Zabaleta I, Bizkarguenaga E, Prieto A, Ortiz-Zarragoitia M, Fernández L A, Zuloaga O
Department of Analytical Chemistry, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), P.O. Box 644, 48080 Bilbao, Spain.
Department of Analytical Chemistry, Faculty of Science and Technology, University of the Basque Country (UPV/EHU), P.O. Box 644, 48080 Bilbao, Spain.
J Chromatogr A. 2015 Mar 27;1387:13-23. doi: 10.1016/j.chroma.2015.01.089. Epub 2015 Feb 7.
An analytical method for the simultaneous determination in fish liver and muscle tissue and mussel samples of 14 perfluorinated compounds (PFCs), including three perfluoroalkylsulfonates (PFSAs), seven perfluorocarboxylic acids (PFCAs), three perfluorophosphonic acids (PFPAs) and perfluorooctanesulfonamide (PFOSA), and 10 potential precursors, including four polyfluoroalkyl phosphates (PAPs), four fluorotelomer saturated acids (FTCAs) and two fluorotelomer unsaturated acids (FTUCAs), was developed in the present work. Different clean-up strategies by means of solid-phase extraction (SPE) using a mix-mode weak anion exchanger (WAX), reverse phase Envi-Carb or a combination of them was optimized and evaluated for the clean-up of focused ultrasonic solid-liquid (FUSLE) extracts before the analysis by liquid chromatography-triple quadrupole tandem mass spectrometry (LC-MS/MS). Mix-mode WAX coupled in-line to Envi-Carb was finally selected since it rendered the cleanest extracts and minimum matrix effect. The FUSLE-SPE-LC-MS/MS methodology was validated in terms of recovery, precision and method detection limits (MDLs). Apparent recovery values in the 65-116%, 59-119% and 67-126% range and MDLs in the 0.1-2.7 ng/g, 0.1-3.8 ng/g and 0.2-3.1ng/g range were obtained for liver, mussel and fish muscle tissue samples, respectively. The method developed was applied to the analysis of grey mullet liver (Chelon labrosus) and mussel (Mytilus galloprovincialis) samples from the Basque Coast (North of Spain) and Yellowfin tuna muscle tissue (Thunnus albacares) samples from the Indian Ocean. To the best of our knowledge this is the first method that describes the simultaneous determination of 14 PFCs and 10 potential precursors in fish liver, fish muscle tissue and mussel samples. Besides, this is the first time that 8:2 monosubstituted polyfluorodecyl phosphate (8:2 monoPAP) and 8:2 disubstituted polyfluorodecyl phosphate (8:2 diPAP) were detected in mussel and tuna samples, respectively.
本研究建立了一种分析方法,用于同时测定鱼肝、肌肉组织和贻贝样品中的14种全氟化合物(PFCs),包括3种全氟烷基磺酸盐(PFSAs)、7种全氟羧酸(PFCAs)、3种全氟膦酸(PFPAs)和全氟辛烷磺酰胺(PFOSA),以及10种潜在前体,包括4种多氟烷基磷酸盐(PAPs)、4种氟调聚物饱和酸(FTCAs)和2种氟调聚物不饱和酸(FTUCAs)。通过使用混合模式弱阴离子交换剂(WAX)、反相Envi-Carb或它们的组合进行固相萃取(SPE)的不同净化策略,在液相色谱-三重四极杆串联质谱(LC-MS/MS)分析之前,对聚焦超声固液(FUSLE)提取物的净化进行了优化和评估。最终选择了与Envi-Carb在线联用的混合模式WAX,因为它能提供最纯净的提取物和最小的基质效应。FUSLE-SPE-LC-MS/MS方法在回收率、精密度和方法检测限(MDLs)方面得到了验证。鱼肝、贻贝和鱼肉组织样品的表观回收率分别在65-116%、59-119%和67-126%范围内,MDLs分别在0.1-2.7 ng/g、0.1-3.8 ng/g和0.2-3.1 ng/g范围内。所建立的方法应用于来自巴斯克海岸(西班牙北部)的乌鱼肝脏(Chelon labrosus)和贻贝(Mytilus galloprovincialis)样品以及来自印度洋的黄鳍金枪鱼肌肉组织(Thunnus albacares)样品的分析。据我们所知,这是第一种描述同时测定鱼肝、鱼肉组织和贻贝样品中14种PFCs和10种潜在前体的方法。此外,这是首次分别在贻贝和金枪鱼样品中检测到8:2单取代多氟癸基磷酸盐(8:2 monoPAP)和8:2二取代多氟癸基磷酸盐(8:2 diPAP)。