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固相萃取-气相色谱-质谱联用法测定水产品中邻苯二甲酸酯的残留量
引用本文:姜琳琳.固相萃取-气相色谱-质谱联用法测定水产品中邻苯二甲酸酯的残留量[J].福建水产,2014(2):132-140.
作者姓名:姜琳琳
作者单位:福建省水产研究所,福建厦门361013
基金项目:福建省省属公益类科研院所基本科研专项(2012R1101-3).
摘    要:建立了测定水产品中常见的6种邻苯二甲酸酯类化合物( PAEs)的气相色谱-质谱(GC-MS)分析方法。样品经环己烷:乙酸乙酯(V/V,1∶1)混合溶液超声提取,用乙腈饱和的正己烷除脂,再用正己烷饱和的乙腈反提,过PAE30006-C固相萃取小柱净化,用1%乙酸乙酯的正己烷淋洗,再用正己烷:乙酸乙酯(V/V,1∶1)混合溶液洗脱,洗脱液浓缩后,正己烷定容,供GC-MS测定。结果显示:6种邻苯二甲酸酯类化合物( PAEs)在10-5000 ng/mL的线性范围内,相关系数在0.9992-0.9998,线性良好,检出限( LOD )在0.62-2.96μg/kg,定量限( LOQ)在2.0-9.0μg/kg。选择罗非鱼样品为测试对象,按照10μg/kg、50μg/kg和100μg/kg 的添加量做加标回收试验,平均回收率在70.5%-105.4%之间,相对标准偏差在3.78%-7.57%之间;选用南美白对虾、草鱼、锯缘青蟹、大黄鱼和牡蛎样品对此方法进行验证,在添加浓度为50 ug/kg的水平上进行加标回收实验,6种PAEs的平均加标回收率在71.5%-102.5%之间,相对标准偏差在3.25%-7.86%之间。该方法提取效率高,净化效果好,可操作性强,符合水产品中药物残留检测的要求。

关 键 词:固相萃取  水产品  邻苯二甲酸酯类  残留量  气相色谱-质谱联用法

Determination of phthalate esters residue in aquatic products by solid phase extraction with gas chromatography-mass spectrometry
JIANG Lin-lin.Determination of phthalate esters residue in aquatic products by solid phase extraction with gas chromatography-mass spectrometry[J].Journal of Fujian Fisheries,2014(2):132-140.
Authors:JIANG Lin-lin
Institution:JIANG Lin-lin (Fisheries Research Institute of Fujian, Xiamen 361013, China )
Abstract:A method was developed for the determination of 6 common phthalate esters ( PAEs ) in aquatic products by gas chromatography-mass spectrometry ( GC-MS) . The PAEs were extracted by cyclohexane-ethyl acetate (1∶1) mixed solution, degreased by acetonitrile saturated n-hexane, then extracted by N-hexane saturation of acetonitrile, and purified by PAE30006-C SPE glass column, washed by 1% ethyl ace-tate and eluted by hexane-ethyl acetate (1∶1), the eluent was concentrated and dissolved in hexane, and analyzed by GC-MS. The results showed that the linear range of 6 PAEs were 10-5 000 ng/mL, and the correlation coefficients were 0. 9992-0. 9998, limits of detection (LOD) were 0. 62-2. 96 μg/kg, limits of quantificat ions (LOQ ) were 2. 0 -9. 0 μg/kg, The average recovery of the added test in tilapia from 10, 50, 100 μg/kg was 70. 5% -105. 4%, and the relative standard deviations ( RSD) was 3. 78% -7. 57%. The average recovery of the added test with 50 ug/kg in pacific white shrimp, grass carp, mud crab, yellow croaker and oyster was 71. 5% -102. 5%, and the RSD was 3. 25% -7. 86%. The method was suitable for the determination of PAEs in aquatic products with high extraction efficiency and purification effect.
Keywords:SPE  aquatic products  PAEs  residue  GC-MS
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