Kobe University Graduate School of Maritime Sciences, 5-1-1 Fukaeminami-machi, Higashinada-ku, Kobe 658-0022, Japan.
Kobe University Graduate School of Maritime Sciences, 5-1-1 Fukaeminami-machi, Higashinada-ku, Kobe 658-0022, Japan.
J Chromatogr A. 2014 Jan 24;1326:130-3. doi: 10.1016/j.chroma.2013.12.013. Epub 2013 Dec 16.
We elucidated theoretically and experimentally that counter-ions in background electrolyte (BGE) play a role of booster for electrokinetic injection (EKI) for the determination of cationgenic weak electrolytes and amino acids in neutral aqueous solutions using capillary electrophoresis (CE). The pH change in the sample solution caused by the migration of counter-ions resulted in the increase of analyte mobility and hence the increase of the amount of analyte injected into the capillary. This type of EKI was named as counter-ion boosted EKI. Using the counter-ion boosted EKI-capillary zone electrophoresis (CZE), the limit of detections (LODs, S/N=3) for creatinine (4.8nM) and l-histidine (9.0nM) were lowest ever achieved by CE with UV detection. The RSDs (n=3) of the migration time for creatinine and l-histidine were obtained as 0.35% and 0.34%, for peak areas of 13% and 12%, and for peak heights of 12% and 8.5%, respectively. The concentrations of creatinine and l-histidine in a urine sample obtained by the proposed method were within those reported with a good recovery.
我们从理论和实验上阐明了背景电解质(BGE)中的抗衡离子在使用毛细管电泳(CE)测定中性水溶液中阳离子弱电解质和氨基酸时对电动进样(EKI)具有促进作用。抗衡离子的迁移导致样品溶液的 pH 值发生变化,从而增加了分析物的迁移率,因此注入毛细管的分析物的量增加。这种类型的 EKI 被命名为抗衡离子增强的 EKI。使用抗衡离子增强的 EKI-毛细管区带电泳(CZE),通过 CE 与 UV 检测,可实现肌酐(4.8nM)和 l-组氨酸(9.0nM)的检测限(LOD,S/N=3)达到前所未有的最低水平。肌酐和 l-组氨酸的迁移时间的 RSD(n=3)分别为 0.35%、0.34%,峰面积的 RSD 分别为 13%、12%,峰高的 RSD 分别为 12%、8.5%。用所提出的方法得到的尿液样品中肌酐和 l-组氨酸的浓度与文献报道的浓度接近,回收率良好。