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最大限度地利用体外ADMET工具预测体内生物利用度和安全性。

Maximising use of in vitro ADMET tools to predict in vivo bioavailability and safety.

作者信息

Wang Jianling, Urban Laszlo, Bojanic Dejan

机构信息

Novartis Institutes for Biomedical Research, Metabolism and Pharmacokinetics, 250 Massachusetts Avenue, Cambridge, MA 02139, USA.

出版信息

Expert Opin Drug Metab Toxicol. 2007 Oct;3(5):641-65. doi: 10.1517/17425255.3.5.641.

Abstract

The drastic increase in the costs for discovering and developing a new drug and the high attrition rate of development candidates led to shifting of drug discovery strategy to parallel assessment of comprehensive drug properties along with efficacy. The article reviews the benefits and caveats of implementing comprehensive in vitro tools in early drug discovery and their impact on addressing in vivo ADMET issues. With the proposal of four-barrier profiling paradigm and employment of integrated risk assessment, one can exponentially enhance the predictive power of those in vitro tools by taking into consideration the interplays among those profiling parameters. An 'Exposure Cube' is proposed to promote collective employment of solubility/dissolution, permeability and metabolic clearance to address in vivo exposure and to direct optimization of new chemical entities in drug discovery.

摘要

发现和开发新药的成本急剧增加,以及开发候选药物的高淘汰率,导致药物发现策略转向在评估疗效的同时并行评估药物的综合性质。本文综述了在早期药物发现中应用综合体外工具的益处和注意事项,以及它们对解决体内ADMET问题的影响。随着四屏障分析范式的提出和综合风险评估的应用,通过考虑这些分析参数之间的相互作用,可以成倍提高这些体外工具的预测能力。本文提出了一个“暴露立方体”,以促进溶解度/溶出度、渗透性和代谢清除率的综合应用,以解决体内暴露问题,并指导药物发现中新化学实体的优化。

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