食品科学 ›› 2025, Vol. 46 ›› Issue (21): 275-283.doi: 10.7506/spkx1002-6630-20250611-079

• 安全检测 • 上一篇    

羧甲基滤纸-MOFs分子印迹膜净化-超高效液相色谱-串联质谱法检测水产品中6 种四环素类抗生素残留

牛灿杰,叶素丹,周晓红   

  1. (浙江经贸职业技术学院,浙江?杭州 310012)
  • 发布日期:2025-11-10
  • 基金资助:
    浙江省基础公益研究计划项目(自然科学基金探索项目)(LTGC24C200003); 浙江经贸职业技术学院省属高校基本科研业务费专项(23SBYB01);浙江省教育厅科研资助项目(Y202353372); 中华全国供销合作总社科技创新课题(GXKJ-2024-056);教育部高等学校科学研究发展中心专项(ZJXF2022188); 浙江省教规办学教学创新团队专项(2022JCD014)

Rapid Determination of Six Tetracycline Residues in Aquatic Products by Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry after Cleanup with Carboxymethyl Filter Paper-based Metal-Organic Framework/Molecularly Imprinted Polymer Film

NIU Canjie, YE Sudan, ZHOU Xiaohong   

  1. (Zhejiang Institute of Economics and Trade, Hangzhou 310012, China)
  • Published:2025-11-10

摘要: 以羧甲基化滤纸为载体,通过原位生长法制备一种新型滤纸基金属有机骨架分子印迹膜,用于水产品中6 种四环素类抗生素残留的高通量特异性检测。该材料结合了金属有机骨架的高比表面积和分子印迹物的特异性识别能力,相较于传统固相萃取方法,富集洗脱时间从45 min缩短至15 min,并避免了固相萃取柱堵塞问题。优化后的方法采用0.1 mol/L Mcllvaine-Na2EDTA缓冲液(pH 4.0)提取,调节pH值至6.0后,以3 片膜材料吸附9 min,5%乙酸-甲醇(V/V)超声洗脱6 min,结合超高效液相色谱-串联质谱检测。6 种四环素类抗生素在2~500 μg/L范围内线性良好(R2≥0.999 8),检出限低至0.62~0.95 μg/kg,加标回收率82.5%~96.8%(相对标准偏差≤4.13%),显著优于国家标准固相萃取方法。该材料可重复使用5 次以上,有效降低了成本。本研究为水产品多残留检测提供了高效、低成本的前处理方案,在食品安全监测领域具有重要应用价值。

关键词: 滤纸基;金属有机骨架;分子印迹聚合物;超高效液相色谱-串联质谱;水产品;四环素

Abstract: A novel metal-organic framework/molecularly imprinted polymer (MOF/MIP) membrane based on carboxymethylated filter paper (CMFP) for the high-throughput and specific detection of six tetracycline residues in aquatic products was prepared by an in-situ growth method. The material combined the high specific surface area of MOF and the specific recognition capacity of MOF. Compared with traditional solid-phase extraction (SPE) methods, the enrichment and elution time was shortened from 45 to 15 minutes, and the problem of SPE column blockage was avoided. In the optimized method, extraction was performed using 0.1 mol/L Mcllvaine-Na2EDTA buffer (pH 4.0), and after pH adjustment to 6.0, adsorption onto three pieces of the CMFP@UiO-66-NH2@MIP membrane was performed for 9 min, followed by ultrasonic-assisted elution with 5% (V/V) acetic acid in methanol for 6 min; detection was carried out using ultra-high liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). All analytes showed good linearity in the concentration range of 2–500 μg/L (R2 ≥ 0.999 8), and the detection limit was as low as 0.62–0.95 μg/kg. Spiked recovery rates were in the range of 82.5%–96.8% with relative standard deviation (RSD) ≤ 4.13%. These figures of merit were significantly better than those of the national standard method with SPE. This material could be reused for more than 5 times, effectively reducing costs. This study provides an efficient and low-cost pretreatment method for the multiresidue detection of tetracyclines in aquatic products, which has important application value in the field of food safety monitoring.

Key words: filter paper-based; metal-organic frameworks; molecularly imprinted polymer; ultra-high liquid chromatography-tandem mass spectrometry; aquatic products; tetracyclines

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