李少晖,任丹丹,谢云峰,杨永坛.超高效液相色谱-串联质谱法测定猪肝中14种喹诺酮类药物残留[J].食品安全质量检测学报,2018,9(4):851-857
超高效液相色谱-串联质谱法测定猪肝中14种喹诺酮类药物残留
Determination of 14 kinds of quinolones residues in pig liver by ultra performance liquid chromatography-tandem mass spectrometry
投稿时间:2017-12-04  修订日期:2018-01-19
DOI:
中文关键词:  兽药残留  喹诺酮  超高效液相色谱串联质谱法  固相萃取  液液萃取
英文关键词:veterinary drug residues  quinolone  ultra performance liquid chromatography-tandem mass spectrometry  solid phase extraction  liquid-liquid extraction
基金项目:国家重点研发计划(2017YFC1600404)
作者单位
李少晖 中粮营养健康研究院, 北京市营养健康与食品安全重点实验室 
任丹丹 中粮营养健康研究院, 北京市营养健康与食品安全重点实验室 
谢云峰 中粮营养健康研究院, 北京市营养健康与食品安全重点实验室 
杨永坛 中粮营养健康研究院, 北京市营养健康与食品安全重点实验室 
AuthorInstitution
LI Shao-Hui Beijing Key Laboratory of Nutrition Health and Food Safety, COFCO Nutrition & Health Research Institute 
REN Dan-Dan Beijing Key Laboratory of Nutrition Health and Food Safety, COFCO Nutrition & Health Research Institute 
XIE Yun-Feng Beijing Key Laboratory of Nutrition Health and Food Safety, COFCO Nutrition & Health Research Institute 
YANG Yong-Tan Beijing Key Laboratory of Nutrition Health and Food Safety, COFCO Nutrition & Health Research Institute 
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中文摘要:
      目的 建立猪肝中14种喹诺酮类抗生素残留的提取、净化和超高效液相色谱串联质谱测定的方法。方法 样品采用EDTA缓冲溶液提取、经正己烷除脂、固相萃取柱净化后, 利用超高效液相色谱串联质谱法检测。结果 本方法显著地除去了动物内脏中的磷脂类杂质的干扰, 待测物均获得了良好的信号响应。方法回收率为72.7%~116.8%、相对标准偏差(relative standard deviation, RSD)为1.6%~19.5%、定量限均为1.0 μg/kg。结论 本方法前处理简单、重复性好、定量限低, 适合作为猪肝中喹诺酮类抗生素残留的日常检测方法。
英文摘要:
      Objective To establish an analytical method for extraction, purification and detection of 14 kinds of quinolone residues in pig liver by ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Methods Samples were extracted by EDTA buffer, the fat was removed by n-hexane, then purified by solid phase extraction column and detected by ultra performance liquid chromatography tandem mass spectrometry. Results This method significantly removed the interference of phospholipid impurities in the animal's liver, and a good signal response was obtained. The recoveries of the method were 72.7%~116.8%, the relative standard deviations (RSDs) were 1.6%~19.5%, and the limit of quantitation was 1 μg/kg. Conclusion The established method is simple, well repeatable and sensitive, which is suitable for routine detection of quinolones residues in pig liver.
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