姚帮本,乔东晴,童 宁,陈 伟.超高效液相色谱串联质谱法同时检测13种植物生长激素残留物[J].食品安全质量检测学报,2020,11(11):3500-3507
超高效液相色谱串联质谱法同时检测13种植物生长激素残留物
Simultaneous determination of 13 plant growth regulators residues by ultra performance liquid chromatography/tandem mass spectrometry
投稿时间:2020-02-26  修订日期:2020-04-02
DOI:
中文关键词:  超高效液相色谱串联质谱法  植物源性食品  植物生长激素  植物营养剂
英文关键词:ultra performance liquid chromatography/tandem mass spectrometry  plant-based foods  plant growth regulators  plant nutrients
基金项目:
作者单位
姚帮本 安徽省产品质量监督检验研究院;合肥工业大学食品与生物工程学院 
乔东晴 安徽省产品质量监督检验研究院 
童 宁 安徽省产品质量监督检验研究院 
陈 伟 合肥工业大学食品与生物工程学院 
AuthorInstitution
YAO Bang-Ben Anhui Province Product Quality Supervision and Inspection Institute;College of Food and Biologic Technology, Hefei University of Technology 
QIAO Dong-Qing Anhui Province Product Quality Supervision and Inspection Institute 
TONG Ning Anhui Province Product Quality Supervision and Inspection Institute 
CHEN Wei College of Food and Biologic Technology, Hefei University of Technology 
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中文摘要:
      目的 采用超高效液相色谱-三重四极杆质谱技术, 建立促进农作物生长的13种植物生长激素残留的检测方法。方法 样品加甲醇超声提取, 离心净化后进样分析, 分析物经C18色谱柱分离, 以甲酸铵-乙腈溶液作为流动相梯度洗脱, 在电喷雾正、负离子扫描、多反应监测模式下, 外标法定量分析, 同时探讨了前处理和仪器分析条件对检测的影响。结果 13种常见植物生长调节剂在1~1000 μg/L范围内, 峰面积与质量浓度的线性关系良好; 当添加浓度水平在50、100、500 μg/kg时, 13种植物生长调节剂的平均回收率为92.5%~103.5%, 相对标准偏差(relative standard deviation, RSD)为1.7%~5.6%, 检出限(limit of detection, LOD)为0.8~4.2 μg/kg。结论 本方法简化了样品前处理步骤, 具有良好的可靠性和灵敏度, 适于植物源性食品中植物生长激素的快速检验与分析。
英文摘要:
      Objective To establish a method for the detection of 13 kinds of plant growth hormone residues by ultra performance liquid chromatography-triple quadrupole mass spectrometry. Methods The samples were extracted by ultrasonic extraction with methanol and purified by centrifugation. The analytes were separated by C18 chromatographic column and eluted by ammonium formate-acetonitrile solution as mobile phase gradient. In the mode of electrospray positive and negative ion scanning and multi-reaction monitoring, the external standard method was used for quantitative analysis. The influence of pretreatment and instrumental analysis conditions on the detection was also discussed. Results The linear relationship of 13 plant growth regulators was good in the range of 1?1000 μg/L between peak area and mass concentration. When the concentration levels were 50, 100 and 500 μg/kg, the average recoveries of 13 plant growth regulators were 92.5%?103.5%, the relative standard deviations (RSDs) was 1.7%?5.6%, and the limits of detection (LODs) was 0.8?4.2 μg/kg. Conclusion This method simplifies the sample pretreatment procedure, has good reliability and sensitivity, and it is suitable for rapid detection and analysis of plant growth regulators in plant nutrients.
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