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dc.contributor.authorRusolahti, Erkki
dc.contributor.authorBhatia, Sangeeta N.
dc.date.accessioned2011-01-18T15:33:11Z
dc.date.available2011-01-18T15:33:11Z
dc.date.issued2010-03
dc.date.submitted2009-10
dc.identifier.issn1540-8140
dc.identifier.issn0021-9525
dc.identifier.urihttp://hdl.handle.net/1721.1/60655
dc.description.abstractThe various types of cells that comprise the tumor mass all carry molecular markers that are not expressed or are expressed at much lower levels in normal cells. These differentially expressed molecules can be used as docking sites to concentrate drug conjugates and nanoparticles at tumors. Specific markers in tumor vessels are particularly well suited for targeting because molecules at the surface of blood vessels are readily accessible to circulating compounds. The increased concentration of a drug in the site of disease made possible by targeted delivery can be used to increase efficacy, reduce side effects, or achieve some of both. We review the recent advances in this delivery approach with a focus on the use of molecular markers of tumor vasculature as the primary target and nanoparticles as the delivery vehicle.en_US
dc.description.sponsorshipUnited States. National Cancer Institute. Bioengineering Research Partnership (grant CA-122427)en_US
dc.description.sponsorshipUnited States. Dept. of Defense (Innovator Award W81XWH-08-1-0727)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant No. DMR-0806859)en_US
dc.language.isoen_US
dc.publisherRockefeller University Pressen_US
dc.relation.isversionofhttp://dx.doi.org/10.1083/jcb.200910104en_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.sourceRockefeller UPen_US
dc.titleTargeting of drugs and nanoparticles to tumorsen_US
dc.typeArticleen_US
dc.identifier.citationRuoslahti, Erkki, Sangeeta N. Bhatia, and Michael J. Sailor. “Targeting of drugs and nanoparticles to tumors.” The Journal of Cell Biology 188.6 (2010): 759 -768.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.approverBhatia, Sangeeta N.
dc.contributor.mitauthorBhatia, Sangeeta N.
dc.relation.journalJournal of Cell Biologyen_US
dc.eprint.versionFinal published versionen_US
dc.identifier.pmid20231381
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsRuoslahti, E.; Bhatia, S. N.; Sailor, M. J.en
dc.identifier.orcidhttps://orcid.org/0000-0002-1293-2097
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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