University of Connecticut School of Medicine, Farmington.
ProHealth, Ear, Nose and Throat, Farmington, Connecticut.
JAMA Otolaryngol Head Neck Surg. 2020 Nov 1;146(11):1054-1058. doi: 10.1001/jamaoto.2020.3053.
Research is needed to demonstrate the efficacy of nasal povidone-iodine (PVP-I) against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
To evaluate the in vitro efficacy of PVP-I nasal antiseptic for the inactivation of SARS-CoV-2 at clinically significant contact times of 15 and 30 seconds.
The SARS-CoV-2, USA-WA1/2020 strain, virus stock was tested against nasal antiseptic solutions consisting of aqueous PVP-I as the sole active ingredient. Povidone-iodine was tested at diluted concentrations of 0.5%, 1.25%, and 2.5% and compared with controls. The test solutions and virus were incubated at mean (SD) room temperature of 22 (2) °C for time periods of 15 and 30 seconds.
This controlled in vitro laboratory research study used 3 different concentrations of study solution and ethanol, 70%, as a positive control on test media infected with SARS-CoV-2. Test media without virus were 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 primary study outcome measurement was the log reduction value after 15 seconds and 30 seconds of given treatment. Surviving virus from each sample was quantified by standard end point dilution assay, and the log reduction value of each compound was compared with the negative (water) control.
Povidone-iodine nasal antiseptics at concentrations (0.5%, 1.25%, and 2.5%) completely inactivated SARS-CoV-2 within 15 seconds of contact as measured by log reduction value of greater than 3 log10 of the 50% cell culture infectious dose of the virus. The ethanol, 70%, positive control did not completely inactivate SARS-CoV-2 after 15 seconds of contact. The nasal antiseptics tested performed better than the standard positive control routinely used for in vitro assessment of anti-SARS-CoV-2 agents at a contact time of 15 seconds. No cytotoxic effects on cells were observed after contact with each of the nasal antiseptics tested.
Povidone-iodine nasal antiseptic solutions at concentrations as low as 0.5% rapidly inactivate SARS-CoV-2 at contact times as short as 15 seconds. Intranasal use of PVP-I has demonstrated safety at concentrations of 1.25% and below and may play an adjunctive role in mitigating viral transmission beyond personal protective equipment.
需要研究证明鼻腔聚维酮碘(PVP-I)对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的疗效。
评估 PVP-I 鼻腔抗菌剂在 15 和 30 秒临床显著接触时间下对 SARS-CoV-2 的体外灭活效果。
用含有唯一活性成分的水性 PVP-I 的鼻腔抗菌溶液测试 SARS-CoV-2,美国 WA1/2020 株病毒株病毒库存。将聚维酮碘测试为 0.5%、1.25%和 2.5%的稀释浓度,并与对照进行比较。测试溶液和病毒在平均(SD)室温 22(2)°C 下孵育 15 和 30 秒。
本控制体外实验室研究使用 3 种不同浓度的研究溶液和乙醇(70%)作为 SARS-CoV-2 感染测试介质的阳性对照。未感染病毒的测试介质添加到 2 管化合物中,作为毒性和中和对照。同时测试乙醇(70%)作为阳性对照,水作为阴性对照。
主要研究结果测量是 15 秒和 30 秒给予治疗后的对数减少值。通过标准终点稀释测定法定量测定每个样本中的存活病毒,并用每个化合物的对数减少值与阴性(水)对照进行比较。
聚维酮碘鼻腔抗菌剂在 15 秒接触时间内,浓度为(0.5%、1.25%和 2.5%)即可完全灭活 SARS-CoV-2,病毒的 50%细胞培养感染剂量的对数减少值大于 3 对数 10。接触 15 秒后,70%乙醇阳性对照未能完全灭活 SARS-CoV-2。与用于评估抗 SARS-CoV-2 制剂的常规体外标准阳性对照相比,测试的鼻腔抗菌剂在 15 秒接触时间内表现更好。接触测试的每种鼻腔抗菌剂后,均未观察到细胞的细胞毒性作用。
浓度低至 0.5%的聚维酮碘鼻腔抗菌溶液可在 15 秒的短接触时间内迅速灭活 SARS-CoV-2。PVP-I 鼻内使用在 1.25%及以下浓度下已证明安全,并且可能在个人防护设备之外在减轻病毒传播方面发挥辅助作用。