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Simulated Gastric Digestion and In Vivo Intestinal Uptake of Orally Administered CuO Nanoparticles and TiO(2) E171 in Male and Female Rat Pups

Oral exposure to nanoparticles (NPs) during early life is an understudied area. The goals of this study were to evaluate the effect of pre-weaned rat gastric fluids on 50 nm CuO NPs and TiO(2) E171 in vitro, and to evaluate uptake in vivo. The NP uptake was studied in vivo in male and female Sprague...

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Autores principales: Mortensen, Ninell P., Moreno Caffaro, Maria, Aravamudhan, Shyam, Beeravalli, Lakshmi, Prattipati, Sharmista, Snyder, Rodney W., Watson, Scott L., Patel, Purvi R., Weber, Frank X., Montgomery, Stephanie A., Sumner, Susan J., Fennell, Timothy R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230348/
https://www.ncbi.nlm.nih.gov/pubmed/34199726
http://dx.doi.org/10.3390/nano11061487
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author Mortensen, Ninell P.
Moreno Caffaro, Maria
Aravamudhan, Shyam
Beeravalli, Lakshmi
Prattipati, Sharmista
Snyder, Rodney W.
Watson, Scott L.
Patel, Purvi R.
Weber, Frank X.
Montgomery, Stephanie A.
Sumner, Susan J.
Fennell, Timothy R.
author_facet Mortensen, Ninell P.
Moreno Caffaro, Maria
Aravamudhan, Shyam
Beeravalli, Lakshmi
Prattipati, Sharmista
Snyder, Rodney W.
Watson, Scott L.
Patel, Purvi R.
Weber, Frank X.
Montgomery, Stephanie A.
Sumner, Susan J.
Fennell, Timothy R.
author_sort Mortensen, Ninell P.
collection PubMed
description Oral exposure to nanoparticles (NPs) during early life is an understudied area. The goals of this study were to evaluate the effect of pre-weaned rat gastric fluids on 50 nm CuO NPs and TiO(2) E171 in vitro, and to evaluate uptake in vivo. The NP uptake was studied in vivo in male and female Sprague-Dawley rat pups following oral administration of four consecutive daily doses of 10 mg/kg CuO NPs, TiO(2) E171, or vehicle control (water) between postnatal day (PND) 7–10. Rat pups were sacrificed on either PND10 or PND21. Simulated digestion led to dissolution of CuO NPs at the later ages tested (PND14 and PND21, but not PND7). In vivo intestinal uptake of CuO NPs and TiO(2) E171 was observed by hyperspectral imaging of intestinal cross sections. Brightfield microscopy showed that the number of immune cells increased in the intestinal tissue following NP administration. Orally administered NPs led to low intestinal uptake of NPs and an increase in immune cells in the small and large intestine, suggesting that oral exposure to NPs during early life may lead to irritation or a low-grade inflammation. The long-term impact of increased immune cells in the intestinal tract during early life is unknown.
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spelling pubmed-82303482021-06-26 Simulated Gastric Digestion and In Vivo Intestinal Uptake of Orally Administered CuO Nanoparticles and TiO(2) E171 in Male and Female Rat Pups Mortensen, Ninell P. Moreno Caffaro, Maria Aravamudhan, Shyam Beeravalli, Lakshmi Prattipati, Sharmista Snyder, Rodney W. Watson, Scott L. Patel, Purvi R. Weber, Frank X. Montgomery, Stephanie A. Sumner, Susan J. Fennell, Timothy R. Nanomaterials (Basel) Article Oral exposure to nanoparticles (NPs) during early life is an understudied area. The goals of this study were to evaluate the effect of pre-weaned rat gastric fluids on 50 nm CuO NPs and TiO(2) E171 in vitro, and to evaluate uptake in vivo. The NP uptake was studied in vivo in male and female Sprague-Dawley rat pups following oral administration of four consecutive daily doses of 10 mg/kg CuO NPs, TiO(2) E171, or vehicle control (water) between postnatal day (PND) 7–10. Rat pups were sacrificed on either PND10 or PND21. Simulated digestion led to dissolution of CuO NPs at the later ages tested (PND14 and PND21, but not PND7). In vivo intestinal uptake of CuO NPs and TiO(2) E171 was observed by hyperspectral imaging of intestinal cross sections. Brightfield microscopy showed that the number of immune cells increased in the intestinal tissue following NP administration. Orally administered NPs led to low intestinal uptake of NPs and an increase in immune cells in the small and large intestine, suggesting that oral exposure to NPs during early life may lead to irritation or a low-grade inflammation. The long-term impact of increased immune cells in the intestinal tract during early life is unknown. MDPI 2021-06-04 /pmc/articles/PMC8230348/ /pubmed/34199726 http://dx.doi.org/10.3390/nano11061487 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mortensen, Ninell P.
Moreno Caffaro, Maria
Aravamudhan, Shyam
Beeravalli, Lakshmi
Prattipati, Sharmista
Snyder, Rodney W.
Watson, Scott L.
Patel, Purvi R.
Weber, Frank X.
Montgomery, Stephanie A.
Sumner, Susan J.
Fennell, Timothy R.
Simulated Gastric Digestion and In Vivo Intestinal Uptake of Orally Administered CuO Nanoparticles and TiO(2) E171 in Male and Female Rat Pups
title Simulated Gastric Digestion and In Vivo Intestinal Uptake of Orally Administered CuO Nanoparticles and TiO(2) E171 in Male and Female Rat Pups
title_full Simulated Gastric Digestion and In Vivo Intestinal Uptake of Orally Administered CuO Nanoparticles and TiO(2) E171 in Male and Female Rat Pups
title_fullStr Simulated Gastric Digestion and In Vivo Intestinal Uptake of Orally Administered CuO Nanoparticles and TiO(2) E171 in Male and Female Rat Pups
title_full_unstemmed Simulated Gastric Digestion and In Vivo Intestinal Uptake of Orally Administered CuO Nanoparticles and TiO(2) E171 in Male and Female Rat Pups
title_short Simulated Gastric Digestion and In Vivo Intestinal Uptake of Orally Administered CuO Nanoparticles and TiO(2) E171 in Male and Female Rat Pups
title_sort simulated gastric digestion and in vivo intestinal uptake of orally administered cuo nanoparticles and tio(2) e171 in male and female rat pups
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230348/
https://www.ncbi.nlm.nih.gov/pubmed/34199726
http://dx.doi.org/10.3390/nano11061487
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