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Published on: June 13, 2014
Nickel Single-Atom Nanozyme for Multimodal Cancer Therapy
Jiwon Woo1, Hojeong Shin1, Seongin Hong1
1Department of Chemistry, Seoul National University, Seoul 08826, Republic of Korea.
This study introduces a novel nickel-based single-atom nanozyme for cancer therapy. It combines catalytic reactive oxygen species generation with photothermal therapy for synergistic antitumor effects with minimal toxicity.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Materials Science
Background:
- Nickel is a promising catalytic center for single-atom catalysts due to its biological relevance and redox versatility.
- Developing targeted nanozymes for cancer therapy is crucial for improving treatment efficacy and reducing side effects.
Purpose of the Study:
- To synthesize and characterize a multifunctional nanozyme (Ni/PEG-FA) for targeted cancer therapy.
- To evaluate the synergistic antitumor effects of combining catalytic reactive oxygen species generation and photothermal therapy.
Main Methods:
- Synthesis of atomically dispersed nickel sites on nitrogen-doped carbon support, functionalized with poly(ethylene glycol) and folic acid.
- Assessment of dual enzyme-mimicking activity (peroxidase-like and superoxide dismutase-like) and photothermal conversion.
- In vitro and in vivo evaluations of synergistic antitumor effects and systemic toxicity.
Main Results:
- Ni/PEG-FA nanozyme demonstrated dual enzyme-mimicking activity and efficient photothermal conversion.
- The nanozyme selectively targeted cancer cells overexpressing folate receptors.
- Synergistic antitumor effects were observed through combined catalytic oxidative stress and photothermal therapy.
- Minimal systemic toxicity was noted in in vitro and in vivo studies.
Conclusions:
- Ni-based single-atom nanozymes offer a safe and effective platform for reactive oxygen species-powered cancer therapy.
- The multifunctional Ni/PEG-FA nanozyme shows significant potential for synergistic cancer treatment by combining catalytic and photothermal modalities.
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