Engineered liver-on-a-chip platform to mimic liver functions and its biomedical applications: A review

  • Jiu Deng
  • , Wenbo Wei
  • , Zongzheng Chen
  • , Bingcheng Lin
  • , Weijie Zhao
  • , Yong Luo
  • , Xiuli Zhang

Research output: Contribution to journalReview articlepeer-review

213 Scopus citations

Abstract

Hepatology and drug development for liver diseases require in vitro liver models. Typical models include 2D planar primary hepatocytes, hepatocyte spheroids, hepatocyte organoids, and liver-on-a-chip. Liver-on-a-chip has emerged as the mainstream model for drug development because it recapitulates the liver microenvironment and has good assay robustness such as reproducibility. Liver-on-a-chip with human primary cells can potentially correlate clinical testing. Liver-on-a-chip can not only predict drug hepatotoxicity and drug metabolism, but also connect other artificial organs on the chip for a human-on-a-chip, which can reflect the overall effect of a drug. Engineering an effective liver-on-a-chip device requires knowledge of multiple disciplines including chemistry, fluidic mechanics, cell biology, electrics, and optics. This review first introduces the physiological microenvironments in the liver, especially the cell composition and its specialized roles, and then summarizes the strategies to build a liver-on-a-chip via microfluidic technologies and its biomedical applications. In addition, the latest advancements of liver-on-a-chip technologies are discussed, which serve as a basis for further liver-on-a-chip research.

Original languageEnglish
Article number676
JournalMicromachines
Volume10
Issue number10
DOIs
StatePublished - 1 Oct 2019
Externally publishedYes

Keywords

  • Drug hepatotoxicity
  • Drug metabolism
  • Liver-on-a-chip

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