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首页> 外文期刊>International Journal of Biomedical and Advance Research >DESIGN, IN VITRO EVALUATION AND IN VIVO STUDIES OF NOVEL DELAYED RELEASE TABLETS OF PANTOPRAZOLE
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DESIGN, IN VITRO EVALUATION AND IN VIVO STUDIES OF NOVEL DELAYED RELEASE TABLETS OF PANTOPRAZOLE

机译:泮托拉唑的新型延迟释放片的设计,体外评估和体内研究

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摘要

In an effort to reduce production costs, a simple, direct compression delayed release formulation consisting of pantoprazole was investigated. Pantoprazole is a proton pump inhibitor belongs to group of benzimidazole. It is very efficient for the treatment of gastric and duodenum ulcers. Even in solid state pantoprazole is sensitive to heat, humidity, light and especially to substances containing an acidic group. For such types of drugs, enteric coating added to the formulation tends to avoid the stomach's acidic exposure, delivering them instead to a basic pH environment where they do not degrade, and give their desired action. Subcoating is desirable to protect the enteric coating. Opadry and Acryl-EZE systems have been utilized for subcoating and enteric coating respectively. Delayed-release tablets with good physical, mechanical and technological properties were obtained with use of different combinations of diluents, binders, superdisintegrants and lubricants. A comparative kinetic study of the present tablets and commercial tablets was established. The value for the similarity factor (f2 = 71.6) suggested that the dissolution profile of the present two delayed-release oral dosage forms are similar. Hixon–Crowell (erosion) kinetic profiles were achieved
机译:努力降低生产成本,研究了由泮托拉唑组成的简单直接压缩延迟释放制剂。 PantoPrazole是质子泵抑制剂属于苯并咪唑的组。它对于治疗胃和十二指肠溃疡是非常有效的。即使在固态的泮托拉唑也对热,湿度,光而敏感,尤其是含有酸性基团的物质。对于这种类型的药物,添加到制剂中的肠溶包衣易于避免胃的酸性暴露,而是将它们递送到它们不会降解的基本pH环境,并给出所需的作用。亚涂层是理想的,以保护肠溶涂层。 OPADRY和ACRYL-EZE系统已分别用于底涂层和肠涂层。利用不同组合的稀释剂,粘合剂,超级分体剂和润滑剂,获得具有良好物理,机械和技术性质的延迟释放片。建立了本片剂和商业片剂的比较动力学研究。相似性因子(F2 = 71.6)的值表明,本两个延迟释放口服剂型的溶出曲线是相似的。赫森 - 挤压(侵蚀)动力学型材是实现的

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