Hara S, Yamaguchi M, Takemori Y, Nakamura M, Ohkura Y
J Chromatogr. 1986 Apr 25;377:111-9. doi: 10.1016/s0378-4347(00)80766-5.
A simple, rapid and highly sensitive high-performance liquid chromatographic method for the determination of N-acetyl- and N-glycolylneuraminic acids in serum and urine is described. The neuraminic acids, released by hydrolysis of serum and urine, are converted in dilute sulphuric acid with 1,2-diamino-4,5-dimethoxybenzene, a fluorogenic reagent for alpha-keto acids, to highly fluorescent derivatives. The derivatives are separated isocratically within 8 min by reversed-phase chromatography using a Radial-Pak cartridge C18 column and detected fluorimetrically. The limit of detection is 40 fmol (12 pg) for both neuraminic acids in 10-microliters injection volume [0.3 nmol (90 ng)/ml) of serum or urine]. This sensitivity permits the precise determination of the neuraminic acids in 5 microliters of serum or urine. The method was applied to the determination of the neuraminic acids in sera from normal subjects and cancer patients, normal urine and rat serum.
本文描述了一种用于测定血清和尿液中N-乙酰神经氨酸和N-羟乙酰神经氨酸的简单、快速且高灵敏度的高效液相色谱法。血清和尿液经水解释放出的神经氨酸,在稀硫酸中与α-酮酸的荧光试剂1,2-二氨基-4,5-二甲氧基苯反应,转化为高荧光衍生物。使用Radial-Pak C18柱通过反相色谱在8分钟内等度分离这些衍生物,并进行荧光检测。对于10微升进样体积(血清或尿液为0.3纳摩尔/毫升(90纳克/毫升))中的两种神经氨酸,检测限均为40飞摩尔(12皮克)。这种灵敏度使得能够精确测定5微升血清或尿液中的神经氨酸。该方法应用于正常受试者和癌症患者血清、正常尿液及大鼠血清中神经氨酸的测定。