Yoshida Hideyuki, Kido Fumito, Yoshitake Makoto, Todoroki Kenichiro, Nohta Hitoshi, Yamaguchi Masatoshi
Faculty of Pharmaceutical Sciences, Fukuoka University, Fukuoka, Japan.
Anal Sci. 2007 Apr;23(4):485-8. doi: 10.2116/analsci.23.485.
A liquid chromatographic (LC) determination of catecholamines and indoleamines is described. This is based on intramolecular excimer-forming fluorescence derivatization with 4-(1-pyrene)butanoyl chloride, followed by reversed-phase LC. The analytes, containing an amino moiety and phenolic hydroxyl moieties in a molecule, were converted to the corresponding polypyrene-labeled derivatives by one-step derivatization. They afforded intramolecular excimer fluorescence, which can clearly be discriminated from the normal fluorescence emitted from reagent blanks. The detection limits (S/N = 3) for catecholamines and indoleamines were femto-mole levels per 20-microL injection. Furthermore, this method was applied to a urine assay.
本文描述了一种用于测定儿茶酚胺和吲哚胺的液相色谱(LC)方法。该方法基于用4-(1-芘)丁酰氯进行分子内形成准分子的荧光衍生化,随后进行反相液相色谱分析。分析物分子中含有氨基部分和酚羟基部分,通过一步衍生化转化为相应的多芘标记衍生物。它们产生分子内准分子荧光,这可以与试剂空白发出的正常荧光明显区分开来。儿茶酚胺和吲哚胺的检测限(信噪比 = 3)为每20微升进样量的飞摩尔水平。此外,该方法还应用于尿液分析。