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Analytical Procedures for the Determination of Aflatoxin B-1 in Eggs of Laying Hens Using Immunoaffinity Columns and Liquid Chromatography with Post-Column Derivatisation and Fluorescence Detection

机译:免疫亲和柱和液相色谱-柱后衍生和荧光检测法测定蛋鸡中黄曲霉毒素B-1的分析程序

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摘要

An analytical procedure for the determination of aflatoxin B-1 in eggs was introduced and validated in laboratory 1. The method consisted of the extraction of aflatoxin B-1 from a sample, purification of the extract with solvents, immunoaffinity column cleanup and the determination by liquid chromatography with post-column bromination and fluorescence detection at lambda (ex) = 362 nm and lambda (em) = 425 nm. The method was transferred to laboratory 2, where it was modified and validated. The limit of detection (LOD) and limit of quantification (LOQ) obtained in laboratory 1 were 2 and 6 ng/kg, respectively, and 2 and 5 ng/kg in laboratory 2, respectively. The repeatability of measurements in laboratory 1, represented by differences between results of duplicate measurements, was 10 ng/kg at the contamination level of 50 ng/kg. At the same concentration level, the standard deviation (s (R)) and the relative standard deviation (RSD (R)) for the within-laboratory reproducibility were 5.5 ng/kg and 11 %, respectively, and the measurement uncertainty was +/- 10 ng/kg. The mean recovery was 70 %. In laboratory 2, the repeatability of measurements at the contamination level of 20 ng/kg, represented by the standard deviation (s (R)), repeatability (r) and relative standard deviation (RSD (R)) was 4 ng/kg, 11 ng/kg and 20 %, respectively, and the recovery was 67 %. The results indicate that the procedures are suitable for the determination of aflatoxin B-1 in eggs and can be implemented for the routine analysis. Using the procedure validated in laboratory 1, 25 samples from farms in Slovenia were analysed. In none of the analysed samples, aflatoxin B-1 was detected.
机译:介绍了一种测定鸡蛋中黄曲霉毒素B-1的分析方法,并在实验室1中进行了验证。该方法包括从样品中提取黄曲霉毒素B-1,用溶剂纯化提取物,免疫亲和柱净化以及通过液相色谱柱后溴化和荧光检测,λ(ex)= 362 nm,λ(em)= 425 nm。该方法已转移到实验室2,在此进行了修改和验证。在实验室1中获得的检出限(LOD)和定量限(LOQ)分别为2和6 ng / kg,在实验室2中分别为2和5 ng / kg。以重复测量结果之间的差异表示的实验室1中测量的可重复性为10 ng / kg,污染水平为50 ng / kg。在相同浓度水平下,实验室内重现性的标准偏差(s(R))和相对标准偏差(RSD(R))分别为5.5 ng / kg和11%,测量不确定度为+ / -10 ng / kg。平均回收率为70%。在实验室2中,在20 ng / kg污染水平下,测量的可重复性由标准偏差(s(R)),可重复性(r)和相对标准偏差(RSD(R))表示,为4 ng / kg,分别为11 ng / kg和20%,回收率为67%。结果表明该方法适用于鸡蛋中黄曲霉毒素B-1的测定,可用于常规分析。使用在实验室1中验证的程序,分析了来自斯洛文尼亚农场的25个样本。在所有分析样品中均未检测到黄曲霉毒素B-1。

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