STABILITY STUDY OF STAVUDINE SINTERED MATRIX TABLET 

Journal Title: International Research Journal of Pharmacy (IRJP) - Year 2013, Vol 4, Issue 1

Abstract

Stavudine has half life (t1/2) 1.5 hours; therefore it needs to be frequently administered during therapy which gives patient incompliance. In this study attempt has been done to study effect of three different storage conditions on stability of Stavudine sintered matrix tablet. Tablets were prepared using combination of Eudragit RS 100 (22 - 33 %w/w) and Compritol 888 ATO (9-13 %w/w) by direct compression. The prepared tablets were sintered using 400 c temperature for time period of 4 hrs. Prepared Stavudine sintered matrix tablets are then exposed to refrigerated condition, room temperature and elevated temperature of 600C for stability study. The unsintered and sintered tablets were evaluated by organoleptic evaluation, drug content, drug release; percent water uptake and percent matrix erosion. Comparison is made in between results of evaluation parameters of unsintered and sintered formulations. It was evident that different storage conditions for identical formulation significantly impact the release profile of drug.  

Authors and Affiliations

Vaibhav Bhamre, Dipika Sherkar, Dilip Derle, Minal Narkhede

Keywords

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  • EP ID EP140850
  • DOI -
  • Views 98
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How To Cite

Vaibhav Bhamre, Dipika Sherkar, Dilip Derle, Minal Narkhede (2013). STABILITY STUDY OF STAVUDINE SINTERED MATRIX TABLET . International Research Journal of Pharmacy (IRJP), 4(1), 182-185. https://europub.co.uk./articles/-A-140850