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Development and Validation of a High Performance Liquid Chromatographic Method for Simultaneous Determination of Vitamins A and D-3 in Fluid Milk Products

机译:高效液相色谱法同时测定流体乳产品中维生素A和D-3的高效液相色谱法的开发与验证

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An HPLC method for simultaneous determination of vitamins A and D-3 in fluid milk was developed and validated. Saponification and extraction conditions were studied for optimum recovery and simplicity. An RP HPLC system equipped with a C-18 column and diode array detector was used for quantitation. The method was subjected to a single-laboratory validation using skim, 2% fat, and whole milk samples at concentrations of 50, 100, and 200% of the recommended fortification levels for vitamins A and D-3 for Grade "A" fluid milk. The method quantitation limits for vitamins A and D-3 were 0.0072 and 0.0026 mu g/mL, respectively, Average recoveries between 94 and 110% and SD values ranging from 2.7 to 6.9% were obtained for both vitamins A and D-3. The accuracy of the method was evaluated using a National Institute of Standards and Technology standard reference material (1849a) and proficiency test samples.
机译:开发并验证了一种用于同时测定液体乳中维生素A和D-3的HPLC方法。 研究了皂化和提取条件,以获得最佳的恢复和简单性。 配备有C-18柱和二极管阵列检测器的RP HPLC系统用于定量。 使用Skim,2%脂肪和全脂牛奶样品以50,100,200%的浓度为“A”牛奶等级“A”流体牛奶,使用脱脂剂,2%脂肪和全牛奶样品进行单实验室验证。 。 对于维生素A和D-3的方法定量限制分别为0.0072和0.0026μg/ ml,分别为5.7至110%的平均回收率为2.7至6.9%的维生素A和D-3的SD值。 使用国家标准和技术标准参考资料(1849A)和熟练程度测试样品进行评估该方法的准确性。

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