Laboratory of Food Analysis, Faculty of Pharmaceutical Sciences, Ghent University, Harelbekestraat 72, 9000, Ghent, Belgium,
Anal Bioanal Chem. 2013 Sep;405(24):7795-802. doi: 10.1007/s00216-013-7096-6. Epub 2013 Jun 18.
A quantitative fluorescence-labeled immunosorbent assay and qualitative on-site column tests were developed for the determination of aflatoxin M1 in milk products. The use of liposomes loaded with quantum dots as a label significantly increased the assay sensitivity by encapsulating multiple quantum dots in a single liposome and, therefore, amplifying the analytical signal. Two different techniques were compared to obtain aflatoxin-protein conjugates, used for further coupling with the liposomes. The influence of nonspecific interactions of the liposome-labeled conjugates obtained with the surface of microtiter plates and column cartridges was evaluated and discussed. The limit of detection for fluorescence-labeled immunosorbent assay was 0.014 μg kg(-1). For qualitative on-site tests, the cutoff was set at 0.05μg kg(-1), taking into account the EU maximum level for aflatoxin M1 in raw milk, heat-treated milk, and milk for the manufacture of milk-based products. The direct addition of labeled conjugate to the milk samples resulted in an additional decrease of analysis time. An intralaboratory validation was performed with sterilized milk and cream samples artificially spiked with aflatoxin M1 at concentrations less than, equal to and greater than the cutoff level. It is shown that milk products can be analyzed without any sample preparation, just diluted with the buffer. The rates for false-positive and false-negative results were below 5% (2.6% and 3.3%, respectively).
建立了一种用于检测乳制品中黄曲霉毒素 M1 的定量荧光标记免疫吸附测定法和定性现场柱测试法。通过将多个量子点封装在单个脂质体中,使用负载量子点的脂质体作为标记物可显著提高测定法的灵敏度,从而放大分析信号。比较了两种不同的技术来获得黄曲霉毒素-蛋白缀合物,用于进一步与脂质体偶联。评估并讨论了获得的与微量滴定板和柱盒表面的非特异性相互作用的脂质体标记缀合物的影响。荧光标记免疫吸附测定法的检测限为 0.014μgkg(-1)。对于定性现场测试,考虑到欧盟对生奶、热处理奶和用于制造奶制品的奶中黄曲霉毒素 M1 的最大限量,将截止值设定为 0.05μgkg(-1)。将标记的缀合物直接添加到牛奶样品中会进一步缩短分析时间。在实验室内部验证中,使用经过消毒的牛奶和奶油样品进行了人工添加黄曲霉毒素 M1 的实验,添加浓度低于、等于和高于截止值。结果表明,无需进行任何样品制备,只需用缓冲液稀释,即可分析奶制品。假阳性和假阴性结果的比例均低于 5%(分别为 2.6%和 3.3%)。