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中国精品科技期刊2020

超声辅助分散液液微萃取-高效液相色谱法测定蜂蜜中溴氰菊酯残留

于玲

于玲. 超声辅助分散液液微萃取-高效液相色谱法测定蜂蜜中溴氰菊酯残留[J]. 食品工业科技, 2016, (02): 68-72. DOI: 10.13386/j.issn1002-0306.2016.02.005
引用本文: 于玲. 超声辅助分散液液微萃取-高效液相色谱法测定蜂蜜中溴氰菊酯残留[J]. 食品工业科技, 2016, (02): 68-72. DOI: 10.13386/j.issn1002-0306.2016.02.005
YU Ling. Determination of deltamethrin residues in honey by HPLC coupled with ultrasound-assisted dispersive liquid-liquid microextraction[J]. Science and Technology of Food Industry, 2016, (02): 68-72. DOI: 10.13386/j.issn1002-0306.2016.02.005
Citation: YU Ling. Determination of deltamethrin residues in honey by HPLC coupled with ultrasound-assisted dispersive liquid-liquid microextraction[J]. Science and Technology of Food Industry, 2016, (02): 68-72. DOI: 10.13386/j.issn1002-0306.2016.02.005

超声辅助分散液液微萃取-高效液相色谱法测定蜂蜜中溴氰菊酯残留

详细信息
    作者简介:

    于玲(1983-),女,硕士,讲师,主要从事色谱分析方法的研究,E-mail:44427364@qq.com。;

  • 中图分类号: O657.72;S896.1

Determination of deltamethrin residues in honey by HPLC coupled with ultrasound-assisted dispersive liquid-liquid microextraction

  • 摘要: 采用超声辅助分散液液微萃取技术结合高效液相色谱法测定蜂蜜中的溴氰菊酯。蜂蜜样品用乙腈∶水(1∶4,v/v)混合溶液提取,加入氯仿萃取,超声,离心,得到沉积相,进行HLPC分析。溴氰菊酯在10~1000μg/kg范围内线性良好,相关系数r=0.9998,富集倍数高达600倍。当蜂蜜样品的加标浓度为10、50、100μg/kg时,加标回收率为82.6%~97.3%,相对标准偏差为2.1%~3.8%。蜂蜜样品中溴氰菊酯的检出限为8μg/kg,定量限为40μg/kg。本方法具有简便快捷、准确灵敏、萃取效率高、有机溶剂消耗少等特点,可成功地应用于蜂蜜中溴氰菊酯残留的测定。 
    Abstract: A method of HPLC combined with ultrasound-assisted dispersive liquid-liquid microextraction was used for the determination of deltamethrin in honey. The honey sample was extracted with mixed solution of acetonitrile∶water(1∶4,v/v). After the chloroform extraction,ultrasound and centrifugation,sedimentary facies were determined by HPLC. Deltamethrin of 10~1000 μg/kg ranged with good linearity. The correlation coefficient was 0.9998,and the enrichment factor was up to 600. When the spiked concentration of honey samples came to 10,50,100 μg/kg,the recovery rates measured by standard addition method ranged from 82.6% to 97.3%,with the relative standard deviation(RSD) between 2.1% and 3.8%. The detection limit of deltamethrin in honey samples was 8 μg/kg,and the limit of quantification was 40 μg/kg. This method was simple and accurate,with high efficiency of extraction and little consumption of organic solvent. It could be successfully applied to the determination of deltamethrin residues in honey.
  • [1] 顾雪竹,李先端,钟银燕,等.蜂蜜的现代研究及应用[J].中国实验方剂学杂志,2007,13(6):70-72.
    [2] 陈猛,陆婉清,韩燕,等.固相萃取-气相色谱法对河水与海水中36种农药残留的同时测定[J].分析测试学报,2009,28(12):1378-1383.
    [3]

    Hou M Y,Zang X H,Wang C,et al.The use of silica-coated magnetic graphene microspheres as the adsorbent for the extraction of pyrethroid pesticides from orange and lettuce samples followed by GC-MS analysis[J].Journal of Separation Science,2013,36(19):3242-3248.

    [4]

    Dell’Oro D,Casamassima F,Gesualdo G,et al.Determination of pyrethroids in chicken egg samples:development and validation of a confirmatory analytical method by gas chromatography/mass spectrometry[J].International Journa l of Food Science and Technology,2014,49(5):1391-1400.

    [5]

    Jenkins D W,Hensens A,Lloyd J,et al.Development and validation of a‘universal’HPLC method for pyrethroid quantification in long-lasting insecticidal mosquito nets for malaria control and prevention[J].Tropical Medicine&International Health,2013,18(1):2-11.

    [6] 李永夫,高华鹏,张健玲,等.超高效液相色谱-串联质谱法测定鳗鱼中呋线威和溴氰菊酯残留[J].分析化学,2008,36(6):755-759.
    [7]

    Daka P S,Obuseng V C,N Torto,et al.Deltamethrin in sediment samples of the Okavango Delta,Botswana[J].Water SA,2006,32(4):483-488.

    [8]

    Li H P,Lin C H,Jen J F.Analysis of aqueous pyrethroid residuals by one-step microwave-assisted headspace solidphase microextraction and gas chromatography with electron capture detection[J].Talanta,2009,79(2):466-471.

    [9]

    Chen S B,Yu X J,He X Y,et al.Simplified pesticide multiresidues analysis in fish by low-temperature cleanup and solid-phase extraction coupled with gas chromatography/mass spectrometry[J].Food Chemistry,2008,113(4):1297-1300.

    [10] 徐虹,曹文婷,易承学,等.液液萃取气相色谱法测定饮用水中百菌清等12种农药残留[J].中国卫生检验杂志,2014,24(23):3363-3365.
    [11]

    Pinho G P,Neves A A,Queiroz M E L R,et al.Optimization of the liquid-liquid extraction method and low temperature purification(LLE-LTP)for pesticide residue analysis in honey samples by gas chromatography[J].Food Control,2010,21(10):1307-1311.

    [12]

    Rezaee M,Assadi Y,Milani Hosseini M R,et al.Determination of organic compounds in water using dispersive liquid-liquid microextraction[J].Journal of Chromatography A,2006,1116(1-2):1-9.

    [13]

    Maleki R,Farhadi K,Nikkhahi Y.Trace determination of malachite green in water samples using dispersive liquidliquid microextraction coupled with high-performance liquid chromatography-diode array detection[J].International Journal of Environmental Analytical Chemistry,2012,92(9):1026-1035.

    [14]

    Zhou S,Wu B,Ma C,et al.Solid-phase extraction followed by dispersive liquid-liquid microextraction for the sensitive determination of carbamates in environmental water by highperformance liquid chromatography[J].Journal of Liquid Chromatography&Related Technologies,2012,35(20):2860-2872.

    [15]

    Li Y Y,Wei G H,Hu J,et al.Dispersive liquid-liquid microextraction followed by reversed phase-high performance liquid chromatography for the determination of polybrominated diphenyl ethers at trace levels in landfill leachate and environmental water samples[J].Analytica Chimica Acta,2008,615(1):96-103.

    [16] 吴玉环,高晓辉,许月红,等.蜂蜜中溴氰菊酯残留量的测定[J].农药科学与管理,1984(3):16-19.
    [17] 金珍,林竹光,陈美瑜,等.气相色谱-质谱法分析蜂蜜中的多种农药残留[J].色谱,2006,24(5):440-446.
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  • 收稿日期:  2015-05-25

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