张 静,赵立军,岳 琴,李 云,冯 波,林顺全.液相色谱-串联质谱法测定饲料中氢化可的松[J].食品安全质量检测学报,2021,12(11):4358-4364
液相色谱-串联质谱法测定饲料中氢化可的松
Determination of hydrocortisone in feed by liquid chromatography-tandem mass spectrometry
投稿时间:2021-03-03  修订日期:2021-05-31
DOI:
中文关键词:  氢化可的松  液相色谱-串联质谱法  饲料  非法添加物
英文关键词:hydrocortisone  liquid chromatography-tandem mass spectrometry  feed  illegal additives
基金项目:
作者单位
张 静 农业农村部饲料质量监督检验测试中心(成都) 
赵立军 农业农村部饲料质量监督检验测试中心(成都) 
岳 琴 农业农村部饲料质量监督检验测试中心(成都) 
李 云 农业农村部饲料质量监督检验测试中心(成都) 
冯 波 农业农村部饲料质量监督检验测试中心(成都) 
林顺全 农业农村部饲料质量监督检验测试中心(成都) 
AuthorInstitution
ZHANG Jing Feed Products Quality Monitoring Center of the Agriculture and Rural Affairs Ministry of China (Chengdu) 
ZHAO Li-Jun Feed Products Quality Monitoring Center of the Agriculture and Rural Affairs Ministry of China (Chengdu) 
YUE Qin Feed Products Quality Monitoring Center of the Agriculture and Rural Affairs Ministry of China (Chengdu) 
LI Yun Feed Products Quality Monitoring Center of the Agriculture and Rural Affairs Ministry of China (Chengdu) 
FENG Bo Feed Products Quality Monitoring Center of the Agriculture and Rural Affairs Ministry of China (Chengdu) 
LIN Shun-Quan Feed Products Quality Monitoring Center of the Agriculture and Rural Affairs Ministry of China (Chengdu) 
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中文摘要:
      目的 建立液相色谱-串联质谱法(liquid chromatography-tandem mass spectrometry, LC-MS/MS)测定饲料中氢化可的松含量的分析方法。方法 饲料样品中的氢化可的松经甲醇提取、石墨化碳黑固相萃取柱结合氨基固相萃取柱净化, 配制基质匹配标准溶液, 外标法定量。色谱采用乙腈(A)和0.1%甲酸水溶液(B)作为流动相进行梯度洗脱, 质谱采用多反应检测模式(multiple reaction monitoring, MRM)对氢化可的松的定量离子和定性离子进行监测。结果 氢化可的松在5.0~500 ng/mL范围内线性良好, 相关系数r均大于0.9975; 方法定量限为5 μg/kg(配合饲料、浓缩饲料、精料补充料)和10 μg/kg(添加剂预混合饲料); 低中高不同浓度添加水平的回收率为77.0%~103.7%, 相对标准偏差小于10% (n=5)。结论 该方法操作简便、灵敏度高、准确度好, 适合饲料产品中非法添加物氢化可的松药物残留测定。
英文摘要:
      Objective To establish an analytical method for determining hydrocortisone content in feed by liquid chromatography-tandem mass spectrometry. Methods Hydrocortisone in feed samples was extracted with methanol, and purified by using a graphitized carbon black solid-phase extraction column combined with an amino solid-phase extraction column. A matrix-matching standard solution was prepared and quantified by external standard method. The chromatograms were gradient eluted with acetonitrile (A) and 0.1% formic acid in water (B) as mobile phases, and the mass spectrum was used to monitor the quantitative and qualitative ions of hydrocortisone in a multiple reaction monitoring. Results The linearities of hydrocortisone were good in the range of 5.0?500 ng/mL, and the correlation coefficient r were all greater than 0.9975. The limits of quantitation for the method were 5 μg/kg (compound feed, concentrated feed and concentrate supplement) and 10 μg/kg (additive premix feed). The recoveries were 77.0%?103.7% and the relative standard deviations were less than 10% (n=5) at different concentrations at low, medium and high levels. Conclusion This method is simple, sensitive and accurate, and is suitable for the determination of hydrocortisone residues in feed products.
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