王守英,司文帅,杨海锋,李 俊,黄志英,白 冰.高效液相色谱-串联质谱法测定动物尿液中23种β-受体激动剂[J].食品安全质量检测学报,2021,12(14):5620-5628
高效液相色谱-串联质谱法测定动物尿液中23种β-受体激动剂
Determination of 23 kinds of β-receptor agonists in animal urine by high performance liquid chromatography-tandem mass spectrometry
投稿时间:2021-03-04  修订日期:2021-07-17
DOI:
中文关键词:  β-受体激动剂  高效液相色谱-串联质谱法  动物尿液  固相萃取
英文关键词:β-receptor agonists  high performance liquid chromatography-tandem mass spectrometry  animal urine  solid phase extraction
基金项目:上海市科技兴农项目(2019-02-08-00-12-F01144)、农业农村部行业标准制修订项目(14192063)
作者单位
王守英 上海市农业科学院农产品质量标准与检测技术研究所 
司文帅 上海市农业科学院农产品质量标准与检测技术研究所 
杨海锋 上海市农业科学院农产品质量标准与检测技术研究所 
李 俊 中国农业科学院饲料研究所 
黄志英 上海市农业科学院农产品质量标准与检测技术研究所 
白 冰 上海市农业科学院农产品质量标准与检测技术研究所 
AuthorInstitution
WANG Shou-Ying Institute for Agro-Food Standards and Testing Technology of Shanghai Academy of Agricultural Sciences 
SI Wen-Shuai Institute for Agro-Food Standards and Testing Technology of Shanghai Academy of Agricultural Sciences 
YANG Hai-Feng Institute for Agro-Food Standards and Testing Technology of Shanghai Academy of Agricultural Sciences 
LI Jun Feed Research Institute of Chinese Academy of Agricultural Sciences 
HUANG Zhi-Ying Institute for Agro-Food Standards and Testing Technology of Shanghai Academy of Agricultural Sciences 
BAI Bing Institute for Agro-Food Standards and Testing Technology of Shanghai Academy of Agricultural Sciences 
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中文摘要:
      目的 建立高效液相色谱-串联质谱法(high performance liquid chromatography-tandem mass spectrometry, HPLC-MS/MS)快速检测动物尿液中23种β-受体激动剂残留的分析方法。方法 样品经酸解释放结合态药物, 混合型阳离子固相萃取柱富集净化, 5%氨水甲醇洗脱, 浓缩。采用Aglient EC C18 (100 mm× 3.0 mm, 2.7 μm)为色谱柱, 乙腈和5 mmol/L乙酸铵-0.2%甲酸溶液作为流动相进行梯度洗脱, 质谱采用多反应监测模式(multiple reaction monitoring, MRM)对β-受体激动剂的定量离子和定性离子进行监测。结果 本方法在10 min内完成23种兴奋剂的有效分离。在猪尿液、牛尿液、羊尿液中0.2、0.4和2 μg/L添加水平下, 23种β-受体激动剂的平均回收率为65.7%~112.6%, 相对标准偏差≤16.5% (n=6), 方法定量限为0.2 μg/L, 检出限为0.1 μg/L。结论 该方法高效、准确, 适合测定动物尿液中23种β-受体激动剂药物残留, 并为相关标准制修订提供参考。
英文摘要:
      Objective To establish an analytical method for rapid detection of 23 kinds of β-receptor agonists residues in animal urine by high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). Methods The sample was treated with acid to interpret the bound drug, enriched and purified by a mixed cation solid-phase extraction column, followed by elution with 5% ammonia and methanol, and concentrate. Aglient EC C18 (100 mm×3.0 mm, 2.7 μm) was used as the chromatographic column, and acetonitrile and 5 mmol/L ammonium acetate-0.2% formic acid solution were used as the mobile phases for gradient elution. The quantitative and qualitative ions of β-receptor agonists were monitored by multiple reaction monitoring (MRM) using mass spectrum. Results This method completed the effective separation of 23 kinds of agonists within 10 minutes. At the addition levels of 0.2, 0.4 and 2 μg/L in pig, cow and goat urine, the average recoveries of the 23 kinds of β-receptor agonists were 65.7%?112.6%, the relative standard deviations were less than or equal to 16.5% (n=6), the limit of quantitation was 0.2 μg/L and the limit of detection was 0.1 μg/L. Conclusion This method is efficient, accurate and suitable for the determination of 23 kinds of β-receptor agonists drug residues in animal urine, and provides reference for the revision of relevant standards.
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