Abstract:
Sulconazole-b-cyclodextrin water soluble
inclusion complex was prepared by freeze drying method in
distilled water. The formation of inclusion complex between
b-cyclodextrin and sulconazole has been studied in a
previous work. Preliminary pharmacological studies concerning the antifungal activity showed that the minimal
inhibitory concentrations for 90% of the tested strains
decreased. Also, the acute toxicity of the sulconazole-bcyclodextrin complex is smaller comparing with the pure
drug, analyzed alone. These results recommend the described conjugates as future promising therapeutic agents.