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Determination of Ochratoxin A in Ready-To-Drink Coffee by Immunoaffinity Cleanup and Liquid Chromatography Tandem Mass Spectrometry

机译:免疫亲和净化和液相色谱-串联质谱法测定即饮咖啡中的ch曲毒素A

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摘要

We developed a simple and accurate method for determining ochratoxin A (OTA) in ready-to-drink coffee, using an immunoaffinity column for cleanup and liquid chromatography-tandem mass spectrometry (LC/MS/MS) for identification and quantification. When uniformly stable isotope-labeled OTA (U-[13C20]-OTA) was employed as an internal standard, the recovery rate of the method was 97.3% (the spiked OTA level was 0.10 ng/mL), the repeatability (relative standard deviation) was 1.9%, and the intermediate precision (relative standard deviation) was 4.0%. The limit of quantification was 0.0065 ng/mL based on a signal-to-noise ratio in coffee of 10:1. The developed method was used for the determination of OTA in ready-to-drink coffee. A total of 30 ready-to-drink coffee samples commercially available in Japan were analyzed. OTA was detected in all of the samples at concentrations ranging from trace levels (0.0020-0.010 ng/mL) to 0.037 ng/mL. This method was shown to be useful for accurately evaluating the intake of OTA from coffee beverages.
机译:我们开发了一种简单,准确的方法来测定即饮咖啡中的曲霉毒素A(OTA),使用免疫亲和柱进行净化,并使用液相色谱-串联质谱(LC / MS / MS)进行鉴定和定量。当使用统一稳定的同位素标记的OTA(U- [13C20] -OTA)作为内标时,该方法的回收率为97.3%(OTA浓度为0.10 ng / mL),可重复性(相对标准偏差)。 )为1.9%,中间精度(相对标准偏差)为4.0%。基于咖啡中信噪比为10:1的定量限为0.0065 ng / mL。所开发的方法用于测定即饮咖啡中的OTA。分析了总共30种在日本市售的即饮咖啡样品。在所有样品中检测到的OTA浓度范围为痕量水平(0.0020-0.010 ng / mL)至0.037 ng / mL。结果表明,该方法对于准确评估咖啡饮料中OTA的摄入量非常有用。

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