美沙拉胺负载pH依赖性结肠特异性脉动给药系统的研制与评价

P. Pawar, G. Varsha
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引用次数: 2

摘要

这些研究的目的是一种口服结肠特异性,脉冲装置,以获得时间和/或地点特异性释放美沙拉明,基于时间药物的考虑。基本设计包括一个不溶性的硬明胶胶囊体,充满了美沙拉胺的Eudragit微胶囊,并用水凝胶塞密封。整个装置是肠溶包被的,因此可以克服胃排空时间的可变性,并实现结肠特异性释放。采用改变药聚比的方法,以Eudragit L-100和S-100(1:2)为原料,分三批制备美沙拉胺微胶囊,并对其粒径、药物含量和体外释放谱进行评价;选择了一种较好的配方,进一步制备脉动胶囊。采用不同的水凝胶聚合物作为堵塞剂,保持适当的滞滞期,发现药物的释放受聚合物比例的控制。脉冲装置体外释放研究表明,增加亲水聚合物含量可导致美沙拉胺微胶囊的延迟释放。脉动性,结肠特异性释放已从胶囊装置在2-24小时内实现,与时间治疗性药物递送的要求一致。
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Formulation and Evaluation of Mesalamine Loaded pH Dependent Colon Specific Pulsatile Drug Delivery System
The aim of these research of an oral colon specific, pulsatile device to attain time and or site specific release of Mesalamine, based on chronopharmaceutical consideration. The basic design consists of an insoluble hard gelatin capsule body, filled with Eudragit microcapsules of Mesalamine and sealed with a hydrogel plug. The entire device was enteric coated, so that the variability in gastric emptying time can be overcome and a colon-specific release can be achieved. The Mesalamine microcapsules were prepared in three batches, with Eudragit L-100 and S-100 (1:2) by changing drug to polymer ratio and evaluated for the particle size, drug content and in vitro release profile and from the obtained results; one better formulation was selected for further fabrication of pulsatile capsule. Different hydrogel polymers were used as plugs, to maintain a suitable lag period and it was found that the drug release was controlled by the proportion of polymers used. In vitro release studies of pulsatile device revealed that, increasing the hydrophilic polymer content resulted in delayed release of Mesalamine from microcapsules. Pulsatile, colon-specific release has been achieved from a capsule device over a 2–24 h period, consistent with the demands of chronotherapeutic drug delivery.
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