Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric Scaling

Extrapolation of pharmacokinetic (PK) parameters from in vitro or in vivo animal to human is one of the main tasks in the drug development process. Translational approaches provide evidence for go or no-go decision-making during drug discovery and the development process, and the prediction of human...

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Main Authors: Go-Wun Choi, Yong-Bok Lee, Hea-Young Cho
Format: Article
Language:English
Published: MDPI AG 2019-04-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/11/4/168
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spelling doaj-e6f394f0662a49139333aa16e3178d302020-11-25T00:45:51ZengMDPI AGPharmaceutics1999-49232019-04-0111416810.3390/pharmaceutics11040168pharmaceutics11040168Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric ScalingGo-Wun Choi0Yong-Bok Lee1Hea-Young Cho2College of Pharmacy, CHA University, 335 Pangyo-ro, Bundang-gu, Seongnam-si, Gyeonggi-do 13488, KoreaCollege of Pharmacy, Chonnam National University, 77 Yongbong-ro, Buk-Gu, Gwangju 61186, KoreaCollege of Pharmacy, CHA University, 335 Pangyo-ro, Bundang-gu, Seongnam-si, Gyeonggi-do 13488, KoreaExtrapolation of pharmacokinetic (PK) parameters from in vitro or in vivo animal to human is one of the main tasks in the drug development process. Translational approaches provide evidence for go or no-go decision-making during drug discovery and the development process, and the prediction of human PKs prior to the first-in-human clinical trials. In vitro-in vivo extrapolation and allometric scaling are the choice of method for projection to human situations. Although these methods are useful tools for the estimation of PK parameters, it is a challenge to apply these methods since underlying biochemical, mathematical, physiological, and background knowledge of PKs are required. In addition, it is difficult to select an appropriate methodology depending on the data available. Therefore, this review covers the principles of PK parameters pertaining to the clearance, volume of distribution, elimination half-life, absorption rate constant, and prediction method from the original idea to recently developed models in order to introduce optimal models for the prediction of PK parameters.https://www.mdpi.com/1999-4923/11/4/168pharmacokineticsin vitro-in vivo extrapolationallometric scalinganimal scale-uptranslational approachnon-clinical study
collection DOAJ
language English
format Article
sources DOAJ
author Go-Wun Choi
Yong-Bok Lee
Hea-Young Cho
spellingShingle Go-Wun Choi
Yong-Bok Lee
Hea-Young Cho
Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric Scaling
Pharmaceutics
pharmacokinetics
in vitro-in vivo extrapolation
allometric scaling
animal scale-up
translational approach
non-clinical study
author_facet Go-Wun Choi
Yong-Bok Lee
Hea-Young Cho
author_sort Go-Wun Choi
title Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric Scaling
title_short Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric Scaling
title_full Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric Scaling
title_fullStr Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric Scaling
title_full_unstemmed Interpretation of Non-Clinical Data for Prediction of Human Pharmacokinetic Parameters: In Vitro-In Vivo Extrapolation and Allometric Scaling
title_sort interpretation of non-clinical data for prediction of human pharmacokinetic parameters: in vitro-in vivo extrapolation and allometric scaling
publisher MDPI AG
series Pharmaceutics
issn 1999-4923
publishDate 2019-04-01
description Extrapolation of pharmacokinetic (PK) parameters from in vitro or in vivo animal to human is one of the main tasks in the drug development process. Translational approaches provide evidence for go or no-go decision-making during drug discovery and the development process, and the prediction of human PKs prior to the first-in-human clinical trials. In vitro-in vivo extrapolation and allometric scaling are the choice of method for projection to human situations. Although these methods are useful tools for the estimation of PK parameters, it is a challenge to apply these methods since underlying biochemical, mathematical, physiological, and background knowledge of PKs are required. In addition, it is difficult to select an appropriate methodology depending on the data available. Therefore, this review covers the principles of PK parameters pertaining to the clearance, volume of distribution, elimination half-life, absorption rate constant, and prediction method from the original idea to recently developed models in order to introduce optimal models for the prediction of PK parameters.
topic pharmacokinetics
in vitro-in vivo extrapolation
allometric scaling
animal scale-up
translational approach
non-clinical study
url https://www.mdpi.com/1999-4923/11/4/168
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AT yongboklee interpretationofnonclinicaldataforpredictionofhumanpharmacokineticparametersinvitroinvivoextrapolationandallometricscaling
AT heayoungcho interpretationofnonclinicaldataforpredictionofhumanpharmacokineticparametersinvitroinvivoextrapolationandallometricscaling
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