Simultaneous Determination of Tetrabromobisphenol A and Hexabromocyclododecane in Aquatic Products by QuEChERS Extraction/Ultra high Performance Liquid Chromatography-Tandem Mass Spectrometry
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Simultaneous Determination of Tetrabromobisphenol A and Hexabromocyclododecane in Aquatic Products by QuEChERS Extraction/Ultra high Performance Liquid Chromatography-Tandem Mass Spectrometry
于紫玲, 左优, 马瑞雪, 朱晓辉, 朱俊彦, 陈希超, 刘立婷, 向明灯, 于云江. Simultaneous Determination of Tetrabromobisphenol A and Hexabromocyclododecane in Aquatic Products by QuEChERS Extraction/Ultra high Performance Liquid Chromatography-Tandem Mass Spectrometry[J]. 2019, 38(3): 301-306.
DOI:
于紫玲, 左优, 马瑞雪, 朱晓辉, 朱俊彦, 陈希超, 刘立婷, 向明灯, 于云江. Simultaneous Determination of Tetrabromobisphenol A and Hexabromocyclododecane in Aquatic Products by QuEChERS Extraction/Ultra high Performance Liquid Chromatography-Tandem Mass Spectrometry[J]. 2019, 38(3): 301-306.DOI: doi:10.3969/j.issn.1004-4957.2019.03.007.
Simultaneous Determination of Tetrabromobisphenol A and Hexabromocyclododecane in Aquatic Products by QuEChERS Extraction/Ultra high Performance Liquid Chromatography-Tandem Mass Spectrometry
An ultra high performance liquid chromatography-tandem mass spectrometric(UPLC-MS/MS) method was developed for the simultaneous determination of tetrabromobisphenol A(TBBPA) and hexabromocyclododecane(HBCD) in aquatic products.Sample preparation was based on QuEChERS procedure.The target analytes in samples were extracted with acetonitrile,followed by a dispersive solid phase extraction clean up procedure using C18.Separation of TBBPA and HBCD isomers was achieved on a CORTECS- C18(4.6 mm×100 mm×2.7 μm) column with gradient elution using water-methanol as mobile phase at a flow rate of 0.7 mL/min.The MS/MS analysis was performed with electrospray ion source in negative mode under multiple reaction monitoring(MRM) mode.Good linearities for TBBPA and three HBCD isomers were achieved in the concentration range of 0.5-500 μg/L,with their correlation coefficients(r) above 0.998.The limits of detection(LOD) and the limits of quantitation(LOQ) were in the ranges of 0.04-0.16 μg/kg and 0.12-0.55 μg/kg,respectively. Recoveries at three spiked levels of 5,20 and 50 μg/kg ranged from 74.0% to 121%,with relative standard deviations(RSDs) of 0.20%-23%.The developed method was simple,rapid and reliable,and was suitable for the rapid determination of TBBPA and HBCD in aquatic products.
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