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.

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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