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dc.contributor.authorRiccardi, Claudiaes_ES
dc.contributor.authorFàbrega, Carmees_ES
dc.contributor.authorGrijalvo, Santiagoes_ES
dc.contributor.authorVitiello, Giuseppees_ES
dc.contributor.authorD'Errico, Geradinoes_ES
dc.contributor.authorEritja Casadellà, Ramónes_ES
dc.contributor.authorMontesarchio, Danielaes_ES
dc.date.accessioned2018-08-24T06:40:59Z-
dc.date.available2018-08-24T06:40:59Z-
dc.date.issued2018-07-27-
dc.identifier.citationJournal of Materials Chemistry B 6: 5368-5384 (2018)es_ES
dc.identifier.urihttp://hdl.handle.net/10261/169109-
dc.description.abstractNiosomes are self-assembled vesicles made up of single chain non-ionic surfactants combined with appropriate amounts of cholesterol or other lipids, exploited as carriers for hydrophilic or lipophilic drugs. Compared to liposomes, niosomes are typically more stable, less expensive and, being generally obtained from synthetic surfactants, more easily derivatizable, providing vesicular structures with a higher versatility and chemical diversity. Herein, we investigated the physico-chemical and biological properties of niosomes loaded with two active ingredients, i.e. the nucleolipidic Ru(III)-complex HoThyRu, selected as an anticancer agent, and the nucleolin-targeting AS1411 aptamer, allowing selective recognition of cancer cells. The morphology, average size, zeta potential, electrophoretic mobility, and stability over time of the functionalized niosomes were analyzed using different biophysical techniques. These formulations, tested on both cancer and normal cells, showed promising antiproliferative activity on HeLa cells, with a higher efficacy associated with the nanosystems containing both AS1411 and HoThyRu with respect to the controls. In all the tested cell lines, AS1411 proved to markedly enhance the bioactivity of the Ru(III)-containing niosomes.es_ES
dc.description.sponsorshipWe are deeply grateful to dr. Rocco Di Girolamo, from the Department of Chemical Sciences, University of Naples Federico II, for his precious contribution for the TEM images acquisition. This work was supported by the Italian Association for Cancer Research (AIRC) (IG2015 n. 17037 to D. M.). C. R. thanks “Programma di scambi internazionali tra l'Università degli Studi di Napoli Federico II ed Università ed Istituti di ricerca stranieri per la mobilità di breve durata di docenti, ricercatori e studiosi”. Financial support by the Spanish Ministerio de Ciencia e Innovación (MICINN) (Project CTQ2014-52588-R and CTQ2017-84415-R) and Generalitat de Catalunya (2017SGR114) are gratefully acknowledged. CIBER-BBN is an initiative funded by the Instituto de Salud Carlos III with assistance from the European Regional Development Fund.es_ES
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistry (UK)es_ES
dc.relation.isversionofPostprintes_ES
dc.rightsopenAccessen_EN
dc.subjectNiosomeses_ES
dc.subjectAS1411es_ES
dc.titleAS1411-decorated niosomes as effective nanocarriers for Ru(III)-based drugs in anticancer strategieses_ES
dc.typeartículoes_ES
dc.identifier.doi10.1039/C8TB01563E-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversion10.1039/C8TB01563Ees_ES
dc.embargo.terms2019-07-27es_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.pmides_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.languageiso639-1en-
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