新型止吐药胶基给药系统的研制与评价

Rajnikant Vegada, A. Seth, C. Sachin, P. Parikh, Pratik Kheini, Shah Chainesh, Ramani Vinod. Sumandeep Vidyapeeth, Piparia, Waghodiya.
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引用次数: 1

摘要

这项研究是为了制定和评估盐酸美氯嗪口香糖,一种用于恶心、呕吐和晕动病的止吐药物。采用直接压缩法,采用不同比例的可直接压缩胶基(Pharmagum S)制备口香糖,以获得最佳配方。以不同浓度的S型药和豆粉为原料,制备了8种不同配方的盐酸美氯嗪口香糖。对直接压缩法制备的口香糖进行了压缩前特性、压缩后特性、口腔吸收、药物含量和体外释药研究。所有制剂在压缩前性状、压缩后性状、药物含量、体外释放度等方面均取得满意的效果。在胶、豆粉浓度分别为775 mg和140 mg时,MCG5具有最佳的压缩特性和97.88±0.69%的体外释药曲线,FTIR研究表明,优化后的MCG5在药聚合物相容性方面取得了满意的结果。因此以MCG5为优化批
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 Evaluation of Novel Gum Based Drug Delivery System of An Antiemetic Drug
The study was to formulate and evaluate medicated chewing gum of meclizine hydrochloride, an antiemetic drug used in nausea, vomiting and motion sickness. The chewing gums were prepared by direct compression method using different ratio of directly compressible gum base (Pharmagum S) in order to obtain optimized formulation. Eight different formulations of chewing gums of meclizine hydrochloride were prepared, which contained various concentration of pharmagum S and Soya powder. The chewing gums which prepared by direct compression method were characterized by pre- compression characters, post compression character, buccal absorption study, drug content and in vitro drug release studies. All the formulations gave satisfactory results in terms of pre compression characters, post compression character, drug content, and in vitro drug release. The best compression characters and 97.88±0.69 % in vitro drug release profile were achieved in formulation MCG5 with a gum and soya powder concentration of 775 mg and 140 mg and FTIR study of optimized MCG5 has shown satisfactory result in terms of drug: polymer compatibility. So MCG5 was taken as optimized batch
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