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Published on: April 10, 2018
Nanocatalytic Tumor Therapy by Single-Atom Catalysts
Minfeng Huo1,2, Liying Wang1,2,3, Youwei Wang1
1State Key Laboratory of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics , Chinese Academy of Sciences , Shanghai 200050 , P.R. China.
PEGylated single-atom iron nanocatalysts trigger Fenton reactions in the tumor microenvironment (TME). This generates hydroxyl radicals, inducing tumor cell apoptosis and ferroptosis for effective cancer suppression with good biosafety.
Area of Science:
- Biomedical Nanotechnology
- Catalysis
- Cancer Therapeutics
Background:
- Localized catalytic reactions in the tumor microenvironment (TME) offer specific cancer therapy.
- Biomedical nanocatalysts are crucial for effective and safe TME-targeted therapies.
Purpose of the Study:
- To develop and evaluate PEGylated single-atom Fe-containing nanocatalysts (PSAF NCs) for tumor-specific Fenton reactions.
- To investigate the mechanism of nanocatalyst-mediated radical generation in the acidic TME.
Main Methods:
- Synthesis and characterization of PEGylated single-atom Fe-containing nanocatalysts (PSAF NCs).
- Utilizing density functional theory (DFT) to elucidate the Fenton reaction mechanism.
- In vitro and in vivo assessments of nanocatalyst efficacy and biosafety.
Main Results:
- PSAF NCs effectively catalyzed the Fenton reaction in the acidic TME, generating hydroxyl radicals (•OH).
- DFT calculations confirmed a proton-mediated H2O2-homolytic pathway for heterogeneous Fenton catalysis.
- Generated radicals induced both tumor cell apoptosis and ferroptosis, leading to significant tumor suppression.
- PSAF NCs demonstrated favorable biodegradability and biocompatibility, ensuring in vivo and in vitro biosafety.
Conclusions:
- PSAF NCs are highly effective biomedical nanocatalysts for TME-specific cancer therapy.
- The synergistic induction of apoptosis and ferroptosis by PSAF NCs offers a promising therapeutic strategy.
- The developed nanocatalysts exhibit excellent biosafety profiles for potential clinical translation.
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