Reduction of SARS-CoV-2 viral load in exhaled air by antiseptic chewing gum: a pilot trial
Purpose The dominant route of transmission of SARS-CoV-2 is airborne, through respiratory transmission by aerosols or droplets which can be measured by viral load in exhaled air. Several natural substances have shown antiviral activity. The aim of this pilot study was to investigate the effect of a...
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Veröffentlicht in: | Infection 2023-08, Vol.51 (4), p.881-885 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Purpose
The dominant route of transmission of SARS-CoV-2 is airborne, through respiratory transmission by aerosols or droplets which can be measured by viral load in exhaled air. Several natural substances have shown antiviral activity. The aim of this pilot study was to investigate the effect of a chewing gum containing natural antiseptic ingredients (cinnamon-, peppermint- and lemon-oil, quercetin, spermidine, ginger and ginseng) on viral load in exhalative air in patients infected with SARS-CoV-2.
Methods
Nine patients infected with SARS-CoV-2 were enrolled and exhaled forcefully into a special mouthpiece at different time points before and after chewing the antiseptic gum. The mouthpiece contained a filter paper serving for extraction of coronaviruses following real-time PCR to quantify the viral load.
Results and conclusion
Cycle threshold (Ct) values of all patients increased after chewing the gum. The mean difference between the Ct values at baseline (before chewing the antiseptic gum) and time point 30 min (15 min after chewing) was 3.8 ± 2.6; (93% viral load reduction;
p
= 0.002). Time point 15 min (2.7 ± 1.7 (83% viral load reduction;
p
= 0.003)), 60 min (3.0 ± 3.4 (88% viral load reduction;
p
= 0.028)), 90 min (3.7 ± 1.8 (92% viral load reduction;
p
= 0.004)) and 120 min (3.0 ± 3.7 (91% viral load reduction;
p
= 0.05)) showed similar results. The antiseptic chewing gum demonstrated a significant potential to reduce SARS-CoV-2 viral load in exhalative air and, in this way, reduce further spread and infection risk. Larger placebo-controlled clinical trials are required to confirm these findings further. |
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ISSN: | 0300-8126 1439-0973 |
DOI: | 10.1007/s15010-022-01944-2 |