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作 者:段丹丹[1] 马青青[2] 张利锋[2] 高强[1] 张榕杰[2] 吕全军[1]
机构地区:[1]郑州大学公共卫生学院,郑州450001 [2]河南省疾病预防控制中心公共卫生研究所,郑州450016
出 处:《食品工业》2017年第3期265-268,共4页The Food Industry
基 金:河南省医学科技攻关项目资助课题(201203060)
摘 要:建立同时检测豆芽中5种植物生长调节剂残留的固相萃取-气相色谱串联质谱方法。匀浆处理的豆芽试样,用体积分数为0.5%的甲酸乙腈溶液超声提取,经MCS小柱纯化,以HP-5 MS毛细管色谱柱分离,在选择离子监测模式下进行分析,外标法定量。方法可以在26 min内同时检测豆芽中5种植物生长调节剂残留,检出限为3.0~8.0μg/kg,定量限为10.0~25.0μg/kg,相关系数r>0.993,平均加标回收率达到81.4%~101.2%,相对标准偏差为2.4%~7.8%。方法快速、高效、灵敏度高,可用于食品中多种植物生长调节剂残留的同时测定。It was to set up a gas chromatography-tandem mass spectrometric(LC-MS/MS) method with solid phase extraction for the determination of 5 plant growth regulators(PGRs) residues simultaneous. Homogenatized samples were initially extracted with acetonitrile containing 0.5% acetic acid via ultrasonic and cleaned-up by using MCS cartridge, then separated by gas chromatography with capillary column(HP-5MS, 30 m×0.25 mm, 0.25 μm) and determined by a mass spectrometer with electron impact(EI) at selected ion monitoring(SIM) mode. The content was quantified by external standard method. This method could simultaneously detect 5 kinds of plant growth regulators within 26 min. The limits of detection(LOD) were 3.0-8.0 μg/kg and the limits of quantification(LOQ) were 10.0-25.0 μg/kg, the correlation coefficient was greater than 0.993, the average recoveries were 81.4%-101.2% and the relative standard deviations were 2.4%-7.8%. This method is rapid, efficient, and sensitive. It can be used for the determination of multiple plant growth regulators residues in food simultaneously.
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