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Single-Atom Catalysts for Nanocatalytic Tumor Therapy
Xiangyu Lu1,2, Shanshan Gao3, Han Lin1
1State Key Lab of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050, P. R. China.
Single-atom catalysts (SACs) show promise for nanocatalytic tumor therapy, offering a drug-free chemotherapy alternative. This review highlights SAC advancements in chemodynamic, photodynamic, and sonodynamic therapies, focusing on nanoplatform design and mechanisms.
Area of Science:
- Catalysis
- Nanotechnology
- Oncology
Background:
- Single-atom catalysts (SACs) are gaining attention for their unique properties, including precise metal centers and tunable structures.
- Nanocatalytic medicine offers a novel approach to tumor chemotherapy, avoiding toxic chemodrugs.
- SACs possess characteristics ideal for developing effective catalytic tumor therapies.
Purpose of the Study:
- To review recent advancements in nanocatalytic tumor therapy utilizing various single-atom catalysts (SACs).
- To focus on the construction of catalytic nanoplatforms and the underlying catalytic mechanisms.
- To provide an outlook on future design and engineering of SACs for tumor treatment.
Main Methods:
- Review of recent literature on single-atom catalysts (SACs) in nanocatalytic tumor therapy.
- Analysis of SAC applications in chemodynamic therapy (CDT), photodynamic therapy (PDT), and sonodynamic therapy (SDT).
- Focus on nanoplatform design and catalytic mechanisms for tumor treatment.
Main Results:
- SACs demonstrate significant achievements in various nanocatalytic tumor therapy modalities.
- Tumor microenvironment-responsive reactions, photocatalysis, and sonocatalysis are key mechanisms.
- Effective nanoplatform construction is crucial for SAC-based tumor therapy.
Conclusions:
- Single-atom catalysts (SACs) are highly promising for advanced nanocatalytic tumor therapy.
- Further research into nanoplatform design and catalytic mechanisms will enhance SAC efficacy.
- Addressing remaining challenges is key for future clinical translation of SACs in oncology.
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