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作 者:吴春霞[1] 张秋萍[1] 王春民[1] 罗佳 WU Chun-xia;ZHANG Qiu-ping;WANG Chun-min;LUO Jia(Suzhou Municipal Center for Disease Control and Prevention,Jiangsu Key Laboratory of Food Safety Risk Monitoring,Suzhou,Jiangsu 215004,China)
机构地区:[1]苏州市疾病预防控制中心江苏省食品安全风险监测重点实验室,江苏苏州215004
出 处:《中国卫生检验杂志》2022年第19期2310-2314,共5页Chinese Journal of Health Laboratory Technology
基 金:苏州市科技局项目(SS202122)。
摘 要:目的建立一种超高效液相色谱-串联三重四级质谱法测定动物源性食品中6种喹诺酮类(氧氟沙星、培氟沙星、诺氟沙星、洛美沙星、环丙沙星、恩诺沙星)和2种四环素类(强力霉素、土霉素)的残留量。方法样品用0.1 mol/L EDTA-Mcllvaine缓冲液提取后,经过滤和离心后,上清液经HLB固相萃取柱净化,电喷雾正离子模式测定,用外标法定量。结果氧氟沙星、培氟沙星、诺氟沙星、洛美沙星、环丙沙星、恩诺沙星、强力霉素、土霉素在1μg/L~100μg/L浓度内与峰面积具有良好的线性关系,相关系数>0.994,8种抗生素在1.0μg/kg、5.0μg/kg、50.0μg/kg 3个水平加标下,回收率为80.5%~96.2%,相对标准偏差(RSD)为1.95%~4.68%。方法的检出限为0.191μg/kg~0.978μg/kg。结论该方法具有灵敏度高、通用性强、准确度高、稳定性好等优点,满足测定动物源性食品中喹诺酮类和四环素类残留的检测要求。Objective A method for the determination of 6 kinds of quinolones and 2 kinds of tetracyclines residues in animal-origin foods by ultra performance liquid chromatography-tandem triple quaternary mass spectrometry(UPLC-MS/MS)was established.Methods The target analytes were extracted from the samples by 0.1 mol/L EDTA-Mcllvaine buffer extraction solution and purified by HLB solid phase extraction cartridge,and analyzed by UPLC-MS/MS,with positive electrospray ionization(ESI+)in multiple reaction monitoring(MRM)mode,and quantified by external standard method.Results The calibration curves of 8 antibiotics showed good linearities in the range of 1μg/L-100μg/L with correlation coefficients(r)greater than 0.994.The recoveries of 8 antibiotics were between 80.5%-96.2%at the spiked levels of 1.0μg/kg,5.0μg/kg,and50.0μg/kg,and the relative standard deviation was between 1.95%-4.68%.The limits of detection of the method were in the range of 0.191μg/kg-0.978μg/kg.Conclusion The method had many advantages such as high sensitivity,high accuracy,strong versatility,good stability and was suitable for determination of quinolones and tetracyclines residues in animal-origin foods.
关 键 词:喹诺酮类 四环素类 超高效液相色谱-串联三重四级质谱法 残留
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