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dc.contributor.authorVOLKOV, YURIen
dc.date.accessioned2015-12-09T12:40:19Z
dc.date.available2015-12-09T12:40:19Z
dc.date.issued2015en
dc.date.submitted2015en
dc.identifier.citationCalero M, Chiappi M, Lazaro-Carrillo A, Rodríguez M.J, Chichón F.J, Crosbie-Staunton K, Prina-Mello A, Volkov Y, Villanueva A, Carrascosa J.L, Characterization of interaction of magnetic nanoparticles with breast cancer cells, Journal of Nanobiotechnology, 13, 1, 2015, 16-en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description.abstractBackground 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. 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. 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.en
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. We acknowledge Dr. Puerto Morales and Dr. Gorka Salas for providing the SPION samples. The encouragement and continuous support of Rodolfo Miranda is deeply recognized. Authors recognize the valuable contribution of Carmen Moreno-Ortiz (Flow Cytometry, Centro Nacional de Biotecnología, Madrid).en
dc.format.extent16en
dc.relation.ispartofseriesJournal of Nanobiotechnologyen
dc.relation.ispartofseries13en
dc.relation.ispartofseries1en
dc.rightsYen
dc.subjectMCF-7 cells; Superparamagnetic iron oxide nanoparticles; Intracellular trafficking; Transmission electron microscopy; Cellular uptake; Endocytosis; Cytotoxicityen
dc.subject.lcshMCF-7 cells; Superparamagnetic iron oxide nanoparticles; Intracellular trafficking; Transmission electron microscopy; Cellular uptake; Endocytosis; Cytotoxicityen
dc.titleCharacterization of interaction of magnetic nanoparticles with breast cancer cellsen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/yvolkoven
dc.identifier.rssinternalid105574en
dc.identifier.doihttp://dx.doi.org/10.1186/s12951-015-0073-9en
dc.rights.ecaccessrightsopenAccess
dc.identifier.rssurihttp://www.scopus.com/inward/record.url?eid=2-s2.0-84928041057&partnerID=40&md5=7920df2136c684dc0a8e8347f50f70cden
dc.identifier.urihttp://hdl.handle.net/2262/75235


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