卢巧梅. 水产品中多种雌激素残留的质谱分析方法研究[J]. 分析测试技术与仪器, 2016, 22(1): 1-8. DOI: 10.16495/j.1006-3757.2016.01.001
引用本文: 卢巧梅. 水产品中多种雌激素残留的质谱分析方法研究[J]. 分析测试技术与仪器, 2016, 22(1): 1-8. DOI: 10.16495/j.1006-3757.2016.01.001
LU Qiao-mei. Mass Spectrometry Analysis of Diverse Estrogens in Aquatic Products[J]. Analysis and Testing Technology and Instruments, 2016, 22(1): 1-8. DOI: 10.16495/j.1006-3757.2016.01.001
Citation: LU Qiao-mei. Mass Spectrometry Analysis of Diverse Estrogens in Aquatic Products[J]. Analysis and Testing Technology and Instruments, 2016, 22(1): 1-8. DOI: 10.16495/j.1006-3757.2016.01.001

水产品中多种雌激素残留的质谱分析方法研究

Mass Spectrometry Analysis of Diverse Estrogens in Aquatic Products

  • 摘要: 建立了同时测定7种雌激素残留的液相色谱-串联质谱法.在最优条件下, 待测物呈现良好的线性关系, 相关系数均大于0.995 7, 检测限介于0.500 0~50.00 ng/mL范围.鱼肉组织经C18小柱净化浓缩, 4.0 mL乙腈-水(体积比5:95, %)淋洗, 2.0 mL乙腈-水(体积比95:5, %)洗脱.三类鱼肉样品中(鮦鱼、龙胆鱼、多宝鱼)均检出双酚A和己二烯雌酚, 部分样品中检出雌二醇和雌酮, 加标回收率为85.70%~120.9%.方法快速、准确, 适用于水产品中雌激素多残留的高效测定.

     

    Abstract: Simultaneous determination of seven estrogens residue was developed using liquid chromatography tandem mass spectrometry. Under the optimal conditions, target compounds presented good linear relationship with correlation coefficients larger than 0.995 7 and limit of detections in the range of 0.500 0~50.00 ng/mL. Fish tissue was extracted by a C18-solid phase extraction cartridge, washed with 4.0 mL of acetonitrile-H2O (5:95, V/V,%), and then eluted with 2.0 mL of acetonitrile-H2O (95:5, V/V,%). Both bisphenol A and dienestrol were detected in three different fish samples, while estradiol and estrone were detected in part of the samples. Recoveries were in the range of 85.70%~120.9%.The proposed method is rapid, accurate and suitable to analyze diverse residue of estrogens in aquatic products.

     

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