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In Vitro Antifungal Activity of Isavuconazole against Madurella mycetomatis
Author(s) -
Wendy Kloezen,
Jacques F. Meis,
Ilse Curfs-Breuker,
Ahmed Hassan Fahal,
Wendy W. J. van de Sande
Publication year - 2012
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.01170-12
Subject(s) - itraconazole , antifungal , ketoconazole , mycetoma , echinocandins , triazole , biology , medicine , pharmacology , amphotericin b , microbiology and biotechnology , caspofungin , chemistry , dermatology , organic chemistry
Currently, therapy of black-grain mycetoma caused by Madurella mycetomatis consists of extensive debridement of the infected tissue combined with prolonged antifungal therapy with ketoconazole or itraconazole. In the present study, the in vitro activity of the new triazole isavuconazole toward M. mycetomatis was evaluated. Isavuconazole appeared to have high activity against M. mycetomatis, with MICs ranging from ≤0.016 to 0.125 μg/ml. Due to its favorable pharmacokinetics, isavuconazole could be a promising antifungal agent in the treatment of mycetoma.

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