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Anti-viral organic coatings for high touch surfaces based on smart-release, Cu(2+) containing pigments
Viruses such as SARS-CoV-2 can remain viable on solid surfaces for up to one week, hence fomites are a potential route of exposure to infectious virus. Copper has well documented antiviral properties that could limit this problem, however practical deployment of copper surfaces has been limited due...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier B.V.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393488/ https://www.ncbi.nlm.nih.gov/pubmed/36035655 http://dx.doi.org/10.1016/j.porgcoat.2022.107135 |
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author | Saud, Zack Richards, Calvin A.J. Williams, Geraint Stanton, Richard J. |
author_facet | Saud, Zack Richards, Calvin A.J. Williams, Geraint Stanton, Richard J. |
author_sort | Saud, Zack |
collection | PubMed |
description | Viruses such as SARS-CoV-2 can remain viable on solid surfaces for up to one week, hence fomites are a potential route of exposure to infectious virus. Copper has well documented antiviral properties that could limit this problem, however practical deployment of copper surfaces has been limited due to the associated costs and the incompatibility of copper metal in specific environments and conditions. We therefore developed an organic coating containing an intelligent-release Cu(2+) pigment based on a cation exchange resin. Organic coatings containing a 50 % weight or higher loading of smart-release pigment were capable of completely inactivating (>6 log reduction in titre) SARS-CoV-2 within 4 h of incubation. Importantly these organic coatings demonstrated a significantly enhanced ability to inactivate SARS-CoV-2 compared to metallic copper and un-pigmented material. Furthermore, the presence of contaminating proteins inhibited the antiviral activity of metallic copper, but the intelligent-release Cu(2+) pigment was unaffected. The approach of using a very basic paint system, based on a polymer binder embedded with “smart release” pigment containing an anti-viral agent which is liberated by ion-exchange, holds significant promise as a cost effective and rapidly deployed coating to confer virus inactivating capability to high touch surfaces. |
format | Online Article Text |
id | pubmed-9393488 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Authors. Published by Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93934882022-08-22 Anti-viral organic coatings for high touch surfaces based on smart-release, Cu(2+) containing pigments Saud, Zack Richards, Calvin A.J. Williams, Geraint Stanton, Richard J. Prog Org Coat Article Viruses such as SARS-CoV-2 can remain viable on solid surfaces for up to one week, hence fomites are a potential route of exposure to infectious virus. Copper has well documented antiviral properties that could limit this problem, however practical deployment of copper surfaces has been limited due to the associated costs and the incompatibility of copper metal in specific environments and conditions. We therefore developed an organic coating containing an intelligent-release Cu(2+) pigment based on a cation exchange resin. Organic coatings containing a 50 % weight or higher loading of smart-release pigment were capable of completely inactivating (>6 log reduction in titre) SARS-CoV-2 within 4 h of incubation. Importantly these organic coatings demonstrated a significantly enhanced ability to inactivate SARS-CoV-2 compared to metallic copper and un-pigmented material. Furthermore, the presence of contaminating proteins inhibited the antiviral activity of metallic copper, but the intelligent-release Cu(2+) pigment was unaffected. The approach of using a very basic paint system, based on a polymer binder embedded with “smart release” pigment containing an anti-viral agent which is liberated by ion-exchange, holds significant promise as a cost effective and rapidly deployed coating to confer virus inactivating capability to high touch surfaces. The Authors. Published by Elsevier B.V. 2022-11 2022-08-22 /pmc/articles/PMC9393488/ /pubmed/36035655 http://dx.doi.org/10.1016/j.porgcoat.2022.107135 Text en © 2022 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Saud, Zack Richards, Calvin A.J. Williams, Geraint Stanton, Richard J. Anti-viral organic coatings for high touch surfaces based on smart-release, Cu(2+) containing pigments |
title | Anti-viral organic coatings for high touch surfaces based on smart-release, Cu(2+) containing pigments |
title_full | Anti-viral organic coatings for high touch surfaces based on smart-release, Cu(2+) containing pigments |
title_fullStr | Anti-viral organic coatings for high touch surfaces based on smart-release, Cu(2+) containing pigments |
title_full_unstemmed | Anti-viral organic coatings for high touch surfaces based on smart-release, Cu(2+) containing pigments |
title_short | Anti-viral organic coatings for high touch surfaces based on smart-release, Cu(2+) containing pigments |
title_sort | anti-viral organic coatings for high touch surfaces based on smart-release, cu(2+) containing pigments |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393488/ https://www.ncbi.nlm.nih.gov/pubmed/36035655 http://dx.doi.org/10.1016/j.porgcoat.2022.107135 |
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