4.3 Article

An acetylcholinesterase-based biosensor for isoprocarb using a gold nanoparticles-polyaniline modified graphite pencil electrode

Journal

ANALYTICAL SCIENCES
Volume 39, Issue 6, Pages 911-923

Publisher

SPRINGERNATURE
DOI: 10.1007/s44211-023-00296-7

Keywords

Acetylcholinesterase; Acetylthiocholine; Isoprocarb; Gold nanoparticle; Graphite pencil

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A biosensor system based on enzymatic inhibition of acetylcholinesterase (AChE) by isoprocarb has been developed. The system utilizes a gold nanoparticles-polyaniline modified graphite pencil electrode (AuNPs-PANI-GPE) to detect thiocholine changes caused by isoprocarb. The electrode, prepared through electro-polymerization of aniline and the deposition of gold nanoparticles, showed enhanced detection capabilities compared to unmodified electrodes. Under optimal conditions, the system provided a linear calibration curve for isoprocarb in the concentration range of 0.05-1.0 mu M, with limits of detection and quantification of 0.1615 nM and 0.5382 nM, respectively.
An analysis tool for isoprocarb has been successfully developed as a biosensor system based on enzymatic inhibition of acetylcholinesterase (AChE) by isoprocarb. A gold nanoparticles-polyaniline modified graphite pencil electrode (AuNPs-PANI-GPE) was utilized to detect the change of thiocholine in the presence of isoprocarb. This electrode was prepared by two cyclic voltammetry steps, including the electro-polymerization of aniline on a graphite pencil and the electro-deposition of gold nanoparticles on the polyaniline surface. Characterization performed by SEM-EDX indicates that 8-80 nm size of gold nanoparticles could be deposited on the surface of polyaniline-modified graphite pencil (PANI-GPE). Electrochemical characterization using cyclic voltammetry suggested that the active surface area of the prepared electrode was 0.17019 cm(2), which was about 4 times higher than (PANI-GPE) and 13 times higher than the unmodified GPE. Furthermore, an oxidation peak of thiocholine could be observed at the modified GPE at a potential of + 0.675 V (vs. Ag/AgCl), formed by an enzymatic reaction of AChE in the presence of acetylthiocholine. This peak current was found to linearly increase with acetylthiocholine concentrations, while in the presence of isoprocarb in a constant concentration of AChE and acetylthiocholine the peak linearly decreases. At the optimum condition of 0.1 M phosphate buffer solution pH 7.4 containing 0.1 M KCl; 100 mU/ml AChE; and 1 mM acetylthiocholine chloride in an inhibition and contact time of 25 and 15 min, respectively, a linear calibration curve of isoprocarb in the concentration range of 0.05-1.0 mu M could be provided. Estimated limits of detection and quantifications of 0.1615 nM and 0.5382 nM, respectively, with a sensitivity of 1.7771 mu A/mu M.mm(2) could be achieved. Furthermore, an excellent stability for 8 times measurements was observed with an RSD of 4.87%, suggesting that the developed tool is promising for the real detection of isoprocarb.

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