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Determination of polycyclic aromatic hydrocarbons, azaarenes, and aminoazaarenes in meat samples by solid-phase extraction (SPE) and HPLC

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A study has been conducted to determine the optimum conditions for selective enrichment, by use of coupled solid-phase extraction (SPE) cartridges, of mutagenic and/or carcinogenic organic compounds from meat samples, before qualitative and/or quantitative analysis. Such compounds, generated during heat-processing of meat, can be polycyclic aromatic hydrocarbons (PAH), polycyclic aromatic heterocyclic nitrogen compounds (azaarenes, PANH), or heterocyclic aromatic amines (HAA). To determine the optimum conditions for the clean-up procedure three kinds of Extrelut-type diatomaceous earth columns were tested. The aminoazaarene fraction was analyzed by reversed-phase high-performance liquid chromatography (RP HPLC) on a chemically bonded C8 column and isocratic elution with 10% (v/v) acetonitrile in triethylamine-phosphate buffer (pH 3.2). Analysis of the PAH and PANH fractions was performed by RP HPLC on a C18 column with acetonitrile-water, 84:16 (v/v), as mobile phase. The identities of HPLC peaks were confirmed by GC-MS for both PAH and PANH. The clean-up procedure was used to analyze samples of roasted chicken breast meat. The aminoazaarenes 2-amino-3-methylimidazo[4,5-f]quinoline (IQ), 2-amino-3,4-dimethylimidazo[4,5-f]quinoline (MeIQ), 2-amino-3,4,8-tri-methylimidazo[4,5-f]quinoxaline (4,8-DiMeIQx), and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) were detected in such samples, at total levels from 8.6-13.9 ng g-1. Polycyclic aromatic hydrocarbons identified included benzo(a)anthracene (6.5-7.5 ng g-1) and benzo(a)pyrene (4.9-7.6 ng g-1). Among the azaarenes benzo(a)acridine was found at concentrations of 10.3-12.9 ng g-1.
Słowa kluczowe
Rocznik
Tom
Strony
104--121
Opis fizyczny
Bibliogr. 17 poz., rys., tab.
Twórcy
autor
  • Medical University of Silesia, Faculty of Medicine, Department of Chemistry, Jordana 19, 41-808 Zabrze, Poland
autor
  • Department of Molecular Biology, Centre of Oncology, M. Skłodowska – Curie Institute, Wybrzeże Armii Krajowej 15, 44-101 Gliwice, Poland
autor
  • Medical University of Silesia, Faculty of Medicine, Department of Chemistry, Jordana 19, 41-808 Zabrze, Poland
  • Medical University of Silesia, Faculty of Medicine, Department of Biochemistry, Jordana 19, 41-808 Zabrze, Poland
autor
  • Medical University of Silesia, Faculty of Medicine, Department of Chemistry, Jordana 19, 41-808 Zabrze, Poland
Bibliografia
  • [1] H. Vaessen, A. Jekel, and A. Wilbers, Toxicol. Environ. Chem., 16, 281 (1998)
  • [2] E. A. Gomaa, J. S. Gray, S. Rabie, C. Lopez-Bote, and A. M. Booren, Food Addit. Contam., 10, 503 (1993)
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  • [5] K. Kikugawa, Cancer Lett., 143, 123 (1999)
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  • [7] R. Edenharder, A. Worf-Wandelburg, M. Decker, and K. L. Platt, Mutat. Res., 444, 235 (1999)
  • [8] T. Sugimura, Mutat. Res., 150, 33 (1985)
  • [9] R. Sinha and N. Rothman, Cancer Lett., 143, 189 (1999)
  • [10] S. S. Thorgeirsson, D. Y. Ryu, V. Weidner, and E. G. Snyderwine, Cancer Lett., 143, 245 (1999)
  • [11] B. Stavric, Food Chem. Toxicol., 32, 977 (1994)
  • [12] L. Rivera, M.J.C. Curto, P. Pais, M. T. Galceron, and L. Puignon, J. Chromatogr. A, 731, 85 (1986)
  • [13] G. A. Gross, Carcinogenesis, 11, 1597 (1990)
  • [14] M. G. Knize, R. Sinha, N. Rothman, E. D. Brown, C. P. Salmon, O. A. Levander, P. L. Cunningham, and J. S. Felton, Food Chem. Toxicol., 33, 545 (1995)
  • [15] L. Warzecha, B. Janoszka, and M. Stróżyk, Acta Chromatogr., 9, 176 (1999)
  • [16] B. H. Chen and D. J. Yang, Chromatographia, 48, 223 (1998)
  • [17] C. P. Chiu, Y. S. Lin, and B. H. Chen, Chromatographia, 44, 497 (1997)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BAT3-0026-0028
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