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Biodegradable CuMoO4 Nanodots with Multienzyme Activities for Multimodal Treatment of Tumor
Jinzha Zhang1, Liqi Peng1, Yijie Hao1
1National and Local Joint Engineering Research Center of Biomedical Functional Materials, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing, 210023, China.
Abstract:
Due to their complexity and variability, tumors need to be treated with multimodal combined therapy, which requires the development of therapeutic agents that can provide multimodal therapeutic effects. Herein, CuMoO4 nanodots smaller than 10 nm that can be prepared by simple hydrothermal method are reported. These nanodots can be well dispersed in water and have good biosafety and biodegradability. Further studies show that these nanodots also present multienzyme activities, such as catalase, peroxidase and glutathione peroxidase. In addition, CuMoO4 nanodots exhibit high photothermal conversion efficiency (41%) under 1064 nm near-infrared laser irradiation. In vitro and in vivo experimental results indicate that CuMoO4 nanodots can effectively inhibit the instinctive regulation of tumor cells to oxidative stress, provide sustained treatment to achieve photothermal synergistic ferroptosis, and trigger immune responses to immunogenic cell death. It is worth mentioning that the CuMoO4 nanodots also cause cuproptosis of tumor cells. This study provides a promising nanoplatform for multimodal combined therapy of cancer.
Insights
Novel copper molybdate (CuMoO4) nanodots offer a multimodal approach to cancer therapy. These biocompatible nanodots exhibit multienzyme activity, photothermal effects, and induce both ferroptosis and cuproptosis for enhanced tumor treatment.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Cancer Therapeutics
Background:
- Tumor complexity necessitates multimodal combination therapies.
- Developing versatile therapeutic agents is crucial for effective cancer treatment.
- Existing treatments face challenges due to tumor heterogeneity and resistance.
Purpose of the Study:
- To synthesize and characterize novel copper molybdate (CuMoO4) nanodots for cancer therapy.
- To evaluate the multimodal therapeutic potential of CuMoO4 nanodots.
- To investigate the synergistic effects of photothermal therapy, enzyme mimetics, and cell death induction.
Main Methods:
- Hydrothermal synthesis of CuMoO4 nanodots (<10 nm).
- Assessment of nanodot dispersion, biosafety, and biodegradability.
- Evaluation of multienzyme activities (catalase, peroxidase, glutathione peroxidase).
- Measurement of photothermal conversion efficiency under near-infrared laser irradiation.
- In vitro and in vivo studies on tumor cell oxidative stress, ferroptosis, cuproptosis, and immunogenic cell death.
Main Results:
- CuMoO4 nanodots are water-dispersible, biocompatible, and biodegradable.
- Nanodots exhibit significant catalase, peroxidase, and glutathione peroxidase-like activities.
- High photothermal conversion efficiency (41%) achieved with 1064 nm laser.
- Effective inhibition of tumor cell oxidative stress response.
- Synergistic photothermal-induced ferroptosis and induction of immunogenic cell death.
- Demonstrated induction of cuproptosis in tumor cells.
Conclusions:
- CuMoO4 nanodots represent a promising platform for multimodal cancer therapy.
- The combination of enzyme mimetics, photothermal therapy, ferroptosis, cuproptosis, and immunotherapy offers a comprehensive treatment strategy.
- This nanoplatform holds potential for overcoming tumor complexity and enhancing therapeutic outcomes.
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