Skip to main content

Pharmacokinetics of Quinidine in Male Patients

A Population Analysis

An Erratum to this article was published on 01 July 1992

Summary

Quinidine pharmacokinetic behaviour was evaluated in 139 adult hospitalised men receiving oral quinidine therapy. A total of 391 serum quinidine concentrations were measured by enzyme immunoassay for routine clinical purposes. The NONMEM programme was used to examine the relationship between quinidine pharmacokinetics and several potential covariates. A 1-compartment open model with first-order absorption and elimination was assumed. The mean apparent volume of distribution (Vd) was about 230L. When measured, α1-acid glycoprotein (AAG) levels were not included in the analysis. Oral quinidine clearance (CL) decreased with age, severe congestive heart failure and renal disease, and increased in patients with a history of alcohol abuse. The interpatient variability in CL and the intrapatient residual variability expressed as coefficients of variation (CV) were 28 and 31%, respectively. When AAG values were incorporated into the analysis, the only important covariates of CL were the AAG measurements and the presence of renal dysfunction as indicated by a calculated creatinine clearance of less than 50 ml/min (3 L/h). The interpatient variability in CL and the residual intrapatient CVs decreased to approximately 24 and 26%, respectively. Improvement of the CL model by inclusion of measured AAG strongly suggests that quinidine elimination is dependent on the free concentration of drug in plasma and supports the use of free serum quinidine concentrations when evaluating and monitoring quinidine therapy.

This is a preview of subscription content, access via your institution.

References

  • Ackerman BH, Olsen KM, Kennedy EE, Taylor EH, Chen BH, et al. Comparison of disposition values obtained by two assay methods for quinidine gluconate in patients with ventricular tachycardia. Pharmacotherapy 9: 22–225, 1989

    Google Scholar 

  • Affrime M, Reidenberg MM. The protein binding of some drugs in plasma from patients with alcoholic liver disease. European Journal of Clinical Pharmacology 8: 267–269, 1975

    PubMed  Article  CAS  Google Scholar 

  • Aronsen KF, Ekelund G, Kindmark CO, Laurell CB. Sequential changes of plasma proteins after surgical trauma. Scandinavian Journal of Clinical and Laboratory Investigations 29 (Suppl. 124): 127–136, 1972

    Article  Google Scholar 

  • Beal SL, Sheiner LB. NONMEM users’ guides, NONMEM project group, University of California, San Francisco, 1985

    Google Scholar 

  • Brosen K, Davidsen F, Gram LF. Quinidine kinetics after a single oral dose in relation to the sparteine oxidation polymorphism in man. British Journal of Clinical Pharmacology 29: 248–253, 1990

    PubMed  Article  CAS  Google Scholar 

  • Cockroft DW, Gault MH. Prediction of creatinine clearance from serum creatinine. Nephron 16: 31–41, 1976

    Article  Google Scholar 

  • Conrad KA, Molk BL, Chidset CA. Pharmacokinetic studies of quinidine in patients with arrhythmias. Circulation 55: 1–7, 1977

    PubMed  CAS  Google Scholar 

  • Covinsky JO. Quinidine. In Taylor & Caviness (Eds) A text book for the clinical application of therapeutic drug monitoring, pp. 161–173, Abbott Laboratories, Diagnostics Division, Irving, 1986

    Google Scholar 

  • Crouthamel WG. The effect of congestive heart failure on quinidine pharmacokinetics. American Heart Journal 90: 335–339, 1975

    PubMed  Article  CAS  Google Scholar 

  • Data JL, Wilkinson GR, Nies AS. Interaction of quinidine with anticonvulsant drugs. New England Journal of Medicine 294: 699–702, 1976

    PubMed  Article  CAS  Google Scholar 

  • Davies RF, Dube LM, Mousseau N, McGilveray I, Beanlands DS. Perioperative variability of binding to lidocaine, quinidine, and propranolol after cardiac operations. Journal of Thoracic and Cardiovascular Surgery 96: 634–641, 1988

    PubMed  CAS  Google Scholar 

  • Drayer DE, Hughes M, Lorenzo B, Reidenberg MM. Prevalence of high (3S)-3hydroxyquinidine/quinidine ratios in serum, and clearance of quinidine in cardiac patients with age. Clinical Pharmacology and Therapeutics 27: 72–75, 1980

    PubMed  Article  CAS  Google Scholar 

  • Drayer DE, Lowenthal DT, Restivo KM, Schwartz A, Cook CE, et al. Steady-state serum levels of quinidine and active metabolites in cardiac patients with varying degrees of renal function. Clinical Pharmacology and Therapeutics 24: 31–39, 1978

    PubMed  CAS  Google Scholar 

  • Edwards DJ, Axelson JE, Slaughter RL, Elvin AT, Lalka D. Factors affecting quinidine protein binding in humans. Journal of Pharmaceutical Sciences 73: 1264–1267, 1984

    PubMed  Article  CAS  Google Scholar 

  • Edwards DJ, Axelson JE, Visco JP, vanEvery S, Slaughter RL, et al. Lack of effect of smoking on the metabolism and pharmacokinetics of quinidine in patients. British Journal of Clinical Pharmacology 23: 351–354, 1987a

    PubMed  Article  CAS  Google Scholar 

  • Edwards DJ, Lalka D, Carra F, Slaughter RL. Alpha-1-acid glycoprotein concentration and protein binding in trauma. Clinical Pharmacology and Therapeutics 31: 62–67, 1982

    PubMed  Article  CAS  Google Scholar 

  • Edwards DJ, Lavoie R, Beckman H, Blevins R, Rubenfire M. The effect of coadministration of verapamil on the pharmacokinetics and metabolism of quinidine. Clinical Pharmacology and Therapeutics 41: 68–73, 1987b

    PubMed  Article  CAS  Google Scholar 

  • Fattinger K, Vožeh S, Ha HR, Borner M, Follath F. Population pharmacokinetics of quinidine. British Journal of Clinical Pharmacology 31: 279–286, 1991

    PubMed  Article  CAS  Google Scholar 

  • Fremstad D, Bergerud K, Haffner JFW, Lunde PKM. Increased plasma protein binding of quinidine after surgery: a preliminary report. European Journal of Clinical Pharmacology 10: 441–444, 1976

    PubMed  Article  CAS  Google Scholar 

  • Fremstad D, Nilsen OG, Storstein L, Amlie J, Jacobsen S. Pharmacokinetics of quinidine related to plasma protein binding in man. European Journal of Clinical Pharmacology 15: 187–192, 1979

    PubMed  Article  CAS  Google Scholar 

  • Fruncillo RJ, Kozin SH, DiGregorio GJ. Effect of amiodarone on the pharmacokinetics of phenytoin, quinidine and lidocaine in the rat. Research Communications in Chemical Pathology and Pharmacology 50: 451–454, 1985

    PubMed  CAS  Google Scholar 

  • Gadeholt G. Ethanol and isoniazid induce a hepatic microsomal cytochrome P-450-dependent activity with similar properties towards substrate and inhibitors and different properties from those induced by classical inducers. Biochemical Pharmacology 33: 3047–3051, 1984

    PubMed  Article  CAS  Google Scholar 

  • Garfinkel D, Mamelok RD, Blaschke TF. Altered therapeutic range for quinidine after myocardial infarction and cardiac surgery. Annals of Internal Medicine 107: 48–50, 1987

    PubMed  CAS  Google Scholar 

  • Giacomini KM, Swezey SE, Giacomini JC, Blaschke TF. Administration of heparin causes in vitro release of non-esterified fatty acids in human plasma. Life Sciences 27: 771–780, 1980

    PubMed  Article  CAS  Google Scholar 

  • Greenblatt DJ, Pfeifer HJ, Ochs HR, Franke K, MacLaughlin DS, et al. Pharmacokinetics of quinidine in humans after intravenous, intramuscular and oral administration. Journal of Pharmacology and Experimental Therapeutics 202: 365–378, 1977

    PubMed  CAS  Google Scholar 

  • Guentert TW, Holford NHG, Coates PE, Upton RA, Riegelman S. Quinidine pharmacokinetics in man: choice of a disposition model and absolute bioavailability studies. Journal of Pharmacokinetics and Biopharmaceutics 7: 315–329, 1979

    PubMed  CAS  Google Scholar 

  • Guentert TW, Oie S. Factors influencing the apparent protein binding of quinidine. Journal of Pharmaceutical Sciences 71: 325–328, 1982

    PubMed  Article  CAS  Google Scholar 

  • Ha HR, Kewitz G, Wenk M, Follath F. Quinidine determination in serum: enzyme immunoassay (EIA) vs HPLC. British Journal of Clinical Pharmacology 11: 312–314, 1981

    PubMed  Article  CAS  Google Scholar 

  • Ha HR, Vožeh S, Follath F. Evaluation of a rapid ultrafiltration technique for determination of quinidine protein binding and comparison with equilibrium dialysis. Therapeutic Drug Monitoring 8: 331–335, 1986

    PubMed  Article  CAS  Google Scholar 

  • Hardy BG, Zador IT, Golden L, Lalka D, Schentag JJ. Effect of cimetidine on the pharmacokinetics and pharmacodynamics of quinidine. American Journal of Cardiology 52: 172–175, 1983

    PubMed  Article  CAS  Google Scholar 

  • Ingelman-Sundberg M, Jornvall H. Induction of the ethanol-inducible form of rabbit liver microsomal cytochrome P-450 by inhibitors of alcohol dehydrogenase. Biochemical and Biophysical Research Communications 124: 375–382, 1984

    PubMed  Article  CAS  Google Scholar 

  • Johansson BG, Kindmark CO, Trell EY, Wollheim FA. Sequential changes of plasma proteins after myocardial infarction. Scandinavian Journal of Clinical and Laboratory Investigations 29 (Suppl. 124): 117–126, 1972

    Article  Google Scholar 

  • Kessler KM, Humphries WC, Black M, Spann JF. Quinidine pharmacokinetics in patients with cirrhosis or receiving propranolol. American Heart Journal 96: 627–635, 1978

    PubMed  Article  CAS  Google Scholar 

  • Kessler KM, Kissane B, Cassidy J, Pefkaros KC, Kozlovskis P, et al. Dynamic variability of binding of antiarrhythmic drugs during the evolution of acute myocardial infarction. Circulation 70: 472–478, 1984a

    PubMed  Article  CAS  Google Scholar 

  • Kessler KM, Leech RC, Spann JF. Blood collection techniques, heparin and quinidine protein binding. Clinical Pharmacology and Therapeutics 25: 204–210, 1979

    PubMed  CAS  Google Scholar 

  • Kessler KM, Lisker B, Conde C, Silver J, Ho-Tung P, et al. Abnormal quinidine binding in survivors of prehospital cardiac arrest. American Heart Journal 107: 665–669, 1984b

    PubMed  Article  CAS  Google Scholar 

  • Kessler KM, Lowenthal DT, Warner H, Gibson T, Briggs W, et al. Quinidine elimination in patients with congestive heart failure or poor renal function. New England Journal of Medicine 290: 706–709, 1974

    PubMed  Article  CAS  Google Scholar 

  • Kessler KM, Perez GO. Decreased quinidine plasma protein binding during hemodialysis. Clinical Pharmacology and Therapeutics 30: 121–126, 1981

    PubMed  Article  CAS  Google Scholar 

  • Lieber CS. Metabolism and metabolic effects of alcohol. Medical Clinics of North America 68: 3–31, 1984

    PubMed  CAS  Google Scholar 

  • MacKichan JJ. Pharmacokinetic consequences of drug displacement from blood and tissue proteins. Clinical Pharmacokinetics 9 (Suppl. 1): 32–41, 1984

    PubMed  Article  CAS  Google Scholar 

  • Mahon WA, Leeder JS, Brill-Edwards MM, Correia J, MacLeod SM. Comparative bioavailability study of three sustained release quinidine formulations. Clinical Pharmacokinetics 13: 118–124, 1987

    PubMed  Article  CAS  Google Scholar 

  • Naranjo CA, Sellers EM, Khouw V, Alexander P, Fan T, et al. Variability in heparin effect on serum drug binding. Clinical Pharmacology and Therapeutics 28: 545–550, 1980

    PubMed  Article  CAS  Google Scholar 

  • Nilsen OG, Storstein L, Jacobsen S. Effect of heparin and fatty acids on the binding of quinidine and warfarin in plasma. Biochemical Pharmacology 26: 229–235, 1977

    PubMed  Article  CAS  Google Scholar 

  • Ochs HR, Greenblatt DJ, Woo E, Franke K, Pfeifer HJ, et al. Single and multiple dose pharmacokinetics of oral quinidine sulfate and gluconate. American Journal of Cardiology 41: 770–777, 1978a

    PubMed  Article  CAS  Google Scholar 

  • Ochs HR, Greenblatt DJ, Woo E, Smith TW. Reduced quinidine clearance in elderly persons. American Journal of Cardiology 42: 481–485, 1978b

    PubMed  Article  CAS  Google Scholar 

  • Pardee HEB. Physical capacity with heart disease. In Diseases of the heart and blood vessels: nomenclature and criteria for diagnosis, 6th ed., pp. 110–114, Little, Brown & Co, Boston, 1964

    Google Scholar 

  • Paxton JW. Alpha-1-acid glycoprotein and binding of basic drugs. Methods and Findings of Experiments in Clinical Pharmacology 5: 635–648, 1983

    CAS  Google Scholar 

  • Perez-Mateo M, Erill S. Protein binding of salicylate and quinidine in plasma from patients with renal failure, chronic liver disease and chronic respiratory insufficiency. European Journal of Clinical Pharmacology 11: 225–231, 1977

    PubMed  Article  CAS  Google Scholar 

  • Piafsky KM, Borga O. Plasma protein binding of basic drugs II: importance of alpha-1-acid glycoprotein for interindividual variation. Clinical Pharmacology and Therapeutics 22: 545–549, 1977

    PubMed  CAS  Google Scholar 

  • Pike E, Skuterud B, Kierulf P, Fremstad D, Abdel Sayed SM, et al. Binding and displacement of basic, acidic and neutral drugs in normal and orosomucoid-deficient plasma. Clinical Pharmacokinetics 6: 367–374, 1981

    PubMed  Article  CAS  Google Scholar 

  • Pike E, Skuterud B, Kierulf P, Lunde PKM. Significance of lipoproteins in serum binding variations of amitriptyline, nortriptyline, and quinidine. Clinical Pharmacology and Therapeutics 32: 599–606, 1982

    PubMed  Article  CAS  Google Scholar 

  • Powell JR, Cates EW. Induction and inhibition of drug metabolism. In Evans et al. (Eds) Applied pharmacokinetics: principles of therapeutic drug monitoring, 2nd ed., pp. 139–186, Applied Therapeutics, Spokane, 1986

    Google Scholar 

  • Reidenberg MM, Affrime M. Influence of disease on binding of drugs to plasma proteins. Annals of the New York Academy of Science 226: 115–126, 1973

    Article  CAS  Google Scholar 

  • Rakhit A, Holford NHG, Guentert TW, Maloney K, Reigelman S. Pharmacokinetics of quinidine and three of its metabolites in man. Journal of Pharmacokinetics and Biopharmaceutics 12: 1–21, 1984

    PubMed  CAS  Google Scholar 

  • Rodgers GC, Blackman MS. Quinidine interaction with anticonvulsants. Drug Intelligence and Clinical Pharmacy 17: 819–820, 1983

    PubMed  CAS  Google Scholar 

  • Saal AK, Werner JA, Greene HL, Sears GK, Graham EL. Effect of amiodarone on serum quinidine and procainamide levels. American Journal of Cardiology 53: 1264–1267, 1984

    PubMed  Article  CAS  Google Scholar 

  • Schwartz A, Brown JR. Quinidine-rifampin interaction. American Heart Journal 107: 789–790, 1984

    PubMed  Article  CAS  Google Scholar 

  • Sheiner LB, Rosenberg B, Marathe VV. Estimation of population characteristics of pharmacokinetic parameters from routine clinical data. Journal of Pharmacokinetics and Biopharmaceutics 5: 445–479, 1977

    PubMed  CAS  Google Scholar 

  • Tozer TN. Implications of altered plasma protein binding in disease states. In Benet et al. (Eds) Pharmacokinetic basis for drug treatment, pp. 173–193, Raven Press, New York, 1984

    Google Scholar 

  • Trohman RG, Estes DM, Castellanos A, Palomo AR, Myerburg RJ, et al. Increased quinidine plasma concentrations during administration of verapamil: a new quinidine-verapamil interaction. American Journal of Cardiology 57: 706–707, 1986

    PubMed  Article  CAS  Google Scholar 

  • Ueda CT. Quinidine. In Evans et al. (Eds) Applied pharmacokinetics; principles of therapeutic drug monitoring, 2nd ed., pp. 712–727, Applied Therapeutics, Spokane, 1986

    Google Scholar 

  • Ueda CT, Dzindzio BS. Quinidine kinetics in congestive heart failure. Clinical Pharmacology and Therapeutics 23: 158–164, 1978

    PubMed  CAS  Google Scholar 

  • Ueda CT, Hirschfeld DS, Scheinman MM, Rowland M, Williamson BJ, et al. Disposition kinetics of quinidine. Clinical Pharmacology and Therapeutics 19: 30–36, 1976

    PubMed  CAS  Google Scholar 

  • Verme CN, Ludden TM, Harris SC. Immunoassay of alpha-1-acid glycoprotein in the COBAS BIO centrifugal analyzer. Clinical Chemistry 34: 2316–2320, 1988

    PubMed  CAS  Google Scholar 

  • Woo E, Greenblatt DJ. Pharmacokinetic and clinical implications of quinidine protein binding. Journal of Pharmaceutical Sciences 68: 466–469, 1979

    PubMed  Article  CAS  Google Scholar 

  • Wooding-Scott RA, Visco J, Slaughter RL. Total and unbound concentrations of quinidine and 3-hydroxyquinidine at steady-state. American Heart Journal 113: 302–306, 1987

    PubMed  Article  CAS  Google Scholar 

  • Wooding-Scott RA, Darling IM, Slaughter RL. Comparison of assay procedures used to measure total and unbound concentrations of quinidine. DICP: Annals of Pharmacotherapy 23: 999–1004, 1989

    PubMed  CAS  Google Scholar 

Download references

Author information

Affiliations

Authors

Additional information

An erratum to this article is available at http://dx.doi.org/10.1007/BF03259377.

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Verme, C.N., Ludden, T.M., Clementi, W.A. et al. Pharmacokinetics of Quinidine in Male Patients. Clin. Pharmacokinet. 22, 468–480 (1992). https://doi.org/10.2165/00003088-199222060-00005

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.2165/00003088-199222060-00005

Keywords

  • Quinidine
  • American Heart Journal
  • Severe Congestive Heart Failure
  • Quinidine Concentration
  • Serum Quinidine