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Kinetic analysis of the fate of methyl parathion in the dog

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Abstract

Methyl parathion (1, 3, 10 and 30 mg · kg−1) was injected intravenously in dogs and the serum concentrations were followed in function of time. For each dose the serum level data were fitted to a two- or tri-exponential equation by means of a non-linear least-squares regression analysis computer program.

During the first hours after injection a rapid and important decrease of the serum levels was observed, whereas afterwards the levels decreased more slowly with a harmonic mean terminal half-life of 7.2 h (range 6.6–8.8 h) for the 10 mg · kg−1 dose. Simulations using the kinetic parameters obtained for the dose of 10 mg · kg−1 show that elimination of methyl parathion from the body is fast (5 h after injection only 30% of the dose is still present in the body) and that the fraction remaining is mainly located in the peripheral compartments.

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References

  • Boelcke, G., Butigan, N., Davar, H., Erdmann, W. D., Gaaz, J. W., Nenner, M.: Neue Erfahrungen bei der toxikologisch kontrollierten Therapie einer ungewöhnlich schweren Vergiftung mit Nitrostigmin (E 605 forte). Dtsch. Med. Wochenschr. 95, 2516–2521 (1970)

    Google Scholar 

  • Boxenbaum, H. G., Riegelman, S., Elashoff, R. M.: Statistical estimations in pharmacokinetics. J. Pharmacokin. Biopharm. 2, 123–148 (1974)

    Google Scholar 

  • De Potter, M., Muller, R., Willems, J.: A method for the determination of some organophosphorus insecticides in human serum. Chromatographia 11, 220–222 (1978)

    Google Scholar 

  • Gupta, P. K., Paul, B. S.: Biological fate of 32P malathion in Gallus domesticus (desi poultry birds). Toxicology 7, 169–177 (1977)

    Google Scholar 

  • Gupta, P. K., Paul, B. S., Ehrnebo, M.: Absorption and elimination kinetics of 32P malathion in the hen. Acta Pharmacol. Toxicol. (Kbh.) 40, 65–69 (1977)

    Google Scholar 

  • Hobbiger, F.: Reactivation of phosphorylated acetylcholinesterase. In: Cholinesterases and anticholinesterase agents. Handbuch der experimentellen Pharmakologie. Ergänzungswerk (G. B. Koelle, Hrsg.), vol. 15, chap. 21, p. 947. Berlin-Göttingen-Heidelberg: Springer 1963

    Google Scholar 

  • Hollingworth, R. M., Metcalf, R. L., Fukuto, T. R.: The selectivity of sumithion compared with methyl parathion. Metabolism in the white mouse. J. Agric. Food. Chem. 15, 242–249 (1967)

    Google Scholar 

  • Karlog, O., Nielsen, P., Rasmussen, F.: Toxicokinetics. Arch. Toxicol. (Suppl.) 1, 55–67 (1978)

    Google Scholar 

  • Kramer, W. G., Lewis, R. P., Cobb, T. C., Forester, W. F., Visconti, J. A., Wanke, L. A., Boxenbaum, H. G., Reuning, R. H.: Pharmacokinetics of digoxin: a comparison of a two- and three-compartment model in man. J. Pharmacokin. Biopharm. 2, 299–312 (1974)

    Google Scholar 

  • Kramer, W. G., Kolibash, A. J., Lewis, R.P., Bathala, M. S., Visconti, J. A., Reuning, R. H.: Pharmacokinetics of digoxin: relationship between response intensity and predicted compartimentai drug levels in man. J. Pharmacokin. Biopharm. 7, 47–61 (1979)

    Google Scholar 

  • Luzhnikov, E. A., Yaroslavsky, A. A., Molodenkov, M. N., Shurkalin, B. K., Evseev, N. G., Barsukov, U. F.: Plasma perfusion through charcoal in methyl parathion poisoning. Lancet 1977 I, 38–39

  • Metzler, C. M., Elfring, G. L., McEwen, A. J.: A package of computer programs for pharmacokinetic modeling. Biometrics 30, 562 (1974)

    Google Scholar 

  • Okonek, S., Kilbinger, H.: Determination of acetylcholine, nitrostigmine and acetylcholinesterase activity in four patients with severe nitrostigmine (E 605 forte) intoxication. Arch. Toxicol. 32, 97–108 (1974)

    Google Scholar 

  • Okonek, S.: Probable progress in the therapy of organophosphate poisoning. Arch. Toxicol. 35, 221–227 (1976)

    Google Scholar 

  • Okonek, S.: Elimination of parathion by hemoperfusion in severe E 605 forte intoxication in vivo. Naunyn-Schmiedebergs Arch. Pharmacol. 302, R66 (1978)

    Google Scholar 

  • Riegelman, S., Loo, J. C. K., Rowland, M.: Shortcomings in pharmacokinetic analysis by conceiving the body to exhibit properties of a single compartment. J. Pharm. Sci. 57, 117–123 (1968)

    Google Scholar 

  • Thron, C. D.: Linearity and superposition in pharmacokinetics. Pharmacol. Rev. 26, 3–31 (1974)

    Google Scholar 

  • Tilstone, W. J., Winchester, J. F., Reavey, P. C.: Pharmacokinetic concepts. The use of pharmacokinetic principles in determining the effectiveness of removal of toxins from blood. Clin. Pharmacokinet. 4, 23–37 (1979)

    Google Scholar 

  • Wagner, J. G.: Fundamentals of clinical pharmacokinetics. Hamilton, Illinois: Drug Intelligence Publ., Inc. 1975

    Google Scholar 

  • Wagner, J. G.: Linear pharmacokinetic equations allowing direct calculation of many needed pharmacokinetic parameters from the coefficients and exponents of polyexponential equations which have been fitted to the data. J. Pharmacokin. Biopharm. 4, 443–467 (1976)

    Google Scholar 

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Braeckman, R.A., Godefroot, M.G., Blondeel, G.M. et al. Kinetic analysis of the fate of methyl parathion in the dog. Arch. Toxicol. 43, 263–271 (1980). https://doi.org/10.1007/BF00366182

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