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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.
  • Stockslager MA; EmitBio Inc., 4222 Emperor Blvd, Suite 470, Durham, NC 27703, United States. Electronic address: mstockslager@emitbio.com.
  • Kocher JF; EmitBio Inc., 4222 Emperor Blvd, Suite 470, Durham, NC 27703, United States.
  • Arwood L; EmitBio Inc., 4222 Emperor Blvd, Suite 470, Durham, NC 27703, United States.
  • Stasko N; EmitBio Inc., 4222 Emperor Blvd, Suite 470, Durham, NC 27703, United States.
  • McDonald RA; EmitBio Inc., 4222 Emperor Blvd, Suite 470, Durham, NC 27703, United States.
  • Tapsak MA; EmitBio Inc., 4222 Emperor Blvd, Suite 470, Durham, NC 27703, United States.
  • Emerson D; EmitBio Inc., 4222 Emperor Blvd, Suite 470, Durham, NC 27703, United States.
J Dent ; 123: 104203, 2022 08.
Article in English | MEDLINE | ID: covidwho-1895174
ABSTRACT

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/cm2 delivered at irradiance less than 200 mW/cm2. A non-hazardous 425 nm light dose in this range (30 J/cm2 at 50 mW/cm2) 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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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies / Prognostic study Limits: Animals / Humans Language: English Journal: J Dent Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies / Prognostic study Limits: Animals / Humans Language: English Journal: J Dent Year: 2022 Document Type: Article