학술논문

Urinary Benzo[a]pyrene and Its Metabolites as Molecular Biomarkers of Asphalt Fume Exposure Characterized by Microflow LC Coupled to Hybrid Quadrupole Time-of-Flight Mass Spectrometry.
Document Type
Article
Source
Analytical Chemistry. 11/1/2003, Vol. 75 Issue 21, p5953-5960. 8p.
Subject
*BIOMARKERS
*ASPHALT
*LIQUID chromatography
*QUADRUPOLES
*TIME-of-flight mass spectrometry
Language
ISSN
0003-2700
Abstract
As a step to study the health effects of asphalt fume exposure, an analytical method was developed to characterize benzo[a]pyrene and its hydroxy metabolites in the urine of asphalt fume-exposed rats. This method is based on microflow liquid chromatography (LC) coupled to hybrid quadrupole orthogonal acceleration time-of-flight mass spectrometry (Q-TOFMS). Twenty-four female Sprague-Dawley rats were used in the experiment, with 8 as controls and 16 exposed to asphalt fumes in a whole-body inhalation chamber for 10 days (4 h/day). Generated at 150°C, the asphalt fume concentration in the animal exposure chamber ranged 76-117 mg/m[SUP3]. In the urine of the asphalt fume-exposed rats, benzo[a]pyrene and its metabolites of 3-hydroxybenzo[a]pyrene, benzo[a]pyrene7,8-dihydrodiol(±), and benzo[a]pyrene-7,8,9,10-tetrahydrotetrol(±) were identified, and their concentrations were determined at 2.19 ± 0.49, 16.17 ± 0.3, 6.28 ± 0.36, and 29.35 ± 0.26 ng/100 mL, respectively. The metabolite concentrations from the controlled group, however, were either under the detection limits or at a relatively very low level (0.19 ± 0.41 ng/100 mL for benzo[a]pyrene-7,8,9,10-tetrahydrotetrol metabolite). The results clearly indicate that the benzo[a]pyrene and its hydroxy metabolites were significantly elevated (p < 0.001) in the urine of asphalt fume-exposed rats relative to controls. The study also demonstrated that the combination of microflow LC separation and collision-induced dissociation leading to a characteristic fragmentation pattern by hybrid Q-TOFMS offers a distinct advantage for the identifications and characterizations of the benzo[a]pyrene metabolites. [ABSTRACT FROM AUTHOR]