The constituents of the neutral aromatic polar subfractions of two coal-derived oils, a shale-derived oil and a petroleum oil wereanalysed and compared. Chemical ionization massspectra, using methanol and ammonia as reagent gases, were used to characterize the oxygen-and nitrogen-containing constitu
Mutagenicity and chemical characterization of two petroleum distillates
β Scribed by June H. Carver; Judith A. Macgregor; R. W. King
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 763 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0260-437X
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β¦ Synopsis
Abstract
To investigate if the Salmonella/microsome assay could reliably screen complex petroleum samples for their carcinogenic potential, two high boiling (700β1070 Β°F) petroleum distillates with known activity in a dermal carcinogenesis bioassay were fully characterized with respect to their hydrocarbon composition and polynuclear aromatic hydrocarbon (PNA) content and assayed for mutagenic activity. Mutagenicity assays were also carried out on the aromatic hydrocarbon aggregates separated from these oils by adsorption chromatography. The composition of the distillates differed substantially, and reflected the fact that they were derived from crude oils that were extremely divergent in hydrocarbon character. Both the distillate and aromatic samples consistently induced a very slight increase in revertant TA98 and TA100 colonies; however, an increase of 2β4βfold over background was observed when the Sβ9 concentration was increased 5β10 times that of the standard assay. The maximal response was less than that expected from the samples' known PNA content and observed potency in the dermal carcinogenesis bioassay. In the Salmonella/microsome assay, all samples inhibited the mutagenic activity of added benzo[a]pyrene. Discordance between the magnitude of the samples' mutagenic activity and their known PNA content may be related to direct or indirect inhibition of sample PNAs by other components of the complex petroleum fractions. Observed inhibitory effects support the use of elevated Sβ9 concentration in the in vitro assays assessing the carcinogenic potential of petroleumβderived materials.
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