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Formulation and In-Vitro evaluation of Aceclofenac Controlled release tablets by wet granulation method and solid dispersion technique

机译:湿法制粒和固相分散技术制备醋氯芬酸控释片的处方及体外评价

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摘要

The objective of the present study was to develop controlled release matrix tablets of Aceclofenac by wet granulation method and solid dispersion technique using Eudragit RL100 as a rate controlled material. Drug-excipient computability studies were conducted by FT-IR and DSC, results showed no chemical interaction was observed between drug and excipient. The granules were evaluated found free flow properties. The tablets were subjected to thickness, hardness, friability weight variation and in-vitro drug release studies. Results of in vitro drug release studies revealed that drug release was controlled for 12hrs prepared by wet granulation method over the formulations by solid dispersion technique. The drug release pattern followed zero order kinetics and the mechanism of drug release was governed by peppas model. The 'n' values were found to be more than 1 (n>1) which indicated that the drug release was predominately controlled by super case II diffusion.
机译:本研究的目的是通过湿法制粒和采用Eudragit RL100作为速率控制材料的固体分散技术开发醋氯芬酸控释基质片剂。通过FT-IR和DSC进行了药物-赋形剂可计算性研究,结果表明在药物和赋形剂之间未观察到化学相互作用。评估颗粒发现自由流动性。对片剂进行厚度,硬度,易碎重量变化和体外药物释放研究。体外药物释放研究的结果表明,通过固体分散技术,通过湿法制粒制备的制剂对药物的释放控制了12小时。药物释放规律遵循零级动力学,药物释放机理受peppas模型控制。发现“ n”值大于1(n> 1),这表明药物释放主要由超级病例II扩散控制。

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