秋葵胶改性卡波醇941生物胶粘剂对吲哚美辛的释放研究

Bollettino chimico farmaceutico Pub Date : 2003-09-01
A A Attama, M U Adikwu, C J Amorha
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引用次数: 0

摘要

以卡波波941 (C-941)和秋秋草胶(AEG)为生物胶粘剂,制备吲哚美辛黏附片。根据聚合物的不同组合比例配制不同批次的片剂。用张力计研究了片剂的生物粘附性能,制备了以50% w/v的Eudragit I. 100溶液包被的片剂,并对其进行了评价。考察其硬度、重量均匀性、崩解时间、脆碎度和绝对药物含量。在不含胰酶的模拟肠液(SIF pH 7.2)和0.1 N盐酸溶液中测定释放研究。结果表明,C-941与AEG的比例为1:1时,包衣片和非包衣片的生物黏附强度最高。在0.1盐酸和SIF中,无包衣片剂的药物释放率为53-90%,包衣片剂在0.1盐酸中释放率为9-16%,包衣片剂在SIF中释放率为63-100%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Release of indomethacin from bioadhesive tablets containing carbopol 941 modified with Abelmuschus esculentus (okra) gum.

Carbopol 941 (C-941) and Abelmuschus esculentus gum (Okra gum, AEG) were used as bioadhesive polymers in the formulation of mucoadhesive indomethacin tablets. Different batches of the tablet compacts were formulated based on different combination ratios of the polymers. The bioadhesive properties of the tablets were studied using a tensiometer: Tablets coated with 50% w/v solution of Eudragit I. 100 in ethanol, were also prepared and evaluated. The following tablet physical properties were evaluated: hardness, uniformity of weight, disintegration time, friability, and absolute drug content. Release studies were determined in simulated intestinal fluid (SIF pH 7.2) without pancreatin, and in 0.1 N solution of HCl. Result obtained indicated that tablets with equal ratio of C-941 and AEG (1:1) gave the highest bioadhesive strength for both the coated and uncoated tablets. The percentage of drug released ranged from 53-90% for uncoated tablets in 0.1 N HCl and SIF, and 9-16% for coated tablets in 0.1 N HCl, and 63-100% for coated tablets in SIF after 8 hrs.

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