4.7 Article

Efficient acetylcholinesterase immobilization for improved electrochemical performance in polypyrrole nanocomposite-based biosensors for carbaryl pesticide

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 339, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2021.129875

关键词

Polypyrrole nanocomposite; Carbaryl; Biosensor for pesticide; Enzyme immobilization

资金

  1. CNPq [303439/2015-7, 141492/2016-3, 423244/2016-7, 141655/2017-8, 305875/2019-1]
  2. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior - Brasil [001]
  3. CAPES-PDSE [88881.132060/2016-01, 88881.135800/2016-01]

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Efficient and portable sensors are needed for monitoring pesticide contaminants in various environments. This study focused on a biocomposite film, which optimized surface conditions for enzyme immobilization and showed improved catalytic performance. The biosensor demonstrated linear responses for carbaryl detection with good repeatability and reproducibility, and improved stability at lower temperatures.
Efficient and portable sensors are required to monitor and evaluate pesticide contaminants in the environment, food supply and biological fluids. In this work, a study of indigo carmine and dodecyl sulphate doped polypyrrole - gold nanoparticle nanocomposite films revealed changes during the polymerization that optimized the surface conditions for the immobilization of acetylcholinesterase enzyme (from electric eel), leading to improved catalytic performance. The results suggest a similar behavior to AChE from electric ray, as previously reported in a theoretical study, where the active site is orientated closer to the electrode when the enzyme is immobilized on a positively charged surface, promoting faster direct electron transfer. In addition, this interaction allows the immobilization of an expressive amount of active enzymes. The lack of hindrance led to a high binding interaction of the analyte (carbaryl) towards the adsorption sites of the enzyme (Langmuir isotherm constant of 7.39 x 108). This electrochemical enzymatic biosensor presented linear responses ranging from 0.05 to 0.25 ng mL-1 for carbaryl (a wide spectrum insecticide), with a detection limit of 0.033 ng cm2 mL-1, quantification limit of 0.11 ng cm2 mL-1 and sensitivity of -59.5 x 103A cm-2 mL g-1. The biosensor showed good intraelectrode repeatability and inter-electrode reproducibility with the relative standard deviation of 1.8 % and 3.7 % towards thiocholine oxidation and carbaryl pesticide detection, respectively. The biosensor stability improved when stored at lower temperature (-15 ?C).

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