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Distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate

BACKGROUND: The study investigated the distribution of silver after 28 days repeated oral administration of silver nanoparticles (AgNPs) and silver acetate (AgAc) to rats. Oral administration is a relevant route of exposure because of the use of silver nanoparticles in products related to food and f...

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Autores principales: Loeschner, Katrin, Hadrup, Niels, Qvortrup, Klaus, Larsen, Agnete, Gao, Xueyun, Vogel, Ulla, Mortensen, Alicja, Lam, Henrik Rye, Larsen, Erik H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123173/
https://www.ncbi.nlm.nih.gov/pubmed/21631937
http://dx.doi.org/10.1186/1743-8977-8-18
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author Loeschner, Katrin
Hadrup, Niels
Qvortrup, Klaus
Larsen, Agnete
Gao, Xueyun
Vogel, Ulla
Mortensen, Alicja
Lam, Henrik Rye
Larsen, Erik H
author_facet Loeschner, Katrin
Hadrup, Niels
Qvortrup, Klaus
Larsen, Agnete
Gao, Xueyun
Vogel, Ulla
Mortensen, Alicja
Lam, Henrik Rye
Larsen, Erik H
author_sort Loeschner, Katrin
collection PubMed
description BACKGROUND: The study investigated the distribution of silver after 28 days repeated oral administration of silver nanoparticles (AgNPs) and silver acetate (AgAc) to rats. Oral administration is a relevant route of exposure because of the use of silver nanoparticles in products related to food and food contact materials. RESULTS: AgNPs were synthesized with a size distribution of 14 ± 4 nm in diameter (90% of the nanoparticle volume) and stabilized in aqueous suspension by the polymer polyvinylpyrrolidone (PVP). The AgNPs remained stable throughout the duration of the 28-day oral toxicity study in rats. The organ distribution pattern of silver following administration of AgNPs and AgAc was similar. However the absolute silver concentrations in tissues were lower following oral exposure to AgNPs. This was in agreement with an indication of a higher fecal excretion following administration of AgNPs. Besides the intestinal system, the largest silver concentrations were detected in the liver and kidneys. Silver was also found in the lungs and brain. Autometallographic (AMG) staining revealed a similar cellular localization of silver in ileum, liver, and kidney tissue in rats exposed to AgNPs or AgAc. Using transmission electron microscopy (TEM), nanosized granules were detected in the ileum of animals exposed to AgNPs or AgAc and were mainly located in the basal lamina of the ileal epithelium and in lysosomes of macrophages within the lamina propria. Using energy dispersive x-ray spectroscopy it was shown that the granules in lysosomes consisted of silver, selenium, and sulfur for both AgNP and AgAc exposed rats. The diameter of the deposited granules was in the same size range as that of the administered AgNPs. No silver granules were detected by TEM in the liver. CONCLUSIONS: The results of the present study demonstrate that the organ distribution of silver was similar when AgNPs or AgAc were administered orally to rats. The presence of silver granules containing selenium and sulfur in the intestinal wall of rats exposed to either of the silver forms suggests a common mechanism of their formation. Additional studies however, are needed to gain further insight into the underlying mechanisms of the granule formation, and to clarify whether AgNPs dissolve in the gastrointestinal system and/or become absorbed and translocate as intact nanoparticles to organs and tissues.
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spelling pubmed-31231732011-06-25 Distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate Loeschner, Katrin Hadrup, Niels Qvortrup, Klaus Larsen, Agnete Gao, Xueyun Vogel, Ulla Mortensen, Alicja Lam, Henrik Rye Larsen, Erik H Part Fibre Toxicol Research BACKGROUND: The study investigated the distribution of silver after 28 days repeated oral administration of silver nanoparticles (AgNPs) and silver acetate (AgAc) to rats. Oral administration is a relevant route of exposure because of the use of silver nanoparticles in products related to food and food contact materials. RESULTS: AgNPs were synthesized with a size distribution of 14 ± 4 nm in diameter (90% of the nanoparticle volume) and stabilized in aqueous suspension by the polymer polyvinylpyrrolidone (PVP). The AgNPs remained stable throughout the duration of the 28-day oral toxicity study in rats. The organ distribution pattern of silver following administration of AgNPs and AgAc was similar. However the absolute silver concentrations in tissues were lower following oral exposure to AgNPs. This was in agreement with an indication of a higher fecal excretion following administration of AgNPs. Besides the intestinal system, the largest silver concentrations were detected in the liver and kidneys. Silver was also found in the lungs and brain. Autometallographic (AMG) staining revealed a similar cellular localization of silver in ileum, liver, and kidney tissue in rats exposed to AgNPs or AgAc. Using transmission electron microscopy (TEM), nanosized granules were detected in the ileum of animals exposed to AgNPs or AgAc and were mainly located in the basal lamina of the ileal epithelium and in lysosomes of macrophages within the lamina propria. Using energy dispersive x-ray spectroscopy it was shown that the granules in lysosomes consisted of silver, selenium, and sulfur for both AgNP and AgAc exposed rats. The diameter of the deposited granules was in the same size range as that of the administered AgNPs. No silver granules were detected by TEM in the liver. CONCLUSIONS: The results of the present study demonstrate that the organ distribution of silver was similar when AgNPs or AgAc were administered orally to rats. The presence of silver granules containing selenium and sulfur in the intestinal wall of rats exposed to either of the silver forms suggests a common mechanism of their formation. Additional studies however, are needed to gain further insight into the underlying mechanisms of the granule formation, and to clarify whether AgNPs dissolve in the gastrointestinal system and/or become absorbed and translocate as intact nanoparticles to organs and tissues. BioMed Central 2011-06-01 /pmc/articles/PMC3123173/ /pubmed/21631937 http://dx.doi.org/10.1186/1743-8977-8-18 Text en Copyright ©2011 Loeschner 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
Loeschner, Katrin
Hadrup, Niels
Qvortrup, Klaus
Larsen, Agnete
Gao, Xueyun
Vogel, Ulla
Mortensen, Alicja
Lam, Henrik Rye
Larsen, Erik H
Distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate
title Distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate
title_full Distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate
title_fullStr Distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate
title_full_unstemmed Distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate
title_short Distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate
title_sort distribution of silver in rats following 28 days of repeated oral exposure to silver nanoparticles or silver acetate
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123173/
https://www.ncbi.nlm.nih.gov/pubmed/21631937
http://dx.doi.org/10.1186/1743-8977-8-18
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