QuEChERS-超高效液相色谱-串联质谱法测定叶类蔬菜中5种植物生长调节剂的残留
投稿时间:2017-07-17      点此下载全文 HTML
引用本文:叶倩,黄健祥,孙玲,等.QuEChERS-超高效液相色谱-串联质谱法测定叶类蔬菜中5种植物生长调节剂的残留[J].农药学学报,2017,19(5):589-596.
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叶倩 广东省农业科学院 农产品公共监测中心/农业部农产品质量安全风险评估实验室(广州)/农业部农产品质量安全检测与评价重点实验室, 广州 510640  
黄健祥 广东省农业科学院 农产品公共监测中心/农业部农产品质量安全风险评估实验室(广州)/农业部农产品质量安全检测与评价重点实验室, 广州 510640  
孙玲 广东省农业科学院 农产品公共监测中心/农业部农产品质量安全风险评估实验室(广州)/农业部农产品质量安全检测与评价重点实验室, 广州 510640  
万凯 广东省农业科学院 农产品公共监测中心/农业部农产品质量安全风险评估实验室(广州)/农业部农产品质量安全检测与评价重点实验室, 广州 510640  
朱富伟 广东省农业科学院 农产品公共监测中心/农业部农产品质量安全风险评估实验室(广州)/农业部农产品质量安全检测与评价重点实验室, 广州 510640  
骆冲 广东省农业科学院 农产品公共监测中心/农业部农产品质量安全风险评估实验室(广州)/农业部农产品质量安全检测与评价重点实验室, 广州 510640  
王富华 广东省农业科学院 农产品公共监测中心/农业部农产品质量安全风险评估实验室(广州)/农业部农产品质量安全检测与评价重点实验室, 广州 510640 wfhwqs@163.com 
基金项目:2017年国家蔬菜质量安全风险评估项目(GJFP201700203,GJFP201701104,GJFP201701503);广东省农业科学院院长基金项目(201319);广东省科技计划项目-农产品质量安全风险评价关键技术研究(2013B020204001);广州市科技计划项目(201508020096)
中文摘要:建立了QuEChERS-超高效液相色谱-串联质谱(QuEChERS-UPLC-MS/MS)对叶类蔬菜中极性较弱的氯吡脲、多效唑、烯效唑和丙环唑以及强极性的矮壮素共5种植物生长调节剂多残留的检测方法。样品经QuEChERS法预处理,用含体积分数为1%乙酸的乙腈溶液提取,石墨化碳黑(GCB)和N-丙基乙二胺(PSA)净化,C18色谱柱分离,采用电喷雾离子化正离子扫描和多反应监测模式(MRM)检测,基质匹配标准溶液外标法定量。结果表明:在1~1 000 μg/L范围内,氯吡脲、多效唑、烯效唑、丙环唑和矮壮素5种植物生长调节剂的质量浓度与对应的峰面积间呈良好的线性关系,相关系数均大于0.999 3,检出限(LOD)为0.002~0.04 μg/kg,定量限(LOQ)为0.01 mg/kg。在0.01、0.1和0.5 mg/kg添加水平下,5种植物生长调剂在菜心、芥蓝和普通白菜中的平均回收率为71%~93%,相对标准偏差(RSD)为0.2%~10%。该方法快捷、简便、定量准确,适用于叶类蔬菜中同时检测氯吡脲、多效唑、烯效唑、丙环唑和矮壮素等植物生长调节剂的残留。
中文关键词:QuEChERS  超高效液相色谱-串联质谱 (UPLC-MS/MS)  蔬菜  植物生长调节剂  残留
 
Determination of Five plant growth regulator residues in leafy vegetables by QuEChERS-ultra performance liquid chromatography-tandem mass spectrometry
Abstract:A method for the simultaneous determination of low-polarity pesticide, such as forchlorfenuron, paclobutrazol, uniconazole and propiconazole, and high polarity pesticide, such as chlormequat chloride in leafy vegetables was developed using QuEChERS-ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Vegetable samples were extracted by acetonitrile containing 1% (V%) acetic acid. Then they were cleaned up by GCB and PSA adsorbents before separated on a C18 column and detected under positive polarity multiple reactions monitoring (MRM) mode. The matrix-matched external standard calibration curves were used for quantitative analysis. The linearity of 5 plant growth regulators was in the range of 1-1 000 μg/L, with correlation coefficients higher than 0.999 3. The limits of detection (LOD) of the proposed method were 0.002 to 0.04 μg/kg. The limit of quantification (LOQ) was 0.01 mg/kg which was the lowest spiked concentration. Recoveries at three spiked levels of 0.01, 0.1 and 0.5 mg/kg ranged from 71% to 93% with relative standard deviations (RSDs) from 0.2% to 10% in flowering Chinese cabbage, Chinese kale and pak-choi. The presented method is fast, simple and accurate, which can meet the requirements for the determination of residues of forchlorfenuron, paclobutrazol, uniconazole, propiconazole and chlormequat chloride in leafy vegetables.
Key words:QuEChERS  ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS)  vegetable  plant growth regulator  residue
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