Abstract
1. 14C-DGEBPA dermally applied to mice was only slowly eliminated in the faeces (20% dose) and urine (3%), as a mixture of metabolites, over three days. Most of the applied radioactivity (66% dose) was extracted from the application area and its covering foil. 2. When 14C-DGEBPA was given orally to mice it was rapidly excreted; 80% of the administered 14C was eliminated in the faeces and 11% in the urine 0-3 days after a single oral dose. 3. The urinary and faecal metabolite profiles derived from dermal application and oral dosing were essentially similar.