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

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Abstract

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 (CoFe2O4-NPs) have been used in different industrial fields, and have also various application possibilities in medical and biomedical fields. CoFe2O4-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 CoFe2O4-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 CoFe2O4-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. CoFe2O4-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. CoFe2O4-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 CoFe2O4-NPs should raise concern about their safety in consumer products.

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Abbreviations

8-OHdG:

8-Hydroxy deoxyguanosine

ATCC:

American type culture collection

AV:

Annexin V–FITC

CoFe2O4-NPs:

Cobalt ferrite nanoparticles

DMEM:

Dulbecco’s modified eagle medium

DNA:

Deoxyribonucleic acid

EDTA:

Ethylene diamine tetraacetic acid

ELISA:

Enzyme-linked immune sorbent assay

EMEM:

Eagle’s minimum essential medium

FBS:

Fetal bovine serum

GSH:

Glutathione

H2O2 :

Hydrogen peroxide

IARC:

International Agency for Research on Cancer

ICP-MS:

Inductively coupled plasma-mass spectrometry

MDA:

Malondialdehyde

MTT:

3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyl-tetrazolium bromide

NRU:

Neutral red uptake

OD:

Optical density

PBS:

Phosphate buffered saline

PC:

Protein carbonyl

PI:

Propidium iodide

ROS:

Reactive oxygen species

SD:

Standard deviation

TEM:

Transmission electron microscopy

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Acknowledgment

This work was supported by the Research Fund of Istanbul University (Project No: 40441).

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Correspondence to Gül Özhan.

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Abudayyak, M., Altincekic Gurkaynak, T. & Özhan, G. In Vitro Toxicological Assessment of Cobalt Ferrite Nanoparticles in Several Mammalian Cell Types. Biol Trace Elem Res 175, 458–465 (2017). https://doi.org/10.1007/s12011-016-0803-3

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  • DOI: https://doi.org/10.1007/s12011-016-0803-3

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