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dc.contributor.authorSancho‐Albero, Maríaes_ES
dc.contributor.authorAyaz, Nazeehaes_ES
dc.contributor.authorSebastián, Víctores_ES
dc.contributor.authorChirizzi, Cristinaes_ES
dc.contributor.authorEncinas-Giménez, Migueles_ES
dc.contributor.authorNeri, Giuliaes_ES
dc.contributor.authorChaabane, Lindaes_ES
dc.contributor.authorLuján, Lluíses_ES
dc.contributor.authorMartín-Duque, Pilares_ES
dc.contributor.authorMetrangolo, Pierangeloes_ES
dc.contributor.authorSantamaría, Jesúses_ES
dc.contributor.authorBaldelli Bombelli, Francescaes_ES
dc.date.accessioned2023-10-25T12:24:22Z-
dc.date.available2023-10-25T12:24:22Z-
dc.date.issued2023-
dc.identifier.citationACS Applied Materials and Interfaces 15(7): 8974-8985 (2023)es_ES
dc.identifier.urihttp://hdl.handle.net/10261/337762-
dc.description.abstractExtracellular vesicles (EVs) play a crucial role in cell-to-cell communication and have great potential as efficient delivery vectors. However, a better understanding of EV in vivo behavior is hampered by the limitations of current imaging tools. In addition, chemical labels present the risk of altering the EV membrane features and, thus, in vivo behavior. 19F-MRI is a safe bioimaging technique providing selective images of exogenous probes. Here, we present the first example of fluorinated EVs containing PERFECTA, a branched molecule with 36 magnetically equivalent 19F atoms. A PERFECTA emulsion is given to the cells, and PERFECTA-containing EVs are naturally produced. PERFECTA-EVs maintain the physicochemical features, morphology, and biological fingerprint as native EVs but exhibit an intense 19F-NMR signal and excellent 19F relaxation times. In vivo 19F-MRI and tumor-targeting capabilities of stem cell-derived PERFECTA-EVs are also proved. We propose PERFECTA-EVs as promising biohybrids for imaging biodistribution and delivery of EVs throughout the body.es_ES
dc.description.sponsorshipM.S.-A. thanks the Spanish Government for the FPU PhD research fellowship (reference 15/03419) and the AIRC-Foundation for cancer research for a Postdoctoral fellowship in Italy. P.M.-D. also thanks the Instituto de Salud Carlos III (PI19/01007). The authors gratefully acknowledge financial support from the ERC Advance Grant CADENCE (grant no-ERC-2016-ADG-762684). V.S. acknowledges the financial support from Fundación Ramón Areces (XX Concurso nacional-Ciencias de la Vida y de la Materia) and Beca Leonardo a Investigadores y Creadores Culturales 2021 de la Fundación BBVA. V.S. also acknowledges the ICTS ELECMI (LMA-UNIZAR). N.A., F.B.B., and P.M. acknowledge financial support from Regione Lombardia (NEWMED project, ID: 1175999, POR FESR 2014 2020). F.B.B. and P.M. are also thankful for the projects Hydrogex funded by Cariplo Foundation (grant no. 2018-1720) and NiFTy funded by MUR (PRIN2017, no. 2017MYBTXC). The authors would also like to thank Prof. Jesús Ruiz-Cabello and Dr. Daniel Padro from CICbioMAGUNE for the 19F-MRI analysis and Scientific Services of the Aragon Institute of Health Sciences, specifically to the Microscopy, Pathology and Animal Facilities Services and their specialists. Dr Marina Cretich from “Istituto di Scienze e Tecnologie Chimiche” (SCITEC-CNR) in Milan, Italy, is acknowledged for the use of NTA Instrument. CIBER-BBN is an initiative funded by the VI National R&D&i Plan 2008–2011 financed by the Instituto de Salud Carlos III with the assistance of the European Regional Development Fund. CIBER-BBN (initiative funded by the VI National R&D&i Plan 2008–2011, Iniciativa Ingenio 2010, Consolider Program, CIBER Actions and financed by the Instituto de Salud Carlos III with assistance from the European Regional Development Fund) and Nanbiosis ICTS are gratefully acknowledged. “CIBER-BBN is an initiative funded by the VI National R&D&i Plan 2008–2011 financed by the Instituto de Salud Carlos III with the assistance of the European Regional Development Fund”.es_ES
dc.formatapplication/pdfes_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/742684es_ES
dc.relation.isversionofPublisher's versiones_ES
dc.rightsopenAccesses_ES
dc.subjectBioimaginges_ES
dc.subjectPERFECTAes_ES
dc.subject19F-MRIes_ES
dc.subjectExtracellular vesicleses_ES
dc.subjectFluorinees_ES
dc.titleSuperfluorinated extracellular vesicles for in vivo imaging by 19F-MRIes_ES
dc.typeartículoes_ES
dc.identifier.doi10.1021/acsami.2c20566-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttps://doi.org/10.1021/acsami.2c20566es_ES
dc.identifier.e-issn1944-8252-
dc.rights.licensehttps://creativecommons.org/licenses/by/4.0/es_ES
dc.contributor.funderAssociation for International Cancer Researches_ES
dc.contributor.funderInstituto de Salud Carlos IIIes_ES
dc.contributor.funderEuropean Commissiones_ES
dc.contributor.funderEuropean Research Counciles_ES
dc.contributor.funderFundación Ramón Areceses_ES
dc.contributor.funderFundación BBVAes_ES
dc.contributor.funderRegione Lombardiaes_ES
dc.contributor.funderMinistero dell'Istruzione, dell'Università e della Ricercaes_ES
dc.contributor.funderFondazione Cariploes_ES
dc.relation.csices_ES
oprm.item.hasRevisionno ko 0 false*
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004587es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100008054es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100007406es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100003407es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000781es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100000780es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100004435es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100002803es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100009882es_ES
dc.identifier.pmid36780137-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.grantfulltextopen-
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item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeartículo-
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