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Mimicking exposures to acute and lifetime concentrations of inhaled silver nanoparticles by two different in vitro approaches

In the emerging market of nano-sized products, silver nanoparticles (Ag NPs) are widely used due to their antimicrobial properties. Human interaction with Ag NPs can occur through the lung, skin, gastrointestinal tract, and bloodstream. However, the inhalation of Ag NP aerosols is a primary concern....

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Autores principales: Herzog, Fabian, Loza, Kateryna, Balog, Sandor, Clift, Martin J D, Epple, Matthias, Gehr, Peter, Petri-Fink, Alke, Rothen-Rutishauser, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168965/
https://www.ncbi.nlm.nih.gov/pubmed/25247119
http://dx.doi.org/10.3762/bjnano.5.149
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author Herzog, Fabian
Loza, Kateryna
Balog, Sandor
Clift, Martin J D
Epple, Matthias
Gehr, Peter
Petri-Fink, Alke
Rothen-Rutishauser, Barbara
author_facet Herzog, Fabian
Loza, Kateryna
Balog, Sandor
Clift, Martin J D
Epple, Matthias
Gehr, Peter
Petri-Fink, Alke
Rothen-Rutishauser, Barbara
author_sort Herzog, Fabian
collection PubMed
description In the emerging market of nano-sized products, silver nanoparticles (Ag NPs) are widely used due to their antimicrobial properties. Human interaction with Ag NPs can occur through the lung, skin, gastrointestinal tract, and bloodstream. However, the inhalation of Ag NP aerosols is a primary concern. To study the possible effects of inhaled Ag NPs, an in vitro triple cell co-culture model of the human alveolar/airway barrier (A549 epithelial cells, human peripheral blood monocyte derived dendritic and macrophage cells) together with an air–liquid interface cell exposure (ALICE) system was used in order to reflect a real-life exposure scenario. Cells were exposed at the air–liquid interface (ALI) to 0.03, 0.3, and 3 µg Ag/cm(2) of Ag NPs (diameter 100 nm; coated with polyvinylpyrrolidone: PVP). Ag NPs were found to be highly aggregated within ALI exposed cells with no impairment of cell morphology. Furthermore, a significant increase in release of cytotoxic (LDH), oxidative stress (SOD-1, HMOX-1) or pro-inflammatory markers (TNF-α, IL-8) was absent. As a comparison, cells were exposed to Ag NPs in submerged conditions to 10, 20, and 30 µg Ag/mL. The deposited dose per surface area was estimated by using a dosimetry model (ISDD) to directly compare submerged vs ALI exposure concentrations after 4 and 24 h. Unlike ALI exposures, the two highest concentrations under submerged conditions promoted a cytotoxic and pro-inflammatory response after 24 h. Interestingly, when cell cultures were co-incubated with lipopolysaccharide (LPS), no synergistic inflammatory effects were observed. By using two different exposure scenarios it has been shown that the ALI as well as the suspension conditions for the lower concentrations after 4 h, reflecting real-life concentrations of an acute 24 h exposure, did not induce any adverse effects in a complex 3D model mimicking the human alveolar/airway barrier. However, the highest concentrations used in the ALI setup, as well as all concentrations under submerged conditions after 24 h, reflecting more of a chronic lifetime exposure concentration, showed cytotoxic as well as pro-inflammatory effects. In conclusion, more studies need to address long-term and chronic Ag NP exposure effects.
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spelling pubmed-41689652014-09-22 Mimicking exposures to acute and lifetime concentrations of inhaled silver nanoparticles by two different in vitro approaches Herzog, Fabian Loza, Kateryna Balog, Sandor Clift, Martin J D Epple, Matthias Gehr, Peter Petri-Fink, Alke Rothen-Rutishauser, Barbara Beilstein J Nanotechnol Full Research Paper In the emerging market of nano-sized products, silver nanoparticles (Ag NPs) are widely used due to their antimicrobial properties. Human interaction with Ag NPs can occur through the lung, skin, gastrointestinal tract, and bloodstream. However, the inhalation of Ag NP aerosols is a primary concern. To study the possible effects of inhaled Ag NPs, an in vitro triple cell co-culture model of the human alveolar/airway barrier (A549 epithelial cells, human peripheral blood monocyte derived dendritic and macrophage cells) together with an air–liquid interface cell exposure (ALICE) system was used in order to reflect a real-life exposure scenario. Cells were exposed at the air–liquid interface (ALI) to 0.03, 0.3, and 3 µg Ag/cm(2) of Ag NPs (diameter 100 nm; coated with polyvinylpyrrolidone: PVP). Ag NPs were found to be highly aggregated within ALI exposed cells with no impairment of cell morphology. Furthermore, a significant increase in release of cytotoxic (LDH), oxidative stress (SOD-1, HMOX-1) or pro-inflammatory markers (TNF-α, IL-8) was absent. As a comparison, cells were exposed to Ag NPs in submerged conditions to 10, 20, and 30 µg Ag/mL. The deposited dose per surface area was estimated by using a dosimetry model (ISDD) to directly compare submerged vs ALI exposure concentrations after 4 and 24 h. Unlike ALI exposures, the two highest concentrations under submerged conditions promoted a cytotoxic and pro-inflammatory response after 24 h. Interestingly, when cell cultures were co-incubated with lipopolysaccharide (LPS), no synergistic inflammatory effects were observed. By using two different exposure scenarios it has been shown that the ALI as well as the suspension conditions for the lower concentrations after 4 h, reflecting real-life concentrations of an acute 24 h exposure, did not induce any adverse effects in a complex 3D model mimicking the human alveolar/airway barrier. However, the highest concentrations used in the ALI setup, as well as all concentrations under submerged conditions after 24 h, reflecting more of a chronic lifetime exposure concentration, showed cytotoxic as well as pro-inflammatory effects. In conclusion, more studies need to address long-term and chronic Ag NP exposure effects. Beilstein-Institut 2014-08-26 /pmc/articles/PMC4168965/ /pubmed/25247119 http://dx.doi.org/10.3762/bjnano.5.149 Text en Copyright © 2014, Herzog et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjnano/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Nanotechnology terms and conditions: (https://www.beilstein-journals.org/bjnano/terms)
spellingShingle Full Research Paper
Herzog, Fabian
Loza, Kateryna
Balog, Sandor
Clift, Martin J D
Epple, Matthias
Gehr, Peter
Petri-Fink, Alke
Rothen-Rutishauser, Barbara
Mimicking exposures to acute and lifetime concentrations of inhaled silver nanoparticles by two different in vitro approaches
title Mimicking exposures to acute and lifetime concentrations of inhaled silver nanoparticles by two different in vitro approaches
title_full Mimicking exposures to acute and lifetime concentrations of inhaled silver nanoparticles by two different in vitro approaches
title_fullStr Mimicking exposures to acute and lifetime concentrations of inhaled silver nanoparticles by two different in vitro approaches
title_full_unstemmed Mimicking exposures to acute and lifetime concentrations of inhaled silver nanoparticles by two different in vitro approaches
title_short Mimicking exposures to acute and lifetime concentrations of inhaled silver nanoparticles by two different in vitro approaches
title_sort mimicking exposures to acute and lifetime concentrations of inhaled silver nanoparticles by two different in vitro approaches
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168965/
https://www.ncbi.nlm.nih.gov/pubmed/25247119
http://dx.doi.org/10.3762/bjnano.5.149
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