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Disposition of parathion after dermal application in pigs
L Brimer1, N Gyrd-Hansen, F Rasmussen
1Department of Pharmacology and Pathobiology, Royal Veterinary and Agricultural University, Frederiksberg, Copenhagen, Denmark.
Journal of Veterinary Pharmacology and Therapeutics
|August 1, 1994
Summary
Parathion
Area of Science:
- Veterinary Pharmacology
- Toxicology
- Dermal Absorption Studies
Background:
- Organophosphorus insecticides are widely used in pour-on preparations for ectoparasite control in livestock.
- Understanding the pharmacokinetic behavior of these compounds after dermal application is crucial for assessing efficacy and safety.
Purpose of the Study:
- To investigate the pharmacokinetic parameters of parathion in pigs following intravenous and dermal administration.
- To determine the absorption, distribution, metabolism, and excretion profile of parathion and its metabolites after dermal exposure.
Main Methods:
- Pharmacokinetic analysis of parathion in pigs using both intravenous (i.v.) and dermal administration routes.
- Utilized unlabelled and radiolabeled (14C) parathion to track compound and metabolite concentrations over time.
- Non-compartmental analysis was applied to plasma concentration-time data.
Main Results:
- Intravenous administration yielded a mean residence time (MRT) of 2.15 h, body clearance (ClB) of 4.4 l/kg/h, and volume of distribution (Vss) of 9.8 l/kg.
- Dermal application resulted in a mean absorption time (MAT) of 78 h and a low bioavailability of 9.9%.
- 14C-parathion and its metabolites showed higher and more persistent plasma levels than parathion itself, with significant accumulation in the application site skin.
Conclusions:
- Dermal bioavailability of parathion in pigs is low, suggesting limited systemic absorption.
- The efficacy of pour-on organophosphorus insecticides likely relies on surface spreading rather than systemic distribution to reach ectoparasites.
- Further research into topical distribution mechanisms is warranted.