Oral Bioavailability, Bioaccessibility, and Dermal Absorption of PAHs from Soil-State of the Science

被引:98
|
作者
Ruby, Michael V. [1 ]
Lowney, Yvette W. [2 ]
Bunge, Annette L. [3 ]
Roberts, Stephen M. [4 ]
Gomez-Eyles, Jose L. [5 ,6 ]
Ghosh, Upal [5 ]
Kissel, John C. [7 ]
Tomlinson, Priscilla [8 ]
Menzie, Charles [9 ]
机构
[1] Integral Consulting Inc, Louisville, CO 80027 USA
[2] Alloy LLC, Boulder, CO 80302 USA
[3] Colorado Sch Mines, Golden, CO 80401 USA
[4] Univ Florida, Gainesville, FL 32611 USA
[5] Univ Maryland Baltimore Cty, Baltimore, MD 21228 USA
[6] Integral Consulting Inc, Seattle, WA 98104 USA
[7] Univ Washington, Seattle, WA 98195 USA
[8] Washington Dept Ecol, Seattle, WA 98503 USA
[9] Exponent, Alexandria, VA 22314 USA
关键词
POLYCYCLIC AROMATIC-HYDROCARBONS; PHYSIOLOGICALLY-BASED EXTRACTION; IN-VITRO BIOACCESSIBILITY; NATURAL ORGANIC-MATTER; SOOT-LIKE MATERIALS; CONTAMINATED SOILS; DNA-ADDUCTS; RELATIVE BIOAVAILABILITY; HUMAN EXPOSURE; BLACK CARBON;
D O I
10.1021/acs.est.5b04110
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This article reviews the state of the science regarding oral bioavailability, bioaccessibility, and dermal absorption of carcinogenic polycyclic aromatic hydrocarbons (cPAHs) in soil by humans, and discusses how chemical interactions may control the extent of absorption. Derived from natural and anthropomorphic origins, PAHs occur in a limited number of solid and fluid matrices (i.e., PAH sources) with defined physical characteristics and PAH compositions. Existing studies provide a strong basis for establishing that oral bioavailability of cPAHs from soil is less than from diet, and an assumption of 100% relative bioavailability likely overestimates exposure to cPAHs upon ingestion of PAH-contaminated soil. For both the oral bioavailability and dermal absorption studies, the aggregate data do not provide a broad understanding of how different PAH source materials, PAH concentrations, or soil chemistries influence the absorption of cPAHs from soil. This article summarizes the existing studies, identifies data gaps, and provides recommendations for the direction of future research to support new default or site-specific bioavailability adjustments for use in human health risk assessment.
引用
收藏
页码:2151 / 2164
页数:14
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