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预防医学  2025, Vol. 37 Issue (7): 751-756    DOI: 10.19485/j.cnki.issn2096-5087.2025.07.023
  实验技术 本期目录 | 过刊浏览 | 高级检索 |
超高效液相色谱-串联质谱法同时检测禽蛋禽肉中灭蝇胺和三聚氰胺
张翔, 吴小琼, 葛淼华, 周莹, 欧阳楠
嘉兴市疾病预防控制中心,浙江 嘉兴 314050
Simultaneous determination of cyromazine and melamine in poultry eggs and meat with ultra-high performance liquid chromatography-tandem mass spectrometry
ZHANG Xiang, WU Xiaoqiong, GE Miaohua, ZHOU Ying, OUYANG Nan
Jiaxing Center for Disease Control and Prevention, Jiaxing, Zhejiang 314050, China
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摘要 目的 基于固相萃取柱净化,建立超高效液相色谱-串联质谱法同时检测禽蛋、禽肉中灭蝇胺和三聚氰胺。方法 采集市售鸡蛋、鹌鹑蛋和鸡肉,匀浆后经0.5%甲酸乙腈提取、MCX柱固相萃取和5%氨水甲醇洗脱后,收集洗脱液,氮吹至近干,加10%甲醇水溶液溶解。选择TSKgel Amide-80(2.0 mm×150 mm,5 μm)色谱柱分离,采用串联质谱正离子多反应监测模式同时检测灭蝇胺和三聚氰胺,内标法定量。通过优化样品提取、固相萃取柱和仪器参数等条件提高效率和减少基质干扰。绘制标准曲线,计算灭蝇胺和三聚氰胺的检出限、定量限、加标回收率和相对标准偏差。结果 优化方法后,灭蝇胺和三聚氰胺的基质效应为0.97~1.04,无明显基质抑制或增强效应;灭蝇胺和三聚氰胺在1.0~200.0 ng/mL范围内线性关系良好,相关系数均≥0.999 5,检出限分别为0.3和0.5 μg/kg,定量限分别为1.0和1.5 μg/kg;在1.0、20.0和150.0 μg/kg水平加标,平均加标回收率为78.6%~103.1%,相对标准偏差为3.5%~6.3%。测定95份样品,6份样品检出灭蝇胺,5份样品检出三聚氰胺,未在鸡肉样品中检出灭蝇胺和三聚氰胺。结论 本研究建立的方法可以同时检测禽蛋、禽肉中的灭蝇胺和三聚氰胺,并实现准确定量。
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张翔
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葛淼华
周莹
欧阳楠
关键词 超高效液相色谱-串联质谱灭蝇胺三聚氰胺    
AbstractObjective To establish an ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method based on solid-phase extraction column purification for simultaneous determination of cyromazine and melamine in poultry eggs and meat. Methods Eggs, quail eggs, and chicken were collected from markets. After homogenization, the sample was extracted with 0.5% formic acid in acetonitrile, subjected to solid-phase extraction using an MCX cartridge, and eluted with 5% ammonia in methanol. The eluate was collected, evaporated to near dryness under nitrogen, and reconstituted in a 10% aqueous methanol solution. Separated using TSK gel Amide-80 column (2.0 mm×150 mm, 5 μm), cyromazine and melamine were simultaneously detected in positive ion multiple reaction monitoring mode via tandem mass spectrometry, with quantification achieved by isotope dilution internal standard methods. Efficiency was enhanced and matrix interference minimized by optimizing conditions such as sample extraction, solid-phase extraction cartridge selection, and instrumental parameters. Calibration curves were constructed, and detection limits, quantification limits, spiked recoveries, and relative standard deviations for (RSD) of cyromazine and melamine were calculated. Results After method optimization, matrix effects for cyromazine and melamine ranged from 0.97 to 1.04, indicating no significant matrix suppression or enhancement. Both cyromazine and melamine exhibited excellent linearity within the concentration range of 1.0-200.0 ng/mL, with correlation coefficients ≥0.999 5. The limits of detection were 0.3 μg/kg for cyromazine and 0.5 μg/kg for melamine, the quantification limits were 1.0 and 1.5 μg/kg, respectively. At spiked levels of 1.0, 20.0, and 150.0 μg/kg, the average recoveries ranged from 78.6% to 103.1%, with RSD between 3.5% and 6.3%. Among 95 samples tested, cyromazine was detected in 6 samples and melamine in 5 samples; neither cyromazine nor melamine was detected in chicken samples. Conclusion The UPLC-MS/MS method established in this study enables simultaneous detection and accurate quantification of cyromazine and melamine in poultry eggs and meat.
Key wordsultra-high performance liquid chromatography-tandem mass spectrometry    cyromazine    melamine
收稿日期: 2025-02-13      修回日期: 2025-05-09      出版日期: 2025-07-10
中图分类号:  R994.3  
基金资助:嘉兴市科技计划项目(2023AD11048)
作者简介: 张翔,硕士,主管技师,主要从事理化检验工作
通信作者: 吴小琼,E-mail:285016065@qq.com   
引用本文:   
张翔, 吴小琼, 葛淼华, 周莹, 欧阳楠. 超高效液相色谱-串联质谱法同时检测禽蛋禽肉中灭蝇胺和三聚氰胺[J]. 预防医学, 2025, 37(7): 751-756.
ZHANG Xiang, WU Xiaoqiong, GE Miaohua, ZHOU Ying, OUYANG Nan. Simultaneous determination of cyromazine and melamine in poultry eggs and meat with ultra-high performance liquid chromatography-tandem mass spectrometry. Preventive Medicine, 2025, 37(7): 751-756.
链接本文:  
http://www.zjyfyxzz.com/CN/10.19485/j.cnki.issn2096-5087.2025.07.023      或      http://www.zjyfyxzz.com/CN/Y2025/V37/I7/751
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