4.7 Article

Evaluation and validation of methodologies for the extraction of per- and polyfluoroalkyl substances (PFASs) in serum of birds and mammals

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 414, 期 9, 页码 3017-3032

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-022-03962-3

关键词

Per- and polyfluoroalkyl substance (PFAS); Blood; Avian; Human; Horse; Sample preparation; Solid-phase extraction (SPE)

资金

  1. Melbourne Water
  2. Water Research Australia

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Advances in analytical techniques have allowed for the improved detection of environmental contaminants from small sample volumes. This study evaluated four methodologies for the extraction of per- and polyfluoroalkyl substances (PFASs) from avian and mammal serum samples, with enhanced matrix removal (EMR) and protein precipitation (PPT) proving to be the most effective methods. The study also highlighted that methanol may not be a suitable solvent for the extraction of long-chain PFASs from protein-rich tissues.
Advances in analytical techniques have allowed greater detection of environmental contaminants from small volumes of sample. Four methodologies were evaluated for the extraction of 53 per- and polyfluoroalkyl substances (PFASs) from eight classes in 200 mu L of avian and mammal serum. Spiked serums at four concentrations (0, 0.5, 5.0 and 25 ng mL(-1)) were prepared by protein precipitation (PPT), enhanced matrix removal (EMR), weak anion exchange (WAX), and hydrophilic-lipophilic balance (HLB) solid-phase extraction cartridges. The extract from each methodology was analysed by high-performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS), and concentrations were compared with known concentrations in the spiked media. EMR performed the best overall, with 40 of 53 compounds effectively recovered at 5 ng mL(-1). Furthermore, EMR was effective overall at concentrations ranging from 0.5 to 25 ng mL(-1) for 39 out of 53. Similarly, PPT was effective for 35 of 53 compounds at all spiked serum concentrations. There was a negative correlation between internal standard recovery for compounds with increasing octanol-water coefficients (K-ow) for WAX (R = - 0.65, p = 0.0043) and HLB (R = - 0.62, p = 0.0077) extractions, indicating methanol may not be a suitable solvent for long-chain PFAS extraction from protein-rich tissues. EMR and PPT represent fast and effective methodologies for the extraction of PFASs from low volumes of serum which allows greater accuracy and precision that can be applied to future human and wildlife biomonitoring programmes.

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