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dc.contributor.authorFunamoto, Kenichi
dc.contributor.authorZervantonakis, Ioannis K.
dc.contributor.authorLiu, Yuchun
dc.contributor.authorOchs, Christopher J.
dc.contributor.authorKim, Choong
dc.contributor.authorKamm, Roger Dale
dc.date.accessioned2014-09-10T15:38:33Z
dc.date.available2014-09-10T15:38:33Z
dc.date.issued2012-09
dc.date.submitted2012-03
dc.identifier.issn1473-0197
dc.identifier.issn1473-0189
dc.identifier.urihttp://hdl.handle.net/1721.1/89411
dc.description.abstractLow oxygen tensions experienced in various pathological and physiological conditions are a major stimulus for angiogenesis. Hypoxic conditions play a critical role in regulating cellular behaviour including migration, proliferation and differentiation. This study introduces the use of a microfluidic device that allows for the control of oxygen tension for the study of different three-dimensional (3D) cell cultures for various applications. The device has a central 3D gel region acting as an external cellular matrix, flanked by media channels. On each side, there is a peripheral gas channel through which suitable gas mixtures are supplied to establish a uniform oxygen tension or gradient within the device. The effects of various parameters, such as gas and media flow rates, device thickness, and diffusion coefficients of oxygen were examined using numerical simulations to determine the characteristics of the microfluidic device. A polycarbonate (PC) film with a low oxygen diffusion coefficient was embedded in the device in proximity above the channels to prevent oxygen diffusion from the incubator environment into the polydimethylsiloxane (PDMS) device. The oxygen tension in the device was then validated experimentally using a ruthenium-coated (Ru-coated) oxygen-sensing glass cover slip which confirmed the establishment of low uniform oxygen tensions (<3%) or an oxygen gradient across the gel region. To demonstrate the utility of the microfluidic device for cellular experiments under hypoxic conditions, migratory studies of MDA-MB-231 human breast cancer cells were performed. The microfluidic device allowed for imaging cellular migration with high-resolution, exhibiting an enhanced migration in hypoxia in comparison to normoxia. This microfluidic device presents itself as a promising platform for the investigation of cellular behaviour in a 3D gel scaffold under varying hypoxic conditions.en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/c2lc40306den_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleA novel microfluidic platform for high-resolution imaging of a three-dimensional cell culture under a controlled hypoxic environmenten_US
dc.typeArticleen_US
dc.identifier.citationFunamoto, Kenichi, Ioannis K. Zervantonakis, Yuchun Liu, Christopher J. Ochs, Choong Kim, and Roger D. Kamm. “A Novel Microfluidic Platform for High-Resolution Imaging of a Three-Dimensional Cell Culture Under a Controlled Hypoxic Environment.” Lab Chip 12, no. 22 (2012): 4855.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.mitauthorFunamoto, Kenichien_US
dc.contributor.mitauthorZervantonakis, Ioannis K.en_US
dc.contributor.mitauthorKamm, Roger Daleen_US
dc.relation.journalLab on a Chipen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsFunamoto, Kenichi; Zervantonakis, Ioannis K.; Liu, Yuchun; Ochs, Christopher J.; Kim, Choong; Kamm, Roger D.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-7232-304X
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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