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dc.contributor.authorCalero, Macarena-
dc.contributor.authorChiappi, Michele-
dc.contributor.authorLázaro-Nogal, Ana-
dc.contributor.authorRodríguez, María Josefa-
dc.contributor.authorChichón, Javier-
dc.contributor.authorCrosbie-Staunton, Kieran-
dc.contributor.authorPrina-Mello, Adriele-
dc.contributor.authorVolkov, Yuri-
dc.contributor.authorVillanueva, Ángeles-
dc.contributor.authorCarrascosa, José L.-
dc.date.accessioned2015-11-25T17:56:16Z-
dc.date.available2015-11-25T17:56:16Z-
dc.date.issued2015-02-26-
dc.identifier.citationJournal of Nanobiotechnology 13(1): 16 (2015)-
dc.identifier.issn1477-3155-
dc.identifier.urihttp://hdl.handle.net/10261/125897-
dc.description.abstract[Background] Different superparamagnetic iron oxide nanoparticles have been tested for their potential use in cancer treatment, as they enter into cells with high effectiveness, do not induce cytotoxicity, and are retained for relatively long periods of time inside the cells. We have analyzed the interaction, internalization and biocompatibility of dimercaptosuccinic acid-coated superparamagnetic iron oxide nanoparticles with an average diameter of 15 nm and negative surface charge in MCF-7 breast cancer cells.-
dc.description.abstract[Results] Cells were incubated with dimercaptosuccinic acid-coated superparamagnetic iron oxide nanoparticles for different time intervals, ranging from 0.5 to 72 h. These nanoparticles showed efficient internalization and relatively slow clearance. Time-dependent uptake studies demonstrated the maximum accumulation of dimercaptosuccinic acid-coated superparamagnetic iron oxide nanoparticles after 24 h of incubation, and afterwards they were slowly removed from cells. Superparamagnetic iron oxide nanoparticles were internalized by energy dependent endocytosis and localized in endosomes. Transmission electron microscopy studies showed macropinocytosis uptake and clathrin-mediated internalization depending on the nanoparticles aggregate size. MCF-7 cells accumulated these nanoparticles without any significant effect on cell morphology, cytoskeleton organization, cell cycle distribution, reactive oxygen species generation and cell viability, showing a similar behavior to untreated control cells.-
dc.description.abstract[Conclusions] All these findings indicate that dimercaptosuccinic acid-coated superparamagnetic iron oxide nanoparticles have excellent properties in terms of efficiency and biocompatibility for application to target breast cancer cells.-
dc.description.sponsorshipThe research leading to these results have received partial funding from the European Seventh Framework Programme (FP7/2007-2013) under the project MULTIFUN grant agreement no. 262943, and the project Nanofrontmag-CM (S2013/MIT-2850) from the Comunidad de Madrid. Additional grants were obtained from BFU 2011–29038 and CTQ2013-48767-C3-3-R from the Ministerio de Economia y Competitividad and S2009/Mat 1507 from the Comunidad de Madrid (to JLC), from EU FP7 project NAMDIATREAM (ref 246479) and from “la Caixa” / CNB International PhD Programme Fellowships.-
dc.publisherBioMed Central-
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/262943-
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/246479-
dc.relation.isversionofPublisher's version-
dc.rightsopenAccess-
dc.subjectMCF-7 cells-
dc.subjectSuperparamagnetic iron oxide nanoparticles-
dc.subjectIntracellular trafficking-
dc.subjectTransmission electron microscopy-
dc.subjectCellular uptake-
dc.subjectEndocytosis-
dc.subjectCytotoxicity-
dc.titleCharacterization of interaction of magnetic nanoparticles with breast cancer cells-
dc.typeartículo-
dc.identifier.doi10.1186/s12951-015-0073-9-
dc.relation.publisherversionhttp://dx.doi.org/10.1186/s12951-015-0073-9-
dc.date.updated2015-11-25T17:56:16Z-
dc.language.rfc3066en-
dc.rights.holderCalero et al.; licensee BioMed Central.-
dc.rights.licensehttp://creativecommons.org/licenses/by/4.0-
dc.contributor.funderEuropean Commission-
dc.contributor.funderComunidad de Madrid-
dc.contributor.funderMinisterio de Economía y Competitividad (España)-
dc.contributor.funderCSIC - Centro Nacional de Biotecnología (CNB)-
dc.contributor.funderLa Caixa-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003329es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100012818es_ES
dc.identifier.pmid25880445-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.openairetypeartículo-
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