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dc.contributor.authorShein, Aye Mya Sithu
dc.contributor.authorWannigama, Dhammika Leshan
dc.contributor.authorHurst, Cameron
dc.contributor.authorMonk, Peter N.
dc.contributor.authorAmarasiri, Mohan
dc.contributor.authorBadavath, Vishnu Nayak
dc.contributor.authorPhattharapornjaroen, Phatthranit
dc.contributor.authorDitcham, William Graham Fox
dc.contributor.authorOunjai, Puey
dc.contributor.authorSaethang, Thammakorn
dc.contributor.authorChantaravisoot, Naphat
dc.contributor.authorThuptimdang, Wanwara
dc.contributor.authorLuk-in, Sirirat
dc.contributor.authorNilgate, Sumanee
dc.contributor.authorRirerm, Ubolrat
dc.contributor.authorTanasatitchai, Chanikan
dc.contributor.authorKueakulpattana, Naris
dc.contributor.authorLaowansiri, Matchima
dc.contributor.authorLiao, Tingting
dc.contributor.authorKupwiwat, Rosalyn
dc.contributor.authorRojanathanes, Rojrit
dc.contributor.authorNgamwongsatit, Natharin
dc.contributor.authorThammahong, Arsa
dc.contributor.authorIshikawa, Hitoshi
dc.contributor.authorPletzer, Daniel
dc.contributor.authorLeelahavanichkul, Asada
dc.contributor.authorRagupathi, Naveen Kumar Devanga
dc.contributor.authorWapeesittipan, Pattama
dc.contributor.authorAli Hosseini Rad, Hosseini
dc.contributor.authorKanjanabuch, Talerngsak
dc.contributor.authorStorer, Robin James
dc.contributor.authorMiyanaga, Kazuhiko
dc.contributor.authorCui, Longzhu
dc.contributor.authorHamamoto, Hiroshi
dc.contributor.authorHiggins, Paul G.
dc.contributor.authorKicic, Anthony
dc.contributor.authorChatsuwan, Tanittha
dc.contributor.authorHongsing, Parichart
dc.contributor.authorAbe, Shuichi
dc.date.accessioned2024-08-01T08:57:20Z
dc.date.available2024-08-01T08:57:20Z
dc.date.created2023-11-14T13:57:06Z
dc.date.issued2023
dc.identifier.issn0753-3322
dc.identifier.urihttps://hdl.handle.net/11250/3144011
dc.description.abstractGiven the rise of multidrug-resistant (MDR) Pseudomonas aeruginosa infections, alternative treatments are needed. Anti-pseudomonal phage therapy shows promise, but its clinical application is limited due to the development of resistance and a lack of biofilm penetration. Recently, adjuvants like CaEDTA have shown the ability to enhance the effectiveness of combined antimicrobial agents. Here, we tested a phage-adjuvant combination and demonstrated the effectiveness of intranasally inhaled phage (KKP10) + CaEDTA in addition to ceftazidime/avibactam (CZA) for chronic P. aeruginosa lung infections. The results emphasize that intranasal inhalation of phage along with CaEDTA can successfully re-sensitize MDR P. aeruginosa to CZA in a triple combination treatment. This promising approach shows potential as a therapy for chronic respiratory tract infections.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleNovel intranasal phage-CaEDTA-ceftazidime/avibactam triple combination therapy demonstrates remarkable efficacy in treating Pseudomonas aeruginosa lung infectionen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2023 The Author(s)en_US
dc.source.articlenumber115793en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1016/j.biopha.2023.115793
dc.identifier.cristin2196528
dc.source.journalBiomedicine & Pharmacotherapyen_US
dc.identifier.citationBiomedicine & Pharmacotherapy. 2023, 168, 115793.en_US
dc.source.volume168en_US


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal