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  • 1
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Product ion mass spectral data of [M + H]+ ions of oligosaccharides, mainly tetra- and pentasaccharides, as their dipalmitoyl phosphatidylethanolamine derivatives were obtained using both liquid secondary ion mass spectrometry with B/E linked scanning and fast atom bombardment ionization with collision-induced dissociation/tandem mass spectrometry. Both methods give similar positive product ion spectra of equivalent high sensitivity (detection limits of approximately 50 pmol) that principally contain glycosidic cleavage ions retaining the reducing end of the molecule from which monosaccharide sequence can be deduced. A series of ions from fission of the phosphate ester bond together with glycosidic cleavage are present in the tandem mass spectra and B/E linked scan spectra when helium collision gas is used. Monosaccharide linkage position of isomeric molecules is reflected in the intensity of glycosidic fragmentation, without retention of the oxygen atom, with decreasing cleavage in the order 1-3 〉 1-4 〉 1-6 linkage. Fucose and N-acetylhexosamines show an increased degree of fragmentation over hexose sugars. The application of product ion spectra of derivatized oligosaccharides is demonstrated for characterizing mixed samples and also the acquisition of spectra directly from the silica surface of high-performance thin-layer chromatography plates.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An optimized procedure is reported for the analysis of non-volatile compounds from the surface of silica gel high-performance thin-layer chromatography plates. Following chromatography individual compound bands, excised from the plate with their aluminium support and attached to the normal probe target with an electro-conducting adhesive, were ionized by liquid secondary ion mass spectrometry (LSIMS). Several compound types were analysed to assess sensitivity and specificity of detection. Urinary porphyrins provided molecular weight information from subnanomolar amounts. The detection sensitivities of free, glycine-conjugated and taurine-conjugated bile acids were approximately 125 pmol, 100 pmol and 20 pmol, respectively. A 21-component mixture containing oligosaccharide derivatives was used to evaluate the retention of spatial resolution and specificity achievable by the method. Prevention of diffusion with optimal definition of sample bands, avoidance of electrical insulation between matrix and target probe (particularly in negative ion mode) and matrix conditions were important determinants of sensitivity for in situ LSIMS analysis. Irreversible adsorption levels on the silica gel plate were shown to be greater using solvent extraction of compounds from silica removed from the plate than from in situ LSIMS detection.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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