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dc.contributor.authorSeeherman, H. J.
dc.contributor.authorNevins, M.
dc.contributor.authorSpector, M.
dc.contributor.authorShah, Nisarg J.
dc.contributor.authorHyder, Md Nasim
dc.contributor.authorQuadir, Mohiuddin Abdul
dc.contributor.authorDorval Courchesne, Noemie-Manuelle
dc.contributor.authorHammond, Paula T.
dc.date.accessioned2015-04-28T20:23:57Z
dc.date.available2015-04-28T20:23:57Z
dc.date.issued2014-08
dc.date.submitted2014-05
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/96834
dc.description.abstractTraumatic wounds and congenital defects that require large-scale bone tissue repair have few successful clinical therapies, particularly for craniomaxillofacial defects. Although bioactive materials have demonstrated alternative approaches to tissue repair, an optimized materials system for reproducible, safe, and targeted repair remains elusive. We hypothesized that controlled, rapid bone formation in large, critical-size defects could be induced by simultaneously delivering multiple biological growth factors to the site of the wound. Here, we report an approach for bone repair using a polyelectrolye multilayer coating carrying as little as 200 ng of bone morphogenetic protein-2 and platelet-derived growth factor-BB that were eluted over readily adapted time scales to induce rapid bone repair. Based on electrostatic interactions between the polymer multilayers and growth factors alone, we sustained mitogenic and osteogenic signals with these growth factors in an easily tunable and controlled manner to direct endogenous cell function. To prove the role of this adaptive release system, we applied the polyelectrolyte coating on a well-studied biodegradable poly(lactic-co-glycolic acid) support membrane. The released growth factors directed cellular processes to induce bone repair in a critical-size rat calvaria model. The released growth factors promoted local bone formation that bridged a critical-size defect in the calvaria as early as 2 wk after implantation. Mature, mechanically competent bone regenerated the native calvaria form. Such an approach could be clinically useful and has significant benefits as a synthetic, off-the-shelf, cell-free option for bone tissue repair and restoration.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01 AG029601)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01 EB010246)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant P30 CA014051)en_US
dc.description.sponsorshipNatural Sciences and Engineering Research Council of Canada (Fellowship)en_US
dc.language.isoen_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1408035111en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceNational Academy of Sciences (U.S.)en_US
dc.titleAdaptive growth factor delivery from a polyelectrolyte coating promotes synergistic bone tissue repair and reconstructionen_US
dc.typeArticleen_US
dc.identifier.citationShah, N. J., M. N. Hyder, M. A. Quadir, N.-M. Dorval Courchesne, H. J. Seeherman, M. Nevins, M. Spector, and P. T. Hammond. “Adaptive Growth Factor Delivery from a Polyelectrolyte Coating Promotes Synergistic Bone Tissue Repair and Reconstruction.” Proceedings of the National Academy of Sciences 111, no. 35 (August 18, 2014): 12847–12852.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Laboratory for Manufacturing and Productivityen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorShah, Nisarg J.en_US
dc.contributor.mitauthorHyder, Md Nasimen_US
dc.contributor.mitauthorQuadir, Mohiuddin Abdulen_US
dc.contributor.mitauthorDorval Courchesne, Noemie-Manuelleen_US
dc.contributor.mitauthorHammond, Paula T.en_US
dc.relation.journalProceedings of the National Academy of Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsShah, N. J.; Hyder, M. N.; Quadir, M. A.; Dorval Courchesne, N.-M.; Seeherman, H. J.; Nevins, M.; Spector, M.; Hammond, P. T.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1727-5732
dc.identifier.orcidhttps://orcid.org/0000-0002-5568-6455
dspace.mitauthor.errortrue
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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