首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of nitroimidazole residues in aquaculture tissue using ultra high performance liquid chromatography coupled to tandem mass spectrometry
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Determination of nitroimidazole residues in aquaculture tissue using ultra high performance liquid chromatography coupled to tandem mass spectrometry

机译:超高效液相色谱-串联质谱法测定水产养殖组织中的硝基咪唑残留量

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摘要

An UHPLC-MS/MS method was developed for the quantitative confirmatory analysis of residues of nitroimidazole drugs (dimetridazole, ipronidazole, metronidazole, ornidazole and ronidazole) and their corresponding hydroxy metabolites (HMMNI, ipronidazile-OH and metronidazole-OH) in aquaculture tissue. Samples were extracted by shaking in acetonitrile, water, MgSO_4 and NaCl before being defatted with n-hexane pre-saturated with acetonitrile and concentrated under nitrogen. Nitroimidazole residues were determined by UHPLC-MS/MS operating in positive electrospray ionisation mode using a reversed phase BEH C_(18) column. The method was validated according to the EU Commission Decision 2002/657/EC guidelines. The following performance studies were carried out: specificity, selectivity, linearity, within laboratory repeatability (WLr)/reproducibility (WLR), accuracy, precision, decision limit (CCα), detection capability (CCβ), absolute recovery and stability. The analytical range of the method is 0.1-20 μgkg~(-1). Accuracy and precision of the method, under within-laboratory reproducibility conditions, ranged from 83 to 105% and 2.3 to 14.0%, respectively. CCα were 0.07-1.0 μgkg~(-1) depending on analyte and matrix. A total of 50 samples can be analysed in a single day using the assay. The method has been extensively evaluated through application to real test samples.
机译:开发了UHPLC-MS / MS方法,用于定量验证水产养殖组织中硝基咪唑类药物(二咪唑,ipronidazole,甲硝唑,奥硝唑和ronidazole)及其相应的羟基代谢物(HMMNI,ipronidazile-OH和甲硝唑-OH)的残留量。通过在乙腈,水,MgSO_4和NaCl中振摇萃取样品,然后用预先用乙腈饱和的正己烷脱脂并在氮气下浓缩。使用反相BEH C_(18)柱,通过正电喷雾电离模式下运行的UHPLC-MS / MS测定硝基咪唑残留物。该方法已根据欧盟委员会决定2002/657 / EC指南进行了验证。进行了以下性能研究:特异性,选择性,线性,实验室重复性(WLr)/重现性(WLR),准确性,精密度,决策极限(CCα),检测能力(CCβ),绝对回收率和稳定性。该方法的分析范围为0.1-20μgkg〜(-1)。在实验室内重现性条件下,该方法的准确度和精密度分别为83%至105%和2.3%至14.0%。取决于分析物和基质,CCα为0.07-1.0μgkg〜(-1)。一天之内可以使用该分析方法分析总共50个样品。该方法已通过应用于实际测试样品进行了广泛评估。

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