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生物转化科学现状 - 体外和体内实践、临床转化及未来趋势的行业调查。

The Current State of Biotransformation Science - Industry Survey of In Vitro and In Vivo Practices, Clinical Translation, and Future Trends.

机构信息

AbbVie, Quantitative, Translational & ADME Sciences, North Chicago, IL, USA.

J&J, Translational PKPD & Investigational Toxicology, San Diego, CA, USA.

出版信息

Pharm Res. 2024 Nov;41(11):2079-2093. doi: 10.1007/s11095-024-03787-y. Epub 2024 Nov 4.

Abstract

Embedded within the field of drug metabolism and pharmacokinetics (DMPK), biotransformation is a discipline that studies the origins, disposition, and structural identity of metabolites to provide a comprehensive safety assessment, including the assessment of exposure coverage in toxicological species. Spanning discovery and development, metabolite identification (metID) scientists employ various strategies and tools to address stage-specific questions aimed at guiding the maturation of early chemical matter into drug candidates. During this process, the identity of major (and minor) circulating human metabolites is ascertained to comply with the regulatory requirements such as the Metabolites in Safety Testing (MIST) guidance. Through the International Consortium for Innovation and Quality in Pharmaceutical Development (IQ), the "Translatability of MetID In Vitro Systems Working Group" was created within the Translational and ADME Sciences Leadership Group. The remit of this group was to objectively determine how accurate commonly employed in vitro systems have been with respect to prediction of circulating human metabolites, both qualitatively and quantitatively. A survey composed of 34 questions was conducted across 26 pharmaceutical companies to obtain a foundational understanding of current metID practices, preclinically and clinically, as well as to provide perspective on how successful these practices have been at predicting circulating human metabolites. The results of this survey are presented as an initial snapshot of current industry-based metID practices, including our perspective on how a harmonized framework for the conduct of in vitro metID studies could be established. Future perspectives from current practices to emerging advances with greater translational capability are also provided.

摘要

在药物代谢和药代动力学(DMPK)领域中,生物转化是一门研究代谢物的起源、处置和结构同一性的学科,旨在提供全面的安全性评估,包括在毒理学物种中评估暴露程度。从发现到开发,代谢物鉴定(metID)科学家采用各种策略和工具来解决特定阶段的问题,旨在指导早期化学物质向候选药物的成熟。在这个过程中,确定主要(和次要)循环人体代谢物的身份,以符合法规要求,例如安全性测试中的代谢物(MIST)指南。通过国际药品创新与质量联盟(IQ),在转化和 ADME 科学领导组内成立了“代谢物鉴定体外系统可转化性工作组”。该小组的任务是客观地确定常用的体外系统在定性和定量上预测循环人体代谢物的准确性。对 26 家制药公司进行了一项由 34 个问题组成的调查,以了解当前在临床前和临床阶段进行代谢物鉴定的实践情况,并提供如何成功预测循环人体代谢物的看法。该调查的结果作为当前行业基于代谢物鉴定实践的初始快照呈现,包括我们对如何建立体外代谢物鉴定研究的协调框架的看法。还提供了当前实践向具有更大转化能力的新兴进展的未来展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/261a/11599300/8b0ec3535e4b/11095_2024_3787_Fig1_HTML.jpg

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