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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...

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Autores principales: Zane, Andrew, McCracken, Christie, Knight, Deborah A, Young, Tanya, Lutton, Anthony D, Olesik, John W, Waldman, W James, Dutta, Prabir K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
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.
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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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