Evaluating the mutagenic potential of aerosol organic compounds using informatics-based screening

被引:0
|
作者
Decesari, Stefano [1 ]
Kovarich, Simona [2 ]
Pavan, Manuela [2 ]
Bassan, Arianna [2 ]
Ciacci, Andrea [2 ]
Topping, David [3 ,4 ]
机构
[1] Natl Res Council Italy ISAC CNR, Inst Atmospher Sci & Climate, I-40121 Bologna, Italy
[2] S IN Soluz Informat Srl, I-36100 Vicenza, Italy
[3] Univ Manchester, Sch Earth Atmospher & Environm Sci, Manchester M13 9PL, Lancs, England
[4] Univ Manchester, Natl Ctr Atmospher Sci, Manchester M13 9PL, Lancs, England
关键词
AIRBORNE PARTICULATE MATTER; APPLICABILITY DOMAIN; AIR-POLLUTION; ALPHA-PINENE; ATMOSPHERIC AEROSOLS; OXIDATION-PRODUCTS; OUTDOOR CHAMBER; SOA FORMATION; DNA-DAMAGE; PARTICLES;
D O I
10.5194/acp-18-2329-2018
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Whilst general policy objectives to reduce airborne particulate matter (PM) health effects are to reduce exposure to PM as a whole, emerging evidence suggests that more detailed metrics associating impacts with different aerosol components might be needed. Since it is impossible to conduct toxicological screening on all possible molecular species expected to occur in aerosol, in this study we perform a proof-of-concept evaluation on the information retrieved from in silico toxicological predictions, in which a subset (N = 104) of secondary organic aerosol (SOA) compounds were screened for their mutagenicity potential. An extensive database search showed that experimental data are available for 13% of the compounds, while reliable predictions were obtained for 82 %. A multivariate statistical analysis of the compounds based on their physico-chemical, structural, and mechanistic properties showed that 80% of the compounds predicted as mutagenic were grouped into six clusters, three of which (five-membered lactones from monoterpene oxidation, oxygenated multifunctional compounds from substituted benzene oxidation, and hydroperoxides from several precursors) represent new candidate groups of compounds for future toxicological screenings. These results demonstrate that coupling model-generated compositions to in silico toxicological screening might enable more comprehensive exploration of the mutagenic potential of specific SOA components.
引用
收藏
页码:2329 / 2340
页数:12
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