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高效液相色谱法-柱前衍生化-4-氯-3,5-二硝基苯甲酰氟测定氨基酸。

High-performance liquid chromatographic method for determination of amino acids by precolumn derivatization with 4-chloro-3,5-dinitrobenzotrifluoride.

机构信息

College of Agriculture and Biotechnology, China Agricultural University, No. 2 Yuanmingyuan West Road, Beijing 100193, China.

出版信息

Anal Chim Acta. 2009 Nov 10;654(2):154-61. doi: 10.1016/j.aca.2009.09.027. Epub 2009 Sep 26.

Abstract

This work presents an high-performance liquid chromatography method for the determination of amino acids after precolumn derivatization with 4-chloro-3,5-dinitrobenzotrifluoride (CNBF) which can readily react with both primary and secondary amines. The precolumn derivatization conditions, including the CNBF concentration, reaction pH, temperature and reaction time were investigated for method optimization. In pH 9.0 borate buffer, the reaction of amino acids with CNBF was carried out at 60 degrees C for 30min, the optimized concentration of CNBF was 70mmol L(-1) and the molar ratio of amino acids to CNBF was 1:5.25. The chromatographic separation of 19 amino acids derivatives was performed on a Kromasil ODS C(18) column (250mm x 4.6mm, 5microm) with good reproducibility, and ultraviolet detection was applied at 260 nm. The mobile phase was a mixture of phase A (acetonitrile) and phase B (acetate buffer, acetonitrile, triethylamine; 82.8:17:0.2, pH 4.9), and the flow rate was 0.4mL min(-1). The separation of all the labeled amino acids was achieved within 45min at room temperature by gradient elution mode. The method linearity, calculated for each amino acid, had a correlation coefficient higher than 0.9979, in concentrations ranging from 9.60 to 3330.00 micromol L(-1). The detection limits of amino acids were 2.40-6.50micromol L(-1), at a signal-to-noise ratio of 3. The proposed method was applied for the determination of amino acids in beer with recoveries of 97.0-103.9% and relative standard deviations of 2.62-4.22%, respectively. This method showed good accuracy and repeatability that can be used for the quantification of amino acids in real samples.

摘要

本文提出了一种高效液相色谱法,用于在柱前衍生化后测定氨基酸,衍生化试剂是 4-氯-3,5-二硝基三氟甲苯(CNBF),它可以与伯胺和仲胺迅速反应。本文对柱前衍生化条件,包括 CNBF 浓度、反应 pH 值、温度和反应时间进行了考察,以优化方法。在 pH 值为 9.0 的硼酸缓冲液中,氨基酸与 CNBF 的反应在 60°C 下进行 30min,优化的 CNBF 浓度为 70mmol L(-1),氨基酸与 CNBF 的摩尔比为 1:5.25。19 种氨基酸衍生物的色谱分离在 Kromasil ODS C(18)柱(250mm x 4.6mm,5μm)上进行,具有良好的重现性,并在 260nm 处进行紫外检测。流动相为相 A(乙腈)和相 B(醋酸盐缓冲液、乙腈、三乙胺;82.8:17:0.2,pH 值 4.9)的混合物,流速为 0.4mL min(-1)。在室温下通过梯度洗脱模式,所有标记氨基酸在 45min 内实现了分离。每种氨基酸的线性关系,其相关系数均高于 0.9979,浓度范围为 9.60-3330.00μmol L(-1)。氨基酸的检测限为 2.40-6.50μmol L(-1),信噪比为 3。该方法用于测定啤酒中的氨基酸,回收率为 97.0-103.9%,相对标准偏差为 2.62-4.22%。该方法具有良好的准确性和重复性,可用于实际样品中氨基酸的定量分析。

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