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电喷雾萃取电离质谱法检测1-羟基芘
引用本文:李雪,陈焕文,傅家谟,盛国英,于志强.电喷雾萃取电离质谱法检测1-羟基芘[J].分析化学,2012,40(5):768-772.
作者姓名:李雪  陈焕文  傅家谟  盛国英  于志强
作者单位:1. 上海大学环境与化学工程学院环境污染与健康研究所,上海200444;东华理工大学江西省质谱科学与仪器重点实验室,南昌330013
2. 东华理工大学江西省质谱科学与仪器重点实验室,南昌,330013
3. 上海大学环境与化学工程学院环境污染与健康研究所,上海200444;中国科学院广州地球化学研究所有机地球化学国家重点实验室,广州510640
4. 中国科学院广州地球化学研究所有机地球化学国家重点实验室,广州,510640
基金项目:中国博士后科学基金,上海市博士后科研资助计划,江西省科技计划项目
摘    要:采用电喷雾萃取电离质谱(EESI-MS)分析致癌性环境有机污染物多环芳烃(PAHs)生物标志物1-羟基芘(1-OHP),探究1-OHP在EESI源中电离的可行性,考察ESI溶剂和样品溶液组成对方法灵敏度的影响,初步建立I-OHP的EESI MS半定量分析方法.结果表明,溶液中1-OHP能够在EES1源中有效电离,生成准分子离子M-H]- (m/z 217),并得到其二级质谱特征碎片离子M- H- CO]- (m/z 189);水、甲醇、乙醇、正丙醇和正丁醇5种ESI溶剂中,使用甲醇时,离子峰m/z 217信噪比最大.样品溶液中甲醇含量越高,离子峰m/z 217强度越强.离子峰m/z 217强度与1-OHP浓度在10~200 μg/L内的线性相关性相对最好;相关系数(R)0.982;相对标准偏差(RSD)为3.4%~14.0%(n=5);定量下限约为10 μg/L(S/N=10);单次检测时间小于0.5 min.

关 键 词:电喷雾萃取电离源  质谱  1-羟基芘  多环芳烃  生物标志物

Detection of 1-Hydroxypyrene by Extractive Electrospray Ionization Mass Spectrometry
LI Xue , CHEN Huan-Wen , FU Jia-Mo , SHENG Guo-Ying , YU Zhi-Qiang.Detection of 1-Hydroxypyrene by Extractive Electrospray Ionization Mass Spectrometry[J].Chinese Journal of Analytical Chemistry,2012,40(5):768-772.
Authors:LI Xue  CHEN Huan-Wen  FU Jia-Mo  SHENG Guo-Ying  YU Zhi-Qiang
Institution:1(Institute of Environmental Pollution and Health,School of Environmental and Chemical Engineering, Shanghai University,Shanghai 200444,China) 2(Jiangxi Key Laboratory for Mass Spectrometry and Instrumentation,Nanchang 330013,China) 3(Guangdong Key Laboratory of Environmental Protection & Resource Utilization, State Key Laboratory of Organic Geochemistry,Guangzhou Institute of Geochemistry, Chinese Academy of Sciences,Guangzhou 510640,China)
Abstract:A method for the detection of 1-hydroxypyrene(1-OHP) using extractive electrospray ionization mass spectrometry(EESI-MS) has been investigated,including the ionization of 1-OHP in a home-made EESI source,effects of the composition of ESI solvent and sample solvent on signal intensity,and semi-quantification analysis.The results indicated that,1-OHP can be effectively extracted and ionized in the EESI source,producing the quasi-molecular ion -(m/z 217) and MS/MS fragment ion M-H-CO]-(m/z 189);when water,methanol,ethanol,n-propanol and n-butanol were used as ESI solvents,respectively,the highest signal to noise ratio(S/N) was achieved while using methanol as ESI solvent;with the increase of methanol content in sample solution,the signal intensity increased significantly,and the signal intensity of m/z 217 in methanol was more than 200 times higher than that in water.The signal intensity of m/z 217was linearly related with the concentration of 1-OHP in methanol within the concentration range of 10-200 μg/L;the correlation coefficient(R) was 0.982,the relative standard deviations(RSD) were 3.4%-14.0%(n=5),the quantitative detection limit(LOD) for 1-OHP in methanol was about 10 μg/L(S/N=10),and the analytical time of each detection was less than 0.5 min.
Keywords:Extractive electrospray ionization  Mass spectrometry  1-Hydroxypyrene  Polycyclic aromatic hydrocarbons  Biomarker
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