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Advantages of LC-MS-MS compared to LC-MS for the determination of nitrofuran residues in honey

机译:与LC-MS相比,LC-MS-MS在测定蜂蜜中硝基呋喃残留量方面的优势

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摘要

In the framework of developing analyses for exogenous contaminants in food matrices such as honey, we have compared data obtained by high-performance liquid chromatography coupled with mass spectrometry (LC-MS) to those provided by high-performance liquid chromatography and tandem mass spectrometry (LC-MS-MS). Initial results obtained with LC-MS showed that the technique lacked selectivity, which is why the method was validated by LC-MS-MS. This method involves a solid-phase extraction (SPE) of nitrofuran metabolites and nitrofuran parent drugs, a derivatization by 2-nitrobenzaldehyde for 17 h, and finally a clean-up by SPE. The data obtained show that the limits of detection varied between 0.2 and 0.6 mu g kg(-1) for the metabolites and between 1 and 2 mu g kg(-1) for nitrofuran parent drugs. The method was applied to different flower honeys. The results showed that nitrofurans (used as antibiotics) are consistently present in this matrix, the predominant compound being furazolidone.
机译:在开发对蜂蜜等食品基质中外源污染物进行分析的框架中,我们将高效液相色谱结合质谱(LC-MS)所获得的数据与高效液相色谱和串联质谱所提供的数据进行了比较( LC-MS-MS)。用LC-MS获得的初步结果表明该技术缺乏选择性,这就是为什么该方法已通过LC-MS-MS验证的原因。该方法涉及固相萃取硝基呋喃代谢物和硝基呋喃母体药物(SPE),2-硝基苯甲醛衍生化17 h,最后进行SPE净化。所获得的数据表明,对于代谢产物,检测限为0.2至0.6μg kg(-1),对于硝基呋喃母体药物,检测限为1至2μg kg(-1)。该方法适用于不同的花蜜。结果表明,硝基呋喃(用作抗生素)始终存在于该基质中,主要化合物为呋喃唑酮。

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