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首页> 外文期刊>Journal of AOAC International >Determination of aflatoxin in processed dried cassava root: validation of a new analytical method for cassava flour.
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Determination of aflatoxin in processed dried cassava root: validation of a new analytical method for cassava flour.

机译:木薯干根中黄曲霉毒素的测定:木薯粉新分析方法的验证。

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摘要

A new method using HPLC with a photochemical reactor for enhanced detection was developed and validated for the determination of aflatoxins in cassava meal. Samples were spiked with a mixture of 4 aflatoxins at 5, 10 and 20 mug/kg mixed with either 1 or 5 g NaCl and extracted with methanol-water (80 + 20, v/v) by shaking for 10 or 30 min. An immunoaffinity column was used for cleanup. HPLC with postcolumn derivatization, for enhancement of aflatoxin fluorescence, and fluorescence determination were used for quantitation of the toxin concentration. The method was validated for recovery, linearity and precision at the 3 concentrations tested. Recovery ranges were 52-70, 69-85 and 80-89% for spiking levels of 5.0, 10.0 and 20.0 mug/kg, respectively. Results indicated that the amount of salt (NaCl) added and shaking time are critical factors in this method; optimal performance was achieved when 1 g salt was used and the shaking time was 10 min. The good linearity and precision of the method allowed baseline separation from interference, e.g. from coumarins.
机译:开发了一种使用HPLC和光化学反应器进行增强检测的新方法,并已验证了木薯粉中黄曲霉毒素的测定方法。用5、10和20杯/千克的4种黄曲霉毒素与1或5克氯化钠混合的混合物加标样品,并通过摇动10或30分钟用甲醇-水(80 + 20,v / v)萃取。免疫亲和柱用于清洁。采用柱后衍生化HPLC增强黄曲霉毒素荧光,并使用荧光测定法定量毒素浓度。验证了该方法在3种浓度下的回收率,线性和精密度。峰值浓度分别为5.0、10.0和20.0杯/千克时,回收率分别为52-70%,69-85%和80-89%。结果表明,添加盐(NaCl)的量和振荡时间是该方法的关键因素。当使用1 g盐和振摇时间为10分钟时,可获得最佳性能。该方法具有良好的线性和精密度,可将基线从干扰中分离出来,例如来自香豆素。

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