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Liver microsystems in vitro for drug response

机译:体外肝微系统用于药物反应

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摘要

Engineering approaches were adopted for liver microsystems to recapitulate cell arrangements and culture microenvironments in vivo for sensitive, high-throughput and biomimetic drug screening. This review introduces liver microsystems in vitro for drug hepatotoxicity, drug-drug interactions, metabolic function and enzyme induction, based on cell micropatterning, hydrogel biofabrication and microfluidic perfusion. The engineered microsystems provide varied microenvironments for cell culture that feature cell coculture with non-parenchymal cells, in a heterogeneous extracellular matrix and under controllable perfusion. The engineering methods described include cell micropatterning with soft lithography and dielectrophoresis, hydrogel biofabrication with photolithography, micromolding and 3D bioprinting, and microfluidic perfusion with endothelial-like structures and gradient generators. We discuss the major challenges and trends of liver microsystems to study drug response in vitro.
机译:肝脏微系统采用了工程方法来概括细胞排列并在体内培养微环境,以进行敏感,高通量和仿生药物筛选。这篇综述介绍了基于细胞微模式,水凝胶生物制造和微流体灌注的体外肝微系统,用于药物肝毒性,药物-药物相互作用,代谢功能和酶诱导。工程微系统为细胞培养提供了多种微环境,其特征是在异质细胞外基质中和可控灌注下,与非实质细胞进行细胞共培养。所描述的工程方法包括采用软光刻和介电泳的细胞微图案化,采用光刻技术的水凝胶生物加工,微成型和3D生物打印以及具有内皮样结构和梯度发生器的微流体灌注。我们讨论肝脏微系统的主要挑战和趋势,以研究体外药物反应。

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