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首页> 外文期刊>Research journal of pharmacy and technology >Formulation and Evaluation Study of Azithromycin Tablets by Various Natural Polymers and their Comparative Preformulation Study
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Formulation and Evaluation Study of Azithromycin Tablets by Various Natural Polymers and their Comparative Preformulation Study

机译:各种天然聚合物的阿奇霉素片剂的制定与评价研究及其对比预制研究

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摘要

The present study was to formulate Azithromycin matrix tablet using Xanthan gum, and guar gum as natural polymers and to elucidate the effect of type of polymers and its concentration on release pattern of drug from sustained release matrix tablets. Azithromycin matrix tablets were prepared in two batches (batch number Fl to F2) by direct compression method using xanthan gum and guar gum as natural polymers and microcrystalline cellulose as a binder and pyrolidone as a water soluble polymer. The in vitro drug release studies of all the batches indicated that optimized formulation pertaining to Batch no. F2 was a promising system to provide sustained release effect of drug. The release pattern of the above formulation was best fitted to zero-order model and first order model. Mechanism of drug release followed was non-Fickian (super case-II) transport mechanism. Based on the above studies it can be concluded that this Azithromycin drug can be effectively formulated using different classes of natural polymers which can have greater bioavailability with less dose related side effects having better patient compliance.
机译:本研究是使用黄原胶和瓜尔胶作为天然聚合物配制阿奇霉素基片,并阐明聚合物类型及其浓度对来自缓释基质片的药物释放模式的作用。通过使用黄原胶和瓜尔胶作为天然聚合物和微晶纤维素作为水溶性聚合物,通过直接压缩方法用两批(批次数F1至F2)用两种批次(批次数F1至F2)制备两种批次(批次数Fl至F2)。所有批次的体外药物释放研究表明,优化的配方与分批NO有关。 F2是一种有助于提供药物持续释放效果的有希望的系统。上述配方的释放图案最适合零阶模型和一阶模型。药物释放机制遵循是非Fickian(超级案例-II)的运输机制。基于上述研究,可以得出结论,这种氮霉素药物可以使用不同类别的天然聚合物有效配制,其可以具有更大的生物利用度,具有更好的相关副作用具有更好的患者依从性。

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