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将金超粒子整合到侧向流动免疫分析中,用于快速灵敏地检测牛奶中的大肠杆菌 O157:H7。

Integrated gold superparticles into lateral flow immunoassays for the rapid and sensitive detection of Escherichia coli O157:H7 in milk.

机构信息

State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, P. R. China; School of Food Science and Technology, Nanchang University, Nanchang 330047, P. R. China.

State Key Laboratory of Food Science and Technology, Nanchang University, Nanchang 330047, P. R. China; School of Food Science and Technology, Nanchang University, Nanchang 330047, P. R. China.

出版信息

J Dairy Sci. 2020 Aug;103(8):6940-6949. doi: 10.3168/jds.2019-17934. Epub 2020 May 29.

Abstract

Escherichia coli O157:H7 is a common harmful foodborne pathogen that can cause severe diseases at low infectious doses. Traditional lateral flow immunoassay (LFIA) for the rapid screening of E. coli O157:H7 in food suffers from low sensitivity due to its dependence on 20- to 40-nm gold nanoparticles (AuNP) with insufficient brightness as labels. To address this issue, we reported for the first time the successful synthesis of gold superparticles (GSP) by encapsulating numerous small AuNP into a polymer nanobead using an evaporation-induced self-assembly method. Results indicated that the resultant GSP exhibited remarkably enhanced absorbance compared with the most widely used 40 nm AuNP in LFIA. In addition, the absorbance of GSP could be easily tuned by varying GSP sizes. Under optimized conditions, we achieved a rapid and sensitive determination of E. coli O157:H7 in milk with a detection limit of 5.95 × 10 cfu/mL when using the GSP with a size of 342 nm as LFIA signal reporters, exhibiting improvement of approximately 32-fold relative to the conventional 40 nm AuNP-LFIA method. We further demonstrated the selectivity, accuracy, reliability, and practicality of the proposed GSP-LFIA strip. In summary, this work offers a new strategy for improving LFIA sensitivity using assembled GSP as markers and demonstrates huge potential in rapidly and sensitively detecting foodborne pathogens.

摘要

大肠杆菌 O157:H7 是一种常见的食源性有害病原体,其低传染性剂量即可引发严重疾病。传统的侧向流动免疫分析(LFA)用于快速筛选食品中的大肠杆菌 O157:H7,由于其依赖于亮度不足的 20-40nm 金纳米颗粒(AuNP)作为标记物,因此灵敏度较低。为了解决这个问题,我们首次报道了通过蒸发诱导自组装方法将大量小 AuNP 封装在聚合物纳米珠中成功合成金超粒子(GSP)。结果表明,与 LFA 中最广泛使用的 40nm AuNP 相比,所得 GSP 的吸光度显著增强。此外,通过改变 GSP 的尺寸可以轻松调节 GSP 的吸光度。在优化条件下,当使用尺寸为 342nm 的 GSP 作为 LFA 信号报告物时,我们实现了对牛奶中大肠杆菌 O157:H7 的快速灵敏检测,检测限为 5.95×10 cfu/mL,与传统的 40nm AuNP-LFA 方法相比,灵敏度提高了约 32 倍。我们进一步证明了所提出的 GSP-LFA 条带的选择性、准确性、可靠性和实用性。总之,这项工作提供了一种使用组装的 GSP 作为标记物来提高 LFA 灵敏度的新策略,并展示了在快速灵敏检测食源性病原体方面的巨大潜力。

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