College of Pharmaceutical Sciences, Hebei University, Baoding, P. R. China.
Electrophoresis. 2009 Aug;30(16):2882-9. doi: 10.1002/elps.200800753.
A novel on-column labeling method of amino acid (AA) enantiomers by using dansyl chloride (Dns-Cl) has been explored combined with chiral ligand-exchange CE (CLE-CE) technique and UV detection. Efficient labeling was achieved by sequential injection of buffer, Dns-Cl, AA enantiomers, Dns-Cl and buffer at 0.2 psi for 10.0, 3.0, 24.0, 3.0, and 10.0 s, respectively. After injection, the sandwich sections were allowed to react at room temperature for 35.0 min. With this procedure, successful on-column labeling and CLE-CE separation of 17 pairs AA enantiomers have been achieved with a buffer of 100.0 mM boric acid, 5.0 mM ammonium acetate, 3.0 mM ZnSO4 and 6.0 mM L-Arg at pH 8.4, giving nine pairs fully enantioresolved with resolution in between 2.0 and 5.1. CLE-CE of some individual and mixed pairs was also demonstrated, much the same as using pre-column labeling. As validated by both artificially prepared solutions and serum samples, this new method was shown to be applicable to the quantitative analysis, with a linear range between 14.0 muM and 3.7 mM, correlation coefficient above 0.99 and recovery in between 90.4% and 111.7%. It was also demonstrated that the migration time-temperature based curve allows for temperature determination in CE by using this new method.
一种新的柱上标记氨基酸(AA)对映体的方法,结合手性配体交换毛细管电泳(CLE-CE)技术和紫外检测进行了探索。通过以 0.2psi 的压力分别连续进样缓冲液、Dansyl 氯(Dns-Cl)、AA 对映体、Dns-Cl 和缓冲液 10.0、3.0、24.0、3.0 和 10.0s,实现了有效的标记。进样后,夹心段在室温下反应 35.0min。采用该程序,在 100.0mM 硼酸、5.0mM 乙酸铵、3.0mM ZnSO4和 6.0mM L-Arg 缓冲液(pH8.4)中,成功地对 17 对对映体进行了柱上标记和 CLE-CE 分离,其中 9 对对映体完全分离,分辨率在 2.0 到 5.1 之间。还演示了一些单个和混合对的 CLE-CE,与使用柱前标记非常相似。通过人工配制的溶液和血清样品验证,该方法适用于定量分析,线性范围在 14.0μM 到 3.7mM 之间,相关系数大于 0.99,回收率在 90.4%到 111.7%之间。还证明了该新方法的迁移时间-温度曲线允许通过使用该新方法在 CE 中进行温度测定。