Journal
JOURNAL OF APPLIED GENETICS
Volume 62, Issue 1, Pages 85-92Publisher
SPRINGER HEIDELBERG
DOI: 10.1007/s13353-020-00608-x
Keywords
Genotoxicity; Mitotic index; Nanoparticles; Tungsten; Chromosomal aberrations
Funding
- Scientific and Technological Research Council of Turkey (TUBITAK) [2209-(1919B011603044)]
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Tungsten oxide nanoparticles exhibit cytotoxic and genotoxic effects on Allium cepa cells, leading to a decrease in mitotic index, an increase in chromosomal aberrations, and significant DNA damage at different concentrations. Further investigation at the molecular level is warranted to evaluate the cytogenetic effects of WO(3)NPs.
Tungsten oxide nanoparticles or nanopowder (WO(3)NPs) is commonly used in various industries and also in biomedical applications such as additives, pigments, and biomedical sensors. Non-judicious excessive use of these nanoparticles (NPs) could be a serious human health concern. Therefore, the current study aimed to explore the cytotoxic and genotoxic assessment of WO(3)NPs through Allium cepa anaphase-telophase and comet assays. Nanoparticles were characterized through the scanning and transmission electron microscopy (TEM), zetasizer, and energy-dispersive X-ray spectroscopy. The mean size and the average diameter of WO(3)NPs were determined as 21.57 +/- 2.48 nm and 349.42 +/- 80.65 nm using TEM and a Zetasizer measurement system, respectively. Five concentrations (12.5 mg/L, 25 mg/L, 50 mg/L, 75 mg/L, and 100 mg/L) of WO(3)NPs were employed on the Allium cepa (A. cepa) roots for 4 h. Significant (p <= 0.05) decrease in mitotic index (MI) was shown by WO(3)NPs at all concentrations. The increase of chromosomal aberrations (CAs) was also observed in a concentration-dependent manner due to the WO(3)NPs exposure. There was a significant increase (p <= 0.05) in DNA damage at all concentrations of WO(3)NPs on the A. cepa cells. It was concluded that WO(3)NPs had cytotoxic and genotoxic effects on A. cepa meristematic cells. Moreover, further cytogenetic effects of WO(3)NPs should be investigated at the molecular level to assess its safety margin.
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