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“ THE PREPARATION, PHYSICO-CHEMICAL ANALYSIS OF
YASHADAMRITA MALAHARA AND SINDHOORADI TAILA AND
COMPARATIVE CLINICAL STUDY ON VICHARCHIKA (ECZEMA) ”
By
DR.SOBAGIN.M.V
B.A.M.S DISSERTATION SUBMITTED TO THE
RAJIV GANDHI UNIVERSITY OF HEALTH SCIENCES, KARNATAKA,
BANGALORE
IN PARTIAL FULFILLMENTS FOR THE DEGREE OF “DOCTOR OF MEDICINE”
(AYURVEDA)
In
RASASHASTRA
GUIDE CO-GUIDE DR.M.C.PATIL DR. GIRISH.N.DANAPPAGOUDAR
M.D.(R.S) M.D(R.S) Prof. Head of the Department Lecturer. Department of Rasashastra. of Rasashastra.
DEPARTMENT OF RASASHASTRA, POST GRADUATE STUDIES & RESEARCH
CENTER,
D.G.M. AYURVEDIC MEDICAL COLLEGE. GADAG –582103 FEBRUARY- 2006
J.S.V.V. SAMITE’S
Post Graduate cum Research Center, D.G.M.Ayurvedic Medical College Gadag –582103
Department of Post Graduate Studies in RASASHASTRA
DECLARATION
I here by declare that this dissertation entitled “ THE PREPARATION, PHYSICO-
CHEMICAL ANALYSIS OF YASHADAMRITA MALAHARA AND SINDHOORADI
TAILA AND COMPARATIVE CLINICAL STUDY ON VICHARCHIKA (ECZEMA ” is a bonafide and genuine research work carried out by me under the guidance of
Dr.M.C.Patil. Professor & HOD, Department of Post Graduate Studies in
Rasashastra, Post Graduate cum Research Center, D. G. M Ayurvedic Medical
College, Gadag –582103
Date:
Place: Gadag.
Dr. Sobagin.M.V P.G.Schalor, Dept. of Rasashastra, Post Graduate cum Research Center, D.G.M Ayurvedic Medical College Gadag –582103
Department of Post graduate Studies in RASASHASTRA
Post Graduate cum Research Center, D.G.M.Ayurvedic Medical College Gadag –582103
J.S.V.V. SAMITE’S
I here by declare that this dissertation entitled “ THE PREPARATION, PHYSICO-
CHEMICAL ANALYSIS OF YASHADAMRITA MALAHARA AND SINDHOORADI
TAILA AND COMPARATIVE CLINICAL STUDY ON VICHARCHIKA (ECZEMA ” is a bonafide and genuine research work done by Dr.Sobagin .M.V in partial
fulfillment of the requirement for the degree of Ayurveda Vachaspati (M.D) in
Rasashastra of Rajiv Gandhi University of Health sciences, Bangalore,
Karnataka.
Date:
Place: Gadag.
CERTIFICATE
Guide Dr.M.C.Patil. M.D.(RS) Head of the department Rasashastra, Post Graduate cum Research Center D.G.M. Ayurvedic Medical College Gadag –582103
Department of Post graduate Studies in RASASHASTRA
D.G.M.Ayurvedic Medical College & Post Graduate cum Research Center Gadag –582103 Dist: Gadag
J.S.V.V. SAMITE’S
I here by declare that this dissertation entitled “ THE PREPARATION, PHYSICO-
CHEMICAL ANALYSIS OF YASHADAMRITA MALAHARA AND SINDHOORADI
TAILA AND COMPARATIVE CLINICAL STUDY ON VICHARCHIKA (ECZEMA ” is a bonafide and genuine research work done by Dr.Sobagin.M.V in partial
fulfillment of the requirement for the degree of Ayurveda Vachaspati (M.D) in
Rasashastra of Rajiv Gandhi University of Health sciences, Bangalore,
Karnataka.
Date:
Place: Gadag.
CERTIFICATE
Co-Guide Dr.Girish.N.Danappagoudar M.D.(RS). Lecturer Rasashastra Post Graduate cum Research Center D.G.M. Ayurvedic Medical College Gadag –582103
ENDORSMENT BY THE HOD, PRINCIPAL / HEAD OF THE INSTITUTATION
J.S.V.V. SAMITE’S
I here by declare that this dissertation entitled “ THE PREPARATION, PHYSICO-
CHEMICAL ANALYSIS OF YASHADAMRITA MALAHARA AND SINDHOORADI
TAILA AND COMPARATIVE CLINICAL STUDY ON VICHARCHIKA (ECZEMA)
” is a bonafide and genuine research work done by Dr.Sobagin.M.V under the
guidence of Dr.M.C.Patil Professor, HOD Department of Post Graduate Studies
& Dr.Girish.N.Danappagoudar Lecturer, Department of Rasashastra, Post
Graduate Studies in D.G.M.Ayurvedic Medical College, Gadag.
Seal & Signature of the HOD. Date:
Place: Gadag.
ENDORSEMENT
Seal & Signature of the
Principal:
Date:
Place:
COPYRIGHT
I here by declare that the Rajiv Gandhi University of Health Sciences,
Karnataka shall have the rights to preserve, use and disseminate this dissertation in
print or electronic format for academic / research purpose.
Date:
Place: Gadag
Dr.Sobagin . M.V P.G.Schalor, Dept. of Rasashastra, Post Graduate cum Research Center, D.G.M.Ayurvedic Medical College Gadag –582103
© Rajiv Gandhi University of Health Sciences, Karnataka
ACKNOWLEDGEMENT
My father & mother is the only Inspiration. This work carries some sweat
memories to express & record about some distinguished personalities by whom I had
been inspired during the course of this thesis.
I express my deep sense of gratitude to my respected guide Prof.Dr.M.C.Patil.
MD(Ayu) Head of Dept. of RS, DGMAMC & PGSRC, Gadag. He has been very kind to
guide me in the preparation of thesis & for who extraordinary efforts, tremendous
encouragement & most valuable thought provoking critical suggestions, made me to
complete this work.
I am extremely greatful & obliged to my co-guide Dr.Girish .N
Danappagoudar.MD(Ayu). Lecturer in Rasashastra, PG studies & Research center
DGMAMC, Gadag, for patiently going through the draft of thesis & correcting with
precious remarks which have been very useful.
I am thankful to Dr.G.B.Patil principal, DGMAMC, PGSRC,Gadag,
for providing all necessary facilities for this research work.
I wish to convey thanks to my teacher Prof.Dr.R.K.Gachchinamath
HOD,Rasashastra dept,(UG) DGMAMC, Gadag, for being kind & affectionate through
his valuable suggestions & advises.
It gives me immense pleasure to express my gratitude to Dr. Dilipkumar
B. MD (Ayu). Asst. Prof. PGSRC for kind advise encouragement during the study.
I am greatful for the support and advise given by Dr. S.H.Doddamani
MD (Ayu). Asst. Prof. PGSRC. DGMAMC, Gadag, during my clinical trail and
encouraged me all the time during this work.
I acknowledge the valuable help given to me by Dr.Jagadish Mitti MD
(Ayu).Lecturer, Dr.Shashikant Nidagundi MD(Ayu) Lecturer, Dr.Mulkipatil M.D(Ayu)
for their support during my PG study.
I wish to convey thanks to all UG & PG lectures of DGMAMC, Gadag,
for their timely help & constant co-operation during my PG work.
I sincerely thank my beloved friend Dr. K.S.Santoji, and seniors Dr. P.
Koteshwar Rao, Dr. V.S.Hiremath, Dr. R.B.Paattanashetti, Dr.Jaggal for their deep co-
operation and involvement in the study.
I sincerely thank my beloved classments Dr. Ghanti, Dr.Pradeep,Dr.
Saswihalli.Dr.Hiremath, for their deep co-operation and involvement in the study.
I am also thankful to scholars of PG Dept. of Rasashastra & other P.G
Dept who have directly or indirectly helps my thesis work. & Expected their co-operation
& support during my PG work.
I am glad to express my heartiest thanks to Dr. Chandur,.Dr.Suresh,
Dr.D.N.Patil Medical pharma. J.T.College Gadag, having helped me in carrying out
analytical works, and for giving kind suggestions.
I wish to convey my thanks to beloved librarian, Sri. V.M.Mundinamani,
Asst. S.B.Sureban for providing many valuable references in the study. I am thankful to
Sri. B.S.Tippanagouda, Lab technician, who extended this co-operation in investigations.
I tender my sincere thanks to Nandakumar, statistician for his help in
statistical evaluation & results.
I wish to thank the physicians , House surgeons, Hospital staff, nurses &
non teaching staff for their timely assistance in completion of this work.
Let me express my thanks to all patients, those were on trial for their
consent for enrolling in this clinical study & obedience to advises.
I am highly indebted to my beloved parents, sisters & other family
members for their love & affection rendered through out my career.
I express my thanks to all the persons who have helped me directly &
indirectly with apologies for my ability to identify them individually.
Lastly I prey my deep homage & tribute to my grand parents for the
love & affection rendered through out my career.
Gadag February 2006 Dr: Sobagin.M.V
ABBREVIATION
1. R.T - Rasa Tarangini
2. R.R.S - Rasa ratna Samuchchaya
3. R.P.S - Rasa Prakasha Sudhakara.
4 A.P - Ayurveda Prakash
5. R.M - Rasamritam
6. R.J - Rasa Jala Nidhi
9. R.Chu - Rasendra Chudamani
10. K.N - Kaideva Nighantu
11. M.N - Madanapala Nighantu
12. R.N - Raja Nighantu
13. B.P - Bhava Prakasha Nighantu
14. D.N - Dhanvantari Nighantu
15. Ch.S - Charaka Samhita
16. S.S - Sushruta Samhita
17. A.S - Ashtanga Sangraha
18. A.H - Ashtanga Hridaya
19. B.S – Bela Samhita
20. H.S – Harita Samhita
21. K.S – Kashapa Samhita
22. Y.R - Yogaratnakar
23. B.T – Before treatment
24. A.T – After treatment
25. _ Not mentioned.
26. + Mentioned
LIST OF TABLES
Sl.N0. Topic Page. No.
1. Synonyms of Yashada 27
2. Shodhana media according to various authorities. 30
3. Pharmacological properties 32
4. Indication of Yashada bhasma 33
5. Synonyms of Girirsindhoora 38
6. Guna of Girirsindhoora 39
7. Indications of Sindhuura 40
8. Synonyms of Sasyaka 42
9. Shodhana dravya according to different authorities 43
10. Guna Karma and Rogaghnata 44
11. Showing Aharaja Nidanas According to different authorities 57
12. Showing Viharaja Nidanas According to different authorities 58
13. Showing Daiva Apacharaja According to different authorities 58
14. Showing Usage of Improperly Purified Rasoushadhi leading to Kushta utpatti 58
15. Showing Poorva Roopas common in Kushta According to Various authors 63
16. Showing the Roopas of Vicharchika according to various authors 65
17. Showing Sapeksha Nidana 66
18. Showing Ayurvedic tests of Yashada bhasma 87
19. Observation of patient based on Age 97
20. Observation of patient based on Sex 98
21. Observation of patient based on Education 99
22. Observation of patient based on Marital rates 99
23. Observation of patient based on Religion 100
24. Observation of patient based on Occupation 101
25. Observation of patient based on Economical Status 102
26. Observation of patient based on Vicharchika lakshanas 103
27. Showing grades of “Varna” before treatment in Group A & B 104
28. Showing grades of “Varna” after treatment in Group A & B 104
29. Showing grades of “Pidika” before treatment in Group A & B 104
30. Showing grades of “Pidika” after treatment in Group A & B 104
31. Showing grades of “Srava” before treatment in Group A & B 105
32. Showing grades of “Srava” after treatment in Group A & B 105
33. Showing grades of “Kandu” before treatment in Group A & B 105
34. Showing grades of “Kandu” after treatment in Group A & B 105
35. Showing grades of “Vedana ” before treatment in Group A & B 106
36. Showing grades of “Vedana ” after treatment in Group A & B 106
37. Assessment of Subjective parameters of Group-A 107
38. Assessment of Subjective parameters of Group-B 108
39. Assessment of Objective parameters of Group-A 109
40. Assessment of Objective parameters of Group-B 110
41. Statistical analysis of Subjective parameters (Group-A) 111
42. Statistical analysis of Objective parameters (Group-A) 111
43. Statistical analysis of Subjective parameters (Group-B) 112
44. Statistical analysis of Objective parameters (Group-B) 112
45. Statistical analysis of comparative study of Group –A & B (After Treatment) 113
46. Showing the Result of the study in Group-A 115
47. Showing the Result of the study in Group-B 116
48. Showing overall Result of the study 117
LIST OF GRAPHS Sl.N0. Topic Page. No.
1.Observation of patient based on Age 97
2.Observation of patient based on Sex 98
3.Observation of patient based on Religion 100
4.Observation of patient based on Occupation 101
5.Showing the Result of the study in Group-A 115
6.Showing the Result of the study in Group-B 116
7. Showing overall Result of the study 117
LIST OF PHOTOGRAPHS
1. Raw drugs of the Yashadamrita Malahara and Sindhooradi taila
2. Patients photos with Trail drug.
ABSTRACT
Back ground:
Kushta, skin disease is very common pathological condition. Among this,
Vicharchika can be correlated to eczema, which is one type of the Kshudra Kushta as
explained in classics.
In modern science there are number of drugs for Vicharchika (Eczema), but a
successful remedy is yet to come out. Here Yashadamrita malahara and Sindhooradi taila
are utilized to find out their comparative efficacy in the management of Vicharchika.
Objectives:
a. Preparation of Yashadamrita malahara and Sindhooradi taila.
b. Physico-chemical analysis of Yashadamrita malahara and Sindhooradi taila.
c. Comparative clinical of Yashadamrita malahara and Sindhooradi taila on
Vicharchika (Eczema)
METHODS:
Pharmaceutical study:
a. Yashada shodhana and marana according to Rasatarangini 19 chapter shloka no
b. Preparation of Yashadamrita malahara and Sindhooradi taila according to
Rasatarangini 19 chapter shloka no 146-147 and 21 chapter shloka no 162-163
Analytical study:
Yashadamrita malahara is subjected to physico chemical analysis i.e. , Fineness of
particle test, Flow rate, Ash value, Acid insoluble ash and for Sindhooradi taila Loss
on drying at 1100c, Boiling point, Specific gravity, Refractive index, Acid value,
Saponification value and including organoleptic character .
Clinical study:
30 patients of Vicharchika with confirmed diagnose are taken from the OPD section
of PGRCDGM Ayurvedic medical collage hospital Gadag.
Results:
Individually both groups showed highly significant in subjective as well as
objective parameters. Comparatively group B shows more significant than the group A.
Interpretation & Conclusion:
1. The dravyas which are mentioned in the classical procedure of shodhana definitely
induces the disease curing property
2. Modern physico-chemical analyses are proved that both yogas are slandered.
3. By clinical study and statistical value it is proved that Yashadamrita malahara is
choice remedy in sravi Vicharchika and Sindhooradi taila in rooksha Vicharchika.
Key words:
Vicharchika, Eczema, Yashada, Sasyaka, Girisindhoora, Shodhana, Marana, Malahara kalpana, Taila kalpana, Physico-chemical analysis, Subjective & Objective criteria, Study duration.
CONTENTS Page Number.
I. INTRODUCTION 1-2
II. OBJECTIVES 3
III. REVIEW OF LITERATURE
1. PROCEDURE REVIEW 5-25
2. DRUG REVIEW 26-52
3. DISEASE REVIEW 53-73
IV. METHODOLOGY
1. PHARMACEUTICAL STUDY 74-86
2. ANALYTICAL STUDY 87-92
3. CLINICAL STUDY 93-95
V. OBSERVATION & RESULTS 96-117
VI. DISCUSSION 118-127
VII. CONCLUSION 128-129
VIII. SUMMARY 130-133
BIBLIOGRAPHY
ANNEXURE – 1 MASTER CHART
ANNEXURE – 2 CASE SHEET
Introduction
INTRODUCTION Ayurveda is the most ancient system of medicine. Which is based on its
own fundamental principles theories or concepts. Which are deeply rooted into the oldest
scriptures of Hindu veda i.e. “Atharvanaveda”. It is an encyclopedia of ancient eternal
medical wisdom in spite of its antiquity. (3,000 years old) it is being practicing today all
over the world.
Rasashastra, one of the branch of Ayurveda, which is well, developed by
Nagarjuna the pioneer of Rasashastra. He practiced Ayurveda by using Rasadravya’s i.e
metals, minerals, gems etc, to achieve the aims of Rasashastra. i.e. Lohasiddhi and
Dehasiddhi. Now Rasashastra holds topmost place in Ayurveda due to its unique
preparation’s – Rasabhasma’s, Kharaliya rasayana, Pottali rasayana, Parpati rasayana,
Kupipakwa rasayana and their utility.
Metal and minerals are also used in Bhaishajya Kalpana such as Malahara and
Taila Kalpana, which are used for externally. Eg: Yashadamrita Malahara containing
metal like Yashada and Sindhooradi Taila containing minerals like Sindhoora and
Sasyaka. Both yogas are indicated in Kushta rogas.
Skin has been defined as the mirror of the body. It reflects the Physical, mental
and psychological state of the individual. Skin is not only covering of the body tissues
and organs, but being composed of epithelial, mesenchymal, glandular and
neuromuscular elements is part of the Curparate system. In addition to it being the largest
organ of the body. It is barrier protecting the underlying tissues from physical, chemical
and biological toxic agents. It also excretes some of the wastes of the body metabolism.
In present day the life style of the human being become change. So sometime he
knowingly or unknowingly expose to the certain influences, which causes the skin
disorders.
Kushta, skin disease is very common pathological condition. Among this,
Vicharchika can be correlated to eczema, which is one type of the Kshudra Kushta as
explained in classics.
1
Introduction
It is difficult to determine the true incidence of a disease like eczema. In USA in a
sample population survey of persons aged 1 to 74 years conducted from 1971-74, the
prevalence of eczema was 18.4 /1000 persons. A British study on Hospital attendance
from 1977-1981 showed that 27.5% of patients had atopic dermatitis, 8.2% nummular,
37% gravitational, 11.9% seborrhea and 9.2% exogenous eczemas. In oxford and
Glasgow it is revealed the fact that 26-9% and 33.5% cases respectively were suffering
from eczemas, 63% of them exogenous.
School surveys in India for skin disease in 1986-1990 demonstrated that 2.07%
had lichen simplex chronicus, 0.2% had seborrhea dermatitis and 3% had seborrhea
capotes and 2% dermatitis.
Vicharchika is skin disease which posses a great problem in the skin. This
dermatological problem is difficult to manage along with medicaments of various
prescriptions and methodologies have been tried out but a successful remedy is yet to
come out. Cases when treated by number of medicine have a high rate of relapse and
hypersensitivity in due course. Hence we find no satisfactory remedies for Vicharchika in
cotemporary medical service.
It is causing a peculiar dermatological manifestation, where the skin becomes
discolored causing Shyava varna, surface being exudates and Pidikayukta, these
prominent signs are associated with Kandu.
Eczema is non-contiguous inflammatory disease of the skin responses to
endogenous or exogenous stimuli characterized by erythema, edema, vascularisation,
oozing and crusting.
Ayurveda claims number of therapy for Vicharchika has been explained. But local
applications are more beneficial than the other process. Because they are quick
absorbable, they protect the skin from external irritants and from sunlight, promotes
percutaneous absorption of the incorporated drug, thus allowing an active
pharmacological effect on the skin.
2
Introduction
According to Rasatarangini as indicated the Yashadamrita Malahara and
Sindhoora taila especially in Vicharchika.
The present yogas are acts as a Kaphapittashamaka, Kandughna, Kushtaghna,
Vrunashodhaka and rapaka action. Keeping in the view of the above facts it was felt to
conduct a study to analysis the efficacy of Yashadamrita malahara and Sindhooradi taila
in the management of Vicharchika with a view to find out therapeutically efficacious,
safer and cost effective.
The present work ……
“PREPARATOION, PHYSICO-CHEMICAL STUDY OF YASHADAMRITA
MALAHARA AND SINDHOORADI TAILA AND COMPARATIVE STUDY ON
VICHARCHIKA ”
3
OBJECTIVES
1. Preparation of Yashadamrita Malahara and Sindhooradi taila.
2. Physico-Chemical study of Yashadamrita Malahara and Sindhooradi taila
3. Comparative clinical evaluation of Yashadamrita Malahara and Sindhooradi taila on Vicharchika
Review of Literature. Malahara Kalpana
PROCEDURE REVIEW I. MALAHARA KALPANA
Malahara Kalpana is not explained in Samhita Period. Yogaratnakara adopted
the term ‘Malahara’ from word ‘Malaharam’ – a unani preparation.
As it mentioned in Ayurveda, the treatment is of two types.
1. Antaparimarjan
2. Bahiparimarjan
The later one called Bahiparimarjana means, the medicine intended for external
use only. Different forms of external applications are described for the convenience
of treatment of different diseases like Lepa Kalpana, Upanaha, Malaharakalpana etc.
In between Lepa Kalpana and Malaharakalpana there is no much difference
regarding usage. But preparation of method is different.
Differences.
Lepa Malahara
1. Herbal & mineral drugs are used 1. Metal and Minerals
2. Without Agni samskara 2. With Agni samskara
3. Should be prepared fleshy and used 3. Used up to 2 year
4. It’s reference in Samhita kala 4. After 14th A.D
Similarities:
1. Both are used externally
2. Indications are also same.
5
Review of Literature. Malahara Kalpana
Preparation of malahara: -
Dividing into 3 processes.
1. Poorvakarma
2. Pradhana karma
3. Paschat karma
1. Poorva karma:
a. Collection of equipments
b. Collection of Raw drugs.
c. Shodhana of main drugs.
d. Marana of main drugs.
2. Pradhana karma:
a. Preparation of Sikta taila
b. Mixing of churna / bhasma into sikta taila
3. Paschat karma: -
a. Storage
c. Uses
1. Poorva karma: -
1. Collection of equipments like
a. Chullika
b. Vessel
c. Cloth
d. Spoon
2. Collection of raw drugs like
1. Sikta
2. Tila taila
3. Main drugs
3. Shodhana: Shodhana of main drug, which is taken for Malahara preparation.
In Yashadamrita Malahara – Yashada shodhana in Nirvapa in Taila, Takra,
Gomutra, Kanjike, Kulattha kwatha for 7 times.
4. Marana: If necessary. Eg: Yashada Marana as per classics.
6
Review of Literature. Malahara Kalpana
2. Pradhana Karma:
1. Preparation of Sikta taila.
Sikta Taila is a mixture of bee’s wax and oil. It is soft, smooth ointment like
substance, used as an emollient or as a base in the preparation of different
ointments. Rasatarangini has described 2 methods of preparation of Sikta taila.
Method 11
One part of pure bees wax and 6 parts of Tila taila are mixed and melted over
mild fore. When the wax melts and becomes a homogenous liquid mix well and
stop heating. After cooling it becomes a soft butter like paste.
Method 22
Here, instead of 6 parts of oil, 5 parts of oil is said to be added to 1 part of bees
wax, rest of the procedure is similar to that of first method. If any physical
impurities are seen in the wax (after melting) it should be filtered through a cloth.
The first method is said to be followed during winter season and the second one
during summer season.
2. Mixing of fine powder into Sikta taila:
The base of the Malahara kalpana i.e. Sikta taila, to this, as per the formulation,
add the fine powder of various ingredients and mix well. The fine powder may be
of Tankana, Gandhaka, Kajjali, Mriddara shringa, Gairika, Girisindhoora,
Manashila, Haratala etc.
7
Review of Literature. Malahara Kalpana
3. Paschat Karma:
1. Storage: Prepared malahara must be preserved in wide mouthed plastic or
glass container having tight fitting.
2. Uses: Vruna Shodhaka and Ropaka
Kushtaghna
Varnya etc.
Qualities of Sikta:3
Rasa – Madhura
Guna – Snigdha, Picchila
Karma – Sandhankar, Vrunaropaka
Indications – Bhagna, Visarpa, kandu, Kushta etc.
Self life – 1 year.
Tila taila:4
Nomenclature:-
Latin – Sesamum indicum.
Family – Pedaliaceae
English – Gingelly oil, Sesamum oil.
Sanskrit – Snehapala, Pavitra, Jahla etc.
Kannada – Yellu enni
Tamil – Nallannai
Hindi – Til Ka tail
Properties:
Rasa – Madhura, Tikta, Kashaya
Veerya – Ushna
Vipaka – Madhura
Guna – Sukshma, Vyavayi, Vishada, Guru, Sara, Vikasi,
Teekshna Himasparsha.
8
Review of Literature. Malahara Kalpana
Actions:-
Vataghna, aggravates pitta, does not aggravate kapha, deepana,
pachana, balya, brimhana, balya, preenana, vrushya, lekhana, twachya, netrya,
krimighna. In combination with different drugs, it is said to cure all diseases.
Combination:
Saturated fatty acids.
Palmitic acid – 9.1%
Stearic acid – 4.3%
Aracidic acid – 0.8%
Unsaturated fatty acids.
Oleic acid – 45.4%
Linoleic acid – 40.4%
9
Review of Literature. Malahara Kalpana
OINTMENTS IN MODERN VIEW 5
Ointments are semisolid preparations meant for external application to the
skin or mucous membrane. They usually contain medicament or medicaments
dissolved, subended or emulsified in an ointment base. They may contain a suitable
antimicrobial preservative. The ointments are mainly used as protective or emollient for
the skin.
The absorption of medicaments by the tissues from the ointments, applied to
the skin depends upon different factors as follows.
1. Properties of the drugs incorporated.
2. Properties of the base, used in the formulation.
3. Condition of the patient skin
4. Site of application
5. Duration of application
6. Degree of friction, exerted while applying the ointment.
Classification of Ointments:
I. According to their therapeutic properties based on penetration
1.Epidermic Ointments
These ointments are meant for action on epidermis and produce local
effect. They are not absorbed. These types of ointments are mainly used as
protective, antiseptics, local anti-infectices and parasiticides.
2. Endodermic ointments:
These ointments are meant for action on deeper layers of coetaneous tissues.
They are partially absorbed and act as emollients, stimulants and local irritants.
3. Daidermic ointments:
These ointments are meant for deep penetration and release the
medicaments that pass through the skin and produce systemic effects.
10
Review of Literature. Malahara Kalpana
II. According to their therapeutic uses:
1. Antibiotic ointments
2. Antifungal
3. Anti-inflammatory etc.
Characteristics of an ideal ointment: -
1. It should be chemically and physically stable.
2. It should be smooth and free form grittiness.
3. It should melt or soften at body temperature and be easily applied.
4. The base should be non-irritating and should have no therapeutic action.
5. The medicament must be finely divided and uniform the distributed through the
base.
6. It should not retard healing of the wound.
Ointment bases:-
The ointment base is that substance or part of an ointment, which serves
as carries or vehicle for the medicament while selecting a suitable ointment base.
The factors such as the action desire nature of the medicament to be incorporated
and the stability of an ointment are to be considered.
There are no single ointment bases, which possess all the qualities of an
ideal ointment base. So it becomes necessary to use more than one ointment base in
the preparation of ointments.
Classification of ointment bases: -
1. Oleaginous bases
2. Absorption bases
3. Emulsion bases
4. Water soluble bases
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Review of Literature. Malahara Kalpana
1. Oleaginous bases:-
Their bases consist of water insoluble, hydrocarbons, vegetable oils,
animal fats and waxes. The constituents of hydrocarbon basis are, Soft paraffin
(petrolatum), Hard paraffin, and Liquid paraffin
2. Absorption bases: -
These bases are generally a hydrous substance, which have the property
of absorbing (emulsifying) considerable quantities of water but still retaining their
ointment like consistency.
The Absorption bases are two types:-
1. Non-emulsified bases
2. Water in oil emulsions
The non-emulsified bases absorb water and aqueous solutions producing
w/o emulsions.Eg:- Wool fat, Wool alcohol, Bees wax, Cholesterol
The water in oil emulsions is capable of absorbing more water and has
the property of non-emulsified bases. Eg: Hydrous wool fat (Canolin)
3. Emulsion bases:
These bases are semisolid or have a cream like consistency both o/w and
w/o emulsions are used as ointments base. The oil in water type of emulsions bases
is more popular because there can be easily remove form the skin or cloths by
washing with water. The w/o type of bases are greasy and sticky. The emulsifying
ointment is prepared from emulsifying wax, white soft paraffin and liquid
parathion.
4. Water soluble bases:-
These are commonly known as “Greaseless ointment bases”. The water-
soluble bases consist of water-soluble ingredients. Such as polyethylene glycol
polymers, which are popularly known, as “Carbo-waxes”. The carbo-waxes are
water soluble, non-volatile and inert substances.
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Review of Literature. Malahara Kalpana
Selection of Dermatological Vehicles:-
There are large numbers of ointment bases, which are available in the
market. These have already been discussed. But none of the above discuss ointment
base, fulfills all the requirements of an ideal ointment base, following one the
factors, which govern the selection of an ideal base for ointments –
A. Dermatological factors
B. Pharmaceutical factors
A. Dermatological factors:-
1. Absorption and Penetration:
Absorption means actually entry into blood stream. i.e. Systemic absorption
where as “Penetration” indicates passage through the skin i.e. cuetaneous absorption.
It is proved scientifically that animal fats and fixed oils penetrate more readily
through the skin in comparison to mineral oils (paraffin). The substances, which are
soluble both in oil and water, are most readily absorbed. The o/w emulsion bases
release the medicament more readily than oleaginous bases or w/o emulsion bases.
2. Effect on skin function:
Greasy bases may interfere with the skin function like heat radiation and sweet
excretion. More ever they are irritant to the skin. The water-soluble bases and o/w
emulsion bases provides a cooling effect rather than the heating effect. These bases
mix readily with skin secretions.
3. Miscibility with skin secretions and Serum.
Skin secretions are more rapidly miscible drug in more rapidly and completely
released to the skin. Due to this reason lesser proportions of the medicament is
needed when emulsion bases are used.
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Review of Literature. Malahara Kalpana
4. Compatibility with skin secretion:
Generally neutral ointment bases are preferable because they do not cause
discomfort in use and are compatible with majority of medicaments.
5. Freedom from irritant effect:
The ointment bases used should be non-irritant Greasy bases cause irritation and
may cause Edema. All bases used should be of high standard of purity.
6. Emollient properties:
Under normal conditions, continuous hydration occurs which keeps the skin
sufficiently moist. Dryness and brittleness of the skin cause discomfort to the skin.
Therefore the ointment bases used should possess emollient properties that should be
able to keep the skin moist.
Eg: Glycerin, propylene glycol.
Wool fat, lard and paraffin.
7. Ease of application and removal:
The ointment bases used should be easily applicable and at the same time they
should be easily removable. Stiff and sticky ointment bases are not suitable. Because
they may cause damage to the newly formed tissues of the skin. Due to this the
emulsion bases are preferable as they are softer and spread more readily over the area
to which they are applied. The emulsions particularly o/w type are easily removable
with water.
B. Pharmaceutical factors.
a. Stability:
Fats and oils of animal and vegetable sources are more liable to undergo
oxidation provided. They are preserved properly soft paraffin, liquid paraffin are
comparatively more.
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Review of Literature. Malahara Kalpana
b. Solvent properties: -
Suitable solvents should be selected for the proper dispersement of the
medicaments of an ointment.
c. Emulsifying properties:
Hydrocarbon bases can absorb only a small amount of aqueous
substances where as some animal fats like wool fat can take up about 50% of the
water. Therefore animal fats are used in the preparation of creams.
d. Consistency:
The ointments produced should be of suitable consistency. They should
neither be too hard nor too soft. They should withstand the climatic condition.
Preparation of Ointments:
Ointments are prepared by following methods:
1. Triturating method
2. Fusion
3. Chemical reaction
4. Emulsification
Triturating method:-
It is the most commonly used method for the preparation of ointments.
The method is used when the base is soft and the medicament is insoluble in the
base. The following procedure is used to get a uniform ointment.
a. Finally powder the solid medicaments
b. Weigh the required quality of an ointment base. Triturate the solid
medicaments with a small amount of the base on an ointment slab with
the help of stainless steel ointment spatula until a homogenous product is
formed.
c. Add remaining quantities of the base until the medicament is uniformly
mixed with it.
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Review of Literature. Malahara Kalpana
II. SNEHA KALPANA
Sneha Kalpana is well known since Samhita period. In Charaka Samhita
Kalpasthana 12th chapter, extraction of taila and taila paka including tests and standard
of taila paka are mentioned in detail. Sushruta and Ashtanga hridaya have explained
same as Charaka.
In Sharangadhara Samhita Madhyama Khanda the definition of preparation,
method of preparation, dose and various formulations have been described in detail.
The nomenclature of Sneha Kalpana is sum of words Sneha and Kalpana, where
Sneha means fat or fatty material and Kalpana stands for pharmaceutical process of
medicaments.
The substance, which is called Sneha Dravya, will have Guru, Sheeta, Sara,
Snigdha, Manda, Sukshma, Mrudhu, Drava gunas.
In Ayurveda Ghrita and Taila Kalpana are included is Sneha Kalpana.
Advantages of Sneha Kalpana:
1. To extract the fat Soluble active principles of plants and minerals.
2. To obtain extra benefits of specific Taila or Ghrita used.
3. To preserve the drug or drugs for longer time.
4. To enhance the absorption of drugs, when used topically in fatty medias.
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Review of Literature. Malahara Kalpana
Definition6:-
The medicaments prepared by using 1 part of Kalka dravya, 4 parts of
taila/ghrita and 16 parts of drava dravy as Snehakalpana.
According to Charaka:-
While preparing Sneha Kalpana, quantity of the water, sneha, aoushada dravya
and Kalka is not mentioned, in such conditions one part of the aoushada, 4 parts of
Sneha, 16 parts of water is advised.
According to Sushruta:
When there is no specifications of drava dravyas then water is advised, same
way if there is no specifications of Kalka and Kwatha in such conditions mentioned
dravadravya, Kalka, Kwatha can be prepared.
According to Vagbhata:
In Snehapaka preparation the quantity of water, Sneha, is not mentioned in
such condition 1 part of dravadravya, ¼ part of Sneha, 1/16 part of kalka is advised.
According to Navaparibhasha:-
Murchit Sneha 1 prasta or ½ prasta, 4 parts of water and ¼ part of Sneha Kalka is added. Give mandagni and do stirring continuously with dravi upto Siddi lakshanas are attained.
According to Vaidaka paribhasha pradeep.
¼ reduced Kwatha, ¼ of Kwatha Sneha, ¼ of Sneha Kwatha is advised for
Snehapaka.
According to Bhashajya ratnavali:
Before doing Snehapaka, Sneha murchana should be done. Mentioned
quantity of Kwatha and Swarasaare added, Paka should be done in Mandagni up to
Snehasiddhi lakshanas are seen.
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Review of Literature. Malahara Kalpana
Murchana7:-
Sneha Kalpanas are widely used in Ayurvedic practice both internally and
externally. Such SnehaKalpans should be subjected to a primary process known as
Murchana. It is a refining process of both Sneha (Oil and Ghee), before subjecting the
drug to Snehapaka. Better colour, odour, taste, results and efficacy of drug are expected
from Murchana. It increases solubility of active principles and absorbility to get
maximum property.
There is no reference to Murchana either in Laghutraya or in brihatraya.
Acharya Govinda das the author of Bhaishajya ratnavali is the first personto mention
about this.
The main aim of Snehamurchana is to remove the durgandha, amadosha and
ugrata etc bad characters of crude form of Sneha, by doing Murchana Samskara Sneha
dravya will appreciated with good smell and colour, apart from these becauses of
Murchana Sneha will get such capability to receive more principles while the
preparation
of Snehapaka and also veerya of the Sneha is enhanced, because of Murchana
Samskara, Sneha will get the active principles of Murchana dravyas too.
General Method of Preparation of Snehapaka:
In generally Snehapaka vidhi can be divided into 3 stages.
1. Poorva karma
2. Pradhana karma
3. Paschat karma.
1. Poorva karma:-
a. Collection of equipments:
Sneha patra, Darvi(stirrer), Sieve, Khalvayantra, Tula yantra, Koshti.
b. Collection of drugs:
18
Review of Literature. Malahara Kalpana
Classically mentioned drugs, including mentioned Sneha and jala.
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Review of Literature. Malahara Kalpana
c. Preparation of Kalka:
The drugs from which Kalka is to be prepared if it is fresh or wet should be
washed well and ground into a paste in a khalva yantra. If it is dry, do Yavakuta
choorna of that and prepare paste by mardana with little quantity of water.
2. Pradhana Karma:
a. Systematic mixing of the ingredients:
It is ghritapaka, first Murchita ghrita has to be collected and melted
in a Snehapatra with gentle heat, then the pieces of kalka bolus are added little
by little into the Sneha, stirred continuously with dravi, this is followed because
to avoid over burning of the kalka and over the whole contents is maintained
over Mandagni.
In case of Taila, the kalka and drava dravya are mixed together the
Sneha is then added, boiled and stirred continuously. So that the kalka is not
allowed to adhere the vessel.
b. Heating pattern8:-
Always Taila paka should be prepared mrudu and madhyamagni only.
The preparation like taila, Ghrita and Guda should be completed
within a day to gain more potency by being prepared in more than a day. Time
taken for the completion of Snehapaka varies according to nature of dravyas.
Duration Dravadravya
1. 1 day Vrihi and Mamsa rasa
2. 2 days Dugdha
3. 3 days Swarasa
4. 5 days Takra and Aranal
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Review of Literature. Malahara Kalpana
c. Factors to be known while preparing Sneha Kashaya.
1. If decoction is drava dravya, then padavashta Kashaya should be prepared from
mrudu, madhyama and kathina dravyas by adding 4,8 and 16 parts of water
respectively. Regarding the proportion of Kalka, Sneha and dravadravyas there
is an identical opinion in Brihatrayas9-11.
2. When dravadravyas more than 5, then each drava dravya should be taken in the
same quantity as that of Sneha. If drava dravyas are less than 5 then the total
quantity of all the liquids should be 4 times to that of Sneha dravya12.
3. If dravadravyas are not mentioned in any of the Sneha preparations, then water
to be used to replace the drava. It should be 4 times the quantity of oil used13.
4. If Kalka dravya is not mentioned in any Sneha preparations, then it must be
prepared by using the dravya itself 14.
5. When flower is used as Kalka dravya, in any of the Sneha preparation then its
quantity should be 1/8th of that of oil 15.
d. Sneha Siddhi Lakshana16:-
When Snehapaka Completes, the following confirmation tests can be
observed.
a. Snehakalpa becomes wick like (Varti) when rolled between two fingers.
b. There should not be any sound when Sneha kalka is sprinkled over fire.
c. Foam is observed when taila paka completes. On the contrary it subsides in
ghee.
d. Specific colour, odour and taste of the ingredients become marked when
Snehapaka is over.
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Review of Literature. Malahara Kalpana
e. Types of Snehapaka17:-
Through Snehapakas are five in number; the most important once are
only three.
1. Mrudu
2. Madhyama
3. Khara
Remaining two are Ama and Dagdha paka
Mrudu paka Sneha will have Kalka with little quantity of moisture
Kalka of Madhyama paka Sneha will be soft, but avoid of moisture content.
Kharapaka Sneha will have slightly hard. Dagdhapaka Sneha will have hard and
brittle kalka. It causes burning sensation and is unfit for therapeutic use. Sneha with
Amapaka will not have any potency and heavy for digestion.
Paschat Karma:-
a. Collection:
In order to obtain optimum quantity of Sneha, the Kalka should be squeezed
(after the paka) at hot stage only Gandha paka dravyas should be added gently with
stirring, when the Sneha is in luke warm state.
b. Preservation:-
Ghrita can be preserved in glass or polythene containers and usually tailas are
preserved in glass or plastic bottles. Usually glass jars (wide mouth) are used for
packing purpose of Ghrita. Where as taila preservation narrow mouthed glass or
plastic bottles are used.
c. Expiry date18:
a. According to Sharangadara expiry date of Snehakalpana is mentioned as 4
months.
b. According to pharmacopia in Ayu, part-I
Ghrita and taila preparations, maintains the potency for about 16 months.
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Review of Literature. Malahara Kalpana
Precautions should be taken for the preparation of Snehakalpa19:
1. Sneha should be pure, clear and without sturry.
2. Taila patra should be wide mouthed, because during the process, taila may come
out if it is having narrow mouth. Depending upon the quantity of Sneha, the size
of the Sneha patra should be selected.
3. During Snehapaka maintain the intensity of fire through the operation in order
to get desirable grade of temperature.
4. Gentle boiling of Sneha is to be maintained continuously. Always Snehapaka
should be prepared in mridu and madhyamagni only.
5. If taila is hot suddenly kwatha should not be poured, if it is poured taila may
come out from the vessel. Hence while stirring only kwatha has to be added
slowly.
6. The mixture is stirred constantly and carefully to ensure that the kalka does not
stick to the bottom of the vessel resulting into a carbonization.
7. When all drava dravya have evaporated, the moisture in the kalka also becomes
to evaporate, at this stage; it has to be stirred more often and carefully to ensure
that the kalka does not stick to the bottom of the vessel. The kalka is taken out
from the ladle and tested from time to time to know the condition and stage of
the paka.
8. Sneha required preparing with Gomutra like kshara dravya combination Sneha
may produce excessive phena. Thus Sneha may come out of the Snehapatra
during pakavasta.
9. In particular Snehakalpana whatever the quantity of Sneha is prescribed that
much quantity of Sneha only is supposed to be taken. Increasing or decreasing
order should not alter the quantity.
10. If in particular formulation Sneha quantity is not mentioned then one seru
Sneha has to be taken and on the bases of Sneha quantity, the kalka, drava
dravya quantity also to estimated.
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Review of Literature. Malahara Kalpana
Liquid dosage form20:-
Liquid dosage forms commonly used in pharmacy are either monophasic or
biphasic.
Monophasic liquid dosage form refers to liquid preparation in which there is
only one phase. It is represented by true solution. A true solution is a clear
homogenous mixture. That is prepared by dissolving a solid, liquid or gas in a liquid.
Classification:-
Classification into 2 groups.
1. Liquids meant for internal administration, for eg, mixtures, syrups and elixirs.
2. Liquids meant for external administrations.
Eg: Gargles, mouth wastes, throat pains, douches, nasal drops, eye drops,
eardrops, liniments and lotions.
Monophasic Liquid dosage form
1.1.
Internal External
1.Mixture
2. Syrup Application on skin used in Mouth Instilled into body
3. Elixir 1. Liniment 1. Gargles 1. Douche
4. Linctus 2. Lotion 2. Mouth wash 2. Ear drop
3. Throat paint 3. Nasal drop
4. Nasal spray
24
Review of Literature. Malahara Kalpana
Liquid to be applied to the skin:-
1. Liniments:
The liniments are liquid or semi-liquid preparations meant for
application to the skin. The liniments are usually applied to the skin with friction
and rubbing of the skin. The liniments may be alcoholic or oily solutions or
emulsions. In alcoholic liniment, alcohol helps in the penetration of medicament
into the skin and also increases its counter irritant and rubefacient action.
In oily liniments arachis oil is commonly used which spreads more
easily on the skin. Soap is also included as on the ingredient in some of the
liniments, which help, in easy application of liniment on the skin.
Generally, liniments contain medicaments possessing analgesic,
rubefacient, soothing and counter irritant or stimulating properties.
A liniment should not be applied to the broken skin because it may
cause excessive irritation.
Container: -The liniment should be dispensed in coloured fluted bottles in order to
distinguish it from preparations meant for internal use.
Labeling: - The label must state “for external use only” and shake the bottle well
before use. “The label should carry the warning. Not to be applied to open
wound or broken skin.”
Storage: - Liniment should be stored in tightly closed air tight containers in a cool place.
25
Review of Literature. Malahara Kalpana
2. Lotions:-
Lotions are liquid preparations meant for external application without
friction. They are applied direct to the skin with the help of some absorbent
material, such as cotton wool or gauze soaked in it. Lotions may be used for local
action as cooling, soothing or protective purposes. They are generally applied for
antiseptic action. (Eg- Calamine lotion)
Alcohol is sometimes included in aqueous lotions for its cooling and
soothing effect Eg. -Salicylic acid lotion.
Where as the addition of glycerin in a lotion keeps the skin moist for
sufficient long time and does not allow the preparation to dry.
Bacterial and molds grow in certain lotions is no preservative is added
care must be taken to avoid contamination during preparation of the lotion.
Containers:- Lotion should be dispensed in coloured fluted bottles in order to
distinguish them from preparations meant for internal use.
Labeling:- The containers should be labeled “ For external use only”. Some times on
long standing lotion have a tendency to separate out. Therefore the
container must be labeled “Shake well before use”
Storage: - Lotion should be stored in well filled, well closed in an air tight container
in a cool place.
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Review of Literature. Drug
DRUG REVIEW YASHADA:
Historical background:
Yashada as ancient Indian chemists knew a metal from the 15th A.D as
Madanapala the author of Madanapala Nighantu is the first scholar to mention it, as the
7th dhatu or metal in his text. Bhavamishra and others followed him in a later period.
Through it was used for making an alloy known as Pittala (Brass) for long as a separate
metallic element it was known much later. Before the 15th A.D it was used and known
by the name of Rasaka or Kharpara satwa that is quite evident from the synonyms
(Ritikrit, Ritihetu, Tamra, Ranjaka) attributed to Rasaka and Kharpara. As regards
Rasaka and Kharapara, the minerals of Yashada they were known even in the Samhita
period.
In Rasashastra period following Rasa-texts are explained Yashada,
1. Ayurveda prakasha
2. Rasajalanidhi
3. Rasatarangini
4. Rasamrita
5. Rasadarpana
Vernacular names:
Latin – Zincum
Sanskrit – Yashada
Hindi – Jasta
English – Zinc
Bengal – Dasta
Gujarat – Jasad
Tamil – Tulanagam
Malayalam – Nagam
Chinese - Tutenague
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Review of Literature. Drug
Synonyms of Yashada 21-26
Table No-1
Prapti Sthana:
Usually Yashada is not available in muktavasta (native form) but in the
form of mineral like Zinc blende (ZnS), Oxide (Zno), Carbonate (ZnCO3)
It is found in Canada, Russia, Australia, Peru, U.S.A, Mexico, China, Japan, Spain,
and Sweden. In India Bihar, Rajasthan, Madras, Punjab, Kashmir.
Description:
±dg®dPdaTdz§Sd £dd«T®da›da ¡d¯dQ±df±dI¶a |
¬ddîUµaŸdz£dy «d£dZ ±d§£dQd£d®ddye›deT±daªd®dZ || Ad.§d � 3/2�
According to ancient classics Yashada is one among the sapta dhatus and
belongs to pootiloha group. It melts quickly on heating and produces bad smell
(Loathsome) while being melted.
Sl.No Name M.N A.P R.T R.M R.D B.P.N
1 Yashada - + + - + -
2 Yasada - - + + - -
3 Jashada - - + - - -
4 Jasada + - + - + -
5 Ritihetu - + + + + -
6 Kharparaja - - + - + -
7 Rangasankamsh - + - - - -
8 Yashaka - - - - + -
9 Rangasadrasha + - - - - +
10 Ditihetu + - - - - +
11 Yashaja - - - - - +
12 Kharapara Satva - - - + - -
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Review of Literature. Drug
Bhoutika gunas of Yashada: -
Varna (colour) – Shweta
Sparsha (Touch) – Mrudu, snigdha
Apekshita gurutwa – 7.1
Melting point – 4290C
Boiling point – 9800C
Grahya Yashada Lakshana:-
According to Rasatarangini the Yashada, which is having following
characters, is best one. i.e. Yashada must be bright and shining on cutting, snigdha,
mrudu, nirmala, dhrutadrava (easily melting) and guru in nature.
CONCEPT OF SHODHANA AND MARANA
Invention of metal brought a great change in the life style of early man. As he
went on investing various metals, he understood their uses and utilized them for various
purposes. When observed medicinal values in metals he started using them as medicine.
During Samhita period metals were used only in the form of raja (churna) but
after the 8th century a scientific study of metals was carried out for their therapeutic
values. Till last century even in western medical sciences, metals were used for
therapeutic purposes but after observing some of their toxic effects, the usage of some
metals was ceased.
Rasavaidyas too had the knowledge of toxic effects of metals and minerals but
were using Rasoushadhies, which are free from adverse effects by virtue of unique
procedures (Shodhana and Marana) adopted by them in detoxifying the metals, these
procedures not only make a mineral or metal free from the toxic effects but also make
them to absorbable and therapeutically effective with a minimum dose for a maximum
and quick result. Hence Rasoushadhies are widely used by Ayurvedic physicians without
the fear of adverse effects.
A¬§d «ddÎddî§dSddye›d£®dd£dŠ AèŸdyT§d‚±da›d£ddZ | e´d§d‚«ddTdy›SdQdSd£®dd£dŠ Adz°d¥dªãdye¥dI¶TdyT±dZ || T.±dd.±da
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Review of Literature. Drug
While preparing medicine, Ayurvedic acharyas were of opinion that when a
medicine is administered in a particular disease it should only cure that disease but should
not cause any other diseases or adverse effect.
Keeping the above in consideration various Shodhana and Marana procedure are
explained in Rasashastra classics.
Merits: -
1. These procedures involve physico-chemical action in order to activate the
inorganic substances (may be from nireendriya state to sendriya state).
2. These procedures not only remove the toxic effects of a drug but also the various
herbs used to act on metals, so as to enhance the pharmacological action of a
drug.
Shodhana28: -
DeÔÝzTdz°d¥dzZ ±ddØa e¸¶Sd£dy §dy°d¦ddeQI¶a |
«d¬de®deŸJµ¦£d¤dy Sdd£dg ¯ddy¥d¦da £deQUµdyŸŸSd£dy || T.£d-2/52 µ
Shodhana is a process by which impurities are removed from a substance by
implementing prescribed methods like Mardana etc. This indicates by shodhana,
impurities and toxic qualities are removed from the drug and to induce certain
qualities, which are essential for further procedures.
Classification: - Shodhana has been divided into two.
1. Samanya shodhana
2. Vishesha shodhana.
Yashada has an explosive tendency, while pouring in shodhana dravya it may
cause injury, to avoid this, one special apparatus is designed and this is known as
Pithara yantra.
Pithara yantra: - It contains mainly one metal (loha) bhanda and is covered with iron or
mud lid having 2 cms hole at its center.
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Review of Literature. Drug
1.Samanya shodhana of Yashada29: -
The common procedure for group of dravya or metal is called Samany shodhana.
£dz¬dy £d¸y¶ ›d®dd«dgÎdy UµT¦dd¬dy Ig¶¬d£¤dŠ¡dy | ¸¶«dde¦d°dyŸSd£d§£da Q„d®dy Q„d®dy £dg ±d§£d¥dd || ±®dPdd‰eQ¬ddyUµ§dÎddPdda ¯dgeÔTy°dda §d‚¯d±Sd£dy || T.T.±d 5/13
In this Yashada is melted and poured in medias like Tila taila (Sesame oil), Takra
(Butter milk), Gomootra (Cow’s urine), Aranala/kanjika (Weak organic acid),
Kulaththa (Horse gram decoction), 7 times in each media.
2. Vishesha shodhana30-34: -
Generally samanya shodhana is planted to remove certain impurities but Vishesha
shodhana is a plan to induce certain therapeutic values in particular drug.
In rasagranthas explained vishesha shodhana by nirvapana in different shodhana
media mentioned below, each time fresh drava dravya is to be taken.
Shodhana media according to different authorities.
Sl.No Drug RT AP RJ RD RM Duration
1 Godugdha + - + + + 21 times
2 Kadalimula swarasa - - + - - 7 times
3 Sudhajala + - - - - 7 times
4 Nirgundi swarasa + - - - - 7 times
5 Snuhi dugdha + - - - - 7 times
6 Arka dugdha + - - - 7 times
Table No-2
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Review of Literature. Drug
Marana:
Marana means “Killing” and converting a metal into non-reversible and final
form i.e. bhasma.
Definition:
The process by which metals, minerals or any hard substance is subjected to
soaking, drying and ignition to convert bhasma is known as Marana. This Marana
process converts into fine state of smaller molecules and makes the light as to be
highly absorbable and assimilated after administration.
1. Marana is process by which metal looses its original state still retains its
originality.
2. Marana converts process drug into a biological acceptable form.
Marana of Yashada:
As the melting point of Yashada is low, it melts easily when subjected to puta
after shodhana. So does not reduce to bhasma. This is convenience can be rectified
adopt another procedure known as Jarana. By this molten metal is converted into a
powder form.
Pootiloha marana generally consists of following steps.
1. Jarana
2. Bhavana
3. Formation of Chakrika
4. Arranging the chakrikas in Sharava.
5. Sealing of Sharava
6. Puta (heatings)
But Rasatarangini has explained a different method for the Yashada marana in
4th method 35 .
In this method shodhita Yashada put into loha patra and subjected to Agni.
After melting the Yashada, stirred it carefully with loha shalaka till Yashada
completely converts into powder form. Then filtered through the cloth when cooling
31
Review of Literature. Drug
and again remaining part of Yashada is subjected to Agni, repeat the process till
whole Yashada is converted completely into bhasma form.
In Rasamrita also explained, research work has been done on this metal and on
that basis this metal needs 7000C temperature maintained for 1 hour for its marana
and to make its bhasma completely free from the presence of free metal content.
Further 7 to 10 heating at the above-mentioned temperature range was found
necessary for its complete marana.
Pharmacological Properties36-41
Sl.No Name of classics Kashaya Tikta Katu Sheeta Sheeta veerya KP hara
1 R.T + + + + + +
2 A.P + + - + + +
3 R.J + + - + + +
4 R.M + + - + + +
5 B.N + + - + + +
6 M.N + + + + + +
Table No. 3
By observing the above table Yashada bhasma is having the following properties.
Rasa – Kashayatikta
Guna – Sheeta
Veerya – Sheeta
Doshaghnata – Kaphapittashamaka
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Review of Literature. Drug
Therapeutic Uses:
Yashada bhasma was chiefly used for external application in some disease. In
Rasagranthas and Nighantu Yashada bhasma is used in various disease listed as
below.
Indication of Yashada bhasma40-47.
Sl.No Disease RT AP RJ RM B.N M.N
1 Prameha + + + + + +
2 Pandu + + + + + +
3 Shwasa + + + + + +
4 Vruna and Vrunasrava + - - - - -
5 Rajasrara + - - - - -
6 Netraroga + + + + - -
Table No-4
Indication of yashadamrita Malahara48:
1. Vruna
2. Vicharchika
3. Agnidagda Vruna
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Review of Literature. Drug
MODERN DESCRIPTION OF ZINC 49:
Zinc is a metal, which resembles tin in many respects and is used for making
alloys. Now a day it is used mostly for coating for coating iron vessels to prevent them
from roasting. In addition it is also one of the constituents of dry cell batteries. Zinc
minerals are generally found associated with lead and Copper-minerals.
Occurrence:
Zinc is not found in native forms rather it is obtained almost from minerals. It is
usually found in native in the form of
1. Sulphide – ZnS (Zinc blends)
2. Oxide –ZnO (Zinc cite)
3. Carbonate –ZnCO 3 (Calamine)
4. Zinc Silicate – ZnSiO4
The major producers of Zinc are Canada, Russia, Australia, Peru, USA, Mexico,
China, Japan, China, Spain, and Sweden.
In India found in Rajasthan. A belt of Zinc covers an area of about 30 square
meters in the Zawar and Udaipur region of Rajasthan. It has also been located in certain
parts of Kashmir.
Extraction:
An extensive community followed by floatation is directed at separating Zinc
from lead, copper and as far as possible from Iron. The process involves the following
operations.
1. Concentration.
2. Roasting
3. Smelting and Distillation
4. Refining
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Review of Literature. Drug
Roasting to ZnO is essential for all-purpose. Further, the heating at high
temperature with Coal converts them into Zinc. The chemical reactions in the process are
as under.
2 ZnS+3O2 2 ZnO+2SO2
ZnCO3 ZnO+CO2
ZnO+C Zn+CO
Outline of extraction of Zinc metal.
Distillation
Properties:
1. Zinc is shiny, bluish, white brittle metal.
2. Zinc possesses a crystalline structure.
3. Zinc melts at 419.58 0C
4. It has specific gravity at about 7.15 gm/ cubic centimeter at 200C
5. Zinc may be rolled out into sheets or drawn into wire between 1000C and
1500C, but it reverts to a brittle condition and may be readily powdered under
the hammer.
6. It is unaffected by dry air, but becomes superficially tarnished in moist air.
7. It is highly acted upon by acids and alkalis.
8. It is soluble in dilute acids.
9. At high temperature it burns in air producing a greenish white flame.
Roasting Refining
Ore Zinc blende
Concentrated Ore Zinc Oxide
Crude Zinc Pure Zinc
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Review of Literature. Drug
ZINC OXIDE (Yashada bhasma)
It is prepared by burning Zinc in air or by igniting Zinc carbonate. The white
fumes of Zinc oxide are condensed and collected.
2 Zn+O2 2ZnO
ZnCO3 ZnO+CO2
Properties:
1. It is a white powder it is known as Philosopher’s wool.
It is attached by acids to form corresponding salts ZnO+H2SO4 ZnSO4+H2O
It is attached by acids to form soluble alkali Zincates ZnO+2NaOH Na2
ZnO2+H2O
Therapeutic properties:
Absorption: Zinc salts are absorbed from GI tract and stored in liver, spleen and
kidney.
Elimination: Through stool, small amount by bile and urine.
Uses50:
1. Good antiseptic, Astringent, Mild soothing local sedative.
2. Emetic like copper.
3. Relieves chronic inflammation like gonorrhea, leucorrhoea, otitis and even
eye disorders.
4. It checks the bleeding and secretion from the broken skin by precipitating the
secretion and providing soothing and protective effects. So it is used in most
of the skin disease and varicose ulcer
5. Even zinc enhances the insulin binding capacity so used in Diabetic mellitus.
6. It acts as nervine tonic, sedative, antispasmodic and astringent.
36
Review of Literature. Drug
GIRISINDHOORA51:
Girisindhoora is well known in ancient days, most of Rasagranthas mentioned as
a Sadharana rasa. But Bhavaprakasha, Rasataranginikara included in Upadhatu. Some
authors are called it is a red oxide of mercury. But Rasataranginikara clearly mentioned
that it is lead oxide and addition to it by seeing the synonyms it is originated from Naga.
And also it is prepared from the Mriddarshringa (PbO) by heating 400 to 450C it
becomes red colour called Sindhoora. Now a day what type of Sindhoora available in
market is chemically lead proxide.
Vernacular name:
Sans - Raktanga, Sindhoora, Nagasambhava etc.
Eng - Read lead, Red oxide of lead.
Arab - Isrenj
Bengali
Gujarat Sindhoora
Kannada
Marathi
Tamilu - Sagappusindhooram
Telagu - Yerrasindhooram
Malayalam - Chinturam
Persi - Suraj-Sang
Hindi - Inglur
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Review of Literature. Drug
Synonyms of Girisindhoora51-58:
Sl.No Synonyms RT RRS RM RJ BP KN MN RD
1 Sindhoora + + +
2 Nagaja +
3 Nagagarbhaja + + + + +
4 Nagarenuka +
5 Mangalya +
6 Bhalasoubhagya +
7 Ganeshabhoosham +
8 Shringarabhooshana + +
9 Rakarenu + + + + + +
10 Sisaka +
11 Sisaja +
12 Rasagarbha + +
13 Rasasindhoora + +
14 Nagaja +
15 Nagarakta +
16 Sriman + +
17 Vasantamangal + +
18 Raktaraja + +
19 Vanapishta +
Table No-5
Occurrence:
It is found in the form of mineral. In India found in Kashmir, Punjab, Rajasthan.
This is found in small quantities inside rocks in big mountains. It is dry red. This is
compound of lead and other things.
Grahya lakshana59:
Sukshma kanayukta, Snigdha, Guru, Bright in colour, Mrudu, Clear.
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Review of Literature. Drug
Shodhana and Marana:
Most of Authorities are not mentioned Shodhana and Marana because it is in
oxide form. Few authors are mentioned about Shodhana, subjected to bhavana with
Godugdha60 and Amladravya61.
Guna62-66:
No were mentioned internal administration, but can be used external only.
Rasa – Katu, Tikta
Veerya – Ushna
Guna – Ushna
Doshaghnata – Tridosha shamaka
Guna of Girisindhoora
Sl.No Text Katu
rasa
Tikta
rasa
Ushna
Guna
Ushna
Veerya
Dosha
Shamaka
1 RRS + + + + Tridosha
2 DN + - - + -
3 BP - - + + -
4 RN + + - + -
5 RC - - + - -
Table No-6
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Review of Literature. Drug
Rogaghnata67-74
Indications of Sindhoora.
Sl.No Disease RRS RT RC BP MN MN KN DN
1 Netra + +
2 Kushta + +
3 Kandu + + +
4 Vruna shodana, ropana + + + + +
5 Bhagna sandhana + + +
6 Visha + + + + + + +
7 Kshudra kushta +
8 Pama,Sidma Vicharchika +
9 Visarpa + + + + +
Table No-7
Description75 :
Sindhoora is prepared from lead. For this lead is kept in crucible or iron pan and
heated in an open atmosphere, to get it reached with oxygen and form a red colour
covering on the external surface of lead. This is known as Sindhoora. While collecting
the material initial and last portions should be discarded and remaining portion is then
washed with water and dried. The Sindhoora, which is red, heavy, fine and smooth, is
considered best.
40
Review of Literature. Drug
MODERN DESCRIPTION OF RED LEAD 76: (PB 3O4 )
It is prepared by heating lead monoxide in a reverberate furnace to a temperature
of 450 0C
2 Pb O+O2 2Pb 3O4
Properties:
1. It is a mixed oxide and is regarded to be a mixture of lead monoxide and lead
dioxide -2 PbO.PbO2
2. It is bright, orange, red, granular, crystalline powder.
3. On heating it turns violet & then black but regains its original colour on cooling.
4. It is insoluble in water.
5. On heating to 600 C it decomposes to give lead monoxide.
2 Pb 3O4+O2 6Pb O+O2
6. It is reduced to metallic lead on heating to carbon, carbon monoxide or hydrogen.
Pb 3O4+4C 3Pb+4CO
Pb 3O4+4CO 3Pb+4CO.
Therapeutic properties77:
Absorption:
Lead salts are absorbed in the blood from GIT tract, skin and stored in central
nervous system, kidneys, liver and bone. In the blood 90% is present in RBC’s.
Elimination: Slowly by the urine, sweat and stool.
Uses:
1. Have feeble action on the broken skin.
2. Good astringent, antiphlogistic, local sedative and stimulant, Allays itching
and control excessive discharge.
3. Used as ointment or liniment in eruptive skin disease as eczema, pustular
eruption etc, to promote maturities of boils and abscesses and the healing
processes in all kinds of ulcers and wounds.
4. An ointment made of Sindhoora and Pippali powder with Navaneeta is
applied in chronic eczema.
41
Review of Literature. Drug
SASYAKA:
Sasyaka is well known drug from ancient time. In Charaka and Sushruta in the
name of Tuttha and Amrutasanga used in various places. By the evidence of Charaka
Samhita from 3200 years used as medicine and most of Rasagranthas are explained
Sasyaka as a Maharasa.
Vernacular names: -
Hindi – Nilottha, Tuttiya
Marati – Moracute
Gujarathi – Morathuthu
Telagu – Mailututham
Eng – Copper Sulphate, Blue vitriol
Latin – Cupri Sulphus.
Synonyms of Sasyaka 78-84: Sl.No Table No-8
Paryaya RM RT RD RN BN DN MN
1 Tuttha + + + + + + +
2 Tutthaka - + + + - - -
3 Tuttyanjana - + + - - - -
4 Mayuraka - + + - + - -
5 Mayurtutthka - + - + - - -
6 Shitthagriva + + - + + + +
7 Tamragarbha - + - + - - -
8 Amritasanga + + - - - + +
9 Vitunnaka - - - - + - -
10 Amritodbhava - - - + - - -
11 Neelashmaja - - - + - - -
12 Shilakantha - - - + - + +
13 Haritashma - - - + - - -
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Review of Literature. Drug
Origin85: -
The Garuda consumed Harital visha after drinking the Amrita. Hence he
vomited the poison mixed with the Amrita on Niligiri Mountain. Later it solidified and
turned into Sasyaka.
Praptisthana:-
It is occurs in the form of native & artificial. Germany, Sweden, Spain,
France, England. In India Bihar and Rajasthan.
Grahyalakshanas86:-
That which looks like the colour of Mayurakantha , snigdha and guru..
That which occurs in nature is called Swabhavaja and that which is made
artificially is called Tuttha. Both yield copper as their Satwa.
Shodhana87-91:-
Shodhana dravya according to different authorities
Sl.No Dravya/Method RRS RT RSS RJ RM
1 Raktavargadravya bhavana + + + +
2 Snehadravya sinchana + +
3 Nimbuswarasa bhavana + +
4 Gomutra swedhana + +
Table No-9
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Review of Literature. Drug
Guna Karma of Sasyaka 92-102
Sl.N
o
Gra
ntha
Kat
u ra
sa
Kas
haya
Ksh
ara
Mad
hura
Lagh
u
Stul
a
Ush
ana
veer
ya
Shee
ta
veer
ya
Kap
ha
pitta
Vam
aka
Lekh
ana
Bhe
dana
Ras
ayan
a ch
aksh
usy
1 RT + + + + + + + +
2 RRS + +
3 AP + + + + + + + + + +
4 RM + + + + + + + + + +
5 RD + + + + + + + + + +
6 RJ + + + + + + + + + +
7 R.Cu + +
8 RN + + + + +
9 DN + +
10 BN + + + + + + + +
11 MN +
Table No-10
Rogaghnata 103-113:-
Indications of Sasyaka
Table No-11
Sl.No Disease RT RRS RM RJ RD RC AP RN DM BN MN
1 Krimi + + + +
2 Shula + +
3 Kushta + + + + + + + + +
4 Switra + + + + + + +
5 Amlapitta + +
6 Ashmari +
7 Kandu + + + + + +
8 Arsha + + + + +
9 Vruna + + +
10 Visha + + + + + + + + + +
44
Review of Literature. Drug
MODERN DESCRIPTION OF COPPER SULPHATE 114(CUSO4. 5H2O)
It is a blue coloured crystalline copper mineral, which is available
occasionally in nature form also. Now a day it is prepared artificially by combining
Copper with Sulphuric acid.
Laboratory preparation:
It is prepared by the action of cupric oxide, Carbonate or hydroxide in dilute
Sulphuric acid followed by evaporation & crystallization.
CuO+H2SO4 CuSo4+H2O
CuCO3+ H2SO4 CuSo4+H2O+CO2
Cu (OH) 2+ H2SO4 CuSo4+2.H2O
Manufacture:
On a large scale Copper Sulphate is obtained by boiling copper tailings with
Conc. H2SO4. Blue solution of Copper Sulphate is formed.
Cu+ 2H2SO4 CuSo4+SO4+2H2O.
Treating copper scrapping in hot dilute. Sulphuric acid in presence of air also obtains it.
2Cu+2H2SO4+O2 2CuSo4+2H2O.
In another process, the mineral Copper Pyrites (Cu2S, Fe2 S3) is roasted in
air, Iron oxide and Copper Sulphate is formed. The roasted mass is treated with water,
copper sulphate dissolves and is separated by filtration. On crystals of CuSO4.5H2O. is
formed.
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Review of Literature. Drug
Properties:
1. Specific gravity 2.1 to 2.3
Hardness – 2.5
2. It is bluish green in colour.
3. Synthetic form is only bluish in colour and opaque.
4. It is easily soluble in water.
5. It looses all the water of crystallization when heated up to 250 C & forms white
amorphous powder.
CuSO4. 5H2O CuSO4 +5H2O
It becomes blue when few drops of water added to it.
6. On electrophoresis, Copper gets separated from its solution.
7. Its solution is acidic; hence blue litmus turns red, when dipped in its solution.
Chemical Composition:-
Mineral form of Blue vitriol has chemical composition Cu2 FeSO4. It
contains 50-70% Copper, 15-16% iron and sulphur.
Synthetic form is-
CuSO4. 5H2O– CuO – 31.8% SO3 – 32.1%
H2O – 36.1%
Therapeutic properties:
Absorption: Copper Sulphate absorbed with difficulty in minute quantities either when
given by mouth or from wounds and other mucous surfaces. And stored in
liver, spleen and kidneys.
Elimination: Through stool, urine, bile, saliva and sweat.
Uses115:
1. It is powerful astringent, antiseptic, stimulant, styptic and mild caustic.
2. It is applied indolent ulcers, exuberant granulations, sinuses and fistula in ano,
eczema, impetigo and eye disorders.
3. As emetic.
46
Review of Literature. Drug
ARKA116:
Gana – Bhedaneeya, Swedopaga Family – Asclepiaceac
Kula – Arka Kula Latin – Calotropis
English – Madar
Sanskrit – Red calotropis - Toolaphala, Ksheeraparna, Shwetarka, Mandur, Vasuka,
Alarka, Raktarka, Arkaparna, Arkanama
White calotropis - Shuklarka, Japan, Supushpa, Vrittamallika
Varities:- There are two varieties depending on the colour of the flowers.
1. White 2. Bluish red.
According to Rajanighantu- 1. Arka 2. Rajarka 3. Shuklarka 4. Shweta mandar
Habitat: - All over India in dry & pungent soil, Srilanka, Iron, Africa.
Chemical composition:
Small amount of yeast, madar alban, madar fluabil, resin & rubber. Some
plants have sugarika gum, Trypsin, Catorropin.
Properties:
Guna - Laghu, Rooksha, Teekshna Vipaka – Katu
Rasa – Katu, Tikta Veerya – Ushna
Dosha – Kaphapitta shamaka.
Uses:-
Externaly – Vedana sthapana, Shothahara, Vrunashodhana, Kushtaghna, Jantughna
Internally – Deepaka, Pachaka, Raktashodhaka etc.
Modern:117
1. It is laxative and is beneficial in skin diseases and ulcers.
2. Research works reported the presence of a powerful bacteriocytic and
vermicidal action.
3. Anti-Inflammatory, antihelmentic and Procoagulant activity.
4. It is showing healing potential on dermal wound.
47
Review of Literature. Drug
HARIDRA118: -
Gana – Kushtaghna, Kandughna, Vishaghna
Kula – Haridra Kula
Family – Scitaminae
Latin – Curcuma longa
English – Turmeric
Sanskrit – Haridra, Harita, Jayanti, Kanchani, Nisha, Krumighna
Habitat – All over India, In Maharashtra, Sangli is an important marketing center.
Chemical Composition:- 1% Volatile oil, Curcumin is responsible for its colour.
Turmeric oil has a peculiar odour & taste.
Properties:-
Guna – Ruksha, Laghu Veerya – Ushna
Rasa – Tikta, Katu Vipaka – Katu
Dosha – Kaphavatashamaka
Uses:-
External use – Shothahara, Vedanasthapana, Varnya, Kushtagna, Vrunashodhana
and Ropana, Krimighna.
Internal – Raktaprasadana, Raktashodhaka, Deepana, Jantughna.
Modern:119
1. It is used in disorders of blood, liver and certain skin disorders.
2. It is applied in pains and as an antiparacytic for many skin affections.
3. Showed significant anti-inflammatory activity in both exudative and proliferative
inflammation.
4. Another work reported that the alcohol extract and essential oil from curcuma
longa showed bactericidal activity.
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Review of Literature. Drug
SARSHAPA TAILA 120:-
Kula – Rajika
Family – Crucifereae
Latin – Brassica alba
Sanskrit – Sarshapa, Katuka, Sneha, Tantubha, Kadambak, Siddhartha.
Verities:-
1. Shweta - Superior
2. Rakta
Habitat:- All over India.
Chemical Composition:-
Glycocides of arachidic (0.5%), behenic(2-3%), eicosenoic (7-8%), erusic(40-
60%), legnoceric(1-2%), linoleic(14-18%), oleic (20-22%), myristic(0.5-10%)acids.
Properties:
Guna - Snigdha, Laghu
Rasa - Katu, Tikta
Veerya - Ushna
Vipaka - Katu
Dosha - Vatakaphashamaka
Uses:-
Raktashodhaka, Kandughna, Kothaghna, Krimighna, Kushtaghna.
Modern:121 Research works shows
1. Highly successful in promoting the absorption of scar tissue.
2. Powerful disinfect or antiseptic.
3. Improved epidermal barrier function.
4. Vasodilatation by stimulation of afferent A beta fibers.
5. Antihistamine and anti pruratic.
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Review of Literature. Drug
Description of drugs used for Shodhana:-
1. Tila taila 122
Rasa – Madhura, Tikta, Kashaya
Guna – Ushna, Teekshna, Sukshma, Vishada, Vyavayi
Vipaka – Madhura
Veerya – Ushna
Doshakarma – Kaphavata Shamaka
Karma – Vrishya, Amapachaka
2. Takra 123
Rasa – Madhura, Amla, Kashaya
Guna – Laghu, Ushna
Dosha – Kaphavata shamaka
Karma – Deepana, Shotha, Udara, Grahini, Arsha, Mootraroga,
Aruchi, Gulma, Pleeha, Panduroga nashaka
3. Gomutra124 :-
Guna – Laghu, Teekshna, Ushna, Kshariya
Karma – Deepana, Medhya.
According to Indian matria medica, Gomutra contains ammonia in
concentrated form it is used in both internal and external medication. It also has a
laxative & purgative nature. So it is used in various medicinal preparations like
Punarnava mandoor, Marichadi taila. It is good bioavailability enhancing drug.
4. Kanji 125 :-
Kanji prepared with the manda of half boiled kulmash dhanya is khanji.
Guna - Teekshna, Laghu
Rasa - Amla
Dosha - Kaphavatashamaka
Karma - Rechana, Pachana
When applied externally it cures Daha and Jwara.
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Review of Literature. Drug
5. Kulattha 126 :-
Guna – Ushna
Rasa – Kashaya
Vipaka – Katu
Dosha – Kaphavata shamaka
Karma – Gulma, Grahim, penasa, Kasahara
6. Nirgundi 127 :-
Latin name - Vites nigundo
Family - Verbinaceae
Sanskrit - Sephalika
English - Five leaved chaste French tree
Kan - Bili yakki
Useful part – Root, fruit, flower & leaves
Properties:-
Rasa - Tikta, Kashaya and Katu
Guna - Rooksha
Dosha - Kaphavata shamaka
Veerya - Ushna
Vipaka - Katu
Chemical composition: - Leaves contain a colourless essential oil of the odour of
drug and a resin, fruit contain an acid, traces of alkaloid & a colouring matter.
Action:- Leaves are externally used as a ant parasitic and powerful discutient,
Internally expectorant, nerving.
51
Review of Literature. Drug
7. Nimbuka128
Kula - Jambur
Family - Rutaceae
English - Lime
Latin name - Citrus acid
Sanskrit - Nimbuka, Amlajambeera, Vahni, Deepana,
Shodhana, Vahnibeja, Amlasara, Rochana,
Jantunmari, Rajnimbuka
Habitat - All over India, specially in Himalaya pradesh, Bengal, Assam, Maharashtra.
Chemical composition:-
7-10% Citric acid, phosphoric acid, malic acid, citrate, sugar, mucin and
alkaloids.
Properties:-
Guna – Laghu
Rasa – Amla
Veerya – Anushna
Vipaka – Madhura
Dosha – Kaphavatashamaka
Karma – Deepaka, Virechaka, Raktastambhaka, Kasa
Chardihara.
52
Review of Literature. Disease
VICHARCHIKA
Vicharchika is one of the most commonly encountered skin diseases, which
comes under Kshudra Kushta. The affected individual undergoes severe discomfort and
disfigurement.
Historical Review
The historical aspects of the disease Vicharchika in terms of Kushta can be traced
from Vedic period itself.
Vedic Period (2500BC-100BC)
The earliest knowledge of Ayurveda is derived from the Vedas, especially from
Athrvaveda. In Athrvaveda the disease Kushta is explained and mentioned that Pama is a
variety of Kushta. In Amarakosha129 Pama, Kacchu, Vicharchika are quoted as
synonyms. In Vishnupurana, Vayupurana, Markandeya Purana the description of Kushta
and its Chikitsa are available.
In Panineeyakala, while naming the Rogas the particular style was adopted, by
adding NUL Pratyaya and making the names to be similar as Prachardika, Pravahika and
Vicharchika. In Brihat Samhita. Vicharchika is explained as variety of Kushta.
Samhita Kala (1000BC-100AD)
Maximum contribution towards Ayurveda was given during this period. The
explanation and treatment of Vicharchika is available in Nidana Sthana 5th chapter and in
Chikitsa Sthana 7th chapter of Charaka Samhita.
Sushrutha Samhita deals with Vicharchika, its Symptomatology and its Chikitsa
in Nindana Sthana 5th chapter and Chikitsa Sthana 9th chapter.
Astanga Hrudaya also deals Vicharchika as a variety of Kshudra Kushta and few
Yogas have been indicated for the treatment of Vicharchika in Nidana Sthana 14th and
Chikitsa Sthana 19th chapter.
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Review of Literature. Disease
Bhela Samhita, Hareetha Samhita, Kashyapa Samhita all has dealt Vicharchika as
a variety of Kshudra Kushta and separate Yogas have been explained under its context.
Nighantu Kala (800AD – 1700AD)
In Madhava Nidana, description on Vicharchika, its Symptomatology is available.
Sharagadhara deals only the varieties of Kushta under which Vicharachika are also
mentioned.
Bhavaprakasha, Yogaratnakara, Vangasena, Gadanigraha, Basavarajeeyam,
Kalyanakaraka, Vrindavaidyaka, and Chakradatta in all these books the description of
Vicharchika and its treatment is available.
Adhunika Kala (1700 AD onwards)
Books like Bhaishajya Ratnavali, Vaidya Vinoda, Ayurveda Prakasha,
Siddhaprayoga Latika, Sidda Bheshaja Manimala, Rasayoga Sagara, Brihat Yoga
Tarangini etc., were written in this period. These books include chiefly the Chikitsa
aspect where the particular Chikitsa for Vicharchika is also available.
Nirukti
According to Monier Williams Sanskrit – English dictionary, the word
Vicharchika comprises of root word "Charcha" with "Vi" Upasarga, which means that
cutaneous eruption with, itch and scab.
Paribhasha
The term Vicharchika is defined as one of the variety of Ekadasha Kushta, in
which the main clinical manifestations are Kandu, Pidaka, Shyava Varna and Srava.
' ±d I¶¦Ngµ §dfdNµI¶, ¯Sdd®d, ©dUgµàd®d, e®dŸddeŸd‰I¶d¶’ 130.
Acharya Charaka, Vagbhata, Bhavamishra, Yogaratnakara, Kashyapa, and
Madhavakara give same opinion.
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Where as Acharya Sushruta defines Vicharchika as
"T¡Sddyíe£d I¶¦Ngµ®díe£d è¡ddZ ±d é´d: ªd®de¦£d ›dÎdyd°dgg e®dŸddeŸd‰I¶dSd«dŠ "131
i.e. a skin disorder associated with Atikandu, Atiruja and Rookshata of the Twacha.
Bhedas
The Bhedas of Vicharchika can be made on the basis of guna and doshic
predominance.
On the basis of Guna - Rooksha Vicharchika
Sravi Vicharchika
On the basis of Doshic predominance - Pitta Pradhana
Kapha Pradhana
Nidana
Specific Nidanas for each variety of Kushta are not described in Ayurvedic
classic. As Vicharchika is one among the different types of Kushta, the Samanya Nidanas
described in the context of Kushta holds good for Vicharchika also.
The various causative factors responsible for Kushta can be categorized as follows
• Aharaja.
• Viharaja.
• Daiva Apacharaja.
• Oushadhi Kritha.
• Panchakarma Apacharaja.
Aharaja, Viharaja and Daiva Apacharaja Nidanas according to different authors
shown in table No 11,12 and 13 respectively.
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Review of Literature. Disease
Oushadhikritha
Some of the Rasadravyas when used in impure state though being Kushtaghna
Dravyas, may result in Kushta. In table No.14 different Oushadhikrita Nidanas are
shown.
Panchakarma Apacharaja
The Panchakarma procedures are adopted to eliminate the Aggravated Doshas,
but by improper application of Panchakarma measures, there will be residual Doshas in
the body, which again aggravates and accumulated in the Shakadi Marga. Such
accumulation results in Shithilata of Dhatus leading to manifestation of Kushta.
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Review of Literature. Disease
Showing Aharaja Nidanas According to Different Authors.
SL No. Type of Ahara Ch.S Su.S B.S. A.H. H.S.
1. Viruddahara + + + + + 2. Ajeerna, Adhyashana + + + - - 3. Matsya + + + - - 4. Dugdati Sevana + + - - + 5. Amlati Sevana + - - - + 6. Guru Ahara + - - - + 7. Gramya Udaka with Anupamamsa
Sevana - + + - -
8. Sneha + - + - - 9. Dadhi Sevana + - + - - 10. Lakucha & Kakamachi + - + - - 11. Matsya and Payasa + - + - - 12. Ahitashana - + - - - 13. Drava Snigdha Ahara + - - - - 14. Navanna, Kulattha, Yavaka + - - - - 15. Lavana, Atasi + - - - - 16. Moolaka, Satata Madhu Sevana + - - - - 17. Tila, Pista, Guda + - - - - 18. Chilichima with Milk + - - - - 19. Madya Amla Dravya with Milk - - + - - 20. Guda with Milk - - + - - 21. Matsya Nimba with Milk - - + - - 22. Mamsa with Madhu - - + - - 23. Papodaka - - - - + 24. Vidagdha Ahara Sevana - - + - - 25. Guda with Mulaka - - + - - 26. Havi Prashana + - - - -
Table No-11
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Review of Literature. Disease
Showing Viharaja Nidanas According to Different Authors.
Sl.No
. Type of Ahara Ch.Su Su.Su B.S. A.H. H.S.
1. Chardi Nigraha, + + - + - 2. Vegavarodha + + - + - 3. Sheetambu Snana after Atapa Sevana + - + - 4. Diva Swapna + - - + + 5. Mithya Vihara - + + - - 6. Vyavaya, Atisantapa + - - - - 7. Shrama. Bhaya. Sheetambu Sevana + - - - - 8. Ratri Jagarana - - - - + 9. Ajeernepi Vyayamam + - - - - 10. Vyavaya after Vidahi Ahara Sevana - - - + - 11. Gramya Dharma Sevana - + - - -
Table No-12
Showing Daiva Apacharaja Nidanas According to Different Authors.
Sl.No. Types of Daiva Apacharaja Nidanas Ch.S Su.S AH B.S H.S. 1. Papakarma + + + - - 2. Vipran Gurun Garshayatan + + + - - 3. Poorvakruta Karma + + + - - 4. Gohatya - - - - + 5. Use of money acquired by theft. - + + - - 6. Sadhu Ninda and Vadha + + + - -
Table No-13
Showing Usage of Improperly Purified Rasaushadhi Leading to Kushta Utpatti.
Sl. No. Rasa Oushdhi Nidanas Kushta Utpatti Reference 1. Parada Kushta Utpatti AP.19, RT5/8
2. Abhraka Kushta Utpatti AP. 2/103
3. Roupya Makshika Mandala Utpatti AP 4/11
4. Gandhaka Kushta Utpadaka AP. 2/18
5. Haratala Sphota Utpadaka R.R S 3/69
6. Vanga Kilasa Kushta R.T. 28/7
7. Vaikranta Kilasa Kushta A.P 5/160
8. Loha Kushta Utpadaka A.P 3/224
Table No-14
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Twacha Shareera Vivechana
Twacha is considered one among the sapta dravya responsible for the
manifestation of Kushta. So the knowledge of twacha and kriya is important. According
to charaka and Vagbhata Twacha is divided into six layers, whereas Sushrutha describes
7 layers.
Twak is considered as Upadhatu of Mamsa Dhatu and one among the Pancha
Jnanendriya, Vayu and Akasha are the Indriya Dravyas present in Twacha, Sparsha is
Indriyartha, and Sparshagnana is Indriya buddhi. It is the seat of Bhrajaka Pitta. During
the process of Parinama of Shukra and Shonita and after the formation of Garbha Twak
and all other Dhatus begin to form just as the cream of milk being formed during boiling
of milk.
Vagbhatacharya mentioned that all types Kushta occurs in fourth layer.
As the adhisthana of Vicharchika is not mentioned by any Acharyas and
considering Vagbhata’s opinion that fourth layer of Twacha is the Adhishtana of various
types of Kushta. The Adhishtana of Vicharchika can be inferred as the fourth layer.
Rakta Vivechana
Rakta is one among the Kushtakaraka sapta drayas. While describing Rakta
Pradoshaja Vyadhis, Charaka mentions Kushta one among them. He also mentions some
specific varieties of Kushta like Dadru, Charmadala, Switra etc., but has not included
Vicharchika. Vicharchika being a variety of Kushta can be considered as Rakta
Pradoshaja Vyadhi.
Mamsa Vivechana
Mamsa, one among the Sapta Dravyas causing Kushta. Twacha is the Sarabhaga
of Mamsa Dhatu. The maintenance of healthy skin depends on the state of Mamsa Dhatu.
Meda Pusti and Mala Pusti are the functions of Mamsa Dhatu. When Mamsa Dhatu is
involved in the pathogenesis of skin disorders it may manifest as Vicharchika.
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Review of Literature. Disease
Laseeka
It is a kind of Udakamsha and is included among the Dravyas resulting in Kushta.
It is a Mala of Rasadhatu and stays in Twak.
Samprapti
All the classical textbooks of Ayurveda have explained common Samprapti of
Kushta. Even though Kushta is classified into Maha Kushta and Kshudra Kushta. There
is no separate Samprapti emphasized by any author. So that the Kushta Samanya
Samprapti should be considered for Vicharchika also.
Kushta Samprapti According to Different Acharyas
According to Charakacharya
The vitiated Sapta Dravyas are considered as Sannikrusta Hetus for Kushta. The
vitiated Doshas vitiate Twacha, Rakta, Mamsa and Ambu and combination of these Sapta
Dravyas will be localized in between Twak and Mamsa and produce different varieties of
lesion at different sites over the skin. They are named differently based on the site and
nature of skin.
‘®d|£ddQSd±ÎdSddy QgÝ£®d›d‚™£d «dda±dda©dg Ÿd Qdy°dSde¦£d ±dd Ig¶Ýd¦ddaa ±d§£dI¶dy Q„®Sd ±da›dUµ‚’ 132.
According to Sushruta
The deranged Vata along with Pitta and Kapha enters into the Siras, which are
transversely spread over the surface of the body. Thus the vitiated Vata deposits Pitta and
Kapha on the skin through the medium of their channels and spread them over the surface
of the body. The areas of the skin in which the morbid Doshas are deposited become
marked with Mandalas or skin patches. If these vitiated Doshas are not brought into
normalcy, they enter into deeper and deeper Dhatus.133
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According to Vagbhatacharya
Due to Nidana Sevana the Doshas gets vitiated and spread to Tiryakgata Siras and
vitiates Twacha, Laseeka and Asruk. This produces Shithilikarana and Vaivarnya. The
disease Kushta manifests wherever the morbid Doshas get lodged.134
Madhavakara , Bhavapraksha and Yogaratnakara explains Samprapti similar to
that of Charaka .
After going through the Samanya Samprapti of Kushta Vicharchika Samprapti
can explained as follows.
"By Nidana Sevana Agnimandya takes place leading to vitiation of three Doshas
with the predominance of Pitta and Kapha. Mainly Pitta and Kaphakara Nidanas result in
the vitiation of Kleda initiating the process of Pathogenesis. These vitiated Doshas with
Dhatus, i.e., Rakta, Mamsa and Ambu enter the Tiryakgata Siras and lodges in the
Twacha".
Kleda plays an important role in the pathogenesis because both Pitta and Kapha
being Drava Dhatus are considered as Kleda karaka Sannikrishta Nidanas. Kapha Dosha
due to Sneha, Sheeta and Pichchila Guna and Pitta by Sneha, Drava and Ushna Guna
leads to accumulation of Kleda. Along with Kleda vitiated doshas takes Ashraya in
Twacha leading to the clinical manifestation of Vicharchika.
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Review of Literature. Disease
Schematic Presentation of Samprapti
Nidana Sevana
Dosha Prakopa
Doshas moves in Tiryakgata Siras
Srotodusti (Sanga and Atipravrutti)
Doshas lodges in Twacha
Vitiation of Twacha, Rakta ,Mamsa and Ambu
Vicharchika
( Kandu, Pidaka, Shyavata, Sravata, / Rookshta)
Samprapti Ghatakas Of Vicharchika
Dosha : Pitta pradhana Tridosha/ Kapha pradhana Tridosha
Dooshya : Twak, Rakta, Mamsa and Ambu
Agni : Jataragni, Dhatwagni
Ama : Jataragni mandyajanya, Dhatwagni mandyajanya.
Srotas : Rasavaha, Raktavaha, Swedovaha
Srotodusti : Sanga and Atipravrutti
Udbhava sthana : Amashaya and Pakwashaya
Sanchara Sthana : Tiryakgata sira
Adishtana : 4th layers of Twacha
Vyakta sthana : Twacha
Rogamarga : Bahya
Swabhava : Chirakari
Purva Roopa
The common purvaroopas are mentioned in the context of Kushta. Which are
applicable to all eighteen varieties of Kushta. The same also applies to Vicharchika.
Different Purva Roopas common in Kushta according to different authors is
shown in table No.15.
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Showing Purva Roopas Common in Kushta According to Various Authors.
Sl. No. Purvaroopas Ch.S Su.S AH KaS
1. Asweda + + + -
2. Atisweda + + + +
3. Parushya + + - -
4. Atislakshnata + - + +
5. Vaivarnya + - + +
6. Kandu + + + -
7. Nistoda + - + -
8. Suptata + + + -
9. Paridaha + + + -
10. Ushmayana + - - -
11. Gourava + - - -
12. Shwayathu + + - -
13. Visarpagamana + + - -
14. Shrama + - + -
15. Kota + - + -
16. Rookshatwa - - + -
17. Pipasa - - - +
18. Raga - - - +
19. Dourbalya - + - +
20. Pariharsha + - - -
21. Pidaka - - - +
22. Ativedana - - - +
Table No. 15
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Roopa
In our classics the specific lakshanas of Vicharchika are mentioned.
Acharya Charaka, Bhavaprakasha and Yogaratnakara describes Vicharchika as
' ±d I¶¦Ngµ §dfdNµI¶, ¯Sdd®d, ©dUgµàd®d, e®dŸddeŸd‰I¶d¶’ 135.
According to Charaka it is a kapha pradhana vyadhi ( Kapha praya Vicharchika).
According to Sushruta, Vicharchika is pitta pradhana vyadhi
"T¡Sddyíe£d I¶¦Ngµ®díe£d è¡ddZ ±d é´d: ªd®de¦£d ›dÎdyd°dgg e®dŸddeŸd‰I¶dSd«dŠ " 136
According to Vagbhata
"±d I¶¦Ngµ §dfdNµI¶, ¯Sdd®d, ¬de±dI¶dQSd e®dŸddeŸd‰I¶d¶ "137
Acharya Vagbhata instead of Srava, he used the word Laseeka.
So each lakshanas can be analyzed as follows:
Kandu
Kandu is one among the Kapha Vruddhi Lakshana, here Karmataha Vruddhi of
Kapha. Acharya Kashyapa mentions that Kandu is due to Ambu. Kandu is also Vruddhi
Lakshana of Sweda.
Shyavata
Shayava Varna could be due to the vitiation of Rakta by Dosha. Acharya
Vagbhata has mentioned that Rakta becomes blackish colour in Purvaroopavastha as Pitta
Pradhana Tridosha vitiates it. Pitta Dushti leads to Krishna Varna.
Pidakas
Pidakas are the characteristic feature of Vicharchika, when the vitiated Pitta,
localise in twacha and Rakta, the Pidakas manifest.
Srava
It occurs because of Dravyataha Vruddhi of Pitta.
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Raji
The fissure formed at the affected part of Twacha is called Raji. It is due to
Gunataha Vruddhi of Vata.
Atiruja
Acharya Sushruta tells Ruja attributed to Vedana. This symptom is due to Vikruta
Vata Dosha. When the lesion of Vicharchika are extensive , Vedana may be felt.
Rookshata
As Acharya Sushruta has mentioned that the Vicharchika is a Rooksha variety,
the aggravated Vata Dosha may play a predominant role.
Showing the Roopas of Vicharchika According to Various Authors.
Sl. No. Lakshanas Cha.S Su.S AH B.S K.S B.P Y.R
1. Kandu + + + - - + +
2. Pidaka + - + + - + +
3. Shyava varna + + + + + + +
4. Srava + - + + + + +
5. Atiruja - + - - - - -
6. Rookshata - + - - - - -
7. Raji - + - - - - -
8. Praklinnata - - - + - - -
9. Paka - - - - + - -
10. Rakta Varna - - - + + - -
Table No. 16 Upashaya Anupashaya
After investigating a disease with the help of Nidana, Samprapti, Purvaroopa and
Roopa, one may be still doubt in diagnosing the disease and also to adopt the proper line
of treatment. In such case Upashaya and Anupashaya will help us to some extent.
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Review of Literature. Disease
The Oushadhas, Ahar, Viharas which is comfortable or gives relief either by
acting directly the cause of the disease or the disease itself or to both, are called
Anupashaya138.
The opposite of Upashaya i.e., if the patient feels discomfort by the use of
Oushadha, Ahara and Vihara is called Anupashaya.
In our classics, the Pratyatma Lakshanas can make the Upashaya Anupashaya of
Vicharchika and which relieves such Symptom are considered as Upashaya.
However, the causative factors themselves may be taken as Anupashaya, as these
may also act as the aggravating factors of the presenting symptoms.
Sapeksha Nidana
Certain diseases though they are different from Vicharchika but exhibits some
similar signs and symptoms. So it is necessary to rule out such possible disease to obtain
right diagnosis.
Showing the Sapeksha Nidana
Sl. No. Name Dosha Vedana Varna Pidaka Sthanas
1. Dadru Pitta , Kapha Kandu Tamra Ustanna,
Mandalavata -
2. Pama Pitta, Kapha
Kandu, Ruja, Daha
Shweta, Aruna
Sravayukta Bahu
Sphik, Pani,
Koorpara
3. Shataru Pitta, Kapha
Daha, Arati
Neela, Lohita, Peeta, Asita
Sthoolamoola Bahu Srava Bahupidaka
Parva
4. Kachchu Pitta Teevra Daha - - Sphik,
Pani, Pada
Table No.17
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Sadhyasadhyata
Various authors mentioned, on the basis of involvement of Doshas, Dooshya and
signs and symptoms have explained Sadhyasadhyata of Kushta. According to Charaka
Ekadoshaja and Vata Kaphaja Kushta are Sadhya, Kapha Pittaja and Vata Pittaja Kashta
are Kashta Sadhya. Kushta having all signs and symptoms with Bala Kshaya, Trishna,
Daha, Agnimandya and Krimi is Asadhya.139
According to Sushruta, the patient who has got full control over his sense organs
and the disease pathogenesis is affecting only twak. Rakta and Mamsa are Sadhya. If the
disease pathogenesis reaches to the Medodhatu it is Yapya. If it proceeds to further
Dhatus it becomes Asadhya.
Madhavakara has accepted the Sushrutas explanation but he has considered those
varieties of Kushta in which Meda, Asthi and Majja Dhatu are involved as Yapya.
Acharya Vagbhata gives the same opinion like that of Charaka and Sushruta.
Along with this he adds, Raktaja and Mamasagata Kushta is Kashta Sadhya and
Twakstha Kushta is Sadhya.
By looking at the above explanations Vicharchika that is Pitta and Kapha
Pradhana Vyadhi with the involvement of Twak, Rakta Mamsa can be considered as
Kashta Sadhya Vyadhi.
Chikitsa
The general line of treatment explained for Kushta is applicable to Vicharchika
also. As per Charka, according to the Doshic predominance Shodhana has to be adopted.
In Vata Pradhana Kushta Sarpi Pana should be done, in Kapha Pradhana Kushta Vamana
should be done and in Pitta Pradhana Kushta Virechana and Raktamokshana should be
done140.
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A specific periodicity for conducting Shodhana karma is mentioned by Sushruta
which is supported by most of the scholars of Ayurveda. Vamana karma has to be carried
out once in a fort night, Virechana once in a month, Nasyakarma has to be carried out on
every third day and Raktamokshana is advocated biannually141.
Sushruta further explains Chikitsa of Kushta based on the involvement of Dhatus.
If Kushta lodges in
Twak : Samshodhana.
Rakta : Samshodhana, Lepana, Kashayapana and Shonita
Avasechana.
Mamsa : along with Raktagata line of treatment Arishta,
Mantha should be administered.
When it involves Medo Dhatu the disease is considered as Yapya. But depending
on the patient’s condition Samshodhana and Raktavasechana should be done and the
Dravyas like Bhallataka, Shilajatu, etc., must be administered142
Acharya Vagbhata opines that, the Kushta must be treated with Snehapana
primarily. In Vata Pradhana Kushta the Taila or Ghrita prepared by Dashamoola,
Erandadi Dravyas must be administered. In Pitta Pradhana Kushta Ghrita prepared out of
Patola, Nimbadi Dravyas must be administered and in Kapha Pradhana Kushta Saptahva,
Chitraka Siddha Ghrita must be administered143.
So after attaining Koshta Shuddi by repeated Vamana and Virechana and
undergoing Raktamokshana, the usage of Lepa and other Shamanoushadhi will definitely
relieve Vicharchika.
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The most commonly used palliative medicines and external applications are as
follows 144 :
Madhusnuhi Rasayana Siva Gutika Patola Muladi Kwatha Churna Brhat Manjishtadi Kwatha Churna Nimbadi Churna Nalapamaradi taila Kushtarakshasa taila Tamra Bhasma Swarna Makshika Bhasma Haratala Bhasma Arogya Vardhini Gutika Gandhaka Rasayana Manjishtadi Taila Chitrakadi Taila etc.
Pathyapathya
Our Acharyas have not dealt with precise Pathya Apathya of Vicharchika
Separately. So the Pathya Apathya explained under Kushta can be considered here.
Pathya.
Ahara
Shookadhanya Varga : Purana Shali, Shastika Shali, Godhuma, Shyamaka
Shamidhanya Varga : Mudga, Masoora, Adaka and Bakuchi.
Mamsa Varga : Jangala Pashu Pakshi
Shaka Varga : Patola, Nimba, Chitraka, Hingu, Punarnava, Kakamachi
and Brihati, Lashuna, Khadira and Chakramarda.
Phala Varga : Triphala, Sarshapa and Agaru
Mootra varga : Gomutra, Ustra and Ashwa.
Apathya
Rasa : Amla, Lavana
Shamidhanya Varga : Masha, Tila and Kulattha
Shookadhanya Varga : Navanna
Mamsa Varga : Mamsa, Matsya and Anoopamamsa
Ahara Yoni Varga : Tila taila
Ikshu Varga : Guda, Ikshurasotpanna Varga
Gorasa Varga : Dugdha, Dadhi
Madya Varga : Madyas
Vihara: Divaswapna, Vyavaya, Vyayama, Soorya Tapa, Swedana, Papakarma,
Guruninda and Guru Gharshana.
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ECZEEMA (ALLERGIC DERMATITIS)
With a background of comprehensive descriptions on Vicharchika by Ayurvedic
Classics, let us now Review the explanations on Allergic Dermatitis.
The term Allergy was introduced in 1906 by von parquet to designate
‘uncommitted’ biologic response, which may lead either to immunity or allergic diseases,
but over a period of time the term allergy is taken to mean IgE Mediated allergic
disease145.
Allergic Dermatitis is inflammation of the skin due to hypersensitivity.
Dermatitis 146-148
The term Eczema and Dermatitis are being used Synonymously and referred to
distinctive patterns of the skin which can be either acute or chronic due to number of
causes including Allergy. It is thus synonymous with dermatitis. However, according to
some only those dermatitis, which have allergy at the background should be called
eczema and others should be termed dermatitis.
Both these terms applied to variety of skin diseases with the specific
histopathological changes though originally applied to large number of skin diseases of
unknown origin now a day the term is more restrictive since many diseases have been
identified and classified. It has been seen almost all the cases of dermatitis are due to
hypersensitivity to various allergens that are, absorbed or in close proximity with the skin
or other wise due to peculiar Idiosyncrasies.
Allergy or hypersensitivity 149,150.
Allergy is the term applied to the natural or spontaneous manifestations of
hypersensitiveness in man, which include asthma, hay fever, eczema, urticaria and
migraine.
A person who is overly reactive to a substance that is tolerated by other people is
said to be hypersensitive.
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A hyper sensitive person starts secreting IgE antibodies those bind to allergens
forming IgE–allergen complex. In response the mast cells and basophiles secrete
histamines, which initiate allergic inflammatory manifestations like skin or lungs. Once
sensitized the individual remains hyper sensitive to that particular antigen. Whenever the
allergen gets into the system the body reacts immediately through inflammation these
reactions can be systemic or local.
Common allergens include
i) Food : Milk, Peanuts, Egg, Fish, Corn, Soya, Wheat etc.
ii) Drugs : Almost all drugs are capable of inducing allergy. Popular drugs
include penicillin, anti hypertensives, and other antibiotic.
iii) Vaccines : Pertusis, Typhoid.
iv) Venoms : Honybee, Wasp, Snake
v) Cosmetics : Hairdye, Nail polish, Perfumes, Deodorant.
vi) Chemical in plants : Poison ivy, Pollen, Dust.
vii) Microbes : Salmonella typhi.
viii) Substances : Leather, Clothing, Plants, Vegetables, Detergents, Chemicals,etc
Cardinal clinical features 151 of Allergic Dermatitis
The vesicle is a constant primary lesion. In some instances a vesicle is so minute
has not to be obvious. The first sign is the patch of erythema, accompanied by itching and
burning; this is soon covered with numerous tiny vesicles. These enlarge and often
coalesce. Later a rupture either spontaneously or by scratching and a clear serous fluid
exudes. Exudation continues once the surface of the skin has been broken and the exuded
serum then dries to form crusts, the more acute dermatitis, the greater degree of
enythema, pruritis or itching and vesiculation. As the disease subsides there is less
erythema and vesicle formation later papules and scales begin to form. In mild cases the
inflammation subsides rapidly, at much more frequently fresh crop of vesicles start up
around the edge of earlier patches while new lesions formed in other parts, some times
nearly whole skin is involved.
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If the disease becomes chronic patches of Lichenification due to long scratching
are formed. Thus the cardinal features of Allergic dermatitis what ever the type or
whatever the cause are erythema, pruritis, vesicle formation, rupture of vesicles, crusting,
scale formation, healing and Lichenification. Itching is a constant symptom and varies
more with the temperament of individual than the stage of disease.
Classification 142,153.
I. Histological
i) Acute - Characterized by considerable spongiosis (intercellular oedema) leading to
formation of intraepidermal vesicles or bullas, these are permeated by acute inflammatory
cells. The upper dermis shows congested blood vessels and mononuclear inflammatory
cell infiltrates or eosinophil especially or around small capillaries.
ii) Subacute – Many follow acute stage, here spongiosis and vesicles are smaller and
epidermis shows moderate acanthuses, varying degree of paracaratosis in the horny layer
and formation of surface crusts containing degenerated leucocytes, bacteria and fibrin.
Here dermis contains perivascular nuclear infiltrate or eosinophil.
iii) Chronic – Shows hyper caratosis, acanthuses, paracaratosis, elongation of Retie
ridges and broadened dermal papillae, vesicles are absent but slight spongiosus may be
present. The upper dermis shows perivascular chronic infiltrate fibrosis.
II. Based on Etiology.
i) Endogenous – Here the dermatitis is as a result of endogenous cause where the
pathology is dominated by hypersensitivity reactions or atopy without an external cause.
Ex : Atopic dermatitis, Seborrhoeic eczema, Infectious eczematous dermatitis, Nummular
dermatitis.
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Review of Literature. Disease
ii) Exogenous – As the name implies is inflammation of the skin from an external source
it may either be localized to a small area of skin or general in its distribution. Depending
on the intensity of the irritating factor it can be acute, sub-acute or chronic. There are
literally hundreds of Substances that can be produce dermatitis and they may act by direct
irritation or by effected individual having become sensitized to them or due to a personal
idiosyncrasy. Ex : Allergic contact dermatitis, Irritant Contact dermatitis, phyto and photo
dermatitis, drug allergy.
iii) Occupation – Usually is a result of continuous exposure to skin irritants in many
occupations.
Ex : Strong cleaning agents or soaps, in laundry work, wet works, solvents, detergents,
vegetable juices, plants, weeds insecticides different dyes, chemicals etc.
Investigations 154
Patch testing to allergies
This is used in suspected cases of allergic contact dermatitis. Patch testing to
irritants (Which cause reactions in everybody) is not advised.
Prick testing
This is used for few patients with stubborn atopic dermatitis if found or inhalant
allergens are suspected an exacerbating factor. Radio allergosorbent Test (RAST) is done
for the levels of allergen specific IgE.
Routine blood test
A specific type of blood cell called an eosinophil is elevated in allergic
conditions.
Management 155, It includes
• Explanation, reassurance and encouragement.
• Avoidance of contact with allergens / irritants.
• Anti inflammatory like cortisone, Antihistamines and Antibiotics.
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Methodology – Pharmaceutical study
METHODOLOGY
PHARMACEUTICAL STUDY
Collection of drugs used in the preparation of Yashada bhasma:
All the raw drugs needed for the preparation for the compound are collected
from local market and some drugs are collected from college garden as well as
pharmacy section of DGMAMC GADAG. Every drug was identified according to
Ayurvedic standards.
Practical study:
The things, which are mentioned in Ayurveda, are better understood by getting
the knowledge in two ways i.e. Theoretical study and Practical. Because as saying, as
doing is very difficult task. This theory is especially applicable to Rasashastra,
because the drugs, which are mentioned in Rasashastra, are considered as visha or
they have visha guna, but after processing some processes those drugs become
‘Amruta’. So this denotes the importance of practical knowledge. The processes,
which are mentioned in the Rasagranthas, seem to be very easy, but they will prove
difficult during the practical.
A detailed description of the steps taken to prepare the trial formulations
includes different processes like Shodhana, Jarana and Marana, Malahara and Taila
kalpana.
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Methodology – Pharmaceutical study
Practical no.1:
1. Name of the preparation: Yashada samanya shodhana in Tila taila for 7 times.
Date of commencement : 10 – 03 -- 2005
Date of completion : 10 – 03 - 2005
Reference : R.R.S - 5/ 13
2. Equipments: Small iron pan with long handle, cloth.
Iron vessel with lid having hole about 2-cm.at center (pithara yantra), Burner.
3. Drugs: 1. Raw Yashada - 500 gms
2. Tila taila - 2.5 lt
3. Water - Q.S
4. Procedure:
a. Sufficient quantity of taila to immerse the metal was taken in Pithara yantra.
b. Raw Yashada about ½ kg was heated in iron pan till it melts.
c. Molten Yashada was immediately poured into Pitharayantra and allowed for self-
cooling which took about 15 to 20 minutes.
d. Cooled metal was taken out, washed with hot water to remove the oiliness and
wiped with cotton and cloth.
e. Dried metal was once again subjected to above said procedure for 6 more times,
each time fresh taila was taken for the procedure.
f. Second process onwards during melting, scum with oil was observed on the
surface of molten Yashada, which has been removed by iron spoon.
5. Observations:
1. Time taken for melting was 13 – 15 minutes on medium flame.
2. When molten Yashada was poured in Tila taila it produced crackling sound.
3. Second process onwards scum with oil was observed on the surface of molten
metal.
4. Colour of the oil becomes slightly blackish.
5. After the above procedure the metal was golden colour coating, but the shining is
decreased slightly.
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Methodology – Pharmaceutical study
6. Precaution:
1. Melting should be done on medium flame.
7. Result:
Initial weight of the metal – 500 gms
Final weight of the metal – 490 gms
Weight loss – 10 gms
Practical no. 2
1. Name of the preparation: Samanya shodhana of Yashada in Takra for 7 times.
Date of commencement : - 11 – 3 – 05
Date of completion : - 11 – 3 – 05
Reference : – R.R.S 5 / I3
2. Equipmnts: - Small iron pan with long handle, Cloth
Iron vessel with lid having hole of 2 cm.diameter at the center ( Pithara yantra ), Burner
3. Drugs: -
a.Taila shodita Yashada - 490 gms
b.Takra - 5 ltr
c. Water - q.s
4.Procedure:
a. Sufficient quantity of Takra was taken in Pithara yantra.
b. Taila shodhita Yashada was heated in iron pan till it melts.
c. Molten Yashada was poured immediately to the Pithara yantra and
allowed for self-cooling.
d. Cooled metal was taken out washed with hot water & wiped with cotton
cloth.
e. Dried metal was once again subjected to above said procedure for 6 more
times each time fresh Takra was taken for the procedure.
5. Observation:
a. Time taken for melting was 13 - 15 minutes on medium flame.
b. When molten Yashada was poured in Takra crackling sound was heard.
76
Methodology – Pharmaceutical study c. Second time onwards while melting the crackling sound was heard due to
presence of water molecules and scum was observed on the surface of
molten Yashada
d. The colour of Takra turned to yellowish and maximum quantity of Takra
reduced due to evaporation.
e. After the above procedure the metal became brittle rough disintegrated
surfaced, the shining of metal was increased.
6. Precaution:
a. Medium flame should be maintained.
b. Care should be taken while pouring into Takra to avoid explosion.
7. Result:
Initial weight of metal – 490 gms
Final weight of the metal – 480 gms
Weight Loss – 010 gms
Practical no. 3
1. Name of the preparation: - Samanya shodhana of Yashada in Gomutra for 7 times.
Date of commencement : - 12 – 3 – 05
Date of completion : - 12 – 3 – 05
Reference :– R.R.S 5 / I3
2. Equipments: - Small iron pan with long handle, Cloth
Iron vessel with lid having holed about 2cm.at center (Pithara yantra), Burner
3. Drugs: - a. Takra shodhita Yashada - 480 gms
b. Gomutra - 6 ltr
c. Water - q.s
4. Procedure:
a. Sufficient quantity of Gomutra was taken in Pithara yantra.
b. Takra shodhita Yashada was heated in iron pan till it melts.
c. Molten Yashada was poured immediately to the Pithara yantra & allowed
for self-cooling.
77
Methodology – Pharmaceutical study
d. Cooled metal was taken out washed with hot water & wiped with cotton
cloth.
e. Dried metal was once again subjected to above said procedure for 6 more
times each time fresh Gomutra was taken for the procedure.
f. Scum formation on the surface of molten Yashada was removed by iron
spoon.
5. Observation:
a. Yashada melts within 13-15 minutes producing crackling sound.
b. Explosive sound was heard when molten Yashada poured in Gomutra.
c. Scum was formed on the surface of molten Yashada
d. The colour of Gomutra turned in to blackish and quantity was reduced.
e. After the above procedure the metal became brittle, the shining of metal
was reduced.
6. Precaution:
a. Medium flame should be maintained.
b. To avoid explosion the lid of the Pithara yantra should be sealed properly
7. Result
Initial weight of metal – 480 gms
Final weight of the metal – 470 gms
Weight loss – 10 gms Practical no.4
1. Name of the preparation :- Samanya shodhana of Yashada in Kanji for 7 times.
Date of commencement : - 13 – 3 – 05
Date of completion :- 13 – 3 –05
Reference :– R.R.S 5/ I3
2. Equipments :- Small iron pan with long handle, Cloth
Iron vessel with lid having hole of 2 cm.diameter at the center (pithara yantra),
Burner
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Methodology – Pharmaceutical study 3. Drugs :- a.Gomootra shodita Yashada – 470 gms
b.Kanji - 3 ltr
c.Water - q.s
4. Procedure:
a. Sufficient quantity of Kanji was taken in Pithara yantra.
b. Gomutra shodhita Yashada was heated in iron pan till it melts.
c. Molten Yashada was poured immediately to the Pithara yantra and
allowed for self-cooling.
d. Cooled metal was taken out washed with hot water & wiped with cotton
cloth.
g. Dried metal was once again subjected to above said procedure for 6 more
times each time fresh Kanji was taken for the procedure.
f. Scum formation on the surface of molten Yashada was removed by iron
spoon.
6. Observation:
a. Explosive sound was heard when molten Yashada poured in Gomutra.
b. Second time onwards scum was formed on the surface of molten Yashada
and was removed by iron spoon.
c. The colour of kanji became dark & more quantity was evaporated.
e. After the above procedure the metal turned to a shining big granule.
7. Precaution: a. Medium flame should be maintained.
8. Result:
Initial weight of metal – 470 gms
Final weight of the metal – 455 gms
Weight loss – 15 gms
Practical no.5
1. Name of the preparation :-Samanya shodhana of Yashada in Kulattha kwatha for 7
times.
Date of commencement : - 14 – 3 – 05
Date of completion :- 14 – 3 –05
79
Methodology – Pharmaceutical study Reference :– R.R.S 5 / I3
2. Equipments :- Small iron pan with long handle, Cloth, Burner and Pithara yantra
3. Drugs :- a. Kanji shodhita Yashada - 455 gms
b. Kulattha kwatha - 8 ltr
c. Water - Q.S
4. Preparatory procedure: 1part of yavakuta churna of Kulattha was boiled with 16
parts of water in earthen pot over a mrudu agni till liquid is reduced to ¼ of the
original quantity.
5. Procedure:
a. Sufficient quantity of Kulaththa kwatha was taken in Pithara yantra.
b. Kanji shodhita Yashada is melted in iron pan on medium flame.
c. Molten Yashada was poured immediately to the Pithara yantra & allowed
for self-cooling.
d. Cooled metal was taken out washed with hot water & wiped with cotton
cloth.
f. Dried metal was once again subjected to above said procedure for 6 more
times, each time fresh Kulaththa kwatha was taken for the procedure.
6. Observation:
a. Yashada melts within 13 - 15 minutes producing crackling sound.
b. When molten Yashada was poured in Pithara yantra explosive sound was
heard.
c. The colour of Kwatha turned in to dark & much quantity was evaporated.
d. After the above procedure some part of the Yashada became powder form.
7. Precaution: Explosive chances are avoided by sealing the lid of Pithara yantra.
8. Result
Initial weight of metal – 455 gms
Final weight of the metal – 435 gms
Weight Loss – 20 gms
Practical No. 6
1. Name of the preparation :- Vishesha shodhana of Yashada in Haridrayukta Nirgundi
swarasa for 3 times.
80
Methodology – Pharmaceutical study Date of commencement : - 15 – 3 – 05
Date of completion :- 15 – 3 –05
Reference :– .R.R.S 5/156
2. Equipments: - Small iron pan with long handle, Cloth, Burner
Iron vessel with lid having hole of 2 cm diameter at the center (Pithara yantra),
Burner
3. Drugs :- a. Samanya shodhita Yashada – 435 gms
b. Nirgundi swarasa - 1.5liters
c. Haridra churna - 30 grams
d. Water - Q.S
4. Preparatory procedure: Nirgundi swarasa preparation.
Fresh Nirgundi leaves were taken and subjected to mardana till it became
fine kalka, later putapakwa vidhi was followed to obtain swarasa.
5. Procedure:
a. Half liter of Nirgundi swarasa was mixed with 10 gms of Haridra churna
and was taken in Pithara yantra.
b. Samanya shodhita Yashada is melted in iron pan on medium flame.
c. Molten Yashada was poured immediately to the Pithara yantra and allowed
for self-cooling.
d. Cooled metal was taken out washed with hot water up to removal of
yellowish tinge of metal and wiped with cotton cloth.
e. Dried Yashada was once again subjected to above said procedure for two
more times. Each time fresh Nirgundi swarasa with Haridra churna was
taken.
6. Observation:
a. Yashada melts within 13 - 15 minutes producing crackling sound.
b. When molted Yashada was poured in Pithara yantra more explosive sound
was heard.
c. Scum formation on the surface of molten Yashada was removed by iron
spoon.
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Methodology – Pharmaceutical study d. The colour of swarasa turned in to dark green and much quantity was
reduced.
e. After this procedure the Yashada became thorny, brittle and most of it became powder.
7. Precautions: Because of throny surface proper care should be taken while removing
the metal from shodhana media.
8. Result: Initial weight of metal - 435 gms
Final weight of the metal - 415 gms
Weight Loss - 20 gms
Practical No.7
1.Name of the preparation :- Marana of Yashada
Date of commencement : - 18 – 3 – 05
Date of completion :- 23 – 3 –05
Reference :– RT 19/116-119
2. Equipments :- Big iron pan with long handle, Cloth, Burner, Chalani.
3. Drug :-
a..Shodhita Yashada - 415gms
4. Procedure:
a. Vishesha shodhita Yashada about 415gms was taken in big iron pan and
melted on medium flame.
b. After complete melting of Yashada, the process is continued with stirred
through chalani until complete Yashada is converted into powder. (At 7500 c)
c. Then the heat was stopped and allowed to self-cooling, and then collecting the
fine powder by sieving through the cloth.
d. Remaining part of course powder of Yashada was once again subjected to
above said procedure continued until complete Yashada was converted into
fine powder.
5. Observations:
a. Yashada starts became into powder form within 1hour (7500c). It is
completely converted into bhasma form at the end of 8th hour.
b. The colour of Yashada turned into Grayish.
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Methodology – Pharmaceutical study
6. Precautions:
a. Care should be taken while stirring with chalani for avoided hot Yashada
course powder damaged to skin or cloth.
b. Medium flame should be maintained.
7. Result
Initial weight of Yashada – 415 gms
Final weight of the metal – 320 gms
Weight loss – 95gms
Practical No.8
1.Name of the preparation :- Shodhana of Girisindhoora in Nimbu swarasa for 3 times.
Date of commencement : - 25 -3 -05
Date of completion :- 26-3 -05
Reference :– RJ -3
2. Equipments :-Khalvayantra, spoon
3. Drugs :- a. Girisindhoora – 200 gms
b. Nimbu swarasa –100ml
4. Procedure:
a. Girisindhoora was taken in the Khalva yantra.
b. Nimbuswarasa was added in the Khalva yantra.
c. Initially Mardana was done slowly to avoid the spillage of material.
d. When it attained semisolid consistency the mardana was carried out continuously
until it becomes powder form.
e. Girisindhoora was once again subjected above said procedure for 2 more times.
5. Observations:-
a. After 1 hour material was become semisolid consistency.
b. Girisindhoora completely turned into fine powder form after six hours.
c. The colour of Girisindhoora turned into bright red.
6. Precaution:-
a. Care should be taken while doing the Mardana for avoids the wastage.
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Methodology – Pharmaceutical study
7. Result:
Initial weight of Girisindhoora – 200 gms.
Final weight - 230 gms
Weight gained - 30 gms.
Practical No.9
1.Name of the preparation :- Shodhana of Sasyaka in Nimbu swarasa
Date of commencement : - 27-3-05
Date of completion :- 27-3-05
Reference :– RT 21/112
2. Equipments :- Khalva yantra
3. Drugs :- a. Sasyaka – 20gms
b. Nimbusarasa – 10 ml
4. Procedure:
a. Sasyaka was taken in the Khalva yantra.
b. Nimbu swarasa added into the Sasyaka.
c. Initially mardana was done slowly to avoid the spillage of material.
d. When it attained semisolid consistency the mardana was carried out
continuously until it became powder form.
e. Sasyaka was once again subjected above said procedure for 2 more times.
5. Observation:
a. After 20 minutes was became semisolid consistency.
b. Sasyaka completely turned into powder form after 1 hour.
c. The colour of Sasyaka turned into green colour.
6. Precaution:
a. Care should be taken while doing the mardana for avoided the wastage.
7. Result:
Initial weight of Sasyaka – 20 gms.
Final weight - 25 gms
Weight gained - 5 gms.
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Methodology – Pharmaceutical study
Practical No.10
1. Name of the preparation :- Preparation of Yashadamrita malahara
Date of commencement : - 28-3-05
Date of completion :- 28-3-05
Reference :– RT 19/146-147
2. Equipments :- Khalva yantra,Vessel, Cloth, Spoon, Burner
3. Drugs :-
a. Sikta – 150gms
b. Tila taila – 750 gms
c. Yashada bhasma.- 300 gms
4. Procedure:
a. Above-mentioned quantity of Sikta and Tila taila was taken into vessel.
b. This vessel was subjected over mild fire.
c. Yashada bhasma was added into Sikta taila after melting and stirred well.
d. Then vessel was removed from the agni and allowed for self cooling.
5. Observation:
d. Sikta was melts in Tila taila within few seconds.
e. After cooling it becomes a soft butter like paste.
6. Precaution:
a. Care should be taken while doing the mardana for avoided the wastage of
the material.
7. Result:
Final product – 1180 gms.
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Methodology – Pharmaceutical study
Practical No.11
1.Name of the preparation :- Preparation of Sindhooradi Taila
Date of commencement : - 29 -3 -05
Date of completion :- 30 –3 -05
Reference :– RT – 21/162-163
2. Equipments :- Ulukula yantra, Vessel, Cloth, Spoon, Burner
3. Drugs :- a. Shodhita Sindhoora – 200 gms
b. Shodhita Sasyaka - 2 gms
c. Sarshapa taila - 2 lts
d. Arka - 480gms
e. Haridra - 480gms
f. Jala - 16 lts
4. Procedure:
a. Arka patra and Haridra was taken in Khalva yantra and prepared kalka.
b. Shodhita Sindhoora and Sasyaka were added into kalka.
c. The whole kalka and dravadravya are mixed together.
d. Sarshapa taila was then added, boiled and stirred continuosly.
e. After getting the Snehasiddi lakshana, Sneha was filtered at hot stage
through the cloth.
5. Observation:
a. Foam was observed when taila paka completed.
b. The colour of taila was become into green colour.
c. Taila paka was completed in two days.
6. Precaution:
a. During Sneha paka stirring was done continuosly for avoided kalka is
adhere the vessel.
b. Taila paka should be prepared madhyamagni only.
c. Kalka should be squeezed at hot stage.
7. Result: Final weight of product – 1900 ml
86
Methodology – Analytical Study
ANALYTICAL STUDY
The metallic and mineral preparation of Ayurvedic pharmacopoeia should be
analyzed for physical and chemical properties to confirm the genuinely & safety before
administration to the patients. Hence it is essential to adopt modern analytical
methodology for better understanding and interpretation of physico - chemical changes
occurred during the process.
Organoleptic characters and Physico chemical analysis done J.T Pharmacy college
Gadag, like Finess of particle test, Flow rate, Ash value, Acid insoluble ash of Yashada
bhasma and Boiling point, Specific gravity, Refractive index, Loss on drying at 1100c
Acid value and Saponification value of Sindhooradi Taila.
Yashada bhasma also assessed according to the Ayurvedic parameters also.
Showing Ayurvedic tests of Yashada bhasma
Name of the sample Varitaratwa Rekhapurnatwa Shlakshnatwa Nischandra
Yashada bhasma + + + +
Table No-18
1. The Finess of particle test:
It can be possible to use the ordinary microscope for particle size measuring
in the range of 0.2 micrometer to about 100 micrometer. According to microscope
method the fine powder was sprinkled on the slide covered with covering slip &
placed on a mechanical stage. In initially standardization of minometer was carried
out by coinciding the lines of both oculo minometer style minometer and standardized
by using the formula
SM -------- X 10 = m OM
In the next step, the style minometer was removed & the mounted slide
was placed on a mechanical stage & focused. The particles are measured alops an
orbitarily chosen fixed lines covered by the particles using the oculominometers. The
size of the particle was calculated using the standard value.
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Methodology – Analytical Study
2. Flow property:
Yashada bhasma is very fine powder so to maintain the actual dose and for
better dispensing, bhasma is subjected to flow property test i.e. “ Angle of repose ” by
which we can analyze either the powder having very good flow property, good
property or a bad flow property.
Angle of repose (θ): - It is the maximum angle that can be obtained between the free
standing surface of a powder heap & the horizontal plane i.e. tan θ = 2h / D
Where D is the diameter of the circle & ‘h’ is the height of the powder heap
This test involves the hollow cylinder half is filled with Yashada bhasma
with one end sealed by transparent plate. The cylinder is rotated about its horizontal
axis until the powder surface cascades. The curved wall is lined with sand paper to
prevent preferential slip at this surface. If the value comes between 200– 400 indicates
reasonable flow potential.
3. Flow rates:
A simple indication of the ease with which a material can be induced to flow
is given by application of a compressibility index “ I ”
I = [1 – V ] x 100 Vo Where ‘ v ‘ is the volume occupied by sample of the powder after being
subjected to a standardized tapping procedure.
Vo = volume before tapping procedure
In this procedure one measuring cylinder is taken and is filled with Yashada
bhasma. The level of the Yashada bhasma should be noted. Then at a height of 2 cm
continuous 10 tapping should be done, after that the level of the Yashada bhasma in
the cylinder is once again noted & the value ‘I ’ is calculated with respect to the Vo &
V value. If the value
‘ I ’ is below 15% usually having good flow rates.
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Methodology – Analytical Study
4. Determination of Ash:
Method:
Incinerate about 2 to 3 g, accurately weighed, of the prepared sample in a tarred
platinum or silica dish at low temperature until free from carbon, cool and weigh. If a
carbon free ash cannot be obtained in this way, extract the charred mass with hot
water, collect the residue on an ashless filter paper, incinerate the residue and filter
paper add the filtrate, evaporate to dryness and ignite to constant weight at a low
temperature. Calculate the percentage of ash with reference to the moisture free drug.
5. Acid insoluble ash:
Boil the ash for 5 minutes with 25ml of dilute hydrochloric acid, collect the
insoluble matter in a Gooch crucible, or on an ashless filter paper, wash with hot
water and ignite to constant weight at a low temperature. Calculate the percentage of
acid insoluble ash with reference to the moisture free drug.
6. Boiling point:
An organic liquid boils at a fixed temperature, which is characteristic of that
substance. The presence of impurities raises its boiling point.
Method: Capillary tube method.
A few drops of the liquid are placed in a thin walled small test tube. A capillary
tube sealed at about 1 cm from one end, is dropped into it. The glass tube containing
the liquid and capillary is then tied along side a thermometer so the liquid stands just
near the bulb. The thermometer is then lowered in a beaker containing water or
Sulphuric acid.
The beaker is heated and the bath liquid stirred continuously with a ring stirrer.
When the boiling point is reached, bubbles issue in a rapid stream from the lower end
of the capillary. The thermometer is read when the evaluation of bubbles just stops.
The experiment is repeated with a fresh liquid in a new capillary and the boiling point
recorded as before. The mean of the two readings is taken to be correct boiling point
of the liquid under examination.
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Methodology – Analytical Study
7. Specific gravity:
The specific gravity of a liquid is the weight of a given volume of the
liquid at the specific temperature compared with the weight of an equal volume of
water at the same temperature, all weighing being taken in air.
Procedure:
A pycnometer of 25 ml. Capacity is cleaned, dried and weighed. It is
filled up to the mark of water at the required temperature and weighed. The
pycnometer is next filled up to the mark with the sample, filtered with necessary, at
the same temperature and weighed. The specific gravity is determined by dividing the
weight of the sample expressed in grams.
8. Refractive Index:
The Refractive index (n) of a substance is the ratio of the velocity of light
in a vacuum to its velocity in the substance. It varies with the wavelength of the light
used in the measurement.
It may also be defined as the ratio of the sine of the angle of incidence to
the since of angle of refraction. Refractive indices are started in terms of sodium light
of wavelength 9893A at a temperature of 200 unless otherwise specified.
Refractometers:
Commercial instruments are normally constructed for use with white light but are
calibrated to give the refractive index in terms of the sodium D wavelength. The
maker’s instructions relating to a suitable light source should be followed.
Temperature control: A suitable device should be used for circulating water at the
required temperature through the Refractometer. The sample is filtered through a dry
filter.
Procedure:-
Circulate water through the instrument at the required temperature. Place a drop
of the liquid between the prisms, and take the reading after half a minute.
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Methodology – Analytical Study
9. Loss on drying at1100:
One gram of Yashada bhasma accurately weighed, heated on electric oven up to
1100 c and again weighed. The difference in weighed was calculated & the result is
attached.
10. Acid Value:
The Acid value of an oil or fat is defined, as the number of milligrams of
Potassium hydroxide required neutralizing the free acid in one gram of the sample.
Method :
Mix 25ml Ether with 25ml alcohol (95%) and 1ml of 1% phenolphthalein
solution and neutralize with N/10 alkali (few drops). Dissolve about 5gm of the fat
or oil. Accurately weighed, in the mixed neutral solvent, and titrate with N/10
Potassium hydroxide, and shaking constantly until a pink colour which persists for
15seconds is obtained.
The titration should preferably not exceed about 10ml.
No. of ml of N/10 alkali used X 5.61 Acid value = Weight of sample in gm.
The free fatty acid content is also express as FFA, calculated as oleic acid%
(1ml. N/10) alkali = 0.028 gm oleic acid.
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Methodology – Analytical Study
11. Saponification value:
The saponification value of an oil or fat is defined as the number of
milligrams of potassium hydroxide required to neutralize the fatty resulting acids
from the complete hydrolysis of 1 gram of the sample.
Alcoholic solution of potassium hydroxide:
Dissolve 35-40 g. potassium hydroxide in 20 ml of water and dilute to one
liter with alcohol (95%) Allow standing overnight and decanting off the pure liquid.
Method:
Weight 2g. of the oil or fat into a conical flask and add exactly 25ml of the
alcoholic potassium hydroxide solution. Attack a reflux condenser and heat the flask
in boiling water for one hour, shaking frequently. Add 1 ml of phenolphthalein (1%)
solution and titration the excess alkali with N/2 hydrochloric acid (titration=a ml)
carry out a blank at the same time (titration=b ml).
(b-a) x 56.1 Saponification value = Wt. In g. of sample
92
Methodology – Clinical Study
CLINICAL STUDY
This clinical study was conducted after proper understanding of classical
explanations, observations and management of Vicharchika. For this clinical study
clinical symptoms and the management of Vicharchika are taken into consideration.
Objectives of the study:
1. Preparation of Yashadamrita Malahara and Sindhooradi taila
2. Physico- chemical analysis of Yashadamrita Malahara and Sindhooradi taila
3. Clinical- evaluation of Yashadamrita Malahara and Sindhooradi taila on
Vicharchika.
The materials are studied as under:
1. Literary aspect of the study regarding the drug was collected from the
Rasatarangini, Rasamrita, Rasaratna samuchchaya etc Rasagranthas and modern
inorganic chemistry and processed in pharmacy section of P.G.R.C.DGM
Ayurvedic medical collage according to the classical methods.
2. Literary aspect of disease was collected from the various Ayurvedic classics,
magazines and journals. The information regarding the disease is updated from
Internet search.
3. Patients: The patients with confirmed diagnosis of Vicharchika (Eczema) were
selected from the O.P.D. Section of P.G.R.C.D.G.M. Ayurvedic medical college
hospital Gadag.
Methods of collection of data:
a. Inclusive criteria:
1. The patients of Vicharchika will be diagnosed according classical features and
dermatological studies.
2. Irrespective of sex, patients will be selected between the age of 16 years to 60 years.
93
Methodology – Clinical Study
b. Exclusive criteria:
The patients who are suffering from any other systematic disorder will be excluded.
c. Study design:
Patients of Vicharchika with confirmed diagnosis selected as for simple
random sampling method with pretest and post test design all patients will be
assigned to a two group.
d. Sample size:
A minimum of 30 patients are selected and 15 in each group randomly selected.
The grouping is as follows:
Group A – Yashadamrita malahara
Group B – Sindhooradi taila
e. Posology: For external application, as required.
f. Duration of treatment: 21days.
g. Follow up: 15 days.
h. Assessment of result:
Results of the treatment were assessed on the basis of difference between the
baseline data and assessment data of the subjective and objective parameters. These
differences are subjected for the statistical analysis by applying paired and unpaired
‘t’test and nonparametric test (if necessary) if ‘p’ value is less than 0.05 the test is
highly significant.
Subjective parameters: As designated in texts
1. Varna
2. Pidaka
3. Srava
4. Kandu
5. Vedana vishesha
94
Methodology – Clinical Study
Objective parameters:
1. Hemoglobin
2. Total count
3. Differential count
4. Erythrocyte sedimentation rate
5. Absolute eosinophile count
Grades of subjective Parameters:
1. Varna: 0 - Normal 1- Mild 2 – Moderate 3 - Severe
2. Kandu: 0 - Normal 1- Mild 2 – Moderate 3 - Severe
3. Pidika: 0 - Normal 1- Mild 2 – Moderate 3 - Severe
4. Srava: 0 - Normal 1- Mild 2 – Moderate 3 - Severe
5. Vedana vishesha: 0 - Normal 1- Mild 2 – Moderate 3 - Severe
As the objective parameters are not suggesting any role in the assessment
of results in this study, so here assessment of results is made only with subjective
parameters.
Over all Assessment of results:
The overall assessments of results in the present study were grouped into
the following categories.
Cured : Complete subsidence of all the subjective symptoms.
Much responded : Complete subsidence of 3 or 4 subjective symptoms.
Moderately responded : Reduction of 2 subjective symptoms.
Responded : Reduction of only one subjective symptom.
Not responded : No reduction of subjective symptoms.
95
Discussion
DISCUSSION
The study entitled “ The Preparation, physico chemical study of Yashadamrita
malahara and Sindhooradi taila and comparative clinical study on Vicharchika” is
presented in 4 parts for both preparations.
1. Literary study
2. Pharmaceutical study
3. Analytical study
4. Clinical study
YASHADAMRITA MALAHARA 1. Literary study:
Literary study explained under two headings.i.e Drug review and Disease
review. In drug review Yashada is discussed according to ayurvedic as well as modern
concept.
a. Yashada might knew to the ancient Ayurvedic scholars, because its alloys are
already mentioned before 15 AD and only its medicine value may be detected
later. So in 15th AD it is mentioned by Madanapala and next by Bhavamisra.
b. When Arabians comes to India for business, then this metal became popular by
name the “Jashada” due to its multidimensional pharmacological property and
they used it for preparing ornaments.
c. Even modern science believed that zinc is a one of the trace elements of the body.
Many times they used it as a nutritive, antioxidant etc.
d. Yogaratnakara was the first person who mentioned Malahara kalpana and
Rasataranginikara was the only one person who mentioned Yashadamrita
malahara.
Under disease review Ayurvedic concept of Vicharchika and modern concept of
Eczema (allergic dermatitis) is discussed.
118
Discussion
Vicharchika is said to be exist since Vedic period. Our Acharyas like Charaka,
Sushruta and Vagbhata described Vicharchika as a variety of Kshudra Kushta. For the
present study Yashadamrita malahara and Sindhooradi taila are selected due to their
Vicharchikahara property.
Although Vicharchika is Tridoshaja Vyadhi it is Pitta and Kapha pradhana
Vyadhi. The lakshana of Vicharchika are Varna, Kandu, Pidika, Srava and Vedana
vishesha
According to modern science the Eczema and dermatitis are being used
synonymously and referred to distinctive pattern of the skin which can be either acute
or chronic due to number of causes including allergy.
Allergy is the term applied to the natural or spontaneous manifestations of
hypersensitiveness in man, which includes Asthma, Hay fever and Eczema, Urticaria
and Migraine.
The clinical features of allergy are erythema, itching, burning, oozing etc. 2.Pharmaceutical study.
Shodhana:
Shodhana not only intended to remove the impurities or toxic material, but also
makes the metal suitable for further procedure & enhances its potency.
In present study samanya shodhana was carried out by doing nirvapana in Tila
taila, Takra, Gomutra, Kanji, Kulaththa kwatha for 7 times in each. and Vishesha
shodhana with nirvapana in Haridrayukta Nirgundi swarasa for 3 times.
In the above said medias Tila taila is neutral where as other medias contain
several acidic compounds, hence some of them are acidic in nature. During processing
with these drugs the organic acids act slowly on metal and help in attainment of
brittleness.
119
Discussion
Scum was observed in molten surface, this is because of high temperature molten Zinc
reacts with external air (steam) and liberates hydrogen forming Zinc oxide (scum).
Explosive sound is produced because
Melting & pouring Zn ZnO2 + H2
In shodhana media (Aqueous in nature) When molten metal was poured in shodhana media, it breaks the water
molecules & releases hydrogen gas immediately this produces explosive sounds. The
intensity of sound depends upon the concentration of hydrogen gas released at that
time. At the same time oxygen is reacts with the metal forms Zinc oxide i.e. ZnO.
Weight loss after shodhana might be due to scum formation on molten surface
that is removed.
Vishesha shodhana is intended to bring diseases specification to drug. In
Yashada vishesha shodhana, Nirgundi & Haridra are used where Nirgundi is best
Kapha vata shamaka & Raktashodhaka. Haridra used for shodhana not only converts
Yashada into shodhita form but also helpful in Vicharchika, as it has a kapha shamaka,
Raktashodhaka, kushtaghna, krimighna, varnya etc. properties. Hence Nirgundi and
Haridra are selected for this procedure.
Marana:
For pootilohas one intermediate procedure is mentioned prior to prepare the
bhasma. Several jarana methods mentioned for Yashada, but in this study I have taken
agnijarita yashada bhasma preparation. In this procedure Yashada is heated in an iron
pan for a long duration i.e. more than 7500c. Due to continuous heat specific gravity of
a metal may decrease, and mass volume increases. Hence metal looses its metallic
bonds. Rubbing with iron ladle vigorously create a pressure on brittle elements
converting into powder form i.e.bhasma form. This is irreversible phenomenon.
120
Discussion
Weight loss of bhasma after marana due to oxidation process, the elements are
definitely looses their atomic weight.
Preparation of Yashadamrita Malahara.
Here sikta taila is used as a base and the main ingredient is Yashada bhasma. Tila
taila is best kapha shamaka, lekhana, krimighna, and twachya, where as sikta is
sandhanakara, vrunaropaka, kandughna and kushtanashaka. That’s why sikta taila is
taken as base for the Yashadamrita Malahara. So it not only acts as a base it also helps
in the curing disease.
3. Analytical study:
1. The end product is subjected for organoleptic characters it is inert, smooth, free
from greasy. So it is easily applicable and does not produce irritation or
sensitization of the skin.
2. This malahara contain Yashada bhasma so to confirm the standared and completion
of oxidation of Yashada. Agnijarita Yashada bhasma is subjected to “Total ash and
Acid insoluble ash test”, the values are Total ash 100% and Acid insoluble ash 29%
so it is proved that bhasma prepared by Agnijarita method is genuine one and it is
completely converted into Vijatiya to Sajatiya i.e. completely oxide form.
3. This compound is only indicated externally so to know either the bhasma is
absorbable through normal skin orifices or not. To confirm the particle size of the
Yashada bhasma, sample is subjected for “Fineness of particle test”. This test was
done in microscope it is evident that the particle sizes of Yashada bhasma
Arithmetic mean is 5.4 micrometer. Mean volume surface diameter is 1.57
micrometer. So by this it is know that Yashada bhasma particles are very fine in
nature, which definitely absorbs through normal skin orifices.
121
Discussion
4. Clinical study:
In this clinical study out of 30 patients 15 patients were selected for the
treatment of Yashadamrita Malahara in the management of Vicharchika.
The demographic data shows that most of the patients comes under middle
age group (73.33%) and male patients (73.33%), which suggests that it was seen more
in middle age and males.
All the 15 patients presented with subjective symptoms like Varna, Kandu
and Pidika. Out of 15 patients, 6 patients have srava and 7 patients have Vedana
vishesha of varying degree before and after the treatment.
Yashadamrita malahara was found highly significant with P<0.001 in Varna
with 33.33% of the patients completely relieved from Varna, 40% were relieved from
Pidaka and 40% were relieved from Kandu and 93.33% in Srava(P<0.02).
In this group out of 15 patients 5 patients (33.33%) have been cured, 5 patients
(33.33%) have been much responded, 3 patients (20%) have been moderately
responded, 2 patients (13.33%) have responded and no patients were found
unresponded.
In objective parameters variations are not more, which are found in normal range
comparing to before and after treatment.
Probable mode of action of Yashadamrita Malahara.
In the present study an effect has been made to discuss the probable mode of
action of Yashadamrita malahara on Vicharchika.The pharmacodynamic properties of
Yashada bhasma is
Rasa – Kashaya, Tikta Guna – Sheeta
Veerya – Sheeta Doshaghnata – Kapha pitta shamaka
Karma – Vrunaropaka, Vrunashamaka
Tila taila,
Rasa – Madhura, Kashaya, Tikta Veerya – Ushna
Guna – Sukshma, Vyavayi, Vikasi, Sara, Guru, Teekshna, Vishada.
Karma – Lekhana, Twachchya, Krimighna
122
Discussion
Sikta,
Rasa - Madhura Guna – Snigdha, Pichchala
Karma – Sandhanakara, Vrunaropaka, Kandughna, Kushtaghna.
The drugs used in the shodhana also induce the kapha pitta property in the
Yashada bhasma.
Even in modern science also, it is expected to be zinc has a good
antiseptic, astringent, local sedative action, it reduces the chronic inflammation it
checks the bleeding and secretion from broken skin by precipitating the secretions, it
provides soothing and protective effect to skin.
So by this yoga main dominated doshas i.e. Kapha pitta in sravi Vicharchika.
So it is best in srava, kandu, pidikayukta Vicharchika.
SINDHOORADI TAILA
1. Literary study:
In drug review ingredients of Sindhooradi taila are discussed according to
Ayurvedic as well as modern concept.
a. Girisindhoora is well known to ancients and they included it in sadharanarasa,
where as Bhavaprakasha and Rasataranginikara consider it as a upadhatu. By this it
may be argued that Girisindhoora might be the derivative of the metal and even
chemical analysis also proved that it is lead pro oxide.
b. Sindhoora found in mineral form, but most of the authorities not mentioned
shodhana and Marana. But some authorities mention bhavana with godugdha or
amlavarga dravya. It may be due to its external limitation.
c. Sasyaka is well known ancient Ayurvedic authorities and it is used in various
pathological conditions. Many times Sasyaka and Tutthya used synonymsly but
both are different. Because grahyalakshana of sasyaka do not correlate with the
tutthya, that means tutthya is artificial form of copper sulphate. Where as sasyaka is
natural, both are used internal as well as external followed by shodhana, marana,
amritikarana n various pathological condition.
123
Discussion
d. Arka, Haridra and Sarshapa are used as a traditional medicine in various
pathological conditions.
Disease review is done in last chapter.
2. Pharmaceutical study.
a. Various types of Taila kalpanas mentioned in the classics. In Sindhooradi taila
Rasataranginikara used sarshapa taila because it mitigates the vata and kapha, it is
best Raktashodhaka, Kandughna, Kushtaghna, Kothaghna and Krimighna.
b. Girisindhoora is Tridoshashamaka, Kushtaghna, Kandughna, Vrunaropana and
shodhana. Even modern science also used in various ointments and liniments,
which are indicated in eczema, eruptive skin disease, ulcers etc.
c. Sasyaka has Kaphapittashamaka, Krimihara, Kushtaghna, Kandughna, and
Vrunaropaka karma. Even modern science also used as local astringent on broken
Skin, antiseptic, it can kill the bacteria fungi and protozoa, it is used to destroy
excerbent granulations, ulcers, eczema, trachoma, as a lotion. Even it can be used
internally.
d. Arka and Haridra, these two drugs used as a kalka dravya along with Sindhoora
and Sasyaka in the preparation Sindhooradi taila. Arka has Kapha pitta shamaka,
Vedanashamaka, Shothahara, Vrunashodhaka and Kushtaghna. Haridra has
Kaphavatashamaka, Vedanashamaka, Shothahara, Vrunashodhana and ropana,
Krimighna and Kushtaghna.
The intention is the preparation of taila of the above combination might be to
store the active principle of compound drug and make it suitable for application.
e. Girisindhoora is red in colour, but the colour of Sindhooradi taila was changed
might be due to chemical reaction with organic matter and also quantity of
Sindhoora is less than kalka dravya.
124
Discussion
3. Analytical study.
1. To know the concentration of saturated or unsaturated fatty acid, compound is
subjected to “Acid value test and Saponification test”, and then it is comes to
know that the compound has Acid value 5.865 i.e. unsaturated fatty acid
concentrations and Saponification value 200 that is saturated fatty acid. So this
taila only indicated externally then also it will not produces any free radicals by
the absorption. There by it is confirmed that classically prepared this taila is
samyak siddha taila, because by this procedure unsaturated taila is converted into
saturated fatty acid.
2. To confirm either taila is highly viscid or the clear solution, compound is
subjected to “Refractive index test”, the value of this test is 1.608 and “Specific
gravity test”, value is 0.86. By this it is confirmed that taila is very clear and not
viscid, their by is absorbed very quickly.
3. When the compound is subject to the test “Loss on 1100c”, the value of this test is
0.86% w/ w and boiling point is 1200c to 1250c. So it is confirmed that taila is free
from water molecule and no chance of microorganism growth.
4. Clinical study.
In this clinical study out of 30 patients 15 patients were selected for the treatment
of Sindhooradi taila in the management of Vicharchika.
The demographic data shows that most of the patients come under middle age
group (93.33%) and male patients (73.33%), which suggests that it was seen more in
middle age and males.
All the 15 patients presented with subjective symptoms like Varna, Kandu and
Pidika. Out of 15 patients, 3 patients have srava and 9 patients have vedana vishesha
of varying degree before and after the treatment.
Sindhooradi taila was found highly significant with P<0.001 in Varna with
46.66% of the patients completely relieved from Varna, 80% were relieved from
Pidaka and 80% were relieved from Kandu and not significant with P>0.05 in Srava.
125
Discussion
In this group out of 15 patients 7 patients (46.66%) have been cured, 6 patients
(40%) have been much responded, 2 patients (13.33%) have been moderately
responded, and no patients were found doesn’t responded.
In objective parameters variations are not more, which are found in normal range
comparing to before and after treatment.
Probable mode of action of Sindhooradi taila.
In the present study an effect has been made to discuss the probable mode of
action of Sindhooradi taila on Vicharchika.The pharmacodynamic properties of
Girisindhoora is
Rasa – Katu, Tikta Guna – Ushna
Veerya – Ushna Doshaghnata – Tridosha shamaka
Karma – Vrunaropaka & shodhaka, Kushtaghna, Kandughna etc
It is a local stimulant and indicated in eczema, eruptive skin disease, ulcers etc
Sasyaka
Rasa – Kashaya, kshara Guna – Laghu, Sheeta
Veerya – Sheeta Doshaghnata – Kaphapitta shamaka
Karma – Vrunaropaka, Kushtaghna, Kandughna, Krimighna etc
Act as local astringent on broken skin, antiseptic, destroy excerbent
granulations, ulcers, eczema,
Arka
Guna: Laghu, ruksha, teekshan Vipaka – Katu
Rasa – Katu, Tikta Veerya – Ushna
Doshaghnata – Kaphapitta shamaka.
Karma - Vedana sthapana, Shothahara, Vrunashodhana, Kushtaghna, Jantughna
Haridra:
Guna – Ruksha, Laghu Vipaka – Katu
Rasa – Tikta, Katu Veerya – Ushna
Doshaghnata – Kaphavatashamaka
Karma- Shothahara, Vedanasthapana, Varnya, Kushtagna, Vrunashodhana &
Ropana.
126
Discussion
Sarshapa:
Guna –Snigdha laghu(oil) Veerya – Ushna
Rasa- Katu, Tikta Vipaka – katu
Doshaghnata – Vatakaphashamaka
Karma - Raktashodhaka, Kandu & Kothaghna, Krimighna, Kushtaghna.
By observing these properties all drugs are having kapha shamaka and
Kushta, Kandu and shothahara etc properties. So this yoga is best in the Vicharchika,
which is Kapha pradhana Kushta vyadhi.
DISCUSSION ON COMPARATIVE CLINICAL STUDY
This study is conducted as a comparative clinical study on Vicharchika by
observing above all data and by statistical result. It is proved that, both the formulations
are having similar significant value for Kandu. But group A (Yashadamrita malahara) is
highly significant for Sravi Vicharchika and group B (Sindhooradi taila) is significant for
Rooksha Vicharchika.
127
Conclusion
CONCLUSION
1. As Rasaushadies are mainly meant for asadhya vyadhis, and it is proved by these
two formulation containing Rasadravya on Vicharchika.
2. The drugs used in shodhana definitely modify the drug suitable for further
procedure and induce the disease curing property.
3. Agnijarita Yashada bhasma mainly indicated in external use. But by physico –
chemical analysis it is proved that even agnijarita Yashada bhasma as it passes all
the bhasma pariksha same as Yashada bhasma which is prepared by following
Jarana as a intermediate procedure.
1. By physico – chemical analysis it is proved that Sindhooradi taila is very clear and
not viscid, their by is absorbed very quickly without producing any free radical
and is free from water molecule, so no chance of microorganism growth.
2. These two formulations quoted by Rasataranginikara in Vicharchika, but by
statistical value it is proved that Yashadamrita malahara is choice remedy in Sravi
Vicharchika and Sindhooradi taila in Rooksha Vicharchika
128
Conclusion
SCOPE OF THE FURTHER STUDY
1. Agnijarita Yashada bhasma mainly indicated in external use. As it passes all the
bhasma pariksha same as Yashada bhasma which is prepared by following Jarana
as a intermediate procedure. So it needs animal experiment for its toxicity study.
2. In Kushtaroga repeated shodhana followed by shamanoshadhi is mentioned. But
by rasadravyayukta yogas disease is subsided. So in this view a comparative
clinical study with big size sample with long duration can be carried out.
129
Observation and Results
OBSERVATION AND RESULTS
The present comparative clinical study was meant for evaluation of efficacy of
Yashadamrita malahara and Sindhooradi taila in the management of Vicharchika. Total
30 patients were taken randomly selected for the above mentioned study. The entire
patients were assessed before and after treatment. Both subjective and objective changes
were recorded according to the performa of case sheet. The collective data is grouped
into 8 categories.
1. Observation based on age.
2. Observation based on sex.
3. Observation based on education.
4. Observation based on marital status.
5. Observation based on religion.
6. Observation based on occupation.
7. Observation based on economical status.
8. Observation based on Vicharchika lakshanas
96
Observation and Results
Observations of patients based on Age.
Age
in years
No.of patients
Group A
%
No.of patients
Group B
%
Total
%
16-20 02 13.33 00 00.00 02 06.66
21-30 01 06.66 04 26.66 05 16.66
31-40 05 33.33 03 20.00 08 26.66
41-50 05 33.33 07 46.66 02 40.00
51-60 02 13.33 01 06.66 03 10.00
Total 15 99.98 15 99.98 30 99.98
Table No.19
In the present observation from both groups maximum number of patients 8
(26.66 %) belongs to the age group 31- 40, 5 patients belongs to 21-30, 3 patients belongs
to 51-60, and 2 patients comes under 16-20 and 41-50 age group
6.66
16.66
26.66
40
10
05
1015202530354045
16-20 21-30 31-40 41-50 51-60Age
Perc
enta
ge
%
Graph-1
97
Observation and Results
Observations of patients based on Sex
Sex No.of patients
Group A
% No.of patients
Group B
% Total %
Male 11 73.33 11 73.33 22 73.33
Female 04 26.66 04 26.66 08 26.66
Total 15 99.99 15 99.99 30 99.99
Table No.-20
From the both groups a total of 22 male (73.33%) and 8 females (26.66%) are
reported. This shows that the exposure for the disease Vicharchika is more in males
because they work outside exposing to different Nidana.
73.33
26.66
0
10
20
30
40
50
60
70
80
Male FemaleSex
Perc
enta
ge
%
Graph-2
98
Observation and Results
Observations of patients based on Education
Education No.of patients
Group A
% No.of patients
Group B
% Total %
Educated 10 66.66 09 60 19 63.33
Un-Educated 05 33.33 06 40 11 36.66
Total 15 99.99 15 100 30 99.99
Table No.-21
Even though there is no specific relation to the disease, but awareness to the
Ayurvedic treatment and faith is observed in this study. It explains that educated 19
patients (63.33) and uneducated 11 patients (36.66) from both groups are reported.
Observations of patients based on marital rates:
Marriage No.of patients
Group A
% No.of patients
Group B
% Total %
Married 12 80 10 66.66 22 73.33
Un-Married 03 20 05 33.33 08 26.66
Total 15 100 15 99.99 30 99.99
Table No.-22
In this study many are married i.e.22 patients (73.33) and unmarried are rest of 8
patients from both groups.
99
Observation and Results
Observations of patients based on Religion
Religion No.of patients
Group A
% No.of patients
Group B
% Total %
Hindu 13 86.66 12 80 25 83.33
Muslim 02 13.33 03 20 05 16.66
Others 00 00.00 00 00 00 00.00
Total 15 99.99 15 100 30 99.99
Table No.-23
Present study explains Hindu, Muslim are reported with problem of Vicharchika.
It does not mean that others are not having this problem. The area in which study
undertook has 2 groups of populations. Out of 30 patients 25 patients (83.33%) belongs
to Hindu religion and 5 patients (16.66 %) belong to Muslim religion.
0
83.33
16.66
0102030405060708090
Hindu Muslim OthersReligion
Perc
enta
ge
%
Graph-3
100
Observation and Results
Observations of patients based on Occupation
Occupation No.of patients
Group A
% No.of patients
Group B
% Total %
Agriculture 04 26.66 03 20.00 07 23.33
Student 03 20.00 01 06.66 04 13.33
Housewife 04 26.66 04 26.66 08 26.66
Employee 03 20.00 02 13.33 05 16.66
Business 01 06.66 05 33.33 06 20.00
Total 15 99.98 15 99.98 30 99.98
Table No.-24
In this study we consider the 5 categories of occupation for the convenience of
studies. Out of 30 patients 8 patients (26,66 %) belongs to the housewife, 7 patients
(23.33%) belongs to the agriculture, 6 patients (20%) belongs to business, 5 patients
belongs to the employee 4 patients (13.33) belongs to the student.
23.33
13.33
26.66
2016.66
05
1015202530
Agricu
lture
Studen
t
House
wife
Employe
e
Busine
ss
Occupation
Perc
enta
ge %
Graph - 4
101
Observation and Results
Observations of patients based on Economical status
Status No.of patients
Group A
% No.of patients
Group B
% Total %
Pour 50 33.33 20 13.33 07 23.33
Middle class 10 66.66 13 86.66 23 76.66
Higher class 00 00.00 00 00.00 00 00.00
Total 15 99.99 15 99.99 30 99.99
Table No.-25
It refers to the physical and psychological status of an individual patient. Out of
30 patients 23 patients (76.66%) belong to middle class, 7 Patients (23.33%) belong to
poor class and no patients belong to higher class.
76.66
23.33
00
102030405060708090
Pour Middle class Higher classStatus
Perc
enta
ge
%
Graph - 5
102
Observation and Results
Observations based on Vicharchika lakshanas
Group A Group B Symptoms
B % A % B % A %
Varna 15 100 10 66.66 15 100 7 46.66
Pidika 15 100 09 60.00 15 100 3 20.00
Srava 06 040 01 06.66 03 020 1 06.66
Kandu 15 100 09 60.00 15 100 3 20.00
Vedana 07 46.66 01 06.66 06 040 0 00.00
Table No.-26
The above table shows the number percentage of the patients complaining the
Vicharchika lakshana before & after the treatment. Before the treatment 15 patients have
the complaint Varna, Pidika, Kandu in both groups. After the treatment 10 and 7 patients
have Varna, 9 and 3 patients have Pidika and Kandu in group A and group B
respectively.
Before the treatment 6 patients have the complaint Srava in-group A and 3
patients in group B. After treatment 1 patient in-group A and I patient in-group B has the
same complaint.
Before the treatment 7 patients have the complaint Vedana in group A and 6
patients in-group B. After the treatment 1 patient complaint in-group A and no patients
have same complaint in-group B.
103
Observation and Results
Observation related to response to the treatment
Showing the grades of “Varna” Before treatment in group A & B No.of patients Group Grade
0 % 1 % 2 % 3 %
15 A - - 3 20.00 6 40 06 40.00
15 B - - 2 13.33 3 20 10 66.66
Table No.-27
Showing the grades of “Varna” After treatment in group A & B
No.of patients Group Grade
0 % 1 % 2 % 3 %
15 A 5 33.33 7 46.66 3 20 - -
15 B 7 46.66 7 46.66 1 6.66 - -
Table No.-28
Showing the grades of Pidika before treatment in Group A & Group B.
No. of patients Group Grade
0 % 1 % 2 % 3 %
15 A - - 4 26.66 8 53.22 3 20
15 B - - 2 13.33 7 46.66 6 40
Table No.-29
Showing the grades of Pidika After treatment in group A & B
Table No.-30
0 – Normal 1 – Mild 2 – Moderate 3 - Severe
No. of patients Group Grade
0 % 1 % 2 % 3 %
15 A 6 40 9 60 - - - -
15 B 12 80 3 20 - - - -
104
Observation and Results
Showing the grades of Srava before treatment in Group A & Group B.
No. of patients Group Grade
0 % 1 % 2 % 3 %
15 A 9 60 4 26.66 2 13.33 - -
15 B 12 80 1 06.66 2 13.33 - -
Table No.-31
Showing the grades of Srava after treatment in Group A & Group B.
No. of patients Group Grade
0 % 1 % 2 % 3 %
15 A 14 93.33 1 6.6 - - - -
15 B 14 93.33 1 6.6 - - - -
Table No.-32
Showing the grades of Kandu before treatment in Group A & Group B.
No. Of patients Group Grade
0 % 1 % 2 % 3 %
15 A 2 13.33 5 33.33 8 53.22
15 B 1 6.66 2 13.33 12 80
Table No.-33
Showing the grades of Kandu after treatment in Group A & Group B.
Table No.-34
0 – Normal 1 – Mild 2 – Moderate 3 - Severe
No. Of patients Group Grade
0 % 1 % 2 % 3 %
15 A 06 40 8 53.22 1 6.66 - -
15 B 12 80 3 20.00 - - - -
105
Observation and Results
Showing the grades of Vedana before treatment in Group A & Group B.
No. Of patients Group Grade
0 % 1 % 2 % 3 %
15 A 8 53.22 7 46.66 - - - -
15 B 6 40.00 9 60.00 - - - -
Table No.-35
Showing the grades of Vedana after treatment in Group A & Group B.
Table No.-36
0 – Normal 1 – Mild 2 – Moderate 3 - Severe
No. Of patients Group Grade
0 % 1 % 2 % 3 %
15 A 14 93.33 1 6.66 - - - -
15 B 15 100.0 - - - - - -
106
Observation and Results
RESULTS
30 patients were studied in two groups with 15 patients in each. Group A
patients treated with Yashadamrita Malahara and group B patients were treated with
Sindhooradi taila. The results obtained in the two groups were assessed on the basis of
Varna, Kandu, Pidika, Srava and Vedana vishesha. and Hb%, TC, DC, ESR and AEC
Assessment Of Subjective Parameters Of Group A
(Yashadamrita Malahara)
Sl.No O P D Varna Pidika Srava Kandu Vedana Vishesha
BT AT BT AT BT AT BT AT BT AT
1 1154 3 2 3 1 0 0 3 1 1 0
2 1198 2 1 2 0 1 0 3 2 1 0
3 2351 2 2 3 1 2 1 3 1 1 1
4 2490 3 1 2 1 0 0 3 1 0 0
5 2553 3 0 3 1 0 0 3 0 0 0
6 2600 1 0 1 0 0 0 2 0 0 0
7 2948 3 1 2 1 1 0 3 1 1 0
8 3153 2 0 1 0 0 0 1 0 0 0
9 3432 2 1 2 1 1 0 2 1 1 0
10 3908 1 0 2 1 0 0 2 1 0 0
11 3922 3 2 2 1 0 0 3 1 0 0
12 3985 2 1 2 0 2 0 2 0 1 0
13 4115 1 0 1 0 0 0 1 0 0 0
14 4051 3 1 2 1 0 0 3 1 0 0
15 4118 2 1 1 0 1 0 2 0 1 0
Table No.-37
BT-Before Treatment, AT-After Treatment
0 – Normal, 1 – Mild, 2 – Moderate, 3 - Severe
107
Observation and Results
Assessment of Subjective Parameters of Group B
(Sindhooradi taila)
Sl.No O P D Varna Pidika Srava Kandu Vedana
Vishesha
BT AT BT AT BT AT BT AT BT AT
1 1102 3 2 3 1 0 0 3 1 1 0
2 1179 3 1 2 0 1 0 3 2 1 0
3 2320 2 2 3 1 2 1 3 1 1 0
4 2484 3 1 2 1 0 0 3 1 0 0
5 2545 1 0 3 1 0 0 3 0 0 0
6 2557 3 0 1 0 0 0 2 0 0 0
7 2837 2 1 2 1 1 0 3 1 1 0
8 3103 3 0 1 0 0 0 1 0 0 0
9 3430 3 1 2 1 1 0 2 1 1 0
10 3635 3 0 2 1 0 0 2 1 0 0
11 3436 1 2 2 1 0 0 3 1 0 0
12 3439 3 1 2 0 2 0 2 0 1 0
13 4043 3 0 1 0 0 0 1 0 0 0
14 4068 2 1 2 1 0 0 3 1 0 0
15 4132 3 1 1 0 1 0 2 0 1 0
Table No.-38
BT-Before Treatment, AT-After Treatment
0 – Normal, 1 – Mild, 2 – Moderate, 3 - Severe
108
Observation and Results
Assessment of Objective Parameters of Group A
(Yashadamrita Malahara)
Sl.No O P D AEC Hb% ESR TC DC (E)
BT AT BT AT BT AT BT AT BT AT
1 1154 580 560 12 11.8 12 11 5300 5100 1 22
2 1198 520 530 11.5 12 14 13 6200 6300 5 4
3 2351 480 460 10 10 13 14 4800 5000 3 3
4 2490 550 560 10.5 10 18 16 6200 6400 4 4
5 2553 600 580 11 10.8 20 18 5400 5200 6 5
6 2600 450 440 9.8 10 12 13 5200 5300 2 2
7 2948 500 490 10.2 10.4 10 11 6800 7000 3 2
8 3153 400 430 13 12.8 08 10 7200 7100 4 4
9 3432 450 460 12 13 09 10 9800 9600 1 2
10 3908 480 460 11.5 12 07 08 4500 4600 5 4
11 3922 540 520 12.4 12 06 06 5400 5500 3 2
12 3985 450 410 10.4 10 11 12 8800 9000 3 2
13 4115 240 250 12 11 15 14 8500 8200 2 3
14 4051 360 320 13 13.2 13 14 7900 8000 2 2
15 4118 390 410 12.5 13 12 12 6300 6400 1 2
Table No.-39
BT-Before Treatment, AT-After Treatment
0 – Normal, 1 – Mild, 2 – Moderate, 3 - Severe
109
Observation and Results
Assessment of objective parameters of Group B
(Sindhooradi taila)
Sl.No O P D AEC Hb% ESR TC DC (E)
BT AT BT AT BT AT BT AT BT AT
1 1102 600 590 10 102 16 12 4000 4200 5 4
2 1179 602 600 12 12.4 20 18 6700 6500 4 4
3 2320 500 480 10.5 11 14 14 5000 5200 4 3
4 2484 525 510 11 11 12 12 5500 5300 6 6
5 2545 450 438 10.8 10.5 10 12 6400 6500 2 3
6 2557 475 468 10 10.2 14 12 6600 6400 3 5
7 2837 430 418 11.5 12 8 06 6800 6700 4 3
8 3103 498 470 12.4 12.5 10 08 6300 6400 5 4
9 3430 503 494 13 13 12 10 3500 4000 3 3
10 3635 550 536 12 12.4 14 12 3800 4000 6 5
11 3436 302 295 10 10.2 6 04 7000 6800 1 2
12 3439 465 460 10.5 10 14 12 8500 8200 2 2
13 4043 256 248 9.8 10 08 06 9200 9000 3 4
14 4068 230 225 10 10.5 12 12 7100 7200 1 3
15 4132 403 328 11 11.4 10 10 5400 5500 4 6
Table No.-40
BT-Before Treatment, AT-After Treatment
0 – Normal, 1 – Mild, 2 – Moderate, 3 - Severe
110
Observation and Results
Statistical analysis of Subjective parameters (Group-A)
Parameters
Mean S.D S.E T.Value P.Value Remarks
Varna
1.333 0.723 0.186 7.166 < 0.001 H.S
Pidika
1.333 0.487 0.125 10.664 < 0.001 H.S
Srava
0.466 0.639 0.165 2.824 < 0.02 H.S
Kandu
1.733 0.593 0.153 11.32 < 0.001 H.S
Vedana vishesha
0.4 0.507 0.130 3.076 < 0.01 H.S
Table No.-41
Subjective parameters in Group – A statistical analysis showed highly significant
Statistical analysis of Objective parameters (Group-A)
Parameters
Mean S.D S.E T.Value P.Value Remarks
AEC
20.66 10.32 2.666 7.751 < 0.001 H.S
Hb%
0.4 0.287 0.074 5.45 < 0.001 H.S
ESR
1.113 0.639 0.165 6.866 < 0.02 H.S
TC
173.33 70.37 18.17 9.53 < 0.001 H.S
DC
0.733 0.457 0.118 6.211 < 0.001 H.S
Table No.-42
Objective parameters in Group – A statistical analysis showed highly significant.
111
Observation and Results
Statistical analysis of Subjective parameters (Group-B)
Table No.-43
Subjective parameters in Group – B statistical analysis showed highly significant
Statistical analysis of Objective parameters (Group-B)
Parameters
Mean S.D S.E T.Value P.Value Remarks
Varna
15.26 17.76 4.587 3.326 < 0.001 H.S
Pidica
0.293 0.179 0.046 6.36 < 0.001 H.S
Srava
1.6 1.121 0.289 5.536 > 0.05 H.S
Kandu
206.66 103.27 26.66 7.75 < 0.001 H.S
Vedana vishesha
0.933 0.703 0.181 5.154 < 0.05 H.S
Table No.-44
Objective parameters in Group – B statistical analysis showed highly significant
Parameters
Mean S.D S.E T.Value P.Value Remarks
Varna
1.933 0.703 0.181 10.67 < 0.001 H.S
Pidika
2.06 0.593 0.153 13.46 < 0.001 H.S
Srava
0.266 0.593 0.153 1.738 > 0.05 H.S
Kandu
2.533 0.639 0.165 15.35 < 0.001 H.S
Vedana vishesha
0.4 0.507 0.130 3.07 < 0.05 H.S
112
Observation and Results
Statistical analysis of comparative study of Group-A & B (After Treatment)
Parameters
Group Mean S.D S.E P.S.E t.value p.value Ramarks
A
0.866 0.743 0.191 Varna
B
0.6 0,632 0.163
0.251
1.05
>0.05
N.S
A
0.6 0.507 0.130 Pidika
B
0.333 0.723 0.186
0.22
1.22
>0.05
N.S
A
0.066 0.258 0.06 Srava
B
0.066 0.258 0.06
0.084
A
0.666 0.617 0.159 Kandu
B
0.2 0.414 0.106
0.191
2.439
< 0.05
H.S
A
0.066 0.258 0.066 Vedana
Vishesha B
0.00 0.00 00.00
0.066
1.00
> 0.05
N.S
A
458.66 90.14 23.27 A E C
B
437.33 115.21 29.74
37.76
0.564
> 0.05
N.S
A
11.466 12.20 0.315
Hb% B
11.15 1.048 0.27
0.414
0.763
> 0.05
N.S
A
12.133 3.020 0.779 E S R
B
10.133 3.518 0.908
1.196
1.231
> 0.05
N.S
A
10.666 1547.44 399.54 T C
B
6580.0 1454.28 375.49
548.29
0.826
> 0.05
N.S
A
6126.66 1.06 0.273 D C
B
2.866 1.264 0.326
0.425
2.197
< 0.05
H.S
Table No.-45
113
Observation and Results
When compare the mean effects of two groups after the treatment, except the
parameter Kandu all other parameters shows not significant. The Kandu shows highly
significant (P < 0.05). The mean effect of the parameter Srava is same in both the groups.
Individually both groups show highly significant, but over all group B
performance is better than group A in all the parameters except Srava.
In subjective parameters (as P< 0.01 by comparing t - value), the parameter
Varna, Kandu, Pidika shows more highly significant in-group B than group A before and
after the treatment. The parameter Vedana vishesha shows same effect in both the groups.
(By comparing t – value, p – value, mean and SD)
In objective parameters in both groups show highly significant.
Comparative overall Assessment of therapeutic response of Group A & group B “ Evaluation of efficacy of Yashadamrita Malahara and Sindhooradi taila in the
management of Vicharchika” has the following data of result assessed on the basis of
subjective and objective parameters. Statistical evaluation is done carefully. The final
result in the study is declared. For the declaration it is classified as
a. Cured
b. Much responded
c. Moderately responded
d. Responded
e. Not responded
114
Observation and Results
Showing the result of the study in Group-A
Result Patients %
Cured 5 33.33
Much responded 5 33.33
Moderate 3 20.33
Responded 2 13.33
Not responded 0 00.00
Total 15 99.00
Table No.-46
In-group A there is no patient who doesn’t not responded. 5 (33.33%) patients
have cured. Much responded in the schedule are 5 (33.33%) patients. Moderate
responded in the schedule are 3 (20%) patients and responded 2 (13.33%) patients
showed significant improvement.
0
33.33
20.33
13.33
33.33
05
101520253035
Cured
Much r
espon
ded
Modera
te
Respon
ded
Not res
pond
ed
Result
Perc
enta
ge
%
Graph-5
115
Observation and Results
Showing the result of the study in Group-B.
Result Patients %
Cured 7 46.66
Much responded 6 40.00
Moderate responded 2 13.33
Responded 0 00.00
Not responded 0 00.00
Total 15 99.99
Table No.-47
In-group B there is no patient who doesn’t respond. 7 (46.66%) patients have
cured. Much responded in the schedule are 6 (40%) patients. Moderate responded in the
schedule are 2 (13.33%) patients showed significant improvement.
0 0
13.33
40
46.66
0
10
20
30
40
50
Cured Muchresponded
Moderateresponded
Responded Not responded
Result
Perc
enta
ge
%
Graph-6
116
Observation and Results
Showing overall result of the study
Result Patients.
Group. A % Patients
Group. B % Total %
Cured 5 33.33 7 46.66 12 40.00
Much responded 5 33.33 6 40.00 11 36.66
Moderate 3 13.33 2 13.33 05 16.66
Responded 2 00.00 0 00.00 02 06.66
Not responded 0 00.00 0 00.00 - -
Total 15 99.99 15 99.99 30 99.98
Table No.-48
In this study there is no patient who comes under not responded. 12 (40%)
patients have cured. Much responded in the schedule are 11 (36.66%) patients and
Moderate responded in the schedule are 5 (16.66%) and 2 (6.66%) patients show
significant improvement and fall under responded.
06.66
16.66
36.6640
0
10
20
30
40
50
Cured Muchresponded
Moderate Responded Notresponded
Result
Perc
enta
ge
%
Graph-7
117
Observation and Results
118
Observation and Results
119
Observation and Results
120
Observation and Results
121
Summary
SUMMARY
The present study entitled “The preparation of physico-chemical analysis of
Yashadamrita malahara and Sindhooradi taila and comparative clinical study on
Vicharchika.”
In this study an attempt was made to prepare genuine Yashadamrita malahara
and Sindhooradi taila by following the classical procedures, its genuinity was
confirmed by physico-chemical analysis, and its clinical efficacy was evaluated
checked by clinical study.
1. In the introduction Aims & objectives of the Rasashastra, importance of Malahara
and Taila kalpanas, description of Vicharchika & necessity for the assortment of
this research work is explained in brief.
2. Aims & Objectives of the present study are mentioned in the Objective chapter.
3. Review of Literature is dealt in two main headings i.e. Drug review and Disease
review and Procedure review.
a) The chapter Drug review deals about the ingredients of the Malahara and
Tailakalpana both in ayurveda & modern view, i.e about the first reference, its
first material, occurrence, synonyms according to different authorities, grahya &
agrahy lakshana, classification, pharmacological properties and pharmaceutical
processes according to different acharyas i.e shodhana, and marana, including its
indication in different diseases explained in detail.
b) Disease review deals about etomology, definition of Vicharchika, direct and
indirect references including its historical background, nidana, roopa, samprapti
and line of treatment according to various authorities.
c) In the same chapter next part deals about the modern concept of Vicharchika i.e.
Eczema starting from definition, causative factors, signs & symptoms and
treatment.
130
Summary
4. METHODOLOGY:- It deals about pharmaceutical, analytical & clinical study.
a. In pharmaceutical study detail explanation about Yashada shodhana,
Agnijarita Marana, Girisindhoora and Sasyaka shodhana, preparation of
Yashadamrita malahara and Sindhooradi taila is explained.
b. The analytical study deals about chemical analysis of Yashada bhasma,
Yashadamrita malahara and Sindhooradi taila carried out in Sri JT
pharmacy collage Gadag
c. In clinical study, repeated special camps were conducted by postgraduate
department of Rasashastra. D.G.M.A.M.C and Hospital Gadag. The
patients of Vicharchika after the complete diagnose were selected. The
clinical study was done application of the Yashadamrita malahara and
Sindhooradi taila in two groups for 21 days and the patients were accessed
for the same.
5. Results: Patients were observed on the basis of various angle i.e. demographic and
various disease relevant points. The patients were assessed according to the subjective
& objective criteria and results are given with the help of statistical values P & S.D
etc.
6. Discussion: First drug & disease discussion has been done in both the view i.e
ayurvedic as well as modern aspect. In the part of pharmaceutical discussion,
rationalities behind shodhana, marana, malahara and taila kalpana were discussed
appropriately. In analytical discussion role of physico-chemical analysis of Yashada
bhasma, malahara and taila kalpana is discussed and in clinical discussion, discussion
about the Vicharchika patients as well as probable mode of action of Yashadamrita
malahara and Sindhooradi taila in Vicharchika is explained.
7. Conclusion: The essence of the research work has been reported.
131
Bibilography
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41. Madanapala Madanapala nighantu 4th chapter shloka 12, Khemraj Krishnadas,
Mumbai; Sarvadhika prakashana; page 99. 42. Shri Sadhanandha sharma Rasatarangini 19th chapter shloka 121-123, Kashinath
shastri 11th edition, Varanasi; Motilal Bhanarasidas; 2000 pp-479. 43. Shri Madavachrya Ayurveda prakash 3rd chapter shloka 183, Shri Gulraj Sharma
mishra 1st edition, Varanasi; Chawkhambha samscrit bharati academy; 1999 pp-381. 44. Budheva mukharji Rasajala nidhi vol 3. 2nd chapter, Siddhinandana mishra
2nd edition, Varanasi; Chawkhambha Samskrita bhavana; 1998 pp-96. 45. Jadavaji Trikamaji Rasamritam 25th chapter shloka 116, Dr Damodara joshi 1st
edition, Varanasi; Chawkhambha samskrit bhavan; 1998 pp-83. 46. Sri Bhavamishra Bhavaprakasha Nighantu 7th chapter shloka 33, Sri Brahmashankar
mishra 6th edition, Varanasi; chawkhambha Sanskrit samsthana ; 1984 pp 606. 47. Nrupamadanapala Madanapala nighantu 4th chapter shloka 12, Khemraj Krishnadas,
Mumbai; Sarvadhika prakashana; page 99. 48. Shri Sadhanandha sharma Rasatarangini 19th chapter shloka 148, Kashinath shastri
11th edition, Varanasi; Motilal Bhanarasidas; 2000 pp-483. 49. B.S.Bowl and G.D.Sharma Modern approach alimentary inorganic chemistry
chapter 2nd edition, New delhi;S.Chand and company;1980 pp-235-37 50. R.Ghosh’s Pharmacology Materia medica and therapeutics 5th chapter, S.S.Senagupta
23rd edition, Culcutta;Hilton and company;1976 pp-894-895. 51. Shri Sadhanandha sharma Rasatarangini 21st chapter shloka 148-149, Kashinath
shastri 11th edition, Varanasi; Motilal Bhanarasidas; 2000 pp-547. 52. Rasa vagabhata Rasa ratna Samuchchaya 3rd chapter shloka 145, Pandit
Dharmanandha Sharma 2nd edition, Varanasi; Motilal Banarasidas; 1996 pp-41. 53. Jadavaji Trikamaji Rasamritam 18th chapter shloka 108, Dr Damodara joshi 1st
edition, Varanasi; Chawkhambha samskrit bhavan; 1998 pp-76. 54. Budheva mukharji Rasajala nidhi vol 2. 3rd chapter, Siddhinandana mishra
2nd edition, Varanasi; Chawkhambha Samskrita bhavana; 1998 pp-222. 55. Sri Bhavamishra Bhavaprakasha Nighantu 7th chapter shloka 76, Sri Brahmashankar
mishra 6th edition, Varanasi; chawkhambha Sanskrit samsthana ; 1984 pp 611.
Bibilography
56. Kaidevacharya Kaideva nighantu 2nd chapter shloka 66-67, Proff.P.V.Sharma 1st
edition, Varanasi; Choukumba orientalia; 1979 pp-284. 57. Nrupaadanapala Madanapala nighantu 4th chapter shloka 35, Khemraj Krishnadas,
Mumbai; Sarvadhika prakashana; page 103. 58. Bajandas swami Dadupant Rasadarpana voll 1st 6th chapter, 3rd edition, Rohatak; Nath
pustak bhandar; pp-139. 59. Shri Sadhanandha sharma Rasatarangini 21st chapter shloka 150, Kashinath shastri
11th edition, Varanasi; Motilal Bhanarasidas; 2000 pp-547. 60. Rasa vagabhata Rasa ratna Samuchchaya 3rd chapter shloka 157, Pandit
Dharmanandha Sharma 2nd edition, Varanasi; Motilal Banarasidas; 1996 pp-42. 61. Budheva mukharji Rasajala nidhi vol 2. 3rd chapter, Siddhinandana mishra
2nd edition, Varanasi; Chawkhambha Samskrita bhavana; 1998 pp-224. 62. Rasa vagabhata Rasa ratna Samuchchaya 3rd chapter shloka 146, Pandit
Dharmanandha Sharma 2nd edition, Varanasi; Motilal Banarasidas; 1996 pp-41. 63. Shri Dhanvantari Dhanvantari nighantu 3rd chapter shloka 98, Dr. P.V.Sharma 1st
edition, Varanasi; Choukumba orintalia; 1982 pp-108. 64. Sri Bhavamishra Bhavaprakasha Nighantu 7th chapter shloka 77, Sri Brahmashankar
mishra 6th edition, Varanasi; chawkhambha Sanskrit samsthana ; 1984 pp 611. 65. Narahari Rajnighantu 13th chapter shloka 52, Indradev tripati 2nd edition, Varanasi;
chawkhambha Sanskrit series; 1998 pp 439. 66. Acharya somadheva Rasendra chudamani 10th chapter shloka 106, Dr Siddinandan
mishra 2nd edition, Varanasi; Chawkhambha orientalia; 1999 pp-195. 67. Rasa vagabhata Rasa ratna Samuchchaya 3rd chapter shloka 146, Pandit
Dharmanandha Sharma 2nd edition, Varanasi; Motilal Banarasidas; 1996 pp-41. 68. Shri Sadhanandha sharma Rasatarangini 21st chapter shloka 151, Kashinath shastri
11th edition, Varanasi; Motilal Bhanarasidas; 2000 pp-548. 69. Acharya somadheva Rasendra chudamani 10th chapter shloka 106, Dr Siddinandan
mishra 2nd edition, Varanasi; Chawkhambha orientalia; 1999 pp-195. 70. Sri Bhavamishra Bhavaprakasha Nighantu 7th chapter shloka 77, Sri Brahmashankar
mishra 6th edition, Varanasi; chawkhambha Sanskrit samsthana ; 1984 pp 611.
Bibilography
71. Nrupaadanapala Madanapala nighantu 4th chapter shloka 36, Khemraj Krishnadas,
Mumbai; Sarvadhika prakashana; page 103. 72. Jadavaji Trikamaji Rasamritam 18th chapter shloka 109, Dr Damodara Joshi 1st
edition, Varanasi; Chawkhambha samskrit bhavan; 1998 pp-77. 73. Kaidevacharya Kaideva nighantu 2nd chapter shloka 67-68, Prof. P.V.Sharma 1st
edition, Varanasi; Choukumba orientalia; 1979 pp-284. 74. Shri Dhanvantari Dhanvantari nighantu 3rd chapter shloka 98, Dr. P.V.Sharma 1st
edition, Varanasi; Choukumba orintalia; 1982 pp-108. 75. Jadavaji Trikamaji Rasamritam 18th chapter, Dr Damodara joshi 1st edition, Varanasi;
Chawkhambha samskrit bhavan; 1998 pp-77. 76. B.S.Bowl and G.D.Sharma Modern approach alimentary inorganic chemistry
chapter 2nd edition, New delhi;S.Chand and company;1980 pp-293-94 77. R.Ghosh’s Pharmacology Materia medica and therapeutics 5th chapter, S.S.Senagupta
23rd edition, Culcutta;Hilton and company;1976 pp-889. 78. Jadavaji Trikamaji Rasamritam 22nd chapter shloka 72, Dr Damodara Joshi 1st
edition, Varanasi; Chawkhambha samskrit bhavan; 1998 pp-57. 79. Shri Sadhanandha sharma Rasatarangini 21st chapter shloka 71, Kashinath shastri
11th edition, Varanasi; Motilal Bhanarasidas; 2000 pp-533. 80. Bajandas swami Dadupant Rasadarpana voll 1st 4th chapter, 3rd edition, Rohatak;
Nath pustak bhandar; pp-196. 81. Narahari Rajnighantu 13th chapter shloka 101, Indradev tripati 2nd edition, Varanasi;
chawkhambha Sanskrit series; 1998 pp 448. 82. Sri Bhavamishra Bhavaprakasha Nighantu 7th chapter shloka 66, Sri Brahmashankar
mishra 6th edition, Varanasi; chawkhambha Sanskrit samsthana ; 1984 pp 610. 83. Shri Dhanvantari Dhanvantari nighantu 3rd chapter shloka 130, Dr. P.V.Sharma 1st
edition, Varanasi; Choukumba orintalia; 1982 pp-114. 84. Nrupaadanapala Madanapala nighantu 4th chapter shloka 30, Khemraj Krishnadas,
Mumbai; Sarvadhika prakashana; page 102. 85. Rasa vagabhata Rasa ratna Samuchchaya 2rd chapter shloka 119, Pandit
Dharmanandha Sharma 2nd edition, Varanasi; Motilal Banarasidas; 1996 pp-21.
Bibilography
86. Shri Sadhanandha sharma Rasatarangini 21st chapter shloka 72, Kashinath shastri
11th edition, Varanasi; Motilal Bhanarasidas; 2000 pp-534. 87. Rasa vagabhata Rasa ratna Samuchchaya 2rd chapter shloka 123, Pandit
Dharmanandha Sharma 2nd edition, Varanasi; Motilal Banarasidas; 1996 pp-22. 88. Shri Sadhanandha sharma Rasatarangini 21st chapter shloka 106-112, Kashinath
shastri 11th edition, Varanasi; Motilal Bhanarasidas; 2000 pp-541. 89. Acharya somadheva Rasendra chudamani 10th chapter shloka 75, Dr Siddinandan
mishra 2nd edition, Varanasi; Chawkhambha orientalia; 1999 pp-152. 90. Budheva mukharji Rasajala nidhi vol 2. 1st chapter, Siddhinandana mishra
2nd edition, Varanasi; Chawkhambha Samskrita bhavana; 1998 pp-111. 91. Jadavaji Trikamaji Rasamritam 22nd chapter shloka 74, Dr Damodara Joshi 1st
edition, Varanasi; Chawkhambha samskrit bhavan; 1998 pp-58. 92. Shri Sadhanandha sharma Rasatarangini 21st chapter shloka 127-129, Kashinath
shastri 11th edition, Varanasi; Motilal Bhanarasidas; 2000 pp-543. 93. Rasa vagabhata Rasa ratna Samuchchaya 2rd chapter shloka 122, Pandit
Dharmanandha Sharma 2nd edition, Varanasi; Motilal Banarasidas; 1996 pp-22. 94. Shri Madavachrya Ayurveda prakash 4rd chapter shloka 38, Shri Gulraj Sharma
mishra 1st edition, Varanasi; Chawkhambha samscrit bharati academy; 1999 pp-417. 95. Jadavaji Trikamaji Rasamritam 22nd chapter shloka 73, Dr Damodara Joshi 1st
edition, Varanasi; Chawkhambha samskrit bhavan; 1998 pp-58. 96. Bajandas swami Dadupant Rasadarpana voll 1st 4th chapter, 3rd edition, Rohatak;
Nath pustak bhandar; pp-198. 97. Budheva mukharji Rasajala nidhi vol 2. 1st chapter, Siddhinandana mishra
2nd edition, Varanasi; Chawkhambha Samskrita bhavana; 1998 pp-111. 98. Acharya somadheva Rasendra chudamani 10th chapter shloka 74, Dr Siddinandan
mishra 2nd edition, Varanasi; Chawkhambha orientalia; 1999 pp-152. 99. Narahari Rajnighantu 13th chapter shloka 102, Indradev tripati 2nd edition,
Varanasi; chawkhambha Sanskrit series; 1998 pp 448. 100. Shri Dhanvantari Dhanvantari nighantu 3rd chapter shloka 131-132, Dr. P.V.Sharma
1st edition, Varanasi; Choukumba orintalia; 1982 pp-114.
Bibilography
101. Shri Bhavamishra Bhavaprakasha Nighantu 7th chapter shloka 67-68, Sri
Brahmashankar mishra 6th edition, Varanasi; Chawkhambha Sanskrit samsthana; 1984 pp 611.
102. Nrupaadanapala Madanapala nighantu 4th chapter shloka 31, Khemraj Krishnadas,
Mumbai; Sarvadhika prakashana; page 102. 103. Shri Sadhanandha sharma Rasatarangini 21st chapter shloka 129, Kashinath shastri
11th edition, Varanasi; Motilal Bhanarasidas; 2000 pp-543. 104. Rasa vagabhata Rasa ratna Samuchchaya 2rd chapter shloka 122, Pandit
Dharmanandha Sharma 2nd edition, Varanasi; Motilal Banarasidas; 1996 pp-22. 105. Jadavaji Trikamaji Rasamritam 22nd chapter shloka 73, Dr Damodara Joshi 1st
edition, Varanasi; Chawkhambha samskrit bhavan; 1998 pp-58. 106. Budheva mukharji Rasajala nidhi vol 2. 1st chapter, Siddhinandana mishra
2nd edition, Varanasi; Chawkhambha Samskrita bhavana; 1998 pp-111. 107. Bajandas swami Dadupant Rasadarpana voll 1st 4th chapter, 3rd edition, Rohatak;
Nath pustak bhandar; pp-198. 108. Acharya somadheva Rasendra chudamani 10th chapter shloka 74, Dr Siddinandan
mishra 2nd edition, Varanasi; Chawkhambha orientalia; 1999 pp-152. 109. Shri Madavachrya Ayurveda prakash 4rd chapter shloka 39, Shri Gulraj Sharma
mishra 1st edition, Varanasi; Chawkhambha samscrit bharati academy; 1999 pp-417.
110. Narahari Rajnighantu 13th chapter shloka 102, Indradev tripati 2nd edition, Varanasi;
chawkhambha Sanskrit series; 1998 pp 448. 111. Shri Dhanvantari Dhanvantari nighantu 3rd chapter shloka 131-132, Dr. P.V.Sharma
1st edition, Varanasi; Choukumba orintalia; 1982 pp-114. 112. Sri Bhavamishra Bhavaprakasha Nighantu 7th chapter shloka 67-68, Sri
Brahmashankar mishra 6th edition, Varanasi; chawkhambha Sanskrit samsthana; 1984 pp 611.
113. Nrupaadanapala Madanapala nighantu 4th chapter shloka 31, Khemraj Krishnadas,
Mumbai; Sarvadhika prakashana; page 102. 114. B.S.Bowl and G.D.Sharma Modern approach alimentary inorganic chemistry
chapter 2nd edition, New delhi;S.Chand and company;1980 pp-326-327.
Bibilography
115. R.Ghosh’s Pharmacology Materia medica and therapeutics 5th chapter,
S.S.Senagupta 23rd edition, Culcutta;Hilton and company;1976 pp-897-898. 116. Vaidya V.M.Gogate Ayurvedic pharmacology and therapeutic uses of medicinal
plants, Shri Ramakrishnan 1st edition, Mumbai;Bharatiya vaidya bhavana; 2000 pp-296.
117. Internet PMID, 16192673, 16085379, 10624886 (indexed for medicine) 118. Vaidya V.M.Gogate Ayurvedic pharmacology and therapeutic uses of medicinal
plants, Shri Ramakrishnan 1st edition, Mumbai;Bharatiya vaidya bhavana; 2000 pp-524.
119. K Raghunath and Miss Rama mitra Pharmacognacy of indigenous drugs voll II, Ist
edition, New Delhi; central council for reference in Ayurveda and sidda; 1982 pp-389.
120. Vaidya V.M.Gogate Ayurvedic pharmacology and therapeutic uses of medicinal
plants, Shri Ramakrishnan 1st edition, Mumbai;Bharatiya vaidya bhavana; 2000 pp-736.
121. Internet PMID,12113324, 11731065, 6526069 ( indexed for medicine) 122. Shri Sadhanandha sharma Rasatarangini 18th chapter shloka 47 to 67, Kashinath
shastri 11th edition, Varanasi; Motilal Bhanarasidas; 2000 pp- 446 to 449. 123. Sushruta Acharya Sushruta samhita suthra 46th chapter shloka 39 to 40, Abikadatta
shastri 12th edition, Varanasi; Chawkahmbha samskrita bhavana; 2001 pp-178. 124. Vagabhatacharya Astanga sangraha 6th chapter shloka 69 to 70, Dr Ravidatta tripati
3rd edition, New delhi; Chawkhambha samskrita pratisthana; 2001 pp- 101 to 102. 125. Sushruta Acharya Sushruta samhita suthra 46th chapter shloka 128, Abikadatta
shastri 12th edition, Varanasi; Chawkahmbha samskrita bhavana; 2001 pp-186. 126. Bhavamishra Bhavaprakash 21st chapter shloka 2 , Shri Bhramha shankara shastri
5th edition, Varanasi; Chawkhambha samskrit series; 1969 pp-783. 127. Sushruta Acharya Sushruta samhita suthra 46th chapter shloka 37, Abikadatta
shastri 12th edition, Varanasi; Chawkahmbha samskrita bhavana; 2001 pp-191. 128. Vaidya V.M.Gogate Ayurvedic pharmacology and therapeutic uses of medicinal
plants, Shri Ramakrishnan 1st edition, Mumbai;Bharatiya vaidya bhavana;2000 pp-412.
Bibilography
129. Amarasimha, Amarakosha, Varanasi, Chaukhamba Sanskrit series, 1970, 2-6-53.
130. Agnivesha, Charaka Samhita Part-II, Chikitsa Sthana 7th chapter Sloka 13 &26, Ganga Sahaya Pandya ed,Varanasi; Chaukhamba Sanskrit Samsthana; 1994 pp-250-252.
131. Acharya Sushruta Sushruta Samhita Part-I, Nidana Sthana 5th chapter, Sloka13 Ambikadatta Sastry 11th edition, Varanasi; Chaukhamba Sanskrit Samsthan; 1997 pp- 247-248.
132. Agnivesha Charka Samhita Redacted by Charaka and Dridabala with Ayurveda Dipika Commentary by Chakrapanidatta, Chikitsa Sthana 7th chapter 9th Sloka, Y.T. Acharya ed, Varanasi; Chaukhamba Surabharati Prakashana; 2000 pp-450.
133. Acharya Sushruta Sushruta Samhita Nibanda Sangraha Commentary by Dalhanacharya, Chikitsa Sthana, 5th chapter, 3rd Sloka, Y.T. Achary ed, Varanasi; Krishnadas Academy; 1998 pp424.
134. Vagbhata Ashtanga Hrudaya Commentaries of Arunadatta Hemadri Nidana Sthana 14th chapter 3rd Sloka, Sadashiva Shastry ed, Varanasi; Chaukhamba Surabharati Prakashana;2002 pp 524.
135. Agnivesha Charaka Samhita Part-II Chikitsa Sthana 7th chapter 26th Sloka, Ganga Sahaya Pandya ed, Varanasi; Chaukhamba Sanskrit Samsthana; 1994 pp-252.
136. Acharya Sushruta Sushruta Samhita Part-I Nidana Sthana 5th chapter 13th Sloka, Ambikadatta Shastry 11th edition, Varanasi; Chaukhamba Sanskrit Samsthan; 1997 pp-248.
137. Vagbhata Ashtanga Hrudaya Commentaries of Arunadatta Hemadri Nidana Sthana 14th chapter 18th Sloka, Sadashiva Shastry ed, Varanasi; Chaukhamba Surabharati Prakashana;2002 pp 525.
138. Agnivesha Charka Samhita Redacted by Charaka and Dridabala with Ayurveda Dipika Commentary by Chakrapanidatta, Chikitsa Sthana 1st chapter 10th Sloka, Y.T. Acharya ed, Varanasi; Chaukhamba Surabharati Prakashana; 2000 pp-195.
139. Ibid 7th chapter, 37-38 Slokas, pp-452.
140. Ibid 7th chapter, 39th Sloka, pp-452.
141. Acharya Sushruta Sushruta Samhita Nibanda Sangraha Commentary by Dalhanacharya, Chikitsa Sthana 9th chapter 43rd Sloka, Y.T. Achary ed, Varanasi; Krishnadas Academy; 1998 pp-446.
142. Ibid 6th Sloka, pp-442p.
Bibilography
143. Vagbhata Ashtanga Hrudaya Commentaries of Arunadatta Hemadri Nidana sthana 19th chapter 1-3 Sloka, Sadashiva Shastry ed, Varanasi; Chaukhamba Surabharati Prakashana;2002 pp-711.
144. Department of Health, The Ayurvedic Formulary of India Part-I, 1st edition, Delhi; Controller of publications; 1978 pp-300.
145. API Text book of Medicine, Siddartha N. Shah, 7th edition, Published by physicians of India, Mumbai; pp-187.
146. Practice of Dermatology by P.N. Behl, 7th edition, CBS Publishers and distributors, New Delhi; pp-129.
147. David Sons Principles and Practice of Medicine, Christopher Haslett, Edvin R Chilvers, John A.A. Hunter, Churchil living stone, 19th ed, Edinburgh; pp-1072.
148. Ibid
149. Recent Advances in Allergy, George W. Bray, 2nd ed, London; J and A Churchill Ltd., 1934 pp-5.
150. Principles of Anatomy and Physiology, Gerard J. Tortora, Bonnie Roesch ed, Johnwiley and sons Inc, New York; 2001 pp-798.
151. Frenchs index of Differential Diagnosis 11th edition, F.Dudley Heart ed, Great Briton, Bristol, John right and Sons Ltd; 1979 pp-821.
152. Text book of Pathology, Harshmohan, Jaypee brothers Medical Publisher Pvt. Ltd, 5th ed, New Delhi; 2005 pp-796.
153. Frenchs index of Differential Diagnosis, F.Dudley Heart 11th edition, Great Briton, Bristol, John right and Sons Ltd; 1979 pp-821-822.
154. David Sons Principles and Practice of Medicine, Christopher Haslett Edvin R Chilvers, John A.A. Hunter,19th edition, Churchil living stone Edinburgh; pp-896, 1055,1056.
155. Ibid pp-1074.
Bibilography
Special clinical trial proforma for Vicharchika
Post graduate and research center (Rasashastra)
Shri D.G.M. Ayurvedic Medical College,Gadag.
Guide : Dr.M.C.Patil Dr. Sobagin.M.V M.D(Ayu) P.G.Scholar Co guide: Dr.G.N.Danappagoudar M.D.(Ayu) Sl.No. 1.Name of the patient: O.P.D. No. 2.Father’s Name/ Husband’s Name: D.O.I. D.O.C
3.Age: 4. Sex:
Male Female
Hindu Muslim Christian Others 5. Religion:
Student House wife Agriculture Others 6. Occupation 7.Educational status:
Poor Middle Higher 8.Economical status: 9.Marital status: Married Unmarried 10.Address: Tel- 11. Result: Well responded Responded Not responded 12.Concent: I -------- -------- Son / Daughter / Wife of----------- Exercise my free will in
the said study, I have been informed to my satisfaction by attending the purpose of the clinical evaluation and nature of drug treatment. I am also aware of my right to quit at any time during the schedule.
Investigator’s signature Patient’s signature
A) Pradhana Vedana
Sl.No. Complaints P/A Duaration 1 Varna 2 Pidika 4 Srava 5 Kandu 6 Vedana vishesha
B) Anubandhi Vedana (Savadhi). C) Vedana Vrittanta. Specific enquires in following headings:
Sudden Gradual Insidious Mode of onset: Course: Episodic Continous Initially episodic
Duration: Periodicity: Seasonal Irregular Aggravating Trauma Climate Infections Drugs Others Factors: D) Poorva Vyadhi Vrittanta. E) Chikitsa Vrittanta: F) Koutumbika Vrittanta:
G) Vayaktika vrittanta: 1) Ahara: Vegetarian Mixed diet Dominant Rasa in food 2) Vihara: Tea Coffee Tobacco Alcohol
Smoking Gutaka Others 3) Vyasana: 4) Jataragni bala: Pravara Madhyama Avara Sama 5)Rajaha: Regular Irregular Menopause H) Rogi pareeksha: Samanya pareeksha:
Pulse rate bpm Blood Pressure mm of Hg
Pulse rhythm Heart rate /min
Respiration rate /min Skin(hard/smooth)
Temparature oF Skin colour
Ashtasthana pareeksha:
Sl.No. Sl.No.
1 Nadi 5 Shabdha
2 Mala 6 Sparsha
3 Mootra 7 Drika
4 Jivha 8 Akruti
Dashavidha Pareeksha: 1) Shareera prakriti: V P K VP KP VK VPK
2) Manasa prakriti: V P K VP KP VK VPK
Pravara Madhyma Avara 3) Sara:
4) Samhanana: Pravara Madhyma Avara
5) Satmya: Pravara Madhyma Avara
Pravara Madhyma Avara 6) Satwa: 7) Vyayama shakti: Pravara Madhyma Avara 8) Vaya: Bala Youvana Vrudda
Jangala Anupa Sadharana 9) Desha:
10) Akriti:
Vikrititaha pareeksha: 1) Nidana: 2) Poorva Roopam: 3) Roopa:
4) Samprapti: Dosha Dushya
Adhistana Srotas Srotodusti Rogamarga
5) Upashaya & Anupashaya:
Upashaya Anupashaya
6. Upadrava:
Jwara Hrillasa Kshaya Arochaka Swarabheda
7. Arista Lakshanas: 8. Sadhyasadhyata: I) Special examination of Vicharchika
Treatment shedule
After
Before 7th day 21st day Fallow up
VARNA Shyava Shyvalohita Rakta Tamra PIDIKA Swabhava
Sankhya
Sthana Akara Varna SRAVA Varna Gandha Pramana Swaroopa KANDU Adhishtana Avadhi Prakopaka kala VEDANA VISHESHA
Adhishtana Avadhi Prakopaka kala
J) Lab Investigations:
Before After DC Before After Hb % gm % gm % N % % ESR mm/h mm/h E % % RBS mg/dl mg/dl B % % TC % % M % % AEC Cells/Cumm Cells/Cumm L % %
K) Chikithsa: Yoga : Yashdamrita Malahara & Sindhooradi taila
Posology : Required quantity
Duration of treatment: 21 days . Follow Up -15 days
L) Pathya: M) Apathya: N) Investigators Note: Signature of Guide Signature of Scholar
MASTER CHART-I
Demographic Data of GROUP-A
Sex
Education
Marital
status
Religion
Occupation
Economical Status
OPD
Age
M F Ed UEd M Un M H M O A ST HW E Bu PC MC HC
1154 42 + - + + - + - - - - - + - - + -
1198 35 + - + - + - + - - + - - - - + - -
2351 55 + - - + + - + - - + - - - - - + -
2490 45 + - + - + - + - - - - - - + - + -
2553 38 - + - + + - + - - - - + - - + - -
2600 37 + - - + + - + - - + - - - - - + -
2948 22 + - + - - + + - - - + - - - - + -
3153 44 - + - + + - + - - - - + - - - + -
3432 45 + - + - + - + - - - - - + - - + -
3908 60 - + - + + - + - - - - + - - + - -
3922 40 + - + + - + - - - - - + - - + -
3985 17 + - + - - + + - - - + - - - + - -
4051 40 + - + - + - + - - + - - - - - + -
4115 18 + - + - - + + - - - + - - - - + -
4118 48 - + + - + - - + - - - + - - + - -
M=Male, F=Female, Ed=Education, UEd=Uneducated, M=Muslim, H=Hindu, O=Others, HW=House Wife, E=Employee,
Bu=Business, PC=Poor Class, MC=Middle Class, HC=High Class, A=Agriculture, ST=Student, SE=Secondary Education
MASTER CHART-II Demographic Data of GROUP-B.
Sex Education Marital status Religion Occupation Economical Status
OPD
Age
M F Ed UEd M Un M H M O A ST HW E Bu PC MC HC
1102 27 + + - - + - - + - - - - + - + -
1179 50 + + - + - + - - - - - + - - + -
2320 60 + - + - + - + - - - - - - + - + -
2484 38 + - - + + - + - - + - - - - - + -
2545 25 + - - + - + + - - - - - + - + - -
2557 45 - + - + + - + - - - - + - - - + -
2837 32 + - + - + - + - - + - - - - + - -
3103 41 + - - + + - - + - - - - - + - + -
3430 22 + - + - - + + - - - + - - - - + -
3635 48 - + + - - + + - - - - + - - - + -
3436 50 - + - + + - + - - - - + - - - + -
3439 25 + - + - - + - + - - - - - + - + -
4043 50 + - + - + - - + - - - - - + - + -
4068 37 + - + - + - + - - + - - - - - + -
4132 44 - + - + + - + - - - - + - - - + -
M=Male, F=Female, Ed=Education, UEd=Uneducated, M=Muslim, H=Hindu, O=Others, HW=House Wife, E=Employee,
Bu=Business, PC=Poor Class, MC=Middle Class, HC=High Class, A=Agriculture, ST=Student, SE=Secondary Education
UnM= Un Married
SHLOKA
Preparation of Yashadamrita malahara:
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£ddy¬dIz¶I¶e«d£da QØd£dŠ Sd¯dQa ®de²¦d¡ddeT£d«dŠ ||
šd¬®dyíe£d«d±dmPddy ´dgQy„ «dQ‰SdyQe£dSd£¦d£dZ |
±d«ddšSdd£ddy «d¬ddUµTdy Sd¯dQd«dm£d ±daëdI¶Z ||
RT 19/146-147 Preparation of Sindhooradi taila
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e¦d¯ddI‰¶§dÎdI¶¬I¶¦£dg QS¥ddeÙa¯de£d£ddy¬dI¶«dŠ ||
§d¬ddye¦«d£da¢Ÿd e±daQjTa £dg£Sda Te™£dŸd£dgÝSd«dŠ |
£dz¬d§ddI¶e®d¥dd¦dy¦d §ddŸdSdyÏdz¬d§ddI¶e®d£dŠ ||
e±daQjTd¥Sde«dQa £dz¬da eªd°de›ªdZ §deTI¶fe£d‰£d«dŠ |
§dd«dde®dŸdeŸd‰I¶|±R¶dyLµ´d£dI¶PNjµe£dI¶d§dUµ«dŠ ||
RT- 21/162-164