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Heavy-atom-free π-twisted photosensitizers for fluorescence bioimaging and photodynamic therapy.
Sánchez, Darío Puchán; Morice, Korentin; Mutovska, Monika G; Khrouz, Lhoussain; Josse, Pierre; Allain, Magali; Gohier, Frédéric; Blanchard, Philippe; Monnereau, Cyrille; Le Bahers, Tangui; Sabouri, Nasim; Zagranyarski, Yulian; Cabanetos, Clement; Deiana, Marco.
Afiliação
  • Sánchez DP; Univ Angers, CNRS, MOLTECH-ANJOU, SFR MATRIX, F-49000 Angers, France. clement.cabanetos@univ-angers.fr.
  • Morice K; Univ Angers, CNRS, MOLTECH-ANJOU, SFR MATRIX, F-49000 Angers, France. clement.cabanetos@univ-angers.fr.
  • Mutovska MG; Faculty of Chemistry and Pharmacy, University of Sofia, 1 James Bourchier blvd., 1164 Sofia, Bulgaria. zagranyarskiyulian@gmail.com.
  • Khrouz L; ENS de Lyon, CNRS, Laboratoire de Chimie UMR 5182, F-69342 Lyon, France.
  • Josse P; Univ Angers, CNRS, MOLTECH-ANJOU, SFR MATRIX, F-49000 Angers, France. clement.cabanetos@univ-angers.fr.
  • Allain M; Univ Angers, CNRS, MOLTECH-ANJOU, SFR MATRIX, F-49000 Angers, France. clement.cabanetos@univ-angers.fr.
  • Gohier F; Univ Angers, CNRS, MOLTECH-ANJOU, SFR MATRIX, F-49000 Angers, France. clement.cabanetos@univ-angers.fr.
  • Blanchard P; Univ Angers, CNRS, MOLTECH-ANJOU, SFR MATRIX, F-49000 Angers, France. clement.cabanetos@univ-angers.fr.
  • Monnereau C; ENS de Lyon, CNRS, Laboratoire de Chimie UMR 5182, F-69342 Lyon, France.
  • Le Bahers T; ENS de Lyon, CNRS, Laboratoire de Chimie UMR 5182, F-69342 Lyon, France.
  • Sabouri N; Institut Universitaire de France, 5 rue Descartes, 75005 Paris, France.
  • Zagranyarski Y; Department of Medical Biochemistry and Biophysics, Umeå University, SE-901 87, Umeå, Sweden.
  • Cabanetos C; Faculty of Chemistry and Pharmacy, University of Sofia, 1 James Bourchier blvd., 1164 Sofia, Bulgaria. zagranyarskiyulian@gmail.com.
  • Deiana M; Univ Angers, CNRS, MOLTECH-ANJOU, SFR MATRIX, F-49000 Angers, France. clement.cabanetos@univ-angers.fr.
J Mater Chem B ; 12(33): 8107-8121, 2024 Aug 22.
Article em En | MEDLINE | ID: mdl-39041337
ABSTRACT
As the field of preclinical research on photosensitizers (PSs) for anticancer photodynamic therapy (PDT) continues to expand, a focused effort is underway to develop agents with innovative molecular structures that offer enhanced targeting, selectivity, activation, and imaging capabilities. In this context, we introduce two new heavy-atom-free PSs, DBXI and DBAI, characterized by a twisted π-conjugation framework. This innovative approach enhances the spin-orbit coupling (SOC) between the singlet excited state (S1) and the triplet state (T1), resulting in improved and efficient intersystem crossing (ISC). Both PSs are highly effective in producing reactive oxygen species (ROS), including singlet oxygen and/or superoxide species. Additionally, they also demonstrate remarkably strong fluorescence emission. Indeed, in addition to providing exceptional photocytotoxicity, this emissive feature, generally lacking in other reported structures, allows for the precise monitoring of the PSs' distribution within specific cellular organelles even at nanomolar concentrations. These findings underscore the dual functionality of these PSs, serving as both fluorescent imaging probes and light-activated therapeutic agents, emphasizing their potential as versatile and multifunctional tools in the field of PDT.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fotoquimioterapia / Fármacos Fotossensibilizantes / Imagem Óptica Limite: Humans Idioma: En Revista: J Mater Chem B Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fotoquimioterapia / Fármacos Fotossensibilizantes / Imagem Óptica Limite: Humans Idioma: En Revista: J Mater Chem B Ano de publicação: 2024 Tipo de documento: Article