Design and Characterization of Effervescent Gastro Retentive Floating Tablets by Using Venlafaxine Hcl as a Model Drug

A. Kauser, A. Haseena, Faheem Unnisa Begum, Taiyaba Fatima
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Abstract

In the present research work the gastro retentive floating matrix formulation of Venlaflaxine hydrochloride by using various hydrophillic polymers. Initially analytical method development was done for the drug molecule. Absorption maxima was determined based on that calibration curve was developed by using different concentrations. Gas generating agent sodium bicarbonate concentration was optimized. Then the formulation was developed by using different concentrations of polymers of various grades of HPMC and Guar gum. The formulation blend was subjected to various preformualation studies, flow properties and all the formulations were found to be good indicating that the powder blend has good flow properties. Among all the formulations the formulations prepared by using Guar gum were in the concentration of 120mg (F4) showed maximum drug release 99.76% in 12 hours with good floating lag time and duration of floating.The formulations prepared with HPMC K 15 M retarded the drug release up to 12 hours in the concentration of 120 mg (F8).The formulations prepared with HPMC K100M were also retarded the drug release for more than 12 hours. Hence they were not considered. The optimized formulation dissolution data was subjected to release kinetics; from the release kinetics data it was evident that the formulation followed peppas mechanism of drug release.
以盐酸文拉法辛为模型药物的泡腾式胃保留漂浮片的设计与表征
本文研究了利用各种亲水性聚合物制备盐酸文拉法欣的胃保留漂浮基质配方。最初的分析方法开发是针对药物分子的。在此基础上确定了不同浓度下的最大吸收曲线。对瓦斯生成剂碳酸氢钠浓度进行了优化。然后用不同等级的HPMC和瓜尔胶的不同浓度的聚合物进行配方研制。该配方共混物进行了各种预配方研究,流动性能和所有配方都很好,表明该粉末共混物具有良好的流动性能。其中瓜尔胶制备的配方在浓度为120mg (F4)时,12 h释药量达到99.76%,具有良好的漂浮滞滞期和漂浮持续时间。用HPMC k15m配制的制剂在120 mg (F8)浓度下可延缓药物释放达12小时。用HPMC - K100M配制的制剂也能延缓药物释放12小时以上。因此,他们没有被考虑。对优化后的配方进行了释放动力学考察;释放动力学数据表明,该制剂符合peppas的药物释放机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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