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Polymer coating on carbon nanotubes into Durobeads is a novel strategy for human environmental safety
Carbon nanotubes (CNTs) have attracted much business interest in industrial applications due to their high electrical and heat conductivities while being both durable and versatile. However, multiwall CNTs (MWCNTs) of ~50 nm diameter (NT50) have been shown to cause mesothelioma in rodents after dire...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nagoya University
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295439/ https://www.ncbi.nlm.nih.gov/pubmed/30587874 http://dx.doi.org/10.18999/nagjms.80.4.597 |
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author | Ito, Fumiya Hisashi, Hideyuki Toyokuni, Shinya |
author_facet | Ito, Fumiya Hisashi, Hideyuki Toyokuni, Shinya |
author_sort | Ito, Fumiya |
collection | PubMed |
description | Carbon nanotubes (CNTs) have attracted much business interest in industrial applications due to their high electrical and heat conductivities while being both durable and versatile. However, multiwall CNTs (MWCNTs) of ~50 nm diameter (NT50) have been shown to cause mesothelioma in rodents after direct exposure to mesothelial cells, and thus were classified as a Group 2B carcinogen to humans, which requires considerable regulations for use. In contrast, tangled MWCNTs of ~15 nm diameter (NTtngl) are not carcinogenic to rats, indicating that the physical dimension linked with mesothelial cellular uptake is an important factor for human environmental risk. In the present study, hypothesizing that dustability is another distinct risk factor, for the first time, we evaluated the toxicity of CNT granules (Durobeads) that were generated with a polymer coating to mesothelial cells. Polymer coating induced prominent agglomeration and significantly suppressed the dustability of CNTs in a dose-dependent manner, with a 10% polymer coating resulting in 730 times less dustability. These CNT granules revealed significantly lower mesothelial uptake and cytotoxicity in comparison to NT50 in in vitro assays. Similarly, in in vivo analyses, CNT granules induced limited peritoneal inflammation 4 weeks after intraperitoneal injection, whereas NT50 caused severe fibrosing inflammation. Previously, we demonstrated that the severity of inflammation by intraperitoneal injection in the subacute studies are in agreement with the mesothelial carcinogenicity by CNTs. Therefore, we suggest that adding a polymer coating to CNTs provides another smart strategy for the safe use of CNTs. |
format | Online Article Text |
id | pubmed-6295439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nagoya University |
record_format | MEDLINE/PubMed |
spelling | pubmed-62954392018-12-26 Polymer coating on carbon nanotubes into Durobeads is a novel strategy for human environmental safety Ito, Fumiya Hisashi, Hideyuki Toyokuni, Shinya Nagoya J Med Sci Original Paper Carbon nanotubes (CNTs) have attracted much business interest in industrial applications due to their high electrical and heat conductivities while being both durable and versatile. However, multiwall CNTs (MWCNTs) of ~50 nm diameter (NT50) have been shown to cause mesothelioma in rodents after direct exposure to mesothelial cells, and thus were classified as a Group 2B carcinogen to humans, which requires considerable regulations for use. In contrast, tangled MWCNTs of ~15 nm diameter (NTtngl) are not carcinogenic to rats, indicating that the physical dimension linked with mesothelial cellular uptake is an important factor for human environmental risk. In the present study, hypothesizing that dustability is another distinct risk factor, for the first time, we evaluated the toxicity of CNT granules (Durobeads) that were generated with a polymer coating to mesothelial cells. Polymer coating induced prominent agglomeration and significantly suppressed the dustability of CNTs in a dose-dependent manner, with a 10% polymer coating resulting in 730 times less dustability. These CNT granules revealed significantly lower mesothelial uptake and cytotoxicity in comparison to NT50 in in vitro assays. Similarly, in in vivo analyses, CNT granules induced limited peritoneal inflammation 4 weeks after intraperitoneal injection, whereas NT50 caused severe fibrosing inflammation. Previously, we demonstrated that the severity of inflammation by intraperitoneal injection in the subacute studies are in agreement with the mesothelial carcinogenicity by CNTs. Therefore, we suggest that adding a polymer coating to CNTs provides another smart strategy for the safe use of CNTs. Nagoya University 2018-11 /pmc/articles/PMC6295439/ /pubmed/30587874 http://dx.doi.org/10.18999/nagjms.80.4.597 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Paper Ito, Fumiya Hisashi, Hideyuki Toyokuni, Shinya Polymer coating on carbon nanotubes into Durobeads is a novel strategy for human environmental safety |
title | Polymer coating on carbon nanotubes into Durobeads is a novel strategy for human environmental safety |
title_full | Polymer coating on carbon nanotubes into Durobeads is a novel strategy for human environmental safety |
title_fullStr | Polymer coating on carbon nanotubes into Durobeads is a novel strategy for human environmental safety |
title_full_unstemmed | Polymer coating on carbon nanotubes into Durobeads is a novel strategy for human environmental safety |
title_short | Polymer coating on carbon nanotubes into Durobeads is a novel strategy for human environmental safety |
title_sort | polymer coating on carbon nanotubes into durobeads is a novel strategy for human environmental safety |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6295439/ https://www.ncbi.nlm.nih.gov/pubmed/30587874 http://dx.doi.org/10.18999/nagjms.80.4.597 |
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