DETERMINATION OF MARINE MONOSACCHARIDES BY HIGH-PH ANION-EXCHANGE CHROMATOGRAPHY WITH PULSED AMPEROMETRIC DETECTION

Citation
P. Kerherve et al., DETERMINATION OF MARINE MONOSACCHARIDES BY HIGH-PH ANION-EXCHANGE CHROMATOGRAPHY WITH PULSED AMPEROMETRIC DETECTION, Journal of chromatography, 718(2), 1995, pp. 283-289
Citations number
36
Categorie Soggetti
Chemistry Analytical","Biochemical Research Methods
Journal title
Volume
718
Issue
2
Year of publication
1995
Pages
283 - 289
Database
ISI
SICI code
Abstract
In this study, a method was developed for the determination of ten mon osaccharides in marine particulate matter utilizing high-pH anion-exch ange chromatography (HPAEC) with pulsed amperometric detection (PAD). Samples were analyzed using a Dionex CarboPac PA1 column with a flow-r ate of 1 ml/min and addition of 380 mM NaOH post-column. The effect of NaOH concentration (between 0.5 and 50 mM) on the monosaccharide sepa rations expressed by the capacity factor (k') was tested. The results showed that one isocratic elution was unfit to discriminate properly a rabinose, fructose, fucose, galactose, glucosamine, glucose, mannose, ribose, rhamnose and xylose. Thus, two isocratic elutions, at 2.5 and 15 mM NaOH, were necessary to separate and quantify with significant s electivity (alpha) and resolution terms (R(s)), respectively, glucose, mannose, xylose and fucose, rhamnose, arabinose, glucosamine, galacto se, fructose and ribose. The method is linear for all sugars over the concentration range tested (25-250 ng per injection or 1-10 mg/g) expe cted in marine concentrated samples, and reproducibility was found to be satisfactory (1.7-4.8%), except for ribose (27%). Monosaccharide de terminations from two kinds of marine matrix (hydrolyzates of surface sediment and of suspended particulate matter) are presented.