首页> 外文会议>Symposium on Mycotoxin Prevention and Control in Agriculture >LC/Ultraviolet/Fluorescence and LC/MS/MSAnalyses of Multiple Mycotoxins in SpikedBeer Using Immunoaffinity Column Clean-Up
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LC/Ultraviolet/Fluorescence and LC/MS/MSAnalyses of Multiple Mycotoxins in SpikedBeer Using Immunoaffinity Column Clean-Up

机译:使用免疫亲和柱清理,LC /紫外/荧光和LC / MS / MSANALYSES在Spikedbeer中的尖刺毒素

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Ten different mycotoxins namely deoxynivalenol (DON), aflatoxins B_1, B_2, G_1, G_2, fumonisins B_1, B_2, B_3, zearalenone (ZON), and ochratoxin A (OTA) present in fortified beer matrices were extracted using mixed-bed ("Myco5inl") Immunoaffinity columns and were detected using both the classical LC/Ultraviolet/Fluorescence with post-column derivatization and modern LC/MS/MS techniques. HPLC separations were performed using a reverse phase C_(18) column. Mass Spectroscopy measurements were done in the positive ESI mode. Multiple reaction monitoring (MRM) analyses were performed for each mycotoxin. The LC/u.v./Fluorescence method detection limit (MDL) ranged from 0.02 to 6 ppb and the LC/MS/MS MDL ranged from 0.5 to 2.5 ppb, respectively. The recoveries of multi-mycotoxin fortified triplicate beer samples using the "Myco5inl" column ranged from 73% to 102%. Both analytical methods achieved good separations and detections.
机译:用混合床(“MyCO5Inl”提取强化啤酒基族脱氧毒素(Don),黄曲霉毒素B_1,B_2,G_1,G_2,B_3,Zearalenone(oon),B_3,Zearalenone(oon)和ochratoxin a(ota)的脱氧毒素(Don),黄曲霉毒素b_1,b_2,b_3,zearalenone(ota)(“myco5inl “)免疫亲和力柱,并使用具有柱柱衍生化和现代LC / MS / MS技术的经典LC /紫外/荧光检测。使用反相C_(18)柱进行HPLC分离。在正ESI模式下进行质谱测量。对每种霉菌毒素进行多次反应监测(MRM)分析。 LC / U.V. /荧光方法检测限(MDL)范围为0.02至6ppb,LC / MS / MS MDL分别为0.5至2.5ppb。使用“MyCO5InL”柱的多霉菌毒素强化三份啤酒样品的回收率范围为73%至102%。两种分析方法都取得了良好的分离和检测。

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