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Online background cleanup followed by high-performance liquid chromatography with tandem mass spectrometry for the analysis of perfluorinated compounds in human blood

机译:在线背景清理,然后进行高效液相色谱-串联质谱分析人血中的全氟化合物

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摘要

In this study, a novel method for the analysis of perfluorinated compounds in whole blood has been developed and validated. The method was developed by using a conventional reversed-phase C-18 column as a trapping column for the elimination of background contamination and high-performance liquid chromatography with tandem mass spectrometry for the target compounds analysis. The trapping column provided fast online separation of the background contamination of perfluorinated compounds. In this developed method, the limits of detection for different perfluorinated compounds ranged from 0.06 to 0.14 ng/mL. It is notable that the limit of detection (0.07 ng/mL) for perfluorooctanoic acid was improved significantly after the elimination of background contamination. The method was also validated in terms of sensitivity, accuracy, and precision. The recoveries ranged from 66.8 to 111.9%, with relative standard deviations from 2.1 to 15.3%. Our preliminary data suggest that the novel method based on trapping column cleanup followed by high-performance liquid chromatography with tandem mass spectrometry could be applied in studies on the human exposure to perfluorinated compounds.
机译:在这项研究中,已经开发并验证了一种用于分析全血中全氟化合物的新颖方法。该方法是通过使用常规的反相C-18色谱柱作为捕集柱来消除背景污染以及采用串联质谱进行高效液相色谱分析目标化合物来开发的。捕集柱可快速在线分离全氟化合物的背景污染物。在这种发达的方法中,不同全氟化合物的检出限范围为0.06至0.14 ng / mL。值得注意的是,消除背景污染后,全氟辛酸的检出限(0.07 ng / mL)得到了显着提高。该方法还通过了灵敏度,准确性和精度方面的验证。回收率范围为66.8至111.9%,相对标准偏差为2.1至15.3%。我们的初步数据表明,基于捕集柱净化再结合高效液相色谱和串联质谱联用的新方法可用于人体暴露于全氟化合物的研究。

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