Literature DB >> 15506208

Toxicity characterization of complex mixtures using biological and chemical analysis in preparation for assessment of mixture similarity.

Leslie Cizmas1, Thomas J McDonald, Tracie D Phillips, Annika M Gillespie, Rebecca A Lingenfelter, Leon F Kubena, Timothy D Phillips, Kirby C Donnelly.   

Abstract

In the United States, several proposed approaches for using bioassays for the risk assessment of complex hazardous mixtures require that selected mixtures be "sufficiently similar" to each other. The goal of this research was to evaluate the utility of a protocol using in vitro bioassays and chemical analysis as a basis for assessing mixture similarity. Two wood preserving wastes (WPWs) containing polycyclic aromatic hydrocarbons and pentachlorophenol were extracted and fractionated to generate potentially similar mixtures. Chemical analysis was conducted using gas chromatography/mass spectrometry. Genotoxicity was evaluated using the Salmonella/microsome and Escherichia coli prophage induction assays. The crude extract of one WPW was also tested in the chick embryotoxicity screening test (CHEST) assay. The CHEST assay provided the most sensitive measurement of toxicity. Overall, the biological potency of the samples was not well correlated with predicted potency based on chemical analysis. Although several mixtures appeared similar based on chemical analysis, the magnitude of the response in bioassays was often dissimilar. Fractionation was required to detect the genotoxicity of mixture components in vitro. The results confirm the need for an integrated protocol, combining chemical analysis, fractionation, and biological testing to characterize the risk associated with complex mixtures.

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Year:  2004        PMID: 15506208     DOI: 10.1021/es035287p

Source DB:  PubMed          Journal:  Environ Sci Technol        ISSN: 0013-936X            Impact factor:   9.028


  4 in total

1.  Method to assess component contribution to toxicity of complex mixtures: Assessment of puberty acquisition in rats exposed to disinfection byproducts.

Authors:  Shahid Parvez; Glenn E Rice; Linda K Teuschler; Jane Ellen Simmons; Thomas F Speth; Susan D Richardson; Richard J Miltner; E Sidney Hunter; Jonathan G Pressman; Lillian F Strader; Gary R Klinefelter; Jerome M Goldman; Michael G Narotsky
Journal:  J Environ Sci (China)       Date:  2017-06-07       Impact factor: 5.565

2.  Long-term Coexposure to Hexavalent Chromium and B[a]P Causes Tissue-Specific Differential Biological Effects in Liver and Gastrointestinal Tract of Mice.

Authors:  Francisco Javier Sánchez-Martín; Yunxia Fan; Vinicius Carreira; Jerald L Ovesen; Andrew Vonhandorf; Ying Xia; Alvaro Puga
Journal:  Toxicol Sci       Date:  2015-03-29       Impact factor: 4.849

3.  Long-term exposure to hexavalent chromium inhibits expression of tumor suppressor genes in cultured cells and in mice.

Authors:  Yunxia Fan; Jerald L Ovesen; Alvaro Puga
Journal:  J Trace Elem Med Biol       Date:  2012-05-19       Impact factor: 3.849

4.  Long-term exposure to low-concentrations of Cr(VI) induce DNA damage and disrupt the transcriptional response to benzo[a]pyrene.

Authors:  Jerald L Ovesen; Yunxia Fan; Jing Chen; Mario Medvedovic; Ying Xia; Alvaro Puga
Journal:  Toxicology       Date:  2013-12-26       Impact factor: 4.221

  4 in total

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