Affiliation:
1. College of Science Huazhong Agricultural University Wuhan 430070 China
2. Laboratory for Biological Effects of Nanomaterials and Nanosafety National Center for Nanoscience and Technology (NCNST) Beijing 100190 China
3. Beijing Institute of Nanoenergy and Nanosystems Chinese Academy of Sciences Beijing 101400 China
4. National Key Laboratory of Crop Genetic Improvement and National Center of Plant Gene Research Huazhong Agricultural University Wuhan 430070 China
Abstract
AbstractChemodynamic 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 H2O2, 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‐C3N4 (Au‐Fe‐g‐C3N4) nanosheet is developed via sono‐activated synergistic effect/H2O2 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‐C3N4 nanosheet oxidizing H2O to highly reactive H2O2 from the valence band, Fe3+/Fe2+ cycling activated by conduction band to generate ·OH, and Au nanoparticles that lower the bandgap and further adopt electrons to generate more 1O2, resulting in improved CDT and sonodynamic therapy (SDT). Moreover, the Au–Fe–g‐C3N4 nanosheet is further modified by the targeted peptide to obtain P–Au–Fe–g‐C3N4, 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.
Funder
National Natural Science Foundation of China
Subject
Pharmaceutical Science,Biomedical Engineering,Biomaterials
Cited by
7 articles.
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