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dc.contributor.authorGrønseth, Torstein
dc.contributor.authorOvchinnikov, Kirill
dc.contributor.authorCarlsen, Harald
dc.contributor.authorSaltyte Benth, Jurate
dc.contributor.authorDiep, Dzung B.
dc.contributor.authorVon Unge, Magnus
dc.contributor.authorSilvola, Juha Tapio
dc.date.accessioned2023-04-03T12:15:03Z
dc.date.available2023-04-03T12:15:03Z
dc.date.created2022-08-30T11:16:40Z
dc.date.issued2022
dc.identifier.citationInternational Wound Journal. 2022, .
dc.identifier.issn1742-4801
dc.identifier.urihttps://hdl.handle.net/11250/3061842
dc.description.abstractThe study aimed to evaluate the antibacterial efficacy of Lugol's solution 5% and Gentian violet 1% against methicillin-resistant Staphylococcus aureus (MRSA) biofilm in vivo. The bactericidal efficacy for treatment of MRSA-biofilm skin wound infection was tested in a murine model. Luciferase-tagged S. aureus Xen31, a MRSA-strain derived from S. aureus ATCC-3359130, was used for infection. Wounds were made in the skin of mice and infected with MRSA. The mice were treated with Lugol's solution and Gentian violet. Application of the antimicrobial agents started 24 hours post infection and was repeated daily for five-days. The antimicrobial effect on the biofilm bacteria was evaluated by measuring bioluminescence from MRSA daily for seven-days. Lugol's solution and Gentian violet showed a significant reduction in luminescent signals from the first assessment day to all subsequent days (P < .001). Lugol's solution and Gentian violet effectively eradicated MRSA in biofilm in vivo and could be alternatives or in addition to topical antibiotics when MRSA-biofilm wound infection is suspected.
dc.language.isoeng
dc.titleLugol's solution and Gentian violet eradicate methicillin-resistant Staphylococcus aureus biofilm in skin wound infections
dc.title.alternativeLugol's solution and Gentian violet eradicate methicillin-resistant Staphylococcus aureus biofilm in skin wound infections
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersion
dc.source.pagenumber11
dc.source.journalInternational Wound Journal
dc.identifier.doi10.1111/iwj.13846
dc.identifier.cristin2047111
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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