Chiral separation of bupivacaine enantiomers by capillary electrophoresis partial-filling technique with human serum albumin as chiral selector

• Published in: Journal of Chromatography A 2004-09, Vol.1048 (1), p.111-118
• Main Authors: Martínez-Pla, J.J., Martín-Biosca, Y., Sagrado, S., Villanueva-Camañas, R.M., Medina-Hernández, M.J.
• Format: Article
• Language: English
• Subjects: Analysis; Analytical chemistry; Anesthetics, Local - isolation & purification; Biological and medical sciences; Bupivacaine; Bupivacaine - isolation & purification; Chemistry; Chromatographic methods and physical methods associated with chromatography; Electrophoresis, Capillary - methods; Enantiomers; Exact sciences and technology; General pharmacology; Human serum albumin (HSA); Medical sciences; Other chromatographic methods; Partial filling technique; Pharmaceutical Preparations - chemistry; Pharmacology. Drug treatments; Stereoisomerism
• ISSN: 0021-9673
• DOI: 10.1016/j.chroma.2004.07.024

Capillary electrophoresis (CE) is a powerful technique for enantiomer separations due to its intrinsic high separation efficiencies, speed of analysis, low reagent consumption and small sample requirements. However, some chiral selectors present strong background UV absorption providing high detection limits. The present paper deals with the application of the partial-filling technique to the separation of bupivacaine enantiomers by capillary electrophoresis using human serum albumin (HSA) as chiral selector. In this procedure the cationic surfactant cetyltrimethylammonium bromide (CTAB) was used as a dinamic capillary coating in order to reduce the electro-osmotic flow and detect both bupivacaine enantiomers out of the chiral selector plug. Several experimental conditions such as CTAB concentration, pH, HSA concentration and plug length, background electrolyte concentration, temperature and voltage were studied. Under the selected conditions it is possible to detect the separated enantiomers out of the HSA plug in less than 4 min using 50 mM Tris pH 8 as background electrolyte with 50 μM CTAB, at 30 °C and using a separation voltage of 25 kV. The proposed methodology was then validated for analytical purpouses and applied to the analysis of pharmaceutical preparations commercially available. The results obtained with the proposed methodology were in good agreement with those declared by the manufacturers. The simplicity, sample throughput, accuracy, reproducibility and low cost of the proposed method make it suitable for the control of the enantiomeric composition of bupivacaine in pharmaceuticals.