Abstract
This work focuses on the characterization of the rosmarinic acid (RA)-b-cyclodextrin (CD) complex in aqueous solution by 1H NMR (1D- and 2D-ROESY), completed with studies by capillary electrophoresis (CE). From the 1H NMR data, the stoichiometry of the complex was determined by a Job’s plot and the binding constant was estimated from a linear regression (Scott’s method). At pH 2.9, the results showed that RA binds CD with a 1:1 stoichiometry and a binding constant Kb of 445 (±53) M-1 or 465 (±81) M-1 depending on the CD protons (H-5 or H-3) selected for the evaluation. The Kb value was also calculated from the CD-induced chemical shifts of each RA proton in order to collect information on the structure of the complex. The pH dependence of Kb revealed that the RA carboxylic form displays the highest affinity for CD. An investigation by capillary electrophoresis fully confirmed these results. 2D ROESY analysis provided detailed structural information on the complex and showed a strong correlation between H-3 and H-5 of CD and most RA protons. In conclusion, RA, an efficient phenolic antioxidant from rosemary with a marketing authorization, spontaneously forms a relatively stable inclusion complex with CD in water.