Literature DB >> 15470233

Pharmacokinetics of perfluorooctanoate in cynomolgus monkeys.

J L Butenhoff1, G L Kennedy, P M Hinderliter, P H Lieder, R Jung, K J Hansen, G S Gorman, P E Noker, P J Thomford.   

Abstract

The pharmacokinetics of perfluorooctanoate (PFOA) in cynomolgus monkeys were studied in a six-month oral capsule dosing study of ammonium perfluorooctanoate (APFO) and in a single-dose iv study. In the oral study, samples of serum, urine, and feces were collected every two weeks from monkeys given daily doses of either 0, 3, 10, or 20 mg APFO/kg. Steady-state was reached within four weeks in serum, urine, and feces. Serum PFOA followed first-order elimination kinetics after the last dose, with a half-life of approximately 20 days. Urine was the primary elimination route. Mean serum PFOA concentrations at steady state in the 3, 10, and 20 mg/kg-day dose groups, respectively, were 81, 99, and 156 microg/ml in serum; 53, 166, and 181 microg/ml in urine; and, 7, 28, and 50 microg/g in feces. Mean liver concentrations reached 16, 14, and 50 microg/g in the 3, 10, and 20 mg/kg groups, respectively. In the iv study, three monkeys per sex were given a single dose of 10 mg/kg potassium PFOA. Samples were collected through 123 days. The terminal half-life of PFOA in serum was 13.6, 13.7, and 35.3 days in the three male monkeys and 26.8, 29.3, and 41.7 days in the three females. Volume of distribution at steady state was 181 +/- 12 and 198 +/- 69 ml/kg for males and females, respectively. Based on the result of both the oral and iv studies, the elimination half-life is approximately 14-42 days, and urine is the primary route of excretion.

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Year:  2004        PMID: 15470233     DOI: 10.1093/toxsci/kfh302

Source DB:  PubMed          Journal:  Toxicol Sci        ISSN: 1096-0929            Impact factor:   4.849


  24 in total

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Authors:  Kyra Kimberly Kieskamp; Rachel Rogers Worley; Eva D McLanahan; Marc-André Verner
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6.  Perfluoroalkyl chemicals and chronic kidney disease in US adults.

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7.  Physiologically based pharmacokinetic modeling of human exposure to perfluorooctanoic acid suggests historical non drinking-water exposures are important for predicting current serum concentrations.

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Journal:  Toxicol Appl Pharmacol       Date:  2017-07-03       Impact factor: 4.219

8.  Congenital anomalies, labor/delivery complications, maternal risk factors and their relationship with perfluorooctanoic acid (PFOA)-contaminated public drinking water.

Authors:  Lynda A Nolan; John M Nolan; Frances S Shofer; Nancy V Rodway; Edward A Emmett
Journal:  Reprod Toxicol       Date:  2009-11-06       Impact factor: 3.143

9.  Variability and epistemic uncertainty in water ingestion rates and pharmacokinetic parameters, and impact on the association between perfluorooctanoate and preeclampsia in the C8 Health Project population.

Authors:  Raghavendhran Avanasi; Hyeong-Moo Shin; Veronica M Vieira; Scott M Bartell
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10.  Roles of rat renal organic anion transporters in transporting perfluorinated carboxylates with different chain lengths.

Authors:  Yi M Weaver; David J Ehresman; John L Butenhoff; Bruno Hagenbuch
Journal:  Toxicol Sci       Date:  2009-11-13       Impact factor: 4.849

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