Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.11851/8635
Title: Disposable electrochemical immunosensor for prostate cancer detection
Authors: Kabay, Gözde
Yin Y.
Singh C.K.
Ahmad N.
Gunasekaran S.
Mutlu M.
Keywords: Electrochemical
Gold nanoparticles
Immunosensor
Prostate cancer
PSMA
Screen-printed electrode
Antigens
Biomarkers
Body fluids
Electrochemical electrodes
Fiber optic sensors
Gold nanoparticles
Immunosensors
Metal nanoparticles
Proteins
Urology
Voltammetry
Antigen proteins
Cancer biomarkers
Differential pulse voltammetry
Disposables
Electrochemical immunosensors
Electrochemicals
Prostate cancer cells
Prostate cancers
Prostate-specific membrane antigens
Screen printed electrodes
Diseases
Issue Date: 2022
Publisher: Elsevier B.V.
Source: Kabay, G., Yin, Y., Singh, C. K., Ahmad, N., Gunasekaran, S., & Mutlu, M. (2022). Disposable electrochemical immunosensor for prostate cancer detection. Sensors and Actuators B: Chemical, 360, 131667.
Abstract: Prostate cancer (PCa) is the second most common cancer amongst men worldwide; hence its early and accurate diagnosis is crucial. Due to the lacking current diagnostic approaches, an urgent need arises for an alternating analytical platform targeting selective PCa biomarkers while testing in body fluids, such as urine and serum. With this motivation, we established a disposable and label-free electrochemical immunosensor for sensitive detection of the selective PCa biomarker, prostate-specific membrane antigen (PSMA). A screen-printed gold electrode (SPGE), with its working electrode functionalized by cysteamine-modified gold nanoparticles (Cys-AuNPs), served as the sensor platform. The PSMA was detected by introducing PSMA protein/PSMA-expressing PCa cells with various concentrations and performing differential pulse voltammetry (DPV) measurements. The established biosensor has detection limits of 0.47 ng/mL for PSMA proteins (0–5 ng/mL range) and 5 cells/mL (0–100 cells/mL range) for PSMA-expressing PCa cells. The corresponding limit of quantification (LOQ) and detection sensitivities were calculated as 2.20 ng/mL and 4 cells/mL; 1.71 ?A·mL/ng and 0.15 ?A·mL/cell, respectively. The selectivity studies confirmed that the DPV signals exerted by PSMA (+) cells were statistically significant in comparison to the PSMA (-) groups (p = 0.012, p * < 0.05). The developed immunosensor platform offers a feasible alternative to facilitate PCa diagnosis. Also, to the best of our knowledge, it displayed the highest analytical performance for PSMA-expressing PCa cells detection amongst its peers. Therefore, it can be adapted for different proteins, particularly for cell detection, to facilitate other types of cancerous cells’ diagnosis soon. © 2022 Elsevier B.V.
URI: https://doi.org/10.1016/j.snb.2022.131667
https://hdl.handle.net/20.500.11851/8635
ISSN: 0925-4005
Appears in Collections:Biyomedikal Mühendisliği Bölümü / Department of Biomedical Engineering
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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