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dc.contributor.authorWang, J.en_US
dc.contributor.authorKutter, J.P.en_US
dc.contributor.authorMu, H.en_US
dc.contributor.authorMoodley, Arshneeen_US
dc.contributor.authorYang, M.en_US
dc.date.accessioned2020-10-26T13:06:31Zen_US
dc.date.available2020-10-26T13:06:31Zen_US
dc.identifier.urihttps://hdl.handle.net/10568/109977en_US
dc.titleSynergistic antibacterial effect of inhaled aztreonam and tobramycin fixed dose combination to combat multidrug-resistant Gram-negative bacteriaen_US
cg.authorship.typesCGIAR and developing country instituteen_US
cg.authorship.typesCGIAR and advanced research instituteen_US
dcterms.abstractThe limited therapeutic option for respiratory infections caused by multi-drug resistant microbial pathogens is a major global health threat. Topical delivery of antibacterial combinations to the lung could dramatically enhance antibacterial activities and provide a means to overcome bacterial resistance development. The aim of the study was to investigate the potential of new inhalable dry powder combinations consisting of a fixed dose of aztreonam (Azt) and tobramycin (Tob) using a spray drying process, against antibiotic resistant Gram-negative respiratory pathogens. The interactions of Azt with Tob on resistant Pseudomonas aeruginosa, Klebsiella pneumoniae and Acinetobacter baumannii were determined by calculating factional inhibitory concentration indices (FICI). A fixed concentration ratio of Azt and Tob that exhibited a synergistic antimicrobial effect was selected and formulated into inhalable dry powders by co-spray drying with and without L-leucine. The obtained dry powders were characterized with respect to the morphology, particle size distribution, solid state, moisture sorption behaviour, and in vitro dissolution. Storage stability, aerosol performance, and in vitro antibacterial activity were also evaluated. Inhalable dry powders consisting of Azt, Tob and L-leucine could be readily obtained via the spray drying process with a fine particle fraction of above 40% as determined using a next generation impactor. The co-spray drying process resulted in amorphous Azt/Tob dry powders with or without the addition of L-leucine as indicated by X-ray powder diffraction. The dissolution rates of the co-spray dried Azt/Tob dry powders were decreased, and the storage stability was improved with an increase in the proportion of L-leucine in the formulations. The inclusion of L-leucine did not affect the minimum inhibitory concentration and the co-spray dried powders reserved the synergistic antibacterial effects and exhibited enhanced antibacterial activities as compared to the individual antibiotic used alone on multidrug-resistant (Azt and Tob resistant) P. aeruginosa 25756 and A. baumannii K31. This study demonstrates that inhalable Azt/Tob dry powders using L-leucine as a moisture protector as well as a dispersing agent can be readily prepared by the spray drying process. This new inhalable fixed dose combinational dry powders may represent an alternative treatment against multidrug-resistant Gram-negative respiratory pathogens.en_US
dcterms.accessRightsLimited Accessen_US
dcterms.audienceScientistsen_US
dcterms.bibliographicCitationWang, J., Kutter, J.P., Mu, H., Moodley, A. and Yang, M. 2020. Synergistic antibacterial effect of inhaled aztreonam and tobramycin fixed dose combination to combat multidrug-resistant Gram-negative bacteria. International Journal of Pharmaceutics 590: 119877.en_US
dcterms.issued2020-11en_US
dcterms.languageenen_US
dcterms.licenseOtheren_US
dcterms.publisherElsevier BVen_US
dcterms.subjectantimicrobial resistanceen_US
dcterms.typeJournal Articleen_US
cg.subject.ilriAMRen_US
cg.contributor.affiliationUniversity of Copenhagenen_US
cg.contributor.affiliationInternational Livestock Research Instituteen_US
cg.contributor.affiliationShenyang Pharmaceutical Universityen_US
cg.identifier.doihttps://doi.org/10.1016/j.ijpharm.2020.119877en_US
cg.isijournalISI Journalen_US
cg.contributor.crpAgriculture for Nutrition and Healthen_US
cg.creator.identifierArshnee Moodley: 0000-0002-6469-3948en_US
cg.contributor.donorChina Scholarship Councilen_US
cg.reviewStatusPeer Reviewen_US
cg.howPublishedFormally Publisheden_US
cg.journalInternational Journal of Pharmaceuticsen_US
cg.issn0378-5173en_US


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