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dc.contributor.authorBanerjee, Deboshri
dc.contributor.authorHarfouche, Rania
dc.contributor.authorSengupta, Shiladitya
dc.date.accessioned2011-02-23T14:21:35Z
dc.date.available2011-02-23T14:21:35Z
dc.date.issued2011-01
dc.date.submitted2010-08
dc.identifier.urihttp://hdl.handle.net/1721.1/61155
dc.description.abstractAbstract Angiogenesis is disregulated in many diseased states, most notably in cancer. An emerging strategy for the development of therapies targeting tumor-associated angiogenesis is to harness the potential of nanotechnology to improve the pharmacology of chemotherapeutics, including anti-angiogenic agents. Nanoparticles confer several advantages over that of free drugs, including their capability to carry high payloads of therapeutic agents, confer increased half-life and reduced toxicity to the drugs, and provide means for selective targeting of the tumor tissue and vasculature. The plethora of nanovectors available, in addition to the various methods available to combine them with anti-angiogenic drugs, allows researchers to fine-tune the pharmacological profile of the drugs ad infinitum. Use of nanovectors has also opened up novel avenues for non-invasive imaging of tumor angiogenesis. Herein, we review the types of nanovector and therapeutic/diagnostic agent combinations used in targeting tumor angiogenesis.en_US
dc.description.sponsorshipNational Institutes of Health (U.S) (1R01CA135242-01A2)en_US
dc.description.sponsorshipUnited States. Dept. of Defense (BCRP Era of Hope Scholar Award W81XWH-07-1-0482)en_US
dc.description.sponsorshipUnited States. Dept. of Defense (BCRP Innovator Collaborative Award)en_US
dc.publisherBioMed Central Ltden_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/2045-824X-3-3en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceBioMed Central Ltden_US
dc.titleNanotechnology-mediated targeting of tumor angiogenesisen_US
dc.typeArticleen_US
dc.identifier.citationVascular Cell. 2011 Jan 31;3(1):3en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.approverSengupta, Shiladitya
dc.contributor.mitauthorSengupta, Shiladitya
dc.relation.journalVascular Cellen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2011-02-22T17:07:55Z
dc.language.rfc3066en
dc.rights.holderBanerjee et al.; licensee BioMed Central Ltd.
dspace.orderedauthorsBanerjee, Deboshri; Harfouche, Rania; Sengupta, Shiladityaen
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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