<p>Zn<sup>2+</sup>-doped cobalt ferrite nanoparticles were prepared by the solution combustion method using hexamine as fuel. The observed X-ray diffraction patterns were shifted slightly when increasing the concentration of Zn<sup>2+</sup> ions because the structure was shrank. The structural parameters were modified by changing the concentration of Zn<sup>2+</sup> ions. The porous nature of the as-synthesized samples was confirmed by scanning electron micrographs. Magnetization was increased from 42 to 63&#xa0;emu/g with the increasing concentration of Zn<sup>2+</sup> ions in cobalt ferrite nanoparticles. Antimicrobial activity was assessed against the Co<sub>1-<i>x</i></sub>Zn<sub><i>x</i></sub>Fe<sub>2</sub>O<sub>4</sub> magnetic nanoparticles, and it was confirmed that the prepared material could be used as an antimicrobial agent. It was found that 50% of cancer cells were inhibited by using 600&#xa0;μg/ml Co<sub>0.8</sub>Zn<sub>0.2</sub>Fe<sub>2</sub>O<sub>4</sub> magnetic nanoparticles (IC<sub>50</sub>).</p>

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Evaluation of antimicrobial and anti-cancer activity of Zn2+ doped cobalt ferrite (Co1-xZnxFe2O4) magnetic nanoparticles prepared by self-sustained solution combustion synthesis (SCS)

  • K. Venkatesan,
  • D. Rajan Babu,
  • R. Vidya

摘要

Zn2+-doped cobalt ferrite nanoparticles were prepared by the solution combustion method using hexamine as fuel. The observed X-ray diffraction patterns were shifted slightly when increasing the concentration of Zn2+ ions because the structure was shrank. The structural parameters were modified by changing the concentration of Zn2+ ions. The porous nature of the as-synthesized samples was confirmed by scanning electron micrographs. Magnetization was increased from 42 to 63 emu/g with the increasing concentration of Zn2+ ions in cobalt ferrite nanoparticles. Antimicrobial activity was assessed against the Co1-xZnxFe2O4 magnetic nanoparticles, and it was confirmed that the prepared material could be used as an antimicrobial agent. It was found that 50% of cancer cells were inhibited by using 600 μg/ml Co0.8Zn0.2Fe2O4 magnetic nanoparticles (IC50).