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UPLC-MS/MS测定猪肉中头孢类药物的残留量

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本文采用超高效液相色谱-串联质谱对猪肉中头孢类药物残留量进行分析.样品经乙腈-水溶液和磷酸盐缓冲溶液提取,HLB固相萃取柱纯化后用超高效液相色谱质谱联用仪进行测定.结果表明,3 种头孢类药物浓度在0~200 ng·mL-1 时,相关系数大于0.996,线性关系良好;检出限为0.001~0.365 μg·kg-1,定量限为 0.003~1.220 μg·kg-1.不同浓度下样品的加标回收率为 83.2%~95.2%,相对标准偏差为 1.9%~7.5%,标准偏差为 0.078~2.817 μg·kg-1.
Determination of Cephalosporin Residues in Pork by UPLC-MS/MS
This article uses ultra high performance liquid chromatography tandem mass spectrometry to analyze the residual levels of cephalosporins in pork.The sample was extracted by acetonitrile aqueous solution and phosphate buffer solution,purified by HLB solid-phase extraction column,and determined by ultra-high performance liquid chromatography mass spectrometry.The results showed that the correlation coefficient(R2)of the three cephalosporin drugs was greater than 0.996 within 0~200 ng·mL-1,indicating a good linear relationship;the detection limit is 0.001~0.365 μg·kg-1,with a quantification limit is 0.003~1.220 μg·kg-1.The spiked recovery rates of samples at different concentrations is 83.2%~95.2%,with a relative standard deviation is 1.9%~7.5%and a standard deviation is 0.078~2.817 μg·kg-1.

porkcephalosporinsultra performance liquid chromatography tandem mass spectrometrysolid-phase extraction column

孙钰莹、李启卉、陈月

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国家轻工业食品质量监督检测南京站,江苏南京 211816

猪肉 头孢类药物 超高效液相色谱-串联质谱 固相萃取柱

2024

食品安全导刊
商业科技质量中心 北京肉类食品协会

食品安全导刊

影响因子:0.065
ISSN:1674-0270
年,卷(期):2024.(7)
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