Sonoactivated Cascade Fenton Reaction Enhanced by Synergistic Modulation of Electron-Hole Separation for Improved Tumor Therapy.
basic_science · Level V
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- Record sourced from PubMed, PMID 37439543.
- Also identified by DOI 10.1002/adhm.202300982.
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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.
Medical subject headings
- Metal Nanoparticles
- Nanoparticles
- Neoplasms