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全身药代动力学模型。

Whole body pharmacokinetic models.

作者信息

Nestorov Ivan

机构信息

Pharmacokinetics and Drug Metabolism, Amgen Inc., 30-O-B, One Amgen Center Drive, Thousand Oaks, CA 91320-1789, USA.

出版信息

Clin Pharmacokinet. 2003;42(10):883-908. doi: 10.2165/00003088-200342100-00002.

Abstract

The aim of the current review is to summarise the present status of physiologically based pharmacokinetic (PBPK) modelling and its applications in drug research, and thus serve as a reference point to people interested in the methodology. The review is structured into three major sections. The first discusses the existing methodologies and techniques of PBPK model development. The second describes some of the most interesting PBPK model implementations published. The final section is devoted to a discussion of the current limitations and the possible future developments of the PBPK modelling approach. The current review is focused on papers dealing with the pharmacokinetics and/or toxicokinetics of medicinal compounds; references discussing PBPK models of environmental compounds are mentioned only if they represent considerable methodological developments or reveal interesting interpretations and/or applications.The major conclusion of the review is that, despite its significant potential, PBPK modelling has not seen the development and implementation it deserves, especially in the drug discovery, research and development processes. The main reason for this is that the successful development and implementation of a PBPK model is seen to require the investment of significant experience, effort, time and resources. Yet, a substantial body of PBPK-related research has been accumulated that can facilitate the PBPK modelling and implementation process. What is probably lagging behind is the expertise component, where the demand for appropriately qualified staff far outreaches availability.

摘要

本综述的目的是总结基于生理的药代动力学(PBPK)建模的现状及其在药物研究中的应用,从而为对该方法感兴趣的人提供一个参考点。该综述分为三个主要部分。第一部分讨论了PBPK模型开发的现有方法和技术。第二部分描述了一些已发表的最有趣的PBPK模型应用。最后一部分专门讨论了PBPK建模方法当前的局限性以及可能的未来发展。本综述重点关注处理药用化合物药代动力学和/或毒代动力学的论文;只有在讨论环境化合物的PBPK模型代表了重大方法学进展或揭示了有趣的解释和/或应用时,才会提及相关参考文献。该综述的主要结论是,尽管PBPK建模具有巨大潜力,但它尚未得到应有的发展和应用,尤其是在药物发现、研究和开发过程中。主要原因是,人们认为成功开发和应用PBPK模型需要投入大量经验、精力、时间和资源。然而,已经积累了大量与PBPK相关的研究,这些研究可以促进PBPK建模和应用过程。可能滞后的是专业知识部分,对合格人员的需求远远超过了供应。

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