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    Smartphone Detection of UV LED-Enhanced Particle Immunoassay on Paper Microfluidics

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    Yoon_UV_LED_UA_Repository.pdf
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    Final Accepted Manuscript
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    Author
    Park, Tu San
    Cho, Soohee
    Nahapetian, Tigran G.
    Yoon, Jeong-Yeol
    Affiliation
    Department of Agricultural and Biosystems Engineering, University of Arizona
    Biomedical Engineering Graduate Interdisciplinary Program, University of Arizona
    Issue Date
    2017-02
    Keywords
    light scatter
    Escherichia coli
    whole blood
    UVA
    CMOS camera
    
    Metadata
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    Publisher
    SLAS TECHNOLOGY
    Citation
    Smartphone Detection of UV LED-Enhanced Particle Immunoassay on Paper Microfluidics 2017, 22 (1):7 SLAS Technology
    Journal
    SLAS Technology
    Rights
    © 2016 Society for Laboratory Automation and Screening.
    Collection Information
    This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
    Abstract
    Use of a smartphone as an optical detector for paper microfluidic devices has recently gained substantial attention due to its simplicity, ease of use, and handheld capability. Utilization of a UV light source enhances the optical signal intensities, especially for the particle immunoagglutination assay that has typically used visible or ambient light. Such enhancement is essential for true assimilation of assays to field deployable and point-of-care applications by greatly reducing the effects by independent environmental factors. This work is the first demonstration of using a UV LED (UVA) to enhance the Mie scatter signals from the particle immunoagglutination assay on the paper microfluidic devices and subsequent smartphone detection. Smartphone's CMOS camera can recognize the UVA scatter from the paper microfluidic channels efficiently in its green channel. For an Escherichia coli assay, the normalized signal intensities increased up to 50% from the negative signal with UV LED, compared with the 4% to 7% with ambient light. Detection limit was 10 colony-forming units/mL. Similar results were obtained in the presence of 10% human whole blood.
    ISSN
    2472-6303
    2472-6311
    DOI
    10.1177/2211068216639566
    Version
    Final accepted manuscript
    Sponsors
    Seoul VioSys, Ansan, Gyeonggi, Republic of Korea; Richard A. Harvill graduate fellowship
    Additional Links
    http://journals.sagepub.com/doi/10.1177/2211068216639566
    ae974a485f413a2113503eed53cd6c53
    10.1177/2211068216639566
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    UA Faculty Publications

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