Cited by 61Pharmacogenetics and Drug MetabolismDrug Transport and Resistance MechanismsPharmaceutical studies and practices

Advanced pharmacokinetic models based on organ clearance, circulatory, and fractal concepts

Open access
Pang, K. Sandy, Weiss, Michael, Macheras, Panos·2007·The AAPS Journal

Abstract

Three advanced models of pharmacokinetics are described. In the first class are physiologically based pharmacokinetic models based on in vitro data on transport and metabolism. The information is translated as transporter and enzyme activities and their attendant heterogeneities into liver and intestine models. Second are circulatory models based on transit time distribution and plasma concentration time curves. The third are fractal models for nonhomogeneous systems and non-Fickian processes are presented. The usefulness of these pharmacokinetic models, with examples, is compared.

Integrity signals

Registry

Crossref · 10.1208/aapsj0902030

Cites

3 of 3 references verified0 citation errors · 0 not checkable

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Authors
Pang, K. S., Weiss, M., & Macheras, P.
Affiliations
  • University of Toronto (CA)
  • Martin Luther University Halle-Wittenberg (DE)
  • National and Kapodistrian University of Athens (GR)
Corresponding author
Pang, K. Sandy
Venue
The AAPS Journal
Published
2007-06
Volume
9
Issue
2
Pages
E268-E283
ISSN
1550-7416 (ISSN-L)
OpenAlex
W2012792624
Cited by
61
References
3
Citations by year
2026: 2 · 2023: 2 · 2021: 3 · 2020: 3 · 2019: 5 · 2018: 6 · 2017: 2 · 2016: 5 · 2015: 1 · 2014: 3 · 2013: 2 · 2012: 7
FWCI
0.62
Type
journal article
Language
en
Open access
Locations
  • The AAPS Journal (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmacogenetics and Drug Metabolism
  • Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
  • Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Pharmaceutical studies and practices
Keywords
pharmacokinetic modeling, circulatory model, fractal model, physiologically based pharmacokinetic modeling, enzyme heterogeneity, hepatic clearance, intestinal clearance, transit time distribution, plasma concentration-time curve, non-Fickian diffusion, inhomogeneous systems
MeSH terms
Animals, Blood Circulation, Pharmaceutical Preparations, Humans, Metabolic Clearance Rate, Models, Biological, Organ Specificity, Pharmacokinetics, Tissue Distribution

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