Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/164768
Title: Surface-enhanced Raman scattering (SERS) spectroscopy platforms for enhanced detection at the nanobio interface: from metabolites to microorganisms
Authors: Leong, Shi Xuan
Keywords: Science::Chemistry
Issue Date: 2023
Publisher: Nanyang Technological University
Source: Leong, S. X. (2023). Surface-enhanced Raman scattering (SERS) spectroscopy platforms for enhanced detection at the nanobio interface: from metabolites to microorganisms. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/164768
Abstract: Surface-enhanced Raman scattering (SERS) spectroscopy is a powerful spectroscopic technique that enhances molecules’ weak Raman signals for ultrasensitive identification and quantification. However, molecule detection at the nanobio interface is hindered by challenges including poor surface affinities, complex sample matrices, and analogous chemical structures. In this thesis, we overcome these roadblocks by synergizing designer plasmonic platforms with emerging strategies to expand the analyte scope, ranging from small-molecule metabolites to microorganisms. Here, we successfully design direct enantiospecific nanoparticle-analyte interactions for label-free, generic chiral differentiation. We also leverage pattern-based recognition of differential probe-analyte interactions to distinguish small-molecule metabolites, both as individual molecules and in complex mixtures, such as the human breath, as well as microorganisms with complex surface biomolecular architectures. We thus showcase the immense potential of the novel and strategic combination of various techniques in advancing SERS beyond the current state-of-the-art toward real-life detection of a broader analyte scope.
URI: https://hdl.handle.net/10356/164768
DOI: 10.32657/10356/164768
Schools: School of Chemistry, Chemical Engineering and Biotechnology
Rights: This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:CCEB Theses

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