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dc.contributor.authorNeiman, Jaclyn A. Shepard
dc.contributor.authorHughes, David J.
dc.contributor.authorGriffith, Linda G.
dc.contributor.authorEbrahimkhani, Mohammad Reza
dc.contributor.authorRaredon, Micha Sam Brickman
dc.date.accessioned2015-10-21T11:56:40Z
dc.date.available2015-10-21T11:56:40Z
dc.date.issued2014-03
dc.identifier.issn0169409X
dc.identifier.urihttp://hdl.handle.net/1721.1/99380
dc.description.abstractLiver is a central nexus integrating metabolic and immunologic homeostasis in the human body, and the direct or indirect target of most molecular therapeutics. A wide spectrum of therapeutic and technological needs drives efforts to capture liver physiology and pathophysiology in vitro, ranging from prediction of metabolism and toxicity of small molecule drugs, to understanding off-target effects of proteins, nucleic acid therapies, and targeted therapeutics, to serving as disease models for drug development. Here we provide perspective on the evolving landscape of bioreactor-based models to meet old and new challenges in drug discovery and development, emphasizing design challenges in maintaining long-term liver-specific function and how emerging technologies in biomaterials and microdevices are providing new experimental models.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (R01 EB010246)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (P50-GM068762-08)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (R01-ES015241)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (P30-ES002109)en_US
dc.description.sponsorship5UH2TR000496-02en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Emergent Behaviors of Integrated Cellular Systems (CBET-0939511)en_US
dc.description.sponsorshipUnited States. Defense Advanced Research Projects Agency. Microphysiological Systems Program (W911NF-12-2-0039)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.addr.2014.02.011en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleBioreactor technologies to support liver function in vitroen_US
dc.typeArticleen_US
dc.identifier.citationEbrahimkhani, Mohammad R., Jaclyn A. Shepard Neiman, Micha Sam B. Raredon, David J. Hughes, and Linda G. Griffith. “Bioreactor Technologies to Support Liver Function in Vitro.” Advanced Drug Delivery Reviews 69–70 (April 2014): 132–157.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Center for Gynepathology Researchen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Materials Science and Engineeringen_US
dc.contributor.mitauthorEbrahimkhani, Mohammad Rezaen_US
dc.contributor.mitauthorNeiman, Jaclyn A. Sheparden_US
dc.contributor.mitauthorRaredon, Micha Sam Brickmanen_US
dc.contributor.mitauthorGriffith, Linda G.en_US
dc.relation.journalAdvanced Drug Delivery Reviewsen_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.orderedauthorsEbrahimkhani, Mohammad R.; Neiman, Jaclyn A. Shepard; Raredon, Micha Sam B.; Hughes, David J.; Griffith, Linda G.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1441-6122
dc.identifier.orcidhttps://orcid.org/0000-0002-1801-5548
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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