研究目的
To develop a low-cost, high-throughput nanofabrication methodology for producing large-area plasmonic nanogap antennas for sensitive label-free biosensing, specifically targeting the detection of miRNA-210, a biomarker for lung cancer.
研究成果
The developed method allows for the production of large-area plasmonic nanogap antennas with features suitable for direct label-free biosensing. The biosensing performance was demonstrated by the direct detection of miRNA-210, achieving a LOD of 0.78 nM without amplification steps, indicating promising applications in clinical biosensing.
研究不足
The fabrication method exhibits slightly lower resolution than more expensive methods like e-beam lithography. Variations in the dimensions of the antennas arms and the gap size are observed, attributed to the size dispersion of the latex NPs.
1:Experimental Design and Method Selection:
A modified protocol of the colloidal hole-mask lithography (HCL) process was used to fabricate nanoplasmonic chips of randomly distributed arrays of gold nanogap antennas on glass substrates.
2:Sample Selection and Data Sources:
Glass substrates were cleaned and silanized, followed by the deposition of a PMMA layer and the application of a cationic solution to fix nanoparticles.
3:List of Experimental Equipment and Materials:
Equipment included an e-gun evaporator, reactive ion etcher, and optical setup components. Materials included gold, titanium, PMMA, and latex nanoparticles.
4:Experimental Procedures and Operational Workflow:
The process involved the evaporation of a Ti sacrificial layer, selective etching of PMMA, tilted metal e-beam evaporation of Au, and a lift-off process to expose the Au nanogap antennas.
5:Data Analysis Methods:
Optical characterization was performed using an ATR configuration, and numerical simulations were conducted using FDTD methods.
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