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Enrichment and separation of cationic, neutral, and chiral analytes by micelle to cyclodextrin stacking−micellar electrokinetic chromatography


Ghiasvand, A and Feng, Z and Quirino, JP, Enrichment and separation of cationic, neutral, and chiral analytes by micelle to cyclodextrin stacking−micellar electrokinetic chromatography, Analytical Chemistry, 91, (3) pp. 1752−1757. ISSN 0003-2700 (2019) [Refereed Article]

Copyright Statement

Copyright 2018 American Chemical Society

DOI: doi:10.1021/acs.analchem.8b03542


Analyte focusing by micelle to cyclodextrin stacking (MCDS) in micellar electrokinetic chromatography (MEKC) using sodium dodecyl sulfate (SDS) and fused silica capillaries is demonstrated for neutral, cationic, and chiral analytes. The stacking was at a dynamic boundary formed between the injected charged SDS micelles and neutral γ-cyclodextrin (γ-CD) zones, where the analytes bound inside micelles were released due to the formation of stable SDS-CD inclusion complexes. The complex formation reduced or eliminated the affinity of the analytes to the micellar phase. There was reversal (for charged) or nulling (for neutrals) of the analyte's effective electrophoretic mobility that caused the analytes to accumulate at the boundary. Under the conditions where the SDS micelles velocity is faster than the electroosmotic flow (using acidic buffer), MCDS was conducted by injection of a long plug of sample in a micellar diluent after injection of a CD solution plug into a capillary that was filled with MEKC background solution. By simply extending the length of the CD plug, chiral separations of chlorpheniramine and phenoxyacid herbicides were achieved without optimizing the MEKC conditions. The analytical figures of merit including linearity and repeatability for the tested compounds were found acceptable, and the sensitivity enhancement factors were up to 171. The stacking strategy in MEKC was applied to metabolic stability studies of small molecules with HepG2 cell line, where the samples were only treated with acetonitrile and then diluted with the micellar diluent (demonstrating the reduction of tedious sample preparation requirements for biological samples prior to chemical analysis).

Item Details

Item Type:Refereed Article
Keywords:capillary electrophoresis; micellar electrokinetic chromatography
Research Division:Chemical Sciences
Research Group:Analytical chemistry
Research Field:Separation science
Objective Division:Expanding Knowledge
Objective Group:Expanding knowledge
Objective Field:Expanding knowledge in the chemical sciences
UTAS Author:Ghiasvand, A (Professor Alireza Ghiasvand)
UTAS Author:Feng, Z (Mr Zikai Feng)
UTAS Author:Quirino, JP (Associate Professor Lito Quirino)
ID Code:134482
Year Published:2019
Funding Support:Australian Research Council (DP180102810)
Web of Science® Times Cited:22
Deposited By:Chemistry
Deposited On:2019-08-14
Last Modified:2022-08-29

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