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同位素稀释固相微萃取-气相色谱-质谱联用(SPME-GC-MS)快速测定加热食品中的呋喃

Rapid determination of furan in heated foodstuffs by isotope dilution solid phase micro-extraction-gas chromatography--mass spectrometry (SPME-GC-MS).

作者信息

Goldmann Till, Périsset Adrienne, Scanlan Francis, Stadler Richard H

机构信息

Nestlé Research Center, Nestec Ltd., Vers-chez-les-Blanc, CH-1000 Lausanne 26, Switzerland.

出版信息

Analyst. 2005 Jun;130(6):878-83. doi: 10.1039/b419270b. Epub 2005 Apr 12.

DOI:10.1039/b419270b
PMID:15912236
Abstract

An analytical method is reported to determine trace amounts of furan in several different commercial foodstuffs that are subjected to thermal treatment. The SPME-GC-MS method is rapid and robust, and entails the following steps: addition of deuterated furan to the sample, sodium chloride-assisted extraction into the headspace, cryofocussing, and finally fibre desorption and GC-MS analysis. Furan is quantified by the use of an external calibration curve, achieving a decision limit (CC alpha) and detection capability (CC beta) of 17 pg and 43 pg, respectively, as absolute furan concentration in a 10 ml headspace vial. The method is applicable to a wide variety of foods, including fruits juices, baby foods in jars, canned foods, pet food, coffee and coffee substitutes. Typical amounts of furan found in selected foodstuffs range from about 1 microg kg(-1) (fruit juice) to 110 microg kg(-1) (baby food containing cooked vegetables). In-house validation data show good precision and accuracy of the method, with a typical repeatability of between 5 and 16% in different food matrices, and trueness determined in orange juice and coffee as 87 and 93%, respectively. Moreover, the measurement uncertainty has been evaluated for two matrices (fruit juice and coffee). Studies on short-term stability of furan in certain foods are also presented, and show that the furan content decreases in food while heating for preparation or reconstitution.

摘要

据报道,有一种分析方法可用于测定经过热处理的几种不同商业食品中的痕量呋喃。固相微萃取-气相色谱-质谱联用(SPME-GC-MS)方法快速且可靠,包括以下步骤:向样品中添加氘代呋喃,氯化钠辅助萃取至顶空,低温聚焦,最后纤维解吸和气相色谱-质谱分析。呋喃通过使用外标校准曲线进行定量,在10 ml顶空瓶中,绝对呋喃浓度的决策限(CCα)和检测能力(CCβ)分别为17 pg和43 pg。该方法适用于多种食品,包括果汁、罐装婴儿食品、罐头食品、宠物食品、咖啡和咖啡替代品。在选定食品中发现的呋喃典型含量范围约为1 μg kg-1(果汁)至110 μg kg-1(含煮熟蔬菜的婴儿食品)。内部验证数据表明该方法具有良好的精密度和准确度,在不同食品基质中的典型重复性在5%至16%之间,在橙汁和咖啡中测定的准确度分别为87%和93%。此外,还评估了两种基质(果汁和咖啡)的测量不确定度。还介绍了某些食品中呋喃短期稳定性的研究,结果表明,在加热制备或复溶过程中,食品中的呋喃含量会降低。

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