Thyroxine T4 and its derivatives (T3, T2) are very sparingly soluble in aqu
eous solutions even in the form of salts. In the presence of beta or gamma-
cyclodextrins and in buffered basic solution, their solubilities are increa
sed by inclusion in the cavity. The inclusion of these hormones in cyclodex
trins was investigated by H-1-NMR in order to derive the influence of the n
umber and position of the iodine atoms, and of the ionization state of the
phenol group on the inclusion geometries.