色谱

色谱 ›› 2012, Vol. 30 ›› Issue (06): 568-571.DOI: 10.3724/SP.J.1123.2012.02003

• 研究论文 • 上一篇    下一篇

高效液相色谱-串联质谱法检测奶中克拉维酸残留

杨刚1,黄显会2,郭春娜1,方秋华1,贺利民3   

  1. 华南农业大学国家兽药残留基准实验室, 广东 广州 510642
  • 收稿日期:2012-02-06 修回日期:2012-03-19 出版日期:2012-06-28 发布日期:2012-06-20
  • 通讯作者: 黄显会,博士,高级兽医师,主要从事兽医药理学与毒理学研究. E-mail: xhhuang@scau.edu.cn.
  • 基金资助:

    2010年农业行业标准制修订项目.

Determination of clavulanic acid residue in milk by high performance liquid chromatography-tandem mass spectrometry

YANG Gang, HUANG Xianhui*, GUO Chunna, FANG Qiuhua, HE Limin   

  1. National Reference Laboratory of Veterinary Drug Residues (SCAU), South China Agricultural University, Guangzhou 510642, China
  • Received:2012-02-06 Revised:2012-03-19 Online:2012-06-28 Published:2012-06-20
  • Contact: Xian-Hui HUANG

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369

被引次数

22

摘要： 采用高效液相色谱-串联质谱(HPLC-MS/MS)建立了克拉维酸在奶中的残留检测方法。2 g样品经乙醇沉淀蛋白质后,转入鸡心瓶中旋转蒸发浓缩至0.5 mL左右,用乙酸铵定容,净化后检测。流动相为乙腈和0.1%甲酸水,梯度洗脱,经Luna 5u C8色谱柱分离,采用电喷雾电离,多反应监测负离子模式对克拉维酸进行定量分析。采用基质匹配法对奶中克拉维酸的含量进行标准校正,在克拉维酸含量为10～400 μg/kg范围内呈现良好的线性关系,相关系数大于0.999;奶中加标样品的检出限(LOD,按信噪比(S/N)≥3计)为10 μg/kg,定量限(LOQ, S/N≥10)为20 μg/kg。在定量限、1/2最高残留限量、最高残留限量、2倍最高残留限量添加水平下,奶中克拉维酸的平均回收率为80.00%～91.25%,相对标准偏差为5.60%～8.77%。该方法可用于奶中克拉维酸残留的分析检测。

关键词: 高效液相色谱-串联质谱, 克拉维酸, 奶

Abstract: An analytical method was developed for the determination of clavulanic acid (CLAV) in milk by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). A 2 g milk sample was deproteinized by ethanol. The supernatant was transferred into a pear-shaped bottle to be evaporated to about 0.5 mL, and the residue was dissolved with ammonium acetate solution. The sample was determined by HPLC-MS/MS after the purification. The chromatographic separation was achieved on a Luna 5u C8 column using 0.1% formic acid in water and acetonitrile as mobile phases with gradient elution. The identification of CLAV was carried out by MS/MS equipped with electrospray ionization in negative scanning and multiple reaction monitoring (MRM) modes. Matrix-matched calibration standard was used for the quantification. The calibration curve showed perfect linear in the range of 10-400 μg/kg with the correlation coefficient of 0.999. The limit of detection (LOD, S/N≥3) was 10 μg/kg in milk, and the limit of quantification (LOQ, S/N≥10) was 20 μg/kg. The mean recoveries varied from 80.00% to 91.25% at the four spiked levels of LOQ, 1/2MRL (the maximum residue limit), MRL, and 2MRL with the relative standard deviations of 5.60%-8.77%. In conclusion, the established method can be applied for the determination of CLAV residues in milk.

Key words: clavulanic acid, milk, high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS)