ABSTRACT
Through the use of alpha-, beta-, gamma- and heptakis(2,6-di-O-methyl)-beta-cyclodextrin as stereospecific selectors or electrolyte modifiers, both in capillary zone electrophoresis and isotachophoresis, selected model isomeric compounds (including optical isomers) were resolved. Soluble alkylhydroxyalkylcellulose derivatives were further added to the cyclodextrin-modified background electrolytes under study. Their presence was found to be essential, as demonstrated by improvements in both enantioselectivity and separation efficiency. The results obtained in both electrophoretic modes, under optimized conditions, are compared and discussed.
Subject(s)
Cyclodextrins , Electrophoresis/methodsABSTRACT
Commercially available phenothiazine derivatives were used for the study of cyclodextrin complex formation by cationic isotachophoresis with alpha-, beta- and gamma-cyclodextrin and methylated analogues of beta-cyclodextrin as leading electrolyte additives. The relationships between the type of solute substituent in the 10- and/or 2-position and the stability of the created cyclodextrin complex were studied and the results were utilized for the optimization of isotachophoretic conditions suitable for the resolution of the studied phenothiazine derivatives. Successful resolution of three racemic solutes was achieved.
Subject(s)
Phenothiazines/analysis , Chemical Phenomena , Chemistry , Cyclodextrins , Electrophoresis , Indicators and Reagents , StereoisomerismABSTRACT
Cyclodextrins (CDs) and some of their methyl derivatives have been used for the optimization of the isotachophoretic separation of bile acids in aqueous electrolyte systems. The addition of heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin to the leading electrolyte proved useful for both the solubilization and the structural differentiation of the solutes studied and led to the successful separation of their mixtures. Other CDs tested, even if they gave a satisfactory solubilization effect, did not support the resolution of bile acid mixtures.