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Novel lanthanide-labeled metal oxide nanoparticles improve the measurement of in vivo clearance and translocation
The deposition, clearance and translocation of europium-doped gadolinium oxide nanoparticles in a mouse lung were investigated experimentally. Nanoparticles were synthesized by spray flame pyrolysis. The particle size, crystallinity and surface properties were characterized. Following instillation,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560106/ https://www.ncbi.nlm.nih.gov/pubmed/23305071 http://dx.doi.org/10.1186/1743-8977-10-1 |
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author | Abid, Aamir D Anderson, Donald S Das, Gautom K Van Winkle, Laura S Kennedy, Ian M |
author_facet | Abid, Aamir D Anderson, Donald S Das, Gautom K Van Winkle, Laura S Kennedy, Ian M |
author_sort | Abid, Aamir D |
collection | PubMed |
description | The deposition, clearance and translocation of europium-doped gadolinium oxide nanoparticles in a mouse lung were investigated experimentally. Nanoparticles were synthesized by spray flame pyrolysis. The particle size, crystallinity and surface properties were characterized. Following instillation, the concentrations of particles in organs were determined with inductively coupled plasma mass spectrometry. The protein corona coating the nanoparticles was found to be similar to the coating on more environmentally relevant nanoparticles such as iron oxide. Measurements of the solubility of the nanoparticles in surrogates of biological fluids indicated very little propensity for dissolution, and the elemental ratio of particle constituents did not change, adding further support to the contention that intact nanoparticles were measured. The particles were intratracheally instilled into the mouse lung. After 24 hours, the target organs were harvested, acid digested and the nanoparticle mass in each organ was measured by inductively coupled plasma mass spectrometry (ICP-MS). The nanoparticles were detected in all the studied organs at low ppb levels; 59% of the particles remained in the lung. A significant amount of particles was also detected in the feces, suggesting fast clearance mechanisms. The nanoparticle system used in this work is highly suitable for quantitatively determining deposition, transport and clearance of nanoparticles from the lung, providing a quantified measure of delivered dose. |
format | Online Article Text |
id | pubmed-3560106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35601062013-02-04 Novel lanthanide-labeled metal oxide nanoparticles improve the measurement of in vivo clearance and translocation Abid, Aamir D Anderson, Donald S Das, Gautom K Van Winkle, Laura S Kennedy, Ian M Part Fibre Toxicol Research The deposition, clearance and translocation of europium-doped gadolinium oxide nanoparticles in a mouse lung were investigated experimentally. Nanoparticles were synthesized by spray flame pyrolysis. The particle size, crystallinity and surface properties were characterized. Following instillation, the concentrations of particles in organs were determined with inductively coupled plasma mass spectrometry. The protein corona coating the nanoparticles was found to be similar to the coating on more environmentally relevant nanoparticles such as iron oxide. Measurements of the solubility of the nanoparticles in surrogates of biological fluids indicated very little propensity for dissolution, and the elemental ratio of particle constituents did not change, adding further support to the contention that intact nanoparticles were measured. The particles were intratracheally instilled into the mouse lung. After 24 hours, the target organs were harvested, acid digested and the nanoparticle mass in each organ was measured by inductively coupled plasma mass spectrometry (ICP-MS). The nanoparticles were detected in all the studied organs at low ppb levels; 59% of the particles remained in the lung. A significant amount of particles was also detected in the feces, suggesting fast clearance mechanisms. The nanoparticle system used in this work is highly suitable for quantitatively determining deposition, transport and clearance of nanoparticles from the lung, providing a quantified measure of delivered dose. BioMed Central 2013-01-10 /pmc/articles/PMC3560106/ /pubmed/23305071 http://dx.doi.org/10.1186/1743-8977-10-1 Text en Copyright ©2013 Abid 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 Abid, Aamir D Anderson, Donald S Das, Gautom K Van Winkle, Laura S Kennedy, Ian M Novel lanthanide-labeled metal oxide nanoparticles improve the measurement of in vivo clearance and translocation |
title | Novel lanthanide-labeled metal oxide nanoparticles improve the measurement of in vivo clearance and translocation |
title_full | Novel lanthanide-labeled metal oxide nanoparticles improve the measurement of in vivo clearance and translocation |
title_fullStr | Novel lanthanide-labeled metal oxide nanoparticles improve the measurement of in vivo clearance and translocation |
title_full_unstemmed | Novel lanthanide-labeled metal oxide nanoparticles improve the measurement of in vivo clearance and translocation |
title_short | Novel lanthanide-labeled metal oxide nanoparticles improve the measurement of in vivo clearance and translocation |
title_sort | novel lanthanide-labeled metal oxide nanoparticles improve the measurement of in vivo clearance and translocation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560106/ https://www.ncbi.nlm.nih.gov/pubmed/23305071 http://dx.doi.org/10.1186/1743-8977-10-1 |
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