Melati Permata Hati, Yandi Syukri, Bambang Hernawan Nugroho
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引用次数: 1

摘要

本研究旨在制备漂浮体系盐酸二甲双胍缓释片并对其进行评价。以HPMC K4M和壳聚糖为基质,w/w分别为17.78%和4.44%,采用湿法制粒;14.44%: 7.78%;11.11%: 11.11%, 7.78%, 14.44%;4.44%: 17.78%。对其重量变化、药物含量、硬度、脆性、体外漂浮和释放度进行了评价。使用USP溶出仪II(桨),在37±0.50℃下900 ml HCl pH 3.0介质中进行6小时的溶出研究。所有片剂的处方均与美国药典(USP)和印尼Farmakope参考标准的要求物理片具有密切的相似性。高HPMC K4M和低壳聚糖的基质均表现出悬浮滞后时间缩短、持续时间延长的特点。同时,片剂崩解程度最低。释放度试验表明,所有处方的溶出度均不符合盐酸二甲双胍缓释片的要求。实验结果表明,以HPMC - K4M和壳聚糖为基质的盐酸二甲双胍缓释片能漂浮,但不形成缓释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pengaruh Kombinasi Matriks terhadap Karakter Tablet Metformin HCl Lepas Lambat Sistem Floating Effervescent
The research aimed to prepare and evaluate of sustained release metformin HCl tablet with floating system. The tablets were prepared by wet granulation using HPMC K4M and chitosan as matrixes with proportions (w/w) 17.78%:4.44%; 14.44%:7.78%; 11.11%:11.11% ;7.78%;14.44%; 4.44%:17.78%. The tablets were evaluated of weight variation, drug content, hardness, friability, and in vitro floating and drug release studies. The dissolution study had been carried out for 6 hours using USP dissolution apparatus II (paddle) in 900 ml HCl pH 3.0 media at 37±0.50C. All tablet formulas showed closed similarity with the requirement physical tablet of United State Pharmacopea (USP) and Farmakope Indonesia reference. The matrixes containing higher HPMC K4M, and lower chitosan showed floating lag time decreased and duration time increased. Meanwhile, tablet disintegration was the lowest. The release test showed that all formulas did not meet the requirements dissolution metformin HCl sustained release tablet. The result of this study is sustained release tablet metformin HCl with matrixes HPMC K4M and chitosan able to float, but it did not form sustained release.
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