Pan Yuchen, Yi Xionghai, Deng Xiaojun, Zhao Shanzhen, Chen Shunsheng, Yang Huiqin, Han Li, Zhu Jian
Shanghai Ocean University, Shanghai 201306, China.
Se Pu. 2012 Nov;30(11):1159-65. doi: 10.3724/sp.j.1123.2012.06033.
A gas chromatography-tandem mass spectrometry (GC-MS/MS) method with subcritical water extraction was developed for the determination of 21 organochlorine and pyrethroid pesticides in black tea. Under the extraction pressure of 5 MPa, the target compounds were extracted with subcritical water at the temperature of 150 degrees C for 15 min, transferred into acetone-n-hexane (1:1, v/v), and cleaned-up by an ENVI-Carb solid phase extraction (SPE) column. The GC separation was performed on a DB-5 capillary column. The pesticides were determined by MS/MS in multiple reaction monitoring (MRM) mode and quantified by matrix-matched internal standard method. The calibration curves showed good linearities in the range of 5.0-320.0 microg/L with the correlation coefficients greater than 0.99. The limit of quantification (S/N > 10) was 50 ng/g, and the limit of detection (S/N > 3) was 10 ng/g. The recoveries of pesticides spiked in the tea at three levels of 50, 100 and 200 ng/g were ranged from 70. 18% to 119.98% with the relative standard deviations (RSDs) of 5.01%-11.76%. The sensitivity, accuracy and precision of the method meet the technical standard of the pesticide determination. The method can be applied to the determination of organochlorine and pyrethroid pesticides in black tea.
建立了一种采用亚临界水萃取的气相色谱 - 串联质谱(GC-MS/MS)法测定红茶中21种有机氯和拟除虫菊酯类农药的方法。在5 MPa的萃取压力下,目标化合物在150℃的温度下用亚临界水萃取15 min,转移至丙酮 - 正己烷(1:1,v/v)中,并用ENVI-Carb固相萃取(SPE)柱进行净化。GC分离在DB-5毛细管柱上进行。农药通过MS/MS在多反应监测(MRM)模式下测定,并采用基质匹配内标法进行定量。校准曲线在5.0 - 320.0 μg/L范围内具有良好的线性,相关系数大于0.99。定量限(S/N > 10)为50 ng/g,检测限(S/N > 3)为10 ng/g。在50、100和200 ng/g三个加标水平下,茶叶中农药的回收率在70.18%至119.98%之间,相对标准偏差(RSD)为5.01% - 11.76%。该方法的灵敏度、准确度和精密度符合农药测定的技术标准。该方法可用于红茶中有机氯和拟除虫菊酯类农药的测定。