In vitro toxicity assessment of zinc and nickel ferrite nanoparticles in human erythrocytes and peripheral blood mononuclear cell

Toxicol In Vitro. 2019 Jun:57:54-61. doi: 10.1016/j.tiv.2019.02.011. Epub 2019 Feb 13.

Abstract

Ferrite nanoparticles (NPs) have gained attention in biomedicine due to their many potential applications, such as targeted drug delivery, their use as contrast agents for magnetic resonance imaging and oncological treatments. The information about the risk effects of ferrite NPs in human blood cells is, however, scarce. To assess their potential toxicity, in vitro studies were carried out with magnetite and zinc, nickel and nickel‑zinc ferrites NPs at different concentrations (50, 100 and 200 μg·ml-1). The toxicity of the ferrite NPs was evaluated in humans by determining red blood hemolysis, by measuring the content of total proteins, and by assaying catalase and glutathione-S-transferase activities. Our results show that nickel‑zinc ferrite lead to hemolysis, and that magnetite, zinc and nickel‑zinc ferrites increase glutathione-S-transferase activity. No significant changes in human peripheral blood mononuclear cells viability were observed after the treatment with the four different ferrite NPs in vitro.

Keywords: Ferrite nanoparticles; Nickel; PBMCs; RBCs; Toxicity; Zinc.

MeSH terms

  • Adult
  • Catalase / metabolism
  • Cell Survival / drug effects
  • Cells, Cultured
  • Erythrocytes / drug effects*
  • Erythrocytes / physiology
  • Ferric Compounds / toxicity*
  • Ferrosoferric Oxide / toxicity*
  • Glutathione Transferase / metabolism
  • Humans
  • Leukocytes, Mononuclear / drug effects*
  • Male
  • Metal Nanoparticles / toxicity*
  • Nickel / toxicity*
  • Zinc Compounds / toxicity*

Substances

  • Ferric Compounds
  • Zinc Compounds
  • nickel ferrite
  • nickel-zinc ferrite
  • Nickel
  • Catalase
  • Glutathione Transferase
  • Ferrosoferric Oxide