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首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >APPLICATION OF CENTRAL COMPOSITE DESIGN FOR OPTIMIZATION OF EFFERVESCENT FLOATING TABLETS USING HYDROPHILIC POLYMERS
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APPLICATION OF CENTRAL COMPOSITE DESIGN FOR OPTIMIZATION OF EFFERVESCENT FLOATING TABLETS USING HYDROPHILIC POLYMERS

机译:中心复合材料设计在亲水性聚合物泡腾片优化中的应用

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The aim of the present study was to optimize effervescent floating tablets of Cefixime Trihydrate as model drug by optimization of polymers concentration using central composite design. Mean dissolution time (MDT), time required to release 50% of drug ( t 50% ), drug release at 2?h ( R 2h ) and dissolution efficiency in 2 h (DE 2h ) were taken as target responses, where as the quantity of different polymers such as Carbopol 934P (viscoelastic agent), Sod.CMC (swelling agent) were considered as independent variables. A second-order polynomial equation was determined by the multiple regression analysis of the experimental data. The best fitting model was selected based on the comparisons of the coefficient of determination (r 2 ), adjusted coefficient of determination (adj. r 2 ). In addition, analysis of variance (ANOVA) was used to evaluate the statistical significance of the quadratic polynomial model. The optimum values for the critical components were obtained as 13.151% Carbopol 934P and 4.08% of Sod.CMC with predicted value of 4.926 h MDT, 5.257 h t 50% , 27.6316% R 2h and 16.5951% DE 2h from desirability and overlay plot. Further the reliability of the model was checked by validating the observed responses from optimized formula. The drug release from characteristics of all formulations followed Higuchi model with a non-Fickian diffusion mechanism. Further the data of FTIR study showed there was no interaction of drug and excipients used for the preparation of floating tablets.
机译:本研究的目的是通过使用中心复合设计优化聚合物浓度来优化头孢克肟三水合物泡腾片作为模型药物。将平均溶解时间(MDT),释放50%的药物所需的时间(t 50%),在2?h的药物释放(R 2h)和在2 h的溶解效率(DE 2h)作为目标响应,其中诸如Carbopol 934P(粘弹性剂),Sod.CMC(膨胀剂)之类的不同聚合物的数量被视为独立变量。通过对实验数据进行多元回归分析,确定了二阶多项式方程。基于确定系数(r 2)和调整后的确定系数(adr。r 2)的比较,选择最佳拟合模型。另外,使用方差分析(ANOVA)来评估二次多项式模型的统计显着性。关键成分的最佳值分别为13.151%Carbopol 934P和Sod.CMC的4.08%,根据合意度和覆盖图,预测值为4.926 h MDT,5.257 h t 50%,27.6316%R 2h和16.5951%DE 2h。此外,通过验证来自优化公式的观察响应来检查模型的可靠性。所有制剂特性的药物释放均遵循Higuchi模型,并具有非Fickian扩散机制。 FTIR研究的进一步数据表明,用于制备浮片的药物和赋形剂没有相互作用。

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