FLUOROMETRIC STUDIES OF THE FORMATION OF RIBOFLAVIN-BETA-CYCLODEXTRININCLUSION COMPLEX - DETERMINATION OF THE STABILITY CONSTANT BY USE OFA NONLINEAR LEAST-SQUARES MODEL
Yl. Loukas et al., FLUOROMETRIC STUDIES OF THE FORMATION OF RIBOFLAVIN-BETA-CYCLODEXTRININCLUSION COMPLEX - DETERMINATION OF THE STABILITY CONSTANT BY USE OFA NONLINEAR LEAST-SQUARES MODEL, Journal of Pharmacy and Pharmacology, 49(2), 1997, pp. 127-130
The non-linear least-squares model for calculation of the stability co
nstant (K-st) of a drug-cyclodextrin complex has been used in fluorime
try studies. Complexation of riboflavin with beta-cyclodextrin (beta-C
yD) was monitored fluorimetrically by measuring changes in the fluores
cence intensity of the vitamin in the presence of various amounts of b
eta-CyD. Formation of an inclusion complex was confirmed in the solid
state by differential scanning calorimetry (DSC) and in aqueous soluti
on by proton nuclear magnetic resonance spectroscopy (H-1 NMR). The ex
perimental K-st value (2112 M(-1)) derived from the fluorimetry studie
s appeared to fit well to a 1:1 drug-to-cyclodextrin molar ratio accor
ding to the non-linear mathematical model. The model is particularly s
uitable for fluorescent compounds of which fluorescence intensity is i
nfluenced by the presence of cyclodextrins.