Determination of seven mycotoxins in cereals by ultra performance liquid chromatography-quadrupole-time of flight mass spectrometry based on the self-built database

被引:2
|
作者
Zhang Luxing [1 ]
Zhou Zheng [2 ]
Cao Lin [2 ]
Qian Jiang [1 ]
机构
[1] Zhejiang Pharmaceut Univ, Ningbo 315100, Peoples R China
[2] Ningbo Inst Drug Control, Ningbo 315048, Peoples R China
关键词
ultra performance liquid chromatography-quadrupole-time of flight mass spectrometry (UPLC-Q-TOF/MS); QuEChERS; mycotoxins; rice; wheat;
D O I
10.3724/SP.J.1123.2023.07014
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A method for the determination of seven mycotoxins in rice and wheat by ultra performance liquid chromatography-quadrupole-time of flight mass spectrometry (UPLC-Q-TOF/MS) based on self-built database was established. Samples were extracted with 0.2% formic acid aqueous solution-acetonitrile (50:50, v/v), dehydrated and salted according to the QuEChERS method (4 g of magnesium sulfate, 1 g of sodium chloride, 1 g of sodium citrate, 0.5 g of citrate disodium salt), and separated on an HSS T3 column (100 mmx2.1 mm, 1.8 mu m). UPLC-Q-TOF/MS with MSE screening was performed, and the positive and negative ions of the screened mycotoxins were calibrated and quantified using matrix-matched standard curves with time of flight multiple reaction monitoring (TOF-MRM). The results showed that aflatoxin G(1) (AFG(1)), aflatoxin G(2) (AFG(2)), aflatoxin B-1 (AFB(1)), aflatoxin B-2 (AFB(2)), and ochratoxin A (OTA) exhibited moderate matrix effects in rice, while OTA and zearalenone (ZEN) exhibited moderate matrix effects in wheat. The seven mycotoxins showed good linearities in their respective concentration ranges, with correlation coefficients (r) of 0.9900-0.9998. The limits of detection (LODs) for rice and wheat were 0.50-400 and 0.50-200 mu g/kg, respectively, and the limits of quantification (LOQs) for both cereals were 1.00-800 mu g/kg. In rice, the average recoveries at three spiked levels of low, medium, and high were 88.1%-123.9%, with relative standard deviations (RSDs) of 0.2%-13.6%. In wheat, the average recoveries at three spiked levels of low, medium, and high were 102.0%-123.4%, with RSDs of 0.8%-14.8%. As a result, one batch of 46 batches of rice was screened out for AFB1 and AFB2, with a screening rate of 2.2%, of which the measured values were 10.8 mu g/kg and 1.2 mu g/kg, respectively. According to GB 2761-2017, the maximum allowable level of AFB1 in rice is 10 mu g/kg; thus, the exceeding rate for AFB1 is 2.2%. Deoxynivalenol (DON) was screened out in 9 out of 24 batches of wheat (screening rate, 37.5%), while ZEN was screened out in 19 batches (screening rate, 79.2%). According to GB 2761-2017, the maximum allowable levels of DON and ZEN in wheat are 1000 and 60 mu g/kg, respectively. The levels of DON and ZEN detected in the wheat samples did not exceed these limits. The proposed method uses MSE for qualitative screening to avoid the occurrence of false positives caused by interfering compounds with mass numbers and retention times similar to those of the analytes. TOF-MRM mode is then used to quantify the positively screened mycotoxins. The method is fast, accurate, sensitive, and suitable for the isolation and quantitative detection of mycotoxin residues in rice and wheat samples. The findings provide powerful technical support for mycotoxin contamination monitoring in rice and wheat and early risk-warning efforts.
引用
收藏
页码:1002 / 1009
页数:8
相关论文
共 14 条
  • [1] [Anonymous], 2011, GB 2761-2011
  • [2] Development and validation of a methodology based on Captiva EMR-lipid clean-up and LC-MS/MS analysis for the simultaneous determination of mycotoxins in human plasma
    Arce-Lopez, Beatriz
    Lizarraga, Elena
    Flores-Flores, Myra
    Irigoyen, Angel
    Gonzalez-Penas, Elena
    [J]. TALANTA, 2020, 206
  • [3] Catherine F, 2020, J Chromatogr B, V1152
  • [4] Determination of 16 mycotoxins in drug and food homologous products by ultra performance liquid chromatography-tandem mass spectrometry combined with accelerated solvent extraction and QuEChERS
    Fang Zhen
    Qu Li
    Gu Shuqing
    Chen Rouhan
    Li You
    Deng Xiaojun
    Guo Dehua
    Feng Feng
    [J]. CHINESE JOURNAL OF CHROMATOGRAPHY, 2020, 38 (07) : 782 - 790
  • [5] Multi-mycotoxin stable isotope dilution LC-MS/MS method for Fusarium toxins in beer
    Habler, Katharina
    Gotthardt, Marina
    Schueler, Jan
    Rychlik, Michael
    [J]. FOOD CHEMISTRY, 2017, 218 : 447 - 454
  • [6] Rapid screening and confirmation of 20 mycotoxins in grain products by ultrahigh performance liquid chromatography-quadrupole/electrostatic field orbitrap highresolution mass spectrometry
    Hu Qiaoru
    Cao Peng
    Cong Zhongxiao
    Liang Junni
    Sha Meilan
    Li Xiaoyu
    Yin Dalu
    Lu Min
    [J]. CHINESE JOURNAL OF CHROMATOGRAPHY, 2019, 37 (11) : 1241 - 1248
  • [7] Development of a rapid multi-mycotoxin LC-MS/MS stable isotope dilution analysis for grain legumes and its application on 66 market samples
    Kunz, Birgitta Maria
    Wanko, Felicitas
    Kemmlein, Sabine
    Bahlmann, Arnold
    Rohn, Sascha
    Maul, Ronald
    [J]. FOOD CONTROL, 2020, 109
  • [8] Multi-mycotoxin detection and human exposure risk assessment in medicinal foods
    Liao, Xiaofang
    Li, Ying
    Long, Nan
    Xu, Qingbin
    Li, Peng
    Wang, Jiabo
    Zhou, Lidong
    Kong, Weijun
    [J]. FOOD RESEARCH INTERNATIONAL, 2023, 164
  • [9] Sun H Y, 2023, Biol Trace Elem Res, DOI [10.1007/s12011.023.03576.5, DOI 10.1007/S12011.023.03576.5]
  • [10] Sun J, 2014, The Crop Journal, V40, P691