Tateda N, Matsuhisa K, Hasebe K, Kitajima N, Miura T
Asahikawa National College of Technology, Shunkodai, Japan.
J Chromatogr B Biomed Sci Appl. 1998 Nov 6;718(2):235-41. doi: 10.1016/s0378-4347(98)00373-9.
A high-performance liquid chromatographic method was developed for the rapid and sensitive determination of histidine. The method is based on separation by reversed-phase ion-pair chromatography followed by highly selective fluorescence derivatization of histidine with o-phthaldialdehyde. A linear calibration curve was obtained over the range of 0.25-200 pmol per injection (10 microl) with the coefficient of variation of 0.9% at 2 pmol (n=10) and with the detection limit (SIN=8) of 25 fmol. The method was applicable to the assay of histidine in human serum. Serum histidine values obtained by the present method were in good agreement with values obtained with an amino acid analyzer.
建立了一种高效液相色谱法,用于快速、灵敏地测定组氨酸。该方法基于反相离子对色谱分离,然后用邻苯二甲醛对组氨酸进行高选择性荧光衍生化。每次进样(10微升)在0.25 - 200皮摩尔范围内获得线性校准曲线,在2皮摩尔时变异系数为0.9%(n = 10),检测限(S/N = 8)为25飞摩尔。该方法适用于人血清中组氨酸的测定。用本法获得的血清组氨酸值与用氨基酸分析仪获得的值高度一致。