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首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >FORMULATION AND EVALUATION OF SUSTAINED RELEASE FLOATING TABLETS OF PIOGLITAZONE EMPLOYING OLIBANUM GUM AND HPMC
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FORMULATION AND EVALUATION OF SUSTAINED RELEASE FLOATING TABLETS OF PIOGLITAZONE EMPLOYING OLIBANUM GUM AND HPMC

机译:使用奥利巴姆胶和HPMC的吡格列酮缓释漂浮片的配方与评价

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The objective of the study is to formulate and evaluate floating tablets of pioglitazone employing olibanum gum, a natural gum resin in comparison to HPMC K15 M, a synthetic cellulose derivative. Floating tablets of pioglitazone were prepared employing olibanum gum and HPMC K15 M as matrix formers, sodium bicarbonate as gas generating agent and bees wax and ethyl cellulose as floating enhancers and the tablets were evaluated for In vitro buoyancy and drug release characteristics. The floating characteristics of the formulations which contained sodium bicarbonate (15%) alone were not satisfactory with both the two polymers and need to be improved. Increasing the strength of sodium bicarbonate from 15% to 20% has not much improved the floating characteristics. Addition of beeswax (15%) and ethyl cellulose (5%) has significantly enhanced the buoyancy of the tablets formulated with both the two polymers. Pioglitazone release from the floating tablets prepared was slow and spread over 24 h and depended on the polymer used and composition of the tablets. Drug release was diffusion controlled and followed zero order kinetics. Non-Fickian diffusion was the drug release mechanism from all the tablets formulated. Pioglitazone release from the tablets containing beeswax and ethyl cellulose along with the matrix forming polymers was slow and spread over more than 24 h. The T90 values were in the range 19 – 24 h with these tablets. These tablets exhibited a floating time of 44 h after a floating lag time in the range 2-6 min. Olibanum is found suitable as matrix former for floating tablets and is comparable to HPMC K15M, a widely used polymer for floating tablets and for controlled release. Since olibanum gum is of natural origin it is non-toxic biocompatable and cheaper.
机译:该研究的目的是与天然纤维素树脂olibanum胶与合成纤维素衍生物HPMC K15 M相比,配制和评估吡格列酮的漂浮片剂。制备吡格列酮漂浮片剂,以寡聚树胶和HPMC K15 M为基质形成剂,以碳酸氢钠为产气剂,以蜂蜡和乙基纤维素为漂浮增强剂,并对该片剂的体外浮力和药物释放特性进行评估。仅包含碳酸氢钠(15%)的制剂的漂浮特性对于两种聚合物都不令人满意,并且需要改进。将碳酸氢钠的强度从15%增加到20%并没有太大改善漂浮特性。蜂蜡(15%)和乙基纤维素(5%)的加入显着增强了由两种聚合物配制的片剂的浮力。吡格列酮从制备的漂浮片剂中释放缓慢且散布在24小时内,这取决于所用的聚合物和片剂的组成。药物释放受扩散控制,并遵循零级动力学。非菲克扩散是所有配制片剂的药物释放机制。吡格列酮从含有蜂蜡和乙基纤维素以及形成基质的聚合物的片剂中释放缓慢,并且散布超过24小时。这些药片的T90值在19-24小时范围内。这些片剂在2-6分钟范围内的漂浮滞后时间后显示出44 h的漂浮时间。发现奥利巴宁适合用作漂浮片剂的基质形成剂,并且可与HPMC K15M(一种广泛用于漂浮片剂和控释的聚合物)相媲美。由于olibanum胶是天然来源的,因此它是无毒的生物相容性且便宜。

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