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dc.contributor.authorMacdonald, Mara L.
dc.contributor.authorSamuel, Raymond E.
dc.contributor.authorShah, Nisarg J.
dc.contributor.authorPadera, Robert F.
dc.contributor.authorBeben, Yvette M.
dc.contributor.authorHammond, Paula T
dc.date.accessioned2015-10-21T15:41:26Z
dc.date.available2015-10-21T15:41:26Z
dc.date.issued2010-11
dc.date.submitted2010-10
dc.identifier.issn01429612
dc.identifier.issn1878-5905
dc.identifier.urihttp://hdl.handle.net/1721.1/99391
dc.description.abstractDrug eluting coatings that can direct the host tissue response to implanted medical devices have the potential to ameliorate both the medical and financial burden of complications from implantation. However, because many drugs useful in this arena are biologic in nature, a paucity of delivery strategies for biologics, including growth factors, currently limits the control that can be exerted on the implantation environment. Layer-by-Layer (LbL) polyelectrolyte multilayer films are highly attractive as ultrathin biologic reservoirs, due to the capability to conformally coat difficult geometries, the use of aqueous processing likely to preserve fragile protein function, and the tunability of incorporation and release profiles. Herein, we describe the first LbL films capable of microgram-scale release of the biologic Bone Morphogenetic Protein 2 (BMP-2), which is capable of directing the host tissue response to create bone from native progenitor cells. Ten micrograms of BMP-2 are released over a period of two weeks in vitro; less than 1% is released in the first 3 h (compared with commercial collagen matrices which can release up to 60% of BMP-2, too quickly to induce differentiation). BMP-2 released from LbL films retains its ability to induce bone differentiation in MC3T3 E1S4 pre-osteoblasts, as measured by induction of alkaline phosphatase and stains for calcium (via Alizarin Red) and calcium matrix (via Von Kossa). In vivo, BMP-2 film coated scaffolds were compared with film coated scaffolds lacking BMP-2. BMP-2 coatings implanted intramuscularly were able to initiate host progenitor cells to differentiate into bone, which matured and expanded from four to 9 weeks as measured by MicroCT and histology. Such LbL films represent new steps towards controlling and tuning host response to implanted medical devices, which may ultimately increase the success of implanted devices, provide alternative new approaches toward bone wound healing, and lay the foundation for development of a multi-therapeutic release coating.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 1-R01-AG029601-01)en_US
dc.description.sponsorshipDeshpande Center for Technological Innovation (Grant 009216-1)en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Graduate Research Fellowshipen_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.biomaterials.2010.10.052en_US
dc.rightsCreative Commons Attribution-Noncommercial-NoDerivativesen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleTissue integration of growth factor-eluting layer-by-layer polyelectrolyte multilayer coated implantsen_US
dc.typeArticleen_US
dc.identifier.citationMacdonald, Mara L., Raymond E. Samuel, Nisarg J. Shah, Robert F. Padera, Yvette M. Beben, and Paula T. Hammond. “Tissue Integration of Growth Factor-Eluting Layer-by-Layer Polyelectrolyte Multilayer Coated Implants.” Biomaterials 32, no. 5 (February 2011): 1446–1453.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.mitauthorMacdonald, Mara L.en_US
dc.contributor.mitauthorSamuel, Raymond E.en_US
dc.contributor.mitauthorShah, Nisarg J.en_US
dc.contributor.mitauthorBeben, Yvette M.en_US
dc.contributor.mitauthorHammond, Paula T.en_US
dc.relation.journalBiomaterialsen_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.orderedauthorsMacdonald, Mara L.; Samuel, Raymond E.; Shah, Nisarg J.; Padera, Robert F.; Beben, Yvette M.; Hammond, Paula T.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-1727-5732
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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