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Michaelis-Menten Kinetics under Spatially Constrained Conditions: Application to Mibefradil Pharmacokinetics

机译:空间受限条件下的Michaelis-Menten动力学:Mibefradil药代动力学的应用

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摘要

Two different approaches were used to study the kinetics of the enzymatic reaction under heterogeneous conditions to interpret the unusual nonlinear pharmacokinetics of mibefradil. Firstly, a detailed model based on the kinetic differential equations is proposed to study the enzymatic reaction under spatial constraints and in vivo conditions. Secondly, Monte Carlo simulations of the enzyme reaction in a two-dimensional square lattice, placing special emphasis on the input and output of the substrate were applied to mimic in vivo conditions. Both the mathematical model and the Monte Carlo simulations for the enzymatic reaction reproduced the classical Michaelis-Menten (MM) kinetics in homogeneous media and unusual kinetics in fractal media. Based on these findings, a time-dependent version of the classic MM equation was developed for the rate of change of the substrate concentration in disordered media and was successfully used to describe the experimental plasma concentration-time data of mibefradil and derive estimates for the model parameters. The unusual nonlinear pharmacokinetics of mibefradil originates from the heterogeneous conditions in the reaction space of the enzymatic reaction. The modified MM equation can describe the pharmacokinetics of mibefradil as it is able to capture the heterogeneity of the enzymatic reaction in disordered media.
机译:两种不同的方法用于研究异质条件下酶促反应的动力学,以解释米贝拉地尔不同寻常的非线性药代动力学。首先,提出了基于动力学微分方程的详细模型,以研究在空间限制和体内条件下的酶促反应。其次,在二维方格中对酶反应的蒙特卡罗模拟,特别强调了底物的输入和输出,被用于模拟体内条件。酶促反应的数学模型和蒙特卡洛模拟均重现了均相介质中的经典米利斯-门腾(MM)动力学和分形介质中的非寻常动力学。基于这些发现,开发了随时间变化的经典MM方程,用于确定无序培养基中底物浓度的变化速率,并成功地用于描述米贝拉地的血浆浓度-时间数据并得出模型的估计值参数。米贝拉地尔异常的非线性药代动力学起源于酶促反应反应空间中的异质条件。修改后的MM方程可以描述米贝拉地尔的药代动力学,因为它能够捕获无序培养基中酶促反应的异质性。

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