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基于智能手机的读取系统与藻蓝蛋白增强的乳胶纳米球免疫分析集成,用于现场测定食品中的黄曲霉毒素 B1。

Smartphone-based reading system integrated with phycocyanin-enhanced latex nanospheres immunoassay for on-site determination of aflatoxin B1 in foodstuffs.

机构信息

College of Chemistry, Fuzhou University, No. 2 Xueyuan Road, Fuzhou 350108, China.

College of Chemistry, Fuzhou University, No. 2 Xueyuan Road, Fuzhou 350108, China; Fujian Key Laboratory of Medical Instrument and Pharmaceutical Technology, Fuzhou University, No. 2 Xueyuan Road, Fuzhou 350108, China.

出版信息

Food Chem. 2021 Oct 30;360:130019. doi: 10.1016/j.foodchem.2021.130019. Epub 2021 May 6.

Abstract

Traditional methods for aflatoxin B1 (AFB1) detection are complex, time-consuming, labor-intensive, and high cost. Moreover, they require sophisticated large-scale instrumentation, which limits their on-site rapid detection. Herein, phycocyanin fluorescent nanospheres based on fluorescence immunochromatographic assay were developed for quantitative detection of AFB1 at parts-per-billion (ppb) levels in foodstuffs. Phycocyanin and anti-AFB1 monoclonal antibodies were coupled on the surface of latex nanospheres to amplify the fluorescence signal and improve the sensitivity. The fluorescence intensity was measured by a self-developed smartphone-based reading system. Under the optimal conditions, this approach achieved quantitative point-of-care detection of AFB1 within 25 min. The calibration curve for AFB1 was linear in the range of 0.2-48 ppb, and the limit of detection was 0.16 ppb. The practical applicability of the proposed approach was demonstrated by the determination of AFB1 in naturally contaminated samples, and the results were consistent with HPLC detection.

摘要

传统的黄曲霉毒素 B1(AFB1)检测方法复杂、耗时、费力且成本高。此外,它们需要复杂的大型仪器,限制了其现场快速检测。在此,我们基于荧光免疫层析法开发了藻蓝蛋白荧光纳米球,用于定量检测食品中 ppb 级别的 AFB1。藻蓝蛋白和抗 AFB1 单克隆抗体被偶联到乳胶纳米球表面,以放大荧光信号并提高灵敏度。荧光强度通过我们自主研发的基于智能手机的读取系统进行测量。在最佳条件下,该方法可在 25 分钟内实现 AFB1 的现场定量检测。AFB1 的校准曲线在 0.2-48 ppb 范围内呈线性,检出限为 0.16 ppb。该方法在实际污染样品中的应用得到了验证,结果与 HPLC 检测一致。

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