Imprinted Polymer-Based Sensor System for Herbicides Using Differential-Pulse Voltammetry on Screen-Printed Electrodes

1999 ◽  
Vol 71 (17) ◽  
pp. 3698-3702 ◽  
Author(s):  
Silke Kröger ◽  
Anthony P. F. Turner ◽  
Klaus Mosbach ◽  
Karsten Haupt
Sensors ◽  
2019 ◽  
Vol 20 (1) ◽  
pp. 76 ◽  
Author(s):  
Anabela S. Lorenzetti ◽  
Tania Sierra ◽  
Claudia E. Domini ◽  
Adriana G. Lista ◽  
Agustin G. Crevillen ◽  
...  

Disposable electrochemically reduced graphene oxide-based (ERGO) screen-printed electrodes (SPE) were developed for the determination of total tetracyclines as a sample screening approach. To this end, a selective adsorption-detection approach relied on adsorptive transfer stripping differential pulse voltammetry (AdTDPV) was devised, where the high adsorption capacity and the electrochemical properties of ERGO were simultaneously exploited. The approach was very simple, fast (6 min.), highly selective by combining the adsorptive and the electrochemical features of tetracyclines, and it used just 10 μL of the sample. The electrochemical sensor applicability was demonstrated in the analysis of environmental and food samples. The not-fully explored AdTDPV analytical possibilities on disposable nanostructured transducers become a new tool in food and environmental fields; drawing new horizons for “in-situ” analysis.


2017 ◽  
Vol 29 (6) ◽  
pp. 1559-1565 ◽  
Author(s):  
Clara Pérez-Ràfols ◽  
Ana Gómez ◽  
Núria Serrano ◽  
José Manuel Díaz-Cruz ◽  
Cristina Ariño ◽  
...  

2008 ◽  
Vol 61 (12) ◽  
pp. 962 ◽  
Author(s):  
Shao-Hua Zuo ◽  
Ling-Fan Zhang ◽  
Yan-Hui Zhao ◽  
Hui-Hui Yuan ◽  
Min-Bo Lan ◽  
...  

A simple, disposable and inexpensive electrochemical DNA biosensor based on a zirconia (ZrO2) modified thin film screen-printed electrode (ZrO2/SPE) has been developed. Short DNA sequences (21 monomer units) from the Escherichia coli pathogen, modified with a phosphate group at the 5′ end, were attached to the surface of the electrode through the affinity of the phosphate group for zirconia, to produce an effective DNA probe (ssDNA/ZrO2/SPE). DNA immobilization and hybridization were characterized using differential pulse voltammetry by employing methylene blue as redox indicator. Target sequences hybridized with the probe resulted in a decrease of the reduction peak current of methylene blue intercalated into the probe. The response of a non-complementary sequence and a single base pair mismatch sequence were both clearly distinguished from that of a complementary sequence. The developed biosensor had a high selectivity and sensitivity towards hybridization detection (10–10 M complementary DNA detectable). Making use of screen-printed technology, the fabrication of the biosensors exhibited satisfactory reproducibility, investigated by cyclic voltammetry and differential pulse voltammetry. The relative standard deviation was found to be <3.0% for six bare SPEs and six ssDNA-modified SPEs (ssDNA/ZrO2/SPE) from a batch.


2019 ◽  
Vol 2019 ◽  
pp. 1-10 ◽  
Author(s):  
Alina Elena Trofin ◽  
Lucia Carmen Trincă ◽  
Elena Ungureanu ◽  
Adina Mirela Ariton

Measurement of antioxidant capacity represents an analytical major challenge in terms of accuracy, efficiency, rapid response, or low cost of detection methods. Quantification of antioxidant capacity of food samples using disposable screen‐printed microelectrodes (SPMEs) was based on cyclic voltammetry versus open-circuit potential (CV vs OCP) and differential pulse voltammetry (DPV) as compared with spectrophotometric measurement of the CUPRAC reaction with 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (trolox). The SPMEs are organic‐resistant electrodes and thus compatible with food samples and organic solvents used to dissolve trolox. A micropipette was used to release a drop of 50 μL sample on the spotted surface of the SPME sensor/working electrode that was time programmed to function according to the working protocol. The SPME response was linearly correlated with trolox content. This preliminary demonstration was focused on the analysis of tea infusions, due to the simplicity and reproducibility of the samples’ preparations involved. Analytical results of the antioxidant capacity (expressed as mol·L−1 trolox equivalents) of the tea samples showed a good agreement in the case of spectrophotometry and differential pulse voltammetry (R2 > 0.998). DPV with SPME based on CUPRAC reactions was proven to be a promising approach for the characterization of antioxidant capacity of tea samples with rapid response, cost-effectiveness, and simplicity of operation.


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