Makrlíková Anna, Opekar František, Tůma Petr
Department of Analytical Chemistry, Faculty of Science, Charles University in Prague, Prague, Czech Republic.
Institute of Biochemistry Cell and Molecular Biology, Third Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.
Electrophoresis. 2015 Aug;36(16):1962-8. doi: 10.1002/elps.201400613. Epub 2015 May 20.
A computer-controlled hydrodynamic sample introduction method has been proposed for short-capillary electrophoresis. In the method, the BGE flushes sample from the loop of a six-way sampling valve and is carried to the injection end of the capillary. A short pressure impulse is generated in the electrolyte stream at the time when the sample zone is at the capillary, leading to injection of the sample into the capillary. Then the electrolyte flow is stopped and the separation voltage is turned on. This way of sample introduction does not involve movement of the capillary and both of its ends remain constantly in the solution during both sample injection and separation. The amount of sample introduced to the capillary is controlled by the duration of the pressure pulse. The new sample introduction method was tested in the determination of ammonia, creatinine, uric acid, and hippuric acid in human urine. The determination was performed in a capillary with an overall length of 10.5 cm, in two BGEs with compositions 50 mM MES + 5 mM NaOH (pH 5.1) and 1 M acetic acid + 1.5 mM crown ether 18-crown-6 (pH 2.4). A dual contactless conductivity/UV spectrometric detector was used for the detection.
一种用于短毛细管电泳的计算机控制的流体动力学进样方法已被提出。在该方法中,缓冲液从六通进样阀的定量环中冲洗样品,并将其带至毛细管的进样端。当样品区位于毛细管处时,在电解液流中产生一个短的压力脉冲,导致样品注入毛细管。然后停止电解液流动并开启分离电压。这种进样方式不涉及毛细管的移动,并且在进样和分离过程中其两端始终保持在溶液中。引入毛细管的样品量由压力脉冲的持续时间控制。这种新的进样方法在测定人尿中的氨、肌酐、尿酸和马尿酸时进行了测试。测定在总长为10.5 cm的毛细管中进行,使用两种缓冲液,其组成为50 mM MES + 5 mM NaOH(pH 5.1)和1 M乙酸 + 1.5 mM冠醚18-冠-6(pH 2.4)。使用双非接触式电导/紫外光谱检测器进行检测。