Huang Wei, Li Na, Xu Ruihan, Li Ting, Li Chongyong
Hanzhong Control and Testing Center for Food and Drug, Hanzhong 723000, China.
Hanzhong Animal Hygienie Supervision Institute, Hanzhong 723000, China.
Se Pu. 2018 Dec 8;36(12):1303-1310. doi: 10.3724/SP.J.1123.2018.09019.
A method has been developed for the simultaneous detection of nine pyrethroid pesticide residues in tea by gas chromatography-tandem mass spectrometry (GC-MS/MS) combined with accelerated solvent extraction (ASE) and solid-phase extraction (SPE). The pesticide residues in tea were extracted using acetone/-hexane (1:1, v/v) for 5 min at 100℃ before preheating the extraction pool for 3 min, under extractive pressure of 10 MPa for one cycle. After extraction, the extraction pool was washed with acetone/-hexane (1:1, v/v) having volume of 40% of the pool volume, followed by purging for 100 s with nitrogen. The extract was purified by a Cleanert TPT solid-phase extraction column. After purification, the target compounds were detected by GC-MS/MS and quantified by the external standard method. Under the optimized conditions, good linearities were obtained for the nine pyrethroid pesticides in the range of 2-1000 μg/L, with correlation coefficients exceeding 0.99. The limits of detection (LODs) were 0.2-4.5 μg/kg and the limits of quantitation (LOQs) were 0.8-15.0 μg/kg. At four spiked levels (0.02, 0.1, 0.4 mg/kg, and the LOQ level) in green tea and black tea, the recoveries of all the pesticides were between 69.87% and 110.0%, with relative standard deviations (RSDs) varying from 0.7% to 11.2%. This method effectively reduces the matrix interference and shows high sensitivity, good reproducibility, and stable recovery, and can thus be used for the detection of pyrethroid pesticide residues in tea.
建立了一种气相色谱 - 串联质谱法(GC-MS/MS)结合加速溶剂萃取(ASE)和固相萃取(SPE)同时检测茶叶中9种拟除虫菊酯类农药残留的方法。在萃取池预热3分钟后,于100℃下使用丙酮/正己烷(1:1,v/v)在10 MPa的萃取压力下对茶叶中的农药残留进行5分钟的萃取,循环一次。萃取后,用占萃取池体积40%的丙酮/正己烷(1:1,v/v)冲洗萃取池,然后用氮气吹扫100秒。提取物通过Cleanert TPT固相萃取柱进行净化。净化后,采用GC-MS/MS对目标化合物进行检测,并采用外标法进行定量。在优化条件下,9种拟除虫菊酯类农药在2 - 1000μg/L范围内具有良好的线性关系,相关系数超过0.99。检测限(LOD)为0.2 - 4.5μg/kg,定量限(LOQ)为0.8 - 15.0μg/kg。在绿茶和红茶的四个加标水平(0.02、0.1、0.4mg/kg和LOQ水平)下,所有农药的回收率在69.87%至110.0%之间,相对标准偏差(RSD)在0.7%至11.2%之间。该方法有效降低了基质干扰,具有高灵敏度、良好的重现性和稳定的回收率,可用于茶叶中拟除虫菊酯类农药残留的检测。