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

Artificial kidneys and clearance calculations

T P Gibson, E Matusik, L D Nelson

    Clinical Pharmacology and Therapeutics
    |December 1, 1976
    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

    Brazos Valley Medical Association.

    Texas medical journal (Austin, Tex.)·2023
    Same author

    Suboptimal exposure to fluconazole in critically ill patients: Pharmacokinetic analysis and determinants.

    Infectious diseases now·2022
    Same author

    Implementation of active injury management (AIM) in youth with acute concussion: A randomized controlled trial.

    Contemporary clinical trials·2022
    Same author

    [Pharmacokinetic modifications and pharmacokinetic/pharmacodynamic optimization of beta-lactams in ICU].

    Annales pharmaceutiques francaises·2020
    Same author

    The role of the critical care pharmacist during the COVID-19 pandemic.

    Annales pharmaceutiques francaises·2020
    Same author

    Death of the Dental Pulp by External Violence.

    The American journal of dental science·2019
    Same journal

    Epcoritamab Step-Up Dosing Regimen Selection and Optimization Using Repeated Time-to-Event Modeling for Cytokine Release Syndrome Risk Mitigation.

    Clinical pharmacology and therapeutics·2026
    Same journal

    From Executor to Orchestrator: The Pharmacology Scientist in the Age of Agentic AI.

    Clinical pharmacology and therapeutics·2026
    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
    See all related articles

    Artificial kidneys remove procainamide (PA) and N-acetylprocainamide (NAPA) from blood. Clearance calculations indicate these drugs are removed from red blood cells, not just plasma.

    Area of Science:

    • Nephrology
    • Pharmacokinetics
    • Artificial Organ Technology

    Background:

    • Artificial kidneys (dialysis) are crucial for solute removal in patients with renal failure.
    • Accurate clearance calculations are essential for optimizing drug removal during dialysis.
    • Understanding drug removal kinetics, including red blood cell partitioning, is vital for therapeutic drug monitoring.

    Purpose of the Study:

    • To determine the in vivo and in vitro clearance of procainamide (PA) and N-acetylprocainamide (NAPA) using artificial kidneys.
    • To compare different methods of calculating solute clearance during dialysis.
    • To investigate the extent to which PA and NAPA are removed from red blood cells during dialysis.

    Main Methods:

    • In vivo clearance of PA and NAPA was measured in 4 patients undergoing dialysis.

    Related Experiment Videos

  • Calculations utilized plasma flow, whole blood flow, plasma solute concentration, and total solute removed.
  • In vitro clearance was assessed using 11 artificial kidneys and an XAD-4 hemoperfusion column for PA, NAPA, quinidine, and phenobarbital.
  • Main Results:

    • In vivo clearance calculated using total amount recovered was generally higher than methods relying solely on plasma concentration.
    • Clearance determined by total amount recovered was substantially greater than that using plasma flow and plasma levels.
    • In vitro studies revealed significant differences in clearance rates among various artificial kidneys and the hemoperfusion column.

    Conclusions:

    • Both procainamide (PA) and N-acetylprocainamide (NAPA) are removed from red blood cells, in addition to plasma, during dialysis.
    • Calculating clearance based on the total amount of solute recovered provides a more comprehensive assessment of drug removal.
    • Significant variability exists in the solute removal efficiency of different artificial kidney devices.