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In vivo Genotoxicity of Silver Nanoparticles after 90-day Silver Nanoparticle Inhalation Exposure
OBJECTIVES: The antimicrobial activity of silver nanoparticles has resulted in their widespread use in many consumer products. Yet, despite their many advantages, it is also important to determine whether silver nanoparticles may represent a hazard to the environment and human health. METHODS: Thus,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Occupational Safety and Health Research Institute
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431887/ https://www.ncbi.nlm.nih.gov/pubmed/22953185 http://dx.doi.org/10.5491/SHAW.2011.2.1.34 |
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author | Kim, Jin Sik Sung, Jae Hyuck Ji, Jun Ho Song, Kyung Seuk Lee, Ji Hyun Kang, Chang Soo Yu, Il Je |
author_facet | Kim, Jin Sik Sung, Jae Hyuck Ji, Jun Ho Song, Kyung Seuk Lee, Ji Hyun Kang, Chang Soo Yu, Il Je |
author_sort | Kim, Jin Sik |
collection | PubMed |
description | OBJECTIVES: The antimicrobial activity of silver nanoparticles has resulted in their widespread use in many consumer products. Yet, despite their many advantages, it is also important to determine whether silver nanoparticles may represent a hazard to the environment and human health. METHODS: Thus, to evaluate the genotoxic potential of silver nanoparticles, in vivo genotoxicity testing (OECD 474, in vivo micronuclei test) was conducted after exposing male and female Sprague-Dawley rats to silver nanoparticles by inhalation for 90 days according to OECD test guideline 413 (Subchronic Inhalation Toxicity: 90 Day Study) with a good laboratory practice system. The rats were exposed to silver nanoparticles (18 nm diameter) at concentrations of 0.7 × 10(6) particles/cm(3) (low dose), 1.4 × 10(6) particles/cm(3) (middle dose), and 2.9 × 10(6) particles/cm(3) (high dose) for 6 hr/day in an inhalation chamber for 90 days. The rats were killed 24 hr after the last administration, then the femurs were removed and the bone marrow collected and evaluated for micronucleus induction. RESULTS: There were no statistically significant differences in the micronucleated polychromatic erythrocytes or in the ratio of polychromatic erythrocytes among the total erythrocytes after silver nanoparticle exposure when compared with the control. CONCLUSION: The present results suggest that exposure to silver nanoparticles by inhalation for 90 days does not induce genetic toxicity in male and female rat bone marrow in vivo. |
format | Online Article Text |
id | pubmed-3431887 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Occupational Safety and Health Research Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-34318872012-09-05 In vivo Genotoxicity of Silver Nanoparticles after 90-day Silver Nanoparticle Inhalation Exposure Kim, Jin Sik Sung, Jae Hyuck Ji, Jun Ho Song, Kyung Seuk Lee, Ji Hyun Kang, Chang Soo Yu, Il Je Saf Health Work Original Article OBJECTIVES: The antimicrobial activity of silver nanoparticles has resulted in their widespread use in many consumer products. Yet, despite their many advantages, it is also important to determine whether silver nanoparticles may represent a hazard to the environment and human health. METHODS: Thus, to evaluate the genotoxic potential of silver nanoparticles, in vivo genotoxicity testing (OECD 474, in vivo micronuclei test) was conducted after exposing male and female Sprague-Dawley rats to silver nanoparticles by inhalation for 90 days according to OECD test guideline 413 (Subchronic Inhalation Toxicity: 90 Day Study) with a good laboratory practice system. The rats were exposed to silver nanoparticles (18 nm diameter) at concentrations of 0.7 × 10(6) particles/cm(3) (low dose), 1.4 × 10(6) particles/cm(3) (middle dose), and 2.9 × 10(6) particles/cm(3) (high dose) for 6 hr/day in an inhalation chamber for 90 days. The rats were killed 24 hr after the last administration, then the femurs were removed and the bone marrow collected and evaluated for micronucleus induction. RESULTS: There were no statistically significant differences in the micronucleated polychromatic erythrocytes or in the ratio of polychromatic erythrocytes among the total erythrocytes after silver nanoparticle exposure when compared with the control. CONCLUSION: The present results suggest that exposure to silver nanoparticles by inhalation for 90 days does not induce genetic toxicity in male and female rat bone marrow in vivo. Occupational Safety and Health Research Institute 2011-03 2011-03-31 /pmc/articles/PMC3431887/ /pubmed/22953185 http://dx.doi.org/10.5491/SHAW.2011.2.1.34 Text en Copyright © 2011 by Safety and Health at Work (SH@W) http://creativecommons.org/licenses/by-nc/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Jin Sik Sung, Jae Hyuck Ji, Jun Ho Song, Kyung Seuk Lee, Ji Hyun Kang, Chang Soo Yu, Il Je In vivo Genotoxicity of Silver Nanoparticles after 90-day Silver Nanoparticle Inhalation Exposure |
title | In vivo Genotoxicity of Silver Nanoparticles after 90-day Silver Nanoparticle Inhalation Exposure |
title_full | In vivo Genotoxicity of Silver Nanoparticles after 90-day Silver Nanoparticle Inhalation Exposure |
title_fullStr | In vivo Genotoxicity of Silver Nanoparticles after 90-day Silver Nanoparticle Inhalation Exposure |
title_full_unstemmed | In vivo Genotoxicity of Silver Nanoparticles after 90-day Silver Nanoparticle Inhalation Exposure |
title_short | In vivo Genotoxicity of Silver Nanoparticles after 90-day Silver Nanoparticle Inhalation Exposure |
title_sort | in vivo genotoxicity of silver nanoparticles after 90-day silver nanoparticle inhalation exposure |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431887/ https://www.ncbi.nlm.nih.gov/pubmed/22953185 http://dx.doi.org/10.5491/SHAW.2011.2.1.34 |
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