首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Determination of histamine and histidine by capillary zone electrophoresis with pre-column naphthalene-2,3-dicarboxaldehyde derivatization and fluorescence detection
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Determination of histamine and histidine by capillary zone electrophoresis with pre-column naphthalene-2,3-dicarboxaldehyde derivatization and fluorescence detection

机译:柱前萘-2,3-二甲苯甲醛衍生化和荧光检测-毛细管区带电泳测定组胺和组氨酸

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摘要

A rapid and sensitive method was developed for the simultaneous determination of histamine and histidine by capillary zone electrophoresis with lamp-induced fluorescence detection. A fluoregenic derivatization reagent, naphthalene-2,3-dicarboxaldehyde (NDA) was successfully applied to label the histamine and histidine respectively. The derivatization conditions and separation parameters including pH and concentration of electrolyte and sample injection were optimized in detail. The optimal derivatization reaction was performed with 1.0 mM NDA, 20 mM NaCN, and 20 mM borate buffer, pH 9.1 for 15 min. The separation of NDA-tagged histamine and histidine could be achieved in less than 200 s with 40 mM phosphate buffer (pH 5.8) as the running buffer. The detection limits for histamine and histidine were 5.5 x 10(-9) and 3.8 x 10(-9) M, respectively (S/N = 3). The relative standard derivations for migration time and peak height of derivatives were less than 1.5 and 5.0%, respectively. The method was successfully applied to the analysis of histamine and histidine in the PS 15 mastocytoma cells and the beer samples. (C) 2004 Elsevier B.V All rights reserved.
机译:建立了一种快速灵敏的方法,通过毛细管区带电泳和灯诱导的荧光检测同时测定组胺和组氨酸。成功地使用了一种荧光衍生试剂萘-2,3-二二甲醛(NDA)分别标记组胺和组氨酸。详细优化了衍生化条件和分离参数,包括pH和电解质浓度以及进样量。最佳衍生化反应使用1.0 mM NDA,20 mM NaCN和20 mM硼酸盐缓冲液(pH 9.1)进行15分钟。使用40 mM磷酸盐缓冲液(pH 5.8)作为运行缓冲液,可以在不到200 s的时间内分离NDA标记的组胺和组氨酸。组胺和组氨酸的检出限分别为5.5 x 10(-9)和3.8 x 10(-9)M(S / N = 3)。迁移时间和衍生物的峰高的相对标准偏差分别小于1.5%和5.0%。该方法已成功应用于PS 15肥大细胞瘤细胞和啤酒样品中的组胺和组氨酸分析。 (C)2004 Elsevier B.V保留所有权利。

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