Maruta K, Teradaira R, Watanabe N, Nagatsu T, Asano M, Yamamoto K, Matsumoto T, Shionoya Y, Fujita K
Institute for Comprehensive Medical Science, School of Medicine, Fujita-Gakuen Health University, Aichi, Japan.
Clin Chem. 1989 Aug;35(8):1694-6.
This simple, rapid liquid-chromatographic assay of urinary polyamines (putrescine, spermidine, spermine, and cadaverine) involves electrochemical detection with a post-column immobilized enzyme, polyamine oxidase (EC 1.4.3.6) from soybean seedlings. Polyamines are separated by isocratic ion-pairing reversed-phase chromatography, then enzymatically converted, with release of hydrogen peroxide, via the post-column reactor with immobilized polyamine oxidase; the hydrogen peroxide is detected by electrochemical oxidation on a platinum electrode. The detection limits for injected putrescine, spermidine, and spermine were 0.3, 0.5, 0.6, and 4 pmol, respectively, with linear ranges of two to three orders of magnitude. Reproducibility was also good, with CV values less than 7%. The efficiency of the immobilized enzyme column was not decreased after analysis of 300 urine samples. Putrescine and spermidine excretion in urine from patients with blood cancers and solid cancers was significantly increased.
这种简单、快速的尿液多胺(腐胺、亚精胺、精胺和尸胺)液相色谱分析方法采用柱后固定化酶——来自大豆幼苗的多胺氧化酶(EC 1.4.3.6)进行电化学检测。多胺通过等度离子对反相色谱法分离,然后在柱后反应器中经固定化多胺氧化酶酶促转化,释放出过氧化氢;过氧化氢在铂电极上通过电化学氧化进行检测。注入的腐胺、亚精胺和精胺的检测限分别为0.3、0.5、0.6和4皮摩尔,线性范围为两到三个数量级。重现性也很好,CV值小于7%。在分析300份尿液样本后,固定化酶柱的效率没有降低。血液癌症和实体癌症患者尿液中的腐胺和亚精胺排泄量显著增加。