Electrochemical aptamer sensor based on metal ion-labeled polyethyleneimine gold nanoparticles for simultaneous detection of multiple disease markers

2021 ◽  
Vol 399 ◽  
pp. 139423
Author(s):  
Huanan Zhao ◽  
Qingfeng Liu ◽  
Jian Wang ◽  
Aiwen Huang ◽  
Bin Qiu ◽  
...  
2019 ◽  
Vol 76 ◽  
pp. 02001
Author(s):  
Aamir Amanat Ali Khan ◽  
Huma Ajab ◽  
Asim Yaqub ◽  
Mohd Azmuddin Abdullah

Square-wave voltammetric stripping analysis is attractive for environmental monitoring and trace metal ion determination. The sensitivity is a result of analytes preconcentration steps on the electrode and advanced measurement procedures, where metal analytes are stripped away from the electrode at appropriate potential scan. Screen-printed electrode (SPE) has great advantages for in situ assays of heavy metal ions. Modification of SPE with bismuth (Bi) film improves the amalgamation of metal ions and the addition of hydroxyapatite (HA) increases the ion sorption, and enhances the current response due to the large porous structure and surface active sites for the metal ion binding. The ionization of the functional groups on the electrode surface upon contact with the aqueous system further assists the cation binding. The analytical performance of Bi and HA-modified SPE for simultaneous detection of Cd(II) and Pb(II) ions by square wave anodic stripping voltammetry (SWASV) was evaluated. Under the optimized electrochemical working conditions, calibration graph is linear for 240 s deposition time, in 0.1 M acetate buffer at pH 7.6 with the detection limit of 16.8 ppb for Pb(II). Two peaks corresponding to Cd(II) at -0.8 V and Pb(II) at -0.6 V can be discerned suggesting that Bi-HA modification had increased the current responses.


Langmuir ◽  
2011 ◽  
Vol 27 (13) ◽  
pp. 7972-7975 ◽  
Author(s):  
Ryo Shomura ◽  
Keum Jee Chung ◽  
Hideo Iwai ◽  
Masayoshi Higuchi

2020 ◽  
Vol 12 (2) ◽  
pp. 212-217 ◽  
Author(s):  
Juan Du ◽  
Shujing Wu ◽  
Liyuan Niu ◽  
Junguang Li ◽  
Dianbo Zhao ◽  
...  

Unfunctionalized flower-shaped AuNPs is used as colorimetric sensor for PCR product detection by naked eyes.


Sensors ◽  
2020 ◽  
Vol 20 (16) ◽  
pp. 4427
Author(s):  
Daria Minta ◽  
Zoraida González ◽  
Piotr Wiench ◽  
Stanisław Gryglewicz ◽  
Grażyna Gryglewicz

Gold nanoparticles (AuNPs) were homogeneously electrodeposited on nitrogen-doped reduced graphene oxide (N-rGO) to modify a glassy carbon electrode (GCE/N-rGO-Au) in order to improve the simultaneous detection of dopamine (DA), ascorbic acid (AA), and uric acid (UA). N-rGO was prepared by the hydrothermal treatment of graphene oxide (GO) and urea at 180 °C for 12 h. AuNPs were subsequently electrodeposited onto the surface of GCE/N-rGO using 1 mM HAuCl4 solution. The morphology and chemical composition of the synthesized materials were characterized by field-emission scanning electron microscopy and X-ray photoelectron spectroscopy. The electrochemical performance of the modified electrodes was investigated through cyclic voltammetry and differential pulse voltammetry measurements. Compared to GCE/rGO-Au, GCE/N-rGO-Au exhibited better electrochemical performance towards the simultaneous detection of the three analytes due to the more homogeneous distribution of the metallic nanoparticles as a result of more efficient anchoring on the N-doped areas of the graphene structure. The GCE/N-rGO-Au-based sensor operated in a wide linear range of DA (3–100 µM), AA (550–1500 µM), and UA (20–1000 µM) concentrations with a detection limit of 2.4, 58, and 8.7 µM, respectively, and exhibited satisfactory peak potential separation values of 0.34 V (AA-DA), 0.20 V, (DA-UA) and 0.54 V (AA-UA). Remarkably, GCE/N-rGO-Au showed a very low detection limit of 385 nM towards DA, not being susceptible to interference, and maintained 90% of its initial electrochemical signal after one month, indicating an excellent long-term stability.


2017 ◽  
Vol 90 ◽  
pp. 343-348 ◽  
Author(s):  
Xiaoting Li ◽  
Beibei Chen ◽  
Man He ◽  
Han Wang ◽  
Guangyang Xiao ◽  
...  

2012 ◽  
Vol 755 ◽  
pp. 108-114 ◽  
Author(s):  
Haowen Huang ◽  
Fang Liu ◽  
Shaowen Huang ◽  
Shishan Yuan ◽  
Bo Liao ◽  
...  

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