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Derivatization of Hydrophobic Amino Acids in Nonaqueous Media and Separation by Nonaqueous Capillary Electrophoresis with Laser-Induced Fluorescence Detection

机译:非水介质中疏水性氨基酸的衍生化和非水毛细管电泳-激光诱导荧光检测分离

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摘要

A method of nonaqueous capillary electrophoresis was established for the separation and determination of alanine, phenylalanine, isoleucine and valine after derivatization with 4-chloro-7-nitrobenzo-2-oxa-1, 3-diazol in nonaqueous media. The derivatization and separation conditions were optimized. The optimum derivatization conditions were 70 min for the reaction time, 55 °C for the reaction temperature and 20 mM ammonium acetate in methanol for the derivatization buffer. The most suitable running buffer was composed of 60 mM ammonium acetate, 10% acetonitrile in methanol with a fused-silica capillary column (47 cm × 75 µm i.d.), 20 kV applied voltage and 20 °C capillary temperature. The correlation coefficients were better than 0.995 in the investigated concentration ranges. The relative standard deviation (R.S.D.) (n = 5) of the migration times and peak areas were 2.0–4.3% and 1.9–4.5%, respectively. The method was applied to the determination of four compounds in two compound amino acid injections, with the exception of phenylalanine, the recoveries for the other three compounds ranging between 88–116%.
机译:建立了一种非水毛细管电泳方法,用于在非水介质中用4-氯-7-硝基苯并-2-恶唑-1、3-二唑衍生化后分离和测定丙氨酸,苯丙氨酸,异亮氨酸和缬氨酸。优化了衍生化和分离条件。最佳衍生条件为:反应时间为70分钟,反应温度为55°C,衍生缓冲液中甲醇中的20 mM乙酸铵为最佳。最合适的运行缓冲液由60 mM醋酸铵,含10%乙腈的甲醇和熔融石英毛细管柱(内径47 cm×75 µm),施加的电压为20 kV和毛细管温度为20°C组成。在研究的浓度范围内,相关系数优于0.995。迁移时间和峰面积的相对标准偏差(R.S.D.)(n = 5)分别为2.0-4.3%和1.9-4.5%。该方法用于两次氨基酸注射液中四种化合物的测定,苯丙氨酸除外,其他三种化合物的回收率在88–116%之间。

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