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Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature

BACKGROUND: Translocation of nanoparticles (NP) from the pulmonary airways into other pulmonary compartments or the systemic circulation is controversially discussed in the literature. In a previous study it was shown that titanium dioxide (TiO(2)) NP were "distributed in four lung compartments...

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Autores principales: Mühlfeld, Christian, Geiser, Marianne, Kapp, Nadine, Gehr, Peter, Rothen-Rutishauser, Barbara
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2018701/
https://www.ncbi.nlm.nih.gov/pubmed/17727712
http://dx.doi.org/10.1186/1743-8977-4-7
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author Mühlfeld, Christian
Geiser, Marianne
Kapp, Nadine
Gehr, Peter
Rothen-Rutishauser, Barbara
author_facet Mühlfeld, Christian
Geiser, Marianne
Kapp, Nadine
Gehr, Peter
Rothen-Rutishauser, Barbara
author_sort Mühlfeld, Christian
collection PubMed
description BACKGROUND: Translocation of nanoparticles (NP) from the pulmonary airways into other pulmonary compartments or the systemic circulation is controversially discussed in the literature. In a previous study it was shown that titanium dioxide (TiO(2)) NP were "distributed in four lung compartments (air-filled spaces, epithelium/endothelium, connective tissue, capillary lumen) in correlation with compartment size". It was concluded that particles can move freely between these tissue compartments. To analyze whether the distribution of TiO(2 )NP in the lungs is really random or shows a preferential targeting we applied a newly developed method for comparing NP distributions. METHODS: Rat lungs exposed to an aerosol containing TiO(2 )NP were prepared for light and electron microscopy at 1 h and at 24 h after exposure. Numbers of TiO(2 )NP associated with each compartment were counted using energy filtering transmission electron microscopy. Compartment size was estimated by unbiased stereology from systematically sampled light micrographs. Numbers of particles were related to compartment size using a relative deposition index and chi-squared analysis. RESULTS: Nanoparticle distribution within the four compartments was not random at 1 h or at 24 h after exposure. At 1 h the connective tissue was the preferential target of the particles. At 24 h the NP were preferentially located in the capillary lumen. CONCLUSION: We conclude that TiO(2 )NP do not move freely between pulmonary tissue compartments, although they can pass from one compartment to another with relative ease. The residence time of NP in each tissue compartment of the respiratory system depends on the compartment and the time after exposure. It is suggested that a small fraction of TiO(2 )NP are rapidly transported from the airway lumen to the connective tissue and subsequently released into the systemic circulation.
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spelling pubmed-20187012007-10-12 Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature Mühlfeld, Christian Geiser, Marianne Kapp, Nadine Gehr, Peter Rothen-Rutishauser, Barbara Part Fibre Toxicol Research BACKGROUND: Translocation of nanoparticles (NP) from the pulmonary airways into other pulmonary compartments or the systemic circulation is controversially discussed in the literature. In a previous study it was shown that titanium dioxide (TiO(2)) NP were "distributed in four lung compartments (air-filled spaces, epithelium/endothelium, connective tissue, capillary lumen) in correlation with compartment size". It was concluded that particles can move freely between these tissue compartments. To analyze whether the distribution of TiO(2 )NP in the lungs is really random or shows a preferential targeting we applied a newly developed method for comparing NP distributions. METHODS: Rat lungs exposed to an aerosol containing TiO(2 )NP were prepared for light and electron microscopy at 1 h and at 24 h after exposure. Numbers of TiO(2 )NP associated with each compartment were counted using energy filtering transmission electron microscopy. Compartment size was estimated by unbiased stereology from systematically sampled light micrographs. Numbers of particles were related to compartment size using a relative deposition index and chi-squared analysis. RESULTS: Nanoparticle distribution within the four compartments was not random at 1 h or at 24 h after exposure. At 1 h the connective tissue was the preferential target of the particles. At 24 h the NP were preferentially located in the capillary lumen. CONCLUSION: We conclude that TiO(2 )NP do not move freely between pulmonary tissue compartments, although they can pass from one compartment to another with relative ease. The residence time of NP in each tissue compartment of the respiratory system depends on the compartment and the time after exposure. It is suggested that a small fraction of TiO(2 )NP are rapidly transported from the airway lumen to the connective tissue and subsequently released into the systemic circulation. BioMed Central 2007-08-29 /pmc/articles/PMC2018701/ /pubmed/17727712 http://dx.doi.org/10.1186/1743-8977-4-7 Text en Copyright © 2007 Mühlfeld 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
Mühlfeld, Christian
Geiser, Marianne
Kapp, Nadine
Gehr, Peter
Rothen-Rutishauser, Barbara
Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature
title Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature
title_full Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature
title_fullStr Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature
title_full_unstemmed Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature
title_short Re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": Evidence for clearance through microvasculature
title_sort re-evaluation of pulmonary titanium dioxide nanoparticle distribution using the "relative deposition index": evidence for clearance through microvasculature
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2018701/
https://www.ncbi.nlm.nih.gov/pubmed/17727712
http://dx.doi.org/10.1186/1743-8977-4-7
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