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dc.contributor.authorIturrioz Rodríguez, Nerea
dc.contributor.authorMartín Rodríguez, Rosa 
dc.contributor.authorRenero Lecuna, Carlos 
dc.contributor.authorAguado Menéndez, Fernando 
dc.contributor.authorGonzález Legarreta, Lorena 
dc.contributor.authorGonzález Gómez, Jesús Antonio 
dc.contributor.authorLópez Fanarraga, Mónica 
dc.contributor.authorPerdigón Aller, Ana Carmen 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2020-10-01T14:51:25Z
dc.date.available2023-01-31T00:32:15Z
dc.date.issued2021-01-30
dc.identifier.issn0169-4332
dc.identifier.otherPI16/00496es_ES
dc.identifier.otherPI19/00349es_ES
dc.identifier.urihttp://hdl.handle.net/10902/19264
dc.description.abstractLaponite is a nanoplatform that has been successfully used as a new biomaterial for drug delivery, tissue engineering and bioimaging at the nanoscale. In general, a deep knowledge of the mechanism interaction of the nanomaterial with biological components in a physiological environment is highly desirable for properly characterizing its therapeutic efficacy and toxicology. Up to know, the use of fluorescent dyes labelling both, the nanomaterial and cell components, has been a requirement to characterize the cell uptake and to visualize the entrance of the nanomaterial into the cytosol and the cell nucleus. The used of fluorophores usually perturb the physiological medium and can interfere in the nanomaterial cell interaction. A new Raman imaging methodology to track the uptake and internalization of Laponite nanoparticles into J774 macrophages line cells is presented in this work. The combination of Raman spectroscopy and confocal microscopy provides direct information about the localization of the nanoparticle into the cell, through its unique vibrational fingerprint without labelling or adding dyes, and taking advantage of the fact that Laponite and biological molecules bands can be clearly differentiated.es_ES
dc.description.sponsorshipWe would like to thank IDIVAL for financial support, Projects N°NVAL16/17, INNVAL19/18 and NVAL18/07. CRL thanks the MINECO for the Juan de la Cierva Formación grant (ref. FJCI-2015-25306). This work has been supported by the Spanish MINECO, Instituto de Salud Carlos III, the European Union FEDER funds under Projects ref. PI16/00496 (AES 2016), PI19/00349 and DTS19/00033 (AES 2019). The authors are grateful to Dr F Madrazo and the Laser Microscopy Unit of the IDIVAL Institute for the use of the Confocal Raman Imaging Microscope.es_ES
dc.format.extent30 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rights© 2020. This manuscript version is made available under the CC-BY-NC-ND 4.0 licensees_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceApplied Surface Science, 2021, 537, 147870es_ES
dc.subject.otherLaponitees_ES
dc.subject.otherNanomateriales_ES
dc.subject.otherNanocarrieres_ES
dc.subject.otherRaman imaging techniquees_ES
dc.subject.otherNanoclayes_ES
dc.titleFree-labeled nanoclay intracellular uptake tracking by confocal Raman imaginges_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.apsusc.2020.147870es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.apsusc.2020.147870
dc.type.versionacceptedVersiones_ES


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© 2020. This manuscript version is made available under the CC-BY-NC-ND 4.0 licenseExcepto si se señala otra cosa, la licencia del ítem se describe como © 2020. This manuscript version is made available under the CC-BY-NC-ND 4.0 license