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Natural gums as sustained release carriers: development of gastroretentive drug delivery system of ziprasidone HCl

机译:天然胶作为持续释放的载体:盐酸齐拉西酮的胃滞留药物递送系统的开发

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Background Objective of this study is to show the potential use of natural gums in the development of drug delivery systems. Therefore in this work gastro retentive tablet formulations of ziprasidone HCl were developed using simplex lattice design considering concentration of okra gum, locust bean gum and HPMC K4M as independent variables. A response surface plot and multiple regression equations were used to evaluate the effect of independent variables on hardness, flag time, floating time and drug release for 1 h, 2 h, and 8 h and for 24 h. A checkpoint batch was also prepared by considering the constraints and desirability of optimized formulation to improve its in vitro performance. Significance of result was analyzed using ANOVA and p was considered statistically significant. Results Formulation chiefly contains locust bean gum found to be favorable for hardness and floatability but combined effect of three variables was responsible for the sustained release of drug. The in vitro drug release data of check point batch (F8) was found to be sustained well compared to the most satisfactory formulation (F7) of 7 runs. The ‘n’ value was found to be between 0.5 and 1 suggesting that release of drug follows anomalous (non-fickian) diffusion mechanism indicating both diffusion and erosion mechanism from these natural gums. Predicted results were almost similar to the observed experimental values indicating the accuracy of the design. In vivo floatability test indicated non adherence to the gastric mucosa and tablets remain buoyant for more than 24 h. Conclusions Study showed these eco-friendly natural gums can be considered as promising SR polymers.
机译:背景技术本研究的目的是显示天然树胶在药物输送系统开发中的潜在用途。因此,在这项工作中,以黄秋葵胶,刺槐豆胶和HPMC K4M的浓度为自变量,使用单纯形格子设计开发了盐酸齐拉西酮的胃滞留片剂。使用响应曲面图和多元回归方程评估自变量对硬度,f 滞后时间,漂浮时间和药物释放1 h,2的影响。小时,8小时和24小时。还考虑了优化配方的约束条件和合意性以改善其体外性能,从而准备了一个检查点批次。结果的显着性使用ANOVA分析,并且p被认为具有统计学意义。结果制剂主要包含刺槐豆胶,被发现对硬度和漂浮性有利,但是三个变量的综合作用导致药物的持续释放。与最满意的7次运行配方(F7)相比,检查点批次(F8)的体外药物释放数据被发现保持良好。发现“ n”值在0.5到1之间,这表明药物的释放遵循异常(非菲克)扩散机制,表明这些天然胶的扩散和侵蚀机制同时存在。预测结果与观察到的实验值几乎相似,表明设计的准确性。体内漂浮性测试表明不粘连胃粘膜,片剂漂浮超过24小时。结论研究表明,这些生态友好型天然胶可以被认为是有前途的SR聚合物。

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