期刊
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
卷 48, 期 9, 页码 3317-3322出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.48.9.3317-3322.2004
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Candida glabrata has recently emerged as a significant pathogen involved in both superficial and deep-seated infections. In the present study, a checkerboard broth microdilution method was performed to investigate the in vitro activities of voriconazole (VOR) in combination with terbinafine (TRB), amphotericin B (AMB), and flucytosine (5FC against 20 clinical isolates of C. glabrata. Synergy, defined as a fractional inhibitory concentration (FIC index of less than or equal to0.50, was observed in 75% of VOR-TRB, 10% of VOR-AMB, and 5% of VOR-5FC interactions. None of these combinations yielded antagonistic interactions (FIC index > 4). When synergy was not achieved, there was still a decrease in the MIC of one or both drugs used in the combination. In particular, the MICs were reduced to less than or equal to1.0 mug/ml as a result of the combination for all isolates for which the AMB MIC at the baseline was greater than or equal to2.0 mug/ml. By a disk diffusion assay, the halo diameters produced by antifungal agents in combination were greater that those produced by each drug alone. Finally, killing curves showed that VOR-AMB exhibited synergistic interactions, while VOR-5FC sustained fungicidal activities against C. glabrata. These studies demonstrate that the in vitro activity of VOR against this important yeast pathogen can be enhanced upon combination with other drugs that have different modes of action or that target a different step in the ergosterol pathway. Further studies are warranted to elucidate the potential beneficial effects of such combination regimens in vivo.
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