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Factoring-in agglomeration of carbon nanotubes and nanofibers for better prediction of their toxicity versus asbestos

BACKGROUND: Carbon nanotubes (CNT) and carbon nanofibers (CNF) are allotropes of carbon featuring fibrous morphology. The dimensions and high aspect ratio of CNT and CNF have prompted the comparison with naturally occurring asbestos fibers which are known to be extremely pathogenic. While the toxici...

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Autores principales: Murray, Ashley R, Kisin, Elena R, Tkach, Alexey V, Yanamala, Naveena, Mercer, Robert, Young, Shih-Houng, Fadeel, Bengt, Kagan, Valerian E, Shvedova, Anna A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379937/
https://www.ncbi.nlm.nih.gov/pubmed/22490147
http://dx.doi.org/10.1186/1743-8977-9-10
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author Murray, Ashley R
Kisin, Elena R
Tkach, Alexey V
Yanamala, Naveena
Mercer, Robert
Young, Shih-Houng
Fadeel, Bengt
Kagan, Valerian E
Shvedova, Anna A
author_facet Murray, Ashley R
Kisin, Elena R
Tkach, Alexey V
Yanamala, Naveena
Mercer, Robert
Young, Shih-Houng
Fadeel, Bengt
Kagan, Valerian E
Shvedova, Anna A
author_sort Murray, Ashley R
collection PubMed
description BACKGROUND: Carbon nanotubes (CNT) and carbon nanofibers (CNF) are allotropes of carbon featuring fibrous morphology. The dimensions and high aspect ratio of CNT and CNF have prompted the comparison with naturally occurring asbestos fibers which are known to be extremely pathogenic. While the toxicity and hazardous outcomes elicited by airborne exposure to single-walled CNT or asbestos have been widely reported, very limited data are currently available describing adverse effects of respirable CNF. RESULTS: Here, we assessed pulmonary inflammation, fibrosis, oxidative stress markers and systemic immune responses to respirable CNF in comparison to single-walled CNT (SWCNT) and asbestos. Pulmonary inflammatory and fibrogenic responses to CNF, SWCNT and asbestos varied depending upon the agglomeration state of the particles/fibers. Foci of granulomatous lesions and collagen deposition were associated with dense particle-like SWCNT agglomerates, while no granuloma formation was found following exposure to fiber-like CNF or asbestos. The average thickness of the alveolar connective tissue - a marker of interstitial fibrosis - was increased 28 days post SWCNT, CNF or asbestos exposure. Exposure to SWCNT, CNF or asbestos resulted in oxidative stress evidenced by accumulations of 4-HNE and carbonylated proteins in the lung tissues. Additionally, local inflammatory and fibrogenic responses were accompanied by modified systemic immunity, as documented by decreased proliferation of splenic T cells ex vivo on day 28 post exposure. The accuracies of assessments of effective surface area for asbestos, SWCNT and CNF (based on geometrical analysis of their agglomeration) versus estimates of mass dose and number of particles were compared as predictors of toxicological outcomes. CONCLUSIONS: We provide evidence that effective surface area along with mass dose rather than specific surface area or particle number are significantly correlated with toxicological responses to carbonaceous fibrous nanoparticles. Therefore, they could be useful dose metrics for risk assessment and management.
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spelling pubmed-33799372012-06-25 Factoring-in agglomeration of carbon nanotubes and nanofibers for better prediction of their toxicity versus asbestos Murray, Ashley R Kisin, Elena R Tkach, Alexey V Yanamala, Naveena Mercer, Robert Young, Shih-Houng Fadeel, Bengt Kagan, Valerian E Shvedova, Anna A Part Fibre Toxicol Research BACKGROUND: Carbon nanotubes (CNT) and carbon nanofibers (CNF) are allotropes of carbon featuring fibrous morphology. The dimensions and high aspect ratio of CNT and CNF have prompted the comparison with naturally occurring asbestos fibers which are known to be extremely pathogenic. While the toxicity and hazardous outcomes elicited by airborne exposure to single-walled CNT or asbestos have been widely reported, very limited data are currently available describing adverse effects of respirable CNF. RESULTS: Here, we assessed pulmonary inflammation, fibrosis, oxidative stress markers and systemic immune responses to respirable CNF in comparison to single-walled CNT (SWCNT) and asbestos. Pulmonary inflammatory and fibrogenic responses to CNF, SWCNT and asbestos varied depending upon the agglomeration state of the particles/fibers. Foci of granulomatous lesions and collagen deposition were associated with dense particle-like SWCNT agglomerates, while no granuloma formation was found following exposure to fiber-like CNF or asbestos. The average thickness of the alveolar connective tissue - a marker of interstitial fibrosis - was increased 28 days post SWCNT, CNF or asbestos exposure. Exposure to SWCNT, CNF or asbestos resulted in oxidative stress evidenced by accumulations of 4-HNE and carbonylated proteins in the lung tissues. Additionally, local inflammatory and fibrogenic responses were accompanied by modified systemic immunity, as documented by decreased proliferation of splenic T cells ex vivo on day 28 post exposure. The accuracies of assessments of effective surface area for asbestos, SWCNT and CNF (based on geometrical analysis of their agglomeration) versus estimates of mass dose and number of particles were compared as predictors of toxicological outcomes. CONCLUSIONS: We provide evidence that effective surface area along with mass dose rather than specific surface area or particle number are significantly correlated with toxicological responses to carbonaceous fibrous nanoparticles. Therefore, they could be useful dose metrics for risk assessment and management. BioMed Central 2012-04-10 /pmc/articles/PMC3379937/ /pubmed/22490147 http://dx.doi.org/10.1186/1743-8977-9-10 Text en Copyright ©2012 Murray 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 Research
Murray, Ashley R
Kisin, Elena R
Tkach, Alexey V
Yanamala, Naveena
Mercer, Robert
Young, Shih-Houng
Fadeel, Bengt
Kagan, Valerian E
Shvedova, Anna A
Factoring-in agglomeration of carbon nanotubes and nanofibers for better prediction of their toxicity versus asbestos
title Factoring-in agglomeration of carbon nanotubes and nanofibers for better prediction of their toxicity versus asbestos
title_full Factoring-in agglomeration of carbon nanotubes and nanofibers for better prediction of their toxicity versus asbestos
title_fullStr Factoring-in agglomeration of carbon nanotubes and nanofibers for better prediction of their toxicity versus asbestos
title_full_unstemmed Factoring-in agglomeration of carbon nanotubes and nanofibers for better prediction of their toxicity versus asbestos
title_short Factoring-in agglomeration of carbon nanotubes and nanofibers for better prediction of their toxicity versus asbestos
title_sort factoring-in agglomeration of carbon nanotubes and nanofibers for better prediction of their toxicity versus asbestos
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379937/
https://www.ncbi.nlm.nih.gov/pubmed/22490147
http://dx.doi.org/10.1186/1743-8977-9-10
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