Abstract:
Flucytosine-b-cyclodextrin and hydroxypropyl
b-cyclodextrin water soluble inclusion complex were prepared by freeze drying method in distilled water. The
formation of inclusion complex between b-cyclodextrins
and flucytosine has been studied and fully described in our
previous work [1]. In this paper we are describing the
results obtained concerning the antifungal activity of this
new compounds. As expected the new inclusion complexes
presents a semnificative increase of the antifungal activity,
illustrated by the reduction of the minimal inhibitory
concentrations for 50 and 90% of the tested strains
decreased. Also, the acute toxicity of the flucytosine b
cyclodextrin and hydroxypropyl b cyclodextrin complex is
smaller comparing with the pure drug, analyzed alone.
These results recommend the described conjugates as
future promising therapeutic agents.