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A rapid and simple method to quantify per- and polyfluoroalkyl substances (PFAS) in plasma and serum using 96-well plates

机译:使用96孔板量化血浆和血清中的速度和多氟烷基物质(PFAS)的快速简便的方法

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摘要

Per- and polyfluoroalkyl substances (PFAS) are synthetic organic compounds that over the past several years, have witnessed a dramatic increase in scientific attention. As PFAS are predominantly accumulated in plasma, monitoring individual burden levels in plasma are typically achieved via some combination of protein precipitation and/or solid phase extraction (SPE), either in online or offline modes. This work describes an updated PFAS extraction workflow, using 96-well plate technology and protein precipitation that is rapid, simple, inexpensive, and amenable for large cohort studies. In brief, plasma proteins were precipitated using methanol and the resulting centrifuged supernatant was directly analyzed using UHPLC-MS/MS. We monitored 51 PFAS, which were quantified via isotope dilution and the effectiveness of the method was demonstrated by using NIST blood-based Standard Reference Materials (SRMs). This method resulted in recoveries ranging between 70 and 89% for all analytes. The 96-well design exhibited low limits of detection and only required sample volumes of 100 µL, thus resulting in an amenable method for high-throughput plasma/serum PFAS screening.
机译:Per-和多氟烷基物质(PFAS)是人工合成的有机化合物,在过去的几年里,目睹了科学的关注急剧增加。如PFAS在等离子体主要积累,监测血浆个人负担水平通过蛋白质沉淀和/或固相提取(SPE),无论是在在线或离线模式中的某些组合,通常实现。这部作品描述了一个更新的PFAS提取工作流,使用96孔板技术和蛋白质沉淀是快速,简单,价格低廉,并且易于大型队列研究。简言之,血浆蛋白用甲醇沉淀,并使用UHPLC-MS / MS直接分析得到的离心上清液。我们监测51 PFAS,将其通过同位素稀释定量,并且该方法的有效性,通过使用基于血液NIST标准参考物质(SRM的)证明。这种方法导致回收率70至89%不等的所有分析物。由此导致对于适合的方法检测的96孔设计表现出低的限制和100μL的仅需要的样品体积,高通量的血浆/血清PFAS筛选。

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