Sustained Release Matrix Tablets of Furosemide

D. Nagendrakumar, G. KeshavshettiG, G. ShardorA
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引用次数: 3

Abstract

Objective: The objective of the present study was to develop and evaluate once-daily sustained release matrix tablets of furosemide using hydroxypropylmethyl cellulose K4M, xanthan gum and sodium alginate as release retarding polymers. Methodology: The matrix tablet formulations were prepared by using different drug: polymer ratios (1:1, 1:2, 1:3, 1:4 and 1:5). The prepared matrix tablets were evaluated for pre-compression parameters like angle of repose, bulk density, tap density and post-compression parameters like hardness, thickness, weight variation, friability, percent drug content and in vitro drug release studies as per USP guidelines. Results: The in vitro drug release data of all the prepared tablet formulations of furosemide were subjected to goodness of fit test by linear regression analysis according to zeroorder and first-order kinetics. Conclusion: The formulation SF 2 containing drug: sodium alginate ratio of 1:2 offered the required in vitro drug release rate according to the official limits of drug release as per USP and selected as a promising formulation among the fifteen formulations which shows 85% drug release in 12 hrs.
速尿缓释基质片
目的:以羟丙基甲基纤维素K4M、黄原胶和海藻酸钠为缓释聚合物,制备速尿缓释基质片,并对缓释效果进行评价。方法:采用不同药聚合物比(1:1、1:2、1:3、1:4、1:5)制备基质片。根据USP指南对制备的基质片进行静置角、堆积密度、轻叩密度等预压缩参数和硬度、厚度、重量变化、脆性、药物含量百分比和体外药物释放研究等后压缩参数的评价。结果:采用零级和一级动力学线性回归分析,对所制备的呋塞米片剂的体外释放数据进行拟合优度检验。结论:本品与海藻酸钠的比例为1:2,可满足美国药典规定的释药官方限量要求,在15个制剂中以12 h释药85%为理想制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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