食品科学 ›› 2025, Vol. 46 ›› Issue (3): 222-229.doi: 10.7506/spkx1002-6630-20240718-183

• 安全检测 • 上一篇    下一篇

金属有机骨架基固相萃取-高效液相色谱法检测水产品中5 种氟喹诺酮类药物残留

牛灿杰,叶素丹,朱千聪,胡玉霞   

  1. (浙江经贸职业技术学院,浙江 杭州 310012)
  • 出版日期:2025-02-15 发布日期:2024-12-30
  • 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); 教育部高等学校科学研究发展中心《虚拟仿真技术在职业教育教学中的创新应用》专项(ZJXF2022188)

Determination of Five Fluoroquinolones in Aquatic Products by High Performance Liquid Chromatography with Solid Phase Extraction Using Metal-Organic Framework as Sorbent

NIU Canjie, YE Sudan, ZHU Qiancong, HU Yuxia   

  1. (Zhejiang Institute of Economic and Trade, Hangzhou 310012, China)
  • Online:2025-02-15 Published:2024-12-30

摘要: 采用溶剂热法合成新型金属有机骨架材料UiO-66-NH2,建立基于UiO-66-NH2的固相萃取-高效液相色谱同时检测水产品中5 种氟喹诺酮类药物残留的方法。样品经体积分数1.0%甲酸-乙腈溶液提取,正己烷脱脂,提取液旋蒸浓缩后,采用pH 8.0的氨水溶液复溶,经装有30 mg UiO-66-NH2 的固相萃取柱富集净化,6 mL 20%乙酸-甲醇溶液洗脱,氮吹近干复溶后,利用高效液相色谱-荧光检测器检测。在建立的实验条件下,5 种FQs在0.005~0.50 mg/L范围内线性关系良好,决定系数(R2)为0.999 9~1.0,回收率为81.4%~104.8%,相对标准偏差为1.29%~4.93%,检出限为0.21~2.05 μg/kg。制备的固相萃取柱可重复使用达5 次,绿色环保、经济成本低,所建立的方法具有良好的准确度、精密度、重现性及选择性,适用于水产品中多种痕量氟喹诺酮类药残的同时检测。

关键词: 金属有机骨架;固相萃取;高效液相色谱;水产品;氟喹诺酮类药物

Abstract: A novel metal-organic framework (MOF) material, UiO-66-NH2, was synthesized using a solvothermal method. Subsequently, a high performance liquid chromatography (HPLC) method with solid phase extraction using UiO-66-NH2 was established for the simultaneous detection of five fluoroquinolone (FQ) residues in aquatic products. The sample was extracted with acetonitrile in 1.0% formic acid, degreased with n-hexane, and concentrated by rotary evaporation. The extract was then redissolved in aqueous ammonia solution at pH 8.0. The FQs were enriched and purified with a solid phase extraction (SPE) column filled with 30 mg of UiO-66-NH2 using 6 mL of 20% acetic acid-methanol solution as the eluent. The collected eluate was blown to dryness under nitrogen, redissolved and detected by HPLC with a fluorescence detector. Under the established experimental conditions, good linear relationships were achieved for the five FQs in the concentration range of 0.005–0.50 mg/L, with determination coefficients (R2) of 0.999 9–1.0. The recovery rates ranged from 81.4% to 104.8% with relative standard deviation (RSD) of 1.29%–4.93%, and the limits of detection (LOD) were in the range of 0.21–2.05 μg/kg. The prepared SPE column could be reused up to five times, which was environmentally friendly and cost-effective. The established method had good accuracy, precision, reproducibility, and selectivity, and was suitable for the simultaneous detection of various trace FQ residues in aquatic products.

Key words: metal-organic framework; solid phase extraction; high performance liquid chromatography; aquatic products; fluoroquinolones

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