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dc.contributor.authorVacanti, Nathaniel M.
dc.contributor.authorCheng, Hao
dc.contributor.authorHill, Paulina Sierpinski
dc.contributor.authorGuerreiro, Joao D. T.
dc.contributor.authorDang, Tram T.
dc.contributor.authorMa, Minglin
dc.contributor.authorWatson, Shanee
dc.contributor.authorHwang, Nathaniel S.
dc.contributor.authorLanger, Robert
dc.contributor.authorAnderson, Daniel Griffith
dc.date.accessioned2013-05-31T15:52:57Z
dc.date.available2013-05-31T15:52:57Z
dc.date.issued2012-08
dc.date.submitted2012-08
dc.identifier.issn1525-7797
dc.identifier.issn1526-4602
dc.identifier.urihttp://hdl.handle.net/1721.1/79053
dc.description.abstractSynthetic scaffolds are crucial to applications in regenerative medicine; however, the foreign body response can impede regeneration and may lead to failure of the implant. Herein we report the development of a tissue engineering scaffold that allows attachment and proliferation of regenerating cells while reducing the foreign body response by localized delivery of an anti-inflammatory agent. Electrospun fibers composed of poly(l-lactic) acid (PLLA) and poly(ε-caprolactone) (PCL) were prepared with and without the steroid anti-inflammatory drug, dexamethasone. Analysis of subcutaneous implants demonstrated that the PLLA fibers encapsulating dexamethasone evoked a less severe inflammatory response than the other fibers examined. They also displayed a controlled release of dexamethasone over a period of time conducive to tissue regeneration and allowed human mesenchymal stem cells to adhere to and proliferate on them in vitro. These observations demonstrate their potential as a building block for tissue engineering scaffolds.en_US
dc.description.sponsorshipArmed Forces Institute of Regenerative Medicine (award number W81XWH-08-2-0034)en_US
dc.description.sponsorshipU.S. Army Medical Research Acquisition Activityen_US
dc.language.isoen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/bm300520uen_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.sourceAmerican Chemical Societyen_US
dc.titleLocalized Delivery of Dexamethasone from Electrospun Fibers Reduces the Foreign Body Responseen_US
dc.typeArticleen_US
dc.identifier.citationVacanti, Nathaniel M., Hao Cheng, Paulina S. Hill, et al. 2012 Localized Delivery of Dexamethasone from Electrospun Fibers Reduces the Foreign Body Response. Biomacromolecules 13(10): 3031–3038. © 2012 American Chemical Society.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineeringen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorVacanti, Nathaniel M.en_US
dc.contributor.mitauthorCheng, Haoen_US
dc.contributor.mitauthorHill, Paulina Sierpinskien_US
dc.contributor.mitauthorGuerreiro, João D.T.en_US
dc.contributor.mitauthorDang, Tram T.en_US
dc.contributor.mitauthorMa, Minglinen_US
dc.contributor.mitauthorWatson, Shaneeen_US
dc.contributor.mitauthorHwang, Nathaniel S.en_US
dc.contributor.mitauthorLanger, Roberten_US
dc.contributor.mitauthorAnderson, Daniel Griffithen_US
dc.relation.journalBiomacromoleculesen_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.orderedauthorsVacanti, Nathaniel M.; Cheng, Hao; Hill, Paulina S.; Guerreiro, João D.T.; Dang, Tram T.; Ma, Minglin; Watson, Shanée; Hwang, Nathaniel S.; Langer, Robert; Anderson, Daniel G.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5629-4798
dc.identifier.orcidhttps://orcid.org/0000-0003-4255-0492
dspace.mitauthor.errortrue
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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