Post-antifungal effects and time-kill studies of anidulafungin, caspofungin, and micafungin against Candida glabrata and Candida parapsilosis

• Published in: Diagnostic microbiology and infectious disease 2011-10, Vol.71 (2), p.131-138
• Main Authors: Smith, Raymond P, Baltch, Aldona, Bopp, Lawrence H, Ritz, William J, Michelsen, Phyllis P
• Format: Article
• Language: English
• Subjects: Antifungal Agents - pharmacology; Biological and medical sciences; C. glabrata; C. parapsilosis; Candida - drug effects; Candida glabrata; Candida parapsilosis; Echinocandin effects; Echinocandins - pharmacology; Fundamental and applied biological sciences. Psychology; Infectious Disease; Infectious diseases; Internal Medicine; Lipopeptides - pharmacology; Medical sciences; Microbial Sensitivity Tests; Microbiology; Miscellaneous; Mycology; PAFE
• ISSN: 0732-8893; 1879-0070
• DOI: 10.1016/j.diagmicrobio.2011.06.018

Abstract Candida glabrata ( Cgl ) and Candida parapsilosis ( Cpa ) can cause serious infections and can be resistant to some antifungal drugs. In treating infections caused by these organisms, killing rates and post-antifungal effects (PAFE) are important factors in both dose interval choice and outcome. Two strains each of Cgl and Cpa were studied. For PAFE studies, each organism was exposed to micafungin (MCF), anidulafungin (ANF), or caspofungin (CAS) for 1 h at concentrations ranging from 0.25 to 16×MIC. Cell suspensions were then washed 3 times and resuspended in fresh broth. Time 0 was immediately after resuspension of the yeast. Time-kill experiments were done using similar drug concentrations. Samples were removed at each time point (0-120 h) and viable counts determined. PAFE of ANF and CAS were generally very long, were markedly longer than those of MCF, and increased with increased drug concentration. For ANF and CAS, PAFE for Cgl were greater than those for Cpa only at 0.5 to 2 × MIC. Time-kill experiments showed that ANF, CAS, and MCF were fungicidal at 8 to 16 × MIC up to 120 h. CAS had the greatest activity against Cgl , while ANF and MCF were more active than CAS against Cpa . Because of the prolonged PAFE of these echinocandins, especially ANF and CAS, less frequent dosing during therapy of Cpa and Cgl infections could be considered. Further studies are needed to determine the clinical efficacy of longer dosing intervals.