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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of agricultural and food chemistry 14 (1966), S. 496-498 
    ISSN: 1520-5118
    Source: ACS Legacy Archives
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 42 (1977), S. 0 
    ISSN: 1750-3841
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: L-ascorbic acid (AA) plus dehydroascorbic acid (DHAA) in foods were determined manually and with an automated sample processor according to the principles of the 2,4-dinitrophenylhydrazine method of Pelletier [J. Lab. & Clin. Med. (1968), 72: 674] for biological materials but with modifications that rendered the methods simpler and applicable to foods. These methods eliminated interference from reductones (arising from sugars during food processing) and of diketogulonic acid (a product of the oxidation of DHAA). Sucrose in a concentration 30,000 times that of AA did not affect the vitamin C assay values. Fructose and glucose, in concentrations respectively 417 and 1668 times that of AA, increased the vitamin C values by only 2–3%. Since a higher range of concentrations of fructose and glucose together gave rather constant increase (8%) in vitamin C values, possible interference from the sugars in noncitrus fruits was eliminated by incorporating a mixture of these sugars in the solutions of standards and samples. Comparisons of vitamin C values in food between the proposed procedures and a modification of the widely used method of Roe [J. Biol. Chem. (1961b) 236: 1611] showed agreement (±5%) for 70% of the foods analyzed. Values were approximately 10% lower by the proposed procedures in the remaining samples. These differences were attributed to the greater specificity of the new methods. Precision of the new procedures was generally within a coefficient of variation of 6% and values (mean of 4 assays on different days) obtained with an automatic sample processor and with manual analyses agreed within 3%.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 10 (1983), S. 130-135 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: To evaluate the accuracy of glucose methods, we have set up an isotope dilution gas chromatographic mass spectrometric method where methyloxime trimethylsilyl derivatives of monosaccharides were separated with a SP-2100 fused silica column. An autodiluter was found suitable for delivering aliquots for derivatization: CV of 0.13% (aqueous) and 0.24% (serum). Ions at m/z 319 (non-labelled) and 323 (deuterium-labelled) were selected for glucose, galactose and mannose, and at m/z 307 and 311 for fructose. Optimization of ion monitoring with a Finnigan 4000 gas chromatograph mass spectrometer 6110 data system was limited to one scan per second without full compensation for 0.1 u shifts. A CV of 0.65% in isotope ratios was obtained for 30 injections (three per vial) of one glucose standard. A similar variation between duplicate injections was obtained with serum. Glucose measurements on 36 serum specimens (six individuals) were made by gas chromatography mass spectrometry and by both a manual (reference) and a flow-through method using hexokinase and glucose-6-phosphate dehydrogenase. Mean glucose by gas chromatography mass spectrometry was 5.57 mmol l-1; bias was -1.7% manually and +1.2% by the automated method. Average concentrations (mmol l-1) of other hexoses were low: mannose (0.058), fructose (0.015) and galactose (0.005). Glucose measurements of two control sera bracketed with standards showed satisfactory agreeement between the three methods. CV of 1.2 to 1.4% by gas chromatography mass spectrometry indicate that further refinements are required.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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