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Determination of agmatine in biological samples by capillary electrophoresis with chemiluminescence detection

机译:毛细管电泳-化学发光检测法测定生物样品中的胍丁胺

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A fast and simple method based on capillary electrophoresis (CE) with chemiluminescence (CL) detection has been developed for the determination of agmatine, a recently identified neurotransmitter/modulator. The CE run time was approximately 2 min for each sample injected. CL detection employed a lab-built reaction flow cell and a photon counter. The CL reagents used were luminol and NaBrO. The optimized conditions for the CL detection were 5 x 10(-4) M luminol added to the CE running buffer and 5.0 x 10(-4) M NaBrO in 100 mM NaCO3-NaOH buffer solution at pH 12.5 introduced post column. Detection limit for agmatine was 4.3 x 10(-6) M (S/N = 3). The precision (R.S.D.) on peak height (at 1 x 10(-5) M agmatine) and migration time were 3.7 and 2.5%, respectively. The present CE-CL method was evaluated with the determination of agmatine in tissue samples taken from rat brain, and rat and monkey stomachs. Samples were directly injected into the CE-CL system after the removal of proteins. A higher level of agmatine was detected in the stomach samples. Agmatine concentrations in the tissue samples taken from rat and monkey stomachs were similar at similar to 1950 ng/g wet tissue. (c) 2006 Elsevier B.V. All rights reserved.
机译:已经开发了一种基于毛细管电泳(CE)和化学发光(CL)检测的快速简便的方法,用于确定胍丁胺(一种最近鉴定的神经递质/调节剂)。每个进样样品的CE运行时间约为2分钟。 CL检测采用实验室建造的反应流通池和光子计数器。使用的CL试剂是鲁米诺和NaBrO。用于CL检测的优化条件是在柱后引入pH 12.5的100 mM NaCO3-NaOH缓冲溶液中,将5 x 10(-4)M鲁米诺添加到CE运行缓冲液中和5.0 x 10(-4)M NaBrO。胍丁胺的检出限为4.3 x 10(-6)M(S / N = 3)。峰高(1 x 10(-5)胍丁胺)的精密度(R.S.D.)和迁移时间分别为3.7%和2.5%。本CE-CL方法通过测定从大鼠脑,大鼠和猴胃中提取的组织样本中的胍丁胺进行了评估。去除蛋白质后,将样品直接注入CE-CL系统。在胃样品中检测到较高水平的胍丁胺。从大鼠和猴胃中提取的组织样本中的胍丁胺浓度与1950 ng / g湿组织相似。 (c)2006 Elsevier B.V.保留所有权利。

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