1. Disposition and metabolism of 2′,2′'-Dithiobisbenzanilide in rodents following intravenous and oral administration and dermal application
- Author
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J. Michael Sanders, Jacob D. McDonald, Benjamin C. Moeller, Suramya Waidyanatha, Melanie Doyle-Eisele, C. Edwin Garner, and Christopher J. Wegerski
- Subjects
Health, Toxicology and Mutagenesis ,Clinical Sciences ,Urine ,Absorption (skin) ,010501 environmental sciences ,Pharmacology ,Disposition ,Distribution ,Toxicology ,01 natural sciences ,Absorption ,Medicinal and Biomolecular Chemistry ,03 medical and health sciences ,0302 clinical medicine ,lcsh:RA1190-1270 ,Oral administration ,Medicine ,Feces ,lcsh:Toxicology. Poisons ,0105 earth and related environmental sciences ,business.industry ,Regular Article ,Metabolism ,Chemical used ,Other Chemical Sciences ,business ,030217 neurology & neurosurgery - Abstract
Highlights • 2′,2′′′-Dithiobisbenzanilide (DTBBA) is a chemical used as a peptizing agent for rubber. • Humane exposure to DTBBA is possible via oral and dermal routes. • DTBBA is well-absorbed in rodents following oral and dermal administration. • Absorbed DTBBA was extensively metabolized and excreted mainly via urine. • N-(2-mercaptophenyl)benzamide accounted for more than 50% of radioactivity in urine., 2′,2′′′-Dithiobisbenzanilide (DTBBA) is a high-production-volume chemical used as a peptizing agent for rubber. The disposition and metabolism of [14C]DTBBA were determined in male and female rats and mice following oral (4, 40, or 400 mg/kg) and intravenous (IV) (4 mg/kg) administration and dermal application (0.4 or 4 mg/kg). [14C]DTBBA was well absorbed following oral administration (> 60%) and dermal application (∼40–50%) in rats and mice. Following oral administration, the majority of radioactivity was excreted in urine (29 − 70%) and feces (16 − 45%). Unlike rats, mice excreted ∼1-5% of the dose as exhaled CO2. The residual radioactivity in tissues was
- Published
- 2020