Structural and physicochemical characterization of the inclusion complexes of cyclomaltooligosaccharides (cyclodextrins) with melatonin

The stoichiometry, geometry, stability, and solubility of the inclusion complexes of melatonin (MLT) with native cyclomaltooligosaccharides (alfa-, beta- or gamma-cyclodextrins, CDs)
are determined experimentally by high-resolution NMR spectroscopy, calorimetric and solubility measurements, and mass spectrometry.
The observed differences are discussed in terms of molecular recognition expression of the host-guest (h-g) interactions within the hydrophobic CDs cavities of different size.
The 1:1 h-g stoichiometry in water solution prevails at low CD concentrations; the trend to form higher order associations is observed at increasing CD concentrations.
The stability order beta-CD>gamma-CD>alfa-CD for the complexes in water solution and beta-CD>alfa-CD>gamma-CD for the protonated or alkali-cationated complexes
in the gas phase are rationalized on the grounds of the structural data from NMR spectroscopy and of the thermodynamic parameters from calorimetric measurements.