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Surface Enhanced Raman Spectroscopy Detection of Biomolecules Using EBL Fabricated Nanostructured Substrates
Published on: March 20, 2015
Biomembrane-Inspired Plasmonic Superstructures with Phenolic-Resin Artificial Pockets for Enantioselective
Danning Wang1, Siyu Wang1, Wenying Xu1
1Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education Zhejiang Key Laboratory of Organosilicon Material Technology, College of Material, Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou 311121, China.
We developed novel SiO2@Au@RF superstructures for ligand-free chiral discrimination of amino acids using surface-enhanced Raman spectroscopy (SERS). This method enables sensitive and selective enantiomer analysis for pharmaceutical and biomarker applications.
Area of Science:
- Nanotechnology
- Analytical Chemistry
- Biochemistry
Background:
- Chiral discrimination of amino acid enantiomers is crucial for pharmaceuticals and biomarkers.
- Surface-enhanced Raman spectroscopy (SERS) faces challenges in enantioselective sensing due to spectral similarity and analyte localization.
Purpose of the Study:
- To develop a ligand-free chiral SERS discrimination strategy using advanced plasmonic superstructures.
- To enhance sensitivity and selectivity for amino acid enantiomer analysis.
Main Methods:
- Fabrication of SiO2@Au@RF plasmonic superstructures with porous resorcinol-formaldehyde (RF) shells and 3D gold (Au) hotspot amplifiers.
- Utilizing cooperative noncovalent interactions and differential adsorption kinetics within RF nanochannels for chiral recognition.
- Employing confined seed-mediated growth to create a dense 3D Au hotspot matrix for enhanced SERS signals.
Main Results:
- The superstructures demonstrated pronounced discrimination between l- and d-tryptophan.
- Achieved a linear calibration for enantiomeric excess determination.
- Showed successful extension to other amino acid pairs like histidine, arginine, and glutamine.
Conclusions:
- The developed plasmonic superstructures offer a distinct strategy for ligand-free enantioselective SERS sensing.
- This approach expands the capabilities for practical chiral analysis, particularly for amino acid enantiomers.
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