A magnetic beads-based portable flow cytometry immunosensor for in-situ detection of marine biotoxin.

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 detec...

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Publicado en:Biomedical Microdevices Vol. 20; no. 3; pp. 1 - 2
Autores principales: Pan, Yuxiang, Wei, Xinwei, Liang, Tao, Zhou, Jie, Wan, Hao, Hu, Ning, Wang, Ping
Formato: Journal Article
Publicado: Springer Nature Sep2018
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Sep2018
      vid: 20
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s10544-018-0304-6
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        atl: A magnetic beads-based portable flow cytometry immunosensor for in-situ detection of marine biotoxin.
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        au:
          Pan, Yuxiang
          Wei, Xinwei
          Liang, Tao
          Zhou, Jie
          Wan, Hao
          Hu, Ning
          Wang, Ping
        affil: Biosensor National Special Laboratory, Key Laboratory for Biomedical Engineering of Education Ministry, Department of Biomedical Engineering, Zhejiang University, 310027, Hangzhou, China
      sug:
      ab: 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.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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