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1000 Titel
  • Distribution Clearance: Significance and Underlying Mechanisms
1000 Autor/in
  1. Weiss, Michael |
1000 Verlag
  • Springer US
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-07-09
1000 Erschienen in
1000 Quellenangabe
  • 41(7):1391-1400
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s11095-024-03738-7 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11263435/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Purpose</jats:title> <jats:p>Evaluation of distribution kinetics is a neglected aspect of pharmacokinetics. This study examines the utility of the model-independent parameter whole body distribution clearance (<jats:italic>CL</jats:italic><jats:sub><jats:italic>D</jats:italic></jats:sub>) in this respect.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>Since mammillary compartmental models are widely used, <jats:italic>CL</jats:italic><jats:sub><jats:italic>D</jats:italic></jats:sub> was calculated in terms of parameters of this model for 15 drugs. The underlying distribution processes were explored by assessment of relationships to pharmacokinetic parameters and covariates.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>The model-independence of the definition of the parameter <jats:italic>CL</jats:italic><jats:sub><jats:italic>D</jats:italic></jats:sub> allowed a comparison of distributional properties of different drugs and provided physiological insight. Significant changes in <jats:italic>CL</jats:italic><jats:sub><jats:italic>D</jats:italic></jats:sub> were observed as a result of drug-drug interactions, transporter polymorphisms and a diseased state.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusion</jats:title> <jats:p>Total distribution clearance <jats:italic>CL</jats:italic><jats:sub><jats:italic>D</jats:italic></jats:sub> is a useful parameter to evaluate distribution kinetics of drugs. Its estimation as an adjunct to the model-independent parameters clearance and steady-state volume of distribution is advocated.</jats:p> </jats:sec>
1000 Sacherschließung
lokal distribution clearance
lokal distribution kinetics
lokal Humans [MeSH]
lokal Pharmaceutical Preparations/metabolism [MeSH]
lokal Models, Biological [MeSH]
lokal permeability-surface product
lokal Tissue Distribution [MeSH]
lokal Drug Interactions [MeSH]
lokal Pharmacokinetics [MeSH]
lokal compartmental model
lokal Original Research Article
lokal pharmacokinetic analysis
lokal Metabolic Clearance Rate [MeSH]
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  1. https://frl.publisso.de/adhoc/uri/V2Vpc3MsIE1pY2hhZWw=
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1000 Label
1000 Förderer
  1. Martin-Luther-Universität Halle-Wittenberg |
1000 Fördernummer
  1. -
1000 Förderprogramm
  1. -
1000 Dateien
  1. Distribution Clearance: Significance and Underlying Mechanisms
1000 Förderung
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    1000 Förderer Martin-Luther-Universität Halle-Wittenberg |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 Erstellt am 2025-07-06T18:10:53.805+0200
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1000 Zuletzt bearbeitet 2025-07-29T18:38:04.854+0200
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