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Uptake of bright fluorophore core-silica shell nanoparticles by biological systems
Nanoparticles are used in a variety of consumer applications. Silica nanoparticles in particular are common, including as a component of foods. There are concerns that ingested nano-silica particles can cross the intestinal epithelium, enter the circulation, and accumulate in tissues and organs. Thu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345991/ https://www.ncbi.nlm.nih.gov/pubmed/25759579 http://dx.doi.org/10.2147/IJN.S76208 |
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author | Zane, Andrew McCracken, Christie Knight, Deborah A Young, Tanya Lutton, Anthony D Olesik, John W Waldman, W James Dutta, Prabir K |
author_facet | Zane, Andrew McCracken, Christie Knight, Deborah A Young, Tanya Lutton, Anthony D Olesik, John W Waldman, W James Dutta, Prabir K |
author_sort | Zane, Andrew |
collection | PubMed |
description | Nanoparticles are used in a variety of consumer applications. Silica nanoparticles in particular are common, including as a component of foods. There are concerns that ingested nano-silica particles can cross the intestinal epithelium, enter the circulation, and accumulate in tissues and organs. Thus, tracking these particles is of interest, and fluorescence spectroscopic methods are well-suited for this purpose. However, nanosilica is not fluorescent. In this article, we focus on core-silica shell nanoparticles, using fluorescent Rhodamine 6G, Rhodamine 800, or CdSe/CdS/ZnS quantum dots as the core. These stable fluorophore/silica nanoparticles had surface characteristics similar to those of commercial silica particles. Thus, they were used as model particles to examine internalization by cultured cells, including an epithelial cell line relevant to the gastrointestinal tract. Finally, these particles were administered to mice by gavage, and their presence in various organs, including stomach, small intestine, cecum, colon, kidney, lung, brain, and spleen, was examined. By combining confocal fluorescence microscopy with inductively coupled plasma mass spectrometry, the presence of nanoparticles, rather than their dissolved form, was established in liver tissues. |
format | Online Article Text |
id | pubmed-4345991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43459912015-03-10 Uptake of bright fluorophore core-silica shell nanoparticles by biological systems Zane, Andrew McCracken, Christie Knight, Deborah A Young, Tanya Lutton, Anthony D Olesik, John W Waldman, W James Dutta, Prabir K Int J Nanomedicine Original Research Nanoparticles are used in a variety of consumer applications. Silica nanoparticles in particular are common, including as a component of foods. There are concerns that ingested nano-silica particles can cross the intestinal epithelium, enter the circulation, and accumulate in tissues and organs. Thus, tracking these particles is of interest, and fluorescence spectroscopic methods are well-suited for this purpose. However, nanosilica is not fluorescent. In this article, we focus on core-silica shell nanoparticles, using fluorescent Rhodamine 6G, Rhodamine 800, or CdSe/CdS/ZnS quantum dots as the core. These stable fluorophore/silica nanoparticles had surface characteristics similar to those of commercial silica particles. Thus, they were used as model particles to examine internalization by cultured cells, including an epithelial cell line relevant to the gastrointestinal tract. Finally, these particles were administered to mice by gavage, and their presence in various organs, including stomach, small intestine, cecum, colon, kidney, lung, brain, and spleen, was examined. By combining confocal fluorescence microscopy with inductively coupled plasma mass spectrometry, the presence of nanoparticles, rather than their dissolved form, was established in liver tissues. Dove Medical Press 2015-02-20 /pmc/articles/PMC4345991/ /pubmed/25759579 http://dx.doi.org/10.2147/IJN.S76208 Text en © 2015 Zane et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Zane, Andrew McCracken, Christie Knight, Deborah A Young, Tanya Lutton, Anthony D Olesik, John W Waldman, W James Dutta, Prabir K Uptake of bright fluorophore core-silica shell nanoparticles by biological systems |
title | Uptake of bright fluorophore core-silica shell nanoparticles by biological systems |
title_full | Uptake of bright fluorophore core-silica shell nanoparticles by biological systems |
title_fullStr | Uptake of bright fluorophore core-silica shell nanoparticles by biological systems |
title_full_unstemmed | Uptake of bright fluorophore core-silica shell nanoparticles by biological systems |
title_short | Uptake of bright fluorophore core-silica shell nanoparticles by biological systems |
title_sort | uptake of bright fluorophore core-silica shell nanoparticles by biological systems |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4345991/ https://www.ncbi.nlm.nih.gov/pubmed/25759579 http://dx.doi.org/10.2147/IJN.S76208 |
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