盐酸二甲双胍黏合剂片的处方及体外评价

H. Kouser, Santosh kumar Chinnaiyan
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引用次数: 0

摘要

本研究的目的是研制一种口服黏附型盐酸二甲双胍缓释片。盐酸二甲双胍(HCl)是一种双胍类药物,血浆半衰期相对较短,绝对生物利用度较低。以不同浓度的可生物降解黏附聚合物黄原胶和果胶为原料,采用湿法造粒法制备片剂。对各批样品进行厚度、重量变化、硬度、药物含量均匀性、体外释药和黏附强度评价。平均溶出时间用于表征药物从剂型的释放速度,并表示聚合物的药物缓释效率。体外实验表明,含果胶的配方比含黄原胶的配方缓凝效果好。黄原胶有效地控制了二甲双胍在12 h内的释放,可成功地用于制备黏合剂片。将数据拟合为零阶方程和Higuchi方程,说明了药物释放的机理。研究表明,与果胶相比,黄原胶的粘接强度最高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation and in vitro evaluation of Metformin HCl mucoadhesive tablets for NIDDM
The objective of the present work was to develop an oral Mucoadhesive Metformin hydrochloride tablet for the sustained-release. Metformin hydrochloride (HCl), a biguanide, has a relatively short plasma half-life and low absolute bioavailability. The tablets were prepared by the Wet Granulation method, using biodegradable mucoadhesive polymer Xanthan gum and pectin at different concentrations. All the batches were evaluated for thickness, weight variation, hardness, drug content uniformity, in vitro drug release and mucoadhesion strength. Mean dissolution time is used to characterize the drug release rate from a dosage form, and indicates the drug release-retarding efficiency of the polymer. The in vitro studies the formulations containing Pectin showed less retardation than the formulation with Xanthan gum. The Metformin release effectively controlled for 12 h with Xanthan gum, thus, can be successfully employed for formulating mucoadhesive tablets. Fitting the data to the Zero order and Higuchi equation indicated the mechanism of drug release. The study reveals that Xanthan gum highest mucoadhesive strength compared with pectin.
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