R. Pastorelli et al., Benzo(a)pyrene diolepoxide-haemoglobin and albumin adducts at low levels of benzo(a)pyrene exposure, BIOMARKERS, 5(4), 2000, pp. 245-251
A biomonitoring study was conducted to simultaneously measure individual be
nzo(a) pyrene (BaP) exposure in 50 office employees, not occupationally exp
osed to polycyclic aromatic hydrocarbons (PAH), using personal samplers and
the formation of (+) r-7, t-8-dihyroxy-t-9, t-10-epoxy-7,8,9,10-tetrahydro
benzo(a) pyrene (BPDE) adducts to haemoglobin (BPDE-Hb) and serum albumin (
BPDE-SA). The population enrolled was exposed to an average of 0.58 +/- 0.4
6 ng BaP m(-3) (mean +/- SD). The concentration of BaP collected from smoke
rs' samples was double that from non-smokers (P = 0.007). BPDE adducts to H
b and SA were quantified as BaP tetrols released from hydrolysis of macromo
lecules and measured by high-resolution gas chromatography-negative ion che
mical ionization-mass spectrometry. BPDE-Hb adducts were detected in 16% of
the population and BPDE-SA adducts in 28%. Smoking did not affect adduct f
ormation. When BaP personal monitoring data were used as the criterion of e
xposure, no correlation was found with the presence and the levels of BPDE-
Hb and BPDE-SA adducts. Undetected sources of PAH, such as the diet, might
markedly alter the exposure profile depicted by individual air sampling and
affect the frequency and levels of protein biomarkers. This is the first c
omparative analysis of BPDE-Hb and BPDE-SA adducts, providing reference val
ues for these biomarkers in a general urban population. However it is diffi
cult to establish which biomarkers would be the more relevant in assessing
low BaP exposure, due to undetectable factors such as dietary PAHs, that mi
ght have influenced the results to some degree.