首页> 外文期刊>Czech Journal of Food Sciences >Analysis of ochratoxin A in malt beverage samples using dispersive liquid–liquid microextraction coupled with liquid chromatography-fluorescence detection
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Analysis of ochratoxin A in malt beverage samples using dispersive liquid–liquid microextraction coupled with liquid chromatography-fluorescence detection

机译:分散液液微萃取-液相色谱-荧光检测法分析麦芽饮料样品中的och曲霉毒素A

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A simple and economic pro cedure based on dispersive liquid–liquid microextraction has been applied to extract and pre-concentrate trace levels of ochratoxin A (OTA) in malt beverage prior to analysis using high performance liquid chromatography with fluorescence detection. The method was based on the formation of fine droplets of a water-immiscible extraction solvent in the sample solution using a water-miscible disperser solvent. The influences of vari -ous parameters such as the type and volume of extraction and disperser solvents, centrifuging time, sonication time, and salt concentration on the extraction efficiency of ochratoxin A were investigated. Under optimum conditions, the relative standard deviations for five replicates of 2 ng/ml of OTA were 3.4% as within-day and 6.2% as between-day precisions. The detection limit (S/N = 3) was 0.1 ng/ml and the mean recoveries of OTA from malt beverage samples at spiking levels of 0.5, 2, and 4 ng/ml were in the range of 104–108.2%
机译:在使用高效液相色谱和荧光检测进行分析之前,基于分散液-液微萃取的一种简单,经济的方法已被用于提取和预浓缩麦芽饮料中痕量的曲霉毒素A(OTA)。该方法基于使用水混溶分散剂在样品溶液中形成水不混溶萃取溶剂的细小液滴。研究了萃取和分散溶剂的类型和体积,离心时间,超声处理时间和盐浓度等各种参数对曲霉毒素A萃取效率的影响。在最佳条件下,两次重复2 ng / ml OTA的相对标准偏差为日内精度为3.4%,日间精度为6.2%。检出限(S / N = 3)为0.1 ng / ml,加标浓度为0.5、2和4 ng / ml的麦芽饮料样品中OTA的平均回收率在104-108.2%的范围内

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