Determination of [13C]galactose enrichment in human plasma by gas chromatography/positive chemical ionization tandem mass spectrometry

Abstract

Galactosemia is a potentially fatal disease resulting from a deficiency of galactose‐1‐phosphate uridyl transferase. In order to perform mechanistic studies designed to elucidate further the etiology of the disease, we required a method to monitor 13C enrichment in plasma galactose following a single oral dose or intravenous infusion of [1‐13C]galactose. Determinations of plasma [13C]galactose enrichment requires methodolgy with extremely high specificity because of potential interference from other low molecular mass plasma constituents and from glucose, an isomer which is present in much higher concentrations. We have developed a method based on gas chromatography/positive chemical ionization tandem mass spectrometry (GC/PCI‐MS/MS) for the precise and accurate determination of plasma [13C]galactose enrichment. The method employed a pentaacetylaldononitrile derivative of galactose in order to improve its GC and MS characteristics. Peak areas resulting from the transitions m/z 328 → 106 and m/z 329 → 107 were used to quantify the relative abundance of labeled and unlabeled galactose. Validation of the method was performed by determination of the precision and accuracy over a wide range of galactose concentrations and 13C enrichments. The GC/PCI‐MS/MS method was able to determine accurately enrichments at galactose concentrations down to 0.8 µM in the presence of 4 mM glucose, making it both highly selective and the most sensitive method currently available. Copyright © 2000 John Wiley & Sons, Ltd.

Acylic Sugar Derivatives for GC/MS Analysis of 13C-Enrichment during Carbohydrate Metabolism

“…Most derivatives in current usage are well suited for carbohydrate analysis − but are of limited utility for metabolic flux analysis because of inadequate formation of MS fragment ions that retain the charge on the anomeric carbon of the original monosaccharide . Hence, although highly desirable for the estimation of flux into carbohydrate anomeric carbons, selective MS fragmentation across the C1−C2 bond is not readily achieved by current methods.…”