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Evaluating noncancer effects of trichloroethylene: dosimetry, mode of action, and risk assessment.

Alternatives for developing chronic exposure limits for noncancer effects of trichloroethylene (TCE) were evaluated. These alternatives were organized within a framework for dose-response assessment--exposure:dosimetry (pharmacokinetics):mode of action (pharmacodynamics): response. This framework pr...

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Detalles Bibliográficos
Autores principales: Barton, H A, Clewell, H J
Formato: Texto
Lenguaje:English
Publicado: 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637754/
https://www.ncbi.nlm.nih.gov/pubmed/10807562
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author Barton, H A
Clewell, H J
author_facet Barton, H A
Clewell, H J
author_sort Barton, H A
collection PubMed
description Alternatives for developing chronic exposure limits for noncancer effects of trichloroethylene (TCE) were evaluated. These alternatives were organized within a framework for dose-response assessment--exposure:dosimetry (pharmacokinetics):mode of action (pharmacodynamics): response. This framework provides a consistent structure within which to make scientific judgments about available information, its interpretation, and use. These judgments occur in the selection of critical studies, internal dose metrics, pharmacokinetic models, approaches for interspecies extrapolation of pharmacodynamics, and uncertainty factors. Potentially limiting end points included developmental eye malformations, liver effects, immunotoxicity, and kidney toxicity from oral exposure and neurological, liver, and kidney effects by inhalation. Each end point was evaluated quantitatively using several methods. Default analyses used the traditional no-observed adverse effect level divided by uncertainty factors and the benchmark dose divided by uncertainty factors methods. Subsequently, mode-of-action and pharmacokinetic information were incorporated. Internal dose metrics were estimated using a physiologically based pharmacokinetic (PBPK) model for TCE and its major metabolites. This approach was notably useful with neurological and kidney toxicities. The human PBPK model provided estimates of human exposure doses for the internal dose metrics. Pharmacodynamic data or default assumptions were used for interspecies extrapolation. For liver and neurological effects, humans appear no more sensitive than rodents when internal dose metrics were considered. Therefore, the interspecies uncertainty factor was reduced, illustrating that uncertainty factors are a semiquantitative approach fitting into the organizational framework. Incorporation of pharmacokinetics and pharmacodynamics can result in values that differ significantly from those obtained with the default methods.
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spelling pubmed-16377542006-11-17 Evaluating noncancer effects of trichloroethylene: dosimetry, mode of action, and risk assessment. Barton, H A Clewell, H J Environ Health Perspect Research Article Alternatives for developing chronic exposure limits for noncancer effects of trichloroethylene (TCE) were evaluated. These alternatives were organized within a framework for dose-response assessment--exposure:dosimetry (pharmacokinetics):mode of action (pharmacodynamics): response. This framework provides a consistent structure within which to make scientific judgments about available information, its interpretation, and use. These judgments occur in the selection of critical studies, internal dose metrics, pharmacokinetic models, approaches for interspecies extrapolation of pharmacodynamics, and uncertainty factors. Potentially limiting end points included developmental eye malformations, liver effects, immunotoxicity, and kidney toxicity from oral exposure and neurological, liver, and kidney effects by inhalation. Each end point was evaluated quantitatively using several methods. Default analyses used the traditional no-observed adverse effect level divided by uncertainty factors and the benchmark dose divided by uncertainty factors methods. Subsequently, mode-of-action and pharmacokinetic information were incorporated. Internal dose metrics were estimated using a physiologically based pharmacokinetic (PBPK) model for TCE and its major metabolites. This approach was notably useful with neurological and kidney toxicities. The human PBPK model provided estimates of human exposure doses for the internal dose metrics. Pharmacodynamic data or default assumptions were used for interspecies extrapolation. For liver and neurological effects, humans appear no more sensitive than rodents when internal dose metrics were considered. Therefore, the interspecies uncertainty factor was reduced, illustrating that uncertainty factors are a semiquantitative approach fitting into the organizational framework. Incorporation of pharmacokinetics and pharmacodynamics can result in values that differ significantly from those obtained with the default methods. 2000-05 /pmc/articles/PMC1637754/ /pubmed/10807562 Text en
spellingShingle Research Article
Barton, H A
Clewell, H J
Evaluating noncancer effects of trichloroethylene: dosimetry, mode of action, and risk assessment.
title Evaluating noncancer effects of trichloroethylene: dosimetry, mode of action, and risk assessment.
title_full Evaluating noncancer effects of trichloroethylene: dosimetry, mode of action, and risk assessment.
title_fullStr Evaluating noncancer effects of trichloroethylene: dosimetry, mode of action, and risk assessment.
title_full_unstemmed Evaluating noncancer effects of trichloroethylene: dosimetry, mode of action, and risk assessment.
title_short Evaluating noncancer effects of trichloroethylene: dosimetry, mode of action, and risk assessment.
title_sort evaluating noncancer effects of trichloroethylene: dosimetry, mode of action, and risk assessment.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637754/
https://www.ncbi.nlm.nih.gov/pubmed/10807562
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