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dc.contributor.authorCheng, George Z.
dc.contributor.authorGangadharan, Sidharta P.
dc.contributor.authorRagelle, Heloise
dc.contributor.authorTibbitt, Mark W
dc.contributor.authorWu, Shang-Yun
dc.contributor.authorCastillo, Michael A.
dc.contributor.authorAnderson, Daniel Griffith
dc.contributor.authorLanger, Robert S
dc.contributor.authorCima, Michael J.
dc.date.accessioned2018-05-02T13:28:15Z
dc.date.available2018-05-02T13:28:15Z
dc.date.issued2018-12
dc.date.submitted2017-09
dc.identifier.issn2041-1723
dc.identifier.urihttp://hdl.handle.net/1721.1/115149
dc.description.abstractThe proliferation of computer-aided design and additive manufacturing enables on-demand fabrication of complex, three-dimensional structures. However, combining the versatility of cell-laden hydrogels within the 3D printing process remains a challenge. Herein, we describe a facile and versatile method that integrates polymer networks (including hydrogels) with 3D-printed mechanical supports to fabricate multicomponent (bio)materials. The approach exploits surface tension to coat fenestrated surfaces with suspended liquid films that can be transformed into solid films. The operating parameters for the process are determined using a physical model, and complex geometric structures are successfully fabricated. We engineer, by tailoring the window geometry, scaffolds with anisotropic mechanical properties that compress longitudinally (~30% strain) without damaging the hydrogel coating. Finally, the process is amenable to high cell density encapsulation and co-culture. Viability ( > 95%) was maintained 28 days after encapsulation. This general approach can generate biocompatible, macroscale devices with structural integrity and anisotropic mechanical properties.en_US
dc.description.sponsorshipLeona M. and Harry B. Helmsley Charitable Trusten_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/s41467-018-03391-wen_US
dc.rightsAttribution 4.0 International (CC BY 4.0)en_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNature Communicationsen_US
dc.titleSurface tension-assisted additive manufacturingen_US
dc.typeArticleen_US
dc.identifier.citationRagelle, Héloïse, et al. “Surface Tension-Assisted Additive Manufacturing.” Nature Communications, vol. 9, no. 1, Dec. 2018. © 2018 The Authorsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Center for Materials Science and Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorRagelle, Heloise
dc.contributor.mitauthorTibbitt, Mark W
dc.contributor.mitauthorWu, Shang-Yun
dc.contributor.mitauthorCastillo, Michael A.
dc.contributor.mitauthorAnderson, Daniel Griffith
dc.contributor.mitauthorCima, Michael J
dc.contributor.mitauthorLanger, Robert S
dc.relation.journalNature Communicationsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-04-27T15:10:00Z
dspace.orderedauthorsRagelle, Héloïse; Tibbitt, Mark W.; Wu, Shang-Yun; Castillo, Michael A.; Cheng, George Z.; Gangadharan, Sidharta P.; Anderson, Daniel G.; Cima, Michael J.; Langer, Roberten_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-0650-9601
dc.identifier.orcidhttps://orcid.org/0000-0002-4917-7187
dc.identifier.orcidhttps://orcid.org/0000-0001-5629-4798
dc.identifier.orcidhttps://orcid.org/0000-0003-2379-6139
dc.identifier.orcidhttps://orcid.org/0000-0003-4255-0492
mit.licensePUBLISHER_CCen_US


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