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A three-parameter expression, which was already employed before for the prediction of the retention time in gradient mode in reversed-phase high-performance liquid chromatography (RP-HPLC) with satisfactory results, has been tested here under a variety of gradient patterns, using methanol and acetonitrile as the organic modifiers. A wide variety of compounds have been employed as test solutes, including some complex ones used as drugs, such as hydrocortisone and estriol. Simplifications of this expression have been made by considering two- and one-parameter expressions based on the p polarity parameter model, which was successfully employed before in isocratic mode to perform predictions of retention time. The advantages that this model gives in isocratic conditions, namely simplicity and less previous experimental work, have been applied with profit in its application to gradient mode. Good correlations between the experimental retention times and the predicted ones have been obtained with both equations in most cases.

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Three equilibria determine the interaction of a neutral analyte with the detergent in micellar electrokinetic chromatography and therefore its migration: (i) that of the free analyte in the aqueous phase with the micelle, (ii) its association with free detergent monomers in the aqueous phase, and (iii) the partition of the associate of analyte and monomer between the aqueous solution and the micelle. For the first equilibrium, non-stoichiometric partitioning between two phases is preferred in the present work over the assumption of complex formation between one molecule of the analyte with one micelle. The second equilibrium is described by the formation of a 1:1 associate of the analyte and monomer. In this paper, thirdly an additional equilibrium is introduced, namely, the distribution of the analyte-monomer associate between the aqueous and the micelle phase; it is expressed by the according partition coefficient. The three equilibrium constants are interrelated. Mobility data for a lipophilic fluorescent compound and a series of n-alkylphenones (differing in chain length) were measured as a function of the SDS concentration below and above the critical micellar concentration. Curve fitting enabled the derivation of the equilibrium constants. It was found that the association constants of the analytes with the detergent monomers are between 2 and 75 M(-1). Interestingly, the partition coefficient of the analyte-monomer associate between the aqueous and micellar phase is by a factor of 5-200 larger than that of the free analyte.