Chemical Safety for Sustainability (CSS): Human in vivo biomonitoring data for complementing results from in vitro toxicology-A commentary

被引:20
作者
Pleil, Joachim D. [1 ]
Williams, Marc A. [2 ]
Sobus, Jon R. [1 ]
机构
[1] US EPA, Human Exposure & Atmospher Sci Div, Natl Exposure Res Lab, Res Triangle Pk, NC 27711 USA
[2] US EPA, Environm Publ Hlth Div, Natl Hlth & Environm Effects Lab, Res Triangle Pk, NC 27711 USA
基金
美国国家环境保护局;
关键词
Exposure science; Toxicological risk; Computational toxicology; Biomonitoring; Systems biology; High-throughput screening; ADVERSE OUTCOME PATHWAYS; TERTIARY-BUTYL ETHER; AMBIENT PARTICULATE MATTER; VOLATILE ORGANIC-COMPOUNDS; LIQUID-LIQUID-EXTRACTION; RISK-ASSESSMENT; EXPOSURE ASSESSMENT; HUMAN BLOOD; JET FUEL; ENVIRONMENTAL CHEMICALS;
D O I
10.1016/j.toxlet.2012.10.011
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The U.S. Environmental Protection Agency (EPA) has instituted the Chemical Safety for Sustainability (CSS) research program for assessing the health and environmental impact of manufactured chemicals. This is a broad program wherein one of the tasks is to develop high throughput screening (HTS) methods and follow-up confirmation for toxicity at realistic environmental exposure levels. The main tools under this task are in vitro toxicity testing, in silico molecular modeling, and in vivo (systemic) measurements documentation. The in vivo research component is intended to support and corroborate in vitro chemical toxicity prioritization with observations of systemic perturbations and statistical parameters derived from intact (living) organisms. Based on EPA's Biomonitoring Framework for human health research, such observations are intended to link environmental exposures to a cascade of biomarker chemicals to help identify and clarify adverse outcome pathways within the context of systems biology. This commentary discusses the issues regarding interpretation of in vitro changes from HTS as an adverse result, an adaptive (non-adverse) response, or a random/irrelevant occurrence. A second goal is to inform in vitro strategies as to relevant dosing (potency) levels at the cellular level that reflect realistic systemic exposures. Although we recognize the high value of in vivo animal toxicity testing, herein we focus on observational (minimally invasive) human biomonitoring methods and propose complementary in vivo testing that could help guide the design of high-throughput analyses and the ultimate interpretation of their outcomes. Published by Elsevier Ireland Ltd.
引用
收藏
页码:201 / 207
页数:7
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