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在发现和探索性开发中使用放射性标记化合物进行药物吸收、分布、代谢和排泄(ADME)研究。

The use of radiolabeled compounds for ADME studies in discovery and exploratory development.

作者信息

Marathe P H, Shyu W C, Humphreys W G

机构信息

Department of Pharmaceutical Candidate Optimization, Bristol-Myers Squibb Company, Princeton, NJ 08543, USA.

出版信息

Curr Pharm Des. 2004;10(24):2991-3008. doi: 10.2174/1381612043383494.

Abstract

Radiolabeled compounds are excellent investigative tools and widely used to carry out ADME studies during drug discovery and development stages. The most commonly used radioisotopes are 14C and 3H. 3H materials are generally easier to synthesize than 14C materials. Therefore, a variety of probes and substrates used in in vitro assays are labeled with 3H. Since synthesis of 14C material requires intensive resources, it is usually not available until after a molecule is considered for potential development or after the molecule enters the development phase. Improvement in the technology in radiochemistry has enabled the use of radiolabeled compounds earlier in pre-clinical and clinical development to address mechanistic issues. For in vitro studies, radiolabeled probes are utilized to test affinity with various transporters, to perform metabolism comparison among species and to assess possible formation of reactive metabolites. For in vivo studies, radiolabeled compounds are employed to identify and elucidate metabolites formed, to investigate the extent of absorption, bioavailability, tissue distribution, mass balance, routes of excretion, and pre-systemic metabolism. Due to the significant impact of radiolabeled studies on drug development, these studies will be performed earlier than have been in the past and will continue to be an integral part of drug discovery and development.

摘要

放射性标记化合物是出色的研究工具,在药物发现和开发阶段被广泛用于进行药物代谢动力学(ADME)研究。最常用的放射性同位素是碳-14(14C)和氢-3(3H)。一般来说,3H标记的材料比14C标记的材料更容易合成。因此,体外试验中使用的各种探针和底物都用3H进行标记。由于14C材料的合成需要大量资源,通常直到一个分子被考虑进行潜在开发或进入开发阶段后才会有。放射化学技术的改进使得放射性标记化合物能够在临床前和临床开发的早期使用,以解决机制问题。对于体外研究,放射性标记的探针用于测试与各种转运体的亲和力、进行物种间的代谢比较以及评估活性代谢物的可能形成。对于体内研究,放射性标记化合物用于识别和阐明形成的代谢物、研究吸收程度、生物利用度、组织分布、质量平衡、排泄途径和首过代谢。由于放射性标记研究对药物开发有重大影响,这些研究将比过去更早进行,并将继续成为药物发现和开发不可或缺的一部分。

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