Zirconia based monoliths used in hydrophilic-interaction chromatography for original selectivity of xanthines.

Monolithic capillary columns based on zirconia were prepared directly from zirconium alkoxide. They were also prepared coating a classical silica based monolithic column with zirconium butoxide. Using the gradual evolution of the theophylline/caffeine separation factor, it was found that successive zirconia coatings produced the progressive fading of surface silanols replaced by Zr-OH groups. The behavior of a silica monolith coated four times with zirconium butoxide was very similar to that of a pure zirconia monolith. The dramatic change in xanthine separation factor observed with zirconia stationary phases and the theophylline and caffeine probe solutes was used to develop a complete separation of xanthines on zirconia stationary phase in less than 6 min. The three dimethylxanthine isomers, theophylline, theobromine and paraxanthine, are very difficult to separate in RPLC with classical C18 stationary phases. The three isomers were easily separated in HILIC mode on a zirconia based stationary phase.