Selective sample preparation for the analysis of (fluoro) quinolones in baby food: molecularly imprinted polymers versus anion-exchange resins

被引:49
作者
Diaz-Alvarez, Myriam [1 ]
Turiel, Esther [1 ]
Martin-Esteban, Antonio [1 ]
机构
[1] INIA, Dept Medio Ambiente, Madrid 28040, Spain
关键词
Baby food; (Fluoro)quinolones; Ultrasound-assisted extraction; Sample clean-up; Anion exchanger; Molecularly imprinted polymer; SOLID-PHASE EXTRACTION; LIQUID-CHROMATOGRAPHY; RESIDUES; FLUOROQUINOLONES; MILK; FISH; DANOFLOXACIN; ANTIBIOTICS; VALIDATION; RISK;
D O I
10.1007/s00216-008-2300-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this work, an analytical method for simultaneous analysis of several quinolones (cinoxacin, oxolinic acid, nalidixic acid, and flumequine) and fluoroquinolones (norfloxacin, enrofloxacin, enoxacin, ciprofloxacin, and danofloxacin) in baby-food samples is described for the first time. The method is based on isolation of these analytes by ultrasound-assisted extraction procedure followed by a solid-phase extraction sample clean-up step and final determination of the analytes by HPLC using UV detection. For the extraction step, 2 g baby food was mixed with methanol in a centrifuge tube and one single extraction cycle of 15 min at room temperature was carried out. After centrifugation, supernatant was collected and two different solid-phase extraction procedures were developed and evaluated for sample clean-up. The first was based on use of strong anion-exchange cartridges whereas the second was based on use of a ciprofloxacin-imprinted polymer. Both sample clean-up procedures had their own advantages and drawbacks, and the analytical performance and applicability of each procedure was established and properly discussed. The anion-exchange resin-based method enabled simultaneous determination of quinolones and fluoroquinolones, reaching limits of detection ranging from 0.03 to 0.11 mu g g(-1). In contrast, the use of a ciprofloxacin-imprinted polymer did provide selectivity towards fluoroquinolones, leading to chromatograms free from co-extractives reaching limits of detection one order of magnitude lower than those obtained by the first approach.
引用
收藏
页码:899 / 905
页数:7
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