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用于吲哚美辛结肠特定递送的pH调节控释基质系统的设计与评价

Design and evaluation of pH modulated controlled release matrix systems for colon specific delivery of indomethacin.

作者信息

Asghar L F A, Chandran S

机构信息

Formulation Development & Pharmacokinetic Laboratory, Pharmacy Group, Birla Institute of Technology & Science, Pilani, India.

出版信息

Pharmazie. 2008 Oct;63(10):736-42.

PMID:18972836
Abstract

Indomethacin, a potent non steroidal anti-inflammatory drug (NSAID), is indicated for the local treatment of colorectal carcinoma. The aim of the present study was to design and investigate various matrix systems for controlled and site specific delivery of indomethacin to the colon. Various pH sensitive and hydrophobic polymers were investigated for their effect on drug release and site specificity. Effect of proportion of Eudragit L100 and Eudragit S100 in matrix either alone or in combination was evaluated. Effect of hydrophobic non-swellable polymer ethyl cellulose on the release pattern of drug from the Eudragit bases was also investigated. Matrix tablets prepared with Eudragit showed pH dependent release profile with the formulations of Eudragit L100 showing faster rate of drug release than Eudragit S100 in alkaline pH. The release profile from matrix tablets containing Eudragit L100 and Eudragit S100 in combination or with ethyl cellulose correlated well with the relative proportion of the two polymer types in the matrix base. Selected formulations when evaluated in simulated gastric fluid pH without enzymes showed negligible to low drug release (less than 10%) in the first 4-6 h followed with controlled release for 14-16 h. It was concluded that pH sensitive matrix bases in combination with a hydrophobic polymer like ethyl cellulose canbe ideal for site specific delivery of drugs to colon with controlled release profile.

摘要

吲哚美辛是一种强效非甾体抗炎药(NSAID),适用于结直肠癌的局部治疗。本研究的目的是设计并研究各种基质系统,以实现吲哚美辛向结肠的控释和定位释放。研究了各种pH敏感和疏水聚合物对药物释放和定位特异性的影响。评估了尤特奇L100和尤特奇S100单独或组合在基质中的比例的影响。还研究了疏水性非膨胀性聚合物乙基纤维素对药物从尤特奇基质中释放模式的影响。用尤特奇制备的基质片剂显示出pH依赖性释放曲线,在碱性pH条件下,尤特奇L100制剂的药物释放速率比尤特奇S100快。含有尤特奇L100和尤特奇S100组合或与乙基纤维素的基质片剂的释放曲线与基质中两种聚合物类型的相对比例密切相关。在不含酶的模拟胃液pH值下评估选定的制剂时,在前4 - 6小时药物释放可忽略不计至较低(小于10%),随后进行14 - 16小时的控释。得出的结论是,pH敏感的基质与乙基纤维素等疏水聚合物结合,对于药物向结肠的定位释放和控释曲线可能是理想的。

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