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Efficacy and hazards of 425 nm oral cavity light dosing to inactivate SARS-CoV-2

OBJECTIVE: Using a battery of preclinical tests to support development of a light-based treatment for COVID-19, establish a range of 425 nm light doses that are non-hazardous to the tissues of the oral cavity and assess whether a 425 nm light dose in this non-hazardous range can inactivate SARS-CoV-...

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Autores principales: Stockslager, Max A., Kocher, Jacob F., Arwood, Leslee, Stasko, Nathan, McDonald, Rebecca A., Tapsak, Mark A., Emerson, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9212724/
https://www.ncbi.nlm.nih.gov/pubmed/35724941
http://dx.doi.org/10.1016/j.jdent.2022.104203
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author Stockslager, Max A.
Kocher, Jacob F.
Arwood, Leslee
Stasko, Nathan
McDonald, Rebecca A.
Tapsak, Mark A.
Emerson, David
author_facet Stockslager, Max A.
Kocher, Jacob F.
Arwood, Leslee
Stasko, Nathan
McDonald, Rebecca A.
Tapsak, Mark A.
Emerson, David
author_sort Stockslager, Max A.
collection PubMed
description OBJECTIVE: Using a battery of preclinical tests to support development of a light-based treatment for COVID-19, establish a range of 425 nm light doses that are non-hazardous to the tissues of the oral cavity and assess whether a 425 nm light dose in this non-hazardous range can inactivate SARS-CoV-2 in artificial saliva. METHODS: The potential hazards to oral tissues associated with a range of acute 425 nm light doses were assessed using a battery of four preclinical tests: (1) cytotoxicity, using well-differentiated human large airway and buccal epithelial models; (2) toxicity to commensal oral bacteria, using a panel of model organisms; (3) light-induced histopathological changes, using ex vivo porcine esophageal tissue, and (4) thermal damage, by dosing the oropharynx of intact porcine head specimens. Then, 425 nm light doses established as non-hazardous using these tests were evaluated for their potential to inactivate SARS-CoV-2 in artificial saliva. RESULTS: A dose range was established at which 425 nm light is not cytotoxic in well-differentiated human large airway or buccal epithelial models, is not cytotoxic to a panel of commensal oral bacteria, does not induce histopathological damage in ex vivo porcine esophageal tissue, and does not induce thermal damage to the oropharynx of intact porcine head specimens. Using these tests, no hazards were observed for 425 nm light doses less than 63 J/cm(2) delivered at irradiance less than 200 mW/cm(2). A non-hazardous 425 nm light dose in this range (30 J/cm(2) at 50 mW/cm(2)) was shown to inactivate SARS-CoV-2 in vitro in artificial saliva. CONCLUSION: Preclinical hazard assessments and SARS-CoV-2 inactivation efficacy testing were combined to guide the development of a 425 nm light-based treatment for COVID-19. CLINICAL SIGNIFICANCE: The process used here to evaluate the potential hazards associated with 425 nm acute light dosing of the oral cavity to treat COVID-19 can be extended to other wavelengths, anatomical targets, and therapeutic applications to accelerate the development of novel photomedicine treatments.
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spelling pubmed-92127242022-06-22 Efficacy and hazards of 425 nm oral cavity light dosing to inactivate SARS-CoV-2 Stockslager, Max A. Kocher, Jacob F. Arwood, Leslee Stasko, Nathan McDonald, Rebecca A. Tapsak, Mark A. Emerson, David J Dent Article OBJECTIVE: Using a battery of preclinical tests to support development of a light-based treatment for COVID-19, establish a range of 425 nm light doses that are non-hazardous to the tissues of the oral cavity and assess whether a 425 nm light dose in this non-hazardous range can inactivate SARS-CoV-2 in artificial saliva. METHODS: The potential hazards to oral tissues associated with a range of acute 425 nm light doses were assessed using a battery of four preclinical tests: (1) cytotoxicity, using well-differentiated human large airway and buccal epithelial models; (2) toxicity to commensal oral bacteria, using a panel of model organisms; (3) light-induced histopathological changes, using ex vivo porcine esophageal tissue, and (4) thermal damage, by dosing the oropharynx of intact porcine head specimens. Then, 425 nm light doses established as non-hazardous using these tests were evaluated for their potential to inactivate SARS-CoV-2 in artificial saliva. RESULTS: A dose range was established at which 425 nm light is not cytotoxic in well-differentiated human large airway or buccal epithelial models, is not cytotoxic to a panel of commensal oral bacteria, does not induce histopathological damage in ex vivo porcine esophageal tissue, and does not induce thermal damage to the oropharynx of intact porcine head specimens. Using these tests, no hazards were observed for 425 nm light doses less than 63 J/cm(2) delivered at irradiance less than 200 mW/cm(2). A non-hazardous 425 nm light dose in this range (30 J/cm(2) at 50 mW/cm(2)) was shown to inactivate SARS-CoV-2 in vitro in artificial saliva. CONCLUSION: Preclinical hazard assessments and SARS-CoV-2 inactivation efficacy testing were combined to guide the development of a 425 nm light-based treatment for COVID-19. CLINICAL SIGNIFICANCE: The process used here to evaluate the potential hazards associated with 425 nm acute light dosing of the oral cavity to treat COVID-19 can be extended to other wavelengths, anatomical targets, and therapeutic applications to accelerate the development of novel photomedicine treatments. The Authors. Published by Elsevier Ltd. 2022-08 2022-06-17 /pmc/articles/PMC9212724/ /pubmed/35724941 http://dx.doi.org/10.1016/j.jdent.2022.104203 Text en © 2022 The Authors. Published by Elsevier Ltd. 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
Stockslager, Max A.
Kocher, Jacob F.
Arwood, Leslee
Stasko, Nathan
McDonald, Rebecca A.
Tapsak, Mark A.
Emerson, David
Efficacy and hazards of 425 nm oral cavity light dosing to inactivate SARS-CoV-2
title Efficacy and hazards of 425 nm oral cavity light dosing to inactivate SARS-CoV-2
title_full Efficacy and hazards of 425 nm oral cavity light dosing to inactivate SARS-CoV-2
title_fullStr Efficacy and hazards of 425 nm oral cavity light dosing to inactivate SARS-CoV-2
title_full_unstemmed Efficacy and hazards of 425 nm oral cavity light dosing to inactivate SARS-CoV-2
title_short Efficacy and hazards of 425 nm oral cavity light dosing to inactivate SARS-CoV-2
title_sort efficacy and hazards of 425 nm oral cavity light dosing to inactivate sars-cov-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9212724/
https://www.ncbi.nlm.nih.gov/pubmed/35724941
http://dx.doi.org/10.1016/j.jdent.2022.104203
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