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Phosalone
ANALYST · 2020 ·Vol. 145 ·期 9 ·3245-3256 · IF 3.978

A disposable molecularly imprinted electrochemical sensor for the ultra-trace detection of the organophosphorus insecticide phosalone employing monodisperse Pt-doped UiO-66 for signal amplification

Liping Xu,Jiebin Li,Jiajia Zhang,Junyong Sun,Tian Gan,Yanming Liu

In this work, a disposable molecularly imprinted electrochemical sensor was developed towards the highly sensitive and selective detection of the organophosphorus insecticide phosalone (PAS), employing a home-made carbon paste microelectrode (CPME) modified with a Zr-based metal–organic framework catalyst (Pt-UiO-66) and a mesoporous structured conductive molecularly imprinted polymer (MIP). Pt-UiO-66 octahedra with isolated dispersed Pt nanoparticle active sites were firstly incorporated into the CPME to provide a remarkably amplified signal for voltammetric determination. The mesoporous MIP was then synthesized onto the Pt-UiO-66/CPME via electropolymerization and a subsequent sol–gel process, which could bind the PAS template molecules through hydrogen bond, coordinate bonding, hydrophobic interaction, and π–π stacking interaction. Morphological, structural, and electrochemical characterization studies revealed that this nano-sized MIP provided excellent features for PAS detection, including high porosity, large surface area, enhanced electron-transport ability, greatly improved diffusion capacity, and strong recognition specificity. Therefore, the resulting sensor exhibited an outstanding linearly proportional concentration domain of 0.50 nM–20 μM, low detection limit of 0.078 nM, marked selectivity over certain interferences with similar configurations, considerable repeatability, reproducibility, and stability for the analysis of PAS. Moreover, the sensor was successfully applied for the determination of PAS in agricultural products and environmental samples with results in good compatibility with a chromatographic method, indicative of the high reliability and practicability. Such an electrochemical sensor might open a novel window for the investigation of selective sensing of small organic species from their analogues coupled with the molecular imprinting technique.

研究领域: 分析化学 · 环境科学 · 农业科学
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Food Analytical Methods · 2019 ·Vol. 12 ·期 9 ·2094-2105 · IF 2.413

Effects of Ions on Core-Shell Bimetallic Au@Ag NPs for Rapid Detection of Phosalone Residues in Peach by SERS

Yaseen Tehseen,Pu Hongbin,Sun Da-Wen

The sensitivity of surface-enhanced Raman spectroscopy (SERS) extremely relies on experimental parameters including pH and aggregating agents. Using Au@Ag nanoparticles (NPs) with 26 nm Au core size and 6 nm Ag shell thickness as the substrate, the effect of cationic (Ca 2+ , K + , Na + ) and anionic (Cl − , Br − ) aggregating agents was investigated on the SERS detection of phosalone. The optimum concentrations of the aggregating agents in relation to the maximum SERS intensity differed broadly from 1 × 10 −2  mol/L for CaBr 2 to 1 × 10 1  mol/L for KCl. Both anions and cations greatly affected the SERS enhancement. With employing Br − as the anion, Ca 2+ and K + showed the maximum SERS intensities for phosalone, while using Ca 2+ as the cation, Br − produced the maximum SERS enhancement. Among these aggregating agent combinations, the maximum SERS enhancement was achieved by employing 1 × 10 −2  mol/L CaBr 2 at pH 3.0. The detection limits of phosalone in standard solution and peach were 0.02 mg/L and 0.2 mg/kg, respectively. This study demonstrated that the Au@Ag NP-based SERS approach could be used as a sensitive, rapid, and simple method for detecting trace contaminants in food matrices.

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