Derivatization strategies for the determination of biogenic amines in wines by chromatographic and electrophoretic techniques

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 May 15;879(17-18):1270-81. doi: 10.1016/j.jchromb.2010.11.020. Epub 2010 Dec 1.

Abstract

This paper revises the derivatization approaches for the determination of biogenic amines in wines. Since most of these amines display poor spectroscopic features to be detected by UV absorption or emission (fluorescence) spectroscopy, derivatization is necessary to attain the desired sensitivity. Reagents such as o-phthaldialdehyde, fluorenylmethylchloroformate, dansyl-Cl and dabsyl-Cl have widely been used for analytical labeling through amino group. A comparison of features of off- and on-line pre- and post chromatographic/electrophoretic labeling is given using 1,2-naphthoquinone-4-sulfonate (NQS) as an example. The evaluation of the influence of the wine sample composition on the derivatization process indicates that pre-column labeling may undergo more severe matrix effects.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Biogenic Amines / analysis*
  • Chromatography, Liquid / methods*
  • Electrophoresis, Capillary / methods*
  • Naphthoquinones / chemistry
  • Wine / analysis*

Substances

  • Biogenic Amines
  • Naphthoquinones
  • 1,2-naphthoquinone-4-sulfonate