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Detection of peptides by precolumn derivatization with biuret reagent and preconcentration on capillary liquid chromatography columns with electrochemical detection

机译:通过缩二脲试剂进行柱前衍生化并在毛细管液相色谱柱上进行电化学检测预浓缩来检测肽

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The separation and detection of biuret complexes of neuropeptides by capillary liquid chromatography with electrochemical detection was explored. Capillaries of 25-mu m inner diameter packed with base-resistant, polymer-based reversed-phase particles were used for separation, and C-fiber electrodes were used for detection. Detection at the C-fiber electrode was found to have some differences in relative sensitivity for peptides compared to glassy carbon electrodes used previously. On-column preconcentration of preformed complexes allowed up to 1-mu L samples to be injected with minimal band broadening resulting in a 100-fold improvement in concentration detection limit with no effect on mass detection limit. Concentration detection limits ranged from 5 to 59 pM, depending upon the peptide, corresponding to 5-59 amol injected. The low concentration detection limit was possible because of minimal baseline disturbances, minimal formation of unwanted products, and high efficiency of complex formation associated with biuret derivatization. The method was applied to determination of vasopressin and bradykinin in dialysates collected with Ei-min sampling frequency from the rat supraoptic nucleus. [References: 33]
机译:探索了毛细管电泳-电化学检测法分离和检测神经肽缩二脲配合物的方法。内径为25μm的毛细管填充有耐碱的聚合物基反相颗粒,用于分离,C纤维电极用于检测。与以前使用的玻璃碳电极相比,发现在C纤维电极上进行检测对肽的相对灵敏度有一些差异。预先完成的复合物的柱上预富集允许以最小的谱带展宽进样多达1μL的样品,从而使浓度检测极限提高100倍,而对质量检测极限没有影响。取决于肽,浓度检测极限范围为5至59 pM,对应于注射的5-59 amol。低浓度检测极限是可能的,因为最小的基线干扰,最小的不想要的产物形成以及与缩二脲衍生化相关的复杂形成的高效率。该方法适用于以大鼠视上核Ei-min采样频率采集的透析液中加压素和缓激肽的测定。 [参考:33]

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