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Comparative metal oxide nanoparticle toxicity using embryonic zebrafish
Engineered metal oxide nanoparticles (MO NPs) are finding increasing utility in the medical field as anticancer agents. Before validation of in vivo anticancer efficacy can occur, a better understanding of whole-animal toxicity is required. We compared the toxicity of seven widely used semiconductor...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443491/ https://www.ncbi.nlm.nih.gov/pubmed/26029632 http://dx.doi.org/10.1016/j.toxrep.2015.03.015 |
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author | Wehmas, Leah C. Anders, Catherine Chess, Jordan Punnoose, Alex Pereira, Cliff B. Greenwood, Juliet A. Tanguay, Robert L. |
author_facet | Wehmas, Leah C. Anders, Catherine Chess, Jordan Punnoose, Alex Pereira, Cliff B. Greenwood, Juliet A. Tanguay, Robert L. |
author_sort | Wehmas, Leah C. |
collection | PubMed |
description | Engineered metal oxide nanoparticles (MO NPs) are finding increasing utility in the medical field as anticancer agents. Before validation of in vivo anticancer efficacy can occur, a better understanding of whole-animal toxicity is required. We compared the toxicity of seven widely used semiconductor MO NPs made from zinc oxide (ZnO), titanium dioxide, cerium dioxide and tin dioxide prepared in pure water and in synthetic seawater using a five-day embryonic zebrafish assay. We hypothesized that the toxicity of these engineered MO NPs would depend on physicochemical properties. Significant agglomeration of MO NPs in aqueous solutions is common making it challenging to associate NP characteristics such as size and charge with toxicity. However, data from our agglomerated MO NPs suggests that the elemental composition and dissolution potential are major drivers of toxicity. Only ZnO caused significant adverse effects of all MO particles tested, and only when prepared in pure water (point estimate median lethal concentration = 3.5–9.1 mg/L). This toxicity was life stage dependent. The 24 h toxicity increased greatly (∼22.7 fold) when zebrafish exposures started at the larval life stage compared to the 24 h toxicity following embryonic exposure. Investigation into whether dissolution could account for ZnO toxicity revealed high levels of zinc ion (40–89% of total sample) were generated. Exposure to zinc ion equivalents revealed dissolved Zn(2+) may be a major contributor to ZnO toxicity. |
format | Online Article Text |
id | pubmed-4443491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-44434912016-01-01 Comparative metal oxide nanoparticle toxicity using embryonic zebrafish Wehmas, Leah C. Anders, Catherine Chess, Jordan Punnoose, Alex Pereira, Cliff B. Greenwood, Juliet A. Tanguay, Robert L. Toxicol Rep Article Engineered metal oxide nanoparticles (MO NPs) are finding increasing utility in the medical field as anticancer agents. Before validation of in vivo anticancer efficacy can occur, a better understanding of whole-animal toxicity is required. We compared the toxicity of seven widely used semiconductor MO NPs made from zinc oxide (ZnO), titanium dioxide, cerium dioxide and tin dioxide prepared in pure water and in synthetic seawater using a five-day embryonic zebrafish assay. We hypothesized that the toxicity of these engineered MO NPs would depend on physicochemical properties. Significant agglomeration of MO NPs in aqueous solutions is common making it challenging to associate NP characteristics such as size and charge with toxicity. However, data from our agglomerated MO NPs suggests that the elemental composition and dissolution potential are major drivers of toxicity. Only ZnO caused significant adverse effects of all MO particles tested, and only when prepared in pure water (point estimate median lethal concentration = 3.5–9.1 mg/L). This toxicity was life stage dependent. The 24 h toxicity increased greatly (∼22.7 fold) when zebrafish exposures started at the larval life stage compared to the 24 h toxicity following embryonic exposure. Investigation into whether dissolution could account for ZnO toxicity revealed high levels of zinc ion (40–89% of total sample) were generated. Exposure to zinc ion equivalents revealed dissolved Zn(2+) may be a major contributor to ZnO toxicity. Elsevier 2015-05-02 /pmc/articles/PMC4443491/ /pubmed/26029632 http://dx.doi.org/10.1016/j.toxrep.2015.03.015 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Wehmas, Leah C. Anders, Catherine Chess, Jordan Punnoose, Alex Pereira, Cliff B. Greenwood, Juliet A. Tanguay, Robert L. Comparative metal oxide nanoparticle toxicity using embryonic zebrafish |
title | Comparative metal oxide nanoparticle toxicity using embryonic zebrafish |
title_full | Comparative metal oxide nanoparticle toxicity using embryonic zebrafish |
title_fullStr | Comparative metal oxide nanoparticle toxicity using embryonic zebrafish |
title_full_unstemmed | Comparative metal oxide nanoparticle toxicity using embryonic zebrafish |
title_short | Comparative metal oxide nanoparticle toxicity using embryonic zebrafish |
title_sort | comparative metal oxide nanoparticle toxicity using embryonic zebrafish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4443491/ https://www.ncbi.nlm.nih.gov/pubmed/26029632 http://dx.doi.org/10.1016/j.toxrep.2015.03.015 |
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