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dc.contributor.authorGallego-Yerga, Laura-
dc.contributor.authorLomazzi, Michela-
dc.contributor.authorSansone, Francesco-
dc.contributor.authorOrtiz-Mellet, Carmen-
dc.contributor.authorCasnati, Alessandro-
dc.contributor.authorGarcía-Fernández, José Manuel-
dc.date.accessioned2014-07-04T08:44:51Z-
dc.date.available2014-07-04T08:44:51Z-
dc.date.issued2014-
dc.identifier.citationChemical Communications, 50: 7440-7443 (2014)es_ES
dc.identifier.urihttp://hdl.handle.net/10261/99428-
dc.description.abstractStable core–shell nanospheres self-assemble in water from heterodimers combining a hydrophobic calix[4]arene moiety and a hydrophilic β-cyclodextrin head; their potential to encapsulate and provide sustained release of the anticancer drug docetaxel and undergo surface post-modification with glycoligands targeting the macrophage mannose receptor is discussed.es_ES
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistry (UK)es_ES
dc.rightsopenAccesses_ES
dc.titleGlycoligand-targeted core-shell nanospheres with tunable drug release profiles from calixarene-cyclodextrin heterodimerses_ES
dc.typeartículoes_ES
dc.identifier.doi10.1039/C4CC02703E-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1039/c0xx00000xes_ES
dc.relation.csices_ES
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