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A Biopersistence Study following Exposure to Chrysotile Asbestos Alone or in Combination with Fine Particles

In designing a study to evaluate the inhalation biopersistence of a chrysotile asbestos that was used as a component of a joint-compound, a feasibility study was initiated to evaluate the short-term biopersistence of the chrysotile alone and of the chrysotile in combination witht the sanded reformul...

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Autores principales: Bernstein, D. M., Donaldson, K., Decker, U., Gaering, S., Kunzendorf, P., Chevalier, J., Holm, S. E.
Formato: Texto
Lenguaje:English
Publicado: Informa Healthcare 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565272/
https://www.ncbi.nlm.nih.gov/pubmed/18788018
http://dx.doi.org/10.1080/08958370802259053
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author Bernstein, D. M.
Donaldson, K.
Decker, U.
Gaering, S.
Kunzendorf, P.
Chevalier, J.
Holm, S. E.
author_facet Bernstein, D. M.
Donaldson, K.
Decker, U.
Gaering, S.
Kunzendorf, P.
Chevalier, J.
Holm, S. E.
author_sort Bernstein, D. M.
collection PubMed
description In designing a study to evaluate the inhalation biopersistence of a chrysotile asbestos that was used as a component of a joint-compound, a feasibility study was initiated to evaluate the short-term biopersistence of the chrysotile alone and of the chrysotile in combination witht the sanded reformulated joint-compound. Two groups of Wistar rats were exposed to either 7RF3 chrysotile (Group 2) or to 7RF3 chrysotile combined with aerosolized sanded joint-compound (Group 3). In addition, a control group was exposed to flltered-air. The chrysotile used in the Ready Mix joint compound is rapidly removed from the lung. The chrysotile alone exposure group had a clearance half-time of fibers L > 20 μm of 2.2 days; in the chrysotile plus sanded exposure group the clearance half-time of fibers L > 20 μm was 2.8 days. However, across all size ranges there was approximately an order of magnitude decrease in the mean number of fibers remaining in the lungs of Group 3 as compared to Group 2 despite similiar aerosol exposures. Histopathological examination showed that the chrysotile exposed lungs had the same appearance as the flltered-air controls. This study uniquely illustrates that additional concurrent exposure to an aerosol of the sanded joint-compound, with large numbers of fine-particles depositing in the lungs, accelerates the recruitment of macrophages, resulting in a tenfold decrease in the number of fibers remaining in the lung. The increased number of macrophages in the chrysotile/sanded joint exposure group was confirmed histologically, with this being the only exposure-related histological finding reported.
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spelling pubmed-25652722008-11-14 A Biopersistence Study following Exposure to Chrysotile Asbestos Alone or in Combination with Fine Particles Bernstein, D. M. Donaldson, K. Decker, U. Gaering, S. Kunzendorf, P. Chevalier, J. Holm, S. E. Inhal Toxicol Original Article In designing a study to evaluate the inhalation biopersistence of a chrysotile asbestos that was used as a component of a joint-compound, a feasibility study was initiated to evaluate the short-term biopersistence of the chrysotile alone and of the chrysotile in combination witht the sanded reformulated joint-compound. Two groups of Wistar rats were exposed to either 7RF3 chrysotile (Group 2) or to 7RF3 chrysotile combined with aerosolized sanded joint-compound (Group 3). In addition, a control group was exposed to flltered-air. The chrysotile used in the Ready Mix joint compound is rapidly removed from the lung. The chrysotile alone exposure group had a clearance half-time of fibers L > 20 μm of 2.2 days; in the chrysotile plus sanded exposure group the clearance half-time of fibers L > 20 μm was 2.8 days. However, across all size ranges there was approximately an order of magnitude decrease in the mean number of fibers remaining in the lungs of Group 3 as compared to Group 2 despite similiar aerosol exposures. Histopathological examination showed that the chrysotile exposed lungs had the same appearance as the flltered-air controls. This study uniquely illustrates that additional concurrent exposure to an aerosol of the sanded joint-compound, with large numbers of fine-particles depositing in the lungs, accelerates the recruitment of macrophages, resulting in a tenfold decrease in the number of fibers remaining in the lung. The increased number of macrophages in the chrysotile/sanded joint exposure group was confirmed histologically, with this being the only exposure-related histological finding reported. Informa Healthcare 2008-09-11 2008-09 /pmc/articles/PMC2565272/ /pubmed/18788018 http://dx.doi.org/10.1080/08958370802259053 Text en Copyright © Informa UK Ltd. http://creativecommons.org/licenses/by/2.0/ This is an open access article distributed under the Supplemental Terms and Conditions for iOpenAccess articles published in Informa Healthcare journals (http://www.informaworld.com/mpp/uploads/iopenaccess_tcs.pdf) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Bernstein, D. M.
Donaldson, K.
Decker, U.
Gaering, S.
Kunzendorf, P.
Chevalier, J.
Holm, S. E.
A Biopersistence Study following Exposure to Chrysotile Asbestos Alone or in Combination with Fine Particles
title A Biopersistence Study following Exposure to Chrysotile Asbestos Alone or in Combination with Fine Particles
title_full A Biopersistence Study following Exposure to Chrysotile Asbestos Alone or in Combination with Fine Particles
title_fullStr A Biopersistence Study following Exposure to Chrysotile Asbestos Alone or in Combination with Fine Particles
title_full_unstemmed A Biopersistence Study following Exposure to Chrysotile Asbestos Alone or in Combination with Fine Particles
title_short A Biopersistence Study following Exposure to Chrysotile Asbestos Alone or in Combination with Fine Particles
title_sort biopersistence study following exposure to chrysotile asbestos alone or in combination with fine particles
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2565272/
https://www.ncbi.nlm.nih.gov/pubmed/18788018
http://dx.doi.org/10.1080/08958370802259053
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