首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Development and application of salting-out assisted liquid/liquid extraction for multi-mycotoxin biomarkers analysis in pig urine with high performance liquid chromatography/tandem mass spectrometry
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Development and application of salting-out assisted liquid/liquid extraction for multi-mycotoxin biomarkers analysis in pig urine with high performance liquid chromatography/tandem mass spectrometry

机译:高效液相色谱/串联质谱法用于猪尿液中多种霉菌毒素生物标志物分析的盐析辅助液/液萃取技术的开发和应用

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摘要

Direct determination of urinary mycotoxins is a better approach to assess individual's exposure than the indirect estimation from average dietary intakes. In this study, a new analytical method was developed and validated for simultaneous analysis of aflatoxin B_1, deoxynivalenol, fumonisin B_1, ochratoxin A, zearalenone and T2 toxin and their metabolites in pig urine. In total 12 analytes were selected. A salting-out assisted liquid-liquid extraction procedure was used for sample preparation. High performance liquid chromatography/tandem mass spectrometry was used for the separation and detection of all the analytes. The extraction recoveries were in a range of 70-108%, with the intra-day relative standard deviation and inter-day relative standard deviation lower than 25% for most of the compounds at 3 different concentration levels. Meanwhile the method bias for all the analytes did not exceed 20%. The limits of quantification ranged from 0.07ngmL~(-1) for ochratoxin A to 3.3ngmL~(-1) for deoxynivalenol. Matrix effect was evaluated in this study and matrix-matched calibration was used for quantification. The developed method was also validated for human urine as an extension of its application. Finally, the developed method was applied in a pilot study to analyze 28 pig urine samples. Deoxynivalenol, aflatoxin B_1, fumonisin B_1 and ochratoxin A were detected in these samples.
机译:与根据平均饮食摄入量进行间接估算相比,直接测定尿中的霉菌毒素是评估个人暴露的更好方法。在这项研究中,开发了一种新的分析方法,并同时用于猪尿中黄曲霉毒素B_1,脱氧雪腐烯酚,伏马毒素B_1,曲霉毒素A,玉米赤霉烯酮和T2毒素及其代谢物的分析。总共选择了12种分析物。盐析辅助液-液萃取程序用于样品制备。高效液相色谱/串联质谱法用于所有分析物的分离和检测。多数化合物在3种不同浓度水平下的提取回收率均在70-108%的范围内,日内相对标准偏差和日间相对标准偏差低于25%。同时,所有分析物的方法偏差均不超过20%。曲霉毒素A的定量限范围为0.07ngmL〜(-1)至脱氧雪茄烯醇的定量范围为3.3ngmL〜(-1)。在这项研究中评估了基质效应,并将基质匹配的校准物用于定量。该开发的方法还被证实可用于人尿,作为其应用的扩展。最后,将开发的方法用于初步研究中,以分析28头猪尿液样品。在这些样品中检测到了脱氧雪腐烯酚,黄曲霉毒素B_1,伏马菌素B_1和曲霉毒素A。

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