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

机译:预测口服药物的吸收和肝胆清除率:人肠和肝体外细胞模型

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摘要

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.
机译:膜转运蛋白控制着包括肠道,肝脏和肾脏在内的许多药物在组织中的吸收和流出,因此在药物的吸收,分布和排泄中起着重要的作用。随着工业环境中高通量筛选技术的发展,拥有合适的体外系统来研究药物转运蛋白的功能,调节和相互作用的重要性变得非常重要。细胞系是筛选单个运输过程的有效工具。在这篇综述中,我们集中于药物吸收和肝胆清除的过程以及细胞系对这种过程进行建模的潜力,尤其要注意Caco-2和HepG2细胞的使用。

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