Vidal J L Martínez, Vega A Belmonte, López F J Sánchez, Frenich A Garrido
Research Group: Analytical Chemistry of Contaminants, Department of Analytical Chemistry, University of Almería, 04071 Almería, Spain.
J Chromatogr A. 2004 Oct 1;1050(2):179-84. doi: 10.1016/j.chroma.2004.08.023.
A method has been developed for the simultaneous determination of paraquat (PQ), deiquat (DQ), chlormequat (CQ) and mepiquat (MQ) in water samples by liquid chromatography (LC) coupled with electrospray ionization mass spectrometry (MS). The LC separations of the target compounds, as well as their MS parameters, were optimized in order to improve selectivity and sensitivity. Separation was carried out in a Xterra C8 column, using as mobile phase methanol-heptafluorobutyric acid (HFBA) in isocratic mode. The molecular ion was selected for the quantitation in selected ion monitoring (SIM) mode. Off-line solid-phase extraction (SPE) was applied with silica cartridges in order to preconcentrate the compounds from waters. Detection limits were in the range 0.02-0.40 microg l(-1). Recovery range varied between 89 and 99.5% with precision values lower than 6%. The method has been applied successfully to the analysis of both surface and groundwater samples from agricultural areas of Andalusia (Spain), using well defined internal quality control (IQC) criteria. The results revealed the presence of deiquat and paraquat in some samples.
已开发出一种通过液相色谱(LC)与电喷雾电离质谱(MS)联用同时测定水样中百草枯(PQ)、敌草快(DQ)、矮壮素(CQ)和甲哌鎓(MQ)的方法。对目标化合物的LC分离及其MS参数进行了优化,以提高选择性和灵敏度。在Xterra C8柱上进行分离,使用甲醇 - 七氟丁酸(HFBA)作为等度模式的流动相。在选择离子监测(SIM)模式下选择分子离子进行定量。采用硅胶柱离线固相萃取(SPE)以预富集水中的化合物。检测限在0.02 - 0.40 μg l⁻¹范围内。回收率在89%至99.5%之间,精密度值低于6%。该方法已成功应用于西班牙安达卢西亚农业区地表水和地下水样品的分析,并采用了明确的内部质量控制(IQC)标准。结果显示在一些样品中存在敌草快和百草枯。