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A comparison of dispersing media for various engineered carbon nanoparticles

BACKGROUND: With the increased manufacture and use of carbon nanoparticles (CNP) there has been increasing concern about the potential toxicity of fugitive CNP in the workplace and ambient environment. To address this matter a number of investigators have conducted in vitro and in vivo toxicity asse...

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Autores principales: Buford, Mary C, Hamilton, Raymond F, Holian, Andrij
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950524/
https://www.ncbi.nlm.nih.gov/pubmed/17655771
http://dx.doi.org/10.1186/1743-8977-4-6
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author Buford, Mary C
Hamilton, Raymond F
Holian, Andrij
author_facet Buford, Mary C
Hamilton, Raymond F
Holian, Andrij
author_sort Buford, Mary C
collection PubMed
description BACKGROUND: With the increased manufacture and use of carbon nanoparticles (CNP) there has been increasing concern about the potential toxicity of fugitive CNP in the workplace and ambient environment. To address this matter a number of investigators have conducted in vitro and in vivo toxicity assessments. However, a variety of different approaches for suspension of these particles (culture media, Tween 80, dimethyl sulfoxide, phosphate-buffered saline, fetal calf serum, and others), and different sources of materials have generated potentially conflicting outcomes. The quality of the dispersion of nanoparticles is very dependent on the medium used to suspend them, and this then will most likely affect the biological outcomes. RESULTS: In this work, the distributions of different CNP (sources and types) have been characterized in various media. Furthermore, the outcome of instilling the different agglomerates, or size distributions, was examined in mouse lungs after one and seven days. Our results demonstrated that CNP suspended in serum produced particle suspensions with the fewest large agglomerates, and the most uniform distribution in mouse lungs. In addition, no apparent clearance of instilled CNP took place from lungs even after seven days. CONCLUSION: This work demonstrates that CNP agglomerates are present in all dispersing vehicles to some degree. The vehicle that contains some protein, lipid or protein/lipid component disperses the CNP best, producing fewer large CNP agglomerates. In contrast, vehicles absent of lipid and protein produce the largest CNP agglomerates. The source of the CNP is also a factor in the degree of particle agglomeration within the same vehicle.
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spelling pubmed-19505242007-08-22 A comparison of dispersing media for various engineered carbon nanoparticles Buford, Mary C Hamilton, Raymond F Holian, Andrij Part Fibre Toxicol Methodology BACKGROUND: With the increased manufacture and use of carbon nanoparticles (CNP) there has been increasing concern about the potential toxicity of fugitive CNP in the workplace and ambient environment. To address this matter a number of investigators have conducted in vitro and in vivo toxicity assessments. However, a variety of different approaches for suspension of these particles (culture media, Tween 80, dimethyl sulfoxide, phosphate-buffered saline, fetal calf serum, and others), and different sources of materials have generated potentially conflicting outcomes. The quality of the dispersion of nanoparticles is very dependent on the medium used to suspend them, and this then will most likely affect the biological outcomes. RESULTS: In this work, the distributions of different CNP (sources and types) have been characterized in various media. Furthermore, the outcome of instilling the different agglomerates, or size distributions, was examined in mouse lungs after one and seven days. Our results demonstrated that CNP suspended in serum produced particle suspensions with the fewest large agglomerates, and the most uniform distribution in mouse lungs. In addition, no apparent clearance of instilled CNP took place from lungs even after seven days. CONCLUSION: This work demonstrates that CNP agglomerates are present in all dispersing vehicles to some degree. The vehicle that contains some protein, lipid or protein/lipid component disperses the CNP best, producing fewer large CNP agglomerates. In contrast, vehicles absent of lipid and protein produce the largest CNP agglomerates. The source of the CNP is also a factor in the degree of particle agglomeration within the same vehicle. BioMed Central 2007-07-27 /pmc/articles/PMC1950524/ /pubmed/17655771 http://dx.doi.org/10.1186/1743-8977-4-6 Text en Copyright © 2007 Buford et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Buford, Mary C
Hamilton, Raymond F
Holian, Andrij
A comparison of dispersing media for various engineered carbon nanoparticles
title A comparison of dispersing media for various engineered carbon nanoparticles
title_full A comparison of dispersing media for various engineered carbon nanoparticles
title_fullStr A comparison of dispersing media for various engineered carbon nanoparticles
title_full_unstemmed A comparison of dispersing media for various engineered carbon nanoparticles
title_short A comparison of dispersing media for various engineered carbon nanoparticles
title_sort comparison of dispersing media for various engineered carbon nanoparticles
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1950524/
https://www.ncbi.nlm.nih.gov/pubmed/17655771
http://dx.doi.org/10.1186/1743-8977-4-6
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