Drug-Cyclodextrin Association Constants Determined by Surface Tension and Surface Pressure Measurements

The compression of water-insoluble drug monolayers spread on the aqueous subphase containing cyclodextrins (CD) led to a shift of surface pressure (pi)-area (A) isotherms toward smaller molecular areas with respect to the pi-A isotherms on the pure water subphase. The displacement of the compression isotherm obtained for the retinol spread on the beta-CD containing aqueous subphase was used to quantify the depletion process and to determine the drug-CD association constants. The proposed method appeared to be sensitive enough to account for extremely low amounts of sequestered drug molecules. The obtained values of the association constants Ka ranged from about 1.4.10(-2) to 36 m2/mol. The magnitudes of these constants are discussed in terms of drug bioavailability and of the stoichiometry of retinol-beta-cyclodextrin inclusion complex which was shown to have a 1:1 correspondence. Copyright 1999 Academic Press.