Pharmacognosy Lecture # 5+6 (Tannins) [By, Sir Tanveer Khan]

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Tannins Muhammad Tanveer Khan

description

Study of Tannins according to Pharmacognosy. Lecture delivered by Muhammad Tanveer Khan to Batch:01093 (F09) in The University of Lahore, Pakistan.

Transcript of Pharmacognosy Lecture # 5+6 (Tannins) [By, Sir Tanveer Khan]

Page 1: Pharmacognosy Lecture # 5+6 (Tannins) [By, Sir Tanveer Khan]

Tannins

Muhammad Tanveer Khan

Page 2: Pharmacognosy Lecture # 5+6 (Tannins) [By, Sir Tanveer Khan]

Introduction

The term tannin was first time coined by Seguin in 1796. This term was used to denote substances present in plant extract which react with protein of animal hide, prevent their putrefaction and convert hide and skin into leather.

Page 3: Pharmacognosy Lecture # 5+6 (Tannins) [By, Sir Tanveer Khan]

Definition

“Complex substances that usually occur as mixtures of polyphenols that are very difficult to separate since they don't

crystallize, are called tannins”.

OR

“Tannins are polyhydroxy phenolic compounds”.

Page 4: Pharmacognosy Lecture # 5+6 (Tannins) [By, Sir Tanveer Khan]

Physical Properties

Color:

Dark brown or reddish brown

Taste:

Puckering taste

State:

Non-crystalline

Solubility:

Soluble in water, alcohol, dilute alkalis, glycerols and acetone.

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Chemical properties

(i )Precipitation

(ii )Anti-oxidizing properties

(iii )Astringent

(iv )Carcinogenicity

(v )Reaction with salts

(vi )Reaction with potassium ferricyanide and ammonia

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(i )PrecipitationTannins have ability to precipitate solutions of;

Gelatin

Alkaloids

Glycosides

Heavy metals

Proteins

(ii )Anti-oxidizing properties

Because of accumulation of OH group on small size nucleus, these agents have anti-oxidant nature .

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(iii )Astringent

Tannins have property to react with protein of mucous membrane and cause precipitation.

(iv )Carcinogenicity

Prolong use of tannin containing plant material is hazardous because it causes cancer. Habitual use of Areca catechu can cause oral and esophageal cancer.

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(v )Reaction with salts

(vi )Reaction with potassium ferricyanide and ammonia

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Importance of tannins

Medicinal Uses:AntidoteAntisepticAlgicidalsAstringentsAnti-carcinogenic

Industrial Uses:

Ink manufacture

Vegetable tanning

Preservatives

Biological Activities:Inhibition of lipid per oxidationDecrease in blood urea nitrogen contentInhibition of plasminLipolysis in fat cells

Page 10: Pharmacognosy Lecture # 5+6 (Tannins) [By, Sir Tanveer Khan]

Chemical Classification

Based on identity of phenolic nuclei involved and on the way they are joined.

Tannins

Hydrolysable tannins Condensed tannins Complex tannins

Page 11: Pharmacognosy Lecture # 5+6 (Tannins) [By, Sir Tanveer Khan]

(i )Hydrolysable tanninsThese tannins are hydrolyzed by enzymes or acids.

Precursors:Phenolic acid )Gallic acid, Ellagic acid(Glucose residueBetween phenolic acids and glucose sugar, there is ester linkage

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Properties:

Types:

Hydrolysable tannins

Gallitannins Ellagitannins

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GallitanninsEllagitannins

OccurrenceRhubarb

Clove

Hamamelis

Pomegranate

Eucalyptus

HydrolysisUpon acid hydrolysis of Gallitannins, Gallic acid is produces.

Upon acid hydrolysis of Ellagitannins, Ellagic acid is produces.

Properties *Rapidly soluble in water.

*Free Gallic acid, in plant, is converted to gluco Gallitannins.

*Slowly soluble in water.

*Present in plants in open and ring forms as Hexa hydroxy diphenic acid.

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(ii )Condensed tanninsThese tannins are derivatives of Flavonoid, catechin, flavonol-3-4-diol.

Precursors:FlavonoidCatechinFlavonol-3-4-diol

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Properties:

Examples:

Hamamelis

Cinchona

Cinnamon

When heated with acids, these are self condensated, polymerized and converted to insoluble red colored complexes, called Phlobaphenes.

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(iii )Complex tanninsThese tannins are mixtures of both, hydrolysable and condensed tannins

Examples:TeaQuercusCastanea

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2nd ClassificationTannin is a substance which is detected qualitatively by tanning test )The Gold beater’s skin test( and quantitatively by its adsorption on standard hide powder.

Depending upon this, tannins are of two types;

True tannins

Pseudo tannins

Tannins

True tannins Pseudo tannins

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True tanninsPseudo tannins

Polyhydroxy phenolic compounds which convert animal hide to leather by precipitating proteins and give positive Gold beater’s skin test, are called true tannins .

Phenolic compounds of plant origin that don't convert animal hide to leather but do give positive Gold beater’s skin test, are called pseudo tannins.

Molecular weight is 1000-5000Molecular weight is less than true tannins.

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Identification tests

Color reaction:Tannins give color reaction with iron.

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Identification tests

Matchstick test:Dip matchstick in plant extract.Dry it.Moisten it with hydrochloric acid. And warm near flame.Wood will turn pink or red in color due to phloroglucinol.

Gelatin test:Solution of tannin )0.5%-1%( precipitates 1% solution of gelatin containing 10% sodium chloride.

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Identification testsPhenazone test:Take 5ml of aqueous extract of drug.

Add 0.5grams of sodium acid phosphate.

Warm it and cool.

Filter solution.

To the filtrate, add 2%solution of Phenazone.

Tannins will be precipitated.

Precipitates will be bulky and colored.

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Identification tests

Gold beater’s skin test:Gold beater’s skin is a membrane prepared from intestine of Ox and I behaves similarly to un tanned skin.

Soak a small piece of Gold beater’s skin in 2% hydrochloric acid.Rinse it with distilled water.Place it in solution to be tested for 5 minutes.Wash in water and transfer to 1% solution of ferrous sulphate.Black or brown color of skin indicates presence of tannins.

It is a quantitative test and +ive only for true tannins

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Identification tests

Catechin test:Catechin when heated with acid produce phloroglucinol. Phloroglucinol can be detected with matchstick test.

Test for chlorogenic acid:Treat extract containing chlorogenic acid with aqueous ammonia and expose it to air. Green color will appear gradually.

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a( HamamelisBotanical origin:

Hamamelis virginiana

Family:Hamamelidaceae

Part used:Dried leaves

Collection:Leaves are collected throughout summers. Drying is done in open air, preferably under shade to preserve green color.

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Constituents:

Gallitannins

Ellagitannins

Free gallic acid

Pro-anthocyanadins

Hamamelase

Uses:

Astringent

Anti-hemorrhagic

Anti-inflammatory

Anti-carcinogenic

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b( Catechu

Botanical origin:Uncaria gambir

Family:Rubiaceae

Part used:Dried aqueous extract from leaves and young twigs

Collection:Boil leaves and twigs in water. Evaporate to a pasty consistency. Paste is put in cubes and dried in sun.

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Constituents:

Catechin

Catechutannic acid

Catechu red

Quercitin

Gambir flourescin

Uses:

Astringent

Dying

Tanning industry

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c( Nutt gall

Botanical origin:

Quercus infectoria

Family:

Fagaceae

Part used:

Galls obtained from twigs

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Formation of galls:

Galls are pathological outgrowth formed on twigs of tree. Galls arise due to deposition of eggs by small insect Adleria galactinctoria.

Steps are;

Early summers, insects lay eggs on twigs

Larvae come out from eggs and enter soft epidermis.

Larvae secretes enzyme that stimulates abnormal growth around larvae.

Starch in the tissue gets converted to sugars and stimulate cell division.

Disappearance of starch causes cell shrinkage.

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Central cavity is formed in which larvae and pupae grows .

Larvae remains in gall for 5-6months.

Mature insect bores the covering of gall and escapes away.

Galls are collected before escaping of insect.

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Constituents:

Tannic acid

Gallic acid

Ellagic acid

Roburic acid

Syringic acid

Calcium oxalate crystals

Uses:

Haemostatic

Antidote for alkaloidal poisoning

Astringent