Liver Microphysiological System for Drug‐Induced Liver Injury (DILI) Evaluation Based on Kinetic Pump Integrated Microfluidic Plate (KIM‐Plate)

ABSTRACT Prediction of the risk of developing Drug‐induced liver injury (DILI) is very important in drug discovery. Although animal tests usually evaluate DILI, the prediction accuracy of DILI is low because experimental animals have different metabolic pathways from humans. A few microphysiological...

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Published inElectrical engineering in Japan Vol. 218; no. 2
Main Authors Shinha, Kenta, Nakamura, Hiroko, Nishikawa, Masaki, Sakai, Yasuyuki, Kimura, Hiroshi
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc 01.06.2025
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Summary:ABSTRACT Prediction of the risk of developing Drug‐induced liver injury (DILI) is very important in drug discovery. Although animal tests usually evaluate DILI, the prediction accuracy of DILI is low because experimental animals have different metabolic pathways from humans. A few microphysiological systems (MPS) have been developed as novel evaluation systems for DILI evaluation. However, the proposed system is not yet practical due to operability, throughput issues, and prediction accuracy. Our purpose is to develop a practical DILI evaluation system. In this study, we investigate the influence of perfusion culture on hepatotoxicity tests using our previously developed Kinetic pump integrated microfluidic plate (KIM‐Plate). The results of acetaminophen toxicity tests showed that perfusion culture using KIM‐Plate improved the detection sensitivity of hepatotoxicity. We suggest that the liver model MPS based on KIM‐Plate could be a novel DILI evaluation system that integrates highly functional liver models and coculture with immune cells.
Bibliography:10.1541/ieejsmas.145.46
Funding
of
IEEJ Transactions on Sensors and Micromachines
This study was assisted by the AMED Project for Regenerative Medicine and Cell and Gene Therapies (JP17be0304201, JP21be0304201).
Translated from Volume 145 Number 3, pages 46–52, DOI
(Denki Gakkai Ronbunshi E).
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ISSN:0424-7760
1520-6416
DOI:10.1002/eej.23513