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首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Formulation and Evaluation of Floating Tablets of Pioglitazone Employing Calcium Starch
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Formulation and Evaluation of Floating Tablets of Pioglitazone Employing Calcium Starch

机译:钙淀粉吡格列酮漂浮片的研制与评价

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摘要

The objective of the study is to formulate and evaluate floating tablets of pioglitazone employing calcium starch, a new modified starch in comparison to hydroxy propyl methyl cellulose R15M, a synthetic cellulose derivative. Floating tablets of pioglitazone were prepared employing calcium starch and hydroxy propyl methyl cellulose, KI5M as matrix formers, sodium bicarbonate as gas generating agent and bees wax as floating enhancer and the tablets were evaluated for in vitro buoyancy and drug release characteristics. Tablets formulated employing calcium starch (50 %), sodium bicarbonate (10 %) and bees wax (10 %) exhibited floating over 36 h with a floating lag time of 5-10 rain. Pioglitazone release from the floating tablets formulated was slow, spread over more than 24 h and depended on the polymer used and its strength and concentration of sodium bicarbonate in the tablets. Drug release was diffusion controlled and followed first order kinetics. Fickian diffusion was the drug release mechanism from all the tablets formulated. Calcium starch gave slow, controlled and complete drug release in 24 h. Whereas hydroxy propyl methyl cellulose, K15M gave slow but incomplete drug release. Calcium starch was found to be a better matrix former than hydroxy propyl methyl cellulose for floating tablets.
机译:该研究的目的是使用钙淀粉(一种新的改性淀粉,与合成纤维素衍生物羟丙基甲基纤维素R15M相比)配制和评估吡格列酮的漂浮片剂。以钙淀粉和羟丙基甲基纤维素,KI5M为基质形成剂,碳酸氢钠为产气剂和蜂蜡为漂浮增强剂,制备了吡格列酮漂浮片剂,并对片剂的体外浮力和药物释放特性进行了评估。使用淀粉淀粉(50%),碳酸氢钠(10%)和蜂蜡(10%)配制的片剂在36小时内漂浮,漂浮滞后时间为5-10雨。吡格列酮从配制的漂浮片剂中释放缓慢,分布超过24小时,并且取决于所用聚合物及其在片剂中的强度和碳酸氢钠浓度。药物释放受扩散控制,并遵循一级动力学。 Fickian扩散是所有配制片剂的药物释放机制。淀粉淀粉在24小时内释放缓慢,受控且完全。而羟丙基甲基纤维素,K15M释放缓慢但不完全。对于漂浮片剂,发现钙淀粉是比羟丙基甲基纤维素更好的基质形成剂。

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