Yujiao Wu, Guoyan Wang, Wenyan Zhao, Hongfen Zhang, Huanwang Jing, Anjia Chen
Biomed Chromatogr. 2014 May;28(5):610-4. doi: 10.1002/bmc.3078.
In this paper, a simple, effective and green capillary electrophoresis separation and detection method was developed for the quantification of underivatized amino acids (dl-phenylalanine; dl-tryptophan) using β-Cyclodextrin and chiral ionic liquid ([TBA] [l-ASP]) as selectors. Separation parameters such as buffer concentrations, pH, β-CD and chiral ionic liquid concentrations and separation voltage were investigated for the enantioseparation in order to achieve the maximum possible resolution. A good separation was achieved in a background electrolyte composed of 15 mm sodium tetraborate, 5 mm β-CD and 4 mm chiral ionic liquid at pH 9.5, and an applied voltage of 10 kV. Under optimum conditions, linearity was achieved within concentration ranges from 0.08 to 10 µg/mL for the analytes with correlation coefficients from 0.9956 to 0.9998, and the analytes were separated in less than 6 min with efficiencies up to 970,000 plates/m. The proposed method was successfully applied to the determination of amino acid enantiomers in compound amino acids injections, such as 18AA-I, 18AA-II and 3AA.
本文建立了一种简单、有效且绿色的毛细管电泳分离检测方法,用于使用β-环糊精和手性离子液体([TBA][l-ASP])作为选择剂对未衍生化氨基酸(dl-苯丙氨酸;dl-色氨酸)进行定量分析。为了实现尽可能高的分离度,研究了缓冲液浓度、pH值、β-环糊精和手性离子液体浓度以及分离电压等分离参数用于对映体分离。在由15 mM四硼酸钠、5 mM β-环糊精和4 mM手性离子液体组成的背景电解质中,于pH 9.5和10 kV的施加电压下实现了良好的分离。在最佳条件下,分析物在0.08至10 μg/mL的浓度范围内实现线性,相关系数为0.9956至0.9998,且分析物在不到6分钟内分离,塔板效率高达970,000块/米。所提出的方法成功应用于复方氨基酸注射液(如18AA-I、18AA-II和3AA)中氨基酸对映体的测定。