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dc.contributor.author | Lineros-Rosa, Mauricio | es_ES |
dc.contributor.author | Cuquerella Alabort, Maria Consuelo | es_ES |
dc.contributor.author | Francés-Monerris, Antonio | es_ES |
dc.contributor.author | Monari, Antonio | es_ES |
dc.contributor.author | Miranda Alonso, Miguel Ángel | es_ES |
dc.contributor.author | Lhiaubet, Virginie Lyria | es_ES |
dc.date.accessioned | 2022-09-29T18:04:42Z | |
dc.date.available | 2022-09-29T18:04:42Z | |
dc.date.issued | 2021-04-28 | es_ES |
dc.identifier.issn | 1477-0520 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/186748 | |
dc.description.abstract | [EN] Recently, sunscreen-based drug photocages have been introduced to provide UV protection to photoactive drugs, thus increasing their photosafety. Here, combined experimental and theoretical studies performed on a photocage based on the commercial UVA filter avobenzone (AB) and on the photosensitizing non-steroidal anti-inflammatory drug ketoprofen (KP) are presented unveiling the photophysical processes responsible for the light-triggered release. Particular attention is paid to solvent stabilization of the drug and UV filter excited states, respectively, which leads to a switching between the triplet excited state energies of the AB and KP units. Most notably, we show that the stabilization of the AB triplet excited state in ethanol solution is the key requirement for an efficient photouncaging. By contrast, in apolar solvents, in particular hexane, KP has the lowest triplet excited state, hence acting as an energy acceptor quenching the AB triplet manifold, thus inhibiting the desired photoreaction. | es_ES |
dc.description.sponsorship | Support from the Universite de Lorraine, CNRS, regional (Prometeo/2017/075) and Spanish Government (PGC2018-096684-B-I00, CTQ2017-87054-C2-2-P) is kindly acknowledged. A. F.-M. is grateful to Generalitat Valenciana and the European Social Fund (postdoctoral contract APOSTD/2019/149 and project GV/2020/226) for financial support. M. L.-R. acknowledges the Universitat Politecnica de Valencia for the FPI grant. All calculations have been performed on the local LPCT computer center and on the Explor regional center in the framework of the project "Dancing under the light". | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | The Royal Society of Chemistry | es_ES |
dc.relation.ispartof | Organic & Biomolecular Chemistry | es_ES |
dc.rights | Reserva de todos los derechos | es_ES |
dc.subject.classification | QUIMICA ORGANICA | es_ES |
dc.title | Triplet stabilization for enhanced drug photorelease from sunscreen-based photocages | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1039/d0ob02244f | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/CTQ2017-87054-C2-2-P/ES/FOTOFISICA DE SISTEMAS ORGANICOS DE TRANSFERENCIA DE CARGA INNOVADORES/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/GVA//APOSTD%2F2019%2F149/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PGC2018-096684-B-I00/ES/REPARACION DEL ADN POR PROCESOS MULTIFOTONICOS/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/GVA//GV%2F2020%2F226/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/GENERALITAT VALENCIANA//PROMETEO%2F2017%2F075//REACCIONES FOTOQUIMICAS DE BIOMOLECULAS./ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Departamento de Química - Departament de Química | es_ES |
dc.contributor.affiliation | Universitat Politècnica de València. Instituto Universitario Mixto de Tecnología Química - Institut Universitari Mixt de Tecnologia Química | es_ES |
dc.description.bibliographicCitation | Lineros-Rosa, M.; Cuquerella Alabort, MC.; Francés-Monerris, A.; Monari, A.; Miranda Alonso, MÁ.; Lhiaubet, VL. (2021). Triplet stabilization for enhanced drug photorelease from sunscreen-based photocages. Organic & Biomolecular Chemistry. 19(8):1752-1759. https://doi.org/10.1039/d0ob02244f | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.1039/d0ob02244f | es_ES |
dc.description.upvformatpinicio | 1752 | es_ES |
dc.description.upvformatpfin | 1759 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 19 | es_ES |
dc.description.issue | 8 | es_ES |
dc.identifier.pmid | 33355577 | es_ES |
dc.relation.pasarela | S\425470 | es_ES |
dc.contributor.funder | European Social Fund | es_ES |
dc.contributor.funder | GENERALITAT VALENCIANA | es_ES |
dc.contributor.funder | Agencia Estatal de Investigación | es_ES |
dc.contributor.funder | Ministerio de Ciencia, Innovación y Universidades | es_ES |