Samanidou Victoria, Evaggelopoulou Evaggelia, Trötzmüller Martin, Guo Xinghua, Lankmayr Ernst
Aristotle University of Thessaloniki, Laboratory of Analytical Chemistry, GR-54124 Thessaloniki, Greece.
J Chromatogr A. 2008 Sep 5;1203(2):115-23. doi: 10.1016/j.chroma.2008.07.003. Epub 2008 Jul 9.
A sensitive and selective confirmatory analytical method for the multi-residue determination of seven quinolones (ciprofloxacin, enrofloxacin, sarafloxacin, danofloxacin, oxolinic acid, nalidixic acid and flumequine) in gilthead seabream (Sparus aurata) was developed. The sample pre-treatment involves extraction with 0.1 M NaOH and purification by solid-phase extraction (SPE) on Waters Oasis HLB cartridges followed by the determination of all compounds in a single LC-electrospray ionization MS/MS run. Separation was achieved on a Perfectsil ODS-2, 5 microm, 250 mm x 4 mm, analytical column (MZ Analysentechnik) by gradient elution using a mixture of 0.2% (v/v) formic acid, methanol and acetonitrile within 30 min. Multiple reaction monitoring (MRM) was used for selective detection of each quinolone. Accuracy was evaluated through recovery studies at three different fortification levels. The mean recoveries are between 90 and 132% for the selected levels with RSD values lower than 20%. The method presents satisfactory results for linearity, precision and limits of quantification. The latter are much lower than the maximum residue limits (MRLs) established by the European Union for quinolones in fish tissues (6-8 microg/kg).
建立了一种灵敏且具选择性的确证分析方法,用于测定金头鲷(Sparus aurata)中7种喹诺酮类药物(环丙沙星、恩诺沙星、沙拉沙星、达氟沙星、恶喹酸、萘啶酸和氟甲喹)的多残留量。样品预处理包括用0.1 M氢氧化钠萃取,然后在Waters Oasis HLB柱上进行固相萃取(SPE)纯化,随后在一次液相色谱 - 电喷雾电离串联质谱(LC - ESI MS/MS)运行中测定所有化合物。在一根Perfectsil ODS - 2、5微米、250毫米×4毫米的分析柱(MZ Analysentechnik)上,通过梯度洗脱实现分离,使用0.2%(v/v)甲酸、甲醇和乙腈的混合物,在30分钟内完成。采用多反应监测(MRM)对每种喹诺酮进行选择性检测。通过在三个不同加标水平下的回收率研究评估准确度。选定水平下的平均回收率在90%至132%之间,相对标准偏差(RSD)值低于20%。该方法在线性、精密度和定量限方面呈现出令人满意的结果。定量限远低于欧盟规定的鱼类组织中喹诺酮类药物的最大残留限量(MRLs)(6 - 8微克/千克)。