Determination of gentamicin C components in fish tissues through SPE-Hypercarb-HPLC-MS/MS

文献类型: 外文期刊

第一作者: Sun, Xiaojie

作者: Sun, Xiaojie;Shang, Derong;Zhai, Yuxiu;Sun, Xiaojie;Shang, Derong;Zhai, Yuxiu;Yang, Yuanhao;Tian, Qiangbing;Yang, Yuanhao;Tian, Qiangbing;Xing, Jun

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关键词: Gentamicin C components; Fish tissue; Porous graphite carbon column; Strong cation exchange; HPLC-MS/MS

期刊名称:JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES ( 影响因子:3.205; 五年影响因子:3.068 )

ISSN: 1570-0232

年卷期: 2018 年 1093 卷

页码:

收录情况: SCI

摘要: In this work, an HPLC/MS/MS method for determination of gentamicin C components in fish tissues was developed based on strong cation exchange solid-phase extraction (SPE) purification coupled with Hypercarb chromatographic column in separation mode. Sample was extracted using trichloroacetic acid aqueous solution containing EDTA. Ion-pairing reagents were not needed because of the "graphite polarity retention effect" of the Hypercarb chromatographic column. HPLC-MS/MS was performed in multiple reaction monitoring (MRM) mode for simultaneous qualitative and quantitative analyses (using matrix external standard) of gentamicin C components in fish tissues. Good linearity was obtained for the target analytes within the concentration range from 0.0100 to 0.500 mg/L. The limits of quantification (LOQ) of this method were 10.0, 20.0, and 20.0 mu g/kg for C1, C1a, and sum of C2 + C2a, respectively. The average recoveries of gentamicin C components were 80.0%-110% when spiked at three levels with the blank carp (Cyprinus carpio) matrix, and the relative standard deviations (RSD) were all less than 15% (n = 6). In addition, for the features of simple operation, high sensitivity and good reproducibility, the proposed method has been successfully applied for detection of gentamicin residues in fish tissues during actual breeding.

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