Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractLarge-volume injection PTV-GC-MS analysis of polycyclic aromatic hydrocarbons in air and sediment samples    Next AbstractGenetic selection of peptide inhibitors of biological pathways »

Toxicol Sci


Title:Effect of PBPK model structure on interpretation of in vivo human aqueous dermal exposure trials
Author(s):Norman AM; Kissel JC; Shirai JH; Smith JA; Stumbaugh KL; Bunge AL;
Address:"University of Washington, Seattle, Washington 98105, USA"
Journal Title:Toxicol Sci
Year:2008
Volume:20080401
Issue:1
Page Number:210 - 217
DOI: 10.1093/toxsci/kfn070
ISSN/ISBN:1096-0929 (Electronic) 1096-0929 (Linking)
Abstract:"Multiple research teams have reported data from in vivo human trials in which breath was monitored during and after whole-body or partial immersion in aqueous solutions of volatile organic compounds. Estimation of total dermal absorption from exhaled breath measurements requires modeling, a task to which physiologically based pharmacokinetic (PBPK) models have often been applied. In the context of PBPK models, the exposed skin compartment can be modeled in many different ways. To demonstrate potential effects of alternative skin models on overall PBPK model performance, alternative models of skin have been incorporated in a PBPK model used to predict chloroform in breath during and after immersion in aqueous solution. The models investigated include treatment of skin as both a homogeneous phase and as a membrane in which concentration varies with depth. Model predictions are compared with in vivo human experimental results reported in the prior literature. In the example chosen, the common practice of modeling skin as a homogenous phase leads to prediction of more rapid initial uptake and lower cumulative uptake than does modeling skin as a membrane. Numerical estimates of the permeability coefficient are shown to be dependent upon skin model form and temperature of the aqueous solution"
Keywords:"Administration, Cutaneous Chloroform/*pharmacokinetics Exhalation Humans Lung/metabolism *Models, Biological Skin/metabolism *Skin Absorption Temperature;"
Notes:"MedlineNorman, Anayi M Kissel, John C Shirai, Jeffry H Smith, Joseph A Stumbaugh, Kelly L Bunge, Annette L eng T42/CCT010418-11/PHS HHS/ T42/OH008433/OH/NIOSH CDC HHS/ Comparative Study Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. 2008/04/03 Toxicol Sci. 2008 Jul; 104(1):210-7. doi: 10.1093/toxsci/kfn070. Epub 2008 Apr 1"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 27-12-2024