Solid formulas obtained between furosemide and two beta-cyclodextrin deriva
tives (HP-beta-CD and RAMEB) were prepared by different methods and in vari
ous ratios (1:I and 1.2). The inclusion complex formation between the drug
and the beta-CDs of 1:1 ratio was evaluated by mean of thermal analysis (DS
C, TG and EGD). Supplementary techniques, such as X-ray diffraction, were a
lso applied to interpret the results of the thermal study of physically mix
ed and kneaded products. Both studies demonstrated the formation of inclusi
on complexes in all samples except the physical mix samples; formation of t
rue inclusion complexes was then possible only when the components were in
melted form. The complexation increased the solubility and the rate of diss
olution of the drug. RAMEB was found to be a better complexing agent than H
P-beta-CD; in both ratios it can be selected as a vehicle in furosemide tab
let preparations.