乔成奎, 庞涛, 黄玉南, 罗静, 王超, 方金豹, 谢汉忠. 分散固相萃取-高效液相色谱-串联质谱法检测4种果蔬中噻苯隆的残留[J]. 农药学学报, 2015, 17(5): 622-626. DOI: 10.3969/j.issn.1008-7303.2015.05.18
    引用本文: 乔成奎, 庞涛, 黄玉南, 罗静, 王超, 方金豹, 谢汉忠. 分散固相萃取-高效液相色谱-串联质谱法检测4种果蔬中噻苯隆的残留[J]. 农药学学报, 2015, 17(5): 622-626. DOI: 10.3969/j.issn.1008-7303.2015.05.18
    Qiao Chengkui, Pang Tao, Huang Yu'nan, Luo Jing, Wang Chao, Fang Jinbao, Xie Hanzhong. Application of dispersive solid phase extraction for the determination of thidiazuron in four fruits and vegetables samples by high performance liquid chromatography-tandem mass spectrometry[J]. Chinese Journal of Pesticide Science, 2015, 17(5): 622-626. DOI: 10.3969/j.issn.1008-7303.2015.05.18
    Citation: Qiao Chengkui, Pang Tao, Huang Yu'nan, Luo Jing, Wang Chao, Fang Jinbao, Xie Hanzhong. Application of dispersive solid phase extraction for the determination of thidiazuron in four fruits and vegetables samples by high performance liquid chromatography-tandem mass spectrometry[J]. Chinese Journal of Pesticide Science, 2015, 17(5): 622-626. DOI: 10.3969/j.issn.1008-7303.2015.05.18

    分散固相萃取-高效液相色谱-串联质谱法检测4种果蔬中噻苯隆的残留

    Application of dispersive solid phase extraction for the determination of thidiazuron in four fruits and vegetables samples by high performance liquid chromatography-tandem mass spectrometry

    • 摘要: 采用高效液相色谱-串联质谱仪(HPLC-MS/MS)建立了猕猴桃、黄瓜、苹果和葡萄4种果蔬中噻苯隆残留的分析方法。样品经乙腈提取,N-丙基乙二胺(PSA)净化,HPLC-MS/MS测定。结果表明:在0.01~1 mg/L范围内,不同基质中噻苯隆的峰面积与其质量浓度间呈良好线性关系,决定系数均大于0.99;在0.01、0.05和0.5 mg/kg添加水平下,4种果蔬基质中噻苯隆的平均回收率为87%~102%,相对标准偏差(RSD)为0.8%~2.0%;方法定量限(LOQ)为0.01 mg/kg。该方法操作简单、高效、经济,准确度和精密度均满足残留分析的要求,适用于噻苯隆的残留检测。

       

      Abstract: An analytical method for the determination of thidiazuron in kiwi, cucumber, apple and grape was established using high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). The samples were extracted with acetonitrile, purified by primary secondary amine (PSA) and detected with HPLC-MS/MS. The results indicated that in the concentration of 0.01-1 mg/L, the matrix-matched calibration curves showed good linearity and determination coefficients >0.99. In the concentration of 0.01-0.5 mg/kg, the average recoveries of thidiazuron in the four matrices were found between 87% and 102% with 0.8%-2.0% relative standard deviations (RSD).The limits of quantification (LOQ) were 0.01 mg/kg. The method was convenient, efficient, economical, sensitive and accurate, which can be suitable for determination of thidiazuron residues.

       

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