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 AbstractCompound-specific isotope analysis coupled with multivariate statistics to source-apportion hydrocarbon mixtures    Next Abstract"Acute inhalation of 2,2,4-trimethylpentane alters visual evoked potentials and signal detection behavior in rats" »

Environ Toxicol Pharmacol


Title:Applications of dosimetry modeling to assessment of neurotoxic risk
Author(s):Boyes WK; Simmons JE; Eklund C; Benignus VA; Janssen P; Bushnell PJ;
Address:"National Health and Environmental Effects Research Laboratory, B105-05, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, NC 27711, USA"
Journal Title:Environ Toxicol Pharmacol
Year:2005
Volume:19
Issue:3
Page Number:599 - 605
DOI: 10.1016/j.etap.2004.12.025
ISSN/ISBN:1382-6689 (Print) 1382-6689 (Linking)
Abstract:"Risk assessment procedures can be improved through better understanding and use of tissue dose information and linking tissue dose level to adverse outcomes. For volatile organic compounds, such as toluene and trichloroethylene (TCE), blood and brain concentrations can be estimated with physiologically based pharmacokinetic (PBPK) models. Acute changes in the function of the nervous system can be linked to the concentration of test compounds in the blood or brain at the time of neurological assessment. This set of information enables application to a number of risk assessment situations. For example, we have used this approach to recommend duration adjustments for acute exposure guideline levels (AEGLs) for TCE such that the exposure limits for each exposure duration yield identical tissue concentrations at the end of the exposure period. We have also used information on tissue concentration at the time of assessment to compare sensitivity across species, adjusting for species-specific pharmacokinetic differences. Finally this approach has enabled us to compare the relative sensitivity of different compounds on a tissue dose basis, leading to expression of acute solvent effects as ethanol-dose equivalents for purposes of estimating cost-benefit relationships of various environmental control options"
Keywords:
Notes:"PubMed-not-MEDLINEBoyes, William K Simmons, Jane Ellen Eklund, Christopher Benignus, Vernon A Janssen, Paul Bushnell, Philip J eng Netherlands 2005/05/01 Environ Toxicol Pharmacol. 2005 May; 19(3):599-605. doi: 10.1016/j.etap.2004.12.025"

 
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 23-11-2024