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吲哚美辛从含有用黄秋葵胶改性的卡波姆941的生物黏附片中的释放。

Release of indomethacin from bioadhesive tablets containing carbopol 941 modified with Abelmuschus esculentus (okra) gum.

作者信息

Attama A A, Adikwu M U, Amorha C J

机构信息

Drug Delivery Research Unit, Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, University of Nigeria, Nsukka, Nigeria.

出版信息

Boll Chim Farm. 2003 Sep;142(7):298-302.

Abstract

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.

摘要

卡波姆941(C-941)和黄秋葵胶(秋葵胶,AEG)被用作制备吲哚美辛黏膜黏附片的生物黏附聚合物。基于聚合物的不同组合比例制备了不同批次的片剂。使用张力计研究了片剂的生物黏附性能:还制备并评估了用100%乙醇中的50% w/v 丙烯酸树脂I溶液包衣的片剂。评估了以下片剂物理性质:硬度、重量均匀度、崩解时间、脆碎度和药物绝对含量。在不含胰酶的模拟肠液(SIF pH 7.2)和0.1 N HCl溶液中进行了释放研究。所得结果表明,对于包衣片和未包衣片,C-941与AEG比例相等(1:1)的片剂具有最高的生物黏附强度。未包衣片在0.1 N HCl和SIF中的药物释放百分比范围为53-90%,包衣片在0.1 N HCl中的药物释放百分比为9-16%,包衣片在SIF中8小时后的药物释放百分比为63-100%。

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