Quantitative retention–structure and retention–activity relationships of barbiturates by micellar liquid chromatography

Abstract Studies on the structural requirements of chromatographic surfaces to emulate in vitro the partitioning process in biomembranes are of great interest. The use of micellar mobile phases in RPLC modifies the hydrophobicity of the stationary phase and provides hydrophobic and electrostatic sites of interaction as a consequence of the adsorption of surfactant monomers to the chromatographic surface. Modified stationary phases in MLC could be structurally similar to biomembranes, but thorough studies are necessary to confirm this. In this paper we focus our attention on barbiturates. The influence of the nature and concentration of the surfactant (Brij 35, SDS and CTAB) and the mobile p…