Please use this identifier to cite or link to this item: https://doi.org/10.3390/bios11050160
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dc.titleDesign and fabrication of the vertical-flow bioreactor for compaction hepatocyte culture in drug testing application
dc.contributor.authorZhu, Liang
dc.contributor.authorWang, Zhenfeng
dc.contributor.authorXia, Huanming
dc.contributor.authorYu, Hanry
dc.date.accessioned2022-10-26T09:12:10Z
dc.date.available2022-10-26T09:12:10Z
dc.date.issued2021-05-19
dc.identifier.citationZhu, Liang, Wang, Zhenfeng, Xia, Huanming, Yu, Hanry (2021-05-19). Design and fabrication of the vertical-flow bioreactor for compaction hepatocyte culture in drug testing application. Biosensors 11 (5) : 160. ScholarBank@NUS Repository. https://doi.org/10.3390/bios11050160
dc.identifier.issn2079-6374
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/233718
dc.description.abstractThe perfusion culture of primary hepatocytes has been widely adopted to build bioreactors for various applications. As a drug testing platform, a unique vertical-flow bioreactor (VfB) array was found to create the compaction culture of hepatocytes which mimicked the mechanic microenvironment in vivo while maintaining the 3D cell morphology in a 2D culture setup and enhancing the hepatic functions for a sustained culture. Here, we report the methodology in designing and fabricating the VfB to reach ideal bioreactor requirements, optimizing the VfB as a prototype for drug testing, and to demonstrate the enhanced hepatic function so as to demonstrate the performance of the bioreactor. This device enables the modular, scalable, and manufacturable construction of a functional drug testing platform through the sustained maintenance of model cells. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
dc.publisherMDPI
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2021
dc.subjectBioreactor
dc.subjectDesign
dc.subjectDrug testing
dc.subjectFabrication
dc.subjectHepatocytes
dc.subjectMicrofluidics
dc.subjectPerfusion culture
dc.typeArticle
dc.contributor.departmentPHYSIOLOGY
dc.description.doi10.3390/bios11050160
dc.description.sourcetitleBiosensors
dc.description.volume11
dc.description.issue5
dc.description.page160
dc.published.statePublished
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