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A proposed synergetic mechanism for metal fume fever involving ZnO and Fe(3)O(4) nanoparticles

Metal fumes fever (MFF) is an inflammatory condition, whose mechanism is yet unclear, associated with the inhalation of metal fumes, particularly zinc. In this study we investigate experimentally the hypothesis of a two-step mechanism of MFF onset: (1) the photocatalytic production of airborne hydro...

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Autores principales: Suárez, Guillaume, Niculita-Hirzel, Hélène, Correia, Daniela, Pralong, Jacques A., Vernez, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9485229/
https://www.ncbi.nlm.nih.gov/pubmed/36123527
http://dx.doi.org/10.1038/s41598-022-19956-1
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author Suárez, Guillaume
Niculita-Hirzel, Hélène
Correia, Daniela
Pralong, Jacques A.
Vernez, David
author_facet Suárez, Guillaume
Niculita-Hirzel, Hélène
Correia, Daniela
Pralong, Jacques A.
Vernez, David
author_sort Suárez, Guillaume
collection PubMed
description Metal fumes fever (MFF) is an inflammatory condition, whose mechanism is yet unclear, associated with the inhalation of metal fumes, particularly zinc. In this study we investigate experimentally the hypothesis of a two-step mechanism of MFF onset: (1) the photocatalytic production of airborne hydrogen peroxide (H(2)O(2)) via ZnO and (2) the production of hydroxyl radicals (HOׄ) through Fenton reaction via magnetite (Fe(3)O(4)) nanoparticles. Photocatalysis and Fenton reaction products were measured using a multiscattering-enhanced absorbance device and assessing the degradation of bromophenol blue with microplate photometry, respectively. We observed that in the presence of UV, ZnO produces 3 to 4-times more H(2)O(2) than UV alone or that non-UV irradiated ZnO. In the presence of biologically-relevant ligands, we also measured a Fenton reaction at physiological pH with either Fe(II), Fe(III) or Fe(3)O(4) nanoparticles. Our results support the hypothesis of a two-step mechanism of MFF onset, in which the prior presence of Fe in the lungs exacerbates the oxidative stress, triggered by the photocatalysis of ZnO, a situation that could occurs when welding galvanized steel. More broadly, this raises the question of the role of the Fenton mechanism in respiratory exposure to metal particles and its possible contribution to other lung diseases.
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spelling pubmed-94852292022-09-21 A proposed synergetic mechanism for metal fume fever involving ZnO and Fe(3)O(4) nanoparticles Suárez, Guillaume Niculita-Hirzel, Hélène Correia, Daniela Pralong, Jacques A. Vernez, David Sci Rep Article Metal fumes fever (MFF) is an inflammatory condition, whose mechanism is yet unclear, associated with the inhalation of metal fumes, particularly zinc. In this study we investigate experimentally the hypothesis of a two-step mechanism of MFF onset: (1) the photocatalytic production of airborne hydrogen peroxide (H(2)O(2)) via ZnO and (2) the production of hydroxyl radicals (HOׄ) through Fenton reaction via magnetite (Fe(3)O(4)) nanoparticles. Photocatalysis and Fenton reaction products were measured using a multiscattering-enhanced absorbance device and assessing the degradation of bromophenol blue with microplate photometry, respectively. We observed that in the presence of UV, ZnO produces 3 to 4-times more H(2)O(2) than UV alone or that non-UV irradiated ZnO. In the presence of biologically-relevant ligands, we also measured a Fenton reaction at physiological pH with either Fe(II), Fe(III) or Fe(3)O(4) nanoparticles. Our results support the hypothesis of a two-step mechanism of MFF onset, in which the prior presence of Fe in the lungs exacerbates the oxidative stress, triggered by the photocatalysis of ZnO, a situation that could occurs when welding galvanized steel. More broadly, this raises the question of the role of the Fenton mechanism in respiratory exposure to metal particles and its possible contribution to other lung diseases. Nature Publishing Group UK 2022-09-19 /pmc/articles/PMC9485229/ /pubmed/36123527 http://dx.doi.org/10.1038/s41598-022-19956-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Suárez, Guillaume
Niculita-Hirzel, Hélène
Correia, Daniela
Pralong, Jacques A.
Vernez, David
A proposed synergetic mechanism for metal fume fever involving ZnO and Fe(3)O(4) nanoparticles
title A proposed synergetic mechanism for metal fume fever involving ZnO and Fe(3)O(4) nanoparticles
title_full A proposed synergetic mechanism for metal fume fever involving ZnO and Fe(3)O(4) nanoparticles
title_fullStr A proposed synergetic mechanism for metal fume fever involving ZnO and Fe(3)O(4) nanoparticles
title_full_unstemmed A proposed synergetic mechanism for metal fume fever involving ZnO and Fe(3)O(4) nanoparticles
title_short A proposed synergetic mechanism for metal fume fever involving ZnO and Fe(3)O(4) nanoparticles
title_sort proposed synergetic mechanism for metal fume fever involving zno and fe(3)o(4) nanoparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9485229/
https://www.ncbi.nlm.nih.gov/pubmed/36123527
http://dx.doi.org/10.1038/s41598-022-19956-1
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