Pharmacokinetics Study of Metformin – Mathematical Modelling and Simulation

Sukankana Chakraborty , Kriti Arora , Prakash Kumar Sharma , Arijit Nath , Chiranjib Bhattacharjee
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引用次数: 1

Abstract

In the present investigation, a deterministic mathematical model of the pharmacokinetics of Metformin was developed using the first principle of chemical engineering (mass balance). The mathematical model developed with precision, can predict the concentration time history of the drug interest in stomach, liver, intestine, and the peripheral areas. According to this model, after administration, the drug is dissolved in the stomach following first order kinetics. The intestinal absorption of Metformin is majorly mediated by plasma membrane monoamine transporter. In liver Metformin takes part in various metabolic pathways which subsequently aid the adsorption of the drug in different cellular systems. No intermediate metabolites of Metformin have been identified till now. The major route for elimination of Metformin is through tubular secretion, in an unchanged form in the urine. The outcome of the predicted data closely matches the experimental finding, extracted after a meticulous scrutiny of the accessible literature, and results of clinical trials. The model is highly realistic and pragmatic in its practice.

二甲双胍的药代动力学研究——数学建模与模拟
在本研究中,利用化学工程第一原理(质量平衡)建立了二甲双胍药代动力学的确定性数学模型。建立的数学模型能准确预测药物在胃、肝、肠和外周区域的浓度时间史。根据该模型,给药后,药物按照一级动力学溶解在胃中。二甲双胍的肠道吸收主要由质膜单胺转运蛋白介导。在肝脏中,二甲双胍参与各种代谢途径,随后帮助药物在不同细胞系统中的吸附。目前尚未发现二甲双胍的中间代谢物。消除二甲双胍的主要途径是通过小管分泌,以不变的形式在尿液中。预测数据的结果与实验结果密切匹配,实验结果是在对可获得的文献进行细致审查后提取的,以及临床试验的结果。该模型在实践中具有很强的现实性和实用性。
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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