首页> 外文期刊>Central European Journal of Chemistry >Ultra performance liquid chromatography-tandem mass spectrometry for the determination of 5-nitroimidazoles and their metabolites in egg
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Ultra performance liquid chromatography-tandem mass spectrometry for the determination of 5-nitroimidazoles and their metabolites in egg

机译:超高效液相色谱-串联质谱法测定鸡蛋中的5-硝基咪唑及其代谢物

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An ultra performance liquid chromatography (UPLC) coupled to tandem mass spectrometry (MS/MS) procedure was developed for the determination of five 5-nitroimidazoles (dimetridazole, ipronidazole, metronidazole, ronidazole and ternidazole) and three of their metabolites (1-methyl-2-hydroxymethyl-5-nitroimidazole, 1-(2-hydroxyethyl)-2-hydroxymethyl-5-nitroimidazole and 1-methyl-2-(2'-hydroxyisopropyl)-5-nitroimidazole) in egg matrices. Conditions for UPLC separation and electrospray ionization MS/MS in the positive ion mode were optimized. Samples were prepared by liquid-liquid extraction with buffered aqueous 2.5% trichloroacetic acid followed by solid-phase extraction on a Strata-X-C cartridge with reversed-phase and cation-exchange functionalities. The method's performance was evaluated in accordance with Commission Decision 2002/657/EC, applying the alternative matrix-comprehensive in-house validation approach using specially designed InterVal software. The method was robust against different sample matrix and SPE cartridges, operator change, and changes in sample extract storage. Acceptable apparent recoveries (76 to 109%) were obtained for all analytes. The decision limits (CC_α) and detection capabilities (CC_β) were within the ranges of 0.19 - 2.62 and 0.26 - 4.29 μg kg~(-1). For all compounds the calibration curve linearity was good with correlation coefficients greater than 0.99. Fifteen eggs and ten whole egg powder samples obtained commercially in Lithuania were analyzed by UPLC-MS/MS; none were found contaminated by 5-nitroimidazoles or their metabolites.
机译:开发了一种超高效液相色谱(UPLC)和串联质谱(MS / MS)程序,用于测定5种5-硝基咪唑(二甲恶唑,ipronidazole,甲硝唑,ronidazole和ternidazole)及其三种代谢物(1-甲基-鸡蛋基质中的2-羟甲基-5-硝基咪唑,1-(2-羟乙基)-2-羟甲基-5-硝基咪唑和1-甲基-2-(2'-羟基异丙基)-5-硝基咪唑。优化了在阳离子模式下进行UPLC分离和电喷雾电离MS / MS的条件。通过用缓冲的2.5%三氯乙酸水溶液液-液萃取,然后在具有反相和阳离子交换功能的Strata-X-C柱上进行固相萃取,来制备样品。根据委员会决定2002/657 / EC对方法的性能进行了评估,并使用特别设计的InterVal软件采用了替代性的矩阵综合内部验证方法。该方法对于不同的样品基质和SPE柱,操作员变更以及样品提取物存储的变更具有鲁棒性。所有分析物的表观回收率均可接受(76%至109%)。判定极限(CC_α)和检测能力(CC_β)在0.19-2.62和0.26-4.29μgkg〜(-1)范围内。对于所有化合物,相关系数均大于0.99,校准曲线线性良好。通过UPLC-MS / MS分析了在立陶宛商业获得的十五个鸡蛋和十个全蛋粉样品。没有发现被5-硝基咪唑或其代谢物污染。

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