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作 者:荣维广[1] 宋宁慧[2] 吴建[1] 吉文亮[1] 刘华良[1] 马永建[1]
机构地区:[1]江苏省疾病预防控制中心,南京210009 [2]环境保护部南京环境科学研究所,南京210009
出 处:《江苏预防医学》2014年第2期10-12,共3页Jiangsu Journal of Preventive Medicine
基 金:江苏省科技厅科技支撑计划项目(BE2010745);江苏省十二五科教兴卫工程(ZX201109)
摘 要:目的 建立猪肝中三氯氰菊酯农药残留的凝胶渗透色谱净化气相色谱负化学离子源质谱的检测方法.方法 样品经乙酸乙酯为溶剂超声波提取后,凝胶渗透色谱净化处理,采用HP-5MS色谱柱分离,气相色谱-负化学离子源质谱选择离子检测技术检测.结果 0.001、0.005、0.020 mg/kg3个浓度添加回收率在75.3%~]07.6%间,相对标准偏差(RSDs)≤7.1%,最低检出限为0.001 mg/kg.结论 建立的检测方法能够消除油脂类干扰,灵敏度高,选择性好,稳定可靠,适用于猪肝中的三氟氯氰菊酯农药残留的检测.Objective To establish an assay to determine pesticide residue cyhalothrin in pig liver by gel permeation chroma- tography-gas chromatography-mass spectrometry in negative chemical ionization (GC-MS/NCI) mode. Methods Specimens were subjected to ultrasonic-assistant extraction in ethyl acetate solvent, followed by clean-up treatment by gel permeation chromatography (GPC) . The exact was then separated on HP-5MS column Cyhalothrin was analyzed by gas chromatogra- phy-mass spectrometry operated by negative-ion chemical-ionization(GC-MS/NCI) in selected ion monitoring (SIM) mode. Re- sults Recovery efficiency was 75.3%- 107.6% at three spiked levels (0. 001,0. 005,0. 020 mg/kg) , relative standard devia- tion(RSDs) was all ≤ 7.1%. Limit of detection was 0. 001mg/kg. Conclusion The established method was capable to elimi- nate fatty matrix interference, with high sensitivity, excellent selectivity, stability and reliability, and is applicable for analysis of cyhalothrin residue in pig liver.
关 键 词:凝胶渗透色谱 三氟氯氰菊酯 气相色谱-负化学离子源质谱 猪肝
分 类 号:R155.55[医药卫生—营养与食品卫生学]
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