Optimization of a matrix tablet formulation using a mixture design.

Acta pharmaceutica Nordica Pub Date : 1992-01-01
P J Waaler, C Graffner, B W Müller
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Abstract

The simplex centroid design was applied to the optimization of a modified release tablet formulation. A base granulation was made with the active ingredient naftidrofuryl. The variables investigated included fractions of the excipients microcrystalline cellulose, lactose and dicalcium phosphate dihydrate. The release rate, crushing strength, friability and weight variation were determined as response parameters. Mathematical models were fitted to the data obtained by the lattice method, described by Scheffé and by means of multiple linear regression. Regression analysis indicated a relatively good fit of the models. On the basis of the regression models, contour plots were constructed. An increase in the amount of dicalcium phosphate caused lower release rate and increased weight variation. An increase in the content of lactose showed lower strength and increased friability, whereas an increase in the amount of microcrystalline cellulose had the opposite effect.

用混合设计优化基质片的配方。
采用单纯形质心设计对一种改良缓释片的配方进行了优化。以活性成分萘磺呋喃为原料制备碱制粒。研究的变量包括辅料微晶纤维素、乳糖和磷酸二钙二水合物的组分。以释放速率、破碎强度、脆性和重量变化为响应参数。用scheff描述的格法和多元线性回归方法对得到的数据拟合数学模型。回归分析表明模型拟合较好。在回归模型的基础上,构建等高线图。磷酸二钙用量的增加导致释放速率降低,重量变化增大。乳糖含量的增加表明强度降低,脆性增加,而微晶纤维素含量的增加则具有相反的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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