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Fluorescence enhancement and multiple protein detection in ZnO nanostructure microfluidic devices
Chen-Hsiang Sang1, Shu-Jen Chou2, F M Pan1
1Institute of Nanotechnology/Department of Materials Science and Engineering, National Chiao Tung University, 1001 Ta-Hsueh Road, Hsinchu 30050, Taiwan.
Biosensors & Bioelectronics
|September 1, 2015
Summary
Sharp zinc oxide nanowires show superior performance in biomolecule detection within microfluidic channels. These nanostructures offer enhanced sensitivity and dynamic range for detecting proteins and other biomolecules, enabling multiplexed assays.
Area of Science:
- Materials Science
- Nanotechnology
- Biomedical Engineering
Background:
- Microfluidic devices enable precise control over small fluid volumes, crucial for sensitive biomolecule detection.
- Zinc oxide (ZnO) nanostructures offer unique optical and electrical properties suitable for biosensing applications.
- Surface modification is essential for immobilizing biomolecules and ensuring specific binding events.
Purpose of the Study:
- To investigate and compare the biomolecule binding properties of different ZnO nanostructures (nanowires, rods, hexahedral-puncheon) grown in microfluidic channels.
- To evaluate the sensitivity and dynamic range of sharp ZnO nanowires for detecting streptavidin and specific proteins (IgG).
- To demonstrate the capability of sharp ZnO nanowires for multiplexed protein detection in a microfluidic array.
Main Methods:
- Growth of various ZnO nanostructures on glass substrates within microfluidic channels.
- Surface functionalization of ZnO nanostructures using 3-aminopropyl-triethoxysilane (3-APTES) and NHS-biotin.
- Infusion of dye-conjugated streptavidin and anti-IgG antibodies at varying concentrations through orthogonal microfluidic channels.
- Fluorescence intensity measurements at crossover areas to quantify biomolecule binding.
- Characterization of protein detection using sharp ZnO nanowires with varying concentrations of anti-mouse IgG.
- Demonstration of multiplexed detection using a microfluidic array for simultaneous detection of anti-mouse and anti-rabbit IgG.
Main Results:
- Sharp ZnO nanowires exhibited the largest dynamic range and highest fluorescent intensity compared to other ZnO morphologies.
- Simulated and experimental results for biomolecule binding showed good agreement.
- Sharp ZnO nanowires successfully detected protein concentrations ranging from 417 fM to 41.7 nM.
- Multiplexed detection of two different dye-conjugated antibodies (anti-mouse IgG and anti-rabbit IgG) was clearly demonstrated using sharp ZnO nanowires in a microfluidic array.
Conclusions:
- Sharp ZnO nanowires are highly effective for sensitive and specific biomolecule detection in microfluidic systems.
- The morphology of ZnO nanostructures significantly influences their performance in biosensing applications.
- The developed microfluidic platform with sharp ZnO nanowires holds promise for advanced diagnostics and high-throughput screening.

