纳米技术
诱导多能干细胞
药品
微流控
对乙酰氨基酚
肝损伤
化学
药物开发
人体生理学
毒性
细胞
生物医学工程
多细胞生物
干细胞
细胞毒性
药物毒性
药理学
人肝
生物人工肝装置
癌症研究
慢性肝病
细胞生物学
医学
作者
Jun-Qi Zhao,Danqing Huang,Jinglin Wang,Yuanjin Zhao
出处
期刊:Small
[Wiley]
日期:2025-10-14
卷期号:21 (48): e05653-e05653
被引量:2
标识
DOI:10.1002/smll.202505653
摘要
Liver-on-a-chip has emerged as an effective tool for liver disease modeling and new drug development, while the current challenge lies in further mimicking liver physiological conditions. Here, inspired by the intricate architecture of hepatic lobules, a novel biomimetic vascularized liver-on-a-chip fabricated via high-precision 3D printing technology is presented. The chip features a capillary network with multiple micro-pores, ensuring a constant nutrient supply and efficient substance exchange within the cell environment through microfluidic perfusion. Under microperfusion conditions, human induced pluripotent stem cell-derived hepatocytes (hiPSC-Heps) exhibit superior physiological status and biological functionality compared to traditional 2D cultures. In addition, a comprehensive platform for assessing drug-induced liver injury (DILI) is established by integrating a concentration gradient chip, liver chips, and multicellular coculture technologies. This innovative platform effectively validates both acute and chronic hepatotoxic effects of acetaminophen (APAP). These findings demonstrate that the biomimetic vascularized liver-on-a-chip exhibits ideal physiological relevance and holds significant potential for applications in drug development and toxicity screening.
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