Evidence map›Paper›PMID 20072802›Full record

ArticleJournal of pharmacokinetics and pharmacodynamics2010

A new approach to the compartmental analysis in pharmacokinetics: fractional time evolution of diclofenac.

Jovan K Popović, Milica T Atanacković, Ana S Pilipović, Milan R Rapaić, Stevan Pilipović, Teodor M Atanacković

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In one paragraph

Article in Journal of pharmacokinetics and pharmacodynamics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Two compartmental fractional derivative model with general fractional derivative.Journal of pharmacokinetics and pharmacodynamics · 2023
    Review
  5. Article
  6. Article
  7. Article
  8. Fractional calculus in pharmacokinetics.Journal of pharmacokinetics and pharmacodynamics · 2018
    Article
  9. How to avoid unbounded drug accumulation with fractional pharmacokinetics.Journal of pharmacokinetics and pharmacodynamics · 2013
    Article
  10. Individualization of a pharmacokinetic model by fractional and nonlinear fit improvement.European journal of drug metabolism and pharmacokinetics · 2013
    Article
  11. Simulation of Drug Uptake in a Two Compartmental Fractional Model for a Biological System.Communications in nonlinear science & numerical simulation · 2011
    Article
  12. A nonlinear two compartmental fractional derivative model.European journal of drug metabolism and pharmacokinetics · 2011
    Article
  13. Fractional kinetics in multi-compartmental systems.Journal of pharmacokinetics and pharmacodynamics · 2010
    Article
  14. Fractional dynamics pharmacokinetics-pharmacodynamic models.Journal of pharmacokinetics and pharmacodynamics · 2010
    Article
  15. Fractional compartmental models and multi-term Mittag-Leffler response functions.Journal of pharmacokinetics and pharmacodynamics · 2010
    Article
  16. A commentary on fractionalization of multi-compartmental models.Journal of pharmacokinetics and pharmacodynamics · 2010
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Jovan K PopovićDepartment of Pharmacology, Toxicology and Clinical Pharmacology, Faculty of Medicine, University of Novi Sad, Hajduk Veljkova 3, 21000, Novi Sad, Republic of Serbia. jovapop@neobee.net
Milica T Atanacković
Ana S Pilipović
Milan R Rapaić
Stevan Pilipović
Teodor M Atanacković

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study presents a new two compartmental model and its application to the evaluation of diclofenac pharmacokinetics in a small number of healthy adults, during a bioequivalence trial. In the model the integer order derivatives are replaced by derivatives of real order often called fractional order derivatives. Physically that means that a history (memory) of a biological process, realized as a transfer from one compartment to another one with the mass balance conservation, is taken into account. This kind of investigations in pharmacokinetics is founded by Dokoumetzidis and Macheras through the one compartmental models while our contribution is the analysis of multi-dimensional compartmental models with the applications of the two compartmental model in evaluation of diclofenac pharmacokinetics. Two experiments were preformed with 12 healthy volunteers with two slow release 100 mg diclofenac tablet formulations. The agreement of the values predicted by the proposed model with the values obtained through experiments is shown to be good. Thus, pharmacokinetics of slow release diclofenac can be described well by a specific two compartmental model with fractional derivatives of the same order. Parameters in the model are determined by the least-squares method and the Particle Swarm Optimization (PSO) numerical procedure is used. The results show that the fractional order two compartmental model for diclofenac is superior in comparison to the classical two compartmental model. Actually this is true in general case since the classical one is a special case of the fractional one.

Indexed as

Models, BiologicalAdultAnti-Inflammatory Agents, Non-SteroidalChromatography, High Pressure LiquidCross-Over StudiesDelayed-Action PreparationsDiclofenacFemaleHumansMaleTherapeutic EquivalencyTissue DistributionAnti-Inflammatory Agents, Non-SteroidalDelayed-Action PreparationsDiclofenac

Identifiers

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.