Lestingi Carmela, Tavoloni Tamara, Bardeggia Valentina, Perugini Monia, Piersanti Arianna
a Istituto Zooprofilattico Sperimentale dell'Umbria e delle Marche , Laboratorio Controllo Chimico e Biomonitoraggio , Ancona , Italy.
b Università degli Studi di Teramo , Facoltà di Bioscienze e Tecnologie Agroalimentari ed Ambientali , Teramo , Italy.
Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2017 Jul;34(7):1140-1152. doi: 10.1080/19440049.2017.1325969. Epub 2017 Jul 12.
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.
本文介绍了一种气相色谱单四极杆分析方法,用于分析食品中16种欧盟优先控制的多环芳烃(PAHs)。该方法满足欧盟法规836/2011对用于欧盟成员国食品中PAHs官方控制分析程序的要求。样品制备包括采用细胞内净化步骤的加压液体萃取(PLE),随后在苯乙烯二乙烯基苯固定相(SDVB)上使用固相萃取(SPE)去除脂质,以及最后的凝胶渗透色谱(GPC)步骤。为了对所有分析物,包括最后洗脱的最重PAHs,获得更好的灵敏度,使用可编程温度汽化(PTV)进样器以溶剂放空模式注入3 μl纯化提取物。使用安捷伦科技公司的DB-17MS(20 m×0.18 mm×0.18 μm)色谱柱成功分离了等压PAH异构体。该方法采用内部方法进行了全面验证,获得的灵敏度、准确度和精密度令人满意。估计了该方法的扩展不确定度,并验证其低于最大标准测量不确定度。此外,还报告了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的347份肉类和肉类产品、鱼类和鱼类产品以及贻贝样品的结果。没有一个样品超过欧盟法规835/2011规定的最大限量,在所分析的食品基质中,蛤类被证明是污染最严重的。最后,通过与16种致癌PAHs总量比较,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]芘、屈)的总量进行了估计。