Autor: |
Huppert, M., Pappagianis, D., Sun, S. H., Gleason-Jordan, I., Collins, M. S., Vukovich, K. R. |
Zdroj: |
Antimicrobial Agents and Chemotherapy; March 1976, Vol. 9 Issue: 3 p406-413, 8p |
Abstrakt: |
Amphotericin B, the principal drug used for treating systemic mycoses, possesses undesirable toxic properties. The ability of this antibiotic to potentiate antifungal activity of other compounds suggests that lower doses of amphotericin B could be used in combination with a second drug without loss of therapeutic efficacy. In vitro tests demonstrated that amphotericin B potentiated rifampin against the mycelial growth phase of Coccidioides immitisbut not against the spherule-endospore phase. Therapy for murine coccidioidomycosis with a combined amphotericin B-rifampin regimen was not better than treatment with amphotericin B alone; in fact, combined drugs may have been even less effective. This would have clinical significance for therapy of concurrent infections. |
Databáze: |
Supplemental Index |
Externí odkaz: |
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