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Development of Evaluation Methods and Computer Softwares for Pharmacokinetic Analysis

机译:用于药代动力学分析的评估方法和计算机软件的开发

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Som eevaluation methods and computer analysis programs on personal computers have been developed for pharmacokinetic analysis. Akaike's Information Criterion (AIC) was introduced to statistically select an optimum model for drug disposition. The moment analysis ewhich has bee been used in chromatography and chemical engineer was applied to the evaluation of absorption, distribution, metabolism and excretion (ADME) of drugs. A pharmacokinetic analysis program based on nonlinear least squares, MULTI, was developed on a personal computer in the early age. We have made other analysis program MULTI (RUNGE) where a pharmacokinetic model is defined as ordinal differential equations, MULTI (FILT) based on a Fast Inverse Laplace Transform (FILT) and MULTI (FEM) based on the Finite Element Method (FEM). MULT12 (BAYES) based on Bayesian least squares and MULTI (ELS) based on extended least squares were developed for the population pharmacokinetics (PPK).
机译:SOM EEVALUITY方法和计算机分析课程已经开发用于药代动力学分析。 引入了Akaike的信息标准(AIC)以统计选择一种用于药物处理的最佳模型。 蜂蜂仔的瞬间分析应用于色谱和化学工程师的吸收,分布,代谢和排泄(Adme)的吸收,分布,代谢和排泄(Adme)。 基于非线性最小二乘,多,在休眠的个人计算机上开发了一种药代动力学分析程序。 我们已经采取了其他分析程序多(横向),其中药代动力学模型被定义为序数微分方程,基于基于有限元方法(FEM)的快速逆拉普拉斯变换(FILT)和多(FEM)。 基于延长最小二乘基于延伸的最小二乘法的Mult12(贝叶斯)是为人口药代动力学(PPK)开发的。

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