2004
DOI: 10.1016/j.bios.2004.03.039
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Acetylcholinesterase-based biosensor electrodes for organophosphate pesticide detection

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Cited by 47 publications
(42 citation statements)
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“…A similar strategy was employed by Yang et al [108] with the only difference being trans-4-cinnamic acid diazonium tetrafluoroborate was used to modify the electrode. Other workers have modified electrodes with 4-nitrophenyl diazonium salt followed by reductive conversion of the nitro group to an amine followed by attachment of the enzymes, glucose oxidase [71], acetylcholine esterase for the detection of pesticides by enzyme inhibition [109] or tyrosinase [77] for detecting phenols at diamond electrodes. More complicated strategies for enzyme and other proteins attachment to electrodes modified with aryl diazonium salts have also been developed.…”
Section: Aryl Diazonium Salt Modified Carbon Electrodesmentioning
confidence: 99%
“…A similar strategy was employed by Yang et al [108] with the only difference being trans-4-cinnamic acid diazonium tetrafluoroborate was used to modify the electrode. Other workers have modified electrodes with 4-nitrophenyl diazonium salt followed by reductive conversion of the nitro group to an amine followed by attachment of the enzymes, glucose oxidase [71], acetylcholine esterase for the detection of pesticides by enzyme inhibition [109] or tyrosinase [77] for detecting phenols at diamond electrodes. More complicated strategies for enzyme and other proteins attachment to electrodes modified with aryl diazonium salts have also been developed.…”
Section: Aryl Diazonium Salt Modified Carbon Electrodesmentioning
confidence: 99%
“…The enzyme non-covalently immobilized onto polyethyleneimine modified screen-printed carbon electrodes showed an improvement of stability when compared to non-immobilized AChE, AChE covalently immobilized onto dialdehyde and polyethyleneimine modified electrodes. Several stabilizer mixtures were also employed for an additional stabilization of AChE, demonstrating higher storage stability in the dry state with dextran-sulphate/sucrose or polygalacturonic acid/sucrose mixtures [138].…”
Section: Immobilisationmentioning
confidence: 99%
“…amine group, hydroxyl group and carboxy group, are drawn in by the ring-opening reaction of epoxy groups, the chemical property modification of polymer is obtained and the polymer can be changed into functional polymer with biocompatibility. [12][13][14][15] In this work, with glycidyl methacrylate (GMA) as monomer and ethylene glycol dimethylacrylate (EGDMA) as cross linking agent, cross linking microbeads with an average diameter of 100 μm were synthesized by suspension copolymerization. Subsequently, by the active epoxy groups of GMA, the GMA/EGDMA microbeads were modified with aminating agents of hexanediamine and other three kinds of multiethylene multi-amine.…”
Section: Introductionmentioning
confidence: 99%