In vitro and in vivo evaluation of propylene glycol ethers metabolism in humans

Propylene glycol ethers (PGEs) consist of a major α-isomer (secondary alcohol group) and a minor β-isomer (primary alcohol group). Animal studies have reported toxic effects of the β-isomer metabolites, but human metabolism of PGEs remains poorly understood. We aimed to characterize the metabolism of two common PGEs in humans. Nine participants were exposed under controlled conditions (4 h) to propylene glycol ethyl ether (PGEE) or propylene glycol propyl ether (PGPE) (<35 ppm). Blood and urine samples were collected, and the respective β-isomers metabolites; 2-ethoxypropanoic acid (2-EPA) and 2-propoxypropanoic acid (2-PPA) were quantified. The 2-PPA blood absorption rate was 0.0005 ± 0.0002 µg/mL/h*ppm followed by rapid urinary elimination (half-life: 2 h) and slower secondary elimination (half-life: 10 h). No dose-response was observed for 2-EPA; therefore, β-PGEE metabolism was investigated in vitro using human liver S9 fractions. We provide 2-EPA hepatic kinetic and enzyme kinetic parameters. We recommend using of 2-PPA as a biomarker for PGPE exposures.

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Publication Details

Journal
Environmental Toxicology and Pharmacology
Published
2025-08-18
DOI
https://doi.org/10.1016/j.etap.2025.104795
Primary Topic
Pharmacogenetics and Drug Metabolism
Type
article
Field-Weighted Citation Impact
0.00

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article

In vitro and in vivo evaluation of propylene glycol ethers metabolism in humans

Pascal Wild, Nancy B. Hopf, Myriam Borgatta, Sophie Werner et al.
Environmental Toxicology and Pharmacology
Pharmacogenetics and Drug Metabolism
article

In vitro and in vivo evaluation of propylene glycol ethers metabolism in humans

Pascal Wild, Nancy B. Hopf, Myriam Borgatta, Sophie Werner, Laura Suter‐Dick, Hélène P. De Luca, Sylvain Le Gludic
article en

Abstract

Propylene glycol ethers (PGEs) consist of a major α-isomer (secondary alcohol group) and a minor β-isomer (primary alcohol group). Animal studies have reported toxic effects of the β-isomer metabolites, but human metabolism of PGEs remains poorly understood. We aimed to characterize the metabolism of two common PGEs in humans. Nine participants were exposed under controlled conditions (4 h) to propylene glycol ethyl ether (PGEE) or propylene glycol propyl ether (PGPE) (<35 ppm). Blood and urine samples were collected, and the respective β-isomers metabolites; 2-ethoxypropanoic acid (2-EPA) and 2-propoxypropanoic acid (2-PPA) were quantified. The 2-PPA blood absorption rate was 0.0005 ± 0.0002 µg/mL/h*ppm followed by rapid urinary elimination (half-life: 2 h) and slower secondary elimination (half-life: 10 h). No dose-response was observed for 2-EPA; therefore, β-PGEE metabolism was investigated in vitro using human liver S9 fractions. We provide 2-EPA hepatic kinetic and enzyme kinetic parameters. We recommend using of 2-PPA as a biomarker for PGPE exposures.

Environmental Toxicology and PharmacologyVol. 118
FHNW University of Applied Sciences and Arts Northwestern Switzerland (CH), University Centre of Legal Medicine (CH), Centre universitaire de médecine générale et santé publique, Lausanne (CH)
Swiss Centre for Applied Human Toxicology
Zero hunger
Openalex Percentile: Top 72%
Pharmacogenetics and Drug Metabolism
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In vitro and in vivo evaluation of propylene glycol ethers metabolism in humans — Pascal Wild, Nancy B. Hopf, et al. · Environmental Toxicology and Pharmacology (2025) | TGRS Research Map | TGRS