References - Information and Library Network...
Transcript of References - Information and Library Network...
References
References 9
9. References
Ali, H., York, P., Ali, A., & Blagden, N. (2011). Hydrocortisone nanosuspensions for
ophthalmic delivery: A comparative study between microfluidic nanoprecipitation and
wet milling. Journal of Controlled Release, 149, 175–181.
Ammar, H. O., Salama, H. A., Ghorab, M., & Mahmoud, A. A. (2006a). Formulation
and biological evaluation of glimepiride–cyclodextrin–polymer systems. International
Journal of Pharmaceutics 309 129–138.
Ammar, H. O., Salama, H. A., Ghorab, M., & Mahmoud, A. A. (2006b). Implication
of inclusion complexation of glimepiride in cyclodextrin–polymer systems on its
dissolution, stability and therapeutic efficacy. International Journal of Pharmaceutics
320 53–57.
Anton, N., & Vandamme, T. F. (2009). The universality of low-energy nano-
emulsification. International Journal of Pharmaceutics 377, 142-147.
Anton, N., & Vandamme, T. F. (2010). Nano-emulsions andMicro-emulsions:
Clarifications of the Critical Differences. Pharmaceutical Research, 28(5), 978-985.
Atef, E., & Belmonte, A. A. (2008). Formulation and in vitro and in vivo
characterization of a phenytoin self-emulsifying drug delivery system (SEDDS).
European Journal of Pharmaceutical Sciences, 35(4), 257–263.
Babu, R., & Pandit, J. (1999). Effect of aging on the dissolution stability of
glibenclamide/beta-cyclodextrin complex. Drug Developnent and Industrial
Pharmacy, 25(11), 1215-1219.
Bachhav, Y., & Patravale, V. (2009). SMEDDS of glyburide: formulation, in vitro
evaluation, and stability studies. AAPS PharmSciTech, 10(2), 482-487.
Bachhav, Y. G., & Patravale, V. B. (June 2009). SMEDDS of Glyburide:
Formulation, In Vitro Evaluation, and Stability Studies. AAPS PharmSciTech, 10(2),
482-487.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 143
References 9
Bassam M. Tashtoush, Zubaida S. Al-Qashi, & Najib, N. M. (2004). In Vitro and In
Vivo Evaluation of Glibenclamide in Solid Dispersion Systems. Drug Development
and Industrial Pharmacy, 30(6), 601–607.
Bilati, U., Allemann, E., & Doelker, E. (2005). Development of a nanoprecipitation
method intended for the entrapment of hydrophilic drugs into nanoparticles. European
Journal of Pharmaceutical Sciences 24 67–75.
Biradar, S. V., Dhumal, R. S., & Paradkar, A. (2009a). Rheological Investigation of
Self-emulsification Process. Journal of Pharmacy and Pharmaceutical Sciences
(www. cspsCanada.org), 12(1), 17- 31.
Biradar, S. V., Dhumal, R. S., & Paradkar, A. (2009b). Rheological Investigation of
Self-emulsification Process: Effect of Co-surfactant. Journal of Pharmacy and
Pharmaceutical Sciences (www. cspsCanada.org), 12(2), 164-174.
Bonfilio, R., Pires, S. A., Ferreira, L. M. B., Almeida, A. E. d., Doriguetto, A. C.,
Araújo, M. B. d., & Salgado, H. R. N. (2012). A discriminating dissolution method
for glimepiride polymorphs. Journal of Pharmaceutical Sciences, 101(2), 794-804.
Bouchemal, K., Briançon, S., Perrier, E., & Fessi, H. (2004). Nano-emulsion
formulation using spontaneous emulsification: solvent, oil and surfactant
optimisation. International Journal of Pharmaceutics 280, 241–251.
Brannon-Peppas, L., & Blanchette, J. (2004). Nanoparticle and targeted systems for
cancer therapy. Advanced Drug Delivery Reviews, 56, 1649-1659.
Brusewitz, C., Schendler, A., Funke, A., Wagner, T., & Lipp, R. (2007). Novel
poloxamer-based nanoemulsions to enhance the intestinal absorption of active
compounds. International Journal of Pharmaceutics 329, 173–181.
Buchanan, C., Alderson, S., Cleven, C., Dixon, D., Ivanyi, R., Lambert, J., . . . Szente,
L. (2002). Synthesis and characterization of water-soluble hydroxybutenyl
cyclomaltooligosaccharides (cyclodextrins). Carbohydrate Research, 337(6), 493-507.
Cerdeira, A. M., Mazzotti, M., & Gander, B. (2010). Miconazole
nanosuspensions:Influenceof formulation variables on particlesize reduction and
physical stability. International Journal of Pharmaceutics 396 210–218.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 144
References 9
Chakraborty, S., Shukla, D., Mishra, B., & Singh, S. (2009). Lipid – An emerging
platform for oral delivery of drugs with poor bioavailability. European Journal of
Pharmaceutics and Biopharmaceutics, 73, 1–15.
Chan, H. K., & Kwok, P. C. L. (2011). Production methods for nanodrug particles
using the bottom-up approach. Advanced Drug Delivery Reviews 63 406–416.
Chauhan, B., Shimpi, S., & Paradkar, A. (2005). Preparation and evaluation of
glibenclamide-polyglycolized glycerides solid dispersions with silicon dioxide by
spray drying technique. European Journal of Pharmaceutical Sciences, 26(2), 219-
230.
Chen, M.-L. (2008). Lipid excipients and delivery systems for pharmaceutical
development: A regulatory perspective. Advanced Drug Delivery Reviews, 60, 768–
777.
Chen, X., Young, T. J., Sarkari, M., Williams III, R. O., & Johnston, K. P. (2002).
Preparation of cyclosporine A nanoparticles by evaporative precipitation into aqueous
solution. International Journal of Pharmaceutics 242 3–14.
Cho, E., Cho, W., Cha, K.-H., Park, J., Kim, M.-S., Kim, J.-S., . . . Hwang, S.-J.
(2010). Enhanced dissolution of megestrol acetate microcrystals prepared by
antisolvent precipitation processusing hydrophilic additives. International
JournalofPharmaceutics 396 91–98.
Cirri, M., Maestrelli, F., Corti, G., Mura, P., & Valleri, M. (2007). Fast-dissolving
tablets of glyburide based on ternary solid dispersions with PEG 6000 and surfactants.
Drug Delivery 14(4), 247-255.
Cui, J., Yu, B., Zhaoe, Y., Zhu, W., Li, H., Lou, H., & Zhai, G. (2009). Enhancement
of oral absorption of curcumin by self-microemulsifying drug delivery systems.
International Journal of Pharmaceutics 371 148–155.
Cui, S., Zhao, C., Chen, D., & He, Z. (2005). Self-Microemulsifying Drug Delivery
Systems (SMEDDS) for Improving In Vitro Dissolution and Oral Absorption of
Pueraria Lobata Isoflavone. Drug Development and Industrial Pharmacy, 31, 349–
356.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 145
References 9
D'Addio, S. M., & Prud'homme, R. K. (2011). Controlling drug nanoparticle
formation by rapid precipitation. Advanced Drug Delivery Reviews, 63 417–426.
Dabhi, M. R., Limbani, M. D., & Sheth, N. R. (2011). Preparation and In Vivo
Evaluation of Self-Nanoemulsifying Drug Delivery System (SNEDDS) Containing
Ezetimibe. Current Nanoscience, 7, 616-627.
Dastmalchi, S., Garjani, A., Maleki, N., Sheikhee, G., Baghchevan, V., Jafari-Azad,
P., . . . Barzegar-Jalali, M. (2005). Enhancing dissolution, serum concentrations and
hypoglycemic effect of glibenclamide using solvent deposition technique. Journal of
Pharmacy and Pharmaceutical Sciences (www.cspscanada.org) 8(2), 175-181,.
Date, A. A., & Nagarsenker, M. S. (2007). Design and evaluation of self-
nanoemulsifying drug delivery systems (SNEDDS) for cefpodoxime proxetil.
International Journal of Pharmaceutics 329 166–172.
Date, A. A., & Patravale, V. B. (2004). Current strategies for engineering drug
nanoparticles. Current Opinion in Colloid & Interface Science, 9, 222– 235.
Derosa, G., & Sibilla, S. (2007). Optimizing combination treatment in the
management of type 2 diabetes. Vascular Health Risk Management, 3(5), 665–671.
Dhumal, R. S., Biradar, S. V., Yamamura, S., Paradkar, A. R., & York, P. (2008).
Preparation of amorphous cefuroxime axetil nanoparticles by sonoprecipitation for
enhancement of bioavailability. European Journal of Pharmaceutics and
Biopharmaceutics.
Dixit, R. P., & Nagarsenker, M. S. (2008). Self-nanoemulsifying granules of
ezetimibe: Design, optimization and evaluation. European Journal of Pharmaceutical
Sciences 35, 183–192.
Dong, Y., Ng, W., Shen, S., Kim, S., & Tan, R. (2011). Controlled antisolvent
precipitation of spironolactone nanoparticles by impingement mixing. International
JournalofPharmaceutics, 410(1-2), 175-179.
Douroumis, D., & Fahr, A. (2006). Nano- and micro-particulate formulations of
poorly water-soluble drugs by using a novel optimized technique. European Journal of
Pharmaceutics and Biopharmaceutics 63 173–175.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 146
References 9
Eerdenbrugh, B. V., Van den Mooter, G., & Augustijns, P. (2008). Top-down
production of drug nanocrystals: Nanosuspension stabilization, miniaturization and
transformation into solid products. International Journal of Pharmaceutics 364 64–75.
El-Laithy, H. M. (2008). Self-Nanoemulsifying Drug Delivery System for Enhanced
Bioavailability and Improved Hepatoprotective Activity of Biphenyl Dimethyl
Dicarboxylate. Current Drug Delivery, 5, 170-176.
Fukami, T., Furuishi, T., Suzuki, T., Hidaka, S., Ueda, H., & Tomono, K. (2006).
Improvement in Solubility of Poorly Water Soluble Drug by Cogrinding with Highly
Branched Cyclic Dextrin. Journal of Inclusion Phenomena and Macrocyclic
Chemistry, 56, 61–64.
Furlanetto, S., Cirri, M., Piepel, G., Mennini, N., & Mura, P. (2011). Mixture
experiment methods in the development and optimization of microemulsion
formulations. Journal of Pharmaceutical and Biomedical Analysis, 55(4), 610-617.
Galal, S., El- Massik, M., Abdallah, O., & Daabis, N. (2003). Formulation of fast
release glibenclamide liquid and semi-solid matrix filled capsules. Acta
Pharmaceutica 53 57–64.
Galindo-Rodr´ıguez, S. A., Puel, F. o., Brianc¸on, S., All´emann, E., Doelker, E., &
Fessi, H. (2005). Comparative scale-up of three methods for producing ibuprofen-
loaded nanoparticles. European Journal of Pharmaceutical Sciences 25 357–367.
Gao, L., Zhang, D., & Chen, M. (2008). Drug nanocrystals for the formulation of
poorly soluble drugs and its application as a potential drug delivery system. Journal of
Nanoparticle Research, 10, 845–862.
Grbic, S., Parojcic, J., Malenovic, A., Djuric, Z., & Maksimovic, M. (2010). A
Contribution to the Glimepiride Dissociation Constant Determination. Journal of
Chemical & Engineering Data, 55, 1368–1371.
Groop, L. C. (1992). Sulfonylureas in NIDDM. Diabetes Care 15(6), 737-754.
Hardman, J. G., & Limbird, L. E. (Eds.). (2001). Insulin, Oral Hypoglycemic Agents,
And the Pharmacology of the Endocrine Pancreas (10 ed.): McGraw Hill.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 147
References 9
Ilić, I., Dreu, R., Burjak, M., Homar, M., Kerc, J., & Srcic, S. (2009). Microparticle
size control and glimepiride microencapsulation using spray congealing technology.
International Journal of Pharmaceutics 381(2), 176-183.
Itoh, K., Pongpeerapat, A., Tozuka, Y., Oguchi, T., & Yamamoto, K. (2003).
Nanoparticle Formation of Poorly Water-Soluble Drugs from Ternary Ground
Mixtures with PVP and SDS. Chemical and Pharmaceutical Bulletin, 51(2), 171—
174
Ivanova, R., Lindman, B., & Alexandridis, P. (2000). Effect of glycols on the
selfassembly of amphiphilic block copolymers in water. 1. Phase diagrams and
structure identification. Langmuir, 16, 3660-3675.
Iwata, M., Fukami, T., Kawashima, D., Sakai, M., Furuishi, T., Suzuki, T., . . . Ueda,
H. (2009). Effectiveness of mechanochemical treatment with cyclodextrins on
increasing solubility of glimepiride. Pharmazie, 64, 390–394
Jacob, S., Shirwaikar, A., & Nair, A. (2009). Preparation and evaluation of fast-
disintegrating effervescent tablets of glibenclamide. Drug Developnent and Industrial
Pharmacy, 35(3), 321-328.
Joshi, M., Pathak, S., Sharma, S., & Patravale, V. (2008). Solid microemulsion
preconcentrate (NanOsorb) of artemether for effective treatment of malaria.
International Journal of Pharmaceutics 362 172–178.
Kakran, M., Sahoo, N. G., Lia, L., & Judeh, Z. (2010). Dissolution of
artemisinin/polymer composite nanoparticles fabricated by evaporative precipitation
of nanosuspension. Journal of Pharmacy and Pharmacology, 62, 413–421.
Kakran, M., Sahoo, N. G., Lia, L., Judeh, Z., Wang, Y., Chong, K., & Loh, L. (2010).
Fabrication of drug nanoparticles by evaporative precipitation of nanosuspension.
International Journal of Pharmaceutics, 383 285–292.
Kang, B. K., Lee, J. S., Chon, S. K., Jeong, S. Y., Yuk, S. H., Khang, G., . . . Choc, S.
H. (2004). Development of self-microemulsifying drug delivery systems (SMEDDS)
for oral bioavailability enhancement of simvastatin in beagle dogs. International
Journal of Pharmaceutics, 274, 65–73.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 148
References 9
Kawashima, Y. (2001). Nanoparticulate systems for improved drug delivery.
Advanced Drug Delivery Reviews, 47, 1-2.
Keck, C. M., & Müller, R. H. (2006). Drug nanocrystals of poorly soluble drugs
produced by high pressure homogenisation. European Journal of Pharmaceutics and
Biopharmaceutics, 62(1), 3-16.
Kelmann, R. G., Kuminek, G., Teixeira, H. F., & Koester, L. ı. S. (2007).
Carbamazepine parenteral nanoemulsions prepared by spontaneous emulsification
process. International Journal of Pharmaceutics(342 ), 231–239.
Kim, M.-S., Jin, S.-J., Kim, J.-S., Park, H. J., Song, H.-S., Neubert, R. H. H., &
Hwang, S.-J. (2008). Preparation, characterization and in vivo evaluation of
amorphous atorvastatin calcium nanoparticles using supercritical antisolvent (SAS)
process. European Journal of Pharmaceutics and Biopharmaceutics, 69 454–465.
Kipp, J. E., Wong, J. C. T., Doty, M. J., & Rebbeck, C. L. (2004). Microprecipitation
method for preparing submicron suspensions. Journal of Controlled Release, 45.
Klein, S., Wempe, M., Zoeller, T., Buchanan, N., Lambert, J., Ramsey, M., . . .
Buchanan, C. (2009). Improving glyburide solubility and dissolution by complexation
with hydroxybutenyl-beta-cyclodextrin. Journal of Pharmacy and Pharmacology,
61(1), 23-30.
Kohli, K., Chopra, S., & Dhar, D. (2010). Self-emulsifying drug delivery systems : an
approach to enhance oral bioavailability. Drug Discovery Today.
Krause, K. P., Kayser, O., Ma¨der, K., Gust, R., & Mu¨ ller, R. H. (2000). Heavy
metal contamination of nanosuspensions produced by high-pressure homogenisation.
International Journal of Pharmaceutics, 196, 169-172.
Kumar, M., Misra, A., Babbar, A. K., Mishra, A. K., Mishra, P., & Pathak, K. (2008).
Intranasal nanoemulsion based brain targeting drug delivery system of risperidone.
International Journal of Pharmaceutics 358 285–291.
Kumar, M. P., Rao, Y. M., & Apte, S. (2008). Formulation of Nanosuspensions of
Albendazole for Oral Administration. Current Nanoscience, 4, 53-58.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 149
References 9
Kumar, R., Gupta, R., & Betageri, G. (2001). Formulation, characterization, and in
vitro release of glyburide from proliposomal beads. Drug Delivery, 8(1), 25-37.
Li, P., Hynes, S. R., Haefele, T. F., Pudipeddi, M., Royce, A. E., & Serajuddin, A. T.
M. (2009). Development of Clinical Dosage Forms for a Poorly Water-Soluble Drug
II: Formulation and Characterization of a Novel Solid Microemulsion Preconcentrate
System for Oral Delivery of a Poorly Water-Soluble Drug. Journal Of Pharmaceutical
Sciences, 98(5), 1750-1764.
Li, W., Shaoling Yi, Zhouhua Wang, Si Chen, Shuang Xin, Jingwen Xie, & Zhao, C.
(2011). Self-nanoemulsifying drug delivery system of persimmon leaf extract:
Optimization and bioavailability studies. International Journal of Pharmaceutics, 420,
161-171.
Lindenberg, M., Kopp, S., & Dressman, J. B. (2004). Classification of orally
administered drugs on the World Health Organization Model list of Essential
Medicines according to the biopharmaceutics classification system. European Journal
of Pharmaceutics and Biopharmaceutics, 58, 265–278.
Liu, P., Rong, X., Laru, J., Veen, B. v., Kiesvaara, J., Hirvonen, J., . . . Peltonen, L.
(2011). Nanosuspensions of poorly soluble drugs: preparation and development by
wet milling. International Journal of Pharmaceutics.
Liversidge, E. M., & Liversidge, G. G. (2011). Nanosizing for oral and parenteral
drug delivery: A perspective on formulating poorly-water soluble compounds using
wet media milling technology. Advanced Drug Delivery Reviews, 63, 427–440.
Liversidge, G. G., & Conzentino, P. (1995). Drug particle size reduction for
decreasing gastric irritancy and enhancing absorption of naproxen in rats.
International Journal of Pharmaceutics 125 309-313.
Madhusudhan, B., Rambhau, D., Apte, S. S., & Gopinath, D. (2006). Improved in
Vitro Permeation of Nabumetone across Rat Skin from 1-O-Alkylglycerol/Lecithin
Stabilized o/w Nanoemulsions. Journal of Dispersion Science and Technology, 27,
921–926.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 150
References 9
Madhusudhan, B., Rambhau, D., Apte, S. S., & Gopinath, D. (2007). Oral
Bioavailability of Flutamide from 1-O-Alkylglycerol Stabilized o/w Nanoemulsions.
Journal of Dispersion Science and Technology, 28, 1254–1261.
Merisko-Liversidge, E., & Liversidge, G. G. ( 2011). Nanosizing for oral and
parenteral drug delivery: A perspective on formulating poorly-water soluble
compounds using wet media milling technology. Advanced Drug Delivery Reviews
63, 427–440.
Miyahara, R. K. (1992). Pharmacotherapy of Oral Hypoglycemic Agents. Journal of
Pharmacy Pracrice, 5, 271-279.
Mou, D., Chen, H., Du, D., Mao, C., Wan, J., Xu, H., & Yang, X. (2008). Hydrogel-
thickened nanoemulsion system for topical delivery of lipophilic drugs. International
Journal of Pharmaceutics 353 270–276.
Mu¨ller, R. H., Jacobs, C., & Kayser, O. (2001). Nanosuspensions as particulate drug
formulations in therapy Rationale for development and what we can expect for the
future. Advanced Drug Delivery Reviews, 47, 3–19.
Mura, P., Valleri, M., Cirri, M., & Mennini, N. (2010). New solid self-
microemulsifying systems to enhance dissolution rate of poorly water soluble drugs.
Pharmaceutical Development and Technology.
Nathan, D. M., Buse, J. B., Davidson, M. B., Ferrannini, E., Holman, R. R., Sherwin,
R., & Zinman, B. (2009). Medical Management of Hyperglycemia in Type 2
Diabetes: A Consensus Algorithm for the Initiation and Adjustment of Therapy A
consensus statement of the American Diabetes Association and the European
Association for the Study of Diabetes. Clinical Diabetes, 14-16.
Nielsen, F. S., Petersen, K. B., & Mullertz, A. (2008). Bioavailability of probucol
from lipid and surfactant based formulations in minipigs: Influence of droplet size and
dietary state. European Journal of Pharmaceutics and Biopharmaceutics, 69 553–562.
Ning, X., Sun, J., Han, X., Wu, Y., Yan, Z., Han, J., & He, Z. (2011). Strategies to
improve dissolution and oral absorption of glimepiride tablets: solid dispersion versus
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 151
References 9
micronization techniques. Drug Development and Industrial Pharmacy, 37(6), 727–
736.
Niwa, T., Miura, S., & Danjo, K. (2011). Universal wet-milling technique to prepare
oral nanosuspension focused on discovery and preclinical animal studies –
Development of particle design method. International Journal of Pharmaceutics 405
218–227.
Okabe, H., Suzuki, E., Sugiura, Y., Yanagimoto, K., Takanashi, Y., Hoshi, M., . . .
Saitoh, E. (2008). Development of an easily swallowed film formulation. International
Journal of Pharmaceutics 355(1-2), 62-66.
Otoom, S., Hasan, M., & Najib, N. (2001). The bioavailability of glyburide
(glibenclamide) under fasting and feeding conditions: a comparative study.
International Journal of Pharmaceutical Medicine 15, 117–120.
Pahovnik, D., Reven, S., Grdadolnik, J., Borštnar, R., Mavri, J., & Zagar, E. (2011).
Determination of the interaction between glimepiride and hyperbranched polymers in
solid dispersions. Journal of Pharmceutical Sciences, 100(11), 4700-4709.
Palamakula, A., Nutan, M. T. H., & Khan, M. A. (2004). Response Surface
Methodology for Optimization and Characterization of Limonene-based Coenzyme
Q10 Self-Nanoemulsified Capsule Dosage Form. AAPS PharmSciTech, 5(4), Article
66.
Patil, P., Joshi, P., & Paradkar, A. (2004). Effect of Formulation Variables on
Preparation and Evaluation of Gelled Self-emulsifying Drug Delivery System
(SEDDS) of Ketoprofen. AAPS PharmSciTech, 5(3), Article 42.
Patil, P., & Paradkar, A. (2006). Porous Polystyrene Beads as Carriers for Self-
Emulsifying System Containing Loratadine. AAPS PharmSciTech, 7(1), Article 28
Patil, P. R., Biradar, S. V., & Paradkar, A. R. (2009). Extended Release Felodipine
Self-Nanoemulsifying System. AAPS PharmSciTech, 10(2).
Patravale, V. B., Date, A., & Kulkarni, R. (2004). Nanosuspensions: a promising drug
delivery strategy. Journal of Pharmacy and Pharmacology., 56, 827-840.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 152
References 9
Peltonen, L., & Hirvonen, J. (2010). Pharmaceutical nanocrystals by nanomilling:
critical process parameters, particle fracturing and stabilization methods. Journal of
Pharmacy and Pharmacology 62(11), 1569-1579.
Pignatello, R., Bucolo, C., Ferrara, P., Maltese, A., Puleo, A., & Puglisi, G. (2002). E
udragit RS100 nanosuspensions for the ophthalmic controlled delivery of ibuprofen.
European Journal of Pharmaceutical Sciences 16 53–61.
Pouton, C. W. (1997). Formulation of self-emulsifying drug delivery systems.
Advanced Drug Delivery Reviews 25 47-58.
Prabu, A. K., Kumarappan, C., Christudas, S., & Kalaichelvan, V. (2012). Effect of
Biophytum sensitivum on streptozotocin and nicotinamide induced diabetic rats.
Asian Pacific Journal of Tropical Biomedicine, 31-35.
Rabinow, B. E. (2004). Nanosuspensions In Drug Delivery. Nature Reviews Drug
Discovery, 3, 785-796.
Ramon, G., Raptis, S. A., & Ravella, R. (2000). Appropriate Timing of Glimepiride
Administration in Patients with Type 2 Diabetes Millitus. Endocrine, 13(1), 117–121.
Rang, H. P., Dale, M. M., Ritter, J. M., & Flower, R. J. (2007). Pharmacology (6 ed.):
Churchil Livingstone.
Rao, S. V. R., & Shao, J. (2008). Self-nanoemulsifying drug delivery systems
(SNEDDS) for oral delivery of protein drugs I. Formulation development.
International Journal of Pharmaceutics 362, 2–9.
Rao, S. V. R., Yajurvedi, K., & Shao, J. (2008). Self-nanoemulsifying drug delivery
system (SNEDDS) for oral delivery of protein drugs III. In vivo oral absorption study.
International Journal of Pharmaceutics, 362, 16–19.
Reven, S., Grdadolnik, J., Kristl, J., & Zagar, E. (2010). Hyperbranched
poly(esteramides) as solubility enhancers for poorly water-soluble drug glimepiride.
International Journal of Pharmaceutics 396(1-2), 119-126.
Reven, S., Homar, M., Peternel, L., Kristl, J., & Zagar, E. (2011). Preparation and
Characterization of Tablet Formulation based on Solid Dispersion of Glimepiride and
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 153
References 9
Poly(ester amide) Hyperbranched Polymer. Pharmaceutical Development and
Technology.
RoIkamp, R., Wernicke-Panten, K., & Draeger, E. (1996). Clinical profile of the
novel sulphonylurea glimepiride. Diabetes Research and Clinical Practice, 3(1), 33-
42.
Salazar, J., Ghanem, A., Müller, R. H., & Möschwitzer, J. (2012). Nanocrystals:
Comparison of the size reduction effectiveness of a novel combinative method with
conventional top-down approaches. European Journal of Pharmaceutics and
Biopharmaceutics.
Sarkari, M., Brown, J., Chen, X., Swinnea, S., Williams III, R. O., & Johnston, K. P.
(2002). Enhanced drug dissolution using evaporative precipitation into aqueous
solution. International Journal of Pharmaceutics 243 17–31.
Sarker, D. K. (2005). Engineering of Nanoemulsions for Drug Delivery. Current Drug
Delivery 0, 297-310.
Seedher, N., & Kanojia, M. (2008). Micellar Solubilization of Some Poorly Soluble
Antidiabetic Drugs: A Technical Note. AAPS PharmSciTech, 9(2), 431-436.
Seedher, N., & Kanojia, M. (2009). Co-solvent solubilization of some poorly-soluble
antidiabetic drugs. Pharmaceutical Development and Technology, 14(2), 185–192.
Shafiq, S., Shakeel, F., Talegaonkar, S., Ahmad, F. J., Khar, R. K., & Ali, M. (2007).
Development and bioavailability assessment of ramipril nanoemulsion formulation.
European Journal of Pharmaceutics and Biopharmaceutics, 66 227–243.
Shah, A., Shah, S., Patel, V., & Potdar, A. (2012). Nanonization: A Dissolution
Enhancement Approach for BCS Class II Drugs. Drug Development and Delivery,
12(1), 48-52.
Shakeel, F., Baboota, S., Ahuja, A., Ali, J., Aqil, M., & Shafiq, S. (2007).
Nanoemulsions as Vehicles for Transdermal Delivery of Aceclofenac. AAPS
PharmSciTech, 8(4), Article 104.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 154
References 9
Sheehan, M. T. (2003). Current Therapeutic Options in Type 2 Diabetes Mellitus: A
Practical Approach. Clinical Medicine & Research, 1, 189-200.
Sigfridsson , K., Forsse´n, S., Holla¨nder, P., Skantze, U., & Verdier, J. d. (2007). A
formulation comparison, using a solution and different nanosuspensions of a poorly
soluble compound. European Journal of Pharmaceutics and Biopharmaceutics 67
540–547.
Singare, D. S., Marella, S., Gowthamrajan, K., Kulkarni, G. T., Vooturi, R., & Rao, P.
S. (2010). Optimization of formulation and process variable of nanosuspension: An
industrial perspective. International Journal of Pharmaceutics 402 213–220.
Singh, B., Bandopadhyay, S., Kapil, R., Singh, R., & Katare, O. P. (2009). Self-
Emulsifying Drug Delivery Systems (SEDDS): Formulation Development,
Characterization, and Applications. Critical Reviews™ in Therapeutic Drug Carrier
Systems, 26(5), 427–521
Singh, K. K., & Vingkar, S. K. ( (2008) ). Formulation, antimalarial activity and
biodistribution of oral lipid nanoemulsion of primaquine. International Journal of
Pharmaceutics, 347 136–143.
Singh, S., Srinivasan, K., Gowthamarajan, K., Prakash, D., Gaikwad, N., & Singare,
D. (2012). Influence of formulation parameters on dissolution rate enhancement of
glyburide using liquisolid technique. Drug Developnent and Industrial Pharmacy.
Singh, S., Srinivasan, K., Gowthamarajan, K., Singare, D., Prakash, D., & Gaikwad,
N. (2011). Investigation of preparation parameters of nanosuspension by top-down
media milling to improve the dissolution of poorly water-soluble glyburide. European
Journal of Pharmaceutics and Biopharmaceutics, 78(3), 441-446.
Singh, S., Srinivasan, K., Singare, D., Gowthamarajan, K., & Prakash, D. (2012).
Formulation of ternary complexes of glyburide with hydroxypropyl-β-cyclodextrin
and other solubilizing agents and their effect on release behavior of glyburide in
aqueous and buffered media at different agitation speeds. Drug Developnent and
Industrial Pharmacy.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 155
References 9
Singh, S., Verma, P., & Razdan, B. (2010). Glibenclamide-loaded self-
nanoemulsifying drug delivery system: development and characterization. Drug
Developnent and Industrial Pharmacy, 36(8), 933-945.
Tagne, J.-B., Kakumanu, S., Ortiz, D., Shea, T., & Nicolosi, R. J. (2008). A
Nanoemulsion Formulation of Tamoxifen Increases Its Efficacy in a Breast Cancer
Cell Line. Molecular Pharmaceutics, 5(2), 280–286.
Taha, E. I., Al-Saidan, S., Samy, A. M., & Khan, M. A. (2004). Preparation and in
vitro characterization of self-nanoemulsified drug delivery system (SNEDDS) of all-
trans-retinol acetate. International Journal of Pharmaceutics 285 109–119.
Taha, E. I., Al-Suwayeh, S. A., & Anwer, M. K. (2009). Preparation, in vitro and in
vivo evaluation of solid-state self-nanoemulsifying drug delivery system (SNEDDS)
of vitamin A acetate. Journal of Drug Targeting, 17(6), 468-473.
Tam, J. M., Mcconville, J. T., Williams III, R. O., & Johnston, K. P. (2008).
Amorphous Cyclosporin Nanodispersions for Enhanced Pulmonary Deposition and
Dissolution. Journal of Pharmaceutical Sciences, 97(11), 4915-4933.
Thorat, A. A., & Dalvi, S. V. (2012). Liquid antisolvent precipitation and stabilization
of nanoparticles of poorly water soluble drugs in aqueous suspensions: Recent
developments and future perspective. Chemical Engineering Journal, 181-182, 1-34.
Trimaille, T., Chaix, C., Delair, T., Pichot, C., Teixeira, H., Dubernet, C., &
Couvreur, P. (2001). Interfacial deposition of functionalized copolymers onto
nanoemulsions produced by the solvent displacement method. ColloidS in Polymer
Sciences, 279, 784-792.
Trotta, M., Gallarate, M., Carlotti, M. E., & Morel, S. (2003). Preparation of
griseofulvin nanoparticles from water-dilutable microemulsions. International Journal
of Pharmaceutics 254 235–242.
Trotta, M., Gallarate, M., Pattarino, F., & Morel, S. (2001). Emulsions containing
partially water-miscible solvents for the preparation of drug nanosuspensions. Journal
of Controlled Release 76 119–128.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 156
References 9
USFDA, & Guidelines. Retrieved 13 January, 2009, from
http://www.accessdata.fda.gov/scripts/cder/dissolution/dsp_SearchResults_Dissolutio
ns.cfm
Valleri, M., Mura, P., Maestrelli, F., Cirri, M., & Ballerini, R. (2004). Development
and evaluation of glyburide fast dissolving tablets using solid dispersion technique.
Drug Developnent and Industrial Pharmacy, 30(5), 525-534.
Venkatesh, S., & Lipper, R. A. (2000). Role of the development scientist in
compound lead selection and optimization. Journal of Pharmaceutical Sciences, 89,
145-154.
Verma, S., Huey, B. D., & Burgess, D. (2009). Scanning Probe Microscopy Method
for Nanosuspension Stabilizer Selection. Langmuir, 25(21), 12481–12487.
Verma, S., Kumara, S., Gokhale, R., & Burgess, D. (2010). Physical stability of
nanosuspensions: Investigation of the role of stabilizers on Ostwald ripening.
International JournalofPharmaceutics, 406(1-2), 145–152.
Vyas, T. K., Shahiwala, A., & Amiji, M. M. (2008). Improved oral bioavailability and
brain transport of Saquinavir upon administration in novel nanoemulsion
formulations. International Journal of Pharmaceutics 347, 93–101.
Wang, L., Dong, J., Chen, J., Eastoe, J., & Li, W. (2009). Design and optimization of
a new self-nanoemulsifying drug delivery system. Journal of Colloid and Interface
Science, 330 443–448.
Wang, Z., Sun, J., Wang, Y., Liu, X., Liu, Y., Fu, Q., . . . He, Z. (2010). Solid self-
emulsifying nitrendipine pellets: Preparation and in vitro/in vivo evaluation.
International Journal of Pharmaceutics, 383, 1-6.
Wiedmann, T. S., DeCastro, L., & Wood, R. W. (1997). Nebulization of
NanoCrystals™: Production of a Respirable Solid-inLiquid- in-Air Colloidal
Dispersion. Pharmaceutical Research, 14(1), 112-116.
Yang, J. Z., Young, A. L., Chiang, P.-C., Thurston, A., & Pretzer, D. K. (2008).
Fluticasone and Budesonide Nanosuspensions for Pulmonary Delivery: Preparation,
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 157
References 9
Characterization, and Pharmacokinetic Studies. Journal of Pharmaceutical Sciences,
97(11), 4869-4878.
Zeng, H., Li, X., Zhang, G., & Dong, J. (2008). Preparation and Characterization of
Beta Cypermethrin Nanosuspensions by Diluting O/W Microemulsions. Journal of
Dispersion Science and Technology, 29, 358–361.
Zerrouk, N., Corti, G., Ancillotti S, Maestrelli F, Cirri M, & P., M. (2006). Influence
of cyclodextrins and chitosan, separately or in combination, on glyburide solubility
and permeability. European Journal of Pharmaceutics and Biopharmaceutics, 62(3),
241-246.
Zhang, J.-Y., Shen, Z.-G., Zhonga, J., Hu, T.-T., Chen, J.-F., Ma, Z.-Q., & Yun, J.
(2006). Preparation of amorphous cefuroxime axetil nanoparticles by controlled
nanoprecipitation method without surfactants. International Journal of Pharmaceutics
323 153–160.
Zhang, X., Xia, Q., & Gu, N. (2006). Preparation of All-Trans Retinoic Acid
Nanosuspensions Using a Modified Precipitation Method. Drug Development and
Industrial Pharmacy, 32, 857–863
Zhong, J., Shen, Z., Yang, Y., & Chen, J. (2005). Preparation and characterization of
uniform nanosized cephradine by combination of reactive precipitation and liquid
anti-solvent precipitation under high gravity environment. International Journal of
Pharmaceutics 301, 286–293.
Zhu, S., Hong, M., Liu, C., & Pei, Y. (2009). Application of Box-Behnken design in
understanding the quality of genistein self-nanoemulsified drug delivery systems and
optimizing its formulation. Pharmaceutical Development and Technology, 14(6),
642–649.
Zidan, A. S., Sammour, O. A., Hammad, M. A., Megrab, N. A., Habib, M. J., &
Khan, M. A. (2007). Quality by design: Understanding the formulation variables of a
cyclosporine A self-nanoemulsified drug delivery systems by Box–Behnken design
and desirability function. International Journal of Pharmaceutics, 332, 55-63.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 158
References 9
Zili, Z., Sfar, S., & Fessi, H. (2005). Preparation and characterization of poly--
caprolactone nanoparticles containing griseofulvin. International Journal of
Pharmaceutics 294 261–267.
Department of Pharmacuetical Sciences, Saurashtra University, Rajkot 159