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内源性药物转运体探针:在理想与现实之间寻求平衡。

Endogenous Probes for Drug Transporters: Balancing Vision With Reality.

机构信息

Pharmacokinetics, Dynamics & Metabolism, Medicine Design, Pfizer Inc., Groton, Connecticut, USA.

Mechanistic Safety and Disposition, IVIVT, GlaxoSmithKline, Ware, Hertfordshire, UK.

出版信息

Clin Pharmacol Ther. 2018 Mar;103(3):434-448. doi: 10.1002/cpt.749. Epub 2017 Jul 14.

Abstract

Various endogenous probes have been identified for a number of hepatic and renal drug transporters and available clinical data indicate that they could be leveraged in phase I trials to facilitate subject phenotyping and drug-drug interaction (DDI) assessment. Despite the progress, however, it is recognized that the menu of probes needs expanding, that existing probes need further characterization and validation, and that compound files need to be built in support of probe absorption-metabolism-distribution-excretion-DDI modeling exercises.

摘要

已经确定了许多肝和肾药物转运体的各种内源性探针,并且现有临床数据表明,它们可以在 I 期临床试验中加以利用,以促进受试者表型分析和药物相互作用(DDI)评估。然而,尽管取得了这些进展,但人们认识到需要扩大探针的种类,需要进一步对现有探针进行特征描述和验证,并且需要构建化合物文件以支持探针吸收-代谢-分布-排泄-DDI 模型构建。

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