Dermal Exposure to Cumene Hydroperoxide
Author(s) -
Cynthia V. Rider,
Po C. Chan,
Ron Herbert,
Grace E. Kissling,
Laurene M. Fomby,
Milton R. Hejtmancik,
Kristine L. Witt,
Suramya Waidyanatha,
Greg Travlos,
Maria B. Kadiiska
Publication year - 2016
Publication title -
toxicologic pathology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 0.613
H-Index - 108
eISSN - 1533-1601
pISSN - 0192-6233
DOI - 10.1177/0192623316636712
Subject(s) - cumene hydroperoxide , toxicity , antioxidant , irritation , chemistry , toxicokinetics , hyperplasia , cumene , toxicology , pharmacology , medicine , immunology , biochemistry , biology , catalysis
Cumene hydroperoxide (CHP) is a high production volume chemical that is used to generate phenol and acetone. Dermal exposure to CHP was hypothesized to result in systemic tissue toxicity, production of free radicals, and consequent decrease in plasma antioxidant levels. To evaluate the hypothesis and characterize the toxicity of CHP, male and female B6C3F1/N mice and F344/N rats were exposed to varying doses of CHP applied topically for 14 or 90 days. No significant changes in survival or body weight of mice and rats were observed following 14 days of exposure. However, 90 days of CHP exposure at the high dose (12 mg/kg) triggered a significant decrease (-15%) in the body weight of the male rat group only. Irritation of the skin was observed at the site of application and was characterized by inflammation and epidermal hyperplasia. In treated animals, histology of liver tissue, free radical generation, and antioxidant levels in blood plasma were not significantly changed as compared to the corresponding controls. Consistent with the lack of systemic damage, no increase in micronucleated erythrocytes was seen in peripheral blood. In conclusion, topical CHP application caused skin damage only at the application site and did not cause systemic tissue impairment.
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