Synthesis, Structural Insights, and Biomedical Evaluation of NiCoFe(2)O(4) Nanoparticles for Antioxidant and Cancer Therapeutic Applications

NiCoFe(2)O(4)纳米粒子的合成、结构解析及生物医学评价及其在抗氧化和癌症治疗中的应用

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Abstract

PURPOSE: The study aims to synthesize nickel-cobalt ferrite (NiCoFe(2)O(4)) nanoparticles with controlled Co/Ni precursor ratios and to evaluate how structural, surface, and electronic modifications influence their antioxidant and anticancer performance. MATERIALS AND METHODS: NiCoFe(2)O(4) nanoparticles were synthesized via a co-precipitation route using varying Ni(2)⁺/Co(2)⁺ concentrations (0.025-0.1 M). Structural, morphological, and surface analyses were carried out using X-Ray Diffraction, fourier transform infrared spectroscopy, Raman, scanning electron microscopy, transmission electron microscopy, energy-dispersive X-Ray spectroscopy, Brunauer-Emmett-Teller, and X-Ray photoelectron spectroscopy techniques. Biological functionality was assessed using 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assay for antioxidant activity and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay on MCF-7 breast cancer and L929 fibroblast cells for cytotoxicity evaluation. RESULTS: All samples exhibited a single-phase cubic spinel structure with tunable crystallite size, lattice strain, and mesoporosity. Increasing Co/Ni concentration enhanced cation redistribution, mixed valence states, and pore-volume characteristics, improving redox-active surface behavior. Among all compositions, NC4 showed the highest DPPH radical scavenging efficiency and the strongest anticancer activity, reducing MCF-7 viability to ~ 20%-30% at 100 μg/mL while maintaining >80% viability in normal L929 cells. CONCLUSION: Tailoring the Co/Ni precursor ratio effectively modulates the structural and surface characteristics of NiCoFe(2)O(4) nanoparticles, leading to enhanced antioxidant capacity and selective anticancer activity. These findings establish NiCoFe(2)O(4) as a promising candidate for biomedical applications, particularly in oxidative stress management and targeted cancer therapeutics.

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