Portable Optofluidic Device for Dynamic Binding Analysis in Field-Settings

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Date

2024

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SPIE

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Yes

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Abstract

Compact and portable biosensing technologies play an important role in replacing traditional counterparts that require costly and heavy equipment, as well as complex infrastructure. The integration of these easy-to-use and cheap devices allows for the conducting of biosensing analyses in resource-limited settings. The study produced a portable optofluidic platform that is lightweight (260 g) and compact (16 cm×10 cm×11 cm). It combines subwavelength nanohole arrays, microfluidics technology, and on-chip computational imaging. It records plasmonic diffraction field images with a CMOS imager and an LED light, allowing for a large field of view for refractive index measurement. This LED source generates diffraction patterns on the imager. The microfluidic pump confirms accurate analyte delivery, allowing real-time analysis of diffraction field images to reveal time-dependent binding kinetics of biomolecules. It identifies biomolecular interactions without labelling, allowing for the detection and quantification of biomolecules. Our platform has an outstanding limit-of-detection (LOD) of 5ng/mL for label-free detection of protein IgG. We effectively determined the association and dissociation constants for protein A/G and IgG binding using real-time diffraction field images. The optofluidic biosensor platform is ideal for surface plasmon resonance (SPR) in field applications. It can monitor interactions in real-time, making it useful for studying the way various biological and chemical compounds bind in many areas. © 2024 SPIE.

Description

The Society of Photo-Optical Instrumentation Engineers (SPIE)
Biophotonics in Point-of-Care III 2024 -- 10 April 2024 through 12 April 2024 -- Strasbourg -- 200984

Keywords

Computational imaging, Label-free biosensing, Microfluidics, Plasmonics, Computational Imaging, Diffraction, Dissociation, Light emitting diodes, Microfluidics, Plasmonics, Proteins, Refractive index, Surface plasmon resonance, Biosensing, Computational imaging, Diffraction fields, Dynamic binding, Field images, In-field, Label-free biosensing, Optofluidic devices, Plasmonics, Real- time, Biomolecules

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Q4
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Proceedings of SPIE - The International Society for Optical Engineering

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13008

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