Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/4784
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dc.contributor.authorAntunes, A.-
dc.contributor.authorBotelho, M. F.-
dc.contributor.authorGomes, C.-
dc.contributor.authorLima, J. J. P. de-
dc.contributor.authorSilva, M. L.-
dc.contributor.authorMoreira, J. N.-
dc.contributor.authorSimões, S.-
dc.contributor.authorGonçalves, L.-
dc.contributor.authorProvidência, L. A.-
dc.date.accessioned2008-09-01T14:14:24Z-
dc.date.available2008-09-01T14:14:24Z-
dc.date.issued2004en_US
dc.identifier.citationJournal of Nuclear Cardiology. 11:4 (2004) S21-S21en_US
dc.identifier.urihttp://hdl.handle.net/10316/4784-
dc.description.abstractBackground: A major impediment to drug diagnosis and therapy of myocardial infarction is the limited access that drugs have to ischemic myocardium, dependent on regional myocardial blood flow. Investigators report that some liposomes concentrate in the experimental myocardial infarction, suggesting that they may be used to transport drugs to a region of ischemia. One of the most promising approaches for increasing liposome circulation time is coating them with polyethyleneglycol (PEG).en_US
dc.description.urihttp://www.sciencedirect.com/science/article/B6WKC-4D0XVDT-3B/1/e8e1e8ec0cf1dcf1546291ba169facffen_US
dc.format.mimetypeaplication/PDFen
dc.language.isoengeng
dc.rightsopenAccesseng
dc.titleDevelopment of liposomes with affinity to ischemic myocardiumen_US
dc.typearticleen_US
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.languageiso639-1en-
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
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