Lost in modelling and simulation?

IF 3.4 Q2 CHEMISTRY, MEDICINAL ADMET and DMPK Pub Date : 2021-03-20 DOI:10.5599/ADMET.923
K. Sugano
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引用次数: 18

Abstract

Over the past few decades, physiologically-based pharmacokinetic modelling (PBPK) has been anticipated to be a powerful tool to improve the productivity of drug discovery and development. However, recently, multiple systematic evaluation studies independently suggested that the predictive power of current oral absorption (OA) PBPK models needs significant improvement. There is some disagreement between the industry and regulators about the credibility of OA PBPK modelling. Recently, the editorial board of AMDET&DMPK has announced the policy for the articles related to PBPK modelling (Modelling and simulation ethics). In this feature article, the background of this policy is explained: (1) Requirements for scientific writing of PBPK modelling, (2) Scientific literacy for PBPK modelling, and (3) Middle-out approaches. PBPK models are a useful tool if used correctly. This article will hopefully help advance the science of OA PBPK models.
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迷失在建模和仿真中?
在过去的几十年里,基于生理的药代动力学建模(PBPK)被认为是提高药物发现和开发效率的有力工具。然而,最近,多个独立的系统评价研究表明,目前口服吸收(OA) PBPK模型的预测能力需要显著提高。对于OA PBPK模型的可信度,行业和监管机构之间存在一些分歧。最近,AMDET&DMPK编辑委员会宣布了与PBPK建模(建模与仿真伦理)相关的文章政策。在这篇专题文章中,解释了这一政策的背景:(1)PBPK建模的科学写作要求;(2)PBPK建模的科学素养;(3)Middle-out方法。如果使用得当,PBPK模型是一个有用的工具。本文将有助于推进OA PBPK模型的科学研究。
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来源期刊
ADMET and DMPK
ADMET and DMPK Multiple-
CiteScore
4.40
自引率
0.00%
发文量
22
审稿时长
4 weeks
期刊介绍: ADMET and DMPK is an open access journal devoted to the rapid dissemination of new and original scientific results in all areas of absorption, distribution, metabolism, excretion, toxicology and pharmacokinetics of drugs. ADMET and DMPK publishes the following types of contributions: - Original research papers - Feature articles - Review articles - Short communications and Notes - Letters to Editors - Book reviews The scope of the Journal involves, but is not limited to, the following areas: - physico-chemical properties of drugs and methods of their determination - drug permeabilities - drug absorption - drug-drug, drug-protein, drug-membrane and drug-DNA interactions - chemical stability and degradations of drugs - instrumental methods in ADMET - drug metablic processes - routes of administration and excretion of drug - pharmacokinetic/pharmacodynamic study - quantitative structure activity/property relationship - ADME/PK modelling - Toxicology screening - Transporter identification and study
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