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Combined activity of ketoconazole and 5-fluorocytosine on potentially pathogenic yeasts
Antimicrobial Agents and Chemotherapy
|February 1, 1982
Abstract:
In vitro studies based on periodic viable count determinations indicated that the two antifungal drugs ketoconazole and 5-fluorocytosine generally were at least additive in their combined effect on various opportunistic yeast pathogens, including some resistant to 5-fluorocytosine.
Insights
Ketoconazole and 5-fluorocytosine showed additive antifungal effects against opportunistic yeasts in vitro. This combination therapy is effective, even against some 5-fluorocytosine-resistant yeast strains.
Area of Science:
- Medical Mycology
- Pharmacology
- Infectious Diseases
Background:
- Opportunistic yeast infections pose significant threats, particularly in immunocompromised individuals.
- Emerging resistance to antifungal agents necessitates the exploration of combination therapies.
- Ketoconazole and 5-fluorocytosine are established antifungal drugs with distinct mechanisms of action.
Purpose of the Study:
- To evaluate the in vitro synergistic or additive effects of ketoconazole and 5-fluorocytosine.
- To assess the efficacy of this drug combination against a range of opportunistic yeast pathogens.
- To determine if the combination is effective against yeast strains resistant to 5-fluorocytosine.
Main Methods:
- In vitro experimental design.
- Periodic viable cell count determinations.
- Testing against various opportunistic yeast species.
Main Results:
- The combined use of ketoconazole and 5-fluorocytosine demonstrated at least additive antifungal activity.
- This additive effect was observed across multiple opportunistic yeast pathogens.
- The combination therapy proved effective against some yeast strains exhibiting resistance to 5-fluorocytosine.
Conclusions:
- Ketoconazole and 5-fluorocytosine exhibit additive antifungal effects in vitro.
- Combination therapy with these agents offers a viable strategy against opportunistic yeast infections.
- This approach may overcome resistance issues associated with monotherapy, particularly for 5-fluorocytosine-resistant strains.