Bioassay-Directed Chemical Analysis of Los Angeles Airborne Particulate Matter Using a Human Cell Mutagenicity Assay
The human cell mutagenicity of Los Angeles airborne fine particulate matter is examined via bioassay-directed chemical analysis. A 1993 composite fine particle sample is separated via liquid chromatography into fractions containing organic compounds of varying polarity. Samples are analyzed by the h...
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Published in | Environmental science & technology Vol. 32; no. 22; pp. 3502 - 3514 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
American Chemical Society
15.11.1998
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Subjects | |
Online Access | Get full text |
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Summary: | The human cell mutagenicity of Los Angeles airborne fine particulate matter is examined via bioassay-directed chemical analysis. A 1993 composite fine particle sample is separated via liquid chromatography into fractions containing organic compounds of varying polarity. Samples are analyzed by the h1A1v2 human cell mutagenicity assay to identify those fractions that contain human cell mutagens and by GC/MS to identify the chemical character of those mutagens. Those subfractions that contain unsubstituted polycyclic aromatic compounds (PAC) are responsible for a considerable portion of the mutagenic potency of the whole atmospheric sample. Six unsubstituted PAC (cyclopenta[cd]pyrene, benzo[a]pyrene, benzo[ghi]perylene, benzo[b]fluoranthene, indeno[1,2,3-cd]pyrene, and benzo[k]fluoranthene) account for most of the mutagenic potency that can be assigned to specific compounds within the atmospheric samples. Important semipolar mutagens that are quantified include 2-nitrofluoranthene and 6H-benzo[cd]pyren-6-one. A large number of other aromatic organics are identified as candidates for future testing as pure compounds in the human cell assay, at which time it should be possible to account for more of the mutagenic potency of the atmospheric samples. |
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Bibliography: | istex:C1471DBF910BC2BE5DB6DA2061BD0E7C5893E7D9 ark:/67375/TPS-13BN02SJ-G ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0013-936X 1520-5851 |
DOI: | 10.1021/es9706561 |