An amperometric biosensor based on acetylcholinesterase immobilized onto iron oxide nanoparticles/multi-walled carbon nanotubes modified gold electrode for measurement of organophosphorus insecticides

The stepwise amperometric biosensor fabrication process and immobilized acetylcholinesterase inhibition in pesticide solution. [Display omitted] • Constructed a novel composite material using Fe 3O 4NP and c-MWCNT at Au electrode for electrocatalysis. • The properties of nanoparticles modified elect...

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Veröffentlicht in:Analytica chimica acta 2011-09, Vol.701 (1), p.66-74
Hauptverfasser: Chauhan, Nidhi, Pundir, Chandra Shekhar
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Sprache:eng
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Zusammenfassung:The stepwise amperometric biosensor fabrication process and immobilized acetylcholinesterase inhibition in pesticide solution. [Display omitted] • Constructed a novel composite material using Fe 3O 4NP and c-MWCNT at Au electrode for electrocatalysis. • The properties of nanoparticles modified electrodes were studied by SEM, FTIR, CVs and EIS. • The biosensor exhibited good sensitivity (0.475 mA μM −1) • The half life of electrode was 2 months. • The sensor was suitable for trace detection of OP pesticide residues in milk and water. An acetylcholinesterase (AChE) purified from maize seedlings was immobilized covalently onto iron oxide nanoparticles (Fe 3O 4NP) and carboxylated multi walled carbon nanotubes (c-MWCNT) modified Au electrode. An organophosphorus (OP) biosensor was fabricated using this AChE/Fe 3O 4/c-MWCNT/Au electrode as a working electrode, Ag/AgCl as standard and Pt wire as an auxiliary electrode connected through a potentiostat. The biosensor was based on inhibition of AChE by OP compounds/insecticides. The properties of nanoparticles modified electrodes were studied by scanning electron microscopy (SEM), Fourier transform infrared (FTIR), cyclic voltammograms (CVs) and electrochemical impedance spectroscopy (EIS). The synergistic action of Fe 3O 4NP and c-MWCNT showed excellent electrocatalytic activity at low potential (+0.4 V). The optimum working conditions for the sensor were pH 7.5, 35 °C, 600 μM substrate concentration and 10 min for inhibition by pesticide. Under optimum conditions, the inhibition rates of OP pesticides were proportional to their concentrations in the range of 0.1–40 nM, 0.1–50 nM, 1–50 nM and 10–100 nM for malathion, chlorpyrifos, monocrotophos and endosulfan respectively. The detection limits were 0.1 nM for malathion and chlorpyrifos, 1 nM for monocrotophos and 10 nM for endosulfan. The biosensor exhibited good sensitivity (0.475 mA μM −1), reusability (more than 50 times) and stability (2 months). The sensor was suitable for trace detection of OP pesticide residues in milk and water.
ISSN:0003-2670
1873-4324
DOI:10.1016/j.aca.2011.06.014