Sonoactivated Cascade Fenton Reaction Enhanced by Synergistic Modulation of Electron-Hole Separation for Improved Tumor Therapy.

Zhang, Su-Ling; Liu, Cong; Li, Zhi-Xiang; Guan, Ying-Hua; Ge, Lin; Sun, Qijun; Liu, Jun-An; Lin, Yong-Jun et al. · Adv Healthc Mater · 2023

basic_science · Level V

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Abstract

Chemodynamic therapy (CDT) is an emerging targeted treatment technique for tumors via the generation of highly cytotoxic hydroxyl radical (·OH) governed by tumor microenvironment-assisted Fenton reaction. Despite high effectiveness, it faces limitations like low reaction efficiency and limited endogenous H<sub>2</sub> O<sub>2</sub> , compromising its therapeutic efficacy. This study reports a novel platform with enhanced CDT performance by in situ sono-activated cascade Fenton reaction. A piezoelectric g-C<sub>3</sub> N<sub>4</sub> (Au-Fe-g-C<sub>3</sub> N<sub>4</sub> ) nanosheet is developed via sono-activated synergistic effect/H<sub>2</sub> O<sub>2</sub> self-supply mediated cascade Fenton reaction, realizing in situ ultrasound activated cascade Fenton reaction kinetics by synergistic modulation of electron-hole separation. The nanosheets consist of piezoelectric g-C<sub>3</sub> N<sub>4</sub> nanosheet oxidizing H<sub>2</sub> O to highly reactive H<sub>2</sub> O<sub>2</sub> from the valence band, Fe<sup>3+</sup> /Fe<sup>2+</sup> cycling activated by conduction band to generate ·OH, and Au nanoparticles that lower the bandgap and further adopt electrons to generate more <sup>1</sup> O<sub>2</sub> , resulting in improved CDT and sonodynamic therapy (SDT). Moreover, the Au-Fe-g-C<sub>3</sub> N<sub>4</sub> nanosheet is further modified by the targeted peptide to obtain P-Au-Fe-g-C<sub>3</sub> N<sub>4</sub> , which inhibits tumor growth in vivo effectively by generating reactive oxygen species (ROS). These results demonstrated that the sono-activated modulation translates into a high-efficiency CDT with a synergistic effect using SDT for improved anti-tumor therapy.

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