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作 者:李萍萍[1] 程景[2] 张振山[1] 吴学进[1]
机构地区:[1]中国热带农业科学院分析测试中心,海口571101 [2]黑龙江省农产品质量检验检测中心,哈尔滨150090
出 处:《农药》2016年第8期593-596,共4页Agrochemicals
基 金:农业部农产品质量安全风险评估专项(GJFP201600301-1)
摘 要:[目的]建立同时测定菠萝蜜中百菌清、克菌丹和己唑醇农药残留的气相色谱串联质谱(GC-MS/MS)分析方法。[方法]样品经乙腈提取,采用石墨氨基固相萃取柱浓缩与净化,多反应监测模式(MRM)下进行质谱检测,外标法定量。[结果]百菌清、克菌丹和己唑醇的最低检出限分别为0.002、0.003、0.002 mg/kg,定量限均为0.01 mg/kg。添加质量分数在0.01-0.2 mg/kg时3种供试农药的平均添加回收率为78.3%-86.7%,相对标准偏差(RSD)≤6.2%。[结论]该方法简单可靠、重现性好、灵敏度高,适用于菠萝蜜中百菌清、克菌丹和己唑醇的农药残留检测。[Aims] An analytical method for simultaneous determination of chlorothalonil, captan and hexaconazole residues in jackfi'uit by gas chromatography-tandem mass spectrometry (GC-MS/MS) was developed. [Methods] The jackfi'uit samples were extracted with acetonitrile, and then purified and concentrated on carbon/NH2 SPE column. The target compounds were determinated under multiple reaction monitoring (MRM) mode and quantified by external standard method. [Results] The limits of detection for chlorothalonil, captan and hexaconazole were 0.002, 0.003 and 0.002 mg/kg, respectively, and the limits of quantitation were all 0.01 mg/kg. The average recoveries at the fortified levels of 0.01, 0.05 and 0.2 mg/kg were in the range of 78.3 to 86.7%, and the relative standard deviations (RSDs) were less than 6.2%. [Conclusions] The method is simple, reliable, with good reproducibility and sensitivity, which is applicable for analysis of chlorothalonil, captan and hexaconazole residues in jackfi'uit.
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