Elimination kinetics of perfluorohexanoic acid in humans and comparison with mouse, rat and monkey

•Elimination half-life of PFHxA determined from blood of ski wax technicians.•Geomean human elimination half-life of PFHxA is 32d (range 14–49d).•Elimination half-life of PFHxA in mammalian species is proportional to body weight.•Rate of PFHxA elimination from mammals is useful for subsequent risk a...

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Published inChemosphere (Oxford) Vol. 93; no. 10; pp. 2419 - 2425
Main Authors Russell, Mark H., Nilsson, Helena, Buck, Robert C.
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier Ltd 01.11.2013
Elsevier
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Summary:•Elimination half-life of PFHxA determined from blood of ski wax technicians.•Geomean human elimination half-life of PFHxA is 32d (range 14–49d).•Elimination half-life of PFHxA in mammalian species is proportional to body weight.•Rate of PFHxA elimination from mammals is useful for subsequent risk assessment. Major fluorinated chemical manufacturers have developed new short-chain per- and polyfluorinated substances with more favorable environmental, health and safety profiles. This study provides the first evaluation of the elimination half-life of perfluorohexanoic acid (PFHxA) from the blood of humans. PFHxA biomonitoring data were obtained from a recently published study of professional ski wax technicians. These data were analyzed to provide estimates of the apparent half-life of PFHxA from humans, and comparisons were made with kinetic studies of PFHxA elimination from mice, rats and monkeys. The apparent elimination half-life of PFHxA in highly exposed humans ranged between 14 and 49d with a geomean of 32d. The half-lives of PFHxA in mice, rats, monkeys and humans were proportional to body weight with no differences observed between genders, indicating similar volumes of distribution and similar elimination mechanisms among mammalian species. Compared to long-chain perfluoroalkyl acid analogs, PFHxA is rapidly cleared from biota. The consistent weight-normalized elimination half-lives for PFHxA in mammalian species indicates that results obtained from animal models are suitable for establishment of PFHxA benchmark dose and reference dose hazard endpoints for use in human risk assessments.
Bibliography:http://dx.doi.org/10.1016/j.chemosphere.2013.08.060
ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0045-6535
1879-1298
1879-1298
DOI:10.1016/j.chemosphere.2013.08.060