Triplet stabilization for enhanced drug photorelease from sunscreen-based photocages.

Mauricio Lineros-Rosa, M Consuelo Cuquerella, Antonio Francés-Monerris, Antonio Monari, Miguel A Miranda, Virginie Lhiaubet-Vallet

Journal: Organic & biomolecular chemistry 2021;19(8):1752-1759

PMID: 33355577

Abstract

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.

Address: Instituto Universitario Mixto de Tecnologia Química UPV-CSIC, Universitat Politècnica de València, Consejo Superior de Investigaciones Científicas, Avda de los Naranjos s/n, 46022 Valencia, Spain. [email protected] [email protected].; Université de Lorraine and CNRS, LPCT UMR 7019, F-54000 Nancy, France. [email protected] and Departament de Química Física Universitat de València, 46100 Burjassot, Spain.; Université de Lorraine and CNRS, LPCT UMR 7019, F-54000 Nancy, France. [email protected].

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