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    XU Xiaoying, ZHAO Chaoqun, LIANG Jingjing, ZHOU Xia, LIU Zhu. HPLC-MS/MS Determination of Residual Amounts of 15 Quinolones in Bean Sprouts with Automated Solid Phase Extraction[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2020, 56(5): 583-589. DOI: 10.11973/lhjy-hx202005017
    Citation: XU Xiaoying, ZHAO Chaoqun, LIANG Jingjing, ZHOU Xia, LIU Zhu. HPLC-MS/MS Determination of Residual Amounts of 15 Quinolones in Bean Sprouts with Automated Solid Phase Extraction[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2020, 56(5): 583-589. DOI: 10.11973/lhjy-hx202005017

    HPLC-MS/MS Determination of Residual Amounts of 15 Quinolones in Bean Sprouts with Automated Solid Phase Extraction

    • The bean sprout sample was extracted with EDTA-mcllvaine buffer solution of pH 4.0. MCX solid phase extraction column was used as on-line purification. HPLC-MS/MS was applied to the determination of residual amounts of 15 quinolones in the sample solution. Waters BEH C18 chromatographic column was used as stationary phase, and the mixture of 0.2% (φ, the same below) formic acid solution and 0.2% formic acid acetonitrile solution mixed in different ratios was used as mobile phase in gradient elution. ESI+ and multi-reactions monitor mode were adopted in MS/MS. Linear relationships between values of peak area and mass concentration of 15 quinolones were kept in the same range of 5-120 μg·L-1, with detection limits (3S/N) of 2 μg·kg-1 and lower limits of determination (10S/N) of 6 μg·kg-1. On the base of blank sample, test for recovery was made by standard addition method; values of recovery found were in the range of 62.0%-89.3%, with RSDs (n=6) of determined values in the range of 2.4%-11%.
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