Show simple item record

dc.contributor.authorKastrup, Christian
dc.contributor.authorNahrendorf, Matthias
dc.contributor.authorFigueiredo, Jose Luiz
dc.contributor.authorLee, Haeshin
dc.contributor.authorKambhampati, Swetha
dc.contributor.authorLee, Timothy
dc.contributor.authorCho, Seung Woo
dc.contributor.authorGorbatov, Rostic
dc.contributor.authorIwamoto, Yoshiko
dc.contributor.authorDang, Tram T.
dc.contributor.authorDutta, Partha
dc.contributor.authorYeon, Ju Hun
dc.contributor.authorCheng, Hao
dc.contributor.authorVegas, Arturo
dc.contributor.authorSiegel, Cory D.
dc.contributor.authorMacDougall, Samantha
dc.contributor.authorOkonkwo, Michael E.
dc.contributor.authorThai, Anh
dc.contributor.authorStone, James R.
dc.contributor.authorCoury, Arthur J.
dc.contributor.authorWeissleder, Ralph
dc.contributor.authorLanger, Robert
dc.contributor.authorAnderson, Daniel Griffith
dc.contributor.authorPritchard, Christopher D., (Christopher David)
dc.date.accessioned2013-08-01T18:31:38Z
dc.date.available2013-08-01T18:31:38Z
dc.date.issued2012-12
dc.date.submitted2012-11
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/79758
dc.description.abstractThe treatment of diseased vasculature remains challenging, in part because of the difficulty in implanting drug-eluting devices without subjecting vessels to damaging mechanical forces. Implanting materials using adhesive forces could overcome this challenge, but materials have previously not been shown to durably adhere to intact endothelium under blood flow. Marine mussels secrete strong underwater adhesives that have been mimicked in synthetic systems. Here we develop a drug-eluting bioadhesive gel that can be locally and durably glued onto the inside surface of blood vessels. In a mouse model of atherosclerosis, inflamed plaques treated with steroid-eluting adhesive gels had reduced macrophage content and developed protective fibrous caps covering the plaque core. Treatment also lowered plasma cytokine levels and biomarkers of inflammation in the plaque. The drug-eluting devices developed here provide a general strategy for implanting therapeutics in the vasculature using adhesive forces and could potentially be used to stabilize rupture-prone plaques.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant DE016516)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01HL096576)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant U24- CA92782)en_US
dc.description.sponsorshipMedtronic, Incen_US
dc.description.sponsorshipCanadian Institutes of Health Research (grant MOP119426)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Pioneer Research Program Grant R31-10071)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Pioneer Research Program Grant WCU-2z011-0001696)en_US
dc.description.sponsorshipJuvenile Diabetes Research Foundation Internationalen_US
dc.language.isoen_US
dc.publisherNational Academy of Sciences (U.S.)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1217972110en_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.sourcePNASen_US
dc.titlePainting blood vessels and atherosclerotic plaques with an adhesive drug depoten_US
dc.typeArticleen_US
dc.identifier.citationKastrup, C. J., M. Nahrendorf, J. L. Figueiredo, H. Lee, S. Kambhampati, T. Lee, S.-W. Cho, et al. “Painting blood vessels and atherosclerotic plaques with an adhesive drug depot.” Proceedings of the National Academy of Sciences 109, no. 52 (December 26, 2012): 21444-21449.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.mitauthorLanger, Roberten_US
dc.contributor.mitauthorAnderson, Daniel Griffithen_US
dc.contributor.mitauthorVegas, Arturoen_US
dc.contributor.mitauthorKastrup, Christianen_US
dc.contributor.mitauthorKambhampati, Swethaen_US
dc.contributor.mitauthorLee, Timothyen_US
dc.contributor.mitauthorDang, Tram T.en_US
dc.contributor.mitauthorCheng, Haoen_US
dc.contributor.mitauthorPritchard, Christopher D.en_US
dc.contributor.mitauthorMacDougall, Samanthaen_US
dc.contributor.mitauthorOkonkwo, Michael E.en_US
dc.contributor.mitauthorThai, Anhen_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.orderedauthorsKastrup, C. J.; Nahrendorf, M.; Figueiredo, J. L.; Lee, H.; Kambhampati, S.; Lee, T.; Cho, S.-W.; Gorbatov, R.; Iwamoto, Y.; Dang, T. T.; Dutta, P.; Yeon, J. H.; Cheng, H.; Pritchard, C. D.; Vegas, A. J.; Siegel, C. D.; MacDougall, S.; Okonkwo, M.; Thai, A.; Stone, J. R.; Coury, A. J.; Weissleder, R.; Langer, R.; Anderson, D. G.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-5629-4798
dc.identifier.orcidhttps://orcid.org/0000-0001-9522-8208
dc.identifier.orcidhttps://orcid.org/0000-0003-4255-0492
dspace.mitauthor.errortrue
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record