首页> 外文期刊>Journal of Drug Delivery and Therapeutics >Formulation and evaluation sustained release mucoadhesive gastroretentive pantoprazole sodium sesquihydrate tablets for anti–ulcer
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Formulation and evaluation sustained release mucoadhesive gastroretentive pantoprazole sodium sesquihydrate tablets for anti–ulcer

机译:缓释粘膜粘附胃滞留top托拉唑倍半水合物抗溃疡药的研制与评价

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Objective: The objective of this research work is to develop and evaluate the mucoadhesive gastroretentive tablets of an anti – ulcer drug for sustain release. Materials and Methods: Mucoadhesive tablets were prepared by direct compression method using Hydroxy propyl methyl cellulose K4M, Carbopol 940 NF and Guar gum in the various drug – polymer ratios. The prepared tablets were evaluated for their pre and post compression parameters. In this study the optimized formulation was obtained within the specified limits. Results: The final optimized formulation was showed mucoadhesion time 12 h, mucoadhesive strength of tablets were ready with HPMC K4M, Carbopol 940 NF and gum were found to be 45 g and the extreme proportion of drug release was obtained 97.11% at the completion of 12 h. The drug release mechanism for optimized formulations of pantoprazole mucoadhesive sustain release tablets was observed to be zero order kinetic model. Conclusion: The formulation of hydroxy propyl methyl cellulose showed excellent mucoadhesive ability and a suitable drug release pattern.
机译:目的:这项研究工作的目的是开发和评估一种抗溃疡药物的粘膜粘附胃滞留片,用于持续释放。材料和方法:通过直接压片法,使用羟丙基甲基纤维素K4M,Carbopol 940 NF和瓜尔胶以各种药物-聚合物比率直接制备粘膜粘膜片剂。评价制备的片剂的压缩前后参数。在这项研究中,在规定的限度内获得了最佳配方。结果:最终的优化配方显示粘膜粘附时间为12 h,HPMC K4M制备的片剂的粘膜粘附强度为Carbopol 940 NF和口香糖,为45 g,在12次完成后获得的药物释放极高比例为97.11%。 H。观察到潘托拉唑粘膜持续释放片剂的优化制剂的药物释放机理为零级动力学模型。结论:羟丙基甲基纤维素制剂具有优异的粘膜粘附能力和合适的药物释放方式。

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