首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Simultaneous analysis of free amino acids and biogenic amines in honey and wine samples using in loop orthophthalaldeyde derivatization procedure
【24h】

Simultaneous analysis of free amino acids and biogenic amines in honey and wine samples using in loop orthophthalaldeyde derivatization procedure

机译:使用环邻苯二甲醛衍生化方法同时分析蜂蜜和葡萄酒样品中的游离氨基酸和生物胺

获取原文
获取原文并翻译 | 示例
           

摘要

This work presents a RP-HPLC method for the simultaneous quantification of free amino acids and biogenic amines in liquid food matrices and the results of the application to honey and wine samples obtained from different production processes and geographic origins. The developed methodology is based on a pre-column derivatization with o-phthaldialdehyde carried out in the sample injection loop. The compounds were separated in a Nova-Pack RP-C-18 column (150 mm x 3.9 mm, 4 mu m) at 35 degrees C. The mobile phase used was a mixture of phase A: 10 mM sodium phosphate buffer (pH 7.3), methanol and tetrahydrofuran (91:8:1); and phase B: methanol and phosphate buffer (80:20), with a flow rate of 1.0 ml/min. Fluorescence detection was used at an excitation wavelength of 3 35 nm and an emission wavelength of 440 mn. The separation and quantification of 19 amino acids and 6 amines was carried out in a single run as their OPA/MCE derivatives elute within 80 min, ensuring a reproducible quantification. The method showed to be adequate for the purpose, with an average RSD of 2% for the different amino acids; detection limits varying between 0.71 mg/l (Asn) and 8.26 mg/l (Lys) and recovery rates between 63.0% (Cad) and 98.0% (Asp). The amino acids present at the highest concentration in honey and wine samples were phenylalanine and arginine, respectively. Only residual levels of biogenic amines were detected in the analysed samples. (c) 2007 Elsevier B.V. All rights reserved.
机译:这项工作提出了一种RP-HPLC方法,用于同时定量液体食品基质中的游离氨基酸和生物胺,以及将其应用于从不同生产过程和地理来源获得的蜂蜜和葡萄酒样品的结果。所开发的方法是基于在样品进样回路中对邻苯二甲醛进行的柱前衍生。将化合物在35摄氏度的Nova-Pack RP-C-18色谱柱(150 mm x 3.9 mm,4μm)中分离。使用的流动相是A相的混合物:10 mM磷酸钠缓冲液(pH 7.3) ),甲醇和四氢呋喃(91:8:1); B相:甲醇和磷酸盐缓冲液(80:20),流速为1.0 ml / min。在3 35 nm的激发波长和440 mn的发射波长下使用荧光检测。一次分离和定量分析19种氨基酸和6种胺,因为它们的OPA / MCE衍生物可在80分钟内洗脱,从而确保了可重复的定量。结果表明该方法足以满足要求,不同氨基酸的平均RSD为2%。检出限在0.71 mg / l(Asn)和8.26 mg / l(Lys)之间变化,回收率在63.0%(Cad)和98.0%(Asp)之间。蜂蜜和葡萄酒样品中浓度最高的氨基酸分别是苯丙氨酸和精氨酸。在分析的样品中仅检测到残留的生物胺含量。 (c)2007 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号