Formulation and Evaluation of Cephalexin Extended-release Matrix Tablets Using Hydroxy Propyl Methyl Cellulose as Rate-controlling Polymer

易碎性 聚合物 差示扫描量热法 溶解 乙基纤维素 材料科学 基质(化学分析) 甲基纤维素 色谱法 粒径 化学 纤维素 数学 复合材料 有机化学 物理化学 物理 热力学
作者
J.T. Sahadevan,R. Prabhakaran,J. Vijay,Ritu Gilhotra
出处
期刊:Journal of Young Pharmacists [EManuscript Services]
卷期号:4 (1): 3-12 被引量:14
标识
DOI:10.4103/0975-1483.93570
摘要

The present investigation reports the design and evaluation of six-hour extended release film-coated matrix tablets of cephalexin using different grades of hydrophilic polymer hydroxypropylmethylcellulose (HPMC) employing direct compression method.The preformulation studies performed included the physical compatibility studies, Differential Scanning Calorimetry analysis, drug characterization using Fourier Transform Infra Red spectroscopic analysis and particle size analysis using sieve method.The tablets were evaluated for weight variation, hardness, thickness and friability.Results of the studies indicate that the polymers used have significant release-retarding effect on the formulation.The dissolution profile comparison of the prepared batches P1 to P8 and market preparation (Sporidex AF 375) was done by using Food and Drug Administration-recommended similarity factor (f 2 ) determination.The formulation P8 (10% HPMC K4M, 15% HPMC 15cps) with a similarity factor (f 2 ) of 77.75 was selected as the optimized formulae for scale-up batches.The dissolution data of the best formulation P8 was fitted into zero order, first order, Higuchi and Korsemeyer-Peppas models to identify the pharmacokinetics and mechanism of drug release.The results of the accelerated stability study of best formulation P8 for three months revealed that storage conditions were not found to have made any significant changes in final formulation F3.The release of cephalexin was prolonged for 6 h by using polymer combinations of HPMC and a twice daily matrix tablet was formulated.
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