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PKRD:一种用于重复给药药代动力学曲线的最小二乘法和贝叶斯分析的药代动力学程序。

PKRD: a pharmacokinetic program for least-squares and bayesian analysis of repeated-dose pharmacokinetic curves.

作者信息

Messori A, Bosi A, Guidi S, Longo G, Pistolesi C, Saccardi R, Valenza T, Vannucchi A M

机构信息

Pharmaceutical Service, Borgo Roma University Hospital, Verona, Italy.

出版信息

Comput Methods Programs Biomed. 1992 Jun;38(1):27-35. doi: 10.1016/0169-2607(92)90072-f.

Abstract

A microcomputer program is presented which analyses multiple-dose pharmacokinetic curves using either a least-squares nonlinear analysis or a bayesian fit. The least-squares subroutine is designed to fit retrospective pharmacokinetic curves and can generate the so-called population pharmacokinetic parameters using the Standard Two-Stage method. The bayesian subroutine can instead be used prospectively to individualise the dosage regimen of a patient based on the concentrations measured in the initial phases of the drug treatment. All the pharmacokinetic subroutines of the program use the one-compartment model with either constant-rate intravenous infusion or oral route with zero-order absorption. The program was tested in a series of ten bone marrow transplantation patients treated with cyclosporine. The least-squares estimates of the one-compartment parameters, calculated by the program, were compared with those generated by the SIMKIN program.

摘要

本文介绍了一个微机程序,该程序使用最小二乘非线性分析或贝叶斯拟合来分析多剂量药代动力学曲线。最小二乘子程序旨在拟合回顾性药代动力学曲线,并可使用标准两阶段法生成所谓的群体药代动力学参数。相反,贝叶斯子程序可用于前瞻性地根据药物治疗初始阶段测得的浓度来个体化患者的给药方案。该程序的所有药代动力学子程序均使用单室模型,采用恒速静脉输注或零级吸收的口服途径。该程序在接受环孢素治疗的一系列10例骨髓移植患者中进行了测试。将该程序计算的单室参数的最小二乘估计值与SIMKIN程序生成的估计值进行了比较。

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