Polydopamine‐Capped Bimetallic AuPt Hydrogels Enable Robust Biosensor for Organophosphorus Pesticide Detection
Source abstract
Abstract
Abstract Noble metal hydrogels/aerogels with macroscopic nanoassemblies characterized by ultralow density, profuse continuous porosity, and extremely large surface area have gained abundant interest due to not only their tunable physicochemical properties, but also promising applications in catalysis and sensing. Coupling the increased reaction temperature with dopamine‐induced effect, herein, a one‐step synthetic approach with accelerated gelation kinetics is reported for the synthesis of polydopamine‐capped bimetallic AuPt hydrogels. 3D porous nanowire networks with surface functionalization of polydopamine make them a promising biocompatible microenvironment for immobilizing acetylcholinesterase (AChE) and constructing enzyme‐based biosensors for sensitive detection of organophosphorus compounds. Taking advantage of their favorable structure and composition, the optimized product exhibits superior electrochemical activity toward thiocholine produced by AChE‐catalyzed hydrolysis of acetylthiocholine. Based on the inhibition of organophosphorus pesticide on the enzymatic activity of AChE, the inhibition mode for the detection of paraoxon‐ethyl is established, displaying linear regions over the range of 0.5–1000 ng L−1 with a low detection limit of 0.185 ng L−1.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Electrochemical sensors and biosensors · Carbon and Quantum Dots Applications · Advanced Nanomaterials in Catalysis
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Pesticide and Chemical Biology of Ministry of Education International Joint Research Center for Intelligent Biosensing Technology and Health College of Chemistry Central China Normal University Wuhan 430079 P. R. China
School of Mechanical and Materials Engineering Washington State University Pullman WA 99164 USA
Funding
Project 211
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