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dc.contributor.authorGómez-González, Elisabetes_ES
dc.contributor.authorCaro, Carloses_ES
dc.contributor.authorGarcía-Martín, María L.es_ES
dc.contributor.authorBecerro, Ana Isabeles_ES
dc.contributor.authorOcaña, Manueles_ES
dc.date.accessioned2024-02-19T22:24:36Z-
dc.date.available2024-02-19T22:24:36Z-
dc.date.issued2022-08-11-
dc.identifier.citationNanoscale 31(14): 11461-11470 (2022)es_ES
dc.identifier.issn2040-3364-
dc.identifier.urihttp://hdl.handle.net/10261/347571-
dc.description.abstractThe use of high-field magnets for magnetic resonance imaging (MRI) is expected to experience the fastest growth rate during the present decade. Although several CAs for MRI scanners using high magnetic fields have been reported, they are mostly based on fluoride matrices, which are known for their low chemical stability in aqueous suspensions. Chemically stable MRI CAs for high-field magnets are therefore needed to enable the advances in MRI technique. Herein, we synthesized uniform DyPO4 nanoparticles (NPs) with tuneable sizes between 23 and 57 nm using homogeneous precipitation in butanol. The NPs were successfully functionalized with polyacrylic acid (PAA) and showed good colloidal stability in aqueous suspensions. Chemical stability was also assessed in PBS, showing negligible solubility. The effect of particle size on the transversal relaxivity value (r2) was further explored at 9.4 T, finding a clear increase in r2 with particle size. The r2 value found for the largest NPs was 516 mM-1 s-1, which is, to the best of our knowledge, the highest r2 value ever reported at 9.4 T for any Dy-based nanometric particles in the literature. Finally, the latter NPs were submitted to biosafety studies after polyethylene glycol (PEG) functionalization. Cell morphology, induction of necrotic/late apoptotic cells, and mitochondrial activity were thoroughly analyzed. The results clearly indicated negligible toxicity effects under the assayed conditions. Short- and long-term in vivo pharmacokinetics of the intravenously injected NPs were assessed by dynamic T2-weighted MRI and quantitative T2 mapping, revealing faster liver than spleen uptake, while no accumulation was observed in the kidneys. Finally, no histopathological changes were observed in any of the studied organs, including the liver, kidney, spleen, and lung, which provide further evidence of the biocompatibility of DyPO4 NPs and, therefore, their suitability as bioimaging probes.es_ES
dc.description.sponsorshipFinancial support was provided by Junta de Andalucía (P20_00182). This publication is part of the I + D + I Grants RTI2018-094426-B-I00 and CTQ2017-86655-R funded by MCIN/AEI/10.13039/501100011033 and by “ERDF A way of making Europe”. Grant PRE2019-090170 is funded by MCIN/AEI/10.13039/501100011033 and by “ESF Investing in your future”.es_ES
dc.formatapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherRoyal Society of Chemistry (UK)es_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/RTI2018-094426-B-I00/ES/NANOPARTICULAS MULTIFUNCIONALES PARA LA OBTENCION DE BIOIMAGENES MEDIANTE LUMINISCENCIA, RESONANCIA MAGNETICA Y TOMOGRAFIA COMPUTARIZADA DE RAYOS X/es_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2017-86655-R/ES/NANOMATERIALES MULTIFUNCIONALES DIRIGIDOS A TUMORES GLIALES PARA IMAGEN MOLECULAR Y TRATAMIENTO COMBINADO MEDIANTE LIBERACION CONTROLADA DE FARMACOS Y TERMOTERAPIA/es_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rightsopenAccesses_ES
dc.titleOutstanding MRI contrast with dysprosium phosphate nanoparticles of tuneable sizees_ES
dc.typeartículoes_ES
dc.identifier.doi10.1039/d2nr02630a-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1039/d2nr02630aes_ES
dc.identifier.e-issn2040-3372-
dc.rights.licensehttp://creativecommons.org/licenses/by-nc/3.0/es_ES
dc.contributor.funderJunta de Andalucíaes_ES
dc.contributor.funderMinisterio de Ciencia e Innovación (España)es_ES
dc.contributor.funderAgencia Estatal de Investigación (España)es_ES
dc.contributor.funderEuropean Commissiones_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004837es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100011033es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100011011es_ES
dc.contributor.orcidGómez-González, Elisabet [0000-0003-2978-3494]es_ES
dc.contributor.orcidCaro, Carlos [0000-0003-4758-3816]es_ES
dc.contributor.orcidGarcía-Martín, María L. [0000-0002-2257-7682]es_ES
dc.contributor.orcidOcaña, Manuel [0000-0003-2243-5438]es_ES
dc.contributor.orcidOcaña, Manuel [0000-0001-9989-606X]es_ES
dc.identifier.pmid35904370-
dc.identifier.scopus2-s2.0-85135333918-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85135333918-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.grantfulltextopen-
item.openairetypeartículo-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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