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dc.contributor.authorDomansky, Karel
dc.contributor.authorInman, Samuel Walker
dc.contributor.authorSerdy, James George
dc.contributor.authorDash, Ajit
dc.contributor.authorLim, Matthew H. M.
dc.contributor.authorGriffith, Linda G.
dc.date.accessioned2014-08-15T18:08:00Z
dc.date.available2014-08-15T18:08:00Z
dc.date.issued2010-01
dc.date.submitted2009-07
dc.identifier.issn1473-0197
dc.identifier.issn1473-0189
dc.identifier.urihttp://hdl.handle.net/1721.1/88735
dc.description.abstractIn vitro models that capture the complexity of in vivo tissue and organ behaviors in a scalable and easy-to-use format are desirable for drug discovery. To address this, we have developed a bioreactor that fosters maintenance of 3D tissue cultures under constant perfusion and we have integrated multiple bioreactors into an array in a multiwell plate format. All bioreactors are fluidically isolated from each other. Each bioreactor in the array contains a scaffold that supports formation of hundreds of 3D microscale tissue units. The tissue units are perfused with cell culture medium circulated within the bioreactor by integrated pneumatic diaphragm micropumps. Electronic controls for the pumps are kept outside the incubator and connected to the perfused multiwell by pneumatic lines. The docking design and open-well bioreactor layout make handling perfused multiwell plates similar to using standard multiwell tissue culture plates. A model of oxygen consumption and transport in the circulating culture medium was used to predict appropriate operating parameters for primary liver cultures. Oxygen concentrations at key locations in the system were then measured as a function of flow rate and time after initiation of culture to determine oxygen consumption rates. After seven days of culture, tissue formed from cells seeded in the perfused multiwell reactor remained functionally viable as assessed by immunostaining for hepatocyte and liver sinusoidal endothelial cell (LSEC) phenotypic markers.en_US
dc.description.sponsorshipNational Institute of Environmental Health Sciences (grant number 5P30ES002109-30)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (NIH grant number 5R01ES015241)en_US
dc.description.sponsorshipDuPont MIT Allianceen_US
dc.description.sponsorshipPfizer Inc.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (NSF grant number EEC-9843342)en_US
dc.language.isoen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.isversionofhttp://dx.doi.org/10.1039/b913221jen_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.titlePerfused multiwell plate for 3D liver tissue engineeringen_US
dc.typeArticleen_US
dc.identifier.citationDomansky, Karel, Walker Inman, James Serdy, Ajit Dash, Matthew H. M. Lim, and Linda G. Griffith. “Perfused Multiwell Plate for 3D Liver Tissue Engineering.” Lab Chip 10, no. 1 (2010): 51.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.mitauthorDomansky, Karelen_US
dc.contributor.mitauthorInman, Samuel Walkeren_US
dc.contributor.mitauthorSerdy, James Georgeen_US
dc.contributor.mitauthorDash, Ajiten_US
dc.contributor.mitauthorGriffith, Linda G.en_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.orderedauthorsDomansky, Karel; Inman, Walker; Serdy, James; Dash, Ajit; Lim, Matthew H. M.; Griffith, Linda G.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-1801-5548
dspace.mitauthor.errortrue
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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