PubMed Health⌕ Search

PubMed · 12485708

On-line sample preconcentration techniques in micellar electrokinetic chromatography.

Abstract

This review provides an overview as well as a practical understanding of on-line sample concentration techniques in micellar electrokinetic chromatography (MEKC). MEKC as well as other capillary electrophoretic modes suffer from low concentration sensitivity due to minute sample volume and limited optical pathlength for on-capillary photometric detection. Two on-line sample preconcentration techniques, sample stacking and sweeping are known to be effective techniques for enhancement of the concentration sensitivity in MEKC. Sample stacking occurs as ions cross a boundary that separates regions of the high electric field sample zone and the low electric field background solution zone. The difference in migration velocity of pseudostationary phases within the two zones is the key to achieving the focusing effect. Sweeping is defined as the picking and accumulating of analytes by the pseudostationary phase that penetrates the sample zone devoid of pseudostationary phase. In this review, several examples of the sample stacking and sweeping under different experimental conditions are given, besides many references to applications.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Jong-Bok Kim, Shigeru Terabe. 2003-01-15. On-line sample preconcentration techniques in micellar electrokinetic chromatography.. https://doi.org/10.1016/s0731-7085(02)00509-5

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Recent progress in the use of ionic polymers as pseudostationary phases for EKC.

This review concerns the introduction, characterization, and application of polymeric pseudostationary phases (PSPs) for EKC since 2004. Achiral and chiral polymers and separations are reviewed, as is the application of polymeric PSPs for the combination of EKC with mass spectrometric detection.

Chromatography, Micellar Electrokinetic Capillary↗

MEKC: an update focusing on practical aspects.

This paper reviews recent methodological and instrumental advances in MEKC. Improvements in sensitivity arising from the use of on-line sample concentration (sweeping, stacking, and combination of both protocols) and derivatization (in-capillary reactions and coupling with flow-injection systems) and improvements in resolution obtained by changing the composition of the BGE (e.g., with organic modifiers, ionic liquids, nonionic and zwitterionic surfactants, mixed micelles, and vesicles) or using coated capillaries are discussed in detail. In addition, MS and LIF spectroscopy are examined in relation to their advantages and restrictions as applied to MEKC analysis. Some thoughts on potential future directions are also expressed.

Chromatography, Micellar Electrokinetic Capillary↗

Comparison of migration models for acidic solutes in micellar electrokinetic chromatography.

The validity of two models that explain the migration of ionisable solutes in micellar electrokinetic chromatography (MEKC), mobility model and retention factor model, has been tested. For this purpose, the mobility (mu) and retention factor (k) of a set of 10 phenolic compounds with different hydrophobicity and pKa values have been determined for several sodium dodecyl sulphate (SDS) concentrations and pH values, and fitted to the models. Results show that in general the retention factor model explains better the retention of ionisable solutes, although for hydrophilic compounds at low SDS concentration, mobility model can give better fits. The different drawbacks pointed out by several authors in relation to both models have been checked, and a deep evaluation of each one has been done. As a result we have observed that, while in the retention factor model the variation of k with pH and [SDS] always follows the same trend, the variation of mu with these variables mainly depends on the value of the binding constant of the neutral form of the solutes to the micelles, KHA(m), which plays a critical role in the fit of the mobility model. Also we provide rules and advices to set up the experimental conditions to apply each model to a particular solute.

Chromatography, Micellar Electrokinetic Capillary↗