Disposition and metabolism of ethylene glycol 2-ethylhexyl ether in Sprague Dawley rats, B6C3F1/N mice, and in vitro in rat hepatocytes

Ethylene glycol 2-ethylhexyl ether (EGEHE) is a solvent used in a variety of applications. We report disposition and metabolism of EGEHE following a single gavage or dermal administration of 50, 150 or 500 mg/kg [ 14 C]EGEHE in rats and mice and in vitro in rat hepatocytes. EGEHE was cleared rapidly...

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Bibliographic Details
Published in:Xenobiotica 2021-06, Vol.51 (6), p.689-702
Main Authors: Watson, AtLee T. D., Moeller, Benjamin C., Doyle-Eisele, Melanie, Garner, Edwin, Blystone, Chad R., McDonald, Jacob D., Waidyanatha, Suramya
Format: Article
Language:English
Subjects:
absorption
Administration, Oral
alkoxyacetic acid
Animals
distribution
EGEHE
Ethers
Ethylene glycol 2-ethylhexyl ether
Ethylene Glycols
excretion
Female
glycol ether
Hepatocytes
Male
metabolism
Mice
Rats
Rats, Sprague-Dawley
Tissue Distribution
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Summary:Ethylene glycol 2-ethylhexyl ether (EGEHE) is a solvent used in a variety of applications. We report disposition and metabolism of EGEHE following a single gavage or dermal administration of 50, 150 or 500 mg/kg [ 14 C]EGEHE in rats and mice and in vitro in rat hepatocytes. EGEHE was cleared rapidly in rat hepatocytes (half-life ∼4 min) with no sex difference. EGEHE was well- and moderately absorbed following oral administration (rats: 80-96%, mice: 91-95%) and dermal application (rats: 25-37%, mice: 22-24%), respectively, and rapidly excreted in urine. [ 14 C]EGEHE-derived radioactivity was distributed to tissues (oral: 2.3-7.2%, dermal: 0.7-2.2%) with liver and kidney containing the highest levels in both species. EGEHE was extensively metabolised with little to no parent detected in urine. The alkoxyacetic acid metabolite, which has previously been shown to mediate toxicities of other shorter-chain ethylene glycol ethers, was not detected. There were no apparent dose, species or sex differences in disposition and metabolism of EGEHE, except that the exhaled volatile compounds were greater in mice (19-20%) compared with rats (
ISSN:0049-8254
1366-5928
DOI:10.1080/00498254.2021.1898062