CHARACTERIZATION AND SOLUBILITY ENHANCEMENT OF GLICLAZIDE SOLID DISPERSION USING PVP-K30 & K -90

R. Guleria
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Abstract

The purpose of this study was to design Polyvinylpyrrolidone (PVP) based solid dispersions bearing gliclazide. Polyvinylpyrrolidone (PVP K-30 and K-90) based solid dispersions containing the drug in different mass ratio i.e. 1:1, 1:3, 1:5 and 1:7 were prepared using fusion method. The prepared solid dispersions were characterized for their drug content, phase solubility studies, fourier-transform infrared (FTIR) spectroscopy, differential scanning calorimetry, x-ray diffraction, and in-vitro dissolution studies. All the formulations showed marked improvement in the solubility and dissolution rate of drug from solid dispersion is due to decrease in crystallinity of drug and additives. It was concluded that prepared solid dispersion of the gliclazide with Polyvinylpyrrolidone may improved the solubility and dissolution rate of the drug.
用pvp-k30和k -90表征格列齐特固体分散体及其溶解度
本研究的目的是设计以聚乙烯吡咯烷酮(PVP)为基础的格列齐特固体分散体。采用融合法制备了不同质量比(1:1、1:3、1:5、1:7)的聚乙烯吡罗烷酮(PVP K-30和K-90)基固体分散体。对所制备的固体分散体进行了药物含量、相溶解度、傅里叶变换红外光谱、差示扫描量热、x射线衍射和体外溶出度的表征。由于药物的结晶度和添加剂的结晶度降低,所有制剂的溶解度和药物的固体分散度都有明显的改善。结果表明,聚乙烯吡咯烷酮制备的格列齐特固体分散体可以提高药物的溶解度和溶出率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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