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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Quantification of light polycyclic aromatic hydrocarbons in seafood samples using on-line dynamic headspace extraction, thermodesorption, gas chromatography tandem mass spectrometry, based on an isotope dilution approach
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Quantification of light polycyclic aromatic hydrocarbons in seafood samples using on-line dynamic headspace extraction, thermodesorption, gas chromatography tandem mass spectrometry, based on an isotope dilution approach

机译:用在线动态顶空萃取,热渗透,气相色谱串联质谱法定量浅多环芳烃碳氢化合物,基于同位素稀释方法

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The aim of our work was to develop an analytical strategy to quantify naphthalene, acenaphthylene, acenaphthene, fluorene, phenanthrene and anthracene in fish products by on-line dynamic headspace extraction, followed by thermodesorption injection and gas chromatography analysis coupled with tandem mass spectrometry using electron ionization mode (DHS-TD-GC-EI-MS/MS). The developed protocol used 1 g of freeze-dried or oil sample supplemented with perdeuterated light PAHs. The sample was heated at [90-100 degrees C], the headspace of the sample was swept by nitrogen and the trapping of the PAHs was carried out on a Tenax-type adsorbent placed at 25 degrees C. Analytes were thermodesorbed at 300 degrees C from the dried adsorbant and then cryofocused on a cooled injection system (CIS) at -25 degrees C before injection (12 degrees C s(-1) up to 300 degrees C). The chromatographic separation of PAHs was carried out on a 5-MS type column (30 m x 0.25 mm, 0.25 mu m) and the acquisition of the signals was performed in SRM following the transitions, involving the loss of one or two hydrogen atoms from the molecular ion. In view of the principle of extraction, the calibration curve was performed on a representative matrix or using the standard addition method. Quantification limits were determined between 0.01 and 0.6 ng g(-1) of matrix from the method blank results. The method was validated by a series of multi-level supplemented matrix assays and by the analysis of a reference material from an inter-laboratory test (mussels, IAEA-432). The average of the expanded measurement uncertainty was from 9 to 44% for the four lightest PAHs, except for fluorene when the sample incubation was set at 90 degrees C. Occurrence measurements were performed on almost two hundred samples of molluscs, echinoderms and fish. The results have shown a quantification frequency greater than 66% for naphthalene and fluorene, at concentrations below a few ng g(-1) of dry matter of fishery products. With this methodology, the light PAHs occurrence can now be measured in a wider range of foodstuffs in order to better characterize their contamination trends and the associated risk simultaneously. (C) 2020 Elsevier B.V. All rights reserved.
机译:我们工作的目的是开发一种分析策略通过在线动态顶空萃取量化萘,苊烯,苊,芴,在鱼制品菲和蒽,随后再加上使用电子串联质谱热解吸注入和气相色谱分析电离模式(DHS-TD-GC-EI-MS / MS)。所开发的方案使用1g补充有备用光Pah的冷冻干燥或油样。将样品加热在[90-100℃],样品的顶部空间被氮气扫过,并且在置于25摄氏度的Tenax型吸附剂上进行PAH的捕获。分析物在300摄氏度下热量吸收从干燥的吸附剂然后在注射前(12摄氏度(-1)至300℃),在-25℃下冷冻焦化在冷却的注射系统(CIS)上。 PAHS的色谱分离在5ms型柱上进行(30mL 0.25mm,0.25μm),并在过渡后在SRM中进行信号,涉及从中丧失一个或两个氢原子分子离子。鉴于提取原理,对代表性矩阵或使用标准添加方法进行校准曲线。从方法空白结果中测定量化限制在0.01和0.6ng(-1)基质之间。通过一系列多级补充基质测定和通过从实验室间试验(贻贝,IAEA-432)的参考材料进行分析来验证该方法。扩展测量不确定性的平均值为四个最轻的PAHS的9至44%,除芴设定为90℃时,含有近20次的软体动物,棘鱼胚胎和鱼类的发生测量。结果显示了萘和芴的量化频率大于66%,浓度低于渔业产品干物质的浓度低于几Ng G(-1)。利用这种方法,现在可以在更广泛的食品中测量光PAHs的发生,以便更好地表征它们的污染趋势和相关风险。 (c)2020 Elsevier B.v.保留所有权利。

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