dc.contributor.author | Iturrioz Rodríguez, Nerea | |
dc.contributor.author | Martín Rodríguez, Rosa | |
dc.contributor.author | Renero Lecuna, Carlos | |
dc.contributor.author | Aguado Menéndez, Fernando | |
dc.contributor.author | González Legarreta, Lorena | |
dc.contributor.author | González Gómez, Jesús Antonio | |
dc.contributor.author | López Fanarraga, Mónica | |
dc.contributor.author | Perdigón Aller, Ana Carmen | |
dc.contributor.other | Universidad de Cantabria | es_ES |
dc.date.accessioned | 2020-10-01T14:51:25Z | |
dc.date.available | 2023-01-31T00:32:15Z | |
dc.date.issued | 2021-01-30 | |
dc.identifier.issn | 0169-4332 | |
dc.identifier.other | PI16/00496 | es_ES |
dc.identifier.other | PI19/00349 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10902/19264 | |
dc.description.abstract | Laponite 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.sponsorship | We 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.extent | 30 p. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | Elsevier | es_ES |
dc.rights | © 2020. This manuscript version is made available under the CC-BY-NC-ND 4.0 license | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.source | Applied Surface Science, 2021, 537, 147870 | es_ES |
dc.subject.other | Laponite | es_ES |
dc.subject.other | Nanomaterial | es_ES |
dc.subject.other | Nanocarrier | es_ES |
dc.subject.other | Raman imaging technique | es_ES |
dc.subject.other | Nanoclay | es_ES |
dc.title | Free-labeled nanoclay intracellular uptake tracking by confocal Raman imaging | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.relation.publisherVersion | https://doi.org/10.1016/j.apsusc.2020.147870 | es_ES |
dc.rights.accessRights | openAccess | es_ES |
dc.identifier.DOI | 10.1016/j.apsusc.2020.147870 | |
dc.type.version | acceptedVersion | es_ES |