Abstract

This study will reveal the fabrication and development of an enzyme-less biosensor for creatinine detection. The biosensor involves a periodically patterned nano-porous TiO2 deposited with Au nanoparticles via e-beam evaporation and a layer of Imprinted Polymer (IP) of acrylamide and bis-acrylamide to obtain a heterostructure of I-Au-TiO2. The detection methods of creatinine are based on electrochemical measurements using Cyclic Voltammetry (CV), Electrochemical Impedance Spectroscopy (EIS) and Differential Pulse Voltammetry (DPV). The IP-Au-TiO2 sensor shows a detection LOD of 0.0949ng/mL and 0. 0.218ng/mL for EIS and DPV measurements, respectively. The nanofabricated biosensor was tested in the presents of urea, glucose, lactose, L-valine, and Glutamic acid and shows high specificity for creatinine due to the specific binding of the analyte to the imprinted polymer on the electrode. A comparison test was performed between the imprinted IP-Au-TiO2 versus Non-Imprinted (NI) NI-Au-TiO2 biosensors. the results show no specificity for the creatinine using NI-Au-TiO2 biosensor for the varied concentration from 0.1ng/ml to 1µg/ml compared to the I-Au-TiO2. However, The N-Au-TiO2 show enhanced specificity for creatinine in the presence of Localized Surface Plasmon Resonance (LSPR) at the interface of the Au nanoparticles and TiO2. The generated LSPR on the surface of the biosensor increased the sensitivity for creatinine due to charge separation and solution resistance between the sensor and mixture. This detection platform provided a promising result which can be easily expanded to detecting a variety of biomarkers linked to human diseases or pathogens such as bacteria or viruses for point of care detection.

Notes

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Graduation Date

2020

Semester

Fall

Advisor

Yang, Yang

Degree

Master of Science (M.S.)

College

College of Graduate Studies

Department

Nanoscience Technology Center

Degree Program

Nanotechnology

Format

application/pdf

Identifier

CFE0008299; DP0023736

URL

https://purls.library.ucf.edu/go/DP0023736

Language

English

Release Date

December 2020

Length of Campus-only Access

None

Access Status

Masters Thesis (Open Access)

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