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采用 C 标记内标物的气相色谱/高分辨率质谱法准确测定橄榄油中四种多环芳烃候选参比方法的开发。

Development of candidate reference method for accurate determination of four polycyclic aromatic hydrocarbons in olive oil via gas chromatography/high-resolution mass spectrometry using C-labeled internal standards.

机构信息

Division of Chemical and Medical Metrology, Korea Research Institute of Standards and Science, Yuseong, Daejeon 34113, South Korea; Department of Chemistry, Chungnam National University, Yuseong, Daejon 34134, South Korea.

Division of Chemical and Medical Metrology, Korea Research Institute of Standards and Science, Yuseong, Daejeon 34113, South Korea.

出版信息

Food Chem. 2020 Mar 30;309:125639. doi: 10.1016/j.foodchem.2019.125639. Epub 2019 Oct 10.

Abstract

We developed an isotope-dilution gas chromatography/high-resolution mass spectrometry (ID-GC/HRMS) method for the accurate determination of four polycyclic aromatic hydrocarbons (PAHs) in olive oil. The clean-up steps were optimized to sufficiently remove co-extracted oil matrix using the EZ-POP NP dual-layer and NH solid-phase extraction (SPE) cartridges. However, the cleaned sample still contained some matrix residues, which caused a bias. When C-labeled PAHs were used as the internal standards instead of deuterated PAHs, the recovery results improved in both low- and high-resolution MS conditions. Furthermore, the HRMS analysis facilitated to obtain more accurate results. The accuracy and precision of the optimized ID-GC/HRMS method were validated using PAH-fortified (0.5, 3, and 6 μg/kg) olive oil. The recoveries and relative standard deviations obtained for all the PAHs/levels were 97.5-102% and ~1%, respectively. Measurement uncertainties were generally within 5% (with a 95% confidence level).

摘要

我们开发了一种同位素稀释气相色谱/高分辨率质谱(ID-GC/HRMS)方法,用于准确测定橄榄油中的四种多环芳烃(PAHs)。通过使用 EZ-POP NP 双层和 NH 固相萃取(SPE)小柱优化了净化步骤,以充分去除共提取的油基质。然而,净化后的样品中仍残留一些基质,这导致了一定的偏差。当使用 C 标记的 PAHs 作为内标而不是氘代 PAHs 时,在低分辨和高分辨 MS 条件下,回收率都得到了改善。此外,HRMS 分析有助于获得更准确的结果。使用 PAH 加标(0.5、3 和 6μg/kg)橄榄油对优化后的 ID-GC/HRMS 方法的准确性和精密度进行了验证。所有 PAHs/水平的回收率和相对标准偏差分别为 97.5-102%和~1%。测量不确定度通常在 5%以内(置信水平为 95%)。

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