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Pharmacokinetic model equations for the one- and two-compartment models with first-order processes in which the absorption and exponential elimination or distribution rate constants are equal

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Abstract

In fitting the one-compartment open model with first-order processes to empirical data, it has frequently been found for single-dose administration that the absorption and elimination rate constants approach each other. If these rate constants tend to be equal, such combinations are impossible to solve with the general model equation. In 1968, Dost (1) published a special model function by which the problems associated with the general model function can be circumvented. No solution, however, has been published for multiple-dose functions with the one-compartment model in which the absorption and elimination rate constants are equal. For a two-compartment open model with first-order processes, similar problems arise if the absorption and exponential distribution rate constants approach each other. Although this type of problems is often encountered in pharmacokinetic curve-fitting to empirical data, no exact solution has been published. Equations are given for multiple-dose administration with the one-compartment open model in which the absorption and elimination rate constants are equal, and for single-dose and multiple-dose administration with the two-compartment open model in which the absorption and exponential distribution rate constants are equal. Included are criteria to decide whether the new or the classical model functions should be applied in the case of a two-compartment open model.

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References

  1. F. H. Dost.Grundlagen der Pharmakokinetik, Georg Thieme Verlag, Stuttgart, West Germany, 1968, pp. 42–43.

    Google Scholar 

  2. M. Bialer. A simple method for determining whether absorption and elimination rate constants are equal in the one-compartment open model with first-order processes.J. Pharmacokin. Biopharm. 8:111–113 (1980).

    Article  CAS  Google Scholar 

  3. L. Saunders and T. Natunen. A stable method for calculating drug absorption rate constants with two compartment disposition.J. Pharm. Pharmacol. 25:44P-51P (1973).

    CAS  PubMed  Google Scholar 

  4. M. Weiss. Use of gamma distributed residence times in pharmacokinetics.Eur. J. Clin. Pharmacol. 25:695–702 (1983).

    Article  CAS  PubMed  Google Scholar 

  5. M. E. Wise. Negative power functions of time in pharmacokinetics and their implications.J. Pharmacokin. Biopharm. 13:309–346 (1985).

    Article  CAS  Google Scholar 

  6. J. G. Wagner.Fundamentals of Clinical Pharmacokinetics, Drug Intelligence Publications, Hamilton, IL, 1975, pp. 102–103.

    Google Scholar 

  7. J. C. J. Stiekema, H. N. Magnani, H. P. Wijnand, P. Morrison, K. Kaär, J. Harenberg, E. Weber, C. D. Forbes, and R. V. Johnston. A comparison of the pharmacokinetics of Org 10172 after i.v. and s.c. administration to young and elderly male and female healthy volunteers.J. Int. Soc. Thrombos. Haemostas. 54(1):1–372; p 555:94 (1985).

    Google Scholar 

  8. L. B. Sheiner. Elsfit (Version 3.1), a program for the extended least squares fit to individual pharmacokinetic data.Users Manual. Technical Report of the Division of Clinical Pharmacology, University of California, San Francisco, CA, January 1983.

    Google Scholar 

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Wijnand, H.P. Pharmacokinetic model equations for the one- and two-compartment models with first-order processes in which the absorption and exponential elimination or distribution rate constants are equal. Journal of Pharmacokinetics and Biopharmaceutics 16, 109–128 (1988). https://doi.org/10.1007/BF01061864

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  • DOI: https://doi.org/10.1007/BF01061864

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