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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Analysis of furan in foods by headspace solid-phase microextraction-gas chromatography-ion trap mass spectrometry
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Analysis of furan in foods by headspace solid-phase microextraction-gas chromatography-ion trap mass spectrometry

机译:顶空固相微萃取-气相色谱-离子阱质谱法分析食品中的呋喃

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摘要

A headspace-solid-phase microextraction (HS-SPME) coupled to gas chromatography-ion trap mass spectrometry (GC-IT-MS) method is proposed for the analysis of furan in different heat-treated carbohydrate-rich food samples. The extraction efficiency of six commercially available fibres was evaluated and it was found that a 75 mu m carboxen/polydimethylsiloxane coating was the most suitable for the extraction of the furan. Parameters affecting the efficiency of HS-SPME procedure such as extraction temperature and time, ionic strength, headspace and aqueous volume ratio (V-h/V-w), desorption temperature and time, were optimized. Quality parameters were established using spiked water and food samples. Linearity ranged between 0.02 and 0.5 ng g(-1) and run-to-run and day-to-day precisions for food samples were lower than 6% and 10%, respectively. The limit of detection (LOD) of the method is sample dependent and ranged from 8 to 70 pg g(-1), while the limit of quantification is from 30 to 250 pg g(-1). Isotope dilution using furan-d(4) is proposed for furan determination providing similar results to those obtained by standard addition with internal standard (US Food and Drug Administration method). The developed HS-SPME-GC-IT-MS method was applied to the analysis of furan in different Spanish food samples from a local market, and concentrations ranging from 0.17 to 2279 ng g(-1) were found. (c) 2007 Elsevier B.V. All rights reserved.
机译:提出了一种顶空-固相微萃取(HS-SPME)结合气相色谱-离子阱质谱(GC-IT-MS)方法来分析不同热处理过的富含碳水化合物的食物样品中的呋喃的方法。评价了六种市售纤维的提取效率,发现75μm的羧基/聚二甲基硅氧烷涂层最适合于呋喃的提取。优化了影响HS-SPME方法效率的参数,例如萃取温度和时间,离子强度,顶空和水体积比(V-h / V-w),解吸温度和时间。使用加标的水和食物样品建立质量参数。线性范围在0.02至0.5 ng g(-1)之间,食品样品的逐次运行和日常精度分别低于6%和10%。该方法的检出限(LOD)取决于样品,范围为8到70 pg g(-1),而定量的范围是30到250 pg g(-1)。提出了使用呋喃-d(4)进行同位素稀释以测定呋喃的方法,其结果与通过内标标准添加(美国食品药品管理局方法)获得的结果相似。发达的HS-SPME-GC-IT-MS方法用于分析来自当地市场的不同西班牙食品样品中的呋喃,发现浓度范围为0.17至2279 ng g(-1)。 (c)2007 Elsevier B.V.保留所有权利。

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