Literature DB >> 7012053

The identification of polynuclear aromatic hydrocarbon (PAH) derivatives in mutagenic fractions of diesel particulate extracts.

D Schuetzle, F S Lee, T J Prater.   

Abstract

The soluble organic fraction (SOF) of particulate matter from diesel exhaust (from point sources, ambient air, etc.) contains hundreds of organic constituents. Norman-phase high pressure liquid chromatography (HPLC) has been used to separate the SOF into subfractions suitable for subsequent chemical analysis and bioassays. These fractions consist of non-polar(PAH), moderately polar (transition) and highly polar constituents. The non-polar fractions have been well characterized and consist of PAH and aliphatic hydrocarbons. The specific compounds present in the transition and polar fractions are for the most part unknown. This analytical information has been difficult to obtain since these compounds are highly labile, polar, of low volatility and in very low concentrations when compared to the bulk of material found in the SOF. Mutagenicity tests using the Ames Salmonella typhimurium assay indicate that the transition fraction accounts for most of the mutagenicity when compared to the non-polar (PAH) and polar fractions. A variety of chromatographic and mass spectrometric techniques are described that have been used to determine the composition of the HPLC fractions. More than one hundred species have been identified in the transition fraction of diesel particulate matter using high resolution gas chromatography (HRGC)/high resolution mass spectrometry (HRMS), HPLC and direct-probe high resolution mass spectrometry. It has been found that the transition fraction contains mostly PAH derivatives consisting of hydroxy, ketone, quinone, carboxaldehyde, acid anhydride and dihydroxy derivatives of PAH. Three nitro-PAH species have been tentatively identified and 1-nitropyrene positively identified in the transition fraction. The 1-nitropyrene was found to account for approximately 45% and 30% of the direct-acting mutagenicity observed for the transition fraction and total extract, respectively. The HPLC separation procedure was shown to give better than 95% recovery of the mass and mutagenic activity. The problem of PAH oxidation during the analytical procedures and possible effect on bioassay results are discussed.

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Year:  1981        PMID: 7012053     DOI: 10.1080/03067318108071903

Source DB:  PubMed          Journal:  Int J Environ Anal Chem        ISSN: 0306-7319            Impact factor:   2.826


  33 in total

1.  Chemical and biological characterization of volatile components of environmental samples after fractionation by vacuum line cryogenic distillation.

Authors:  R L Hanson; A R Dahl; S J Rothenberg; J M Benson; A L Brooks; J S Dutcher
Journal:  Arch Environ Contam Toxicol       Date:  1985-05       Impact factor: 2.804

2.  Sub-parts-per-billion determination of nitro-substituted polynuclear aromatic hydrocarbons in airborne particulate matter and soil by electron capture-Tandem mass spectrometry.

Authors:  M Vincenti; C Minero; E Pelizzetti; M Fontana; R De Maria
Journal:  J Am Soc Mass Spectrom       Date:  1996-12       Impact factor: 3.109

3.  Mutagenicity of a polar portion in the neutral fraction separated from organic extracts of airborne particulates.

Authors:  H Matsumoto; K Inoue
Journal:  Arch Environ Contam Toxicol       Date:  1987-07       Impact factor: 2.804

4.  Influence of ethanol and methanol gasoline blends on the mutagenicity of particulate exhaust extracts.

Authors:  C R Clark; J S Dutcher; R O McClellan; T M Naman; D E Seizinger
Journal:  Arch Environ Contam Toxicol       Date:  1983-05       Impact factor: 2.804

5.  Evidence for enzymatic reduction of 1-nitropyrene by rat liver fractions.

Authors:  J P Nachtman; E T Wei
Journal:  Experientia       Date:  1982-07-15

6.  Interactive effects of cerium oxide and diesel exhaust nanoparticles on inducing pulmonary fibrosis.

Authors:  Jane Y C Ma; Shih-Houng Young; Robert R Mercer; Mark Barger; Diane Schwegler-Berry; Joseph K Ma; Vincent Castranova
Journal:  Toxicol Appl Pharmacol       Date:  2014-05-02       Impact factor: 4.219

7.  Mechanism of Error-Free Bypass of the Environmental Carcinogen N-(2'-Deoxyguanosin-8-yl)-3-aminobenzanthrone Adduct by Human DNA Polymerase η.

Authors:  Amritraj Patra; Dustin A Politica; Arindom Chatterjee; E John Tokarsky; Zucai Suo; Ashis K Basu; Michael P Stone; Martin Egli
Journal:  Chembiochem       Date:  2016-09-13       Impact factor: 3.164

8.  The influence of diesel exhaust on polycyclic aromatic hydrocarbon-induced DNA damage, gene expression, and tumor initiation in Sencar mice in vivo.

Authors:  Lauren A Courter; Andreas Luch; Tamara Musafia-Jeknic; Volker M Arlt; Kay Fischer; Robert Bildfell; Cliff Pereira; David H Phillips; Miriam C Poirier; William M Baird
Journal:  Cancer Lett       Date:  2008-03-18       Impact factor: 8.679

Review 9.  Combustion of diesel fuel from a toxicological perspective. II. Toxicity.

Authors:  P T Scheepers; R P Bos
Journal:  Int Arch Occup Environ Health       Date:  1992       Impact factor: 3.015

10.  Exposure to diesel exhaust upregulates COX-2 expression in ApoE knockout mice.

Authors:  Ni Bai; Erin M Tranfield; Terrance J Kavanagh; Joel D Kaufman; Michael E Rosenfeld; Stephan F van Eeden
Journal:  Inhal Toxicol       Date:  2012-07       Impact factor: 2.724

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