Rapid In-Vitro Inactivation of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Using Povidone-Iodine Oral Antiseptic Rinse

被引:102
作者
Bidra, Avinash S. [1 ]
Pelletier, Jesse S. [2 ]
Westover, Jonna B. [3 ]
Frank, Samantha [4 ]
Brown, Seth M. [4 ,5 ]
Tessema, Belachew [4 ,5 ]
机构
[1] Univ Connecticut, Hlth Ctr, Dept Reconstruct Sci, 263 Farmington Ave,L7039, Farmington, CT 06030 USA
[2] Ocean Ophthalmol Grp, Miami, FL USA
[3] Utah State Univ, Inst Antiviral Res, Logan, UT 84322 USA
[4] Univ Connecticut, Hlth Ctr, Dept Otolaryngol, Farmington, CT 06030 USA
[5] ProHlth Phys Ear Nose & Throat, Farmington, CT USA
来源
JOURNAL OF PROSTHODONTICS-IMPLANT ESTHETIC AND RECONSTRUCTIVE DENTISTRY | 2020年 / 29卷 / 06期
关键词
SARS-CoV-2; corona virus; povidone-iodine; dental safety; oral rinse; DENTAL AEROBIOLOGY; ABSORPTION; AEROSOLS; SPLATTER;
D O I
10.1111/jopr.13209
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Purpose To investigate the optimal contact time and concentration for viricidal activity of oral preparation of povidone-iodine (PVP-I) against SARS-CoV-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 (SARS-CoV-2) USA-WA1/2020 strain, virus stock was tested against oral antiseptic solutions consisting of aqueous povidone-iodine (PVP-I) as the sole active ingredient. The PVP-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 degrees 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 mu g/mL gentamicin. Surviving virus from each sample was quantified by standard end-point dilution assay and the log reduction value (LRV) of each compound compared to the negative (water) control was calculated. Results PVP-I oral antiseptics at all tested concentrations of 0.5%, 1%, and 1.5%, completely inactivated SARS-CoV-2 within 15 seconds of contact. The 70% ethanol control group was unable to completely inactivate SARS-CoV-2 after 15 seconds of contact, but was able to inactivate the virus at 30 seconds of contact. Conclusions PVP-I oral antiseptic preparations rapidly inactivated SARS-CoV-2 virus in vitro. The viricidal activity was present at the lowest concentration of 0.5 % PVP-I and at the lowest contact time of 15 seconds. This important finding can justify the use of preprocedural oral rinsing with PVP-I (for patients and health care providers) may be useful as an adjunct to personal protective equipment, for dental and surgical specialties during the COVID-19 pandemic.
引用
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页码:529 / 533
页数:5
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