首页> 外文期刊>Journal of Drug Delivery and Therapeutics >FORMULATION DEVELOPMENT AND EVALUATION OF DILTIAZEM HYDROCHLORIDE GASTRO RETENTIVE FLOATING TABLETS
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FORMULATION DEVELOPMENT AND EVALUATION OF DILTIAZEM HYDROCHLORIDE GASTRO RETENTIVE FLOATING TABLETS

机译:盐酸地尔硫卓胃气固性漂浮片的配方开发和评价

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The investigation was concerned with design and characterization of oral sustained release gastro retentive floating tablets of DiltiazemHCl in order to improve efficacy and better patient compliance. Present investigation was to formulate, evaluate and optimize gastro retentive tablet of DiltiazemHCl. This tablets released drug till 24 hrs due to floating mechanism of polymers. Gastro retentive floating tablets were prepared by direct compression method using various proportions of polymersHPMC K4M, HPMC K100M,Carbopol 934, Ethyl cellulose, Xanthan gum along with Sodium bicarbonatethe sustained release behaviour of the fabricated tablets was investigated. Tablets were prepared by directcompretiontechnique.Formulation was optimized on the basis of acceptable tablet properties and in vitro drug release. The resulting formulation produced robust tablets with optimum hardness, consistent weight uniformity and low friability. All tablets but one exhibited gradual and near-complete sustained release for DiltiazemHCl (90-100%) at the end of 24 h. The results of dissolution studies indicated that formulation Dtz15 was found to be most successful as it exhibits drug release pattern very close to theoretical release profile. A decrease in release kinetics of the drug was observed on increasing polymer ratio.
机译:该研究与盐酸地尔硫卓口服缓释胃滞留漂浮片剂的设计和表征有关,以提高疗效和改善患者依从性。目前的研究是配制,评估和优化盐酸地尔硫卓的胃滞留片。由于聚合物的漂浮机制,该片剂可释放药物直至24小时。采用不同比例的聚合物HPMC K4M,HPMC K100M,Carbopol 934,乙基纤维素,黄原胶和碳酸氢钠,通过直接压片法制备胃滞留性漂浮片剂,研究了制成片剂的缓释性能。通过直接压制技术制备片剂。在可接受的片剂性质和体外药物释放的基础上优化了制剂。所得制剂产生具有最佳硬度,一致的重量均匀性和低脆性的坚固片剂。在24小时结束时,除一种片剂外,所有片剂均显示盐酸地尔硫卓(90-100%)的逐渐和接近完全的持续释放。溶出度研究的结果表明,发现制剂Dtz15最成功,因为它显示的药物释放模式非常接近理论释放曲线。随着聚合物比例的增加,药物的释放动力学下降。

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