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Detection of staphylococcal enterotoxin B in spiked food samples.

机译:加标食品样品中葡萄球菌肠毒素B的检测。

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摘要

Contamination of food with infectious agents, intentional or not, is a global concern with far-reaching economic and social impact. Staphylococcal enterotoxins are a major cause of food poisoning, but most methods for the identification of these agents in food require extensive pretreatment or concentration of the sample prior to analysis. The array biosensor was developed as a portable device for the simultaneous analysis of multiple complex samples for multiple targets with minimal sample preparation. In this study, we use an array biosensor to expand and improve on a staphylococcal enterotoxin B (SEB) assay with the ultimate intent of incorporating testing for SEB into a battery of sensitive and convenient assays for food safety validation. In addition to buffer studies, six different types of food samples, including beverages, homogenates of fruit and meat, and carcass washings, were spiked with SEB, incubated for at least 2 h to permit antigen sequestration, and assayed. For all samples, there were differences in fluorescence intensity, but 0.5 ng of SEB per ml could be detected in <20 min with little if any pretreatment and no sample preconcentration.
机译:食品是否被传染性物质污染,无论是有意还是无意,都是全球性的问题,对经济和社会产生深远影响。葡萄球菌肠毒素是食物中毒的主要原因,但是大多数在食品中鉴定这些物质的方法都需要进行大量的预处理或在分析前对样品进行浓缩。阵列生物传感器被开发为一种便携式设备,可以用最少的样品制备同时分析多个目标的多个复杂样品。在这项研究中,我们使用阵列生物传感器来扩展和改进葡萄球菌肠毒素B(SEB)检测,最终目的是将SEB检测纳入一系列敏感且方便的检测中,以进行食品安全性验证。除缓冲液研究外,还将六种不同类型的食物样品(包括饮料,水果和肉的匀浆以及car体洗液)掺入SEB,孵育至少2小时以进行抗原隔离,并进行分析。对于所有样品,荧光强度都有差异,但是在<20分钟内可以检测到0.5 ng SEB / ml,几乎没有任何预处理,也没有样品预浓缩。

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