PharmacyPharmacokineticsToxicologyDrug MetabolismMetabolismPharmaceutical ToxicologyDrug DispositionHepatic Drug MetabolismMetabolite KineticsPyrethroid Mechanism Of Toxicity
OBJECTIVE: To study the metabolism of 14C-deltamethrin in rats. METHODS: Rats were dosed orally and i.p. with a single dose of 14C-deltamethrin (0.64 mg/Kg) body weight. The required dose was applied daily for 3 days. At the end of the experiment, selected organs, such as liver, kidney, fat, intestine, and blood were excised for radioassay of 14C-content. RESULTS: Deltamethrin was almost eliminated from the body within 1-3 days. The main portion of 14C-residues was extracted from urine (38%, 32%) and feces (20%, 24%) with a little amount remained in various organs. CONCLUSION: The elimination and distribution of 14C-radioactivity in rats treated orally and intraperitoneally signify that deltamethrin is bioavailable in urine and feces.
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Repeated dose toxicity of alfa-cypermethrin in rats
S Manna, Debashis Bhattacharyya, TK Mandal et al. · Journal of Veterinary Science · 2004 · 115 citations · Full text
Medicine, Pharmacology, Toxicology +17