Haedrich Johannes, Stumpf Claudia, Denison Michael S
European Union Reference Laboratory (EU-RL) for Dioxins and PCBs in Feed and Food, CVUA Freiburg, Bissierstraße 5, 79114 Freiburg, Germany.
Ringstr. 5, 79252 Stegen, Germany.
Environ Sci Eur. 2021;33(1):33. doi: 10.1186/s12302-021-00474-2. Epub 2021 Mar 18.
Low maximum and action levels set by the European Union for polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and dioxin-like polychlorinated biphenyls (DL-PCBs) in pig meat (pork) have led to a demand for reliable and cost-effective bioanalytical screening methods implemented upstream of gas chromatography/high-resolution mass spectrometry confirmatory technology, that can detect low levels of contamination in EU-regulated foods with quick turn-around times.
Based on the Chemically Activated LUciferase gene eXpression (CALUX) bioassay, extraction and clean-up steps were optimized for recovery and reproducibility within working ranges significantly lower than in current bioassays. A highly sensitive "3rd generation" recombinant rat hepatoma cell line (H4L7.5c2) containing 20 dioxin responsive elements was exposed to pork sample extracts, and their PCDD/Fs and DL-PCBs levels were evaluated by measuring luciferase activity. The method was validated according to the provisions of Commission Regulation (EU) 2017/644 of 5 April 2017 with spiking experiments performed selectively for PCDD/Fs and DL-PCBs and individual calibration for PCDD/Fs, DL-PCBs and the calculated sum of PCDD/Fs and DL-PCBs. The resulting performance parameters met all legal specifications as confirmed by re-calibration using authentic samples. Cut-off concentrations for assessing compliance with low maximum levels and action levels set for PCDD/Fs and DL-PCBs within a range of 0.50-1.25 pg WHO-TEQ/g fat were derived, ensuring low rates of false-compliant results (ß-error < 1%) and keeping the rate of false-noncompliant results well under control (α-error < 12%).
We present a fast and efficient bioanalytical routine method validated according to the European Union's legal requirements on the basis of authentic samples, allowing the analyst to reliably identify pork samples and any other EU-regulated foods of animal origin suspected to be noncompliant with a high level of performance and turn-around times of 52 h. This was facilitated in particular by a quick and efficient extraction step followed by selective clean-up, use of a highly sensitive "3rd generation" H4L7.5c2 recombinant rat hepatoma cell CALUX bioassay, and optimized assay performance with improved calibrator precision and reduced lack-of-fit errors. New restrictions are proposed for the calibrator bias and the unspecific background contribution to reportable results. The procedure can utilize comparably small sample amounts and allows an annual throughput of 840-1000 samples per lab technician. The described bioanalytical method contributes to the European Commission's objective of generating accurate and reproducible analytical results according to Commission Regulation (EU) 2017/644 across the European Union.
欧盟为猪肉中多氯二苯并 - 对 - 二恶英和二苯并呋喃(PCDD/Fs)以及类二恶英多氯联苯(DL - PCBs)设定了较低的最大限量和行动水平,这使得人们需要一种可靠且具有成本效益的生物分析筛选方法,该方法应用于气相色谱/高分辨率质谱确证技术之前,能够快速周转检测欧盟监管食品中的低水平污染物。
基于化学激活荧光素酶基因表达(CALUX)生物测定法,对提取和净化步骤进行了优化,以在显著低于当前生物测定法的工作范围内实现回收率和重现性。将含有20个二恶英反应元件的高灵敏度“第三代”重组大鼠肝癌细胞系(H4L7.5c2)暴露于猪肉样品提取物中,并通过测量荧光素酶活性评估其PCDD/Fs和DL - PCBs水平。根据欧盟委员会2017年4月5日第2017/644号实施条例的规定对该方法进行了验证,分别针对PCDD/Fs和DL - PCBs进行加标实验,并对PCDD/Fs、DL - PCBs以及计算得出的PCDD/Fs和DL - PCBs总和进行单独校准。使用真实样品重新校准后确认,所得性能参数符合所有法律规范。得出了用于评估是否符合为PCDD/Fs和DL - PCBs设定的低最大限量和行动水平的截断浓度,范围为0.50 - 1.25 pg WHO - TEQ/g脂肪,确保假阳性结果率(β错误<1%)较低,且假阴性结果率得到有效控制(α错误<12%)。
我们提出了一种快速高效的生物分析常规方法,该方法基于真实样品根据欧盟法律要求进行了验证,使分析人员能够可靠地识别猪肉样品以及任何其他疑似不符合规定的欧盟监管动物源性食品,具有高性能和52小时的周转时间。这尤其得益于快速高效的提取步骤,随后进行选择性净化,使用高灵敏度的“第三代”H4L7.5c2重组大鼠肝癌细胞CALUX生物测定法,以及通过提高校准品精度和减少失拟误差优化测定性能。针对校准品偏差和对可报告结果的非特异性背景贡献提出了新的限制。该程序可使用相对少量的样品,每位实验室技术人员每年可处理840 - 1000个样品。所描述的生物分析方法有助于欧盟委员会实现根据第2017/644号实施条例在欧盟范围内生成准确且可重现的分析结果的目标。