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LC-MS-MS测定河口及近岸海水中的氟喹诺酮类药物; Measurement of Fluoroquinolone Antibiotics in Estuarine and Coastal Seawater by Liquid Chromatography-Tandem Mass Spectrometry
杨琳 ; 黄东仁 ; 温裕云
2011
关键词氟喹诺酮 河口及近岸海水 固相萃取 液相色谱 串级质谱 fluoroquinolone antibiotics estuarine and coastal seawater solid phase extraction liquid chromatography tandem mass spectrometry
英文摘要建立了河口及近岸海水中氟喹诺酮类药物残留的固相萃取富集-高效液相色谱-串级质谱测定方法.以WATErS Hlb固相萃取(SPE)小柱富集水样中的氟喹诺酮类药物,用Xdb-C18柱、乙腈、甲酸(体积分数为0.2%)水流动相进行分离,ESI正离子源、三重串级质谱及多反应监测模式(MrM)进行目标物的定性、定量测定.优化实验条件下,方法的检出限(3σ)为0.002~0.010μg/l,定量限(10σ)为0.010~0.050μg/l,样品加标回收率为73.3%(奥比沙星)~119.7%(氧氟沙星),相对标准偏差(rSd)为1.3%~5.8%(2.5μg/l,n=6).; An accurate method was developed for measurement of fluoroquinolone antibiotics in estuarine and coastal seawater by solid phase extraction(SPE) and liquid chromatography-tandem mass spectrometry.The fluoroquinolones were enriched by Waters HLB SPE column,eluted and concentrated before separating with XDB-C18 column with mobile phase of acetonitrile and water containing 0.2 % formic acid.The analytes were then detected with tandem mass spectrometer using positive ESI at MRM mode.Under the optimized operating conditions,relative standard deviation(RSD) for developed method were 1.3 %--5.8 %(2.5 μg/L,n=6),standard added recoveries were 73.3 %(orbifloxacin) --119.7 %(ofloxacin),limits of detection(3σ) were 0.002--0.010 μg/L,limits of quantification(10σ)were 0.010--0.050 μg/L.; 海洋公益性行业科研专项(200705029)
语种zh_CN
内容类型期刊论文
源URL[http://dspace.xmu.edu.cn/handle/2288/104322]  
专题海洋环境-已发表论文
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GB/T 7714
杨琳,黄东仁,温裕云. LC-MS-MS测定河口及近岸海水中的氟喹诺酮类药物, Measurement of Fluoroquinolone Antibiotics in Estuarine and Coastal Seawater by Liquid Chromatography-Tandem Mass Spectrometry[J],2011.
APA 杨琳,黄东仁,&温裕云.(2011).LC-MS-MS测定河口及近岸海水中的氟喹诺酮类药物..
MLA 杨琳,et al."LC-MS-MS测定河口及近岸海水中的氟喹诺酮类药物".(2011).
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