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suck abstract from ncbi


10.1177/0022034520967933

http://scihub22266oqcxt.onion/10.1177/0022034520967933
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33089717!7582358!33089717
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suck abstract from ncbi

pmid33089717      J+Dent+Res 2021 ; 100 (2): 124-132
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  • Antiviral Activity of Reagents in Mouth Rinses against SARS-CoV-2 #MMPMID33089717
  • Carrouel F; Goncalves LS; Conte MP; Campus G; Fisher J; Fraticelli L; Gadea-Deschamps E; Ottolenghi L; Bourgeois D
  • J Dent Res 2021[Feb]; 100 (2): 124-132 PMID33089717show ga
  • The oral cavity, an essential part of the upper aerodigestive tract, is believed to play an important role in the pathogenicity and transmission of SARS-CoV-2. The identification of targeted antiviral mouth rinses to reduce salivary viral load would contribute to reducing the COVID-19 pandemic. While awaiting the results of significant clinical studies, which to date do not exist, the commercial availability of mouth rinses leads us to search among them for reagents that would have specific antiviral properties with respect to SARS-CoV-2. The challenges facing this target were examined for 7 reagents found in commercially available mouth rinses and listed on the ClinicalTrials.gov website: povidone-iodine, chlorhexidine, hydrogen peroxide, cyclodextrin, Citrox, cetylpyridinium chloride, and essential oils. Because SARS-CoV-2 is an enveloped virus, many reagents target the outer lipid membrane. Moreover, some of them can act on the capsid by denaturing proteins. Until now, there has been no scientific evidence to recommend mouth rinses with an anti-SARS-CoV-2 effect to control the viral load in the oral cavity. This critical review indicates that current knowledge of these reagents would likely improve trends in salivary viral load status. This finding is a strong sign to encourage clinical research for which quality protocols are already available in the literature.
  • |Antiviral Agents/*pharmacology[MESH]
  • |COVID-19/*prevention & control[MESH]
  • |Humans[MESH]
  • |Indicators and Reagents[MESH]
  • |Mouth/virology[MESH]
  • |Mouthwashes/*pharmacology[MESH]


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