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

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 a...

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Main Authors: Park, Tu San, Cho, Soohee, Nahapetian, Tigran G., Yoon, Jeong-Yeol
Other Authors: Department of Agricultural and Biosystems Engineering, University of Arizona
Language:en
Published: SLAS TECHNOLOGY 2017
Subjects:
UVA
Online Access:http://hdl.handle.net/10150/623058
http://arizona.openrepository.com/arizona/handle/10150/623058
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spelling ndltd-arizona.edu-oai-arizona.openrepository.com-10150-6230582017-04-09T03:00:43Z Smartphone Detection of UV LED-Enhanced Particle Immunoassay on Paper Microfluidics Park, Tu San Cho, Soohee Nahapetian, Tigran G. Yoon, Jeong-Yeol Department of Agricultural and Biosystems Engineering, University of Arizona Biomedical Engineering Graduate Interdisciplinary Program, University of Arizona light scatter Escherichia coli whole blood UVA CMOS camera 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. 2017-02 Article Smartphone Detection of UV LED-Enhanced Particle Immunoassay on Paper Microfluidics 2017, 22 (1):7 SLAS Technology 2472-6303 2472-6311 10.1177/2211068216639566 http://hdl.handle.net/10150/623058 http://arizona.openrepository.com/arizona/handle/10150/623058 SLAS Technology en http://journals.sagepub.com/doi/10.1177/2211068216639566 © 2016 Society for Laboratory Automation and Screening SLAS TECHNOLOGY
collection NDLTD
language en
sources NDLTD
topic light scatter
Escherichia coli
whole blood
UVA
CMOS camera
spellingShingle light scatter
Escherichia coli
whole blood
UVA
CMOS camera
Park, Tu San
Cho, Soohee
Nahapetian, Tigran G.
Yoon, Jeong-Yeol
Smartphone Detection of UV LED-Enhanced Particle Immunoassay on Paper Microfluidics
description 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.
author2 Department of Agricultural and Biosystems Engineering, University of Arizona
author_facet Department of Agricultural and Biosystems Engineering, University of Arizona
Park, Tu San
Cho, Soohee
Nahapetian, Tigran G.
Yoon, Jeong-Yeol
author Park, Tu San
Cho, Soohee
Nahapetian, Tigran G.
Yoon, Jeong-Yeol
author_sort Park, Tu San
title Smartphone Detection of UV LED-Enhanced Particle Immunoassay on Paper Microfluidics
title_short Smartphone Detection of UV LED-Enhanced Particle Immunoassay on Paper Microfluidics
title_full Smartphone Detection of UV LED-Enhanced Particle Immunoassay on Paper Microfluidics
title_fullStr Smartphone Detection of UV LED-Enhanced Particle Immunoassay on Paper Microfluidics
title_full_unstemmed Smartphone Detection of UV LED-Enhanced Particle Immunoassay on Paper Microfluidics
title_sort smartphone detection of uv led-enhanced particle immunoassay on paper microfluidics
publisher SLAS TECHNOLOGY
publishDate 2017
url http://hdl.handle.net/10150/623058
http://arizona.openrepository.com/arizona/handle/10150/623058
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AT chosoohee smartphonedetectionofuvledenhancedparticleimmunoassayonpapermicrofluidics
AT nahapetiantigrang smartphonedetectionofuvledenhancedparticleimmunoassayonpapermicrofluidics
AT yoonjeongyeol smartphonedetectionofuvledenhancedparticleimmunoassayonpapermicrofluidics
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