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Oral absorption of PEG-coated versus uncoated gold nanospheres: does agglomeration matter?
BACKGROUND: Particle size is thought to be a critical factor affecting the bioavailability of nanoparticles following oral exposure. Nearly all studies of nanoparticle bioavailability focus on characterization of the primary particle size of the material as supplied or as dosed, and not on agglomera...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396175/ https://www.ncbi.nlm.nih.gov/pubmed/25884802 http://dx.doi.org/10.1186/s12989-015-0085-5 |
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author | Hinkley, Georgia K Carpinone, Paul Munson, John W Powers, Kevin W Roberts, Stephen M |
author_facet | Hinkley, Georgia K Carpinone, Paul Munson, John W Powers, Kevin W Roberts, Stephen M |
author_sort | Hinkley, Georgia K |
collection | PubMed |
description | BACKGROUND: Particle size is thought to be a critical factor affecting the bioavailability of nanoparticles following oral exposure. Nearly all studies of nanoparticle bioavailability focus on characterization of the primary particle size of the material as supplied or as dosed, and not on agglomeration behavior within the gastrointestinal tract, which is presumably most relevant for absorption. METHODS: In the study reported here, snapshots of agglomeration behavior of gold nanospheres were evaluated in vivo throughout the gastrointestinal tract using transmission electron microscopy. Agglomeration state within the gastrointestinal tract was then used to help explain differences in gastrointestinal particle absorption, as indicated by tissue levels of gold detected using inductively coupled plasma mass spectrometry. Mice were dosed (10 mg/kg) with either 23 nm PEG-coated or uncoated gold nanospheres. RESULTS: Transmission electron microscopy demonstrates that PEG-coated gold nanoparticles can be observed as primary, un-agglomerated particles throughout the gastrointestinal tract and feces of dosed animals. In contrast, uncoated gold nanoparticles were observed to form agglomerates of several hundred nanometers in all tissues and feces. Inductively coupled plasma mass spectrometry shows significantly higher levels of gold in tissues from animals dosed with PEG-coated versus uncoated 23 nm gold nanoparticles. Retention of particles after a single oral gavage was also very high, with all tissues of animals dosed with PEG-coated particles having detectable levels of gold at 30 days following exposure. CONCLUSIONS: Qualitative observation of these particles in vivo shows that dispersed PEG-coated particles are able to reach the absorptive tissues of the intestine while agglomerated uncoated particles are sequestered in the lumen of these tissues. However, the large differences observed for in vivo agglomeration behavior were not reflected in oral absorption, as indicated by gold tissue levels. Additional factors, such as surface chemistry, may have played a more important role than in vivo particle size and should be investigated further. |
format | Online Article Text |
id | pubmed-4396175 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43961752015-04-15 Oral absorption of PEG-coated versus uncoated gold nanospheres: does agglomeration matter? Hinkley, Georgia K Carpinone, Paul Munson, John W Powers, Kevin W Roberts, Stephen M Part Fibre Toxicol Research BACKGROUND: Particle size is thought to be a critical factor affecting the bioavailability of nanoparticles following oral exposure. Nearly all studies of nanoparticle bioavailability focus on characterization of the primary particle size of the material as supplied or as dosed, and not on agglomeration behavior within the gastrointestinal tract, which is presumably most relevant for absorption. METHODS: In the study reported here, snapshots of agglomeration behavior of gold nanospheres were evaluated in vivo throughout the gastrointestinal tract using transmission electron microscopy. Agglomeration state within the gastrointestinal tract was then used to help explain differences in gastrointestinal particle absorption, as indicated by tissue levels of gold detected using inductively coupled plasma mass spectrometry. Mice were dosed (10 mg/kg) with either 23 nm PEG-coated or uncoated gold nanospheres. RESULTS: Transmission electron microscopy demonstrates that PEG-coated gold nanoparticles can be observed as primary, un-agglomerated particles throughout the gastrointestinal tract and feces of dosed animals. In contrast, uncoated gold nanoparticles were observed to form agglomerates of several hundred nanometers in all tissues and feces. Inductively coupled plasma mass spectrometry shows significantly higher levels of gold in tissues from animals dosed with PEG-coated versus uncoated 23 nm gold nanoparticles. Retention of particles after a single oral gavage was also very high, with all tissues of animals dosed with PEG-coated particles having detectable levels of gold at 30 days following exposure. CONCLUSIONS: Qualitative observation of these particles in vivo shows that dispersed PEG-coated particles are able to reach the absorptive tissues of the intestine while agglomerated uncoated particles are sequestered in the lumen of these tissues. However, the large differences observed for in vivo agglomeration behavior were not reflected in oral absorption, as indicated by gold tissue levels. Additional factors, such as surface chemistry, may have played a more important role than in vivo particle size and should be investigated further. BioMed Central 2015-03-25 /pmc/articles/PMC4396175/ /pubmed/25884802 http://dx.doi.org/10.1186/s12989-015-0085-5 Text en © Hinkley et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Hinkley, Georgia K Carpinone, Paul Munson, John W Powers, Kevin W Roberts, Stephen M Oral absorption of PEG-coated versus uncoated gold nanospheres: does agglomeration matter? |
title | Oral absorption of PEG-coated versus uncoated gold nanospheres: does agglomeration matter? |
title_full | Oral absorption of PEG-coated versus uncoated gold nanospheres: does agglomeration matter? |
title_fullStr | Oral absorption of PEG-coated versus uncoated gold nanospheres: does agglomeration matter? |
title_full_unstemmed | Oral absorption of PEG-coated versus uncoated gold nanospheres: does agglomeration matter? |
title_short | Oral absorption of PEG-coated versus uncoated gold nanospheres: does agglomeration matter? |
title_sort | oral absorption of peg-coated versus uncoated gold nanospheres: does agglomeration matter? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4396175/ https://www.ncbi.nlm.nih.gov/pubmed/25884802 http://dx.doi.org/10.1186/s12989-015-0085-5 |
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