首页|同位素标记法—超高效液相色谱—串联质谱法检测肉类中3种β受体阻断剂

同位素标记法—超高效液相色谱—串联质谱法检测肉类中3种β受体阻断剂

扫码查看
目的:建立Oasis MCX柱净化,超高效液相色谱串联质谱法(UPLC-MS)检测肉类中3种β-受体阻断剂的测定方法.方法:肉类样品经酸解提取后,过Oasis MCX净化柱净化,以0.1%甲酸水和甲醇为流动相梯度洗脱,用ThermocHypersil Gold C18色谱柱分离,ESI+进行多反应监测(MRM),内标法定量.结果:3种β—受体阻断剂的线性范围在0.50~18 μg/L,相关系数 r>0.999,检出限(LOD):0.01~0.06 μg/kg,定量限(LOQ):0.03~0.18 μg/kg.3个加标水平下(0.4、1.6、3.2 μg/kg)的回收率为 82.6%~103.2%,RSD 为 3.10%~11.0%.结论:方法准确可靠,可用于肉制品中β-受体阻断剂的定性、定量检测.
Determination of three β-blocker residues in meat by isotope labeling-ultra performance liquid chromatography-tandem mass spectrometry
Objective:To establish a MCX column purification method for the determination of three β-receptor blockers in meat products by ultra performance liquid chromatography tandem mass spectrometry.Method:After extraction by acid hydrolysis,pork samples were purified by Oasis MCX purification column.The mobile phases were eluted by gradient elution of methanol and 0.1%formic acid water,separated by ThermocHypersil Gold C18 column,multiple reaction monitoring(MRM)with ESI source positive ion mode,and quantified by internal standard method.Result:The linear range of the three β-receptor blockers was 0.5~18 μg/L,the correlation coefficient(r)was>0.999,the LOD was 0.01~0.06 μg/kg,and the LOQ was 0.03~0.18μg/kg.At three spiked levels(0.4、1.6、3.2 μg/kg),the recoveries were 82.57%~103.22%,RSD were 3.10%~11.05%.Conclusion:This method is accurate and reliable,and can be used for qualitative and quantitative determination of β-receptor blockers in meat products.

UPLC-MSβ-receptor blockerMAX column purification

孟春杨、吴玉田、周贻兵、刘文政、刘利亚

展开 >

贵州省疾病预防控制中心,贵阳 550004

UPLC-MS β-受体阻断剂 MAX柱净化

贵州省卫生健康委科学技术基金项目贵州省科学(青年)技术基金项目

gzwkj2022-2682021-E1-2青

2024

微量元素与健康研究
贵阳中医学院

微量元素与健康研究

影响因子:0.457
ISSN:1005-5320
年,卷(期):2024.41(1)
  • 1
  • 6