TY - JOUR
T1 - Enhancement of the Yu and Ledeen gas-liquid chromatographic method for sialic acid estimation
T2 - Use of methane chemical ionization mass fragmentography
AU - Ashraf, J.
AU - Butterfield, D. A.
AU - Jarnefelt, J.
AU - Laine, R. A.
N1 - Copyright:
Copyright 2004 Elsevier B.V., All rights reserved.
PY - 1980
Y1 - 1980
N2 - The sialic acid present in erythrocyte ghosts was estimated by methane chemical ionization mass fragmentography of the trimethylsilyl methyl glycosides. The internal standard was 3,4,6-tris-trimethylsilyl-α-phenyl-2-deoxy-2-acetamide-D-glucosaminide, as proposed by Yu and Ledeen. The [MH-16]+ions (m/e 610 for the TMS-methylglycoside of N-acetylneuraminic acid and m/e 498 for the internal standard) were used for quantifying nanogram levels of sialic acid in the presence of other contaminating substances. This effectively raises the signal-to-noise ratio for the Yu and Ledeen method by at least two orders of magnitude. The sensitivity and linearity of the method, without use of isotopic carriers, were tested using known quantities of N-acetylneuraminic acid. The limit of detection was below 0.4 nanograms (approximately one picomole). The useful range of detection was 10 ng-1 μg, showing a large dynamic range.
AB - The sialic acid present in erythrocyte ghosts was estimated by methane chemical ionization mass fragmentography of the trimethylsilyl methyl glycosides. The internal standard was 3,4,6-tris-trimethylsilyl-α-phenyl-2-deoxy-2-acetamide-D-glucosaminide, as proposed by Yu and Ledeen. The [MH-16]+ions (m/e 610 for the TMS-methylglycoside of N-acetylneuraminic acid and m/e 498 for the internal standard) were used for quantifying nanogram levels of sialic acid in the presence of other contaminating substances. This effectively raises the signal-to-noise ratio for the Yu and Ledeen method by at least two orders of magnitude. The sensitivity and linearity of the method, without use of isotopic carriers, were tested using known quantities of N-acetylneuraminic acid. The limit of detection was below 0.4 nanograms (approximately one picomole). The useful range of detection was 10 ng-1 μg, showing a large dynamic range.
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M3 - Article
C2 - 7462810
AN - SCOPUS:0019162135
SN - 0022-2275
VL - 21
SP - 1137
EP - 1141
JO - Journal of Lipid Research
JF - Journal of Lipid Research
IS - 8
ER -