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In this study, polymyxin analogs designed to have reduced nephrotoxicity, direct activity, and potentiating activity were assessed for inhibition and outer membrane interaction kinetics against wild-type (WT) and polymyxin or multidrug-resistant (MDR)\n                    <jats:named-content content-type=\"genus-species\">Escherichia coli<\/jats:named-content>\n                    ,\n                    <jats:named-content content-type=\"genus-species\">Pseudomonas aeruginosa<\/jats:named-content>\n                    ,\n                    <jats:named-content content-type=\"genus-species\">Acinetobacter baumannii<\/jats:named-content>\n                    , and\n                    <jats:named-content content-type=\"genus-species\">Klebsiella pneumoniae<\/jats:named-content>\n                    .\n                  <\/jats:p>","DOI":"10.1128\/aac.00935-19","type":"journal-article","created":{"date-parts":[[2019,7,23]],"date-time":"2019-07-23T06:47:25Z","timestamp":1563864445000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":63,"title":["Outer Membrane Interaction Kinetics of New Polymyxin B Analogs in Gram-Negative Bacilli"],"prefix":"10.1128","volume":"63","author":[{"given":"Noushin","family":"Akhoundsadegh","sequence":"first","affiliation":[{"name":"Centre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Corrie R.","family":"Belanger","sequence":"additional","affiliation":[{"name":"Centre for Microbial Diseases and Immunity Research, Department of Microbiology and Immunology, University of British Columbia, Vancouver, Canada"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5989-8503","authenticated-orcid":false,"given":"Robert E. 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