CELL-WALL ESTERIFIED PHENOLIC DIMERS - IDENTIFICATION AND QUANTIFICATION BY REVERSE-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY AND DIODE-ARRAY DETECTION
Kw. Waldron et al., CELL-WALL ESTERIFIED PHENOLIC DIMERS - IDENTIFICATION AND QUANTIFICATION BY REVERSE-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY AND DIODE-ARRAY DETECTION, Phytochemical analysis, 7(6), 1996, pp. 305-312
An optimized high performance liquid chromatography (HPLC) procedure h
as been developed for the analysis and quantification of all of the kn
own ferulic acid dehydrodimers, and the principle phenolic aldehydes a
nd acids, found in the cell walls of higher plants. The HPLC system us
es an ODS2 reverse phase column (5 mu m particle size) eluted with a m
ethanol, acetonitrile and water gradient with detection at 280 nm. In
addition to providing baseline resolution of most components, the meth
od employs a spectrometric detector which enables the precise identifi
cation of eluted components through the analysis of their spectral pro
perties, Analysis of the cell wall phenolics of wheat straw stem (Trit
icum vulgare) was carried out using this method which is highly versat
ile and, for certain components, more sensitive than the current gas c
hromatography-mass spectrometry methodology.