Heavy-atom-free π-twisted photosensitizers for fluorescence bioimaging and photodynamic therapy.

Sánchez DP, Morice K, Mutovska MG, Khrouz L, Josse P, Allain M, Gohier F, Blanchard P, Monnereau C, Le Bahers T, Sabouri N, Zagranyarski Y, Cabanetos C, Deiana M

J Mater Chem B 12 (33) 8107-8121 [2024-08-22; online 2024-08-22]

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.

Chemical Biology Consortium Sweden (CBCS) [Service]

PubMed 39041337

DOI 10.1039/d4tb01014k

Crossref 10.1039/d4tb01014k