Wang Z J, Zaitsu K, Ohkura Y
Faculty of Pharmaceutical Sciences, Kyushu University, Fukuoka, Japan.
J Chromatogr. 1988 Sep 9;430(2):223-31. doi: 10.1016/s0378-4347(00)83157-6.
A simple and highly sensitive high-performance liquid chromatographic (HPLC) method for the determination of alpha-keto acids in human serum and urine is described. In an acidic solution, twelve species of alpha-keto acids examined were converted by reaction with 1,2-diamino-4,5-methylenedioxy-benzene into highly fluorescent derivatives. The derivatives were separated isocratically by reversed-phase HPLC on a TSK gel ODS-80TM column and detected fluorimetrically. Eight alpha-keto acids in human serum and eleven alpha-keto acids in human urine can be determined simultaneously. The detection limits (signal-to-noise ratio = 5) are 6-44 fmol in an injection volume of 5 microliters. The intra-assay relative standard deviations for both serum and urine sample analyses are usually ca. 5%.
本文描述了一种用于测定人血清和尿液中α-酮酸的简单且高灵敏度的高效液相色谱(HPLC)方法。在酸性溶液中,所检测的12种α-酮酸与1,2-二氨基-4,5-亚甲基二氧基苯反应转化为高荧光衍生物。这些衍生物在TSK凝胶ODS-80TM柱上通过反相HPLC等度分离,并进行荧光检测。人血清中的8种α-酮酸和人尿液中的11种α-酮酸可同时测定。在进样体积为5微升时,检测限(信噪比 = 5)为6 - 44飞摩尔。血清和尿液样品分析的批内相对标准偏差通常约为5%。