1979
DOI: 10.1093/jaoac/62.6.1292
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High Pressure Liquid Chromatographic Determination of Carbohydrates in Food Products: Evaluation of Method

Abstract: A high pressure liquid chromatographic (HFLC) method for determining 5 common carbohydrates in food products was evaluated. Reproducibility data were generated showing a relative standard deviation of 2.8%. Recovery studies on a variety of foods gave an average recovery of 98.8%. The HPLC data for 3 varieties of ready-to-eat cereals were compared with data from 4 independent laboratories using current AOAC chemical methods. The HPLC mean values differed from the chemical mean values by 3.2%.

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Cited by 10 publications
(9 citation statements)
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“…[ Carbohydrate analysis: For carbohydrate analysis, 2 mL of medium was taken every 2 days, centrifuged for 10 min at 10,000 rpm, and filtered through acrodiscs (0.45-µm pore size, Nalgene®, NY, USA). Sucrose was determined by HPLC according to the previously reported procedure [25].…”
Section: Kinetic Studies and Viability Assaymentioning
confidence: 99%
“…[ Carbohydrate analysis: For carbohydrate analysis, 2 mL of medium was taken every 2 days, centrifuged for 10 min at 10,000 rpm, and filtered through acrodiscs (0.45-µm pore size, Nalgene®, NY, USA). Sucrose was determined by HPLC according to the previously reported procedure [25].…”
Section: Kinetic Studies and Viability Assaymentioning
confidence: 99%
“…Comparisons with other results (DeVries et al 1979;Dunmire and Otto 1979;Iverson and Bueno 1981;Picha 1985) are difficult because different foods were tested and precision data were not reported in detail.…”
Section: Recovery Of Added Solutesmentioning
confidence: 99%
“…In addition, extracting dough in water would allow the measurement of sugars and ethanol in a single extract, which is not possible with ethanolic solvents. DeVries et al (1979) extracted a variety of food products in water at 80-90°C, with good recovery of sugars. The Approved Method 80-04 for measuring simple sugars in cereal products involves extraction in boiling water (AACC International 2000).…”
mentioning
confidence: 99%
“…The isocratic acetonitrile-water (78:22, v/v) mobile phase employed with the ELSD to deter mine fructose and glucose did not adequately resolve both monosaccharides due to the dete rioration of the NH 2 column, which is very sus ceptible to water (19). Several changes in the proportions of the mobile phase components were assayed (acetonitrile-water [80:20,82:18, and 85:15, v/v]), and the flow rate was varied between 0.8-1.2 mL/min.…”
Section: Optimization Of Chromatographic Conditions For Ridmentioning
confidence: 99%