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Development of Sustained Release Drug Delivery System of Lithium Carbonate and in Vitro Evaluation

T.K. Pal1, J. Khanam2 and S. SiddiquE1

1Department of Pharmaceutics, Radharaman College of Pharmacy, Bhopal - 462 003 (India)

2Division of Pharmaceutical Engineering, Department of Pharmaceutical Technology, Jadavpur University, Kolkata - 700 032 (India) 

DOI : http://dx.doi.org/10.13005/msri/032a27

Article Publishing History
Article Received on : 3 Sep 2006
Article Accepted on : 28 Nov 2006
Article Published :
Plagiarism Check: Yes
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ABSTRACT:

The purpose of this study was to investigate the effect of different proportions of HPMC polymer in the release of drug from the hydrophilic matrix tablets. Three formulations were made by wet granulation method 450mg Lithium carbonate and 10%, 20% & 30% HPMC were granulated with Ethanolic solution of Eudragit S100, dried and then compressed to formulate the tablets. In vitro studies were conducted on the three formations. All the three formulations demonstrated relatively sustained release behavior but the matrix tables containing 30% HPMC exhibited suitable release kinetics.

KEYWORDS: Drug delivery system; lithium carbonate; invitro evaluation

Copy the following to cite this article:

Pal T. K, Khanam J, SiddiquE S. Development of Sustained Release Drug Delivery System of Lithium Carbonate and in Vitro Evaluation. Mat.Sci.Res.India;3(2a)


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Pal T. K, Khanam J, SiddiquE S. Development of Sustained Release Drug Delivery System of Lithium Carbonate and in Vitro Evaluation. Mat.Sci.Res.India;3(2a). Available from: http://www.materialsciencejournal.org/?p=3336


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