Department of Analytical Chemistry, Faculty of Chemistry, Universidad Complutense, E-28040 Madrid, Spain; CEI Campus Moncloa, UCM-UPM, Avda Complutense s/n, E-28040 Madrid, Spain.
Institute for Food Research and Technology, -Food Chemistry Programme, Finca Camps i Armet s/n, Monells, 17121 Girona, Spain.
J Chromatogr A. 2014 May 23;1343:1-9. doi: 10.1016/j.chroma.2014.03.045. Epub 2014 Mar 24.
This paper describes the synthesis of novel molecularly imprinted polymer (MIP) micro-beads for the selective extraction (MISPE) of six fluoroquinolone (FQ) antibiotics (enrofloxacin, ciprofloxacin, lomefloxacin, danofloxacin, sarafloxacin and norfloxacin) from chicken muscle samples and further analysis by high-performance liquid chromatography (HPLC) with fluorescence (FLD) or mass spectrometry (MS) detection. A combinatorial screening approach has been applied to select the optimal functional monomer and cross-linker formulation for polymer synthesis. The MIP prepared using enoxacin (ENOX) as the template - a mixture of methacrylic acid (MAA) and trifluoromethacrylic acid (TFMAA) as functional monomers and ethylene glycol dimethacrylate (EDMA) as the cross-linker - showed superior FQ recognition properties than the rest of the materials generated. MIP spherical particles were prepared using silica beads as sacrificial scaffolds. The polymers were packed in solid phase extraction (SPE) cartridges. The optimized MISPE-HPLC method allows the extraction of the antimicrobials from aqueous samples followed by a selective washing with acetonitrile/water (0.005% TFA, pH=3.0), 20:80 (v/v) and elution with 5% trifluoroacetic acid in methanol. Optimum MISPE conditions led to recoveries of the target FQs in chicken muscle samples ranging between 68 and 102% and precisions in the 3-4% range (RSD, n=18). The method has been validated according to European Union Decision 2002/657/EC, in terms of linearity, accuracy, precision, selectivity, decision limit (CCα) and detection capability (CCβ) by HPLC-FLD and HPLC-MS/MS. The limits of detection were improved using HPLC-MS/MS analysis and ranged between 0.2 and 2.7μgkg(-1) (S/N=3) for all the FQs tested.
本文描述了一种新型分子印迹聚合物(MIP)微球的合成方法,用于选择性提取(MISPE)鸡肉样品中的六种氟喹诺酮(FQ)抗生素(恩诺沙星、环丙沙星、洛美沙星、丹诺沙星、沙拉沙星和诺氟沙星),并进一步通过高效液相色谱(HPLC)进行分析,荧光(FLD)或质谱(MS)检测。组合筛选方法已应用于选择用于聚合物合成的最佳功能单体和交联剂配方。以恩诺沙星(ENOX)为模板制备的 MIP-混合甲基丙烯酸(MAA)和三氟甲基丙烯酸(TFMAA)作为功能单体和乙二醇二甲基丙烯酸酯(EDMA)作为交联剂-表现出优于其余材料的 FQ 识别性能。MIP 球形颗粒是使用硅胶珠作为牺牲支架制备的。聚合物填充在固相萃取(SPE)小柱中。优化的 MISPE-HPLC 方法允许从水溶液中提取抗菌剂,然后用乙腈/水(0.005%TFA,pH=3.0)、20:80(v/v)选择性洗涤,然后用甲醇中的 5%三氟乙酸洗脱。最佳 MISPE 条件可使目标 FQs 在鸡肉肌肉样品中的回收率在 68%至 102%之间,精密度在 3-4%范围内(RSD,n=18)。该方法已根据欧盟 2002/657/EC 号决定,通过 HPLC-FLD 和 HPLC-MS/MS 对线性、准确性、精密度、选择性、决策限(CCα)和检测能力(CCβ)进行了验证。使用 HPLC-MS/MS 分析可提高检测限,所有测试的 FQs 的检测限均在 0.2 至 2.7μgkg-1(S/N=3)之间。