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UBC Theses and Dissertations
Label-free electrochemical aptasensor based on gold nanoparticles-modified screen-printed electrodes for detection of cytokines Shieh, Hamed
Abstract
Detection of inflammatory and pro-inflammatory cytokines is of great importance due to their involvement in the pathogenesis of various health conditions. In this thesis, a highly sensitive electrochemical aptamer-based biosensor (aptasensor) is presented for precise and label-free detection of tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6). The aptasensor was fabricated based on a gold screen-printed electrode (GSPE) which was modified by electrochemically-deposited gold nanoparticles (AuNPs). The thiolatedaptamers were anchored on the surface of the aptasensor using gold-sulfur chemistry. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques were employed to characterize the aptasensor through the fabrication process. For measurement of target cytokines square wave voltammetry (SWV) was carried out in a redox electrolyte solution containing [Fe(CN)₆]³⁻/⁴⁻. Based on the results, the aptasesnor was capable of detecting TNF-alpha and IL-6 in a linear range of 1 pg/mL to 1 μg/mL with a detection limit of 0.278 pg/mL. For IL-6 the linear detection range of the patasensor was 1 fg/mL to 1 μg/mL with a detection limit of 1 fg/mL. The label-free sensing scheme of the aptasensor and its simple fabrication procedure make it promising for point-of-care applications.
Item Metadata
Title |
Label-free electrochemical aptasensor based on gold nanoparticles-modified screen-printed electrodes for detection of cytokines
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Creator | |
Supervisor | |
Publisher |
University of British Columbia
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Date Issued |
2021
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Description |
Detection of inflammatory and pro-inflammatory cytokines is of great importance due to
their involvement in the pathogenesis of various health conditions. In this thesis, a highly
sensitive electrochemical aptamer-based biosensor (aptasensor) is presented for precise and
label-free detection of tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6).
The aptasensor was fabricated based on a gold screen-printed electrode (GSPE) which was
modified by electrochemically-deposited gold nanoparticles (AuNPs). The thiolatedaptamers
were anchored on the surface of the aptasensor using gold-sulfur chemistry.
Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques were
employed to characterize the aptasensor through the fabrication process. For measurement
of target cytokines square wave voltammetry (SWV) was carried out in a redox electrolyte
solution containing [Fe(CN)₆]³⁻/⁴⁻. Based on the results, the aptasesnor was capable of
detecting TNF-alpha and IL-6 in a linear range of 1 pg/mL to 1 μg/mL with a detection
limit of 0.278 pg/mL. For IL-6 the linear detection range of the patasensor was 1 fg/mL to
1 μg/mL with a detection limit of 1 fg/mL. The label-free sensing scheme of the aptasensor
and its simple fabrication procedure make it promising for point-of-care applications.
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Genre | |
Type | |
Language |
eng
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Date Available |
2021-08-30
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Provider |
Vancouver : University of British Columbia Library
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Rights |
Attribution-NonCommercial-NoDerivatives 4.0 International
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DOI |
10.14288/1.0401797
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URI | |
Degree | |
Program | |
Affiliation | |
Degree Grantor |
University of British Columbia
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Graduation Date |
2021-09
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Campus | |
Scholarly Level |
Graduate
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Rights URI | |
Aggregated Source Repository |
DSpace
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Item Citations and Data
Rights
Attribution-NonCommercial-NoDerivatives 4.0 International