肖永华,黄常刚,革丽亚,李静娜,粱高道.超高效液相色谱-串联质谱法快速测定稻谷和玉米中伏马毒素[J].食品安全质量检测学报,2020,11(24):9251-9255
超高效液相色谱-串联质谱法快速测定稻谷和玉米中伏马毒素
Rapid determination of fumonisins in paddy and maize by ultra performance liquid chromatography-tandem mass spectrometry
投稿时间:2020-08-03  修订日期:2020-12-07
DOI:
中文关键词:  同位素稀释-超高效液相色谱-串联质谱法  稻谷  玉米  伏马毒素。
英文关键词:isotope dilution-ultra-performance liquid chromatography tandem mass spectrometry  paddy  maize  fumonisins
基金项目:武汉市卫健委项目(WG19C07)、武汉市卫计委项目(WG17B03)
作者单位
肖永华 武汉市疾病预防控制中心 
黄常刚 武汉市疾病预防控制中心 
革丽亚 武汉市疾病预防控制中心 
李静娜 武汉市疾病预防控制中心 
粱高道 武汉市疾病预防控制中心 
AuthorInstitution
XIAO Yong-Hua Wuhan Center for Disease Control and Prevention 
HUANG Chang-Gang Wuhan Center for Disease Control and Prevention 
GE Li-Ya Wuhan Center for Disease Control and Prevention 
LI Jing-Na Wuhan Center for Disease Control and Prevention 
LIANG Gao-Dao Wuhan Center for Disease Control and Prevention 
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中文摘要:
      目的 建立同位素稀释-超高效液相色谱串联质谱法测定稻谷和玉米中伏马毒素(fumonisins, FB)。 方法 样品加入同位素内标后用50%乙腈水溶液(含1%甲酸)提取, 采用ZORBAX Eclipse Plus C18色谱柱分离, 以甲醇?0.1%甲酸水溶液为流动相, 梯度洗脱, 质谱采用电喷雾电离, 负离子模式下, 以多反应监测模式检测, 采用内标法定量。结果 FB1、FB2和FB3在0.5~100.0 μg/L范围内线性关系良好, 相关系数均大于0.995, 检出限均为1.0 μg/kg。在5.0、50.0、500.0 μg/kg 3个加标浓度水平下, FB1、FB2和FB3的回收率为82.5%~107.1%, RSDs为3.9%~6.2%(n=5)。结论 该方法简单快速, 定性定量准确, 有效降低了背景干扰, 可用于粮食中伏马毒素的检测。
英文摘要:
      Objective To establish a method for the determination of fumonisins in rice and corn by isotopic dilution-ultra performance liquid chromatography tandem mass spectrometry. Methods The samples were extracted with 50% acetonitrile aqueous solution (containing 1% formic acid) after adding isotope internal standard. The samples were separated by ZORBAX Eclipse Plus C18 chromatographic column. Methanol?0.1% formic acid aqueous solution was used as mobile phase, gradient elution was performed, electrospray ionization was used for mass spectrometry, and multiple reaction monitoring mode was used for detection under negative ion mode, and internal standard method was used for quantification. Results The linear relationship of FB1, FB2 and FB3 were good in the range of 0.5?100.0 g/L, the correlation coefficient was greater than 0.995, and the limit of detection was 1.0 g/kg. The recoveries of FB1, FB2 and FB3 were 82.5%?107.1%, and RSDs were 3.9%?6.2% at 5.0, 50.0 and 500.0 g/kg standard concentrations (n=5). Conclusion This method is simple and fast, accurate in qualitative and quantitative analysis, and can effectively reduce background interference. It can be used to detect fumonisins in grain.
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