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大学・研究所にある論文を検索できる 「Generation of Tetrafluoroethylene–Propylene Elastomer-Based Microfluidic Devices for Drug Toxicity and Metabolism Studies」の論文概要。リケラボ論文検索は、全国の大学リポジトリにある学位論文・教授論文を一括検索できる論文検索サービスです。

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Generation of Tetrafluoroethylene–Propylene Elastomer-Based Microfluidic Devices for Drug Toxicity and Metabolism Studies

Sano, Emi Deguchi, Sayaka Matsuoka, Naoki Tsuda, Masahiro Wang, Mengyang Kosugi, Kaori Mori, Chihiro Yagi, Keisuke Wada, Aya Yamasaki, Shinsuke Kawai, Tsuyoshi Yodogawa, Masahide Mizuguchi, Hiroyuki Nakazawa, Norihito Yamashita, Fumiyoshi Torisawa, Yu-suke Takayama, Kazuo 京都大学 DOI:10.1021/acsomega.1c03719

2021.09

概要

Polydimethylsiloxane (PDMS) is widely used to fabricate microfluidic organs-on-chips. Using these devices (PDMS-based devices), the mechanical microenvironment of living tissues, such as pulmonary respiration and intestinal peristalsis, can be reproduced in vitro. However, the use of PDMS-based devices in drug discovery research is limited because of their extensive absorption of drugs. In this study, we investigated the feasibility of the tetrafluoroethylene–propylene (FEPM) elastomer to fabricate a hepatocyte-on-a-chip (FEPM-based hepatocyte chip) with lower drug absorption. The FEPM-based hepatocyte chip expressed drug-metabolizing enzymes, drug-conjugating enzymes, and drug transporters. Also, it could produce human albumin. Although the metabolites of midazolam and bufuralol were hardly detected in the PDMS-based hepatocyte chip, they were detected abundantly in the FEPM-based hepatocyte chip. Finally, coumarin-induced hepatocyte cytotoxicity was less severe in the PDMS-based hepatocyte chip than in the FEPM-based hepatocyte chip, reflecting the different drug absorptions of the two chips. In conclusion, the FEPM-based hepatocyte chip could be a useful tool in drug discovery research, including drug metabolism and toxicity studies.

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参考文献

(1) Ewart, L.; Dehne, E.-M.; Fabre, K.; Gibbs, S.; Hickman, J.;

Hornberg, E.; Ingelman-Sundberg, M.; Jang, K.-J.; Jones, D. R.;

Lauschke, V. M.; Marx, U.; Mettetal, J. T.; Pointon, A.; Williams, D.;

Zimmermann, W.-H.; Newham, P. Application of microphysiological

systems to enhance safety assessment in drug discovery. Annu. Rev.

Pharmacol. Toxicol. 2018, 58, 65−82.

(2) Grassart, A.; Malardé, V.; Gobaa, S.; Sartori-Rupp, A.; Kerns, J.;

Karalis, K.; Marteyn, B.; Sansonetti, P.; Sauvonnet, N. Bioengineered

human organ-on-chip reveals intestinal microenvironment and

mechanical forces impacting Shigella infection. Cell Host Microbe

2019, 26, 435−444.

(3) Jang, K.-J.; Otieno, M. A.; Ronxhi, J.; Lim, H.-K.; Ewart, L.;

Kodella, K. R.; Petropolis, D. B.; Kulkarni, G.; Rubins, J. E.;

Conegliano, D.; Nawroth, J.; Simic, D.; Lam, W.; Singer, M.; Barale,

E.; Singh, B.; Sonee, M.; Streeter, A. J.; Manthey, C.; Jones, B.;

Srivastava, A.; Andersson, L. C.; Williams, D.; Park, H.; Barrile, R.;

Sliz, J.; Herland, A.; Haney, S.; Karalis, K.; Ingber, D. E.; Hamilton, G.

A. Reproducing human and cross-species drug toxicities using a LiverChip. Sci. Transl. Med. 2019, 11, aax5516.

(4) Huh, D.; Hamilton, G. A.; Ingber, D. E. From 3D cell culture to

organs-on-chips. Trends Cell Biol. 2011, 21, 745−754.

24865

https://doi.org/10.1021/acsomega.1c03719

ACS Omega 2021, 6, 24859−24865

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