Comparative pharmacokinetics of chlorpyrifos versus its major metabolites following oral administration in the rat

• Published in: Toxicology (Amsterdam) Vol. 268; no. 1; pp. 55 - 63
• Main Authors: Busby-Hjerpe, Andrea L, Campbell, James A, Smith, Jordan Ned, Lee, Sookwang, Poet, Torka S, Barr, Dana B, Timchalk, Charles
• Format: Journal Article
• Language: English
• Published: Kidlington Elsevier Ireland Ltd 31.01.2010; Elsevier
• Subjects: 60 APPLIED LIFE SCIENCES; Administration, Oral; Animals; Biocompatibility; Biological and medical sciences; BIOLOGICAL INDICATORS; Chains; Chlorpyrifos; Chlorpyrifos - administration & dosage; Chlorpyrifos - pharmacokinetics; Diethylthiophosphate; Emergency; ENVIRONMENTAL EXPOSURE; Gas Chromatography-Mass Spectrometry; Half-Life; In Vitro Techniques; IN VIVO; INSECTICIDES; Insecticides - administration & dosage; Insecticides - pharmacokinetics; Male; Medical sciences; METABOLISM; METABOLITES; ORAL ADMINISTRATION; ORGANIC PHOSPHORUS COMPOUNDS; Parents; Pesticides; Pesticides, fertilizers and other agrochemicals toxicology; Pharmacokinetics; PHARMACOLOGY; RATS; Rats, Sprague-Dawley; Toxicology; Trichloropyridinol; URINE; Chlorpyrifos; Diethylthiophosphate; Trichloropyridinol; Pharmacokinetics; Insecticide; Rat; Metabolite; Pesticides; Rodentia; Oral administration; Vertebrata; Mammalia; Animal; Organophosphorus compounds; Comparative study
• ISSN: 0300-483X; 1879-3185
• DOI: 10.1016/j.tox.2009.11.022

Abstract Chlorpyrifos (CPF) is a commonly used diethylphosphorothionate organophosphorus (OP) insecticide. Diethylphosphate (DEP), diethylthiophosphate (DETP) and 3,5,6-trichloro-2-pyridinol (TCPy) are products of both in vivo metabolism and environmental degradation of CPF and are routinely measured in urine as biomarkers of exposure. Hence, urinary biomonitoring of TCPy, DEP and DETP may be reflective of an individual's contact with both the parent pesticide and exposure to these metabolites in the environment. In the current study, simultaneous dosing of13 C- or2 H-isotopically labeled CPF (13 C-labeled CPF, 513 C on the TCPy ring; or2 H-labeled CPF, diethyl-D10 (deuterium labeled) on the side chain) were exploited to directly compare the pharmacokinetics and metabolism of CPF with TCPy, and DETP. The key objective in the current study was to quantitatively evaluate the pharmacokinetics of the individual metabolites relative to their formation following a dose of CPF. Individual metabolites were co-administered (oral gavage) with the parent compound at equal molar doses (14 μmol/kg; ∼5 mg/kg CPF). Major differences in the pharmacokinetics between CPF and metabolite doses were observed within the first 3 h of exposure, due to the required metabolism of CPF to initially form TCPy and DETP. Nonetheless, once a substantial amount of CPF has been metabolized (≥3 h post-dosing) pharmacokinetics for both treatment groups and metabolites were very comparable. Urinary excretion rates for orally administered TCPy and DETP relative to13 C-CPF or2 H-CPF derived13 C-TCPy and2 H-DETP were consistent with blood pharmacokinetics, and the urinary clearance of metabolite dosed groups were comparable with the results for the13 C- and2 H-CPF groups. Since the pharmacokinetics of the individual metabolites were not modified by co-exposure to CPF; it suggests that environmental exposure to low dose mixtures of pesticides and metabolites will not impact their pharmacokinetics.