高效液相色谱-串联质谱法同时测定水产品中7种微囊藻毒素  被引量:6

Determination of 7 Microcystin Variants in Aquatic Products by High Performance Liquid Chromatography-Tandem Triple Quadrupole Mass Spectrometry

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作  者:金玉娥[1] 汪国权[1] 马佳鸣[1] 朱怡平[1] 温忆敏[1] 刘弘[1] 

机构地区:[1]上海市疾病预防控制中心,上海200336

出  处:《环境与职业医学》2012年第6期343-346,共4页Journal of Environmental and Occupational Medicine

基  金:上海市科学技术委员会项目(编号:09411967200)

摘  要:[目的]建立用高效液相色谱一串联质谱法同时测定水产品中7种微囊藻毒素(microcystin,MC)的测定方法。[方法]样品经Tris.HCl(pH=7)缓冲液提取、HLB固相萃取柱(OasisHLB)净化、C18柱分离、电喷雾电离质谱检测、内标法定量。[结果]通过有效的提取和净化,能同时完成水产品中7种微囊藻毒素MC—LR、MC—RR、MC-YR、MC-LA、MC—LW、MC—LY和MC.LF的测定,4种不同水产品基质中10μg/kg、40tc/kg加标回收率为51%~112%和60%.117%,相对标准偏差分别为1.7%~12.7%和0.9%~8.0%(n=6);检出限为0.20—0.40μg/kg。[结论]本研究建立的液相色谱一串联质谱同时测定水产品中7种微囊藻毒素的测定方法是测定水产品中微囊藻毒素残留量快速、有效、实用的方法,能为水产品中微囊藻毒素的监测提供有力的技术保障。[ Objective ] To establish a high performance liquid chromatography-tandem triple quadrnpole mass spectrometry method for simultaneous determination of 7 variants of mierocystins in aquatic products. [ Methods ] All samples were subject to extraction in Tris-HC1 buffer (pH=7), clean-up with Oasis HLB solid phase extraction, C18 separation, mass spectrometry detection and quantification with internal standards. [ Results ] After'effective extraction and purification, 7 mieroeystins of LR, RR, YR, LA, LW, LY and LF were detected simultaneously. The mean recoveries spiked at levels of 10 μg/kg and 40 μg/kg in four matrices were 51%-112% and 60%-117%, with relative standard deviation of 1.7%-12.7% and 0.9%-8.0% (n=6), respeetiveIy. The limits of detection were 0.20-0.40 μg/kg. [ Conclusion ] A rapid and practical method with high efficiency is proposed and provides technical basis for standard determination protocol of mierocystins.

关 键 词:微囊藻毒素 水产品 液相色谱-串联质谱 节球藻毒素 

分 类 号:Q178.51[生物学—水生生物学]

 

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