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Original Research Article | OPEN ACCESS

Formulation of Fast-Release Gastroretentive Solid Dispersion of Glibenclamide with Gelucire 50/13

Prashant Upadhyay1 , Jayanta Kumar Pandit2

1Department of Pharmaceutics, College of Pharmacy, I.F.T.M, Delhi Road, Moradabad-244001 and Gautam Buddh Technical University, Lucknow; 2Department of Pharmaceutics, Institute of Technology, Banaras Hindu University, Varanasi-221005, Uttar Pradesh, India.

For correspondence:-  Prashant Upadhyay   Email: p23upadhyay@yahoo.com   Tel:+919719915567

Received: 18 November 2011        Accepted: 5 April 2012        Published: 15 June 2012

Citation: Upadhyay P, Pandit JK. Formulation of Fast-Release Gastroretentive Solid Dispersion of Glibenclamide with Gelucire 50/13. Trop J Pharm Res 2012; 11(3):361-369 doi: 10.4314/tjpr.v11i3.4

© 2012 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: Fast-release gastroretentive solid dispersions of glibenclamide using gelucire were prepared to achieve improved bioavailability.
Methods: Hot melt granulation technique was adopted to prepare solid dispersions (SDs) of glibenclamide in gelucire 50/13 and were compared with pure glibenclamide and physical mixtures of drug and gelucire using hot stage polarized microscopy, powder x-ray diffraction (PXRD), Fourier-transform infrared spectroscopy FTIR, bouyancy as well as by in vitro release and in vivo studies. Further aging studies were carried out for the samples.
Results: PXRD showed that glibenclamide was present in SD in an amorphous form while FTIR spectroscopy revealed the presence of hydrogen bonding in the SDs. In vitro buoyancy was found for 11 h and there was improvement in solubility and dissolution rate for all test formulations. Formulations were found to follow Zero order kinetic. . During aging study,   no decrease of in vitro drug dissolution was observed over 3-month period.  Crystallinity in the SDs was observed following aging. A more pronounced lowering of blood glucose level in Wistar rats compared with the pure drug, suggests that the test formulations are superior.
Conclusion:  This study demonstrates the high potential of hot melt technique for obtaining stable fast-release gastroretentive solid dispersions of poorly water soluble drug using polyglycolized glycerides as carriers.      

Keywords: Glibenclamide, Gelucire, Solid dispersion, Gastro-retentive multi-particulates, Hot melt technique

Impact Factor
Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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