In vitro susceptibility of chromoblastomicosis and phaehyphomycosis agents to antigungal drugs
s.l; s.n; 1999. 5 p. tab.
Non-conventional
em En
| SES-SP, SESSP-ILSLACERVO, SES-SP
| ID: biblio-1242722
Biblioteca responsável:
BR191.1
Localização: [{"text": "BR191.1", "_a": "09208/s"}]
ABSTRACT
The in vitro susceptibility of chromoblastomycosis and phaeohyphomycosis agents to antifungal drugs was appraised using the reference macrodilution method proposed by the National Committee for Clinical Laboratory Standards (NCCLS) for yeasts modified for filamentos fungi. The antifungal drugs amphotericin B, 5-fluorocytosine, intraconazole and fluconazole were tested agsints one environmental and 18 clinical isolates. This work amented the macrodilution methods proposed by NCCLS and suggests that a conidial suspension free of hyphae leads to a more reliable assay and provides for better reproducibility. The macrodilution method was performed with 10 (elevado ao 4) conidia ml-1. The MIC values ranged from 1.0 to 16.0 ug ml-1 for amphotericin B and 3.12 to 25.0 ug ml-1 for 5-fluorocytosine. A MIC range of 0.06 to 1.95 ug ml-1 was determined for itraconazole while 2.0 to 64.0 ug ml-1 was detected for fluconazole
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Coleções:
06-national
/
BR
Base de dados:
SES-SP
/
SESSP-ILSLACERVO
Assunto principal:
Cromoblastomicose
/
Anticorpos Antifúngicos
Limite:
Humans
Idioma:
En
Ano de publicação:
1999
Tipo de documento:
Non-conventional