FLOATING DRUG DELIVERY SYSTEM OF NSAIDS TO INCREASE GASTRIC RETENTION TIME IN UPPER PART OF GASTROINTESTINAL TRACT

A. Tripathi, Suraj Neupane, K. Bhardwaj, Shivakaht Mishra, Meenakshi Gupta, R. K. Mishra
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Abstract

The purpose of the present work is to prolong the gastric residence time of Lornoxicam by developing gastric floating drug delivery system. Lornoxicam is non-steroidal anti-inflammatory drugs. Its short half life 2 to 3 hrs and maximal absorption of upper part of gastrointestinal tract. The residence time of the dosage form in the stomach depends upon various factors like pH, size of the dosage form, food intake, and biological factors which include age, body weight gender, posture, and diseased states Floating tablet prepared by melt granulation techniques, using bees wax as a binder and the other polymers include HPMC 50cPs,15cPs,5cPs and Sodium Alginate. The Prepared granules were then evaluated for Precompression Properties. The best batches were then tabulated, and Evaluation was carried out for the following parameters with in vitro release, buoyancy, Floating Lag timed. Batch F12 and F13 Showed best Floating time of 12hrs and Floating Lag time of 60 second.
非甾体抗炎药漂浮给药系统增加胃在胃肠道上半部分的停留时间
本研究旨在通过研制胃漂浮给药系统,延长氯诺昔康在胃中的停留时间。氯诺昔康是一种非甾体抗炎药。半衰期短,2 ~ 3小时,最大吸收部位为胃肠道上半部分。剂型在胃中的停留时间取决于多种因素,如pH值、剂型大小、食物摄入量以及年龄、体重、性别、姿势、患病状态等生物因素。浮片采用熔融造粒技术制备,以蜂蜡为粘合剂,其他聚合物包括HPMC 50cPs、15cPs、5cPs和海藻酸钠。然后对制备的颗粒进行预压缩性能评价。然后将最佳批次制成表格,并对体外释放度、浮力、漂浮滞后时间等参数进行评价。F12和F13批次的最佳悬浮时间为12小时,悬浮滞后时间为60秒。
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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