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预测口服药物吸收和肝胆清除率:人肠和肝体外细胞模型。

Predicting oral drug absorption and hepatobiliary clearance: Human intestinal and hepatic in vitro cell models.

机构信息

Institute for Cell and Molecular Biosciences, University of Newcastle, Medical School, Newcastle upon Tyne NE2 4HH, UK.

出版信息

Environ Toxicol Pharmacol. 2006 Feb;21(2):168-78. doi: 10.1016/j.etap.2005.06.002. Epub 2005 Aug 2.

Abstract

Membrane transport proteins control the uptake and efflux of many drugs in tissues including the intestine, liver and kidneys and thus play important roles in drug absorption, distribution and excretion. With the development of high throughput screening in an industrial environment, the importance of having appropriate in vitro systems to study drug transporter function, regulation, and interactions are invaluable. Cell lines are efficient tools in screening individual transport processes. In this review, we focus on the processes involved in the absorption and hepatobiliary clearance of drugs and the potential of cell lines to model such process, paying particular attention to the use of Caco-2 and HepG2 cells.

摘要

膜转运蛋白控制着许多药物在包括肠道、肝脏和肾脏等组织中的摄取和外排,因此在药物吸收、分布和排泄中起着重要作用。随着高通量筛选在工业环境中的发展,拥有适当的体外系统来研究药物转运蛋白的功能、调节和相互作用变得至关重要。细胞系是筛选单个转运过程的有效工具。在这篇综述中,我们重点讨论了药物吸收和肝胆清除过程中涉及的过程,以及细胞系在模拟这些过程中的潜力,特别关注 Caco-2 和 HepG2 细胞的应用。

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