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2 protocols using perfluoroundecanoic acid

1

Plasma Protein Binding of PFAS Compounds

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The molecular structures of the 14 PFAS evaluated are in Figure S1 and physiochemical properties, such as molecular weight (MW) and logD shown in Table S1. The following fourteen PFAS were either obtained from Accustandard, Inc. (New Haven, CT, USA) or Sigma-Aldrich (St. Louis, MO, USA): Perfluorobutanoic acid (PFBA), perfluoropentanoic acid (PFPA), perfluorohexanoic acid (PFHxA), perfluoroheptanoic acid (PFHpA), perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), perfluoroundecanoic acid (PFUDA), perfluorododecanoic acid (PFDoDA), perfluorohexanesulfonic acid (PFHxS), perfluorooctanesulfonamide (PFOSA), 6:2 fluorotelomer sulfonate (6:2 FtS), perfluorobutanesulfonic acid (PFBS), and perfluorooctanesulfonic acid (PFOS). Human, rat (Wistar-Han), and mouse (CD-1; C57BL/6) equal sex pooled (minimum of 3 male and 3 female) plasma was obtained from BioIVT (Hicksville, NY, USA). The equilibrium dialysis device (HTD96) and cellulose membranes with a molecular weight cutoff of 12–14 kDa were obtained from HTDialysis, LLC (Gales Ferry, CT, USA). Human, rat, and mouse albumin, along with all other reagents were obtained from Sigma-Aldrich unless specified otherwise.
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2

Analytical Method for Emerging Contaminants

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Reagents purchased were HPLC grade and the standards used were of high purity grade (>95%): perfluorooctanoic acid (PFOA), perfluoroheptanoic acid (PFHpA), perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), perfluoroundecanoic acid (PFUnDA), bisphenol A (BPA) and acetaminophen (ACT), caffeine (CAF), diclofenac (DCF), lamivudine (LA), triclosan (TS), phenytoin (PHE), sulfamethoxazole (SMX), carbamazepine (CAR), 2nitrophenol, sulfamethoxazole-d 4 and acetaminophen-d 4 from Sigma Aldrich (South Africa). Individual stock standards and isotopically labelled internal standards were prepared in methanol at a concentration of 1000 mg/L. Stock solutions in methanol were stored at À20 C. Working standard solutions were prepared by appropriate dilution of the stock solutions in methanol stored at 4 C in appropriate storage amber container glassware to prevent light degradation. Working standard solutions were used for preparation of the calibration curves and for spiking samples in the validation study. The cartridges Oasis HLB (6 mL, 200 mg) were obtained by Waters Corporation (Mildford, MA, USA). HPLC grade methanol, acetonitrile and acetone from Sigma Aldrich (South Africa), ultrapure water was purified by Milli-Q system (Millipore, Bedford, MA, USA).
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