Abstract
The aim of the study was to evaluate the antifungal activity of a new triazole formulation against 182 clinical isolates of yeasts recovered from blood cultures in three tertiary hospitals in Romania and to compare its activity with those of fluconazole and voriconazole. In vitro susceptibility was assessed by following the guidelines of AFST-EUCAST E. Def. 7.1. The distribution of minimum inhibitory concentrations (MICs) of MXP-4509 was very similar to that of voriconazole (MIC50: 0.0312 mg/l vs. 0.0156 mg/l; MIC90: 0.25 mg/l vs. 0.25 mg/l), but significantly different from that of fluconazole (MIC50: 0.0312 mg/l vs. 0.5 mg/l; MIC90: 0.25 mg/l vs. 32 mg/l). The new triazole MXP-4509 proved to have a good in vitro antifungal activity raising the interest for further pharmacological and microbiological investigations in order to assess its potential advantages for therapy.
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Acknowledgments
The authors are indebted to Maria Mirela Flonta, Ariana Almaş, Maria Cîrlan, Maria Dan, Doina Veronica Bilcă, and Annamaria Foldes, who kindly supplied some of the clinical isolates used in this study, as well as Valeria Harabagiu, Mariana Pinteală, and Narcisa Marangoci for the synthesis of MXP-4509 nanoconjugates. This work was supported by the Ministry of Education and Research from Romania—CNCSIS-UEFISCSU, project number PN II-RU 159/2010.
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Mareş, M., Năstasă, V., Moraru Ramona, F. et al. Comparative In Vitro Activities of Fluconazole, Voriconazole, and MXP-4509 Against Romanian Blood Yeast Isolates. Mycopathologia 172, 487–492 (2011). https://doi.org/10.1007/s11046-011-9455-1
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DOI: https://doi.org/10.1007/s11046-011-9455-1