The paper reports the spectrofluorimetric and calorimetric study of binding of two hydrophobic biologically active molecules with antioxidant ability, flavonoids quercetin, and curcumin, to human serum albumin (HSA) in water, aqueous DMSO (0.05 and 0.1 mol. fraction of DMSO), and aqueous ethanol (0.05 mol. fraction of EtOH). Both flavonoids induce the quenching of HSA fluorescence. The stability constants of associates, as well as the changes in enthalpy of the reaction between quercetin and protein, were evaluated. The influence of solvent composition and additions of hydroxypropyl-β-cyclodextrin as a solubilizer of hydrophobic molecules, on the association processes is discussed.
Supplementary information: The online version contains supplementary material available at 10.1007/s10973-022-11216-8.
Keywords: Albumin; Binding constant; Calorimetry; Curcumin; Enthalpy; Mixed solvents; Quercetin.
© Akadémiai Kiadó, Budapest, Hungary 2022.