Asperger Arndt, Efer Jürgen, Koal Therese, Engewald Werner
Leipzig University, Institute of Analytical Chemistry, Germany.
J Chromatogr A. 2002 Jun 25;960(1-2):109-19. doi: 10.1016/s0021-9673(01)01392-9.
An integrated on-line SPE-HPLC-MS/MS system has been developed for the rapid analysis of various trace level priority pesticides in surface and drinking water. Eleven pesticides were included in this study, with various phenylureas, triazines and organophosphorous species among them. Use of turbulent-flow chromatography columns (TFC, 50 x 1 mm, 30-50 microm particle size) as extraction cartridges enables fast on-line SPE at high sampling flow-rate (5 ml/min). Polymeric and carbon based TFC columns (Oasis HLB, Cyclone, Hypercarb) allow complete extraction with good recoveries from water volumes up to 50 ml. On-line coupling to HPLC is performed with re-mixing of the organic TFC eluate with water in front of the analytical column to ensure efficient band focussing. For fast HPLC analysis, a short monolithic column is applied in combination with highly selective API-MS/MS detection. Matrix effects on the APCI-MS/MS signal were found to be reduced by the system to an acceptable minimum. Limits of detection, determined for 10-ml samples of river water were in the range between 0.4 and 13 ng/l typically, except trifluralin (approximately 280 ng/l), which is less susceptible to ionization under atmospheric pressure conditions. At an enriched water volume of 10 ml, the whole SPE-HPLC-MS/MS procedure requires less than 14 min. The method was successfully applied to the analysis of drinking and surface water samples taken from several sampling sites around the city of Leipzig, Germany. Concentrations measured (maximum: 16 ng/l simazine in river water) were far below the concentration limits scheduled by law.
已开发出一种在线固相萃取-高效液相色谱-串联质谱联用系统,用于快速分析地表水和饮用水中各种痕量优先控制农药。本研究涵盖了11种农药,包括各种苯基脲类、三嗪类和有机磷类农药。使用湍流色谱柱(TFC,50×1mm,粒径30 - 50微米)作为萃取柱,可在高采样流速(5ml/min)下实现快速在线固相萃取。聚合物基和碳基TFC柱(Oasis HLB、Cyclone、Hypercarb)能够从高达50ml的水样中实现完全萃取且回收率良好。在线与高效液相色谱联用是通过在分析柱前将有机TFC洗脱液与水重新混合来进行的,以确保有效的谱带聚焦。为了实现快速高效液相色谱分析,采用了短整体柱并结合高选择性大气压电离串联质谱检测。该系统可将基质对大气压化学电离串联质谱信号的影响降低到可接受的最低水平。对10ml河水样品测定的检测限通常在0.4至13ng/l之间,除了氟乐灵(约280ng/l),其在大气压条件下较不易电离。在10ml富集水样的情况下,整个固相萃取-高效液相色谱-串联质谱分析过程所需时间不到14分钟。该方法已成功应用于分析从德国莱比锡市周边多个采样点采集的饮用水和地表水样品。所测浓度(最高:河水中西玛津为16ng/l)远低于法定浓度限值。