Approaches to carcinogenic risk assessment for polycyclic aromatic hydrocarbons: a UK perspective

被引:103
|
作者
Pufulete, M
Battershill, J
Boobis, A
Fielder, R
机构
[1] Depth Hlth, London SE1 6LH, England
[2] Kings Coll London, Nutr Food & Hlth Res Ctr, London SE1 9NN, England
[3] Imprial Coll London, Dept Hlth Toxicol Unit, Sect Expt Med & Toxicol, London W12 0NN, England
关键词
polycyclic aromatic hydrocarbons; risk assessment; potency equivalency factors; carcinogenicity; DNA adducts;
D O I
10.1016/j.yrtph.2004.04.007
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
This paper reviews the approaches to carcinogenic risk assessment of polycyclic aromatic hydrocarbons (PAHs) in air pollution with emphasis on high potency PAHs such as dibenzo[a,l]pyrene (D13[a,l]P). The potency of DB[a,I]P may be 100-fold greater than benzo[a]pyrene (B[a]P); thus the B[a]P surrogate approach currently used to monitor for compliance with UK air pollution standards may not be appropriate. It is suggested that an approach based on potency equivalency factors (PEFs) could be developed to include highly potent PAHs provided an appropriate reference data set for relevant PAHs using a route acceptable for inhalation risk assessment is selected. Available data suggest that intratracheal administration of low doses of PAHs to rats is likely to simulate the kinetics of inhalation exposure to PAHs in a feasible manner. The use of a measure of total DNA adducts as an endpoint, which correlates well with lung tumourigenicity, would provide surrogate data for setting PEFs without the need for long-term bioassays in rodents. Further, dose-response studies using intratracheal administration of a range of PAHs singly and in combination to assess additivity are required to develop a PEF system for inhalation PEFs derived from DNA adduct measurements. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:54 / 66
页数:13
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