Author
Listed:
- Shiwei Cui
(Key Laboratory of Chemical Safety and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China
National Institute of Occupational Health and Poison Control, Chinese Center for Disease Control and Prevention, Beijing 100050, China
Department of Chemistry, Zhengzhou University, Zhengzhou 450001, Henan province, China)
- Haibin Li
(Key Laboratory of Chemical Safety and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China
National Institute of Occupational Health and Poison Control, Chinese Center for Disease Control and Prevention, Beijing 100050, China
Department of Chemistry, Zhengzhou University, Zhengzhou 450001, Henan province, China)
- Shaojia Wang
(Key Laboratory of Chemical Safety and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China
National Institute of Occupational Health and Poison Control, Chinese Center for Disease Control and Prevention, Beijing 100050, China
College of Public Health, Hebei United University, Tangshan 063009, Hebei province, China)
- Xiao Jiang
(Key Laboratory of Chemical Safety and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China
National Institute of Occupational Health and Poison Control, Chinese Center for Disease Control and Prevention, Beijing 100050, China)
- Shusheng Zhang
(Department of Chemistry, Zhengzhou University, Zhengzhou 450001, Henan province, China)
- Rongjie Zhang
(Henan Center for Disease Control and Prevention, Zhengzhou 450016, Henan province, China)
- Xin Sun
(Key Laboratory of Chemical Safety and Health, Chinese Center for Disease Control and Prevention, Beijing 100050, China
National Institute of Occupational Health and Poison Control, Chinese Center for Disease Control and Prevention, Beijing 100050, China)
Abstract
Etheno-DNA adducts are generated from the metabolism of exogenous carcinogens and endogenous lipid peroxidation. We and others have previously reported that 1, N 6 -ethenodeoxyadenosine (εdA) and 3, N 4 -ethenodeoxycytidine (εdC) are present in human urine and can be utilized as biomarkers of oxidative stress. In this study, we report a new ultrasensitive UPLC-ESI-MS/MS method for the analysis of εdA and edC in human urine, capable of detecting 0.5 fmol εdA and 0.3 fmol εdC in 1.0 mL of human urine, respectively. For validation of the method, 20 human urine samples were analyzed, and the results revealed that the mean levels of εdA and εdC (SD) fmol/µmol creatinine are 5.82 ± 2.11 (range 3.0–9.5) for εdA and 791.4 ± 328.8 (range 116.7–1264.9) for εdC in occupational benzene-exposed workers and 2.10 ± 1.32 (range 0.6–4.7) for εdA and 161.8 ± 200.9 (range 1.8–557.5) for εdC in non-benzene-exposed workers, respectively. The ultrasensitive detection method is thus suitable for applications in human biomonitoring and molecular epidemiology studies.
Suggested Citation
Shiwei Cui & Haibin Li & Shaojia Wang & Xiao Jiang & Shusheng Zhang & Rongjie Zhang & Xin Sun, 2014.
"Ultrasensitive UPLC-MS-MS Method for the Quantitation of Etheno-DNA Adducts in Human Urine,"
IJERPH, MDPI, vol. 11(10), pages 1-13, October.
Handle:
RePEc:gam:jijerp:v:11:y:2014:i:10:p:10902-10914:d:41430
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