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Karaya and ghatti gum as a novel polymer blend in preparation of extended release tablets: optimization by factorial design

机译:Karaya和Ghatti Gum作为一种新型聚合物混合物,用于制备延长释放片剂:通过因数设计优化

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The objective of the study was to formulate sustained release matrix tablets of diclofenac sodium using karaya and ghatti gum as the matrix polymers. 3(2)full factorial design was employed to optimize the drug release profile systematically. Matrix tablets were prepared by the wet granulation technique. The dependent variables selected were, % of drug released in first hour (Y-1). % of drug released in 1211(Y-2), diffusion exponent (n) (Y-3) and time taken for the 50 % of the drug release (T-50%) (Y4). The independent variables are amount of karaya (X-1) and gatti gum (X-2). The FTIR and DSC studies confirmed the drug-polymer compatibility and the pre-compression granular properties were assessed indicating a good flow property. The results of evaluation of the tablets were found to be within the standard limits indicating pharmaco-technical characteristics. The response variables studied were found as follows: 1/2 ranged between 2.57 to 26.74 %. Y-2 was found robe between 61.87 to 101.982 To. Y-3 ranged between 0.45 to 1.26 and Y-1 ranging between 3.98 to 9.56 h, respectively, for batches. The release data showed a good fit in zero order, Higuchi & Peppa's equation with high R-2 value. The best fit was Peppa:s model. It was observed that the rate of swelling and erosion was found to compliment the drug release kinetics which was further confirmed by SEM studies. The experimental values were in close agreement with the predicted response, indicating adequate fitting and validation of formula generated by constrained optimization. Results of the stability studies showed no significant changes in drug content, physical appearance or the dissolution profile of the prepared tablets. Thus, the experimental results obtained indicated that the feasibility of the blend of two gums can be used efficiently in order W formulate a sustained release tablet without any lag effect.
机译:该研究的目的是使用Karaya和Ghatti Gum制备双氯芬酸钠的缓释基质片作为基质聚合物。 3(2)采用完整的因子设计来系统地优化药物释放曲线。通过湿造粒技术制备基质片。选择的依赖变量是在第一小时(Y-1)中释放的药物的百分比。在1211(Y-2)中释放的药物的百分比,扩散指数(N)(Y-3)和用于50%的药物释放(T-50%)(Y4)的时间。独立变量是Karaya(X-1)和Gatti Gum(X-2)的量。 FTIR和DSC研究证实了药物 - 聚合物相容性,评估了预压缩粒状性质,表明良好的流动性质。发现评估片剂的结果是在标准限制内,该标准限制表明药物技术特征。研究的响应变量如下:1/2范围在2.57至26.74%之间。在61.87至​​101.982之间被发现y-2的长袍。 Y-3分别为0.45至1.26和y-1分别为3.98至9.56小时,分批。释放数据显示出良好的零级,HIGUCHI和PEPPA等式具有高R-2值。最合适的是Peppa:S模型。据观察,发现肿胀和腐蚀速率赞美通过SEM研究进一步证实的药物释放动力学。实验值与预测的响应密切一致,表明通过约束优化产生的公式的适当拟合和验证。稳定性研究的结果表明,制备片剂的药物含量,物理外观或溶出曲线没有显着变化。因此,获得的实验结果表明,可以有效地使用两种牙龈混合物的可行性,以便W制备持续释放片剂而无需任何滞后效果。

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