IRSA-CNR, Water Research Institute, Via Mulino 19, 20861 Brugherio, Italy.
Thermo Fisher Scientific, 16 avenue du Québec, Silic 765, Villebon-sur-Yvette, 91963 Courtaboeuf Cedex, France.
J Anal Methods Chem. 2015;2015:942016. doi: 10.1155/2015/942016. Epub 2015 Mar 5.
An UHPLC-MS/MS multiresidue method based on an on-line solid phase extraction (SPE) procedure was developed for the simultaneous determination of 9 perfluorinated carboxylates (from 4 to 12 carbon atoms) and 3 perfluorinated sulphonates (from 4 to 8 carbon atoms). This work proposes using an on-line solid phase extraction before chromatographic separation and analysis to replace traditional methods of off-line SPE before direct injection to LC-MS/MS. Manual sample preparation was reduced to sample centrifugation and acidification, thus eliminating several procedural errors and significantly reducing time-consuming and costs. Ionization suppression between target perfluorinated analytes and their coeluting SIL-IS were detected for homologues with a number of carbon atoms less than 9, but the quantitation was not affected. Total matrix effect corrected by SIL-IS, inclusive of extraction efficacy, and of ionization efficiency, ranged between -34 and +39%. The percentage of recoveries, between 76 and 134%, calculated in different matrices (tap water and rivers impacted by different pollutions) was generally satisfactory. LODs and LOQs of this on-line SPE method, which also incorporate recovery losses, ranged from 0.2 to 5.0 ng/L and from 1 to 20 ng/L, respectively. Validated on-line SPE-LC/MS/MS method has been applied in a wide survey for the determination of perfluoroalkyl acids in Italian surface and ground waters.
基于在线固相萃取(SPE)程序的 UHPLC-MS/MS 多残留方法已被开发出来,用于同时测定 9 种全氟羧酸(碳原子数从 4 到 12)和 3 种全氟磺酸(碳原子数从 4 到 8)。本工作提出在色谱分离和分析之前使用在线固相萃取代替传统的离线 SPE 直接进样到 LC-MS/MS 方法。手动样品制备简化为样品离心和酸化,从而消除了几个程序错误,并显著减少了耗时和成本。在数量少于 9 个碳原子的同系物中检测到目标全氟分析物与其共洗脱 SIL-IS 之间的电离抑制,但定量不受影响。通过 SIL-IS 校正的总基质效应,包括提取效率和电离效率,范围在-34%到+39%之间。在不同基质(自来水和受不同污染影响的河流)中计算的回收率在 76%到 134%之间,总体上令人满意。该在线 SPE 方法(还包括回收率损失)的检出限和定量限范围从 0.2 到 5.0ng/L 和 1 到 20ng/L。已在意大利地表水和地下水的全氟烷基酸广泛调查中应用了经过验证的在线 SPE-LC/MS/MS 方法。