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Simultaneous Determination of Nitroimidazoles and Quinolones in Honey by Modified QuEChERS and LC-MS/MS Analysis

机译:改进的QuEChERS和LC-MS / MS分析同时测定蜂蜜中的硝基咪唑和喹诺酮类药物

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This study reports an analytical method for the determination of nitroimidazole and quinolones in honey using liquid chromatography-tandem mass spectrometry (LC-MS/MS). A modified QuEChERS methodology was used to extract the analytes and determine veterinary drugs in honey by LC-MS/MS. The linear regression was excellent at the concentration levels of 1–100 ng/mL in the solution standard curve and the matrix standard curve. The recovery rates of nitroimidazole and quinolones were 4.4% to 59.1% and 9.8% to 46.2% with relative standard deviations (RSDs) below 5.2% and the recovery rates of nitroimidazole and quinolones by the matrix standard curve ranged from 82.0% to 117.8% and 79% to 115.9% with relative standard deviations (RSDs) lower than 6.3% in acacia and jujube honey. The acacia and jujube honeys have stronger matrix inhibition effect to nitroimidazole and quinolones residue; the matrix inhibition effect of jujube honey is stronger than acacia honey. The matrix standard curve can calibrate matrix effect effectively. In this study, the detection method of antibiotics in honey can be applied to the actual sample. The results demonstrated that the modified QuEChERS method combined with LC-MS/MS is a rapid, high, sensitive method for the analysis of nitroimidazoles and quinolones residues in honey.
机译:这项研究报告了一种使用液相色谱-串联质谱法(LC-MS / MS)测定蜂蜜中硝基咪唑和喹诺酮的分析方法。改良的QuEChERS方法用于提取分析物并通过LC-MS / MS测定蜂蜜中的兽药。在溶液标准曲线和基质标准曲线中的浓度水平为1–100 ng / mL时,线性回归非常出色。硝基咪唑和喹诺酮类化合物的回收率分别为4.4%至59.1%和9.8%至46.2%,相对标准偏差(RSD)低于5.2%,而基质标准曲线测得的硝基咪唑和喹诺酮类化合物的回收率为82.0%至117.8%,金合欢和枣蜂蜜中的相对标准偏差(RSD)低于6.3%,为79%至115.9%。相思和大枣蜂蜜对硝基咪唑和喹诺酮类残留物具有更强的基质抑制作用。枣蜜的基质抑制作用强于相思蜜。基质标准曲线可以有效地校正基质效应。在这项研究中,蜂蜜中抗生素的检测方法可以应用于实际样品。结果表明,改良的QuEChERS方法与LC-MS / MS结合使用是一种快速,高灵敏度的方法,用于分析蜂蜜中的硝基咪唑和喹诺酮类药物残留。

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