化学
色谱法
甲酸铵
质谱法
检出限
乙腈
选择性反应监测
电喷雾电离
高效液相色谱法
三级四极质谱仪
萃取(化学)
固相萃取
串联质谱法
作者
Chenxia Zhang,Yuxiang Ma,Tian-Pei Zhao,Jun Xi,Li Pan,Qing Guo,Lili Shi,Xue‐De Wang
出处
期刊:Sepu
[Science Press]
日期:2020-02-08
卷期号:38 (2): 224-231
被引量:2
标识
DOI:10.3724/sp.j.1123.2019.04046
摘要
An ultra performance liquid chromatography-triple quadrupole mass spectrometry (UPLC-MS/MS) method was developed for the determination of seven heterocyclic aromatic amines (HCAs) in oil and fried food samples. The samples were extracted with acetonitrile containing 1% (v/v) ammonia water, defatted by n-hexane saturated with acetonitrile, and cleaned up with PCX solid phase extraction column. The extracts were separated on a Waters ACQUITY UPLC BEH C18 reversed-phase column (50 mm×2.1 mm, 1.7 μm) with gradient elution by using acetonitrile-10 mmol/L ammonium formate aqueous solution as the mobile phase. Quantitative detection was performed by using a positive-ion electrospray ionization source in the multiple reaction monitoring (MRM) mode, employing an internal isotope standard. The method showed good linear relationships in the range of 0.5-100 μg/L for the seven HCAs with correlation coefficients (R2)>0.999. The average recoveries ranged from 64.31% to 113.8% with the relative standard deviations of 0.18%-9.26% at the three spiked levels in oil and fried food samples. The limits of detection (LODs) and limits of quantification (LOQs) were 0.01-0.14 ng/g and 0.09-0.38 ng/g, respectively. The method is sensitive, accurate, and suitable for the determination and confirmation of the seven HCAs in oil and fried food samples.
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