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首页> 外文期刊>Chemical and Pharmaceutical Bulletin >Implementing PRED Subroutine of NONMEM for Versatile Pharmacokinetic Analysis Using Fast Inversion of Laplace Transform (FILT)
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Implementing PRED Subroutine of NONMEM for Versatile Pharmacokinetic Analysis Using Fast Inversion of Laplace Transform (FILT)

机译:使用LAPLACE变换的快速反转实现多功能药代动力学分析的非谋区的PREG子程序(FILT)

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摘要

In pharmacokinetic (PK) analysis, conventional models are described by ordinary differential equations (ODE) that are generally solved in their Laplace transformed forms. The solution in the Laplace transformed forms is inverse Laplace transformed to derive an analytical solution. However, inverse Laplace transform is often mathematically difficult. Consequently, numerical inverse Laplace transform methods have been developed. In this study, we focus on extending the modeling functions of Nonlinear Mixed Effect Model (NONMEM), a standard software for PK and population pharmacokinetic (PPK) analyses, by adding the Fast Inversion of Laplace Transform (FILT) method, one of the representative numerical inverse Laplace transform methods. We implemented PREDFILT, a specialized PRED subroutine, which functions as an internal model unit in NONMEM to enable versatile FILT analysis with second-order precision. The calculation results of the compartment models and a dispersion model are in good agreement with the ordinary analytical solutions and theoretical values. Therefore, PREDFILT ensures enhanced flexibility in PK or PPK analyses under NONMEM environments.
机译:在药代动力学(PK)分析中,常规模型由普通微分方程(ode)描述,这些方程(ode)通常在其拉普拉斯变换形式中解决。拉普拉斯变换形式中的溶液是逆拉普拉斯变换以导出分析溶液。然而,逆拉普拉斯变换通常困难。因此,已经开发了数值逆拉普拉斯变换方法。在这项研究中,我们专注于扩展非线性混合效果模型(非默米姆)的建模功能,是PK和人口药代动力学(PPK)分析的标准软件,通过增加拉普拉斯变换(FILT)方法,其中一个代表性数值逆拉普拉斯变换方法。我们实现了预先菲尔特,专用PEAM子程序,它用作非梅内的内部模型单元,以使多功能FILT分析以二阶精度实现。隔室模型和分散模型的计算结果与普通的分析解决方案和理论值吻合良好。因此,预先菲尔特可确保在非梅环境下的PK或PPK分析中的增强灵活性。

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