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高效液相色谱-四极杆/静电场轨道阱高分辨质谱对水产品中未知污染物的非定向快速筛查与测定
引用本文:郭思言,丁涛,殷耀,张晓燕,柳菡,沈伟健,林宏,吴斌,邓晓军,伊雄海,杨功俊.高效液相色谱-四极杆/静电场轨道阱高分辨质谱对水产品中未知污染物的非定向快速筛查与测定[J].色谱,2019,37(1):15-20.
作者姓名:郭思言  丁涛  殷耀  张晓燕  柳菡  沈伟健  林宏  吴斌  邓晓军  伊雄海  杨功俊
作者单位:1. 南京海关动植物与食品检测中心, 江苏 南京 210019; 2. 中国药科大学药学院, 江苏 南京 211198; 3. 上海海关动植物与食品检验检疫技术中心, 上海 200135
基金项目:政府间国际科技创新合作重点专项(2017YFE0110800).
摘    要:建立了高效液相色谱-四极杆/静电场轨道阱高分辨质谱对水产品中污染物的非定向快速筛查与测定的方法。筛查时样品用乙腈提取、氮气浓缩吹干、甲醇-水溶液定容,采用全扫描数据依赖二级扫描模式进样分析。利用Trace Finder软件对水产样品中未知污染物的精确质量数、同位素丰度比、二级碎片离子进行数据库检索匹配。定量时样品采用优化的QuEChERS方法净化,对筛查过程确认的三环唑、咖啡因和乙氧基喹啉3种污染物进行目标离子二级扫描模式定量分析。鱼和虾中3种化合物在5~1 000μg/L范围内线性关系良好,相关系数均大于0. 99;方法检出限(LOD)为1μg/kg,定量限(LOQ)为5μg/kg,平均回收率为70. 5~90. 9%,相对标准偏差为5. 4%~12. 8%。筛查方法具有快速、准确、高通量等优点,结合定量方法能够用于实际水产品中未知污染物的筛查与测定。

关 键 词:高效液相色谱  高分辨质谱  非定向筛查  水产品  污染物
收稿时间:2018-08-28

Rapid untargeted screening and determination of unknown contaminants in aquatic products by high performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectrometry
GUO Siyan,DING Tao,YIN Yao,ZHANG Xiaoyan,LIU Han,SHEN Weijian,LIN Hong,WU Bin,DENG Xiaojun,YI Xionghai,YANG Gongjun.Rapid untargeted screening and determination of unknown contaminants in aquatic products by high performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectrometry[J].Chinese Journal of Chromatography,2019,37(1):15-20.
Authors:GUO Siyan  DING Tao  YIN Yao  ZHANG Xiaoyan  LIU Han  SHEN Weijian  LIN Hong  WU Bin  DENG Xiaojun  YI Xionghai  YANG Gongjun
Institution:1. Animal, Plant and Food Inspection Center, Nanjing Customs, Nanjing 210019, China; 2. College of Pharmacy, China Pharmaceutical University, Nanjing 211198, China; 3. Animal, Plant and Food Inspection & Quarantine Center, Shanghai Customs, Shanghai 200135, China
Abstract:A method has been developed for rapid untargeted screening and determination of unknown contaminants in aquatic products by high performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectrometry. The samples were extracted by acetonitrile, dried under nitrogen, dissolved in methanol-water (3:7, v/v), and analyzed via the full MS scan/data dependent MS2 mode during the screening process. The Trace Finder software was used to match the precise mass, the isotope abundance ratio, the fragment ion to search for unknown contaminants in aquatic samples. The optimized QuEChERS method is used to purify the samples when quantifying. The quantitative analyses of triazole, caffeine, and ethoxyquinoline were performed via the target-MS2 mode. The correlation coefficients of the three compounds in fish and shrimp samples were higher than 0.99 in the linear range of 5-1000 μg/L. The limit of detection was 1 μg/kg, and the limit of quantitation was 5 μg/kg. The average recoveries were between 70.5% and 90.9% with the relative standard deviations ranging from 5.4% to 12.8%. The screening method has the advantages of fast, accurate, and high throughput; when combined with the quantitative method, it can be used to screen and determine unknown contaminants in the actual aquatic products.
Keywords:high performance liquid chromatography (HPLC)  high resolution mass spectrometry (HRMS)  untargeted screening  aquatic products  contaminants
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