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3D 肝脏模拟物——需要采用多中心方法。

3D hepatic mimics - the need for a multicentric approach.

机构信息

Department of Biomedical Engineering, Indian Institute of Technology Hyderabad, Sangareddy 502285, Telangana, India. Department of Chemistry and Biotechnology, School of Science, Swinburne University of Technology, Hawthorn, Victoria 3122, Australia.

出版信息

Biomed Mater. 2020 Aug 31;15(5):052002. doi: 10.1088/1748-605X/ab971c.

Abstract

The liver is a center of metabolic activity, including the metabolism of drugs, and consequently is prone to drug-induced liver injury. Failure to detect hepatotoxicity of drugs during their development will lead to the withdrawal of the drugs during clinical trials. To avoid such clinical and economic consequences, in vitro liver models that can precisely predict the toxicity of a drug during the pre-clinical phase is necessary. This review describes the different technologies that are used to develop in vitro liver models and the different approaches aimed at mimicking different functional aspects of the liver at the fundamental level. This involves mimicking of the functional and structural units like the sinusoid, the bile canalicular system, and the acinus.

摘要

肝脏是代谢活动的中心,包括药物代谢,因此容易受到药物引起的肝损伤。如果在药物开发过程中未能检测到药物的肝毒性,将会导致药物在临床试验中被撤回。为了避免这种临床和经济后果,在临床前阶段能够准确预测药物毒性的体外肝脏模型是必要的。本文综述了用于开发体外肝脏模型的不同技术,以及旨在从根本上模拟肝脏不同功能方面的不同方法。这涉及到模拟功能性和结构性单位,如窦状隙、胆小管系统和腺泡。

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