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RECORD NUMBER: 42 OF 103

Main Title Estimating human equivalent no obeserved adverse effect levels for VOC's based on minimal knowledge of physiologic parameters /
Author Overton, J. H. ; Jarabek, A. M.
Other Authors
Author Title of a Work
Jarabek, A. M.
CORP Author Health Effects Research Lab., Research Triangle Park, NC. Environmental Toxicology Div.
Publisher U.S. Environmental Protection Agency, Office of Research and Development, Health Effects Research Laboratory,
Year Published 1989
Report Number EPA600/D-89/097
Stock Number PB89-224588
Additional Subjects Formulas(Mathematics) ; Toxicity ; Blood chemical analysis ; Estimating ; Dosimetry ; Mathematical models ; Air pollution effects(Humans) ; Pharmacokinetics ; Dose-response relationships ; Volatile organic compounds ; No observed adverse effect level
Holdings
Library Call Number Additional Info Location Last
Modified
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Status
NTIS  PB89-224588 Some EPA libraries have a fiche copy filed under the call number shown. 07/26/2022
Collation 15 pages ; 28 cm
Abstract
The U.S. EPA advocates the assessment of health effects data and calculation of 'inhaled reference doses' as benchmark values for gauging systemic toxicity to inhaled gases. The assessment often requires an inter- or intra-species dose extrapolation from 'no observed adverse effect level' (NOAEL) exposure concentrations in animals to human equivalent NOAEL exposure concentrations. To achieve this, a dosimetric extrapolation procedure has been developed based on the form or type of equations that describe the uptake and disposition of inhaled volatile organic compounds (VOCs) in physiologically-based pharmacokinetic (PB-PK) models. The procedure assumes allometric scaling of most physiological parameters and that the value of the time integrated human arterial blood concentration must be limited to no more than to that of experimental animals. The scaling assumption replaces the need for most parameter values and allows the derivation of a simple formula for dose extrapolation of VOCs that gives equivalent or more conservative exposure concentrations values than those that would be obtained using a PB-PK model in which scaling was assumed.
Notes
"Technical paper submitted for 82nd Annual APCA Meeting, June 25-30, 1989, Anaheim, CA." Microfiche.