Health risk assessment on human exposed to environmental polycyclic aromatic hydrocarbons pollution sources

被引:596
作者
Chen, Szu-Chich [1 ]
Liao, Chung-Min [1 ]
机构
[1] Natl Taiwan Univ, Dept Bioenvironm Syst Engn, Ecotoxicol Modeling Ctr, Taipei 10617, Taiwan
关键词
polycyclic aromatic hydrocarbons; benzo[alpha]pyrene; potency equivalency factor; health risk assessment; environmental pollution;
D O I
10.1016/j.scitotenv.2005.08.047
中图分类号
X [环境科学、安全科学];
学科分类号
08 [工学]; 0830 [环境科学与工程];
摘要
To assess how the human exposure to environmental carcinogenic polycyclic aromatic hydrocarbons (PAHs) pollution sources generated from industrial, traffic and rural settings, we present a probabilistic risk model, appraised with reported empirical data. A probabilistic risk assessment framework is integrated with the potency equivalence factors (PEFs), age group-specific occupancy probability and the incremental lifetime cancer risk (1LCR) approaches to quantitatively estimate the exposure risk for three age groups of adults, children, and infants. The benzo[a]pyrene equivalents based PAH concentrations in rural, traffic, and industrial areas associated with age group-specific occupancy probability at different environmental settings are used to calculate daily exposure level through inhalation and dermal contact pathways. Risk analysis indicates that the inhalation-ILCR and dermal contact-ILCR values for adults follow a lognormal distribution with geometric mean 1.04 X 10(-4) and 3.85 x 10(-5) and geometric standard deviation 2.10 and 2.75, respectively, indicating high potential cancer risk; whereas for the infants the risk values are less than 10(-6), indicating no significant cancer risk. Sensitivity analysis indicates that the input variables of cancer slope factor and daily inhalation exposure level have the greater impact than that of body weight on the inhalation-ILCR; whereas for the dermal-ILCR, particle-bound PAH-to-skin adherence factor and daily dermal exposure level have the significant influence than that of body weight. (c) 2005 Elsevier B.V All rights reserved.
引用
收藏
页码:112 / 123
页数:12
相关论文
共 35 条
[1]
CYP1A1 and GSTM1 genotypes affect benzo[a]pyrene DNA adducts in smokers' lung:: comparison with aromatic/hydrophobic adduct formation [J].
Alexandrov, K ;
Cascorbi, I ;
Rojas, M ;
Bouvier, G ;
Kriek, E ;
Bartsch, H .
CARCINOGENESIS, 2002, 23 (12) :1969-1977
[2]
Indoor and outdoor air pollution in Tokyo and Beijing supercities [J].
Ando, M ;
Katagiri, K ;
Tamura, K ;
Yamamoto, S ;
Matsumoto, M ;
Li, YF ;
Cao, SR ;
Ji, RD ;
Liang, CK .
ATMOSPHERIC ENVIRONMENT, 1996, 30 (05) :695-702
[3]
[Anonymous], 1994, HUM RESP TRACT MOD R
[4]
Lung cancer risk after exposure to polycyclic aromatic hydrocarbons: A review and meta-analysis [J].
Armstrong, B ;
Hutchinson, E ;
Unwin, J ;
Fletcher, T .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2004, 112 (09) :970-978
[5]
*ATSDR, 1990, TOX PROF BENZ PYR
[6]
Cancer risk from occupational and environmental exposure to polycyclic aromatic hydrocarbons [J].
Boffetta, P ;
Jourenkova, N ;
Gustavsson, P .
CANCER CAUSES & CONTROL, 1997, 8 (03) :444-472
[7]
RISK ASSESSMENT FOR BENZO[A]PYRENE [J].
COLLINS, JF ;
BROWN, JP ;
DAWSON, SV ;
MARTY, MA .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1991, 13 (02) :170-184
[8]
Potency equivalency factors for some polycyclic aromatic hydrocarbons and polycyclic aromatic hydrocarbon derivatives [J].
Collins, JF ;
Brown, JP ;
Alexeeff, GV ;
Salmon, AG .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 1998, 28 (01) :45-54
[9]
DEUTSCHWENZEL RP, 1983, JNCI-J NATL CANCER I, V71, P539
[10]
Dobson S., 1994, CALCULATION ENV ASSE, P34