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Enhanced anticancer and biological activities of environmentally friendly Ni/Cu-ZnO solid solution nanoparticles
Huma Ayub1, Uzma Jabeen1, Iqbal Ahmad2
1Department of Chemistry, Sardar Bahadur Khan Women University, Quetta, Pakistan.
Heliyon
|December 17, 2024
Summary
Nickel and copper-doped zinc oxide nanoparticles (Ni/Cu-ZnO NPs) show enhanced anticancer and antioxidant properties. These modified nanoparticles exhibit significant efficacy against breast cancer cells with reduced toxicity to normal cells.
Area of Science:
- Materials Science
- Nanotechnology
- Biomedical Engineering
Background:
- Zinc oxide nanoparticles (ZnO NPs) possess therapeutic potential but require enhancement for improved efficacy.
- Incorporating transition metals like Nickel (Ni) and Copper (Cu) can modify ZnO NP properties.
- Developing novel nanomaterials for targeted cancer therapy and antioxidant applications is crucial.
Purpose of the Study:
- To synthesize and characterize Ni/Cu-ZnO NPs.
- To evaluate the anticancer activity of Ni/Cu-ZnO NPs against breast cancer cells.
- To assess the antioxidant capacity of Ni/Cu-ZnO NPs.
Main Methods:
- Synthesis of Ni/Cu-ZnO NPs.
- Characterization using pXRD, FTIR, UV-visible spectroscopy, FESEM, and EDAX.
- In vitro cytotoxicity assays (MDA and BHK-21 cells), antioxidant assays (TAC, FRAP, DPPH), and molecular docking.
Main Results:
- Successful synthesis and structural modification of Ni/Cu-ZnO NPs confirmed.
- Ni/Cu-ZnO NPs demonstrated dose-dependent cytotoxicity against breast cancer cells, with lower toxicity to normal cells.
- Ni/Cu-ZnO NPs exhibited superior antioxidant activity compared to pure ZnO NPs.
- Molecular docking validated the binding affinities and biological activities.
Conclusions:
- Ni/Cu-ZnO NPs exhibit enhanced anticancer and antioxidant properties due to synergistic effects.
- These NPs show promise as therapeutic agents for cancer treatment and antioxidant applications.
- The study highlights the potential of bimetallic doping for improving nanomaterial functionality.

