(Invited) Nanosurface Fluidic Devices for Electrochemical Sensing and Biosensing

2021 ◽  
Vol MA2021-01 (55) ◽  
pp. 1410-1410
Author(s):  
Sara Mahshid
2021 ◽  
Author(s):  
Amanda Roley ◽  
Kaylee Clark ◽  
Alec Richardson ◽  
Brandaise Martinez ◽  
Stuart Tobet ◽  
...  

The growth in fluidic devices, such as organ-on-chip (OOC) technology, comes with a need for growth in sensing capabilities of key biomolecules to help elucidate changes during the time course of experiments. We developed an on-line, easy-to-assemble, 3D-printed electrochemical sensor module that is magnetically sealed for ease of assembly. The sensor module includes a plug-and-play format for electrochemical sensors made in finger-tight fittings to allow for a wide selection of experimental set-ups and target molecules. Here, we report the feasibility of the sensor module as well as demonstrate its use for electrochemical sensing with integrated thermoplastic electrodes (TPEs). The sensor module withstood over 300 kPa of backpressure and demonstrated reliable performance with TPEs when using cyclic voltammetry (CV) and amperometry under flow conditions. CVs using the ferri/ferrocyanide (K3/4[Fe(CN)6]) redox system demonstrate that the sensor module does not hinder the expected linear response with respect to analyte concentration. Further CVs and amperometry demonstrated the use of the sensor module under flow conditions. Such success in device design and usability is promising for future work using the on-line sensor module with a variety of applications.


1969 ◽  
Vol 48 (4) ◽  
pp. 169
Author(s):  
K. Foster ◽  
G.A. Parker
Keyword(s):  

Author(s):  
Xiaoyun Yang ◽  
Ruel Overfelt ◽  
Alice Zitova ◽  
Aleksandr Simonian ◽  
Jeffrey Kirsch ◽  
...  

Author(s):  
Somayeh Tajik ◽  
Hadi Beitollahi ◽  
Fariba Garkani Nejad ◽  
Mohadeseh Safaei ◽  
Peyman Mohammadzadeh Jahani

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Pattan-Siddappa Ganesh ◽  
Ganesh Shimoga ◽  
Seok-Han Lee ◽  
Sang-Youn Kim ◽  
Eno E. Ebenso

Abstract Background A simple and simultaneous electrochemical sensing platform was fabricated by electropolymerization of allura red on glassy carbon electrode (GCE) for the interference-free detection of dihydroxy benzene isomers. Methods The modified working electrode was characterized by electrochemical and field emission scanning electron microscopy methods. The modified electrode showed excellent electrocatalytic activity for the electrooxidation of catechol (CC) and hydroquinone (HQ) at physiological pH of 7.4 by cyclic voltammetric (CV) and differential pulse voltammetric (DPV) techniques. Results The effective split in the overlapped oxidation signal of CC and HQ was achieved in a binary mixture with peak to peak separation of 0.102 V and 0.103 V by CV and DPV techniques. The electrode kinetics was found to be adsorption-controlled. The oxidation potential directly depends on the pH of the buffer solution, and it witnessed the transfer of equal number of protons and electrons in the redox phenomenon. Conclusions The limit of detection (LOD) for CC and HQ was calculated to be 0.126 μM and 0.132 μM in the linear range of 0 to 80.0 μM and 0 to 110.0 μM, respectively, by ultra-sensitive DPV technique. The practical applicability of the proposed sensor was evaluated for tap water sample analysis, and good recovery rates were observed. Graphical abstract Electrocatalytic interaction of ALR/GCE with dihydroxy benzene isomers.


2021 ◽  
Vol 1154 ◽  
pp. 338295
Author(s):  
Wenqi Wang ◽  
Rui Han ◽  
Kai Tang ◽  
Shuju Zhao ◽  
Caifeng Ding ◽  
...  

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