色谱 ›› 2025, Vol. 43 ›› Issue (9): 1045-1052.DOI: 10.3724/SP.J.1123.2024.11012

• 研究论文 • 上一篇    下一篇

超高效液相色谱-四极杆/线性离子阱质谱法同时确证和测定牛源性食品中4种新型异噁唑啉类兽药残留

杨成1, 祝伟霞1, 刘亚风1, 魏蔚1,*(), 赵芳1, 胡锴2,*(), 赵文杰3   

  1. 1.郑州海关技术中心,河南 郑州 450003
    2.河南中医药大学,中医药科学院,河南 郑州 450046
    3.河南工业大学化学化工学院,河南 郑州 450001
  • 收稿日期:2024-11-17 出版日期:2025-09-08 发布日期:2025-09-04
  • 通讯作者: *E-mail:56096231@qq.com(魏蔚);E-mail:hk5268@126.com(胡锴).
  • 基金资助:
    海关总署科研项目(2020HK227)

Simultaneous identification and detection of four novel isoxazoline drugs in bovine-origin foods using ultra-high performance liquid chromatography coupled to quadrupole/linear ion trap mass spectrometry

YANG Cheng1, ZHU Weixia1, LIU Yafeng1, WEI Wei1,*(), ZHAO Fang1, HU Kai2,*(), ZHAO Wenjie3   

  1. 1. Zhengzhou Customs District,Zhengzhou 450003,China
    2. Academy of Chinese Medical Science,Henan University of Chinese Medicine,Zhengzhou 450046,China
    3. School of Chemistry and Chemical Engineering,Henan University of Technology,Zhengzhou 450001,China
  • Received:2024-11-17 Online:2025-09-08 Published:2025-09-04
  • Supported by:
    Scientific Research Project of the General Administration of Customs(2020HK227)

摘要:

异噁唑啉类药物(ISOs)是一类含有N和O原子的五元杂环类化合物,它们能够抑制γ-氨基丁酸门控氯离子通道,被广泛用于家禽寄生虫病的治疗。人类摄入动物源性食品是接触ISOs的重要途径,为解决动物源性食品中ISOs残留带来的安全问题,本研究建立了一种针对牛源性食品(包括牛奶、牛肉和牛肝)中4种新型ISOs(氟雷拉纳、洛替拉纳、沙罗拉纳和阿福拉纳)的超高效液相色谱-四极杆/线性离子阱质谱(UHPLC-Q/Trap MS)分析方法。样品先经乙腈提取,再用PRiME HLB固相萃取小柱净化;以5 mmol/L乙酸铵水溶液和乙腈作为流动相,经Shim-pack GIST C18-AQ (100 mm×2.1 mm, 2.7 μm)色谱柱分离后,在多反应监测(MRM)模式下,采用信息依赖性采集(IDA)、增强子离子扫描(EPI)和谱库检索进行分析,并使用外标法进行定量。结果显示,4种ISOs在各自的质量浓度范围内线性关系良好,相关系数(r)均≥0.993 6,检出限(LOD)和定量限(LOQ)分别为0.2~0.5 μg/kg和0.5~1.0 μg/kg;在低、中、高3个加标水平(1、2、10 μg/kg)下,4种ISOs的回收率为67.6%~118.9%,相对标准偏差(RSD)为2.0%~20.0%。此外,本研究通过MRM-IDA-EPI结合谱库检索对目标化合物进行定性筛查分析,依据色谱保留时间和EPI碎片离子等信息对目标化合物进行双重定性,提高了定性分析的准确性,有效排除了假阳性结果的干扰。该方法具有LOD低、回收率良好等特点,且操作简单、快速,具备高灵敏度和高准确度,能够实现牛源性食品中新型ISOs残留的定性和定量分析。

关键词: 固相萃取, 超高效液相色谱-四极杆/线性离子阱质谱, 异噁唑啉类药物, 氟雷拉纳, 牛源性食品

Abstract:

Isoxazoline drugs (ISOs) are a class of five-membered heterocyclic compounds containing N and O atoms. They can inhibit γ-aminobutyric acid gated chloride channels and are widely used in the treatment of parasitic diseases in poultry. The intake of animal-derived foods by humans is an important way to come into contact with ISOs. Excessive use of ISOs can lead to their residues in animal-derived foods, thereby threatening human health and causing neurotoxicity and hepatotoxicity. To address the safety issues caused by ISO residues in animal-derived foods, an ultra-high performance liquid chromatography-quadrupole/linear ion trap mass spectrometry (UHPLC-Q/Trap MS) analytical method for four novel ISOs (fluralaner, sarolaner, afoxolaner, lotilaner) in bovine-origin foods (including milk, beef and bovine liver) was established. The sample was first extracted with acetonitrile and then purified with PRiME HLB solid phase extraction (SPE) column. Using 5 mmol/L ammonium acetate aqueous solution and acetonitrile as the mobile phase, after separation by Shim-pack GIST C18-AQ (100 mm×2.1 mm, 2.7 μm) chromatography column, the analysis was carried out in the multi-reaction monitoring (MRM) mode by information-dependent acquisition (IDA), enhanced product ion scanning (EPI) and spectral library retrieval, and quantification was performed using the external standard method. The results showed that the four ISOs had good linear relationships within their respective mass concentration ranges. The correlation coefficients (r) were all ≥0.993 6, and the limits of detection (LODs) and quantification (LOQs) were 0.2-0.5 μg/kg and 0.5-1.0 μg/kg, respectively. Under the low, medium and high spiked levels (1, 2 and 10 μg/kg), the recoveries of the four ISOs ranged from 67.6% to 118.9%, and the relative standard deviations (RSDs) ranged from 2.0% to 20.0%. In addition, in this study, qualitative screening and analysis of the target compounds were conducted through MRM-IDA-EPI combined with spectral library retrieval. Dual qualitative analysis of the target compounds was carried out based on information such as retention time and EPI fragment ions, which improved the accuracy of qualitative analysis and effectively eliminated the interference of false positive results. This method features low LODs and good recoveries. It is also simple and rapid to operate, with high sensitivity and accuracy. It can achieve qualitative and quantitative analysis of new ISOs residues in bovine-origin foods. This study can provide technical support for food safety agencies to implement preventive measures against new ISOs in animal foods.

Key words: solid phase extraction (SPE), ultra-high performance liquid chromatography-quadrupole/linear ion trap mass spectrometry (UHPLC-Q/Trap MS), isoxazoline drugs (ISOs), fluralaner, bovine-origin foods

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