Identification of an in vivo chrysene diol epoxide adduct in human hemoglobin

Chem Res Toxicol. 1990 Jul-Aug;3(4):340-3. doi: 10.1021/tx00016a011.

Abstract

Human blood samples were analyzed by fluorescence and mass spectrometry for the presence of polycyclic aromatic hydrocarbon metabolites covalently bound to hemoglobin. Globin was prepared by HCl-acetone precipitation and enzymatically digested. The polycyclic aromatic alcohols generated from ester adducts during digestion were concentrated by monoclonal antibody immunoaffinity chromatography and separated by C-18 HPLC. Analysis of collected fractions by room temperature fluorescence spectroscopy revealed the presence of the anti-tetrahydrotetrols of benzo[a]pyrene and another component possessing a phenanthrene chromophore. Gas chromatographic-mass spectral analysis of the HPLC fractions revealed that the latter compound was r-1,t-2,t-3,c-4-tetrahydroxy-1,2,3,4-tetrahydrochrysene, arising from a hemoglobin-chrysene diol epoxide adduct.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Chromatography, High Pressure Liquid
  • Chrysenes / analysis
  • Chrysenes / metabolism*
  • Hemoglobins / analysis*
  • Hemoglobins / metabolism
  • Humans

Substances

  • Chrysenes
  • Hemoglobins
  • chrysene
  • chrysene,2-diol-3,4-epoxide-1