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dc.contributor.authorPrieto Montero, Ruth ORCID
dc.contributor.authorKatsumiti Kodo Filho, Alberto ORCID
dc.contributor.authorCajaraville Bereciartua, Miren Pilare ORCID
dc.contributor.authorLópez Arbeloa, Iñigo María
dc.contributor.authorMartínez Martínez, Virginia ORCID
dc.date.accessioned2020-10-15T12:19:49Z
dc.date.available2020-10-15T12:19:49Z
dc.date.issued2020-09-29
dc.identifier.citationSensors 20(19) : (2020) // Article ID 5590es_ES
dc.identifier.issn1424-8220
dc.identifier.urihttp://hdl.handle.net/10810/46915
dc.description.abstractFunctionalized fluorescent silica nanoparticles were designed and synthesized to selectively target cancer cells for bioimaging analysis. The synthesis method and characterization of functionalized fluorescent silica nanoparticles (50–60 nm), as well as internalization and subcellular localization in HeLa cells is reported here. The dye, rhodamine 101 (R101) was physically embedded during the sol–gel synthesis. The dye loading was optimized by varying the synthesis conditions (temperature and dye concentration added to the gel) and by the use of different organotriethoxysilanes as a second silica precursor. Additionally, R101, was also covalently bound to the functionalized external surface of the silica nanoparticles. The quantum yields of the dye-doped silica nanoparticles range from 0.25 to 0.50 and demonstrated an enhanced brightness of 230–260 fold respect to the free dye in solution. The shell of the nanoparticles was further decorated with PEG of 2000 Da and folic acid (FA) to ensure good stability in water and to enhance selectivity to cancer cells, respectively. In vitro assays with HeLa cells showed that fluorescent nanoparticles were internalized by cells accumulating exclusively into lysosomes. Quantitative analysis showed a significantly higher accumulation of FA functionalized fluorescent silica nanoparticles compared to nanoparticles without FA, proving that the former may represent good candidates for targeting cancer cells.es_ES
dc.description.sponsorshipThis research was funded by the Basque Government, grant numbers IT912-16 and IT-1302-19; Ministry of Economy and Competitiveness (MINECO), grant numbers MAT2017-83856-C3-3-P and CTM2016-81130-R; and the University of the Basque Country (UPV/EHU), grant number COLAB19/01.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/MAT2017-83856-C3-3-Pes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTM2016-81130-Res_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjecttargetinges_ES
dc.subjectfunctionalized fluorescent silica nanoparticleses_ES
dc.subjectrhodamine 101es_ES
dc.subjectpolyethylene glycoles_ES
dc.subjectfolic acides_ES
dc.subjectHeLa cellses_ES
dc.titleFunctionalized Fluorescent Silica Nanoparticles for Bioimaging of Cancer Cellses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2020-10-13T13:24:15Z
dc.rights.holder2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1424-8220/20/19/5590es_ES
dc.identifier.doi10.3390/s20195590
dc.departamentoesQuímica física
dc.departamentoesZoología y biología celular animal
dc.departamentoeuKimika fisikoa
dc.departamentoeuZoologia eta animalia zelulen biologia


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2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).