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Short- and Long-Term Effects of Prenatal Exposure to Iron Oxide Nanoparticles: Influence of Surface Charge and Dose on Developmental and Reproductive Toxicity

Iron oxide nanoparticles (NPs) are commonly utilized for biomedical, industrial, and commercial applications due to their unique properties and potential biocompatibility. However, little is known about how exposure to iron oxide NPs may affect susceptible populations such as pregnant women and deve...

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Autores principales: Di Bona, Kristin R., Xu, Yaolin, Gray, Marquita, Fair, Douglas, Hayles, Hunter, Milad, Luckie, Montes, Alex, Sherwood, Jennifer, Bao, Yuping, Rasco, Jane F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691173/
https://www.ncbi.nlm.nih.gov/pubmed/26694381
http://dx.doi.org/10.3390/ijms161226231
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author Di Bona, Kristin R.
Xu, Yaolin
Gray, Marquita
Fair, Douglas
Hayles, Hunter
Milad, Luckie
Montes, Alex
Sherwood, Jennifer
Bao, Yuping
Rasco, Jane F.
author_facet Di Bona, Kristin R.
Xu, Yaolin
Gray, Marquita
Fair, Douglas
Hayles, Hunter
Milad, Luckie
Montes, Alex
Sherwood, Jennifer
Bao, Yuping
Rasco, Jane F.
author_sort Di Bona, Kristin R.
collection PubMed
description Iron oxide nanoparticles (NPs) are commonly utilized for biomedical, industrial, and commercial applications due to their unique properties and potential biocompatibility. However, little is known about how exposure to iron oxide NPs may affect susceptible populations such as pregnant women and developing fetuses. To examine the influence of NP surface-charge and dose on the developmental toxicity of iron oxide NPs, Crl:CD1(ICR) (CD-1) mice were exposed to a single, low (10 mg/kg) or high (100 mg/kg) dose of positively-charged polyethyleneimine-Fe(2)O(3)-NPs (PEI-NPs), or negatively-charged poly(acrylic acid)-Fe(2)O(3)-NPs (PAA-NPs) during critical windows of organogenesis (gestation day (GD) 8, 9, or 10). A low dose of NPs, regardless of charge, did not induce toxicity. However, a high exposure led to charge-dependent fetal loss as well as morphological alterations of the uteri (both charges) and testes (positive only) of surviving offspring. Positively-charged PEI-NPs given later in organogenesis resulted in a combination of short-term fetal loss (42%) and long-term alterations in reproduction, including increased fetal loss for second generation matings (mice exposed in utero). Alternatively, negatively-charged PAA-NPs induced fetal loss (22%) earlier in organogenesis to a lesser degree than PEI-NPs with only mild alterations in offspring uterine histology observed in the long-term.
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spelling pubmed-46911732016-01-06 Short- and Long-Term Effects of Prenatal Exposure to Iron Oxide Nanoparticles: Influence of Surface Charge and Dose on Developmental and Reproductive Toxicity Di Bona, Kristin R. Xu, Yaolin Gray, Marquita Fair, Douglas Hayles, Hunter Milad, Luckie Montes, Alex Sherwood, Jennifer Bao, Yuping Rasco, Jane F. Int J Mol Sci Article Iron oxide nanoparticles (NPs) are commonly utilized for biomedical, industrial, and commercial applications due to their unique properties and potential biocompatibility. However, little is known about how exposure to iron oxide NPs may affect susceptible populations such as pregnant women and developing fetuses. To examine the influence of NP surface-charge and dose on the developmental toxicity of iron oxide NPs, Crl:CD1(ICR) (CD-1) mice were exposed to a single, low (10 mg/kg) or high (100 mg/kg) dose of positively-charged polyethyleneimine-Fe(2)O(3)-NPs (PEI-NPs), or negatively-charged poly(acrylic acid)-Fe(2)O(3)-NPs (PAA-NPs) during critical windows of organogenesis (gestation day (GD) 8, 9, or 10). A low dose of NPs, regardless of charge, did not induce toxicity. However, a high exposure led to charge-dependent fetal loss as well as morphological alterations of the uteri (both charges) and testes (positive only) of surviving offspring. Positively-charged PEI-NPs given later in organogenesis resulted in a combination of short-term fetal loss (42%) and long-term alterations in reproduction, including increased fetal loss for second generation matings (mice exposed in utero). Alternatively, negatively-charged PAA-NPs induced fetal loss (22%) earlier in organogenesis to a lesser degree than PEI-NPs with only mild alterations in offspring uterine histology observed in the long-term. MDPI 2015-12-18 /pmc/articles/PMC4691173/ /pubmed/26694381 http://dx.doi.org/10.3390/ijms161226231 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Di Bona, Kristin R.
Xu, Yaolin
Gray, Marquita
Fair, Douglas
Hayles, Hunter
Milad, Luckie
Montes, Alex
Sherwood, Jennifer
Bao, Yuping
Rasco, Jane F.
Short- and Long-Term Effects of Prenatal Exposure to Iron Oxide Nanoparticles: Influence of Surface Charge and Dose on Developmental and Reproductive Toxicity
title Short- and Long-Term Effects of Prenatal Exposure to Iron Oxide Nanoparticles: Influence of Surface Charge and Dose on Developmental and Reproductive Toxicity
title_full Short- and Long-Term Effects of Prenatal Exposure to Iron Oxide Nanoparticles: Influence of Surface Charge and Dose on Developmental and Reproductive Toxicity
title_fullStr Short- and Long-Term Effects of Prenatal Exposure to Iron Oxide Nanoparticles: Influence of Surface Charge and Dose on Developmental and Reproductive Toxicity
title_full_unstemmed Short- and Long-Term Effects of Prenatal Exposure to Iron Oxide Nanoparticles: Influence of Surface Charge and Dose on Developmental and Reproductive Toxicity
title_short Short- and Long-Term Effects of Prenatal Exposure to Iron Oxide Nanoparticles: Influence of Surface Charge and Dose on Developmental and Reproductive Toxicity
title_sort short- and long-term effects of prenatal exposure to iron oxide nanoparticles: influence of surface charge and dose on developmental and reproductive toxicity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691173/
https://www.ncbi.nlm.nih.gov/pubmed/26694381
http://dx.doi.org/10.3390/ijms161226231
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