食品科学 ›› 2020, Vol. 41 ›› Issue (4): 313-318.doi: 10.7506/spkx1002-6630-20190313-167

• 安全检测 • 上一篇    下一篇

基于三重四极杆复合线性离子阱质谱法筛查和确证水产品中多种抗生素残留

孟勇,王静,朱晓华,耿雪冰,杨总,沈美芳   

  1. (1.江苏省淡水水产研究所,江苏 南京 210017;2.江苏省水产质量检测中心,农业农村部渔业产品质量监督检验测试中心(南京),江苏 南京 210017;3. SCIEX亚太应用中心,上海 201206)
  • 出版日期:2020-02-25 发布日期:2020-03-02
  • 基金资助:
    江苏现代农业(鮰鱼)产业技术体系质量控制与饲料创新团队项目(JATS[2019]354); 江苏现代农业产业技术体系建设专项(JATS[2019]384);江苏省农业科技自主创新资金项目(CX(18)2011)

Screening and Confirmation of Multiple Antibiotic Residues in Aquatic Products by Triple Quadrupole-Linear Ion Trap Mass Spectrometry

MENG Yong, WANG Jing, ZHU Xiaohua, GENG Xuebing, YANG Zong, SHEN Meifang   

  1. (1. Fresh Water Fisheries Research Institute of Jiangsu Province, Nanjing 210017, China;2. Quality Control & Inspection Center for Domestic Fishery Products (Nanjing), Ministry of Agriculture and Rural Affairs, Fishery Analysis & Testing Center of Jiangsu Province, Nanjing 210017, China;3. SCIEX Asia Pacific Application Support Center, Shanghai 201206, China)
  • Online:2020-02-25 Published:2020-03-02

摘要: 应用液相色谱-三重四极杆复合线性离子阱质谱技术,建立水产品中38 种抗生素残留的快速筛查确证方法。水产品经酸化乙腈和乙二胺四乙酸二钠提取,浓缩后加正己烷去脂进行样品预处理。检测采用分段时间多反应监测-信息关联采集-增强离子扫描的方式及建立多种抗生素数据谱库,通过对化合物保留时间、离子对信息以及增强离子扫描谱图进行检索比对,完成多种抗生素的筛查和确证,并采用内标法定量,实现水产品中38 种抗生素的同时定性和定量分析。结果表明,38 种抗生素线性相关性良好(r>0.99),方法的定量限在1.0~5.0 μg/kg之间。添加水平在1.0~50.0 μg/kg时,平均回收率为63.5%~117.3%,相对标准偏差为2.6%~14.8%。本实验建立的水产品中抗生素药物残留的液相色谱-三重四极杆复合线性离子阱质谱分析方法,快速、准确、灵敏度高,定性能力强,可以成功应用于水产品中抗生素残留的筛查和确证分析。

关键词: 水产品, 抗生素, 残留, 三重四极杆复合线性离子阱质谱, 筛查, 确证

Abstract: A rapid method for the screening and confirmation of 38 antibiotic residues in aquatic products was developed by high performance liquid chromatography-triple quadrupole-linear ion trap mass spectrometry (HPLC-Q-Trap-MS). The sample was extracted with acidified acetonitrile with EDTA-2Na, and then the extract was concentrated and degreased with n-hexane. Finally, the analytes were detected by HPLC-Q-Trap-MS in the multiple-reaction monitoring with information-dependent acquisition of enhanced product ion (sMRM-IDA-EPI) mode, followed by establishment of a multiple antibiotic database. The 38 antibiotics were confirmed by their retention times and ion pairs through database searching using the EPI library, and quantified by the internal standard method. All the antibiotics showed good linearity with correlation coefficients above 0.99. The limits of quantification (LOQs) for the antibiotics were in the range of 1.0–5.0 μg/kg. The average recoveries ranged from 63.5% to 117.3% with relative standard deviations of 2.6%–14.8% at spiked concentration levels of 1.0–50.0 μg/kg. The method is sensitive and accurate and can be successfully applied to the screening of antibiotic residues in aquatic products.

Key words: aquatic products, antibiotic, residues, triple quadrupole-linear ion trap mass spectrometry, screening, confirmation

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