Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Digoxin bioavailability during quinidine administration

W D Hager, M Mayersohn, P E Graves

    Clinical Pharmacology and Therapeutics
    |November 1, 1981
    PubMed
    Summary
    This summary is machine-generated.

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    Measurement of disposition half-life, clearance, and residence times.

    Current protocols in toxicology·2010
    Same author

    Femoral bone mineral density in patients with heart failure.

    Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA·2006
    Same author

    Factor analysis of asthma and atopy traits shows 2 major components, one of which is linked to markers on chromosome 5q.

    The Journal of allergy and clinical immunology·2001
    Same author

    Genetic variation in beta-adrenergic receptors and their relationship to susceptibility for asthma and therapeutic response.

    Drug metabolism and disposition: the biological fate of chemicals·2001
    Same author

    Pharmacokinetics tricks and traps: drug dosage adjustment in renal failure.

    Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques·2000
    Same author

    Evaluation of a minimal experimental design for determination of enzyme kinetic parameters and inhibition mechanism.

    The Journal of pharmacology and experimental therapeutics·2000
    Same journal

    The Future of Clinical Pharmacology: The Right Medicine at the Right Dose for Each Patient.

    Clinical pharmacology and therapeutics·2026
    Same journal

    Effects of Trimethoprim on Three Previously Proposed Putative Biomarkers for OCT2/MATE-Mediated Renal Drug-Drug Interactions in Healthy Volunteers.

    Clinical pharmacology and therapeutics·2026
    Same journal

    Clinical Characterization of Enzyme and Transporter Precipitants to Evaluate Drug-Drug Interactions for Orforglipron, a Small Molecule Glucagon-Like Peptide-1 Receptor Agonist.

    Clinical pharmacology and therapeutics·2026
    Same journal

    Symposium Report: Stakeholders' Perspectives on Phase 1 Trials in Japanese Prior to Multi-Regional Clinical Trials and Future Pathways.

    Clinical pharmacology and therapeutics·2026
    Same journal

    Resolving CYP2D6 Structural Complexity with Long-Read Sequencing: Implications for Tamoxifen Precision Dosing in Thai Breast Cancer Patients.

    Clinical pharmacology and therapeutics·2026
    Same journal

    Identification of a Functional CYP2C8 Variant Allele that Alters Splicing, Reduces Protein Expression, and Increases Drug Exposure.

    Clinical pharmacology and therapeutics·2026
    See all related articles

    Quinidine does not change how the body absorbs digoxin, despite higher digoxin levels observed. This study found no alteration in digoxin bioavailability when taken with quinidine.

    Area of Science:

    • Pharmacology
    • Drug Interactions
    • Clinical Pharmacology

    Background:

    • Elevated digoxin serum concentrations are observed when co-administered with quinidine.
    • The mechanism behind this interaction, specifically potential alterations in digoxin bioavailability, requires investigation.

    Purpose of the Study:

    • To investigate whether quinidine administration affects the oral bioavailability of digoxin.
    • To determine if altered digoxin absorption contributes to increased serum concentrations in patients taking quinidine.

    Main Methods:

    • Six subjects received intravenous and oral digoxin (1.0 mg) on alternate weeks during steady-state oral quinidine therapy.
    • Digoxin bioavailability was assessed by comparing area under the concentration-time curve (AUC) and urinary excretion (Xxu) after oral versus intravenous administration.

    Related Experiment Videos

  • Serum concentrations of both digoxin and quinidine were monitored over 96 hours post-administration.
  • Main Results:

    • Digoxin bioavailability, assessed via serum AUC (73.5% vs. 79.5%) and urinary excretion (69.8% vs. 70.2%), showed no statistically significant difference between administration with and without quinidine (P > 0.05).
    • Steady-state quinidine serum concentrations remained unchanged during the 4 days following both intravenous and oral digoxin administration.
    • No significant alteration in digoxin absorption or elimination was detected due to concurrent quinidine use.

    Conclusions:

    • Quinidine does not alter the oral bioavailability of digoxin.
    • The observed increase in digoxin serum concentration in the presence of quinidine is not explained by changes in digoxin absorption.
    • Further research is needed to elucidate the mechanism behind the quinidine-induced rise in digoxin serum levels.