Publication | Open Access
In Vitro Susceptibilities of <i>Madurella mycetomatis</i> to Itraconazole and Amphotericin B Assessed by a Modified NCCLS Method and a Viability-Based 2,3-Bis(2-Methoxy-4-Nitro-5- Sulfophenyl)-5-[(Phenylamino)Carbonyl]-2 <i>H</i> - Tetrazolium Hydroxide (XTT) Assay
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References
2004
Year
Pharmaceutical ScienceFungal ViabilityDrug ResistanceMedicinal ChemistryBioanalysisAmphotericin BToxicologyAntimicrobial ResistanceBiochemistryTetrazolium HydroxideModified Nccls MethodPharmacologyMadurella MycetomatisFungal PathogenMycoproteinAntifungal AgentNatural SciencesMicrobiologyMedicineDrug DiscoveryDrug Analysis
Susceptibilities of Madurella mycetomatis against amphotericin B and itraconazole in vitro were determined by protocols based on NCCLS guidelines (visual reading) and a 2,3-bis (2-methoxy-4-nitro-5-sulfophenyl)-5-[(phenylamino) carbonyl]-2H-tetrazolium hydroxide (XTT) assay for fungal viability. The XTT assay was reproducible and sensitive for both antifungals. Itraconazole (MIC at which 50% of the isolates tested are inhibited [MIC(50)]) of 0.06 to 0.13 mg/liter) was superior to amphotericin B (MIC(50) of 0.5 to 1.0 mg/liter).
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