Grimmer G, Brune H, Dettbarn G, Heinrich U, Jacob J, Mohtashamipur E, Norpoth K, Pott F, Wenzel-Hartung R
Biochemical Institute for Environmental Carcinogens, Grosshansdorf, Federal Republic of Germany.
Arch Toxicol. 1988;62(6):401-5. doi: 10.1007/BF00288341.
The urinary and faecal excretion of chrysene and its phenolic metabolites after oral, intraperitoneal, intratracheal, and intrapulmonary administration to rats have been studied by means of gas chromatography/mass spectrometry. The metabolite profile was found to depend on the mode of excretion and on the route of administration. In all cases the oxidation of chrysene in the 1,2- or 3,4-position predominates, whereas oxidation in the 5,6-position (K-region) seems be a minor pathway.