庄宇, 丁琳, 姜楠. 液相色谱—质谱复合扫描模式鉴定水产品中硝基呋喃类药物[J]. 环境卫生学杂志, 2012, 2(6): 303-309.
    引用本文: 庄宇, 丁琳, 姜楠. 液相色谱—质谱复合扫描模式鉴定水产品中硝基呋喃类药物[J]. 环境卫生学杂志, 2012, 2(6): 303-309.
    Zhuang Yu, Ding Lin, Jiang Nan. Compound Scan to Confirm Metabolites of Nitrofurans in Water Products by Combined Liquid Chromatography-Tandem Mass Spectrometry with a Quadrupole /Linear Ion Trap Instrument[J]. Journal of Environmental Hygiene, 2012, 2(6): 303-309.
    Citation: Zhuang Yu, Ding Lin, Jiang Nan. Compound Scan to Confirm Metabolites of Nitrofurans in Water Products by Combined Liquid Chromatography-Tandem Mass Spectrometry with a Quadrupole /Linear Ion Trap Instrument[J]. Journal of Environmental Hygiene, 2012, 2(6): 303-309.

    液相色谱—质谱复合扫描模式鉴定水产品中硝基呋喃类药物

    Compound Scan to Confirm Metabolites of Nitrofurans in Water Products by Combined Liquid Chromatography-Tandem Mass Spectrometry with a Quadrupole /Linear Ion Trap Instrument

    • 摘要: 建立水产品中4种硝基呋喃及其代谢物的液相色谱—三重四极杆/线性离子阱质谱检测方法。方法实验过程中真实样品中存在干扰,利用多反应监控(MRM)信息依赖性(IDA)采集线性离子阱内富集的增强子离子扫描(EPI)的复合扫描模式,建立有效的硝基呋喃及其代谢物的定性、定量方法。结果在0.01~5.0μg/kg浓度范围内4种化合物均有良好的线性(r>0.999)。4种硝基呋喃代谢物AHD、AOZ、SEM、AMOZ的检测限分别为0.01μg/kg、0.001μg/kg、0.01μg/kg、0.001μg/kg,此时S/N均>10,在0.01、0.1和0.5μg/kg3个添加水平重复6次进样测定,平均回收率为76.3%~97.6%,相对标准偏差(CV%)为1.36~5.09。结论该方法采用MRM→IDA→EPI复合扫描模式采集数据,能实现一次进样同时定性、定量分析,有效排除实验中因基质干扰而引起的假阳性结果。

       

      Abstract: Objectives To apply the high-performance liquid chromatography-tandem mass spectrometry with quadrupole / linear ion trap instrument in water products for detection and analysis of 4 nitrofurans and related metabolites. Method Considering the interference in true sample,a compound scan by multiple reaction monitoring ( MRM) with information-dependent acquisition ( IDA ) to trigger enhanced product ion ( EPI ) mode is used for identification and quantification of nitrofurans and related metabolites. Results There are good linear correlations( r > 0. 999) between the peak areas and concentrations of the four metabolites of nitrofuran antibiotics in the range of 0. 01 - 5. 0 μg / kg, the limit of detection of AHD、AOZ、SEM、AMOZ are 0. 01 μg / kg、0. 001 μg / kg、0. 01 μg / kg、0. 001 μg / kg and the S / N are more than 10. The average recoveries ranged from 76. 3% to 97. 6% and the relative standard deviations are between 1. 36 to 5. 09% in 0. 01、0. 1 和 0. 5 μg / kg three levels respectively. Conclusions Application of MRMIDA-EPI for compound scan to collect data can achieve the aim of quantifying and qualifying analysis in one sample,effectively exclude the false positive results caused by matrix inference.

       

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