Obach R Scott, Nedderman Angus N, Smith Dennis A
Pfizer Inc, Groton, CT, USA.
Xenobiotica. 2012 Jan;42(1):46-56. doi: 10.3109/00498254.2011.621985. Epub 2011 Oct 12.
The conduct of excretion and metabolism studies using radiolabelled drugs in multiple laboratory animal species has been a mainstay of the suite of support activities provided by drug metabolism groups within pharmaceutical research and development organizations for decades. Drug metabolism scientists carry out exhaustive analyses of plasma and excretory matrices to comprehensively determine the profiles of metabolites in these species. While these analyses have taught us considerably regarding principles of drug metabolism and excretion, it is our contention that the routine conduct of such studies for every new drug development compound in every laboratory animal species used in toxicology studies is no longer necessary. The recently released regulatory guidance regarding metabolites and safety testing have better defined what we need to know regarding metabolite profiles in humans relative to animals. In this commentary, we propose a strategy wherein a radiolabel metabolism study is conducted only in humans, and that these data are utilized as a springboard to direct the exploration of steady-state human versus animal metabolite exposures. Such a strategy better serves the purpose of what is needed to support our understanding of the safety of a new drug candidate. Valuable expertise in drug metabolism and biotransformation can be redeployed to meet the burgeoning needs in drug design efforts to optimize structures with regard to metabolic clearance properties, understanding pharmacologically active metabolites, and reducing generation of chemically reactive metabolites.
几十年来,在多种实验动物物种中使用放射性标记药物进行排泄和代谢研究,一直是制药研发机构中药物代谢团队提供的一系列支持活动的主要内容。药物代谢科学家对血浆和排泄基质进行详尽分析,以全面确定这些物种中的代谢物谱。虽然这些分析让我们对药物代谢和排泄原理有了相当多的了解,但我们认为,对于毒理学研究中使用的每种实验动物物种的每种新药开发化合物都常规进行此类研究已不再必要。最近发布的关于代谢物和安全性测试的监管指南,已经更明确地界定了我们相对于动物而言需要了解人类代谢物谱的哪些方面。在这篇评论中,我们提出一种策略,即仅在人体中进行放射性标记代谢研究,并将这些数据用作指导探索稳态下人体与动物代谢物暴露情况的跳板。这样一种策略更有助于实现支持我们理解新药候选物安全性所需目标。药物代谢和生物转化方面的宝贵专业知识可以重新调配,以满足药物设计工作中不断涌现的需求,即在代谢清除特性、理解药理活性代谢物以及减少化学反应性代谢物生成方面优化结构。