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Aerogels are not regulated as nanomaterials, but can be assessed by tiered testing and grouping strategies for nanomaterials

Aerogels contribute to an increasing number of novel applications due to many unique properties, such as high porosity and low density. They outperform most other insulation materials, and some are also useful as carriers in food or pharma applications. Aerogels are not nanomaterials by the REACH de...

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Autores principales: Keller, Johannes G., Wiemann, Martin, Gröters, Sibylle, Werle, Kai, Vennemann, Antje, Landsiedel, Robert, Wohlleben, Wendel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: RSC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9419173/
https://www.ncbi.nlm.nih.gov/pubmed/36133012
http://dx.doi.org/10.1039/d1na00044f
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author Keller, Johannes G.
Wiemann, Martin
Gröters, Sibylle
Werle, Kai
Vennemann, Antje
Landsiedel, Robert
Wohlleben, Wendel
author_facet Keller, Johannes G.
Wiemann, Martin
Gröters, Sibylle
Werle, Kai
Vennemann, Antje
Landsiedel, Robert
Wohlleben, Wendel
author_sort Keller, Johannes G.
collection PubMed
description Aerogels contribute to an increasing number of novel applications due to many unique properties, such as high porosity and low density. They outperform most other insulation materials, and some are also useful as carriers in food or pharma applications. Aerogels are not nanomaterials by the REACH definition but retain properties of nanoscale structures. Here we applied a testing strategy in three tiers. In Tier 1, we examined a panel of 19 aerogels (functionalized chitosan, alginate, pyrolyzed carbon, silicate, cellulose, polyurethane) for their biosolubility, and oxidative potential. Biosolubility was very limited except for some alginate and silicate aerogels. Oxidative potential, as by the ferric reduction ability of human serum (FRAS), was very low except for one chitosan and pyrolyzed carbon, both of which were <10% of the positive control Mn(2)O(3). Five aerogels were further subjected to the Tier 2 alveolar macrophage assay, which revealed no in vitro cytotoxicity, except for silicate and polyurethane that induced increases in tumor necrosis factor α. Insufficiently similar aerogels were excluded from a candidate group, and a worst case identified. In the Tier 3 in vivo instillation, polyurethane (0.3 to 2.4 mg) elicited dose-dependent but reversible enzyme changes in lung lavage fluid on day 3, but no significant inflammatory effects. Overall, the results show a very low inherent toxicity of aerogels and support a categorization based on similarities in Tier 1 and Tier 2. This exemplifies how nanosafety concepts and methods developed on particles can be applied to specific concerns on advanced materials that contain or release nanostructures.
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spelling pubmed-94191732022-09-20 Aerogels are not regulated as nanomaterials, but can be assessed by tiered testing and grouping strategies for nanomaterials Keller, Johannes G. Wiemann, Martin Gröters, Sibylle Werle, Kai Vennemann, Antje Landsiedel, Robert Wohlleben, Wendel Nanoscale Adv Chemistry Aerogels contribute to an increasing number of novel applications due to many unique properties, such as high porosity and low density. They outperform most other insulation materials, and some are also useful as carriers in food or pharma applications. Aerogels are not nanomaterials by the REACH definition but retain properties of nanoscale structures. Here we applied a testing strategy in three tiers. In Tier 1, we examined a panel of 19 aerogels (functionalized chitosan, alginate, pyrolyzed carbon, silicate, cellulose, polyurethane) for their biosolubility, and oxidative potential. Biosolubility was very limited except for some alginate and silicate aerogels. Oxidative potential, as by the ferric reduction ability of human serum (FRAS), was very low except for one chitosan and pyrolyzed carbon, both of which were <10% of the positive control Mn(2)O(3). Five aerogels were further subjected to the Tier 2 alveolar macrophage assay, which revealed no in vitro cytotoxicity, except for silicate and polyurethane that induced increases in tumor necrosis factor α. Insufficiently similar aerogels were excluded from a candidate group, and a worst case identified. In the Tier 3 in vivo instillation, polyurethane (0.3 to 2.4 mg) elicited dose-dependent but reversible enzyme changes in lung lavage fluid on day 3, but no significant inflammatory effects. Overall, the results show a very low inherent toxicity of aerogels and support a categorization based on similarities in Tier 1 and Tier 2. This exemplifies how nanosafety concepts and methods developed on particles can be applied to specific concerns on advanced materials that contain or release nanostructures. RSC 2021-05-19 /pmc/articles/PMC9419173/ /pubmed/36133012 http://dx.doi.org/10.1039/d1na00044f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Keller, Johannes G.
Wiemann, Martin
Gröters, Sibylle
Werle, Kai
Vennemann, Antje
Landsiedel, Robert
Wohlleben, Wendel
Aerogels are not regulated as nanomaterials, but can be assessed by tiered testing and grouping strategies for nanomaterials
title Aerogels are not regulated as nanomaterials, but can be assessed by tiered testing and grouping strategies for nanomaterials
title_full Aerogels are not regulated as nanomaterials, but can be assessed by tiered testing and grouping strategies for nanomaterials
title_fullStr Aerogels are not regulated as nanomaterials, but can be assessed by tiered testing and grouping strategies for nanomaterials
title_full_unstemmed Aerogels are not regulated as nanomaterials, but can be assessed by tiered testing and grouping strategies for nanomaterials
title_short Aerogels are not regulated as nanomaterials, but can be assessed by tiered testing and grouping strategies for nanomaterials
title_sort aerogels are not regulated as nanomaterials, but can be assessed by tiered testing and grouping strategies for nanomaterials
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9419173/
https://www.ncbi.nlm.nih.gov/pubmed/36133012
http://dx.doi.org/10.1039/d1na00044f
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