首页> 外文会议>International symposium on controlled release of bioactive materials;Consumer diversified products conference >DEVELOPMENT IN-VITRO EVALUATION OF SUSTAINED RELEASE DILTIAZEM HYDROCHLORIDE TABLETS
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DEVELOPMENT IN-VITRO EVALUATION OF SUSTAINED RELEASE DILTIAZEM HYDROCHLORIDE TABLETS

机译:缓释盐酸地尔硫卓片剂的开发与体外评估

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Diltiazem hydrochloride is a calcium channel blocker widely employed not only in the treatment of cardiovascular disorders like hypertension, angina pectoris & arrythymias but also for the management of migrain, Raynands phenomenon & oesophageal motility disorders. Its water solubility, short elimination half life & therapeutic use in chronic disease, make it suitable as a candidate for prolongation of release from dosage forms. Matrix formulation was prepared to retard the release of drug. Eudragit RS 100,Eudragit RL 100 & Eudragit L were used to prepare matrix tablets. It was found that Eudragit RS 100,Eudragit L & Eudragit RL PM in the ratio of 60:20:20 ; along with plastizers diethyl phthalate (added as 10%dry polymer weight) provided sustained release of drag for period of 12 hours.
机译:盐酸地尔硫卓是一种钙通道阻滞剂,不仅广泛用于治疗高血压,心绞痛和心律失常等心血管疾病,还可以用于治疗偏头痛,雷氏现象和食道运动障碍。它的水溶性,消除半衰期短和在慢性疾病中的治疗用途,使其适合延长剂型的释放。制备基质制剂以延迟药物的释放。用Eudragit RS 100,Eudragit RL 100和Eudragit L制备基质片剂。发现Eudragit RS 100,Eudragit L&Eudragit RL PM的比例为60:20:20;与增塑剂邻苯二甲酸二乙酯(以聚合物干重的10%添加)一起提供了12个小时的持续释放阻力。

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