6533b86dfe1ef96bd12c956b

RESEARCH PRODUCT

Modulation of retention and selectivity in oil-in-water microemulsion liquid chromatography: A review

María-josé Ruíz-angelE. Peris-garcíaSamuel Carda-brochM.c. García-alvarez-coqueN. Pankajkumar-patel

subject

Work (thermodynamics)modulation of selectivity010402 general chemistry01 natural sciencesBiochemistryAnalytical ChemistrySurface-Active AgentsPulmonary surfactantPhase (matter)Microemulsionmicroemulsion liquid chromatographyChromatographyAqueous solutionChemistry010401 analytical chemistryOrganic ChemistryWaterGeneral Medicineoil-in-water microemulsionsexperimental factors0104 chemical sciencesoptimization of resolutionReagentYield (chemistry)SelectivityOilsChromatography Liquid

description

Microemulsions (MEs) are stable, isotropically clear solutions consisting of an oil and water stabilized by a surfactant and a co-surfactant. Oil-in-water microemuslion liquid chromatography (MELC) is a relatively new chromatographic mode, which uses an O/W ME as mobile phase. Retention, selectivity and efficiency can be modified by changing the concentration of the ME components and the ratio between the aqueous and oil phases. This work makes a critical survey on the information found in the literature about the mobile phase compositions that lead to the creation of successful O/W ME mobile phases, as well as the effect of pH for ionizable compounds and temperature. The viability of performing the analyses using isocratic and gradient elution is also considered. The complexity of the composition of a successful ME, and the fact that the different factors interact each other, may require many manipulations during method development to achieve an acceptable separation for complex mixtures. This is the reason of the proposal from several authors of a standard ME as starting point when developing a method for a new separation with no previous reports. Based on these initial conditions, the interest of several authors in applying computer-assisted approaches to optimize the composition of ME mobile phases, and reduce significantly the time and reagent consumption for method development, is described. Some practical tips are given to prepare stable ME mobile phases that yield reproducible results.

https://doi.org/10.1016/j.chroma.2019.01.046