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一种用于即时检测复杂基质中葡萄球菌肠毒素 B 的离心微流控芯片。

A centrifugal microfluidic chip for point-of-care testing of staphylococcal enterotoxin B in complex matrices.

机构信息

Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, P. R. China.

Key Laboratory of Luminescent and Real-Time Analytical System (Southwest University), Chongqing Science and Technology Bureau, College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, P. R. China.

出版信息

Nanoscale. 2022 Jan 27;14(4):1380-1385. doi: 10.1039/d1nr05599b.

Abstract

Staphylococcal enterotoxin B (SEB) is a typical biological toxin that causes food poisoning. Currently reported SEB detection methods have the drawbacks of sophisticated sample preparation and being time-consuming and labor-intensive. Herein, we propose a strategy based on an immune sandwich structure operating on a centrifugal microfluidic chip for point-of-care testing (POCT) of SEB. The fluorescent microparticle-labeled primary antibody (CM-EUs-Ab), capture antibody (CAb), and goat anti-mouse IgG antibody (SAb) were modified on the bond area, T-area, and C-area, respectively. When SEB was added, it first reacted with the CM-EUs-Ab through the specific recognition between SEB and the Ab. Then, under capillarity, the conjugates of SEB and the CM-EUs-Ab were captured by the CAb when they flowed to the T-area, and the remaining CM-EUs-Ab bound with the SAb in the C-area. Finally, this chip was put into a dry fluorescence detection analyzer for centrifugation and on-site detection of SEB. The fluorescence intensity ratio of the T-area to the C-area was positively correlated with the concentration of SEB. The resulting linear range was 0.1-250 ng mL, and the limit of detection (3/) was 68 pg mL. This POCT platform only needs 20 μL of sample and can realize the full process of detection within 12 min. This chip also exhibits good stability for 35 days. Additionally, the proposed method has been successfully utilized for the detection of SEB in urine, milk, and juice without any pre-treatment of the samples. Thus, this platform is expected to be applied to food safety testing and clinical diagnosis.

摘要

金黄色葡萄球菌肠毒素 B(SEB)是一种典型的生物毒素,可引起食物中毒。目前报道的 SEB 检测方法存在样品制备复杂、耗时耗力的缺点。在此,我们提出了一种基于免疫夹心结构的策略,该策略在离心微流控芯片上运行,用于 SEB 的即时检测(POCT)。荧光微粒子标记的一抗(CM-EUs-Ab)、捕获抗体(CAb)和山羊抗小鼠 IgG 抗体(SAb)分别修饰在键合区、T 区和 C 区。当加入 SEB 时,它首先通过 SEB 和 Ab 之间的特异性识别与 CM-EUs-Ab 反应。然后,在毛细作用下,当混合物流到 T 区时,SEB 和 CM-EUs-Ab 的缀合物被 CAb 捕获,而剩余的 CM-EUs-Ab 与 C 区中的 SAb 结合。最后,将该芯片放入干燥荧光检测仪中进行离心和现场检测 SEB。T 区与 C 区的荧光强度比值与 SEB 的浓度呈正相关。所得线性范围为 0.1-250ng mL,检测限(3/)为 68pg mL。这种 POCT 平台仅需 20μL 样品,可在 12min 内完成整个检测过程。该芯片在 35 天内表现出良好的稳定性。此外,该方法已成功用于尿液、牛奶和果汁中 SEB 的检测,无需对样品进行任何预处理。因此,该平台有望应用于食品安全检测和临床诊断。

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