[利用一步式 QuEChERS-气相色谱-三重四极杆质谱法快速测定风干牦牛肉中的 15 种 N-亚硝胺]。

Han Xia, Kai-Xuan Tong, Zhe-Hui Zhu, Yu-Jie Xie, Xing-Qiang Wu, Qiao-Ying Chang, Hong-Yi Zhang, Chun-Lin Fan, Hui Chen
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Favorable recoveries of the 15 <i>N</i>-nitrosamines were obtained when the extraction solution was incompletely dried. Thus, the final extract was dried to below 0.5 mL under a mild nitrogen stream and then redissolved to 0.5 mL with acetonitrile. After filtration, 200 μL of the sample was transferred to an autosampler vial for GC-MS/MS analysis. The 15 <i>N</i>-nitrosamines were determined using GC-MS/MS on a DB-HeavyWAX column (30 m×0.25 mm×0.25 μm) with an electron impact ion source in multiple-reaction monitoring (MRM) mode, and quantified using an external standard method. Under the optimized experimental conditions, the results showed that the calibration curves exhibited good linearities for the 15 <i>N</i>-nitrosamines, with correlation coefficients (<i>r</i><sup>2</sup>) greater than 0.9990. The limits of detection (LODs) and the limits of quantification (LOQs) ranged from 0.05 to 0.20 μg/kg and from 0.10 to 0.50 μg/kg, respectively. At spiked levels of 1LOQ, 2LOQ, and 10LOQ, the average recoveries were 79.4%-102.1%, 80.6%-109.5%, and 83.0%-110.6%, respectively, and the relative standard deviations were in the range of 0.8%-16.0%. The low matrix effects of the 15 <i>N</i>-nitrosamines indicated the high sensitivity of the proposed method. The method was applied to detect representative commercial air-dried yak meat samples obtained using different processing techniques. Seven <i>N</i>-nitrosamines, including <i>N</i>-nitrosodimethylamine, <i>N</i>-nitrosodiisobutylamine, <i>N</i>-nitrosodibutylamine, <i>N</i>-methyl-<i>N</i>-phenylnitrous amide, <i>N</i>-ethyl-<i>N</i>-nitrosoaniline, <i>N</i>-nitrosopyrrolidine, and <i>N</i>-nitrosodiphenylamine were detected in all samples. The average contents of the seven <i>N</i>-nitrosamines was 0.08-20.18 μg/kg. The detection rates and average contents of the <i>N</i>-nitrosamines in cooked air-dried yak meat samples were higher than those in traditional raw air-dried yak meat samples. Compared with the manual QuEChERS method, the one-step QuEChERS method developed integrated the extraction and clean-up procedures into one single run, and the detection efficiency was considerably improved. The developed method is simple, rapid, highly sensitive, and insusceptible to human errors. Thus, it is useful for the determination of <i>N</i>-nitrosamines in air-dried yak meat and can be extended to the qualitative and quantitative analysis of <i>N</i>-nitrosamines in other meat products. 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引用次数: 0

摘要

建立了基于气相色谱-三重四极杆质谱(GC-MS/MS)和一步法 QuEChERS 技术同时测定风干牦牛肉中 15 种亚硝胺的方法。根据亚硝胺和样品基质的特点,对水化体积、萃取溶剂、萃取盐和净化材料进行了优化。优化条件如下10 mL 纯净水用于样品水合,乙腈作为水合后样品的萃取溶剂,4.0 g 无水 MgSO4 和 1.0 g NaCl 作为萃取盐,500 mg MgSO4+25 mg C18+50 mg PSA 作为净化材料。当萃取液未完全干燥时,15 种 N-亚硝胺的回收率较高。因此,在温和的氮气流下将最终提取液干燥至 0.5 mL 以下,然后用乙腈重新溶解至 0.5 mL。过滤后,将 200 μL 样品转移到自动进样器的样品瓶中,进行 GC-MS/MS 分析。采用 DB-HeavyWAX 色谱柱(30 m×0.25 mm×0.25 μm)和电子碰撞离子源,在多重反应监测(MRM)模式下,使用 GC-MS/MS 对 15 种 N-亚硝胺进行测定,并使用外标法进行定量。结果表明,在优化的实验条件下,15 种 N-亚硝胺的定标曲线具有良好的线性关系,相关系数(r2)大于 0.9990。检出限(LOD)和定量限(LOQ)分别为 0.05 至 0.20 μg/kg 和 0.10 至 0.50 μg/kg。在加标水平为 1LOQ、2LOQ 和 10LOQ 时,平均回收率分别为 79.4%-102.1%、80.6%-109.5% 和 83.0%-110.6%,相对标准偏差为 0.8%-16.0%。15 种 N-亚硝胺的基质效应较低,表明该方法具有较高的灵敏度。该方法被用于检测采用不同加工技术获得的具有代表性的商用风干牦牛肉样品。在所有样品中都检测到了七种 N-亚硝胺,包括 N-亚硝基二甲胺、N-亚硝基二异丁胺、N-亚硝基二丁胺、N-甲基-N-苯基亚硝酰胺、N-乙基-N-亚硝基异苯胺、N-亚硝基吡咯烷和 N-亚硝基二苯胺。七种 N-亚硝胺的平均含量为 0.08-20.18 微克/千克。熟风干牦牛肉样品中 N-亚硝胺的检出率和平均含量均高于传统生风干牦牛肉样品。与手工 QuEChERS 方法相比,所开发的一步法 QuEChERS 方法将萃取和净化过程整合为一次运行,大大提高了检测效率。所开发的方法简单、快速、灵敏度高,不易受人为误差的影响。因此,该方法适用于测定风干牦牛肉中的亚硝胺,并可扩展到其他肉制品中亚硝胺的定性和定量分析。它还为亚硝胺的一般测定提供了方法支持和数据参考,对食品安全具有重要意义。
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[Rapid determination of 15 N-nitrosamines in air-dried yak meat using one-step QuEChERS-gas chromatography-triple quadrupole mass spectrometry].

A method based on gas chromatography-triple quadrupole mass spectrometry (GC-MS/MS) coupled with one-step QuEChERS technique was developed for the simultaneous determination of 15 N-nitrosamines in air-dried yak meat. The hydration volume, extraction solvent, extracting salt, and cleaning material were optimized according to the characteristics of the N-nitrosamines and sample matrix. The optimized conditions were as follows: 10 mL of purified water for sample hydration, acetonitrile as the extraction solvent for the sample after hydration, 4.0 g of anhydrous MgSO4 and 1.0 g of NaCl as extracting salts, 500 mg of MgSO4+25 mg of C18+50 mg of PSA as cleaning materials. Favorable recoveries of the 15 N-nitrosamines were obtained when the extraction solution was incompletely dried. Thus, the final extract was dried to below 0.5 mL under a mild nitrogen stream and then redissolved to 0.5 mL with acetonitrile. After filtration, 200 μL of the sample was transferred to an autosampler vial for GC-MS/MS analysis. The 15 N-nitrosamines were determined using GC-MS/MS on a DB-HeavyWAX column (30 m×0.25 mm×0.25 μm) with an electron impact ion source in multiple-reaction monitoring (MRM) mode, and quantified using an external standard method. Under the optimized experimental conditions, the results showed that the calibration curves exhibited good linearities for the 15 N-nitrosamines, with correlation coefficients (r2) greater than 0.9990. The limits of detection (LODs) and the limits of quantification (LOQs) ranged from 0.05 to 0.20 μg/kg and from 0.10 to 0.50 μg/kg, respectively. At spiked levels of 1LOQ, 2LOQ, and 10LOQ, the average recoveries were 79.4%-102.1%, 80.6%-109.5%, and 83.0%-110.6%, respectively, and the relative standard deviations were in the range of 0.8%-16.0%. The low matrix effects of the 15 N-nitrosamines indicated the high sensitivity of the proposed method. The method was applied to detect representative commercial air-dried yak meat samples obtained using different processing techniques. Seven N-nitrosamines, including N-nitrosodimethylamine, N-nitrosodiisobutylamine, N-nitrosodibutylamine, N-methyl-N-phenylnitrous amide, N-ethyl-N-nitrosoaniline, N-nitrosopyrrolidine, and N-nitrosodiphenylamine were detected in all samples. The average contents of the seven N-nitrosamines was 0.08-20.18 μg/kg. The detection rates and average contents of the N-nitrosamines in cooked air-dried yak meat samples were higher than those in traditional raw air-dried yak meat samples. Compared with the manual QuEChERS method, the one-step QuEChERS method developed integrated the extraction and clean-up procedures into one single run, and the detection efficiency was considerably improved. The developed method is simple, rapid, highly sensitive, and insusceptible to human errors. Thus, it is useful for the determination of N-nitrosamines in air-dried yak meat and can be extended to the qualitative and quantitative analysis of N-nitrosamines in other meat products. It also provides method support and a data reference for the general determination of N-nitrosamines, which is of great significance for food safety.

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