Melanson Jeremy E, Lucy Charles A
Department of Chemistry, University of Alberta, Edmonton, Alberta, Canada.
Electrophoresis. 2002 Jun;23(11):1689-94. doi: 10.1002/1522-2683(200206)23:11<1689::AID-ELPS1689>3.0.CO;2-L.
A highly sensitive technique for the analysis of urinary porphyrins using capillary electrophoresis (CE) coupled with laser-induced fluorescence (LIF) detection is reported. Separation of mesoporphyrin IX, coproporphyrin, uroporphyrin and the penta-, hexa- and heptacarboxylic acid porphyrins was achieved in 11 min using a 10 mM 2-(N-cyclohexylamino)ethanesulfonic acid (CHES, pH 10) -75 mM sodium dodecyl sulfate (SDS) buffer. Migration time and peak area repeatability were less than 1 and 5% relative standard deviation (RSD), respectively. Limits of detection of 20 pM (2 x 10(-11) M) were achieved employing the recently introduced Nichia violet diode laser for excitation at 400 nm. This represents an enhancement in sensitivity of over two orders of magnitude compared to previous reports. This high sensitivity for urinary porphyrins was demonstrated through the quantification of coproporphyrin and uroporphyrin in urine samples after up to a 100-fold dilution.
报道了一种使用毛细管电泳(CE)结合激光诱导荧光(LIF)检测来分析尿卟啉的高灵敏度技术。使用10 mM 2-(N-环己基氨基)乙磺酸(CHES,pH 10)-75 mM十二烷基硫酸钠(SDS)缓冲液,在11分钟内实现了中卟啉IX、粪卟啉、尿卟啉以及五、六和七羧酸卟啉的分离。迁移时间和峰面积的重复性相对标准偏差(RSD)分别小于1%和5%。采用最近推出的日亚紫光二极管激光器在400 nm处进行激发,检测限达到20 pM(2×10⁻¹¹ M)。与之前的报道相比,这代表灵敏度提高了两个多数量级。通过对尿液样本中粪卟啉和尿卟啉进行高达100倍稀释后的定量分析,证明了对尿卟啉的这种高灵敏度。