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dc.contributor.authorIturrioz Rodríguez, Nerea
dc.contributor.authorMartín Rodríguez, Rosa 
dc.contributor.authorAguado Menéndez, Fernando 
dc.contributor.authorGonzález Legarreta, Lorena 
dc.contributor.authorGonzález Gómez, Jesús Antonio 
dc.contributor.authorValiente Barroso, Rafael 
dc.contributor.authorLópez Fanarraga, Mónica 
dc.contributor.authorPerdigón Aller, Ana Carmen 
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-06-30T15:02:18Z
dc.date.available2025-06-30T15:02:18Z
dc.date.issued2025-05
dc.identifier.issn0272-8842
dc.identifier.issn1873-3956
dc.identifier.otherTED2021-131305B-I00es_ES
dc.identifier.urihttps://hdl.handle.net/10902/36577
dc.description.abstractLaponite is a synthetic nanoclay highly attractive for medical applications, particularly as a platform for drug delivery and as an active material or bioimaging. The use of fluorescent dyes or even the functionalization of the nanoplatforms is a common practice to visualize the nanosystem within cell structures. However, these practices involve indirect characterization methods or could induce irreversible effects on the nanoparticle-cell interaction. Here, we introduce a methodology combining luminescence and confocal Raman microscopy to track the nanosystem and detect its cargo independently, using Eu3+ as a fluorescent probe. Confocal Raman microscopy allow us to determine the localization of the nanoparticle by its unique Raman spectrum fingerprint while mapping the cell. At the same time, Eu3+ luminescence serves to detect the cargo by its emission spectrum. Speciffically, we describe here the use of Eu-doped Laponite as a fluorescent probe, to track its uptake and incorporation into a macrophage cell line. To discard potential adhesion to the cell membrane, images were taken at different Z planes. In this way, we have observed that the cargo remains attached to the nanoparticle. Finally, the biocompatibility of the nanoplatforms and their cargo has been studied, showing no significant difference in the survival rate.es_ES
dc.description.sponsorshipWe would like to thank IDIVAL for financial support, Projects Nº INNVAL19/18. This work has been supported by the Spanish MCIN and European Union under Project TED2021-131305B-I00 funded by MCIN/ AEI/10.13039/501100011033 and by the European Union -NextGenerationEU/PRTR.es_ES
dc.format.extent8 p.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsAttribution 4.0 Internationales_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceCeramics International, 2025, 51(12,B), 16951-16958es_ES
dc.subject.otherFluorescencees_ES
dc.subject.otherConfocal Raman imaginges_ES
dc.subject.otherLaponitees_ES
dc.subject.otherEuropiumes_ES
dc.subject.otherNanoclayes_ES
dc.titleEu3+-doped Laponite as a new probe for combined confocal Raman imaging fluorescencees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.ceramint.2025.02.246es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.ceramint.2025.02.246
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International