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Bile Salts in Chiral Micellar Electrokinetic Chromatography: 2000–2020

Bile salts are naturally occurring chiral surfactants that are able to solubilize hydrophobic compounds. Because of this ability, bile salts were exploited as chiral selectors added to the background solution (BGS) in the chiral micellar electrokinetic chromatography (MEKC) of various small molecule...

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Autores principales: Yu, Raymond B., Quirino, Joselito P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468585/
https://www.ncbi.nlm.nih.gov/pubmed/34577002
http://dx.doi.org/10.3390/molecules26185531
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author Yu, Raymond B.
Quirino, Joselito P.
author_facet Yu, Raymond B.
Quirino, Joselito P.
author_sort Yu, Raymond B.
collection PubMed
description Bile salts are naturally occurring chiral surfactants that are able to solubilize hydrophobic compounds. Because of this ability, bile salts were exploited as chiral selectors added to the background solution (BGS) in the chiral micellar electrokinetic chromatography (MEKC) of various small molecules. In this review, we aimed to examine the developments in research on chiral MEKC using bile salts as chiral selectors over the past 20 years. The review begins with a discussion of the aggregation of bile salts in chiral recognition and separation, followed by the use of single bile salts and bile salts with other chiral selectors (i.e., cyclodextrins, proteins and single-stranded DNA aptamers). Advanced techniques such as partial-filling MEKC, stacking and single-drop microextraction were considered. Potential applications to real samples, including enantiomeric impurity analysis, were also discussed.
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spelling pubmed-84685852021-09-27 Bile Salts in Chiral Micellar Electrokinetic Chromatography: 2000–2020 Yu, Raymond B. Quirino, Joselito P. Molecules Review Bile salts are naturally occurring chiral surfactants that are able to solubilize hydrophobic compounds. Because of this ability, bile salts were exploited as chiral selectors added to the background solution (BGS) in the chiral micellar electrokinetic chromatography (MEKC) of various small molecules. In this review, we aimed to examine the developments in research on chiral MEKC using bile salts as chiral selectors over the past 20 years. The review begins with a discussion of the aggregation of bile salts in chiral recognition and separation, followed by the use of single bile salts and bile salts with other chiral selectors (i.e., cyclodextrins, proteins and single-stranded DNA aptamers). Advanced techniques such as partial-filling MEKC, stacking and single-drop microextraction were considered. Potential applications to real samples, including enantiomeric impurity analysis, were also discussed. MDPI 2021-09-12 /pmc/articles/PMC8468585/ /pubmed/34577002 http://dx.doi.org/10.3390/molecules26185531 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Yu, Raymond B.
Quirino, Joselito P.
Bile Salts in Chiral Micellar Electrokinetic Chromatography: 2000–2020
title Bile Salts in Chiral Micellar Electrokinetic Chromatography: 2000–2020
title_full Bile Salts in Chiral Micellar Electrokinetic Chromatography: 2000–2020
title_fullStr Bile Salts in Chiral Micellar Electrokinetic Chromatography: 2000–2020
title_full_unstemmed Bile Salts in Chiral Micellar Electrokinetic Chromatography: 2000–2020
title_short Bile Salts in Chiral Micellar Electrokinetic Chromatography: 2000–2020
title_sort bile salts in chiral micellar electrokinetic chromatography: 2000–2020
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468585/
https://www.ncbi.nlm.nih.gov/pubmed/34577002
http://dx.doi.org/10.3390/molecules26185531
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