米格列醇控释微球配方开发与评价

P. K, V. J. Marabathuni, Naidu Narapusetty
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引用次数: 0

摘要

该研究解释了米格列醇在体内的位置,并达到和维持所需的ISD浓度,半衰期为2小时,生物利用度低。本文介绍了用HPMC K15M、乙基纤维素和卡拉亚胶按不同比例配制的9种配方。FTIR光谱显示,聚合物与米格列醇之间没有相互作用。随着聚合物配比的增加,米格列醇微球的平均粒径也随之增大。结果表明,米格列醇在微球中的分布合理,偏差在可接受范围内。在释放数据和图形分析的基础上,含HPMC K15M的配方F6由于聚合物浓度高,在12小时内具有良好的控释曲线,截留效率最高,符合零级动力学,具有超级II型转运机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Controlled release miglitol microspheres formulation development and evaluation
The research explain about Miglitol site in the body and also to achieve and maintain the desired ISD concentration, having 2 hour half-life and low bioavilability. The paper give information about nine formulations formulated by using HPMC K15M, Ethyl cellulose and karaya gum in different proportions. The FTIR Spectra revealed that, there was no interaction between polymers and Miglitol. As the polymer ratio was increased, the mean particle size of Miglitol microspheres was also increased.   From the results it can be inferred that there was a proper distribution of Miglitol in the microspheres and the deviation was within the acceptable limits. On the basis of release data and graphical analysis formulation F6 containing HPMC K15M showed a good controlled release profile up to 12hrs with maximum entrapment efficiency because of high polymer concentration and follows zero order kinetics with super case II transport mechanism.
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