Release characteristics of gliclazide in a matrix system.

In Silico Pharmacology Pub Date : 2021-01-11 eCollection Date: 2021-01-01 DOI:10.1007/s40203-020-00068-5
Mehmet Melih Tatlisoz, Esra Demirturk, Cetin Canpolat
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引用次数: 3

Abstract

In this study, the release characteristics of gliclazide in a polymeric matrix system, which is used for controlled drug release purposes, are conducted experimentally and numerically. A code using the finite element method predicting the drug release behavior of gliclazide matrix system in an aqueous medium is developed. The parameters having significant importance in drug release kinetics, such as structure factor, the slab's size and shape are varied systematically. The consistent reduction in the solid drug during the dissolution process is evaluated. The numerical data agree well with the experimental results. Therefore, the controlled drug release of gliclazide is accurately modeled by the present numerical code. The results imply that the porosity of the matrix system has the most significant effect on the drug dissolution rate. The reduction in the tablet's diameter and utilization of cylindrical slab geometry increases the speed of the drug dissolution in the aqueous medium.

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格列齐特在基质体系中的释放特性。
本研究通过实验和数值方法研究了格列齐特在用于药物控释的聚合物基质体系中的释放特性。编制了用有限元法预测格列齐特基质体系在水介质中的药物释放行为的程序。对药物释放动力学有重要影响的参数,如结构因素、板坯的大小和形状等,是有系统变化的。在溶解过程中,固体药物的一致性减少被评估。数值计算结果与实验结果吻合较好。因此,格列齐特的受控药物释放可以用目前的数字代码精确地模拟。结果表明,基质体系孔隙度对药物溶出率的影响最为显著。片剂直径的减小和圆柱形片剂几何形状的利用增加了药物在水介质中的溶解速度。
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