воскресенье, 17 февраля 2008 г.

Potential synergy activity of the novel ceragenin, csa-13, against clinical isolates of pseudomonas aeruginosa, including multidrug-resistant p. aeruginosa

(2): 365 Journal of Antimicrobial Chemotherapy '); //> Pp.ADVANCE ACCESS ORIGINALLY PUBLISHED ONLINE ON DECEMBER 12, 2007 Journal of Antimicrobial Chemotherapy 2008 61(2):365-370; doi:10.This Article All Versions of this Article: 61/2/365 _most recent_ Services Google Scholar PubMed ORIGINAL RESEARCH POTENTIAL SYNERGY ACTIVITY OF THE NOVEL CERAGENIN, CSA-13, AGAINST CLINICAL ISOLATES OF _PSEUDOMONAS AERUGINOSA_, INCLUDING MULTIDRUG-RESISTANT _P_.JUDY N.RONALD N.HELIO S.PAUL B.AND MICHAEL J._ 1 Anti-infective Research Laboratory, Department of Pharmacy Practice, Eugene Applebaum College of Pharmacy and Health Sciences, Wayne State University, 259 Mack Avenue, Detroit, MI 48201, USA 2 JMI Laboratories, North Liberty, IA, USA 3 Department of Chemistry and Biochemistry, Brigham Young University, Provo, UT 84602, USA _ _Received 15 August 2007;_ _returned 23 September 2007;_ _revised 23 October 2007;_ _accepted 30 October 2007_ Corresponding author.+1-313-577-4376; Fax: +1-313-577-8915; E-mail: m.Previous data from our research had shown that the novel ceragenin, CSA-13, demonstrated concentration-dependent bactericidal activity against glycopeptide-resistant _Staphylococcus aureus_.It is unknown whether CSA-13 demonstrates a similar property against _Pseudomonas aeruginosa_.Evaluated CSA-13 antipseudomonal activitypared with cefepime, meropenem, piperacillin/tazobactam, tobramycin and ciprofloxacin by susceptibility testing as well as inbination with cefepime, tobramycin and ciprofloxacin.Methods: Fifty clinical isolates of _P_.Were analysed by reference broth microdilution methods.Strains with various susceptibilities were evaluated by time-killing curve (TKC) analysis at 0.2x and 4x MIC using an initial inoculum of 106 cfu/mL.Testing, TKC analysis of CSA-13 alone and inbination with cefepime, tobramycin and ciprofloxacin at 0.Was performed.Results: CSA-13 MIC50 and MBC50 were 16 and 16 mg/L, respectively.Demonstrated concentration-dependent activity, with CSA-13 at 4x MIC achieving earliest kill at 1 h (99.Limit).Analysis demonstrated synergy or additive effect with cefepime and ciprofloxacin, in some cases achieving early synergy.Addition of tobramycin to CSA-13 resulted in no difference in kill for two strains.Conclusions: CSA-13 showed concentration-dependent activity against clinical isolates of _P_.Including multidrug-resistant _P_.The addition of cefepime or ciprofloxacin to CSA-13 enhanced bacterial kill, achieving early synergy.
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