Research Institute for Pesticides and Water, University Jaume I, Avda. Sos Baynat, s/n-12071 Castellón, Spain.
Iproma S.L., Camino de la Raya, 46, 12005 Castellón, Spain.
Talanta. 2015 Jan;131:719-27. doi: 10.1016/j.talanta.2014.08.005. Epub 2014 Aug 11.
This work describes a rapid analytical method based on direct sample injection of water samples for the simultaneous identification/quantification of 40 emerging compounds, including pharmaceuticals and drugs of abuse. The water samples were analyzed by ultra-high-performance liquid chromatography coupled to hybrid triple quadrupole mass spectrometer (UHPLC-MS/MS QqQ). Taking profit of the increasing sensitivity of nowadays tandem mass spectrometers, direct sample injection of large volumes has been an attractive alternative to pre-concentration steps. In this work, the developed methodology has been validated at three concentration levels (10, 100 and 1000 ng/L) in 10 different water samples of different types (5 effluent wastewater and 5 surface water samples). The majority of compounds could be satisfactory validated at these concentrations, showing good recoveries and precision. With only few exceptions, the limits of quantification (LOQs), estimated from the sample chromatogram at lowest spiked level tested, were below 3 ng/L. The method was applied to the analysis of 10 effluent wastewater and 10 surface water samples. Venlafaxine was the compound most frequently detected (80%) in surface water, followed by acetaminophen (70%). Regarding effluent wastewater, valsartan and 4-acetyl aminoantipyrine were detected in 9 out of 10 samples analyzed. These two compounds together with 4-formyl aminoantipyrine and naproxen showed the highest concentrations (>2000 ng/L). In these cases, a dilution step was required for a correct quantification. As an additional evaluation of the method performance, the same water samples were analyzed in another laboratory by a second analytical methodology, based on on-line solid-phase-extraction coupled to LC-MS/MS (QqQ).
这项工作描述了一种基于直接进样水样品的快速分析方法,用于同时鉴定/定量 40 种新兴化合物,包括药物和滥用药物。水样品通过超高效液相色谱与混合三重四极杆质谱联用(UHPLC-MS/MS QqQ)进行分析。利用当今串联质谱仪灵敏度的提高,直接进样大体积已成为预浓缩步骤的一种有吸引力的替代方法。在这项工作中,所开发的方法在 10 种不同类型的 10 种不同水样品的三个浓度水平(10、100 和 1000ng/L)下进行了验证。大多数化合物在这些浓度下都可以得到令人满意的验证,显示出良好的回收率和精密度。除了少数例外,从测试的最低加标水平的样品色谱图中估算的定量限(LOQs)均低于 3ng/L。该方法应用于 10 个废水和 10 个地表水样品的分析。文拉法辛是地表水最常检测到的化合物(80%),其次是对乙酰氨基酚(70%)。对于废水,缬沙坦和 4-乙酰氨基安替比林在分析的 10 个样品中的 9 个中被检测到。这两种化合物与 4-甲酰氨基安替比林和萘普生一起显示出最高的浓度(>2000ng/L)。在这些情况下,需要进行稀释步骤才能进行正确的定量。作为对方法性能的额外评估,同样的水样品由另一个基于在线固相萃取与 LC-MS/MS(QqQ)联用的分析方法在另一个实验室进行了分析。