陈 泳,何王福,吴俊杰,徐敦明,胡秋婷,邱伊婷,王瑞龙.高效液相色谱-串联质谱法测定植物源食品中特丁硫磷、特丁硫磷砜和特丁硫磷亚砜的残留量[J].食品安全质量检测学报,2021,12(2):616-622
高效液相色谱-串联质谱法测定植物源食品中特丁硫磷、特丁硫磷砜和特丁硫磷亚砜的残留量
Determination of terbufos, terbufos-sulfone and terbufos-sulfoxide residues in plant origin foodstuffs by high performance liquid chromatography-tandem mass spectrometry
投稿时间:2020-10-10  修订日期:2020-12-26
DOI:
中文关键词:  特丁硫磷  特丁硫磷砜  特丁硫磷亚砜  高效液相色谱-串联质谱法  植物源食品
英文关键词:terbufos  terbufos-sulfone  terbufos-sulfoxide  high performance liquid chromatography-tandem mass spectrometry  plant origin foodstuffs
基金项目:国家重点研发计划(2019YFC1605400)
作者单位
陈 泳 漳州海关综合技术服务中心 
何王福 漳州海关综合技术服务中心 
吴俊杰 厦门海关技术中心 
徐敦明 厦门海关技术中心 
胡秋婷 漳州海关综合技术服务中心 
邱伊婷 漳州海关综合技术服务中心 
王瑞龙 漳州海关综合技术服务中心 
AuthorInstitution
CHEN Yong Integrated Technical Service Center, Zhangzhou Customs 
HE Wang-Fu Integrated Technical Service Center, Zhangzhou Customs 
WU Jun-Jie Technology Center, Xiamen Customs 
XU Dun-Ming Technology Center, Xiamen Customs 
HU Qiu-Ting Integrated Technical Service Center, Zhangzhou Customs 
QIU Yi-Ting Integrated Technical Service Center, Zhangzhou Customs 
WANG Rui-Long Integrated Technical Service Center, Zhangzhou Customs 
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中文摘要:
      目的 建立高效液相色谱-串联质谱法测定植物源食品中特丁硫磷、特丁硫磷砜和特丁硫磷亚砜残留量的分析方法。方法 样品采用乙腈或1%乙酸-乙腈提取, 提取液经分散固相萃取净化。以CORTECS C18 (100 mm×2.1 mm, 2.7 ?m)色谱柱分离待测物, 以0.1%乙酸铵甲醇溶液和0.1%甲酸加乙酸铵水溶液为流动相, 梯度洗脱, 流速为0.3 mL/min, 柱温35 ℃。目标化合物采用电喷雾正离子电离、多反应监测模式检测, 以基质匹配校准曲线外标法进行定量分析。结果 3种化合物的相关系数均大于0.997, 3种化合物的检测定量限均低于0.005 mg/kg。3种化合物在10种基质(柑橘、苹果、大葱、黄瓜、西兰花、菠菜、胡萝卜、花生、大米、茶叶)中3个添加水平(0.005、0.01、0.05 mg/kg)的回收率为79.2%~105%, 相对标准偏差为1.2%~20.1%。结论 该方法简便、灵敏、环保, 回收率和精密度好, 适合于植物源食品中特丁硫磷及其氧类似物(砜、亚砜)残留的检测。
英文摘要:
      Objective To establish a method for the determination of terbufos, terbufos-sulfone and terbufos-sulfoxide residues in plant-based foods by high performance liquid chromatography-tandem mass spectrometry. Methods The samples were extracted with acetonitrile or acetonitrile containing 1% acetic acid, the extracts were cleaned up by dispersive solid phase extraction, and separated by CORTECS C18(100 mm×2.1 mm, 2.7 ?m) column using 0.1% ammonium acetate in methanol and 0.1% formate + ammonium acetate as mobile phase at the flow of 0.3 mL/min by gradient elute, and the column temperature was maintained at 35 ℃. Target compounds were analyzed by positive electrospray ionization tandem mass spectrometry under multiple reaction monitoring mode. Quantification was achieved using matrix-matched standard calibrations as the external standard. Results The correlation coefficients of the 3 compounds were all greater than 0.997, and the limits of quantitation were lower than 0.005 mg/kg. Recoveries of 3 compounds in 10 matrixes (mandarin, apple, shallot, cucumber, brocolli, spinach, carrot, peanut, rice and tea) at fortification levels of 0.005, 0.01, 0.05 mg/kg ranged from 79.2% to 105%, and relative standard deviations (RSDs) were 1.2%?20.1%. Conclusion This method is simple, sensitive, environmentally friendly, with good recovery and precision, which is suitable for detecting terbufos and its oxidative analogues(-sulfone, -sulfoxide) residues in plant origin foodstuffs.
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