Department of Drug Metabolism and Pharmacokinetics, Genentech Inc , South San Francisco , CA , USA.
Department of Medicine - Division of Clinical Pharmacology, The Johns Hopkins University School of Medicine , Baltimore , MD , USA.
Drug Metab Rev. 2019 May;51(2):121-161. doi: 10.1080/03602532.2019.1615937. Epub 2019 Aug 6.
In the past three decades, ADME sciences have become an integral component of the drug discovery and development process. At the same time, the field has continued to evolve, thus, requiring ADME scientists to be knowledgeable of and engage with diverse aspects of drug assessment: from pharmacology to toxicology, and from modeling to models and finally models. Progress in this field requires deliberate exposure to different aspects of ADME; however, this task can seem daunting in the current age of mass information. We hope this review provides a focused and brief summary of a wide array of critical advances over the past year and explains the relevance of this research ( Table 1 ). We divided the articles into categories of (1) drug optimization, (2) metabolites and drug metabolizing enzymes, and (3) bioactivation. This annual review is the fourth of its kind (Baillie et al. 2016 ; Khojasteh et al. 2017 , 2018 ). We have followed the same format we used in previous years in terms of the selection of articles and the authoring of each section. This effort in itself also continues to evolve. I am pleased that Rietjens, Miller, and Mitra have again contributed to this annual review. We would like to welcome Namandjé N. Bumpus, James P. Driscoll, and Donglu Zhang as authors for this year's issue. We strive to maintain a balance of authors from academic and industry settings. We would be pleased to hear your opinions of our commentary, and we extend an invitation to anyone who would like to contribute to a future edition of this review. Cyrus Khojasteh, on behalf of the authors.
在过去的三十年中,ADME 科学已成为药物发现和开发过程的一个组成部分。与此同时,该领域还在不断发展,因此要求 ADME 科学家了解并参与药物评估的各个方面:从药理学到毒理学,从建模到模型,再到模型。该领域的进展需要刻意接触 ADME 的不同方面;但是,在当今信息海量的时代,这项任务似乎令人生畏。我们希望这篇综述能重点而简要地总结过去一年中广泛的关键进展,并解释这项研究的相关性(表 1)。我们将文章分为三类:(1)药物优化,(2)代谢物和药物代谢酶,(3)生物活化。这是该综述的第四版(Baillie 等人,2016 年;Khojasteh 等人,2017 年,2018 年)。在选择文章和撰写每个部分方面,我们遵循了与前几年相同的格式。这项工作本身也在不断发展。我很高兴 Rietjens、Miller 和 Mitra 再次为这项年度综述做出贡献。我们欢迎 Namandjé N. Bumpus、James P. Driscoll 和 Donglu Zhang 成为今年这一期的作者。我们努力在学术和工业环境的作者之间保持平衡。我们将很高兴听取您对我们评论的意见,并邀请任何有兴趣为未来的评论做出贡献的人。Cyrus Khojasteh,代表作者。