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Published on: February 9, 2021
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NIR-II Photoactivatable Cobalt(III) Nanoparticles for Photoactivated Metal Chemo-Immunotherapy
Dongsheng Tang1, Minhui Cui1, Johannes Karges2
1Beijing National Laboratory for Molecular Sciences, Laboratory of Polymer Physics and Chemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, P. R. China.
Advanced Materials (Deerfield Beach, Fla.)
|December 4, 2025
Summary
This study introduces near-infrared II (NIR-II) photoactivated cobalt(III) nanoparticles (NanoCo) for enhanced cancer therapy. NanoCo demonstrates superior efficacy against resistant cancer cells and triggers anti-tumor immune responses, significantly inhibiting tumor growth.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Cancer Therapy
Background:
- Photoactivated cobalt(III) (Co(III)) complexes show promise in cancer therapy but face limitations due to toxicity and lack of spatial-temporal control.
- Developing targeted therapies with improved control is crucial for clinical application.
Purpose of the Study:
- To develop and evaluate novel second near-infrared window (NIR-II) photoactivated cobalt(III) nanoparticles (NanoCo) for cancer treatment.
- To investigate NanoCo's efficacy, mechanisms of action, and synergistic effects with other therapies.
Main Methods:
- Synthesis of Co(III) nanoparticles (NanoCo) activated by NIR-II light (1064 nm).
- Evaluation of NanoCo's photothermal effect, cytotoxicity against platinum-resistant and sensitive cancer cells (A549DDP, CT26).
- Assessment of NanoCo's ability to induce immunogenic cell death and anti-tumor immune responses.
- Combination therapy with Pt(IV) nanoparticles (HSA@Pt) in a 4T1 tumor-bearing mouse model.
Main Results:
- NanoCo generates photothermal heat under 1064 nm irradiation, facilitating Co(III) to Co(II) reduction.
- NanoCo exhibits significantly enhanced efficacy against platinum-resistant A549DDP cells (166x cisplatin) and CT26 cells (5000x oxaliplatin).
- NanoCo triggers immunogenic cell death, enhances dendritic cell maturation, and stimulates anti-tumor immunity.
- Combination therapy with HSA@Pt and NanoCo achieved 99% tumor growth inhibition in a 4T1 mouse model.
Conclusions:
- NIR-II photoactivated NanoCo offers a promising strategy for targeted cancer therapy with improved spatial-temporal control.
- NanoCo demonstrates potent anti-tumor activity, induces immunogenic cell death, and potentiates anti-tumor immune responses.
- The combination of NanoCo and HSA@Pt shows significant therapeutic potential for overcoming tumor resistance and enhancing treatment outcomes.
Keywords:
NIR‐IIcobalt(III) nanoparticlesphotoactivated metal chemo‐immunotherapyphotothermal therapyprodrugs
