Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/87586
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dc.contributorDepartment of Biomedical Engineeringen_US
dc.creatorZhang, Qen_US
dc.creatorSito, Len_US
dc.creatorMao, Men_US
dc.creatorHe, Jen_US
dc.creatorZhang, YSen_US
dc.creatorZhao, Xen_US
dc.date.accessioned2020-07-16T03:59:09Z-
dc.date.available2020-07-16T03:59:09Z-
dc.identifier.urihttp://hdl.handle.net/10397/87586-
dc.language.isoenen_US
dc.publisherAME Publishing Companyen_US
dc.rights© Microphysiological Systems. All rights reserved.en_US
dc.rightsMicrophysiological Systems is a peer reviewed, open access journal. All content of the journal is published under the Creative Commons Attribution-NonCommercial- NoDerivatives 4.0 International License (CC BY-NC-ND 4.0) (https://creativecommons.org/licenses/by-nc-nd/4.0/). All articles published open access will be immediately and permanently free for all to read, download, copy and distribute as defined by the applied license.en_US
dc.rightsThe following publication Zhang Q, Sito L, Mao M, He J, Zhang YS, Zhao X. Current advances in skin-on-a-chip models for drug testing. Microphysiol Syst 2018;2:4 is available at http://mps.amegroups.com/article/view/4737en_US
dc.subjectOrgan-on-a-chipen_US
dc.subjectHuman skin equivalents (HSEs)en_US
dc.subjectSkin-on-a-chipen_US
dc.subjectMicrofluidicsen_US
dc.subjectDrug testingen_US
dc.titleCurrent advances in skin-on-a-chip models for drug testingen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1en_US
dc.identifier.epage9en_US
dc.identifier.volume2en_US
dcterms.abstractSkin-on-a-chip models are highly desirable in drug testing compared to conventional 2D cell culture and animal models as they can replicate organ-specific 3D structural organization and physiological functions at a relatively low cost. To engineer a physiologically relevant skin model, human skin structures have been integrated onto microfluidic platforms to construct skin-on-a-chip systems that can mimic the complex in vivo situation. In this mini-review, we first briefly introduce some critical technologies employed to develop in vitro skin-on-a-chip models. We then review the applications of the state-of-the-art skin-on-a-chip models in drug testing, with a focus on using models of full-thickness skin equivalents (FTSEs), skin models with additional components such as vasculature, immune cells and hair follicles as well as multi-organ-on-a-chip models. Finally, we discuss some current challenges and future directions of development of complex, and in vivo-like skin-on-a-chip models.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationMicrophysiological systems, Aug. 2018, v. 2, 4, p. 1-9en_US
dcterms.isPartOfMicrophysiological systemsen_US
dcterms.issued2018-08-
dc.identifier.eissn2616-275Xen_US
dc.identifier.artn4en_US
dc.identifier.rosgroupid2018003551-
dc.description.ros2018-2019 > Academic research: refereed > Publication in refereed journalen_US
dc.description.validate202007 bcrcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera0596-n36, OA_Others (ROS1819)en_US
dc.identifier.SubFormID480-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextP0006214en_US
dc.description.pubStatusPublisheden_US
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