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Xenobiotica
the fate of foreign compounds in biological systems
Volume 50, 2020 - Issue 12
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Animal Pharmacokinetics and Metabolism

Disposition and metabolism of antibacterial agent, triclocarban, in rodents; a species and route comparison

, , , , , , & show all
Pages 1469-1482 | Received 28 Apr 2020, Accepted 03 Jun 2020, Published online: 24 Jun 2020
 

Abstract

  1. Triclocarban is a residue-producing antibacterial agent used in a variety of consumer products. These studies investigated the disposition and metabolism of [14C]triclocarban.

  2. In male rats following a single gavage administration of 50, 150, and 500 mg/kg, excretion was primarily via feces (feces, 85–86%; urine, 3–6%) with no apparent dose-related effect. In male rats, 29% of the administered dose was excreted in bile suggesting some of the fecal excretion is from the absorbed dose which was excreted to the intestine via bile.

  3. The tissue retention of radioactivity was low in male rats (24 h, 3.9%; 72 h, 0.1%).

  4. Disposition pattern following gavage administration of 50 mg/kg in female rats and male and female mice were similar to male rats.

  5. Plasma elimination half-life of triclocarban in rats following gavage administration was shorter (∼2 h) compared to that based on total radioactivity (≥9 h) which included all products of triclocarban.

  6. Absorption following a single dermal application of 1.5 or 3% was low (≤3%) in rodents.

  7. Hydroxylated and conjugated metabolites of triclocarban predominated in bile.

  8. In hepatocytes, clearance of triclocarban in mouse and human was similar and was faster than in rat.

Acknowledgements

The authors are grateful to Drs Esra Mutlu and Madelyn Huang for their review of this manuscript.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

This work was supported by the Intramural Research Program of the NIH, National Institute of Environmental Health Sciences, Intramural Research project ZIA ES103316-04, and performed for the National Toxicology Program, National Institute of Environmental Health Sciences, National Institutes of Health, U.S. Department of Health and Human Services, under contract HHSN29120077563 (RTI International, RTP, NC).

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