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Disopyramide pharmacokinetics and bioavailability following the simultaneous administration of disopyramide and14C-disopyramide

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The pharmacokinetics and bioavailability of total (bound plus unbound) and unbound disopyramide were compared following the simultaneous administration of an oral dose of disopyramide and an intravenous dose of14C-disopyramide in five normal volunteers and in 11 patients with congestive heart failure. The binding of disopyramide varied between 60 and 92% in patients and between 81 and 88% in normal subjects at postequilibrium drug concentrations of 10−7M. The binding of disopyramide to serum protein was concentration-dependent in all study subjects at serum concentrations achieved following drug administration. The association constant for the first binding site in serum from normal subjects and patients averaged 8.7X105 M−1 and 4.4X10 5 M−1, respectively (p < 0.05). The unbound clearance of disopyramide averaged 277ml/min and 209 ml/min in normal subjects and in patients (p < 0.05). When normalized for body weight, the unbound clearance between patients and normal subjects was not significantly different. The elimination half-life of unbound concentrations in normal subjects and in patients averaged 4.9 and 6.1 h, respectively (p < 0.05). The clearance and elimination half-life of total disopyramide was the same in both groups. Although the bioavailability of disopyramide averaged 0.85 in both groups, it was more variable in patients owing to the variability in the fraction of the dose absorbed. The unbound renal clearance and volume of distribution at steady state of disopyramide was related to cardiac index. The ratio of elimination half-lives of total and unbound disopyramide was related to the extent of serum protein binding.

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References

  1. P. H. Hinderling and E. R. Garrett. Pharmacokinetics of the antiarrhythmic disopyramide in healthy humans.J. Pharmacokin. Biopharm. 4:199–230 (1976).

    Article  CAS  Google Scholar 

  2. J. J. Lima, H. Boudoulas, and M. F. Blandford. Concentration-dependence of disopyramide binding to serum protein and its influence on kinetics and dynamics.J. Pharmacol Exp. Ther. 219:741–747 (1981).

    CAS  PubMed  Google Scholar 

  3. J. L. Cunningham, D. D. Shen, I. Shudo, and D. L. Azarnoff. The effects of urine pH and plasma protein binding on the renal clearance of disopyramide.Clin. Pharmacokin. 2:373–383 (1977).

    Article  CAS  Google Scholar 

  4. J. L. Cunningham, D. D. Shen, I. Shudo, and D. L. Azarnoff. The effects of non-linear disposition kinetics on the systemic availability of disopyramide.Br. J. Clin. Pharmacol. 5:343–346 (1978).

    Article  CAS  PubMed Central  Google Scholar 

  5. P. J. Meffln, E. W. Robert, R. A. Winkle, S. Harapat, F. A. Peters, and D. C. Harison. Role of concentration-dependent plasma protein binding in disopyramide disposition.J. Pharmacokin. Biopharm. 7:29–46 (1979).

    Article  Google Scholar 

  6. K. C. Giacomini, S. E. Swezey, K. Turner-Tamiyasu, and T. F. Blaschke. The effect of saturable binding to plasma proteins on the pharmacokinetic properties of disopyramide.J. Pharmacokin. Biopharm. 10:1–14 (1982).

    Article  CAS  Google Scholar 

  7. P. J. Podrid, A. Schoeneberger, and B. Lown. Congestive heart failure caused by oral disopyramide.N. Engt J. Med. 302:614–617 (1980).

    Article  CAS  Google Scholar 

  8. J. J. Lima, J. J. MacKichan, N. Libertin, and J. R. Sabino, Influence of volume shifts on drug binding during equilibrium dialysis: correction and attenuation.J. Pharmacokin. Biopharm. 11:483–498 (1983).

    Article  CAS  Google Scholar 

  9. H.E. Rosenthal. A graphic method for the determination and presentation of binding parameters in a complex system.Anal. Biochem. 20:525–532 (1967).

    Article  CAS  PubMed  Google Scholar 

  10. R. L. Priore and H. E. Rosenthal. A statistical method for the estimation of binding parameters in a complex system.Anal. Biochem. 70:231–240 (1976).

    Article  CAS  PubMed  Google Scholar 

  11. R. F. Mais, S. Keresztes-Nagy, J. F. Zaroslinski, and Y. T. Vester. Interpretation of protein-drug interaction through fraction bound and relative contribution of secondary sites.J. Pharm. Sci. 63:1423–1427 (1974).

    Article  CAS  PubMed  Google Scholar 

  12. H. Sandler and H. T. Dodge. Angiographic methods for determination of left ventricular geometry and volume. In: I. Mirsky, S. N. Ghista and H. Sandler (eds.),Cardiac Mechanics. Physiological, Clinical and Mathematical Considerations, Wiley, New York, 1974.

    Google Scholar 

  13. J. J. Lima. Liquid Chromatographic analysis of disopyramide and its mono-N-dealkylated metabolite.Clin. Chem. 25:405–508 (1979).

    CAS  PubMed  Google Scholar 

  14. A. Karim.The pharmacokinetics of Norpace. Angiology (suppl.)I (part 2):85–98 (1975).

    Google Scholar 

  15. M. Gibaldi and D. Perrier.Pharmacokinetics, Marcel Dekker, New York, 1982.

    Google Scholar 

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

    Article  Google Scholar 

  17. J. W. Wagner. Statistics. InFundamentals of Clinical Pharmacokinetics. Drug Intelligence Publns., Hamilton, Ill., 1975, Vol. 1, pp. 286–287.

    Google Scholar 

  18. K. Landmark, J. E. Bredesen, E. Thaulow, S. Simonsen, and J. P. Amile. Pharmacokinetics of disopyramide with imminent to moderate cardiac failure.Eur. J. Clin. Pharmacol. 19:187–192 (1981).

    Article  CAS  PubMed  Google Scholar 

  19. G. R. Wilkinson and D. G. Shand. A physiological approach to hepatic drug clearance.Clin. Pharmacol. Ther. 18:377–390 (1975).

    CAS  PubMed  Google Scholar 

  20. L. Z. Benet, A. Greither, and W. Meister. Gastrointestinal absorption of drugs in patients with cardiac failure. In L. Z. Benet (ed.),The Effect of Disease States on Drug Pharmacokinetics. A. Ph. A/Academy of Pharmaceutical Sciences, Washington, D. C., 1976, pp. 33–50.

    Google Scholar 

  21. W. S. Nimmo. Gastric emptying and drug absorption. In L. F. Prescott and W. S. Nimmo (eds.)Drug Absorption. Proceedings of the Edinburgh International Conference Adis Press (Australia), 1979, pp. 11–20.

    Google Scholar 

  22. M. Gibaldi and P. J. McNamara. Apparent volumes of distribution and drug binding to plasma proteins and tissues.Eur. J. Clin. Pharmacol. 13:373–378 (1978).

    Article  CAS  PubMed  Google Scholar 

  23. J. J. Lima and L. Salzer. Contamination of albumin by alpha 1-acid glycoprotein.Biochem. Pharmacol. 30:2633–2636 (1981).

    Article  CAS  PubMed  Google Scholar 

  24. K. Schmid. Alpha 1-acid glycoprotein. In F. W. Putnam (ed.),The Plasma Proteins. Academic Press, New York, 1975, Vol. 1, pp. 183–228.

    Chapter  Google Scholar 

  25. C. Pollick, K. M. Giacomini, T. F. Blaschke, W. L. Nelson, K. Turner-Tamiyasu, V. B. Briskin, and R. L. Popp. The cardiac effects of d-and 1-disopyramide in normal subjects: noninvasive study.Circulation 66:447–453 (1982).

    Article  CAS  PubMed  Google Scholar 

  26. D. B. Haughey and J. J. Lima. Influence of concentration-dependent protein binding on serum concentrations and urinary excretion of disopyramide.Biopharm. Drug Dispos. 4:103–112 (1983).

    Article  CAS  PubMed  Google Scholar 

  27. J. J. Lima. Experimental evidence for concentration-dependent plasma protein binding effects on the apparent half-lives of restrictively cleared drugs.J. Pharm. Sci. 72:461–462 (1983).

    Article  CAS  PubMed  Google Scholar 

  28. P. J. McNamara, G. Levy, and M. Gibaldi. Effect of plasma protein and tissue binding on the time course of drug concentration in plasma.J. Pharmacokin. Biopharm. 7:195–206 (1979).

    Article  CAS  Google Scholar 

  29. S. Oie, T. W. Guentert, and T. Tozer. Effect of saturable binding on the pharmacokinetics of drugs: a simulation.J. Pharm. Pharmacol. 32:471–4771 (1980).

    Article  CAS  PubMed  Google Scholar 

  30. K. Altland, T. H. Roeder, H. M. Jakin, H. G. Zimmer, and V. Neilhoff. Demonstration of alpha 1-acid glycoprotein (orosomucoid) by double one dimensional slab gel electrophoresis: evidence for intra- and interindividual variability of the microheterogeneity pattern in health and disease.Clin. Chem. 28:1000–1010 (1982).

    CAS  PubMed  Google Scholar 

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This work was supported by Grant GM-28424 from the National Institute of General Medical Sciences, National Institutes of Health.

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Lima, J.J., Haughey, D.B. & Leier, C.V. Disopyramide pharmacokinetics and bioavailability following the simultaneous administration of disopyramide and14C-disopyramide. Journal of Pharmacokinetics and Biopharmaceutics 12, 289–313 (1984). https://doi.org/10.1007/BF01061722

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