Evaluation of the whole body physiologically based pharmacokinetic (WB-PBPK) modeling of drugs

被引:1
作者
Munir, Anum [1 ]
Azam, Shumaila [1 ]
Fazal, Sahar [1 ]
Bhatti, A., I [2 ]
机构
[1] Capital Univ Sci & Technol, Fac Hlth & Life Sci, Dept Biosci, Islamabad, Pakistan
[2] Capital Univ Sci & Technol, Dept Elect Engn, Islamabad, Pakistan
关键词
Absorption; Distribution; Elimination; Metabolism; PBPK; WBPBPK; HISTONE DEACETYLASE INHIBITOR; BELINOSTAT PXD101; PRINCIPLES; ALLOPURINOL; VARIABILITY; PREDICTION; CHILDREN; INFANTS; RAT;
D O I
10.1016/j.jtbi.2018.04.032
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Physiologically based pharmacokinetic (PBPK) modeling is a supporting tool in drug discovery and improvement. Simulations produced by these models help to save time and aids in examining the effects of different variables on the pharmacokinetics of drugs. For this purpose, Sheila and Peters suggested a PBPK model capable of performing simulations to study a given drug absorption. There is a need to extend this model to the whole body entailing all another process like distribution, metabolism, and elimination, besides absorption. The aim of this scientific study is to hypothesize a WB-PBPK model through integrating absorption, distribution, metabolism, and elimination processes with the existing PBPK model.Absorption, distribution, metabolism, and elimination models are designed, integrated with PBPK model and validated. For validation purposes, clinical records of few drugs are collected from the literature. The developed WB-PBPK model is affirmed by comparing the simulations produced by the model against the searched clinical data.. It is proposed that the WB-PBPK model may be used in pharmaceutical industries to create of the pharmacokinetic profiles of drug candidates for better outcomes, as it is advance PBPK model and creates comprehensive PK profiles for drug ADME in concentration-time plots. (C) 2018 Elsevier Ltd. All rights reserved.
引用
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页码:1 / 9
页数:9
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