In vivo (human) and in vitro inactivation of SARS-CoV-2 with 0.5% povidone-iodine nasal spray
IF 0.4
P. Friedland, S. Tucker, Stephen Goodall, Justin L Julander, M. Mendenhall, Peter Molloy, Douwe Marcus de Jong, D. Musungaie, C. Sikazwe, Kirtu Panta, A. Levy, David C. Smith
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Abstract
Background: Nasal disinfection with 0.5% povidone-iodine (PVP-I) may be a useful adjunct in the management of COVID-19. The purpose of this article is to confirm the in vitro activity of the PVP-I nasal spray against SARS-CoV-2 and whether that may translate into reduced nasal shedding in vivo. Methods: Two SARS-CoV-2 virus isolates were exposed to 0.5% PVP-nasal spray (Nasodine®) for different times in vitro, with PCR and cell culture used to assess impact on viral infectivity and RNA copies. An open label in vivo single arm pilot study of 14 subjects with positive COVID-19 PCR diagnosis was undertaken. Baseline nasal swabs were collected to quantify SARS-CoV-2 pre-treatment, followed by a single 0.5% PVP nasal spray application (1.12 mL). Nasal swabs were collected at 5, 15, and 60 minutes post-dose to assess immediate and residual impact of treatment. Results: In vitro, the nasal spray reduced infectivity by 3.5 log10 TCID50/mL (99.97%) after 15 seconds exposure and eliminated detectable viral infectivity after 60 seconds;there was no effect on viral RNA detection by PCR. In vivo, culturable virus (VOC beta/B.1.351 variant) was obtained from 6 of 14 PCRconfirmed positive subjects;in these subjects, 5 minutes after the single PVP-I dose, the mean viral titre was reduced by 65% versus baseline and by 79% versus baseline at 60 minutes post-dose. 5 of the 6 subjects (83%), had reduction or cessation of viral shedding at 5 minutes in all 6 subjects, virus titers 60 minutes post-dose were below baseline value. 0.5% PVP-I treatment didn’t interfere with the laboratory diagnosis of COVID-19 via PCR-detection of viral RNA in humans. Conclusions: 0.5% PVP-I nasal spray is rapidly virucidal to SARS-CoV-2 in vitro using exposure times consistent with nasal residence;single in vivo nasal administration reduced infectious viral titers in COVID-19 subjects with culturable virus. A single application of 0.5% PVP-I nasal spray does not interfere with PCR-mediated laboratory diagnosis of COVID-19. We are undertaking a large double blinded randomized controlled trial to confirm if repeated application of 0.5% PVP-I nasal spray over a longer period could be useful in suppressing viral shedding and transmission risk in COVID-positive patients. © Australian Journal of Otolaryngology. All rights reserved.
0.5%聚维酮碘鼻喷雾剂在体内(人)和体外灭活SARS-CoV-2
背景:0.5%聚维酮碘(PVP-I)鼻腔消毒可能是治疗COVID-19的有效辅助手段。本文的目的是确认pvp - 1鼻喷雾剂对SARS-CoV-2的体外活性,以及是否可以转化为体内减少鼻腔脱落。方法:将2株SARS-CoV-2病毒分离株在体外不同时间暴露于0.5% pvp鼻喷雾剂(纳索定®)中,采用PCR和细胞培养方法评估其对病毒传染性和RNA拷贝量的影响。对14名COVID-19 PCR诊断阳性的受试者进行了一项开放标签的体内单臂初步研究。收集基线鼻拭子以量化SARS-CoV-2预处理,然后单次使用0.5% PVP鼻喷雾剂(1.12 mL)。在给药后5分钟、15分钟和60分钟收集鼻拭子,以评估治疗的即时和残余影响。结果:鼻腔喷雾剂在体外暴露15秒后降低3.5 log10 TCID50/mL(99.97%)的传染性,60秒后消除可检测到的病毒传染性;对PCR检测病毒RNA无影响。在体内,从14名pcr确认阳性受试者中的6名获得可培养病毒(VOC β /B.1.351变体);在这些受试者中,在单次PVP-I剂量后5分钟,平均病毒滴度比基线降低了65%,在剂量后60分钟比基线降低了79%。6名受试者中有5名(83%)在5分钟内病毒脱落减少或停止,所有6名受试者的病毒滴度在给药后60分钟低于基线值。0.5% PVP-I治疗不影响通过pcr检测人体内病毒RNA对COVID-19的实验室诊断。结论:0.5% PVP-I鼻喷雾剂在体外对SARS-CoV-2具有快速毒力,暴露时间与鼻腔停留时间一致;单次鼻腔给药可降低携带可培养病毒的COVID-19受试者的传染性病毒滴度。单次应用0.5% PVP-I鼻喷雾剂不会干扰pcr介导的COVID-19实验室诊断。我们正在进行一项大型双盲随机对照试验,以确认在较长时间内重复使用0.5% PVP-I鼻喷雾剂是否有助于抑制新冠病毒阳性患者的病毒脱落和传播风险。©澳大利亚耳鼻喉科学杂志。版权所有。
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