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Simultaneous Determination of Paraquat and Diquat in Environmental Water Samples by HPLC-MS/MS

机译:HPLC-MS / MS的环境水样中同时测定百草枯和肝炎

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Purpose: To develop and evaluate a high throughput quantitative method for paraquat and diquat pesticide residues in environmental water samples using high pressure liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Methods: Environmental water samples were filtered, spiked with internal standards and injected directly for LC-MS/MS analysis. Chromatographic separation was achieved on a prototype column featuring reversed-phase, weak anion exchange and weak cationexchange retention mechanisms. A Thermo Scientific TSQ Quantum Access MAX triple stage quadrupolewas operated in selected reaction monitoring (SRM) mode to provide sensitive and selective detection. Results: Paraquatand diquat were sufficiently retained and completely separated on this prototype column within 5 minutes. Accurate quantitation was achieved through 3 orders of magnitude from 0.1 ng/mL to 100 ng/mL with a coefficient of determination (r2) greater than 0.999. Excellent precision was achieved with %RSD < 10% at 0.5 ng/mL and %RSD < 4% at 50 ng/mL..
机译:目的:使用高压液相色谱 - 串联质谱法(HPLC-MS / MS)开发和评估环境水样中的拟法和达奎特农药残留的高通量定量方法。方法:过滤环境水样,掺入内标并直接注射LC-MS / MS分析。在原型柱上实现了色谱分离,其具有反相,弱阴离子交换和弱阳离子化保留机制。在选定的反应监测(SRM)模式下,Thermo Sciencific TSQ量子接入MAX三级四轮轴运行,提供敏感和选择性检测。结果:在5分钟内充分保留并在该原型柱上充分保留并完全分离。通过从0.1ng / ml的0.1ng / ml至100ng / ml的3个级别实现精确的定量,其测定系数大于0.999。在0.5ng / ml下以0.5ng / ml的%RSD <10%实现优异的精度,并且在50 ng / ml下%RSD <4%。

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