Handheld high-throughput plasmonic biosensor using computational on-chip imaging

被引:0
|
作者
Arif E Cetin
Ahmet F Coskun
Betty C Galarreta
Min Huang
David Herman
Aydogan Ozcan
Hatice Altug
机构
[1] Boston University,Department of Electrical and Computer Engineering
[2] Boston,Departments of Electrical Engineering and Bioengineering
[3] MA 02215,Division of Chemistry and Chemical Engineering
[4] USA,Departamento de Ciencias
[5] University of California,Quimica
[6] Los Angeles (UCLA),Bioengineering Department
[7] Los Angeles,undefined
[8] CA 90095,undefined
[9] USA,undefined
[10] California Institute of Technology,undefined
[11] Pasadena,undefined
[12] CA 91125,undefined
[13] USA,undefined
[14] Pontificia Universidad Catolica del Peru,undefined
[15] Avenida Universitaria 1801,undefined
[16] Ecole Polytechnique Federale de Lausanne (EPFL),undefined
[17] California NanoSystems Institute,undefined
[18] University of California Los Angeles,undefined
[19] Los Angeles (UCLA),undefined
[20] Los Angeles,undefined
[21] CA,undefined
[22] 90095,undefined
[23] USA,undefined
来源
Light: Science & Applications | 2014年 / 3卷
关键词
computational imaging; high-throughput biodetection; lens-free imaging; on-chip sensing; plasmonics; point of care diagnostics; telemedicine;
D O I
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中图分类号
学科分类号
摘要
We demonstrate a handheld on-chip biosensing technology that employs plasmonic microarrays coupled with a lens-free computational imaging system towards multiplexed and high-throughput screening of biomolecular interactions for point-of-care applications and resource-limited settings. This lightweight and field-portable biosensing device, weighing 60 g and 7.5 cm tall, utilizes a compact optoelectronic sensor array to record the diffraction patterns of plasmonic nanostructures under uniform illumination by a single-light emitting diode tuned to the plasmonic mode of the nanoapertures. Employing a sensitive plasmonic array design that is combined with lens-free computational imaging, we demonstrate label-free and quantitative detection of biomolecules with a protein layer thickness down to 3 nm. Integrating large-scale plasmonic microarrays, our on-chip imaging platform enables simultaneous detection of protein mono- and bilayers on the same platform over a wide range of biomolecule concentrations. In this handheld device, we also employ an iterative phase retrieval-based image reconstruction method, which offers the ability to digitally image a highly multiplexed array of sensors on the same plasmonic chip, making this approach especially suitable for high-throughput diagnostic applications in field settings.
引用
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页码:e122 / e122
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