Evaluation of the potential impact of age- and gender-specific pharmacokinetic differences on tissue dosimetry

Clewell, HJ; Gentry, PR; Covington, TR; Sarangapani, R; Teeguarden, JG

HERO ID

56269

Reference Type

Journal Article

Year

2004

Language

English

PMID

15056818

HERO ID 56269
In Press No
Year 2004
Title Evaluation of the potential impact of age- and gender-specific pharmacokinetic differences on tissue dosimetry
Authors Clewell, HJ; Gentry, PR; Covington, TR; Sarangapani, R; Teeguarden, JG
Journal Toxicological Sciences
Volume 79
Issue 2
Page Numbers 381-393
Abstract The physiological and biochemical processes that determine the tissue concentration time courses (pharmacokinetics) of xenobiotics vary, in some cases significantly, with age and gender. While it is known that age- and gender-specific differences have the potential to affect tissue concentrations and, hence, individual risk, the relative importance of the contributing processes and the quantitative impact of these differences for various life stages are not well characterized. The objective of this study was to identify age- and gender-specific differences in physiological and biochemical processes that affect tissue dosimetry and integrate them into a predictive physiologically based pharmacokinetic (PBPK) life-stage model. The life-stage model was exercised for several environmental chemicals with a variety of physicochemical, biochemical, and mode-of-action properties. In general, predictions of average pharmacokinetic dose metrics for a chemical across life stages were within a factor of two, although larger transient variations were predicted, particularly during the neonatal period. The most important age-dependent pharmacokinetic factor appears to be the potential for decreased clearance of a toxic chemical in the perinatal period due to the immaturity of many metabolic enzyme systems, although this same factor may also reduce the production of a reactive metabolite. Given the potential for age-dependent pharmacodynamic factors during early life, there may be chemicals and health outcomes for which decreased clearance over a relatively brief period could have a substantial impact on risk.
Doi 10.1093/toxsci/kfh109
Pmid 15056818
Wosid WOS:000221551200020
Url https://academic.oup.com/toxsci/article-lookup/doi/10.1093/toxsci/kfh109
Is Certified Translation No
Dupe Override No
Comments ECRIB.Toxicol. Sci. 79: 381-383.
Is Public Yes
Language Text English
Keyword pharmacokinetics; PBPK; children; age; gender; dosimetry
Is Qa No