Institute of Pesticide and Environmental Toxicology, Zhejiang University, Hangzhou, P. R. China.
J Agric Food Chem. 2010 Mar 24;58(6):3271-8. doi: 10.1021/jf904045j.
The present study developed an improved analytical method for simultaneous quantification of seven neonicotinoids in food by ultraperformance liquid chromatography combined with electrospray ionization triple quadrupole tandem mass spectrometry (UPLC-MS/MS) under the multiple reaction monitoring (MRM) mode. The optimization of extraction, cleanup, UPLC separation and MS/MS parameters of analytes were especially focused on. The low limits of quantification (LOQs) of neonicotinoids ranged from 0.1 to 6 microg kg(-1). Meanwhile, reasonable recoveries (65-120%) of seven neonicotinoids for food including apple, cabbage, potato, rice, tea, milk, chicken, pork and egg were demonstrated in different spiked levels within their respective linear range (0.025-150 microg kg(-1)). The developed analytical method would be appropriate for the routine, high throughput, high sensitivity quantification of seven neonicotinoids using simple sample pretreatment.
本研究建立了一种超高效液相色谱-电喷雾串联三重四极杆质谱联用(UPLC-MS/MS)在多反应监测(MRM)模式下同时定量分析食品中七种新烟碱类杀虫剂的改进分析方法。重点优化了提取、净化、UPLC 分离和 MS/MS 参数。新烟碱类杀虫剂的定量下限(LOQ)范围为 0.1 至 6 微克/千克。同时,在不同添加水平下(0.025-150 微克/千克),该方法在苹果、白菜、土豆、大米、茶、牛奶、鸡肉、猪肉和鸡蛋等七种食品中表现出合理的回收率(65-120%)。该方法采用简单的样品预处理,适用于七种新烟碱类杀虫剂的常规、高通量、高灵敏度定量分析。