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A fit-for-purpose method to monitor 16 European Union PAHs in food: results of five years of official food control in two Italian regions

机译:一种适合目的的方法来监控食品中的16种欧盟PAH:意大利两个地区五年官方食品控制的结果

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摘要

A gas-chromatographic single-quadrupole analytical method for the analysis of the 16 priority European Union (EU) polycyclic aromatic hydrocarbons (PAHs) in food is presented. The method fulfils the request of Regulation EU 836/2011 for an analytical procedure to be used for official control of PAHs in food in EU member states. The sample preparation involves a pressurised liquid extraction (PLE) with an in-cell clean-up step followed by a lipid removal using solid-phase extraction (SPE) on a styrene divinylbenzene stationary phase (SDVB) and a final gel-permeation chromatography (GPC) step. To reach a better sensitivity for all the analytes, including the heaviest last eluting PAHs, 3 μl of the purified extract were injected in solvent vent mode using a programmable temperature vaporization (PTV) injector. The isobaric PAH isomers were successfully separated using an Agilent Technologies DB-17MS (20 m × 0.18 mm × 0.18 μm) column. The method was fully validated using an in-house approach and the sensitivity, accuracy and precision obtained were satisfactory. The method expanded uncertainty was estimated and it was verified that it was below the maximum standard measurement uncertainty. Moreover, the results of 347 samples of meat and meat products, fish and fish products and mussels collected from January 2012 to December 2016 in the Marche and Umbria regions of Italy are reported. None of the samples exceed the maximum levels fixed by EU Regulation 835/2011, and clams turned out to be the most contaminated among the food matrices analysed. Finally, an estimate of the sum of four marker PAHs (benzo[a]anthracene, benzo[b]fluoranthene, benzo[a]pyrene, chrysene) as indicator of the PAHs contamination was done by comparison with the 16 carcinogenic PAHs sum.
机译:提出了一种气相色谱单四极杆分析方法,用于分析食品中的16种优先级欧盟(EU)多环芳烃(PAHs)。该方法满足欧盟836/2011法规的要求,该分析方法可用于欧盟成员国食品中多环芳烃的官方控制。样品制备涉及带有细胞内净化步骤的加压液体萃取(PLE),然后使用固相萃取(SPE)在苯乙烯二乙烯基苯固定相(SDVB)上进行脂质去除并进行最终的凝胶渗透色谱( GPC)步骤。为了对所有分析物(包括最重的最后洗脱的PAHs)达到更高的灵敏度,使用可编程温度蒸发(PTV)进样器以溶剂排放模式进样3 µl纯化的提取物。使用Agilent Technologies DB-17MS(20 m×0.18 mm×0.18μm)色谱柱成功分离了同量PAH异构体。该方法已使用内部方法进行了充分验证,所获得的灵敏度,准确性和精密度均令人满意。对该方法扩展的不确定度进行了估计,并验证了该不确定度低于最大标准测量不确定度。此外,据报道,2012年1月至2016年12月在意大利马尔凯和翁布里亚地区采集了347个肉类,肉类产品,鱼和鱼产品以及贻贝的样品。样品均未超过欧盟法规835/2011规定的最高含量,在分析的食品基质中,蛤lam是最受污染的。最后,通过与16种致癌PAHs的总和进行比较,对作为PAHs污染指标的四种标记PAHs(苯并[a]蒽,苯并[b]荧蒽,苯并[a] re,)的总和进行了估算。

著录项

  • 来源
    《Food additives & contaminants》 |2017年第7期|1140-1152|共13页
  • 作者单位

    Istituto Zooprofilattico Sperimentale dell’Umbria e delle Marche, Laboratorio Controllo Chimico e Biomonitoraggio, Ancona, Italy;

    Istituto Zooprofilattico Sperimentale dell’Umbria e delle Marche, Laboratorio Controllo Chimico e Biomonitoraggio, Ancona, Italy;

    Istituto Zooprofilattico Sperimentale dell’Umbria e delle Marche, Laboratorio Controllo Chimico e Biomonitoraggio, Ancona, Italy;

    Università degli Studi di Teramo, Facoltà di Bioscienze e Tecnologie Agroalimentari ed Ambientali, Teramo, Italy;

    Istituto Zooprofilattico Sperimentale dell’Umbria e delle Marche, Laboratorio Controllo Chimico e Biomonitoraggio, Ancona, Italy;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    chromatography-GC/MS; fish and fish products; In-house validation; PAH; processed foods; smoked food;

    机译:色谱-GC / MS鱼和鱼制品;内部验证;PAH;加工食品;烟熏食品;

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