Fan Ruifang, Dong Yulian, Zhang Wenbing, Wang Yu, Yu Zhiqiang, Sheng Guoying, Fu Jiamo
Guangdong Key Laboratory of Environmental Protection & Resource Utilization, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2006 May 19;836(1-2):92-7. doi: 10.1016/j.jchromb.2006.03.044. Epub 2006 Apr 17.
A fast analysis method using liquid chromatography-atmospheric pressure chemical ionization tandem mass spectrometry was developed for the simultaneous determination of the 1-hydroxypyrene (1-OHP) and 3-hydroxybenzo[a]pyrene (3-OHBaP) in urine. Mass transitions were monitored at m/z 219.3-200.0 for 1-OHP and m/z 269.2-252.2 for 3-OHBaP. Only 10 min was needed for the analysis. The recovery was 60% for 3-OHBaP and 91% for 1-OHP, respectively. And the method detection limits were 0.49 microg/L for 1-OHP and 1.03 microg/L for 3-OHBaP. The inter- and intra-day relative standard deviations were in the range of 2.8-8.9% for 1-OHP and 9.7-20.8% for 3-OHBaP, respectively. The developed method was successfully used to measure urinary PAH metabolites of student volunteers in a high school.
建立了一种使用液相色谱-大气压化学电离串联质谱的快速分析方法,用于同时测定尿液中的1-羟基芘(1-OHP)和3-羟基苯并[a]芘(3-OHBaP)。对1-OHP监测m/z 219.3-200.0的质量转移,对3-OHBaP监测m/z 269.2-252.2的质量转移。分析仅需10分钟。3-OHBaP的回收率分别为60%,1-OHP的回收率为91%。该方法的检测限1-OHP为0.49μg/L,3-OHBaP为1.03μg/L。1-OHP的日间和日内相对标准偏差分别在2.8-8.9%范围内,3-OHBaP的日间和日内相对标准偏差分别在9.7-20.8%范围内。所建立的方法成功用于测定一所高中学生志愿者尿液中的多环芳烃代谢物。