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A Pilot Study of 0.4% Povidone-Iodine Nasal Spray to Eradicate SARS-CoV-2 in the Nasopharynx
PURPOSE: This study aimed to evaluate the virucidal efficacy of 0.4% povidone-iodine (PVP-I) nasal spray against SARS-CoV-2 in the patients’ nasopharynx at 3 minutes and 4 hours after PVP-I exposure. PATIENTS AND METHODS: The study was an open-label, before and after design, single-arm pilot study o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790155/ https://www.ncbi.nlm.nih.gov/pubmed/36575672 http://dx.doi.org/10.2147/IDR.S391630 |
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author | Sirijatuphat, Rujipas Leelarasamee, Amorn Puangpet, Thanapat Thitithanyanont, Arunee |
author_facet | Sirijatuphat, Rujipas Leelarasamee, Amorn Puangpet, Thanapat Thitithanyanont, Arunee |
author_sort | Sirijatuphat, Rujipas |
collection | PubMed |
description | PURPOSE: This study aimed to evaluate the virucidal efficacy of 0.4% povidone-iodine (PVP-I) nasal spray against SARS-CoV-2 in the patients’ nasopharynx at 3 minutes and 4 hours after PVP-I exposure. PATIENTS AND METHODS: The study was an open-label, before and after design, single-arm pilot study of adult patients with RT-PCR-confirmed COVID-19 within 24 hours. All patients received three puffs of 0.4% PVP-I nasal spray in each nostril. Nasopharyngeal (NP) swabs were collected before the PVP-I spray (baseline, left NP samples), and at 3 minutes (left and right NP samples) and 4 hours post-PVP-I spray (right NP samples). All swabs were coded to blind assessors and transported to diagnostic laboratory and tested by RT-PCR and cultured to measure the viable SARS-CoV-2 within 24 hours after collection. RESULTS: Fourteen patients were enrolled but viable SARS-CoV-2 was cultured from 12 patients (85.7%). The median viral titer at baseline was 3.5 log TCID(50)/mL (IQR 2.8–4.0 log TCID(50)/mL). At 3 minutes post-PVP-I spray via the left nostril, viral titers were reduced in 8 patients (66.7%). At 3 minutes post-PVP-I, the median viral titer was 3.4 log TCID(50)/mL (IQR 1.8–4.4 log TCID(50)/mL) (P=0.162). At 4 hours post-PVP-I spray via the right nostril, 6 of 11 patients (54.5%) had either the same or minimal change in viral titers. The median viral titer 3 minutes post-PVP-I spray was 2.7 log TCID(50)/mL (IQR 2.0–3.9 log TCID(50)/mL). Four hours post-PVP-I spray the median titer was 2.8 log TCID(50)/mL (IQR 2.2–3.9 log TCID(50)/mL) (P=0.704). No adverse effects of 0.4% PVP-I nasal spray were detected. CONCLUSION: The 0.4% PVP-I nasal spray demonstrated minimal virucidal efficacy at 3 minutes post-exposure. At 4 hours post-exposure, the viral titer was considerably unchanged from baseline in 10 cases. The 0.4% PVP-I nasal spray showed poor virucidal activity and is unlikely to reduce transmission of SARS-CoV-2 in prophylaxis use. |
format | Online Article Text |
id | pubmed-9790155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-97901552022-12-26 A Pilot Study of 0.4% Povidone-Iodine Nasal Spray to Eradicate SARS-CoV-2 in the Nasopharynx Sirijatuphat, Rujipas Leelarasamee, Amorn Puangpet, Thanapat Thitithanyanont, Arunee Infect Drug Resist Original Research PURPOSE: This study aimed to evaluate the virucidal efficacy of 0.4% povidone-iodine (PVP-I) nasal spray against SARS-CoV-2 in the patients’ nasopharynx at 3 minutes and 4 hours after PVP-I exposure. PATIENTS AND METHODS: The study was an open-label, before and after design, single-arm pilot study of adult patients with RT-PCR-confirmed COVID-19 within 24 hours. All patients received three puffs of 0.4% PVP-I nasal spray in each nostril. Nasopharyngeal (NP) swabs were collected before the PVP-I spray (baseline, left NP samples), and at 3 minutes (left and right NP samples) and 4 hours post-PVP-I spray (right NP samples). All swabs were coded to blind assessors and transported to diagnostic laboratory and tested by RT-PCR and cultured to measure the viable SARS-CoV-2 within 24 hours after collection. RESULTS: Fourteen patients were enrolled but viable SARS-CoV-2 was cultured from 12 patients (85.7%). The median viral titer at baseline was 3.5 log TCID(50)/mL (IQR 2.8–4.0 log TCID(50)/mL). At 3 minutes post-PVP-I spray via the left nostril, viral titers were reduced in 8 patients (66.7%). At 3 minutes post-PVP-I, the median viral titer was 3.4 log TCID(50)/mL (IQR 1.8–4.4 log TCID(50)/mL) (P=0.162). At 4 hours post-PVP-I spray via the right nostril, 6 of 11 patients (54.5%) had either the same or minimal change in viral titers. The median viral titer 3 minutes post-PVP-I spray was 2.7 log TCID(50)/mL (IQR 2.0–3.9 log TCID(50)/mL). Four hours post-PVP-I spray the median titer was 2.8 log TCID(50)/mL (IQR 2.2–3.9 log TCID(50)/mL) (P=0.704). No adverse effects of 0.4% PVP-I nasal spray were detected. CONCLUSION: The 0.4% PVP-I nasal spray demonstrated minimal virucidal efficacy at 3 minutes post-exposure. At 4 hours post-exposure, the viral titer was considerably unchanged from baseline in 10 cases. The 0.4% PVP-I nasal spray showed poor virucidal activity and is unlikely to reduce transmission of SARS-CoV-2 in prophylaxis use. Dove 2022-12-21 /pmc/articles/PMC9790155/ /pubmed/36575672 http://dx.doi.org/10.2147/IDR.S391630 Text en © 2022 Sirijatuphat et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Sirijatuphat, Rujipas Leelarasamee, Amorn Puangpet, Thanapat Thitithanyanont, Arunee A Pilot Study of 0.4% Povidone-Iodine Nasal Spray to Eradicate SARS-CoV-2 in the Nasopharynx |
title | A Pilot Study of 0.4% Povidone-Iodine Nasal Spray to Eradicate SARS-CoV-2 in the Nasopharynx |
title_full | A Pilot Study of 0.4% Povidone-Iodine Nasal Spray to Eradicate SARS-CoV-2 in the Nasopharynx |
title_fullStr | A Pilot Study of 0.4% Povidone-Iodine Nasal Spray to Eradicate SARS-CoV-2 in the Nasopharynx |
title_full_unstemmed | A Pilot Study of 0.4% Povidone-Iodine Nasal Spray to Eradicate SARS-CoV-2 in the Nasopharynx |
title_short | A Pilot Study of 0.4% Povidone-Iodine Nasal Spray to Eradicate SARS-CoV-2 in the Nasopharynx |
title_sort | pilot study of 0.4% povidone-iodine nasal spray to eradicate sars-cov-2 in the nasopharynx |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790155/ https://www.ncbi.nlm.nih.gov/pubmed/36575672 http://dx.doi.org/10.2147/IDR.S391630 |
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