Abstract
A series of inhalation studies with propylene glycol monomethyl ether (PGME) vapor were undertaken to characterize its subchronic toxicity in mice and chronic toxicity/oncogenicity in rats and mice. Groups of male and female Fischer 344 rats and B6C3F1 mice were exposed to 0,300, 1,000, or 3,000 ppm vapor from 1 week to 2 years. Primary treatment-related effects included: initial sedation of animals exposed to 3,000 ppm and its subsequent resolution correlating with induction of hepatic mixed function oxidase activity and S-phase DNA synthesis; elevated mortality in high-exposure male rats and mice (chronic study); elevated deposition of alpha2U-globulin (α2U-G) and associated nephropathy and S-phase DNA synthesis in male rat kidneys; accelerated atrophy of the adrenal gland X-zone in female mice (subchronic study only); and increased occurrence and/or severity of eosinophilic foci of altered hepatocytes in male rats. No toxicologically relevant statistically significant increases in neoplasia occurred in either species. A numerical increase in the incidence of kidney adenomas occurred in intermediate-exposure male rats; however, the association with α2U-G nephropathy, a male rat specific effect, indicated a lack of relevance for human risk assessment.
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Spencer, P. J., Crissman, J. W., Stott, W. T., Corley, R. A., Cieszlak, F. S., Schumann, A. M., & Hardisty, J. F. (2002). Propylene glycol monomethyl ether (PGME): Inhalation toxicity and carcinogenicity in fischer 344 rats and B6C3F1 mice. Toxicologic Pathology, 30(5), 570–579. https://doi.org/10.1080/01926230290105848
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