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Original Research Article | OPEN ACCESS

Preparation and Characterization of Nitrendipine-loaded Eudragit RL 100 Microspheres Prepared by an Emulsion-Solvent Evaporation Method.

S K Basu1, R . Adhiyaman2

1Division of Pharmaceutics, Department of Pharmaceutical Technology, Jadavpur University, Kolkata, India.; 2School of Pharmacy and Health Sciences, International Medical University, Kuala Lumpur, Malaysia..

For correspondence:-  R Adhiyaman   Email: genomic2002@yahoo.com   Tel:0060-86567229

Published: 20 September 2008

Citation: Basu SK, Adhiyaman R.. Preparation and Characterization of Nitrendipine-loaded Eudragit RL 100 Microspheres Prepared by an Emulsion-Solvent Evaporation Method.. Trop J Pharm Res 2008; 7(3):1033-1041 doi: 10.4314/tjpr.v7i3.5

© 2008 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: The aim of the work was to prepare nitrendipne-loaded Eudragit RL 100 microspheres to achieve sustained release nitrendipine.
Method: Nitrendipne-loaded Eudragit RL 100 microspheres were prepared by an emulsion-solvent evaporation method using ethanol/liquid paraffin system. The resultant microspheres were evaluated for average particle size, drug loading, in vitro drug release and release kinetics. FTIR spectrometry, scanning electron microscopy, differential scanning calorimetry and x-ray powder diffractometry were used to investigate the physical state of the drug in the microspheres.
Result: The mean particle size of the microspheres was influenced by varying drug:polymer ratio and emulsifier concentration while drug loading was dependent on drug:polymer ratio. The results of FTIR spectrometry, differential scanning calorimetry and x-ray diffractometry indicated the stable character of nitrendipne in drug-loaded microspheres and also revealed absence of drug-polymer interaction. The drug release profiles of the microspheres at pH 1.2 showed poor drug release characteristics while at pH 6.8, drug release was extended over a period of 8 h; release was influenced by polymer concentration and particle size. Drug release followed the Higuchi model.
Conclusion: The nitrendipine-loaded Eudragit RL 100 microspheres prepared under optimized conditions showed a good sustained release characteristics and were stable under the conditions studied.

Keywords: Nitrendipine, Eudragit RL 100, Microspheres, Physicochemical characterization, Sustained release.

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Thompson Reuters (ISI): 0.523 (2021)
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