Literature DB >> 25435351

Genotoxicity assessment of cerium oxide nanoparticles in female Wistar rats after acute oral exposure.

Monika Kumari1, Srinivas Indu Kumari2, Sarika Srinivas Kalyan Kamal3, Paramjit Grover4.   

Abstract

Cerium oxide nanoparticles (CeO2 NPs; nanoceria) have demonstrated excellent potential for commercial use in various arenas, such as in biomedical industry in cosmetics and as a fuel additive. However, limited knowledge exists regarding their potential toxicity. In this study, acute oral toxicity of CeO2 NPs and their microparticles (MPs; bulk) was carried out in female albino Wistar rats. The CeO2 NPs and CeO2 MPs were characterized utilizing transmission electron microscopy (TEM), dynamic light scattering (DLS) and laser Doppler velocimetry (LDV) for the size, distribution and surface charge respectively. The genotoxicity studies were conducted using micronucleus test (MNT), comet and chromosomal aberration (CA) assays. Results revealed that at high dose (1000mg/kg bw) CeO2 NPs induced significant DNA damage in peripheral blood leukocytes (PBL) and liver cells, micronucleus formation in bone marrow and blood cells and total cytogenetic changes in bone marrow. However, significant genotoxicity was not observed at 500 and 100mg/kg bw of CeO2 NPs. The findings from biochemical assays depicted significant alterations in ALP and LDH activity in serum and GSH content in liver, kidneys and brain only at the high dose of CeO2 NPs. Tissue biodistribution of both particles was analyzed by inductively coupled plasma optical emission spectrometer (ICP-OES). Bioaccumulation of nanoceria in all tissues was significant and dose-, time- and organ-dependent. Moreover, CeO2 NPs exhibited higher tissue distribution along with greater clearance in large fractions through urine and feces than CeO2 bulk, whereas, maximum amount of micro-sized CeO2 got excreted in feces. The histopathological examination documented alterations in the liver due to exposure with CeO2 NPs only. Hence, the results suggest that bioaccumulation of CeO2 NPs may induce genotoxic effects. However, further research on long term fate and adverse effects of CeO2 NPs is warranted.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Biochemical; Biodistribution; CeO(2) microparticles; CeO(2) nanoparticles; Genotoxicity; Wistar rats

Mesh:

Substances:

Year:  2014        PMID: 25435351     DOI: 10.1016/j.mrgentox.2014.09.009

Source DB:  PubMed          Journal:  Mutat Res Genet Toxicol Environ Mutagen        ISSN: 1383-5718            Impact factor:   3.189


  18 in total

1.  Dermal transfer and environmental release of CeO2 nanoparticles used as UV inhibitors on outdoor surfaces: Implications for human and environmental health.

Authors:  Justin G Clar; William E Platten; Eric J Baumann; Andrew Remsen; Steve M Harmon; Christina L Bennett-Stamper; Treye A Thomas; Todd P Luxton
Journal:  Sci Total Environ       Date:  2017-09-20       Impact factor: 7.963

Review 2.  Cerium oxide nanoparticles in neuroprotection and considerations for efficacy and safety.

Authors:  Beverly A Rzigalinski; Charles S Carfagna; Marion Ehrich
Journal:  Wiley Interdiscip Rev Nanomed Nanobiotechnol       Date:  2016-11-08

3.  Toxicological assessment of tungsten oxide nanoparticles in rats after acute oral exposure.

Authors:  Srinivas Chinde; Naresh Dumala; Mohammed Fazlur Rahman; Sarika Srinivas Kalyan Kamal; Srinivas Indu Kumari; Mohammed Mahboob; Paramjit Grover
Journal:  Environ Sci Pollut Res Int       Date:  2017-04-08       Impact factor: 4.223

Review 4.  Synthesis and biomedical applications of Cerium oxide nanoparticles - A Review.

Authors:  S Rajeshkumar; Poonam Naik
Journal:  Biotechnol Rep (Amst)       Date:  2017-11-29

5.  Primary genotoxicity in the liver following pulmonary exposure to carbon black nanoparticles in mice.

Authors:  Justyna Modrzynska; Trine Berthing; Gitte Ravn-Haren; Nicklas Raun Jacobsen; Ingrid Konow Weydahl; Katrin Loeschner; Alicja Mortensen; Anne Thoustrup Saber; Ulla Vogel
Journal:  Part Fibre Toxicol       Date:  2018-01-03       Impact factor: 9.400

6.  Cerium oxide and barium sulfate nanoparticle inhalation affects gene expression in alveolar epithelial cells type II.

Authors:  Daniela Schwotzer; Monika Niehof; Dirk Schaudien; Heiko Kock; Tanja Hansen; Clemens Dasenbrock; Otto Creutzenberg
Journal:  J Nanobiotechnology       Date:  2018-02-20       Impact factor: 10.435

7.  Effects from a 90-day inhalation toxicity study with cerium oxide and barium sulfate nanoparticles in rats.

Authors:  Daniela Schwotzer; Heinrich Ernst; Dirk Schaudien; Heiko Kock; Gerhard Pohlmann; Clemens Dasenbrock; Otto Creutzenberg
Journal:  Part Fibre Toxicol       Date:  2017-07-12       Impact factor: 9.400

8.  Cerium Oxide Nanoparticles in Lung Acutely Induce Oxidative Stress, Inflammation, and DNA Damage in Various Organs of Mice.

Authors:  Abderrahim Nemmar; Priya Yuvaraju; Sumaya Beegam; Mohamed A Fahim; Badreldin H Ali
Journal:  Oxid Med Cell Longev       Date:  2017-03-14       Impact factor: 6.543

9.  Effect of exposure to CeO2 nanoparticles on ram spermatozoa during storage at 4 °C for 96 hours.

Authors:  Laura Falchi; Grazia Galleri; Gian Mario Dore; Maria Teresa Zedda; Salvatore Pau; Luisa Bogliolo; Federica Ariu; Alessandra Pinna; Stefano Nieddu; Plinio Innocenzi; Sergio Ledda
Journal:  Reprod Biol Endocrinol       Date:  2018-03-06       Impact factor: 5.211

10.  Physiologically based pharmacokinetic modeling of nanoceria systemic distribution in rats suggests dose- and route-dependent biokinetics.

Authors:  Ulrika Carlander; Tshepo Paulsen Moto; Anteneh Assefa Desalegn; Robert A Yokel; Gunnar Johanson
Journal:  Int J Nanomedicine       Date:  2018-05-01
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