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June 4, 2026Electrophoresis0 citationsOpen Access

Cyclodextrins as Chiral Selectors in Capillary Electrophoresis—Recent Developments in Understanding Analyte Complexation and Applications in Pharmaceutical Analysis

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GSGerhard K. E. Scriba

Key Points

  • The review aims to explore recent mechanistic studies on cyclodextrins as chiral selectors in enantioseparation techniques.
  • Review of studies published from January 2023 to March 2026.
  • Analysis of the application of cyclodextrins in determining enantiomeric purity.
  • Combination of capillary electrophoresis with techniques like NMR spectroscopy and molecular modeling.
  • Improved understanding of chiral recognition mechanisms in enantioseparations.
  • Demonstrated efficacy of cyclodextrins in analyzing pharmaceutical formulations.
  • Insights into the role of cyclodextrins in enhancing enantioseparation efficiency.

Abstract

CDs, cyclic oligosaccharides consisting of α-1,4 linked d-glucopyranose units, have been applied in many areas, such as food, cosmetics, environmental, agriculture, textile, pharmaceutical, and chemical industries, due to their ability to form guest-host complexes. Because CDs are chiral compounds, they have also been successfully used as chiral selectors in analytical enantioseparation techniques, especially CE. In the last decades, multidisciplinary approaches have been performed, combining CE with NMR spectroscopy, molecular modeling, and other techniques in order to understand aspects of chiral recognition underlying enantioseparations. The present review focuses on such mechanistic studies published between January 2023 and March 2026 in addition to the application of CD-mediated CE enantioseparations to the determination of the enantiomeric purity of drug substances as well as the analysis of pharmaceutical formulations.

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Cite This Study

Gerhard K. E. Scriba (2026) studied this question.

synapsesocial.com/papers/6a2115d7d499ed480b16eeddhttps://doi.org/10.1002/elps.70116
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