首页> 外文期刊>Journal of liquid chromatography and related technologies >Preparation and characterization of molecularly imprinted monolithic column for on-line solid-phase extraction coupled with hplc for determination of the fluoroquinolone residues in honey samples
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Preparation and characterization of molecularly imprinted monolithic column for on-line solid-phase extraction coupled with hplc for determination of the fluoroquinolone residues in honey samples

机译:在线固相萃取与hplc联用的分子印迹整体柱的制备与表征,用于测定蜂蜜样品中的氟喹诺酮残留

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A new ofloxacin-imprinted monolithic precolumn on-line coupling with reversed-phase high performance liquid chromatography was developed for the determination of the fluoroquinolone residues in honey samples. The molecularly imprinted monolithic column (MIP-MC) was prepared by in situ polymerization in a stainless steel chromatographic column, using methacrylic acid as the functional monomer, ethylene glycol dimethacrylate as the cross-linker, and chloroform and dodecanol as the mixed porogenic solvents. The optimal synthesis conditions and on-line extraction conditions were investigated. The maximum binding capacity (51.50 mg/g) and the dynamic binding capacity (434.92 μg/mL) of the MIP-MC were evaluated by Scatchard analysis and the breakthrough curves, respectively, and they are higher than the non-imprinted monolithic column (43.15 mg/g and 96.52 μg/mL). An enrichment factor of 15.4 along with a good sample cleanup effect was obtained under the optimized conditions. The recoveries of the method for three fluoroquinolones such as ofloxacin, ciprofloxacin, and enrofloxacin were investigated, and high recoveries of 82.0-90.2% from honey samples were obtained with precision between 2.5% and 6.9%. The limits of detection and quantitation of the proposed method were in a range of 5.68-9.71 (μg/kg and 18.93-32.37 (μg/kg, respectively. The method was successfully applied to on-line preconcentration, separation, and determination of the fluoroquinolone residues in food.
机译:建立了一种新的氧氟沙星烙印的整体柱前在线与反相高效液相色谱联用,用于测定蜂蜜样品中的氟喹诺酮残留。分子印迹整体柱(MIP-MC)通过在不锈钢色谱柱中原位聚合制备,使用甲基丙烯酸作为功能单体,乙二醇二甲基丙烯酸酯作为交联剂,氯仿和十二烷醇作为混合成孔剂。研究了最佳合成条件和在线提取条件。通过Scatchard分析和穿透曲线分别评估了MIP-MC的最大结合能力(51.50 mg / g)和动态结合能力(434.92μg/ mL),它们比非印迹整体柱( 43.15 mg / g和96.52μg/ mL)。在优化的条件下获得了15.4的富集因子以及良好的样品净化效果。研究了该方法对三种氟喹诺酮类药物(如氧氟沙星,环丙沙星和恩诺沙星)的回收率,从蜂蜜样品中获得了82.0-90.2%的高回收率,准确度在2.5%至6.9%之间。该方法的检出限和定量限分别为5.68-9.71(μg/ kg)和18.93-32.37(μg/ kg)。该方法已成功地用于在线预浓缩,分离和测定食物中的氟喹诺酮残留物。

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