Date of Award

6-29-2020

Document Type

Thesis and Dissertation

Degree Name

Master of Science (MS)

Department

Department of Chemistry

First Advisor

Jeremy Driskell

Abstract

SERS based immunoassays for point-of-care diagnostics is a promising tool to facilitate biomarker detection for early disease diagnosis and control. The technique is based on a sandwiched system in which antigen is first captured by a selective substrate and then labeled by an extrinsic Raman label (ERL). Here, we report on the use of gold nanoparticle modified filter paper as a novel capture membrane in a vertical flow format. This vertical flow configuration affords reproducible flow of sample and label through the capture substrate to overcome diffusion limited kinetics and significantly reduced assay time. The filter paper was selected due to its affordability and availability, while the embedded AuNPs maximized plasmonic coupling and SERS enhancement. Additionally, the embedded AuNP served as a scaffold to immobilize capture antibody to specifically bind antigen. In this work, a SERS-based rapid vertical flow (SERS-RVF) immunoassay for detection of mouse IgG was developed to establish proof of principle. Optimization of assay conditions led to a limit of detection of 3 ng/mL, which is comparable to more traditional formats carried out in multi-well plates and significantly reduced assay time to less than 2 minutes. Additionally, IgG was accurately quantified in normal serum to validate the SERS-RVF assay for application to the analysis of biological samples. These results highlight the potential advantages of the SERS-RVF platform for point-of-need testing.

KEYWORDS: Immunoassay; surface-enhanced Raman scattering (SERS); plasmonic paper; vertical flow assay; point-of-need (PON) testing;point-of-care (POC) diagnostics.

Comments

Imported from Frimpong_ilstu_0092N_11761.pdf

DOI

https://doi.org/10.30707/ETD2020.1606247535.289026bf

Page Count

83

Included in

Chemistry Commons

Share

COinS