The
effectiveness of photodynamic therapy (PDT) in treating
brain
gliomas is limited by the solubility of photosensitizers and the production
of reactive oxygen species (ROS), both of which are influenced by
the concentration of photosensitizers and catalyst active sites. In
this study, we developed a controllable surface hydroxyl concentration
for the photosensitizer CN11 to address its poor water solubility
issue and enhance PDT efficacy in tumor treatment. Compared to pure
g-C3N4 (CN), CN11 exhibited 4.6 times higher
hydrogen peroxide production under visible light, increased incidence
of the n → π* electron transition, and provided more
available reaction sites for cytotoxic ROS generation. These findings
resulted in a 2.43-fold increase in photodynamic treatment efficacy
against brain glioma cells. Furthermore, in vivo experiments conducted
on mice demonstrated that CN11 could be excreted through normal cell
metabolism with low cytotoxicity and high biosafety, effectively achieving
complete eradication of tumor cells.