Development of methods for the determination of vitamins A, E and β-carotene in processed foods based on supercritical fluid extraction: a collaborative study

L. Mathiasson, C. Turner, H. Berg, L. Dahlberg, A. Theobald, E. Anklam, R. Ginn, M. Sharman, F. Ulberth, R. Gabernig
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引用次数: 24

Abstract

New methodologies based on supercritical fluid extraction (SFE) have been developed for the determination of fat-soluble vitamins in processed foods. The results obtained so far indicate that SFE is well suited to extraction of fat-soluble vitamins from food products, although validation work is required to establish accuracy and precision. The vitamins investigated were A, E and β -carotene, and the processed foods were UHT milk, milk powder, minced meat, liver paste, infant formula, canned baby food and margarine. Extraction equipment employed analyte collection on either a solid-phase trap or in a solvent. After extraction, the samples were saponified and the vitamins determined using reversed-phase liquid chromatography with ultraviolet or fluorescence detection. Sample throughput was at least 12 samples day-1, i.e. at least twice the number achievable with a conventional extraction methodology. The detection limits for the vitamins in different processed foods were well below 0.1 μg g -1. Recoveries (in comparison with vitamin levels obtained using conventional solvent extraction) were close to 100% for experienced personal with access to modern automatic equipment. To reach this level, it was necessary to protect the vitamins with an antioxidant during the different steps of the analysis procedure, to add methanol or ethanol to the extraction cell to facilitate the analyte extraction from the food matrix, and when using a solid-phase trap, to employ a fractionated extraction-elution procedure to prevent breakthrough losses. The developed methods were tested in a validation exercise between five laboratories, which had taken part in the method development, and in an intercomparison between 10 laboratories including laboratories with less experience of vitamin determination. The within-laboratory RSD was generally ≤ 11%. The average of the between-laboratory relative standard deviation (RSD) was about 23% in the validation, and increased to about 40% in the intercomparison. Ruggedness tests performed at different steps of the project showed that different types and models of equipment did not give large differences in recoveries. Thus, the increasing RSD can largely be ascribed to differences in experience in vitamin analysis of the participants.
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基于超临界流体萃取的加工食品中维生素A、E和β-胡萝卜素测定方法的发展:一项合作研究
基于超临界流体萃取(SFE)的新方法已被开发用于测定加工食品中的脂溶性维生素。目前所获得的结果表明,SFE非常适合从食品中提取脂溶性维生素,尽管需要进行验证工作以建立准确性和精密度。研究的维生素为A、E和β -胡萝卜素,加工食品为UHT牛奶、奶粉、肉末、肝膏、婴儿配方奶粉、婴儿罐头食品和人造黄油。在固相阱或溶剂中收集分析物的萃取设备。提取后皂化,反相液相色谱法测定维生素含量,紫外或荧光检测。样品通量至少为第1天12个样品,即至少是传统提取方法的两倍。不同加工食品中维生素的检出限均低于0.1 μg -1。对于使用现代自动设备的有经验的人员,回收率(与使用传统溶剂萃取获得的维生素水平相比)接近100%。为了达到这一水平,有必要在分析过程的不同步骤中用抗氧化剂保护维生素,在提取池中添加甲醇或乙醇以促进从食物基质中提取分析物,当使用固相陷阱时,采用分馏提取-洗脱程序以防止突破损失。所开发的方法在参与方法开发的5个实验室之间进行了验证,并在10个实验室之间进行了相互比较,其中包括在维生素测定方面经验较少的实验室。实验室内RSD一般≤11%。验证时实验室间相对标准偏差(RSD)均值约为23%,比对时RSD均值约为40%。在项目的不同步骤进行的坚固性测试表明,不同类型和型号的设备在回收方面没有太大差异。因此,RSD的增加很大程度上归因于参与者在维生素分析方面的经验差异。
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