转运体检测在药物发现和开发中的应用:文献更新。

IF 6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Donna A Volpe
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引用次数: 0

摘要

导言:确定一种新药是否是外排或吸收膜转运体的底物、抑制剂或诱导剂已成为药物发现和开发过程中的一项常规工作。体外实验用于确定新药是否有可能成为转运体介导的临床药物相互作用的对象(底物)或沉淀物(抑制剂、诱导剂)。然后根据这些体外实验的结果来确定是否有必要对新药进行进一步的体内药物相互作用研究:本文介绍了体外转运体检测的最新进展,重点关注转染细胞的新用途、时间依赖性抑制、转运体诱导和复杂模型系统:较新的体外检测方法增加了将新药定义为转运体底物、抑制剂或诱导剂的工具箱。球体、有机体和微生理系统等复杂模型需要标准化,并需要进一步研究模型转运体底物和抑制剂。在药物发现过程中,可采用较传统的转运体检测方法作为底物和抑制剂筛选检测方法。在药物开发过程中,可在后期药物开发中使用更复杂的细胞模型,以更好地了解转运体如何参与新药的吸收、分布和排泄。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Application of transporter assays for drug discovery and development: an update of the literature.

Introduction: Determining whether a new drug is a substrate, inhibitor or inducer of efflux or uptake membrane transporters has become a routine process during drug discovery and development. In vitro assays are utilized to establish whether a new drug has the potential to be an object (substrate) or precipitant (inhibitor, inducer) in transporter-mediated clinical drug-drug interactions. The findings from these in vitro experiments are then used to determine whether further in vivo drug interaction studies are necessary for a new drug.

Areas covered: This article provides an update on in vitro transporter assays, focusing on new uses of transfected cells, time-dependent inhibition, transporter induction, and complex model systems.

Expert opinion: The newer in vitro assays add to the toolbox in defining new drugs as transporter substrates, inhibitors, or inducers. Complex models such as spheroids, organoids, and microphysiological systems require standardization and further research with model transporter substrates and inhibitors. In drug discovery, the more traditional transporter assays may be employed as substrate and inhibitor screening assays. In drug development, more complex cell models can be employed in later drug development to better understand how transporter(s) are involved in the absorption, distribution, and excretion of new drugs.

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来源期刊
CiteScore
10.20
自引率
1.60%
发文量
78
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Drug Discovery (ISSN 1746-0441 [print], 1746-045X [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles on novel technologies involved in the drug discovery process, leading to new leads and reduced attrition rates. Each article is structured to incorporate the author’s own expert opinion on the scope for future development. The Editors welcome: Reviews covering chemoinformatics; bioinformatics; assay development; novel screening technologies; in vitro/in vivo models; structure-based drug design; systems biology Drug Case Histories examining the steps involved in the preclinical and clinical development of a particular drug The audience consists of scientists and managers in the healthcare and pharmaceutical industry, academic pharmaceutical scientists and other closely related professionals looking to enhance the success of their drug candidates through optimisation at the preclinical level.
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