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  4. Analysis of N7-(benzo[alpyrene-6-yl)guanine in urine using two-step solid-phase extraction and isotope dilution with liquid chromatography/tandem mass spectrometry
 
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Analysis of N7-(benzo[alpyrene-6-yl)guanine in urine using two-step solid-phase extraction and isotope dilution with liquid chromatography/tandem mass spectrometry

Journal
Rapid Communications in Mass Spectrometry
Journal Volume
19
Journal Issue
7
Pages
893-898
Date Issued
2005
Author(s)
Chen Y.-L.
Wang C.-J.
KUEN-YUH WU  
DOI
10.1002/rcm.1868
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-15944373565&doi=10.1002%2frcm.1868&partnerID=40&md5=7aa0a5364374a1768fc65078b28054b0
https://scholars.lib.ntu.edu.tw/handle/123456789/601680
Abstract
Analysis of urinary N7-(benzo[a]pyren-6-yl)guanine (BP-6-N7Gua), a DNA adduct induced by benzo[a]pyrene, may serve as a risk-associated biomarker for exposure to polyaromatic hydrocarbons (PAHs). In this study a highly sensitive and specific analytical method, incorporating on-line sample preparation coupled with isotope-dilution liquid chromatography and tandem mass spectrometry (LC/MS/MS), was developed to quantitate this adduct in human urine. In order to achieve accurate quantitation, 15N5-labeled BP-6-N7Gua was synthesized to serve as the internal standard, and a two-step solid-phase extraction (SPE) procedure using C8 and SCX cartridges was used for sample cleanup. BP-6-7-N7Gua was analyzed using positive ion LC/MS/MS operated in multiple reaction monitoring (MRM) mode. The [M+H]+ ions at m/z 402 and 407 and the common fragment ion of [M+H]+ at m/z 252 were monitored for quantification. The recovery of this analyte after two-step SPE was 90%, and the limit of detection was 2.5 fmol/mL in 10 mL of urine. This highly specific and sensitive method for BP-6-N7Gua in urine may be applied to assess exposure to PAHs in coke-oven workers for future molecular epidemiology studies on health effects of PAHs.
SDGs

[SDGs]SDG3

Type
journal article

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