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Point-of-care molecular diagnostics can provide efficient and cost-effective medical care, and they have the potential to fundamentally change our approach to global health. However, most existing approaches are not scalable to include multiple biomarkers. As a solution, we have combined

Point-of-care molecular diagnostics can provide efficient and cost-effective medical care, and they have the potential to fundamentally change our approach to global health. However, most existing approaches are not scalable to include multiple biomarkers. As a solution, we have combined commercial flat panel OLED display technology with protein microarray technology to enable high-density fluorescent, programmable, multiplexed biorecognition in a compact and disposable configuration with clinical-level sensitivity. Our approach leverages advances in commercial display technology to reduce pre-functionalized biosensor substrate costs to pennies per cm[superscript 2]. Here, we demonstrate quantitative detection of IgG antibodies to multiple viral antigens in patient serum samples with detection limits for human IgG in the 10 pg/mL range. We also demonstrate multiplexed detection of antibodies to the HPV16 proteins E2, E6, and E7, which are circulating biomarkers for cervical as well as head and neck cancers.

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    Title
    • Application of Flat Panel OLED Display Technology for the Point-of-Care Detection of Circulating Cancer Biomarkers
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    Date Created
    2016-07-04
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    Identifier
    • Digital object identifier: 10.1038/srep29057
    • Identifier Type
      International standard serial number
      Identifier Value
      2045-2322
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    • The final version of this article, as published in Scientific Reports, can be viewed online at: https://www.nature.com/articles/srep29057

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    Katchman, B. A., Smith, J. T., Obahiagbon, U., Kesiraju, S., Lee, Y., O’Brien, B., . . . Anderson, K. S. (2016). Application of flat panel OLED display technology for the point-of-care detection of circulating cancer biomarkers. Scientific Reports, 6(1). doi:10.1038/srep29057

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