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Development and validation of a method for the analysis of trifludimoxazin, picarbutrazox, and pyraziflumid residues in cereals, vegetables and fruits using ultra-performance liquid chromatography/tandem mass spectrometry
Microchemical Journal ( IF 4.9 ) Pub Date : 2021-05-29 , DOI: 10.1016/j.microc.2021.106477
Fajun Tian , Chengkui Qiao , Caixia Wang , Jing Luo , Linlin Guo , Tao Pang , Jun Li , Ruiping Wang , Rongli Pang , Hanzhong Xie

A sensitive method for the determination of three new pesticides (trifludimoxazin, pyraziflumid, and picarbutrazox) in cereals, vegetables, and fruits samples has been developed using ultra-performance liquid chromatography/tandem mass spectrometry. The analytes were extracted using acetonitrile containing 1% formic acid, and then the extracts were purified using primary secondary amine and octadecylsilane. The compounds were eluted in < 3.5 min using an electrospray ionization source in positive mode. Good linearities (R2 > 0.9916) were acquired for the analytes in all matrices. The limit of detection and quantification were 0.05 - 5 μg kg-1 and 10 μg kg-1 for all the three target compounds, respectively. The recoveries were 74.4 - 105.1% and the relative standard deviations values were lower than 12.4% at three spiked levels (10, 100, and 500 μg kg-1). The results indicated that the method is reliable for monitoring the three pesticides in cereals, vegetables, and fruits.



中文翻译:

使用超高效液相色谱/串联质谱法分析谷物、蔬菜和水果中的三氟啶虫脒、吡卡布唑和吡嗪虫胺残留的方法的开发和验证

使用超高效液相色谱/串联质谱法开发了一种用于测定谷物、蔬菜和水果样品中三种新农药(三氟嘧啶、吡唑嗪和吡卡布唑)的灵敏方法。分析物用含 1% 甲酸的乙腈提取,然后用伯仲胺和十八烷基硅烷纯化提取物。使用正离子模式的电喷雾电离源在 < 3.5 分钟内洗脱化合物。所有基质中的分析物都获得了良好的线性 (R 2 > 0.9916)。检测限和定量限分别为 0.05 - 5 μg kg -1和 10 μg kg -1分别为所有三个目标化合物。在三个加标水平(10、100 和 500 μg kg -1)下,回收率为 74.4 - 105.1%,相对标准偏差值低于 12.4% 。结果表明,该方法对谷物、蔬菜和水果中的三种农药进行监测是可靠的。

更新日期:2021-05-30
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