Pan Yuxiang, Wei Xinwei, Liang Tao, Zhou Jie, Wan Hao, Hu Ning, Wang Ping
Biosensor National Special Laboratory, Key Laboratory for Biomedical Engineering of Education Ministry, Department of Biomedical Engineering, Zhejiang University, Hangzhou, 310027, China.
State Key Laboratory of Transducer Technology, Chinese Academy of Sciences, Shanghai, 200050, China.
Biomed Microdevices. 2018 Jul 13;20(3):60. doi: 10.1007/s10544-018-0304-6.
Okadaic acid (OA), a representative diarrhetic shellfish poisoning toxin, mainly produced by toxigenic dinoflagellates, has significant hazard to public health. Traditional methods for detection of OA can not give the consideration to the need of rapid, high sensitive, quantitative and in-situ detection at the same time. Herein, a new effective detection method of OA was developed based on fluorescence immunosensor and flow cytometry (FCM). In this assay, Streptavidin-coated magnetic beads (MBs) were used as the supporter to immobilize the biotinylated OA. Modified MBs competed with the free OA in the sample solution to bind with the anti-OA monoclonal antibody (OA-MAb). The R-phycoerythrin (R-PE) dye labeled IgG was served as a secondary antibody to perform fluorescence detection. A portable flow cytometry was applied for the in-situ fluorescence quantification. The results showed that the OA concentration was inversely proportional to the R-PE fluorescence intensity. The detection method took within 50 min with a limit of detection (LOD) was 0.05 μg/L and range from 0.2 to 20 μg/L for OA detection. Moreover, the matrix effect and the recovery rate were assessed during real sample measurement, showing a high recovery. Performance features such as high sensitivity, low LOD, speediness and simplicity of the analysis protocol, shows this biosensing-systems as a promising tool for routine use.
冈田酸(OA)是一种具有代表性的腹泻性贝类中毒毒素,主要由产毒的甲藻产生,对公众健康具有重大危害。传统的OA检测方法无法同时兼顾快速、高灵敏、定量和原位检测的需求。在此,基于荧光免疫传感器和流式细胞术(FCM)开发了一种新的有效的OA检测方法。在该检测中,链霉亲和素包被的磁珠(MBs)用作固定生物素化OA的载体。修饰后的MBs与样品溶液中的游离OA竞争结合抗OA单克隆抗体(OA-MAb)。用藻红蛋白(R-PE)标记的IgG作为二抗进行荧光检测。应用便携式流式细胞仪进行原位荧光定量。结果表明,OA浓度与R-PE荧光强度成反比。该检测方法耗时50分钟以内,检测限(LOD)为0.05μg/L,OA检测范围为0.2至20μg/L。此外,在实际样品测量过程中评估了基质效应和回收率,显示出高回收率。该生物传感系统具有高灵敏度、低检测限、快速和分析方案简单等性能特点,是一种很有前景的常规检测工具。