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dc.contributor.authorDuran-Frigola, Miquel
dc.contributor.authorHernandez, Bryan
dc.contributor.authorNonell, Santi
dc.contributor.authorFosas, Elisabet
dc.contributor.authorSantoma, Pablo
dc.contributor.authorLlinas, Maria C.
dc.contributor.authorRuiz-Gonzalez, Ruben
dc.contributor.authorSanchez-Garcia, David
dc.contributor.authorBalcells-Camps, Mercedes
dc.contributor.authorEdelman, Elazer R
dc.contributor.authorRosas, Elisabet Canyelles
dc.date.accessioned2015-01-13T16:23:29Z
dc.date.available2015-01-13T16:23:29Z
dc.date.issued2013-07
dc.date.submitted2013-07
dc.identifier.issn0743-7463
dc.identifier.issn1520-5827
dc.identifier.urihttp://hdl.handle.net/1721.1/92822
dc.description.abstractInflammation and shear stress can upregulate expression of cellular adhesion molecules in endothelial cells (EC). The modified EC surface becomes a mediating interface between the circulating blood elements and the endothelium, and grants opportunity for immunotherapy. In photodynamic therapy (PDT), immunotargeting might overcome the lack of selectivity of currently used sensitizers. In this study, we hypothesized that differential ICAM-1 expression modulates the effects of a drug targeted to surface ICAM-1. A novel porphycene–anti-ICAM-1 conjugate was synthesized and applied to treat endothelial cells from macro and microvasculature. Results show that the conjugate induces phototoxicity in inflamed, but not in healthy, microvascular EC. Conversely, macrovascular EC exhibited phototoxicity regardless of their state. These findings have two major implications; the relevance of ICAM-1 as a modulator of drug effects in microvasculature, and the potential of the porphycene bioconjugate as a promising novel PDT agent.en_US
dc.description.sponsorshipSpain. Ministerio de Economia y Competividad (Grant BFU2009-0984)en_US
dc.description.sponsorshipSpain. Ministerio de Economia y Competividad (Grant CTQ2010-20870-C03-01)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant NIH/NIGMS RO1/GM049039)en_US
dc.description.sponsorshipFundacio Empreses IQSen_US
dc.description.sponsorshipFundacio Empreses POSIMATen_US
dc.description.sponsorshipMIT-Spain Seed Funden_US
dc.language.isoen_US
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/la401067den_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.sourcePMCen_US
dc.titleModifications of Microvascular EC Surface Modulate Phototoxicity of a Porphycene anti-ICAM-1 Immunoconjugate; Therapeutic Implicationsen_US
dc.typeArticleen_US
dc.identifier.citationRosas, Elisabet, Pablo Santoma, Miquel Duran-Frigola, Bryan Hernandez, Maria C. Llinas, Ruben Ruiz-Gonzalez, Santi Nonell, David Sanchez-Garcia, Elazer R. Edelman, and Mercedes Balcells. “Modifications of Microvascular EC Surface Modulate Phototoxicity of a Porphycene Anti-ICAM-1 Immunoconjugate; Therapeutic Implications.” Langmuir 29, no. 31 (August 6, 2013): 9734–9743.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.mitauthorRosas, Elisabeten_US
dc.contributor.mitauthorSantoma, Pabloen_US
dc.contributor.mitauthorDuran-Frigola, Miquelen_US
dc.contributor.mitauthorHernandez, Bryanen_US
dc.contributor.mitauthorEdelman, Elazer R.en_US
dc.contributor.mitauthorBalcells-Camps, Mercedesen_US
dc.relation.journalLangmuiren_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.orderedauthorsRosas, Elisabet; Santoma, Pablo; Duran-Frigola, Miquel; Hernandez, Bryan; Llinas, Maria C.; Ruiz-Gonzalez, Ruben; Nonell, Santi; Sanchez-Garcia, David; Edelman, Elazer R.; Balcells, Mercedesen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-7832-7156
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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