Ontogeny of Scaling Factors for Pediatric Physiologically Based Pharmacokinetic Modeling and Simulation: Cytosolic Protein Per Gram of Liver.


Journal

Drug metabolism and disposition: the biological fate of chemicals
ISSN: 1521-009X
Titre abrégé: Drug Metab Dispos
Pays: United States
ID NLM: 9421550

Informations de publication

Date de publication:
Dec 2023
Historique:
received: 11 06 2023
accepted: 18 09 2023
pmc-release: 01 12 2024
medline: 16 11 2023
pubmed: 22 9 2023
entrez: 21 9 2023
Statut: ppublish

Résumé

Scaling factors are necessary for translating in vitro drug biotransformation data to in vivo clearance values in physiologically-based pharmacokinetic modeling and simulation. Values for microsomal protein per gram of liver are available from several sources for use as a scaling factor to estimate hepatic clearance from microsomal drug biotransformation data. However, data regarding the distribution of cytosolic protein per gram of liver (CPPGL) values across the lifespan are limited, and sparse pediatric data have been published to date. Thus, CPPGL was determined in 160 liver samples from pediatric (

Identifiants

pubmed: 37735064
pii: dmd.123.001417
doi: 10.1124/dmd.123.001417
pmc: PMC10658907
doi:

Substances chimiques

Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1578-1582

Subventions

Organisme : NICHD NIH HHS
ID : P50 HD090258
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2 TR002367
Pays : United States
Organisme : NICHD NIH HHS
ID : HHSN275200900011C
Pays : United States
Organisme : NIMH NIH HHS
ID : K23 MH130728
Pays : United States
Organisme : NIDDK NIH HHS
ID : HHSN267200700004C
Pays : United States
Organisme : NLM NIH HHS
ID : HHSN267200700004G
Pays : United States

Informations de copyright

Copyright © 2023 by The American Society for Pharmacology and Experimental Therapeutics.

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Auteurs

Stephani L Stancil (SL)

Division of Clinical Pharmacology, Toxicology and Therapeutic Innovation, Department of Pediatrics and Children's Mercy Research Institute, Children's Mercy Kansas City, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri slstancil@cmh.edu.

Robin E Pearce (RE)

Division of Clinical Pharmacology, Toxicology and Therapeutic Innovation, Department of Pediatrics and Children's Mercy Research Institute, Children's Mercy Kansas City, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri.

Vincent S Staggs (VS)

Division of Clinical Pharmacology, Toxicology and Therapeutic Innovation, Department of Pediatrics and Children's Mercy Research Institute, Children's Mercy Kansas City, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri.

J Steven Leeder (JS)

Division of Clinical Pharmacology, Toxicology and Therapeutic Innovation, Department of Pediatrics and Children's Mercy Research Institute, Children's Mercy Kansas City, University of Missouri-Kansas City School of Medicine, Kansas City, Missouri.

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Classifications MeSH