Please use this identifier to cite or link to this item: https://doi.org/10.3390/mi10030165
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dc.titleEngineering microfluidic organoid-on-a-chip platforms
dc.contributor.authorYu, F.
dc.contributor.authorHunziker, W.
dc.contributor.authorChoudhury, D.
dc.date.accessioned2022-01-11T06:21:06Z
dc.date.available2022-01-11T06:21:06Z
dc.date.issued2019
dc.identifier.citationYu, F., Hunziker, W., Choudhury, D. (2019). Engineering microfluidic organoid-on-a-chip platforms. Micromachines 10 (3) : 165. ScholarBank@NUS Repository. https://doi.org/10.3390/mi10030165
dc.identifier.issn2072666X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/213749
dc.description.abstractIn vitro cell culture models are emerging as promising tools to understand human development, disease progression, and provide reliable, rapid and cost-effective results for drug discovery and screening. In recent years, an increasing number of in vitro models with complex organization and controlled microenvironment have been developed to mimic the in vivo organ structure and function. The invention of organoids, self-organized organ-like cell aggregates that originate from multipotent stem cells, has allowed a whole new level of biomimicry to be achieved. Microfluidic organoid-on-a-chip platforms can facilitate better nutrient and gas exchange and recapitulate 3D tissue architecture and physiology. They have the potential to transform the landscape of drug development and testing. In this review, we discuss the challenges in the current organoid models and describe the recent progress in the field of organoid-on-a-chip. © 2019 by the authors.
dc.publisherMDPI AG
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceScopus OA2019
dc.subjectCell culture
dc.subjectDrug screening
dc.subjectMicrobioreactor
dc.subjectMicrofluidics
dc.subjectOrgan-on-a-chip
dc.subjectOrganoids
dc.typeArticle
dc.contributor.departmentPHYSIOLOGY
dc.description.doi10.3390/mi10030165
dc.description.sourcetitleMicromachines
dc.description.volume10
dc.description.issue3
dc.description.page165
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