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In Vitro and In Vivo Short-Term Pulmonary Toxicity of Differently Sized Colloidal Amorphous SiO(2)

In vitro prediction of inflammatory lung effects of well-dispersed nanomaterials is challenging. Here, the in vitro effects of four colloidal amorphous SiO(2) nanomaterials that differed only by their primary particle size (9, 15, 30, and 55 nm) were analyzed using the rat NR8383 alveolar macrophage...

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Autores principales: Wiemann, Martin, Sauer, Ursula G., Vennemann, Antje, Bäcker, Sandra, Keller, Johannes-Georg, Ma-Hock, Lan, Wohlleben, Wendel, Landsiedel, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5869651/
https://www.ncbi.nlm.nih.gov/pubmed/29534009
http://dx.doi.org/10.3390/nano8030160
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author Wiemann, Martin
Sauer, Ursula G.
Vennemann, Antje
Bäcker, Sandra
Keller, Johannes-Georg
Ma-Hock, Lan
Wohlleben, Wendel
Landsiedel, Robert
author_facet Wiemann, Martin
Sauer, Ursula G.
Vennemann, Antje
Bäcker, Sandra
Keller, Johannes-Georg
Ma-Hock, Lan
Wohlleben, Wendel
Landsiedel, Robert
author_sort Wiemann, Martin
collection PubMed
description In vitro prediction of inflammatory lung effects of well-dispersed nanomaterials is challenging. Here, the in vitro effects of four colloidal amorphous SiO(2) nanomaterials that differed only by their primary particle size (9, 15, 30, and 55 nm) were analyzed using the rat NR8383 alveolar macrophage (AM) assay. Data were compared to effects of single doses of 15 nm and 55 nm SiO(2) intratracheally instilled in rat lungs. In vitro, all four elicited the release of concentration-dependent lactate dehydrogenase, β-glucuronidase, and tumor necrosis factor alpha, and the two smaller materials also released H(2)O(2). All effects were size-dependent. Since the colloidal SiO(2) remained well-dispersed in serum-free in vitro conditions, effective particle concentrations reaching the cells were estimated using different models. Evaluating the effective concentration–based in vitro effects using the Decision-making framework for the grouping and testing of nanomaterials, all four nanomaterials were assigned as “active.” This assignment and the size dependency of effects were consistent with the outcomes of intratracheal instillation studies and available short-term rat inhalation data for 15 nm SiO(2). The study confirms the applicability of the NR8383 AM assay to assessing colloidal SiO(2) but underlines the need to estimate and consider the effective concentration of such well-dispersed test materials.
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spelling pubmed-58696512018-03-28 In Vitro and In Vivo Short-Term Pulmonary Toxicity of Differently Sized Colloidal Amorphous SiO(2) Wiemann, Martin Sauer, Ursula G. Vennemann, Antje Bäcker, Sandra Keller, Johannes-Georg Ma-Hock, Lan Wohlleben, Wendel Landsiedel, Robert Nanomaterials (Basel) Article In vitro prediction of inflammatory lung effects of well-dispersed nanomaterials is challenging. Here, the in vitro effects of four colloidal amorphous SiO(2) nanomaterials that differed only by their primary particle size (9, 15, 30, and 55 nm) were analyzed using the rat NR8383 alveolar macrophage (AM) assay. Data were compared to effects of single doses of 15 nm and 55 nm SiO(2) intratracheally instilled in rat lungs. In vitro, all four elicited the release of concentration-dependent lactate dehydrogenase, β-glucuronidase, and tumor necrosis factor alpha, and the two smaller materials also released H(2)O(2). All effects were size-dependent. Since the colloidal SiO(2) remained well-dispersed in serum-free in vitro conditions, effective particle concentrations reaching the cells were estimated using different models. Evaluating the effective concentration–based in vitro effects using the Decision-making framework for the grouping and testing of nanomaterials, all four nanomaterials were assigned as “active.” This assignment and the size dependency of effects were consistent with the outcomes of intratracheal instillation studies and available short-term rat inhalation data for 15 nm SiO(2). The study confirms the applicability of the NR8383 AM assay to assessing colloidal SiO(2) but underlines the need to estimate and consider the effective concentration of such well-dispersed test materials. MDPI 2018-03-13 /pmc/articles/PMC5869651/ /pubmed/29534009 http://dx.doi.org/10.3390/nano8030160 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wiemann, Martin
Sauer, Ursula G.
Vennemann, Antje
Bäcker, Sandra
Keller, Johannes-Georg
Ma-Hock, Lan
Wohlleben, Wendel
Landsiedel, Robert
In Vitro and In Vivo Short-Term Pulmonary Toxicity of Differently Sized Colloidal Amorphous SiO(2)
title In Vitro and In Vivo Short-Term Pulmonary Toxicity of Differently Sized Colloidal Amorphous SiO(2)
title_full In Vitro and In Vivo Short-Term Pulmonary Toxicity of Differently Sized Colloidal Amorphous SiO(2)
title_fullStr In Vitro and In Vivo Short-Term Pulmonary Toxicity of Differently Sized Colloidal Amorphous SiO(2)
title_full_unstemmed In Vitro and In Vivo Short-Term Pulmonary Toxicity of Differently Sized Colloidal Amorphous SiO(2)
title_short In Vitro and In Vivo Short-Term Pulmonary Toxicity of Differently Sized Colloidal Amorphous SiO(2)
title_sort in vitro and in vivo short-term pulmonary toxicity of differently sized colloidal amorphous sio(2)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5869651/
https://www.ncbi.nlm.nih.gov/pubmed/29534009
http://dx.doi.org/10.3390/nano8030160
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