Author: Bidra, Avinash S.; Pelletier, Jesse S; Westover, Jonna B; Frank, Samantha; Brown, Seth M; Tessema, Belachew
Title: Rapid Inâ€Vitro Inactivation of Severe Acute Respiratory Syndrome Coronavirus 2 (SARSâ€CoVâ€2) Using Povidoneâ€Iodine Oral Antiseptic Rinse Cord-id: 87tpjvs6 Document date: 2020_6_16
ID: 87tpjvs6
Snippet: PURPOSE: To investigate the optimal contact time and concentration for viricidal activity of oral preparation of povidoneâ€iodine (PVPâ€I) against SARSâ€CoVâ€2 (‘corona virus’) to mitigate the risk and transmission of the virus in the dental practice. MATERIALS AND METHODS: The severe acute respiratory syndrome coronavirus 2 (SARSâ€CoVâ€2) USAâ€WA1/2020 strain, virus stock was tested against oral antiseptic solutions consisting of aqueous povidoneâ€iodine (PVPâ€I) as the sole active
Document: PURPOSE: To investigate the optimal contact time and concentration for viricidal activity of oral preparation of povidoneâ€iodine (PVPâ€I) against SARSâ€CoVâ€2 (‘corona virus’) to mitigate the risk and transmission of the virus in the dental practice. MATERIALS AND METHODS: The severe acute respiratory syndrome coronavirus 2 (SARSâ€CoVâ€2) USAâ€WA1/2020 strain, virus stock was tested against oral antiseptic solutions consisting of aqueous povidoneâ€iodine (PVPâ€I) as the sole active ingredient. The PVPâ€I was tested at diluted concentrations of 0.5%, 1%, and 1.5%. Test media without any virus was added to 2 tubes of the compounds to serve as toxicity and neutralization controls. Ethanol (70%) was tested in parallel as a positive control, and water only as a negative control. The test solutions and virus were incubated at room temperature (22 ± 2 °C) for time periods of 15 and 30 seconds. The solution was then neutralized by a 1/10 dilution in minimum essential medium (MEM) 2% fetal bovine serum (FBS), 50 µg/mL gentamicin. Surviving virus from each sample was quantified by standard endâ€point dilution assay and the log reduction value (LRV) of each compound compared to the negative (water) control was calculated. RESULTS: PVPâ€I oral antiseptics at all tested concentrations of 0.5%, 1%, and 1.5%, completely inactivated SARSâ€CoVâ€2 within 15 seconds of contact. The 70% ethanol control group was unable to completely inactivate SARSâ€CoVâ€2 after 15 seconds of contact, but was able to inactivate the virus at 30 seconds of contact. CONCLUSIONS: PVPâ€I oral antiseptic preparations rapidly inactivated SARSâ€CoVâ€2 virus in vitro. The viricidal activity was present at the lowest concentration of 0.5 % PVPâ€I and at the lowest contact time of 15 seconds. This important finding can justify the use of preprocedural oral rinsing with PVPâ€I (for patients and health care providers) may be useful as an adjunct to personal protective equipment, for dental and surgical specialties during the COVIDâ€19 pandemic.
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