首页 | 本学科首页   官方微博 | 高级检索  
     检索      

自制混合型小柱净化-高效液相色谱-串联质谱法同时测定尿液中有机磷酸酯代谢物和8-羟基-2'-脱氧鸟苷
引用本文:李栋,张芹,张圣虎,徐诚,陈建秋,刘艳华,宋宁慧,郭瑞昕.自制混合型小柱净化-高效液相色谱-串联质谱法同时测定尿液中有机磷酸酯代谢物和8-羟基-2'-脱氧鸟苷[J].色谱,2020,38(6):647-654.
作者姓名:李栋  张芹  张圣虎  徐诚  陈建秋  刘艳华  宋宁慧  郭瑞昕
作者单位:1 中国药科大学工学院, 江苏 南京 2111982 生态环境部南京环境科学研究所, 江苏 南京 210042
基金项目:国家自然科学基金(21876207);国家自然科学基金(21507165);环境医学工程教育部重点实验室开放课题项目(2017EME001)
摘    要:建立了基于自制混合型小柱的样品净化-高效液相色谱-串联质谱同时测定7种有机磷酸酯(OPEs)主要代谢产物及生物标志物8-羟基-2'-脱氧鸟苷(8-OHdG)的分析方法。样品经乙腈提取后用自制小柱富集净化,以乙腈-0.2%(v/v)氨水溶液作为流动相进行梯度洗脱,在多反应监测模式下进行定性和定量分析。结果显示,8种目标物在0.1~200 μg/L范围内呈良好的线性关系,7种OPEs代谢物的回收率为52.36%~114.56%,8-OHdG回收率为88.63%~97.72%。将该方法应用于人体尿液实际样品中,7种OPEs代谢物和8-OHdG的检出范围分别为6.24~46.07 μg/L和5.90~16.71 μg/L,8-OHdG与7种OPEs代谢物总含量之间存在显著相关性。该方法操作简单、灵敏度高、准确性好、重现性强,可为更全面地评价人体内OPEs暴露水平及机体损伤提供可靠的技术支持。

关 键 词:高效液相色谱-串联质谱法  有机磷酸酯  代谢物  8-羟基-2'-脱氧鸟苷  尿液  
收稿时间:2019-10-22

Simultaneous determination of seven metabolites of organophosphate esters and 8-hydroxy-2'-deoxyguanosine in urine by high-performance liquid chromatography-tandem mass spectrometry with homemade mixed column purification
LI Dong,ZHANG Qin,ZHANG Shenghu,XU Cheng,CHEN Jianqiu,LIU Yanhua,SONG Ninghui,GUO Ruixin.Simultaneous determination of seven metabolites of organophosphate esters and 8-hydroxy-2'-deoxyguanosine in urine by high-performance liquid chromatography-tandem mass spectrometry with homemade mixed column purification[J].Chinese Journal of Chromatography,2020,38(6):647-654.
Authors:LI Dong  ZHANG Qin  ZHANG Shenghu  XU Cheng  CHEN Jianqiu  LIU Yanhua  SONG Ninghui  GUO Ruixin
Institution:1 School of Engineering, China Pharmaceutical University, Nanjing 211198, China2 Nanjing Institute of Environmental Sciences, Ministry of Ecology and Environment, Nanjing 210042, China
Abstract:A method based on high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) with a small homemade mixed column was developed for the simultaneous determination of seven metabolites of organophosphate esters (OPEs) and 8-hydroxy-2'-deoxyguanosine (8-OHdG), an DNA oxidative damage marker, in urine. The urine samples were extracted by acetonitrile and enriched by the self-made column. All the samples were separated by gradient elution with acetonitrile-0.2% (v/v) ammonia solution, and then analyzed by an electrospray ionization source in negative ion multiple reaction monitoring mode. The results showed that the eight targets had good linearities in the range of 0.1-200 μg/L. The recoveries of the seven metabolites of OPEs and 8-OHdG in urine samples were in the ranges of 52.36% to 114.56% and 88.63% to 97.72%, respectively. The established method was successfully applied for the determination of the abovementioned eight target compounds in real urine samples, with the mass concentrations of the seven metabolites of OPEs and 8-OHdG being 6.24-46.07 μg/L and 5.90-16.71 μg/L, respectively. In addition, significant correlations were found between 8-OHdG and the total content of the seven metabolites of OPEs. The established method is simple, sensitive, accurate, and reproducible, and it provides reliable technical support for a more comprehensive evaluation of the level of human exposure to OPEs and the resulting health hazards.
Keywords:high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS)  organophosphate ester (OPEs)  metabolites  8-hydroxy-2'-deoxyguanosine (8-OHdG)  urine  
本文献已被 CNKI 等数据库收录!
点击此处可从《色谱》浏览原始摘要信息
点击此处可从《色谱》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号