| Literature DB >> 31061161 |
Maurizio Sanguinetti1,2, Emilia Cantón3, Riccardo Torelli4, Fabio Tumietto5, Ana Espinel-Ingroff6, Brunella Posteraro7,8.
Abstract
We determined the in vitro activity of fenticonazole against 318 vaginitis isolates of Candida and bacterial species and selected 28 isolates for time-kill studies. At concentrations equal to 4× MIC, fenticonazole reached the 99.9% killing endpoint by ∼10 h for Staphylococcus aureus, Streptococcus agalactiae, and Escherichia coli and by ∼17 h for Candida albicans and Candida parapsilosis; and at concentrations equal to 8× MIC, by ∼19 and ∼20 h for Candida glabrata and Candida tropicalis, respectively. At concentrations equal to 2× MIC, fenticonazole required ∼20 h to reach the above endpoint against C. albicans in mixed culture with S. aureus, S. agalactiae, or E. coli versus ∼17 h against C. albicans in pure culture. Supra-MICs are achievable in topically treated patients' vaginal surfaces.Entities:
Keywords: antimicrobial susceptibility testing; fenticonazole; targeted therapy; vaginal isolates
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Year: 2019 PMID: 31061161 PMCID: PMC6591636 DOI: 10.1128/AAC.02693-18
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191