In Vitro Toxicological Assessment of Cobalt Ferrite Nanoparticles in Several Mammalian Cell Types

• Published in: Biological trace element research 2017-02, Vol.175 (2), p.458-465
• Main Authors: Abudayyak, Mahmoud, Altincekic Gurkaynak, Tuba, Özhan, Gül
• Format: Article
• Language: English
• Subjects: Algae; Animals; Apoptosis; Biochemistry; Biomedical and Life Sciences; Biotechnology; Caco-2 Cells; Carbonyl compounds; Cobalt; Cobalt - toxicity; Consumer products; Cytotoxicity; Cytotoxins - toxicity; Digestive system; DNA Damage; Ferric Compounds - toxicity; Ferrites; Genotoxicity; Hep G2 Cells; Human exposure; Humans; Life Sciences; Mice; Nanoparticles; Nanoparticles - toxicity; Nutrition; Oncology; Physicochemical properties
• ISSN: 0163-4984; 1559-0720
• DOI: 10.1007/s12011-016-0803-3

Nanoparticles have been widely used in various fields due to the superior physicochemical properties and functions. As a result, human exposure to nanoparticles increases dramatically. Previous researches have shown that nanoparticles could travel through the respiratory, digestive system, or skin into the blood and then to the secondary organs such as the brain, heart, and liver. Besides, the nanoparticle toxicity is controversial and dependent on the sensitivity of the cell type, route of exposure, and condition, as well as their characteristics. Similarly, cobalt ferrite nanoparticles (CoFe 2 O 4 -NPs) have been used in different industrial fields, and have also various application possibilities in medical and biomedical fields. CoFe 2 O 4 -NPs induce toxic responses in various organisms such as human, mice, and algae. However, there is a serious deficit of information concerning their effects on human health and the environment. We aimed to investigate the toxic effects of CoFe 2 O 4 -NPs on liver (HepG2), colon (Caco-2), lung (A549), and neuron (SH-SY5Y) cells, which reflect different exposure routes in vitro, by using various toxicological endpoints. The cytotoxicity, genotoxicity, oxidative damage, and apoptosis induction of CoFe 2 O 4 -NPs (39 ± 17 nm) were evaluated. After 24 h, the nanoparticles decreased cell viability at ≤100 μg/mL, while increasing viability at >100 μg/mL. CoFe 2 O 4 -NPs induced DNA and oxidative damage with increased malondialdehyde (MDA) and 8-hydroxy deoxyguanosine (8-OHdG) levels and decreased glutathione (GSH) levels with no change in protein carbonyl (PC) levels. CoFe 2 O 4 -NPs had apoptotic effect in HepG2 and Caco-2 cells in a concentration-dependent manner and necrotic effects on SH-SY5Y and A549 cells. Consequently, the adverse effects of CoFe 2 O 4 -NPs should raise concern about their safety in consumer products.