SrasV1, Main, Curation, bibRecord, 001789

Evaluating the virucidal efficacy of hydrogen peroxide vapour

Identifieur interne : 001789 ( Main/Curation ); précédent : 001788; suivant : 001790

Evaluating the virucidal efficacy of hydrogen peroxide vapour

Auteurs : S. M. Goyal [États-Unis] ; Y. Chander [États-Unis] ; S. Yezli [Royaume-Uni] ; J. A. Otter [Royaume-Uni]

Source :

The Journal of hospital infection [ 0195-6701 ] ; 2014.

RBID : Pascal:14-0118111

Descripteurs français

KwdFr :
- Désinfectants (pharmacologie), Microbiologie de l'environnement, Peroxyde d'hydrogène (pharmacologie), Vapeur, Viabilité microbienne (), Virus ().
MESH :
- pharmacologie : Désinfectants, Peroxyde d'hydrogène.
Pascal (Inist)
- Grippe, Gastroentérite, Microbiologie de l'environnement, Syndrome respiratoire aigu sévère, Antiviral, Peroxyde Hydrogène, Désinfection, Décontamination, Papillomavirus humain, Calicivirus félin, Santé publique, Norovirus, Vapeur, Viabilité microbienne, Virus.
Wicri :
- topic : Santé publique.

English descriptors

KwdEn :
- Antiviral, Decontamination, Disinfectants (pharmacology), Disinfection, Environmental Microbiology, Feline calicivirus, Gastroenteritis, Human papillomavirus, Hydrogen Peroxide (pharmacology), Influenza, Microbial Viability (drug effects), Norovirus, Peroxides Hydrogen, Public health, Severe acute respiratory syndrome, Steam, Viruses (drug effects).
MESH :
- chemical , pharmacology : Disinfectants, Hydrogen Peroxide.
- drug effects : Microbial Viability, Viruses.
- Environmental Microbiology, Steam.

Abstract

Background: Surface contamination has been implicated in the transmission of certain viruses, and surface disinfection can be an effective measure to interrupt the spread of these agents. Aim: To evaluate the in-vitro efficacy of hydrogen peroxide vapour (HPV), a vapour-phase disinfection method, for the inactivation of a number of structurally distinct viruses of importance in the healthcare, veterinary and public sectors. The viruses studied were: feline calicivirus (FCV, a norovirus surrogate); human adenovirus type 1; transmissible gastroenteritis coronavirus of pigs (TGEV, a severe acute respiratory syndrome coronavirus [SARS-CoV] surrogate); avian influenza virus (AIV); and swine influenza virus (SwIV). Methods: The viruses were dried on stainless steel discs in 20- or 40-μL aliquots and exposed to HPV produced by a Clarus L generator (Bioquell, Horsham, PA, USA) in a 0.2-m³ environmental chamber. Three vaporized volumes of hydrogen peroxide were tested in triplicate for each virus: 25, 27 and 33 mL. Findings: No viable viruses were identified after HPV exposure at any of the vaporized volumes tested. HPV was virucidal (>4-log reduction) against FCV, adenovirus, TGEV and AIV at the lowest vaporized volume tested (25 mL). For SwIV, due to low virus titre on the control discs, >3.8-log reduction was shown for the 25-mL vaporized volume and >4-log reduction was shown for the 27-mL and 33-mL vaporized volumes. Conclusion: HPV was virucidal for structurally distinct viruses dried on surfaces, suggesting that HPV can be considered for the disinfection of virus-contaminated surfaces.

Url:

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7132520

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Le document en format XML

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<term>Peroxyde d'hydrogène (pharmacologie)</term>
<term>Vapeur</term>
<term>Viabilité microbienne ()</term>
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<front><div type="abstract" xml:lang="en">Background: Surface contamination has been implicated in the transmission of certain viruses, and surface disinfection can be an effective measure to interrupt the spread of these agents. Aim: To evaluate the in-vitro efficacy of hydrogen peroxide vapour (HPV), a vapour-phase disinfection method, for the inactivation of a number of structurally distinct viruses of importance in the healthcare, veterinary and public sectors. The viruses studied were: feline calicivirus (FCV, a norovirus surrogate); human adenovirus type 1; transmissible gastroenteritis coronavirus of pigs (TGEV, a severe acute respiratory syndrome coronavirus [SARS-CoV] surrogate); avian influenza virus (AIV); and swine influenza virus (SwIV). Methods: The viruses were dried on stainless steel discs in 20- or 40-μL aliquots and exposed to HPV produced by a Clarus L generator (Bioquell, Horsham, PA, USA) in a 0.2-m<sup>3</sup>
 environmental chamber. Three vaporized volumes of hydrogen peroxide were tested in triplicate for each virus: 25, 27 and 33 mL. Findings: No viable viruses were identified after HPV exposure at any of the vaporized volumes tested. HPV was virucidal (>4-log reduction) against FCV, adenovirus, TGEV and AIV at the lowest vaporized volume tested (25 mL). For SwIV, due to low virus titre on the control discs, >3.8-log reduction was shown for the 25-mL vaporized volume and >4-log reduction was shown for the 27-mL and 33-mL vaporized volumes. Conclusion: HPV was virucidal for structurally distinct viruses dried on surfaces, suggesting that HPV can be considered for the disinfection of virus-contaminated surfaces.</div>
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<term>Disinfection</term>
<term>Feline calicivirus</term>
<term>Gastroenteritis</term>
<term>Human papillomavirus</term>
<term>Influenza</term>
<term>Norovirus</term>
<term>Peroxides Hydrogen</term>
<term>Public health</term>
<term>Severe acute respiratory syndrome</term>
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<term>Gastroentérite</term>
<term>Syndrome respiratoire aigu sévère</term>
<term>Antiviral</term>
<term>Peroxyde Hydrogène</term>
<term>Désinfection</term>
<term>Décontamination</term>
<term>Papillomavirus humain</term>
<term>Calicivirus félin</term>
<term>Santé publique</term>
<term>Norovirus</term>
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<front><div type="abstract" xml:lang="en">Background: Surface contamination has been implicated in the transmission of certain viruses, and surface disinfection can be an effective measure to interrupt the spread of these agents. Aim: To evaluate the in-vitro efficacy of hydrogen peroxide vapour (HPV), a vapour-phase disinfection method, for the inactivation of a number of structurally distinct viruses of importance in the healthcare, veterinary and public sectors. The viruses studied were: feline calicivirus (FCV, a norovirus surrogate); human adenovirus type 1; transmissible gastroenteritis coronavirus of pigs (TGEV, a severe acute respiratory syndrome coronavirus [SARS-CoV] surrogate); avian influenza virus (AIV); and swine influenza virus (SwIV). Methods: The viruses were dried on stainless steel discs in 20- or 40-μL aliquots and exposed to HPV produced by a Clarus L generator (Bioquell, Horsham, PA, USA) in a 0.2-m<sup>3</sup>
 environmental chamber. Three vaporized volumes of hydrogen peroxide were tested in triplicate for each virus: 25, 27 and 33 mL. Findings: No viable viruses were identified after HPV exposure at any of the vaporized volumes tested. HPV was virucidal (>4-log reduction) against FCV, adenovirus, TGEV and AIV at the lowest vaporized volume tested (25 mL). For SwIV, due to low virus titre on the control discs, >3.8-log reduction was shown for the 25-mL vaporized volume and >4-log reduction was shown for the 27-mL and 33-mL vaporized volumes. Conclusion: HPV was virucidal for structurally distinct viruses dried on surfaces, suggesting that HPV can be considered for the disinfection of virus-contaminated surfaces.</div>
</front>
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<author><name sortKey="Goyal, S M" sort="Goyal, S M" uniqKey="Goyal S" first="S. M." last="Goyal">S. M. Goyal</name>
<affiliation wicri:level="2"><nlm:aff id="aff1">Department of Veterinary Population Medicine, University of Minnesota, Saint Paul, MN, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Veterinary Population Medicine, University of Minnesota, Saint Paul, MN</wicri:regionArea>
<placeName><region type="state">Minnesota</region>
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<author><name sortKey="Chander, Y" sort="Chander, Y" uniqKey="Chander Y" first="Y." last="Chander">Y. Chander</name>
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<author><name sortKey="Yezli, S" sort="Yezli, S" uniqKey="Yezli S" first="S." last="Yezli">S. Yezli</name>
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<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Bioquell UK Ltd, Andover</wicri:regionArea>
<wicri:noRegion>Andover</wicri:noRegion>
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</author>
<author><name sortKey="Otter, J A" sort="Otter, J A" uniqKey="Otter J" first="J. A." last="Otter">J. A. Otter</name>
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<wicri:noRegion>Andover</wicri:noRegion>
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<affiliation wicri:level="1"><nlm:aff id="aff3">Centre for Clinical Infection and Diagnostics Research (CIDR), Department of Infectious Diseases, King's College London School of Medicine and Guy’s and St Thomas’ NHS Foundation Trust, UK</nlm:aff>
<country xml:lang="fr">Royaume-Uni</country>
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Evaluating the virucidal efficacy of hydrogen peroxide vapour</title>
<author><name sortKey="Goyal, S M" sort="Goyal, S M" uniqKey="Goyal S" first="S. M." last="Goyal">S. M. Goyal</name>
<affiliation wicri:level="2"><nlm:aff id="aff1">Department of Veterinary Population Medicine, University of Minnesota, Saint Paul, MN, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Veterinary Population Medicine, University of Minnesota, Saint Paul, MN</wicri:regionArea>
<placeName><region type="state">Minnesota</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Chander, Y" sort="Chander, Y" uniqKey="Chander Y" first="Y." last="Chander">Y. Chander</name>
<affiliation wicri:level="2"><nlm:aff id="aff1">Department of Veterinary Population Medicine, University of Minnesota, Saint Paul, MN, USA</nlm:aff>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Veterinary Population Medicine, University of Minnesota, Saint Paul, MN</wicri:regionArea>
<placeName><region type="state">Minnesota</region>
</placeName>
</affiliation>
</author>
<author><name sortKey="Yezli, S" sort="Yezli, S" uniqKey="Yezli S" first="S." last="Yezli">S. Yezli</name>
<affiliation wicri:level="1"><nlm:aff id="aff2">Bioquell UK Ltd, Andover, UK</nlm:aff>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Bioquell UK Ltd, Andover</wicri:regionArea>
<wicri:noRegion>Andover</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Otter, J A" sort="Otter, J A" uniqKey="Otter J" first="J. A." last="Otter">J. A. Otter</name>
<affiliation wicri:level="1"><nlm:aff id="aff2">Bioquell UK Ltd, Andover, UK</nlm:aff>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Bioquell UK Ltd, Andover</wicri:regionArea>
<wicri:noRegion>Andover</wicri:noRegion>
</affiliation>
<affiliation wicri:level="1"><nlm:aff id="aff3">Centre for Clinical Infection and Diagnostics Research (CIDR), Department of Infectious Diseases, King's College London School of Medicine and Guy’s and St Thomas’ NHS Foundation Trust, UK</nlm:aff>
<country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Centre for Clinical Infection and Diagnostics Research (CIDR), Department of Infectious Diseases, King's College London School of Medicine and Guy’s and St Thomas’ NHS Foundation Trust</wicri:regionArea>
<wicri:noRegion>King's College London School of Medicine and Guy’s and St Thomas’ NHS Foundation Trust</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series><title level="j">The Journal of Hospital Infection</title>
<idno type="ISSN">0195-6701</idno>
<idno type="eISSN">1532-2939</idno>
<imprint><date when="2014">2014</date>
</imprint>
</series>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Disinfectants (pharmacology)</term>
<term>Environmental Microbiology</term>
<term>Hydrogen Peroxide (pharmacology)</term>
<term>Microbial Viability (drug effects)</term>
<term>Steam</term>
<term>Viruses (drug effects)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Désinfectants (pharmacologie)</term>
<term>Microbiologie de l'environnement</term>
<term>Peroxyde d'hydrogène (pharmacologie)</term>
<term>Vapeur</term>
<term>Viabilité microbienne ()</term>
<term>Virus ()</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Disinfectants</term>
<term>Hydrogen Peroxide</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>Microbial Viability</term>
<term>Viruses</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr"><term>Désinfectants</term>
<term>Peroxyde d'hydrogène</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Environmental Microbiology</term>
<term>Steam</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Microbiologie de l'environnement</term>
<term>Vapeur</term>
<term>Viabilité microbienne</term>
<term>Virus</term>
</keywords>
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<front><div type="abstract" xml:lang="en"><title>Summary</title>
<sec><title>Background</title>
<p>Surface contamination has been implicated in the transmission of certain viruses, and surface disinfection can be an effective measure to interrupt the spread of these agents.</p>
</sec>
<sec><title>Aim</title>
<p>To evaluate the in-vitro efficacy of hydrogen peroxide vapour (HPV), a vapour-phase disinfection method, for the inactivation of a number of structurally distinct viruses of importance in the healthcare, veterinary and public sectors. The viruses studied were: feline calicivirus (FCV, a norovirus surrogate); human adenovirus type 1; transmissible gastroenteritis coronavirus of pigs (TGEV, a severe acute respiratory syndrome coronavirus [SARS-CoV] surrogate); avian influenza virus (AIV); and swine influenza virus (SwIV).</p>
</sec>
<sec><title>Methods</title>
<p>The viruses were dried on stainless steel discs in 20- or 40-μL aliquots and exposed to HPV produced by a Clarus L generator (Bioquell, Horsham, PA, USA) in a 0.2-m<sup>3</sup>
 environmental chamber. Three vaporized volumes of hydrogen peroxide were tested in triplicate for each virus: 25, 27 and 33 mL.</p>
</sec>
<sec><title>Findings</title>
<p>No viable viruses were identified after HPV exposure at any of the vaporized volumes tested. HPV was virucidal (>4-log reduction) against FCV, adenovirus, TGEV and AIV at the lowest vaporized volume tested (25 mL). For SwIV, due to low virus titre on the control discs, >3.8-log reduction was shown for the 25-mL vaporized volume and >4-log reduction was shown for the 27-mL and 33-mL vaporized volumes.</p>
</sec>
<sec><title>Conclusion</title>
<p>HPV was virucidal for structurally distinct viruses dried on surfaces, suggesting that HPV can be considered for the disinfection of virus-contaminated surfaces.</p>
</sec>
</div>
</front>
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   |texte=   Evaluating the virucidal efficacy of hydrogen peroxide vapour
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Evaluating the virucidal efficacy of hydrogen peroxide vapour

Evaluating the virucidal efficacy of hydrogen peroxide vapour

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