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Chiral Separation of Four Stereoisomers of Ketoconazole Drugs Using Capillary Electrophoresis
Author(s) -
Wan Ibrahim Wan Aini,
Arsad Siti Rosilah,
Maarof Hasmerya,
Sanagi Mohd. Marsin,
AboulEnein Hassan Y.
Publication year - 2015
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/chir.22416
Subject(s) - chemistry , capillary electrophoresis , ketoconazole , enantiomer , chromatography , stereochemistry , electrophoresis , antifungal , medicine , dermatology
This work aimed to develop a chiral separation method of ketoconazole enantiomers using electrokinetic chromatography. The separation was achieved using heptakis (2, 3, 6‐tri‐O‐methyl)‐β‐cyclodextrin (TMβCD), a commonly used chiral selector (CS), as it is relatively inexpensive and has a low UV absorbance in addition to an anionic surfactant, sodium dodecyl sulfate (SDS). The influence of TMβCD concentration, phosphate buffer concentration, SDS concentration, buffer pH, and applied voltage were investigated. The optimum conditions for chiral separation of ketoconazole was achieved using 10 mM phosphate buffer at pH 2.5 containing 20 mM TMβCD, 5 mM SDS, and 1.0% (v/v) methanol with an applied voltage of 25 kV at 25 °C with a 5‐s injection time (hydrodynamic injection). The four ketoconazole stereoisomers were successfully resolved for the first time within 17 min (total analysis time was 28 min including capillary conditioning). The migration time precision of this method was examined to give repeatability and reproducibility with RSDs ≤5.80% ( n =3) and RSDs ≤8.88% ( n =9), respectively. Chirality 27:223–227, 2015 . © 2014 Wiley Periodicals, Inc.