Pan Congjie, Lv Wenjuan, Wang Guoxiu, Niu Xiaoying, Guo Heying, Chen Xingguo
State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China; Department of Chemistry, Lanzhou University, Lanzhou 730000, China.
State Key Laboratory of Applied Organic Chemistry, Lanzhou University, Lanzhou 730000, China; Department of Chemistry, Lanzhou University, Lanzhou 730000, China.
J Chromatogr A. 2017 Feb 10;1484:98-106. doi: 10.1016/j.chroma.2017.01.017. Epub 2017 Jan 11.
Developing simple methods for separation of analytes that belong to different classes is of great importance. Herein, we developed a simple one-dimensional (1-D) capillary electrochromatography method to demonstrate the simultaneous separation of target fractions that belong to two different classes (i.e., cationic and neutral analytes) without switching buffer solution by a zeolitic imidazolate framework ZIF-8 coated capillary column. Owing to the difference of charge-to-mass ratio of the cationic analytes, the interaction of the cationic analytes and coating material ZIF-8 and the hydrophobic interactions between the neutral analytes and the microporous framework of ZIF-8, six cationic analytes and four neutral analytes were simultaneously separated in a single run by 1-D capillary electrochromatography. The relative standard deviations (RSDs) of the analytes migration time for intra-day, inter-day and column-to-column were in the range of 0.11-0.87%, 0.54-2.04% and 2.00-6.89% and the RSDs of the analytes peak area for intra-day, inter-day and column-to-column were in the range of 0.70-4.45%, 1.33-6.20% and 2.27-11.88%. Additionally, the developed method was employed in the analysis of urine samples with satisfactory recoveries.
开发用于分离不同类分析物的简单方法非常重要。在此,我们开发了一种简单的一维(1-D)毛细管电色谱方法,以证明通过沸石咪唑酯骨架ZIF-8涂层毛细管柱在不切换缓冲溶液的情况下同时分离属于两种不同类别的目标馏分(即阳离子和中性分析物)。由于阳离子分析物的电荷质量比不同、阳离子分析物与涂层材料ZIF-8的相互作用以及中性分析物与ZIF-8微孔骨架之间的疏水相互作用,通过一维毛细管电色谱在一次运行中同时分离了六种阳离子分析物和四种中性分析物。分析物迁移时间的日内、日间和柱间相对标准偏差(RSD)在0.11 - 0.87%、0.54 - 2.04%和2.00 - 6.89%范围内,分析物峰面积的日内、日间和柱间RSD在0.70 - 4.45%、1.33 - 6.20%和2.27 - 11.88%范围内。此外,所开发的方法用于尿液样品分析,回收率令人满意。