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Rapid, low cost thin-layer chromatographic screening method for the detection of ochratoxin A in green coffee at a control level of 10 mu g/kg

机译:快速,低成本的薄层色谱筛选方法,用于检测生豆中的曲霉毒素A,控制水平为10μg / kg

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摘要

A thin-layer chromatographic (TLC) screening method was developed for the detection of ochratoxin A (OTA) in green coffee at a control level of 10 mug/kg. The method is based on extraction of OTA with a mixture of phosphoric acid and dichloromethane, purification by liquid-liquid partition into sodium hydrogen carbonate, separation by normal-phase TLC, and detection by visual estimation of fluorescence intensity under a UV lamp at 366 nm. The method was validated by performing replicate analyses of uncontaminated green coffee material spiked at 3 different levels of OTA (5, 10, and 20 mug/kg), and also by comparing results obtained on a series of test trial green coffees naturally contaminated with OTA (range 0.2 to 136.7 mug/kg) with those measured by a quantitative immunoaffinity/HPLC method. The agreement between the two methods was excellent, and neither false positive nor false negative results were recorded. This screening method is rapid, simple, robust, and very cheap, which makes it particularly well adapted for implementation in coffee-producing countries.
机译:开发了一种薄层色谱(TLC)筛选方法,用于检测生豆中的曲霉毒素A(OTA),控制水平为10杯/千克。该方法基于以下步骤:用磷酸和二氯甲烷的混合物萃取OTA;通过液-液分配纯化为碳酸氢钠;通过正相TLC进行分离;以及在366 nm的紫外灯下通过目测估计荧光强度进行检测。通过对3种不同水平的OTA(5、10和20杯/千克)加标的未污染生咖啡原料进行重复分析并通过比较一系列被OTA天然污染的试验生咖啡豆获得的结果进行验证,从而验证了该方法的有效性。 (范围0.2至136.7马克杯/千克),并采用定量免疫亲和/ HPLC方法进行测量。两种方法之间的一致性极好,且未记录假阳性或假阴性结果。这种筛选方法快速,简单,耐用且非常便宜,这使其特别适合在咖啡生产国实施。

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