食品科学 ›› 2025, Vol. 46 ›› Issue (16): 353-338.doi: 10.7506/spkx1002-6630-20250301-002

• 安全检测 • 上一篇    

基于金属有机骨架-分子印迹材料的分散固相萃取-液相色谱-串联质谱法检测水产品中氟喹诺酮类药物残留

牛灿杰,叶素丹,胡玉霞,楼佳怡,朱千聪,吕志勇   

  1. (浙江经贸职业技术学院食品健康学院,浙江?杭州 310012)
  • 发布日期:2025-07-22
  • 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项目(GXKJ-2024-056);教育部高等学校科学研究发展中心专项(ZJXF2022188)

Determination of Fluoroquinolone Residues in Aquatic Products by Dispersive Solid Phase Extraction with Metal-Organic Framework-Based Molecularly Imprinted Polymer and Liquid Chromatography-Tandem Mass Spectrometry

NIU Canjie, YE Sudan, HU Yuxia, LOU Jiayi, ZHU Qiancong, LÜ Zhiyong   

  1. (School of Food and Health, Zhejiang Institute of Economics and Trade, Hangzhou 310012, China)
  • Published:2025-07-22

摘要: 以氨基功能化锆基金属有机骨架(UiO-66-NH2)为核,分子印迹聚合物为壳,制备新型金属有机骨架基分子印迹吸附材料,并采用傅里叶变换红外光谱、扫描电镜、透射电镜等进行表征。系统考察样品溶剂、吸附剂用量、吸附时间、解吸附溶剂及时间等关键因素,并与液相色谱-串联质谱仪结合,建立高灵敏度的水产品中氟喹诺酮类药物残留的特异性检测方法。样品提取液氮吹近干后用体积分数10%甲醇-氨水溶液(pH 8.0)复溶,加入30 mg新型吸附材料吸附8 min,再用10%乙酸-甲醇溶液超声解吸附4 min,氮吹近干复溶后使用液相色谱-三重四极杆质谱仪检测。结果表明,10 种氟喹诺酮类药物在0.1~200 μg/L范围内线性关系良好,回收率为84.5%~105.9%,与国标方法相比,所建方法准确度更高,检出限、定量限更低,操作更简单、高效。所制备的新型材料具有良好的选择性和重复使用性,有效降低了检测成本。本研究有助于拓展金属有机骨架基分子印迹聚合物在食品安全检测中的应用范围,可为相关领域的研究和实际检测工作提供参考,具有一定的研究价值和实际应用潜力。

关键词: 金属有机骨架;分子印迹聚合物;分散固相萃取;液相色谱-串联质谱;水产品;氟喹诺酮类药物;特异性检测

Abstract: A novel adsorption material for dispersive solid phase extraction (DSPE) was prepared using amino-functionalized zirconium-based metal-organic framework (UiO-66-NH2) as the core and molecularly imprinted polymer as the shell. Subsequently, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) were used to characterize the material. Key experiential parameters such as solvent, adsorbent concentration, adsorption time, desorption solvent and time were systematically investigated. Furthermore, a highly sensitive method for the determination of fluoroquinolone residues in aquatic products was developed using liquid chromatography-tandem mass spectrometry (LC-MS/MS) with DSPE. The extract was blown to near dryness under nitrogen and re-dissolved with 10% methanol-ammonia solution (pH 8.0). Subsequently, 30 mg of the adsorbent was added for adsorption for 8 minutes. Next, the fluoroquinolones sorbed were ultrasonically desorbed with 10% acetic acid-methanol solution for 4 minutes, blown to near dryness under nitrogen and re-dissolved before analysis by LC-MS/MS. Good linearity was observed all 10 fluoroquinolones in the concentration range of 0.1–200 μg/L, with recovery rates of 84.5%–105.9%. Compared with the national standard method, the established method had higher accuracy, lower limit of detection (LOD) and limit of quantification (LOQ), simpler and more efficient operation. The new material had good selectivity and reusability, effectively reducing the cost of detection. This study helps expand the application scope of metal-organic framework-based molecularly imprinted polymers in food safety detection.

Key words: metal-organic framework; molecularly imprinted polymer; dispersed solid-phase extraction; liquid chromatography-tandem mass spectrometry; aquatic products; fluoroquinolones; specific detection

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