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In Situ Forming Formulation: Development Evaluation and Optimization Using 33 Factorial Design

机译:原位成型配方:使用33因子设计进行开发评估和优化

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摘要

The present investigation concerns with the development and optimization of an in situ forming formulation using 33 full factorial design experimentation. Metformin, an antidiabetic drug with upper part of gastrointestinal tract as absorption window was used as a model drug. The formulations were designed with an objective to retain in stomach for an extended time period. The effect of three independent factors—concentrations of sodium alginate (X1), gellan gum (X2), and metformin (X3) on in vitro drug release were used to characterize and optimize the formulation. Five dependent variables—release exponent (Y1), dissolution efficiency (Y2), drug release at 30 min (Y3), 210 min (Y4), and 480 min (Y5) were considered as optimization factors. The data were statistically analyzed using ANOVA, and a p < 0.05 was considered statistically significant. Three dimensional surface response plots were drawn to evaluate the interaction of independent variables on the chosen dependent variables. Of the prepared 27 formulations, the responses exhibited by batch F17 containing medium level sodium alginate (X1), low level gellan (X2), and medium level metformin (X3) were similar to the predicted responses.
机译:本研究涉及使用3 3 全因子设计实验开发和优化原位成型配方。以胃肠道上部为吸收窗口的抗糖尿病药物二甲双胍用作模型药物。设计该制剂的目的是在胃中保留更长的时间。海藻酸钠(X1),吉兰糖胶(X2)和二甲双胍(X3)的三个独立因素对体外药物释放的影响用于表征和优化制剂。优化因素包括五个因变量-释放指数(Y1),溶出效率(Y2),30分钟(Y3),210分钟(Y4)和480分钟(Y5)的药物释放。使用方差分析对数据进行统计分析,p 0.05被认为具有统计学意义。绘制了三维表面响应图,以评估自变量在所选因变量上的相互作用。在所准备的27种配方中,批次F17所含中度藻酸钠(X1),低度结冷胶(X2)和中度二甲双胍(X3)所显示的响应与预测的响应相似。

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