The National Toxicology Program (NTP) seeks to assess risks associated with possible acute, repeated or chronic exposure to chemicals by investigating a variety of biological effects including carcinogenicity indiced on chronic exposure. Studies of the mechanism(s) of toxicity and the fate of chemicals in intact animals are an integral part of the range of NTP studies designed to characterize chemical toxicity. Data obtained from studies of the fate of chemicals in intact animals, as described in this contract, support NTP objectives by providing the fundation on which extrapolations of risks from laboratory animals to humans are based. Objectives of this project are two fold. Each study is designed to address those physical and chemical properties unique to the compound studied as well as to provide data that will permit structural characterization of the respective chemical calss. These studies may also be designed to address the impact of one or more factors such as does, species, age, sex or route of exposure on the fate and/or toxicity of the chemical(s) studied and thesignificance of thede data to assessments of human helath risks. Thus, the immediate objective of these studies is to determine more accurately the doses for NTP bioassay studies. The long-range objective is the accumulation of data that will permit better assessments of those structure-activity relationships that determine chemical absorption, metabolism and disposition in laboratory animals. The ultimate objective of this project is to provide data that permit better assessments of risks associated with human exposure to chemicals encountered in the environment, home and workplace.

Project Start
1997-03-01
Project End
2002-02-28
Budget Start
1997-03-01
Budget End
1998-02-28
Support Year
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Research Triangle Institute
Department
Type
DUNS #
131606022
City
Research Triangle Park
State
NC
Country
United States
Zip Code
27709
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Black, S R; Decosta, K S; Patel, P R et al. (2007) [14C]bis(2-chloroethoxy)methane: comparative absorption, distribution, metabolism and excretion in rats and mice. Xenobiotica 37:427-40
Mathews, James M; Etheridge, Amy S; Black, Sherry R (2002) Inhibition of human cytochrome P450 activities by kava extract and kavalactones. Drug Metab Dispos 30:1153-7
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Thomas, B F; Burgess, J P; Coleman, D P et al. (1999) Isolation and identification of novel metabolites of gemfibrozil in rat urine. Drug Metab Dispos 27:147-57
Mathews, J M; De Costa, K S (1999) Absorption, metabolism, and disposition of 1,3-diphenyl-1-triazene in rats and mice after oral, i.v., and dermal administration. Drug Metab Dispos 27:1499-504