MTM Research Centre, School of Science and Technology, Örebro University, Örebro, Sweden.
J Chromatogr A. 2013 Aug 30;1305:164-70. doi: 10.1016/j.chroma.2013.07.026. Epub 2013 Jul 10.
To facilitate high-throughput analysis suitable for large epidemiological studies we developed an automated column-switching ultra-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method for determination of perfluorocarboxylic acids (PFCAs; C5, C6, C7, C8, C9, C10, C11, C12, and C13), perfluoroalkyl sulfonic acids (PFSAs; C4, C6, C8, and C10), perfluorooctane sulfonamide (PFOSA), and five groups of structural perfluorooctane sulfonic acid (PFOS) isomers in human serum or plasma. The analytical procedure involves rapid protein precipitation using 96-well plates followed by an automated sample clean-up using an on-line trap column removing many potentially interfering sample components while through the mobile phase gradient the target analytes are eluted onto the analytical column for further separation and subsequent mass detection. The method was linear (R(2)<0.995) at concentrations ranging from 0.01 to 60ngmL(-1) with method detection limits ranging between 0.01 and 0.17ngmL(-1) depending on the analyte. The developed method was precise, with repeatability (n=7) and reproducibility (n=103) coefficients of variation between 2% and 20% for most compounds including PFOS (2% and 8%) and its structural isomers (2-6% and 4-8%). The method was in conformity with a standard reference material. The column-switching HPLC-MS/MS method has been successfully applied for the determination of perfluoroalkyl substances including structural PFOS isomers in human plasma from an epidemiological study.
为了便于适用于大型流行病学研究的高通量分析,我们开发了一种自动化柱切换超高效液相色谱-串联质谱(HPLC-MS/MS)方法,用于测定全氟羧酸(PFCAs;C5、C6、C7、C8、C9、C10、C11、C12 和 C13)、全氟烷基磺酸(PFSAs;C4、C6、C8 和 C10)、全氟辛烷磺酸(PFOSA)和 5 组结构全氟辛烷磺酸(PFOS)异构体在人血清或血浆中的含量。该分析程序涉及使用 96 孔板进行快速蛋白质沉淀,然后使用在线阱柱进行自动样品净化,去除许多潜在的干扰样品成分,同时通过流动相梯度将目标分析物洗脱到分析柱上进行进一步分离和随后的质量检测。该方法在浓度范围为 0.01 至 60ngmL(-1) 时具有线性(R(2)<0.995),取决于分析物,方法检测限在 0.01 至 0.17ngmL(-1) 之间。所开发的方法具有较高的精密度,大多数化合物(包括 PFOS(2% 和 8%)及其结构异构体(2-6%和 4-8%))的重复性(n=7)和再现性(n=103)的变异系数在 2%至 20%之间。该方法符合标准参考物质。该柱切换 HPLC-MS/MS 方法已成功应用于包括结构 PFOS 异构体在内的人类血浆中全氟烷基物质的测定,用于流行病学研究。