GSH-activatable copper-elsinochrome off-on photosensitizer for combined specific NIR-II two-photon photodynamic/chemodynamic therapy

The complexity of cancer therapy has led to the emergence of combination therapy as a promising approach to enhance treatment efficacy and safety. The integration of glutathione (GSH)-activatable two-photon photodynamic therapy (TP-PDT) and chemodynamic therapy (CDT) offers the possibility to advance precision and efficacy in anti-cancer treatments. In this study, a GSH-activatable photosensitizer (PS), namely copper-elsinochrome (CuEC), is synthesized and utilized for combination second near-infrared (NIR-II) TP-PDT/CDT. The Cu2+ acts as a “lock”, suppressing the fluorescence and 1O2 generation ability of EC in a normal physiological environment (“OFF” state). However, the overexpressed GSH in the tumor microenvironment acts as the “key”, resulting in the release of EC (“ON” state) and Cu+ (reduced by GSH). The released EC can be utilized for fluorescence imaging and TP-PDT under NIR-II (λ = 1000 nm) two-photon excitation, while Cu+ can generate highly toxic hydroxyl radicals (•OH) via Fenton-like reaction for CDT. Additionally, this process consumes GSH and diminishes the tumor's antioxidant capacity, thereby augmenting the efficacy of combination therapy. The CuEC achieves significant tumor cell ablation in both 2D monolayer cells and 3D multicellular tumor spheres through the combination of NIR-II TP-PDT and CDT. A novel photosensitizer, CuEC, which can be selectively activated in the tumor microenvironment through overexpressed glutathione (GSH), has been designed and synthesized. The CuEC exhibits a remarkable tumor cell ablation effect through the combined treatment of NIR-II TP-PDT and CDT under two-photon excitation using a 1000 nm laser. [Display omitted]