谷物面粉中微量赭曲霉毒素A含量的快速准确测定:面向现场应用

Chrysoula-Evangelia Karachaliou, G. Koukouvinos, K. Pissaridi, D. Ladikos, D. Goustouridis, I. Raptis, E. Livaniou, S. Kakabakos, P. Petrou
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引用次数: 1

摘要

赭曲霉毒素是一些曲霉和青霉属真菌次生代谢产物产生的一类真菌毒素。赭曲霉毒素A (OTA)是这类毒素中毒性最大的一种,可以在咖啡、可可、葡萄酒和面粉等多种广泛食用的食物中找到。因此,要确保符合国家/欧洲法规规定的最大残留限量,并最大限度地减少消费者的健康风险,就必须可靠地确定食品样品中的OTA水平。本研究展示了一种基于白光反射光谱(WLRS)的无标签生物传感器,用于快速准确地测定谷物面粉样品中的OTA。将OTA -蛋白偶联物固定在硅片表面后,硅片表面覆盖1 μ m厚的热二氧化硅,起到传感器的作用。对于该检测,将内部开发的抗ota抗体与校准器或样品的混合物注射到芯片表面,然后与二级生物素化抗体和链霉亲和素反应以放大信号。通过记录免疫反应引起的反射干扰谱的偏移,实现了对发生在sio2 /Si芯片表面的免疫反应的无标记实时监测。这种位移通过适当的数学处理转换为有效的生物分子层厚度。优化后,该传感器能够在25分钟内检测浓度低至60 pg/mL的小麦粉样品中的OTA。该检测重复性好,内、间CVs分别≤5.9%和≤9.0%。该试验具有优异的分析特性和短的分析时间,再加上设备的小尺寸,使所提出的WLRS系统非常适合在需要的地方定量测定微量OTA水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fast and Accurate Determination of Minute Ochratoxin A Levels in Cereal Flours: Towards Application at the Field
: Ochratoxins are a group of mycotoxins produced as secondary metabolites by several fungi of Aspergillus and Penicillium species. Ochratoxin A (OTA) is the most toxic member of the group and can be found in a large variety of widely consumed foods, such as coffee, cocoa, wine, and flour. Reliable determination of OTA levels in food samples is therefore indispensable to ensure compliance with MRLs set by national/European regulations and minimize health risks for consumers. In the current study, a label-free biosensor based on white light reflectance spectroscopy (WLRS) for the rapid and accurate determination of OTA in cereal flour samples is demonstrated. A Si chip with a 1- µ m-thick thermal SiO 2 on top plays the role of transducer after the immobilization of an OTA– protein conjugate on its surface. For the assay, a mixture of an in-house-developed anti-OTA antibody with the calibrators or the samples is injected over the chip surface, followed by reaction with a secondary biotinylated antibody and streptavidin for signal amplification. The label-free, real-time monitoring of immunoreactions occurring on the SiO 2 /Si chip surface is achieved by recording the shift in the reflected interference spectrum caused by the immunoreactions. This shift is converted through appropriate mathematical processing to an effective biomolecular adlayer thickness. After optimization, the sensor is capable of detecting OTA in wheat flour samples at concentrations as low as 60 pg/mL within 25 min. The assay is repeatable, with intra- and inter-assay CVs ≤ 5.9% and ≤ 9.0%, respectively. The assay’s excellent analytical characteristics and short analysis time, in combination with the small size of the device, render the proposed WLRS system ideal for the quantitative determination of minute OTA levels at the point-of-need.
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