Surface-enhanced Raman scattering (SERS) has been widely used in the detection of targets and strongly depends on the interaction and the distance between the targets and nanoparticles. Herein, metal-organic frameworks (MOFs) were first easily synthesized on a large scale via a water bath method, especially Uio-66 and Uio-67. MOFs embedded with gold nanoparticles (AuNPs) for SERS enhancement were successfully fabricated via an impregnation strategy. The synthesized AuNPs/MOF-199, AuNPs/Uio-66, and AuNPs/Uio-67 composites, with LSPR properties and high adsorption capability of MOFs to preconcentrate the analytes close to the surface of the AuNPs, exhibited excellent SERS activity. The effects of the reducing concentrations of sodium citrate on the SERS activity, and the stability and reproducibility of the AuNP/MOFs have been discussed via the detection of acetamiprid. The SERS intensity enhanced by the composites was retained for more than 40 days under ambient conditions with the reducing concentrations of sodium citrate at 0.16%, 0.20%, and 0.16%. The limits of detection with the signal/noise ratio higher than 3 at the characteristic peak 632 cm were 0.02 μM, 0.009 μM, and 0.02 μM for acetamiprid. Most interestingly, the AuNP/MOF-199 composites, whose morphology was long tube sheet, exhibited excellent SERS activity. These novel composites with high sensitivity, stability, and reproducibility provide a new route for the detection of pesticides via the SERS technology.

The biomimetic enzyme-linked immunosorbent assay (BELISA) is widely used for detection of small-molecule compounds as a result of low cost and reagent stability of molecularly imprinted polymers (MIPs). However, enzyme labels used in BELISA still suffer some drawbacks, such as high production cost and limited stability. To overcome the drawbacks, a biomimetic nanozyme-linked immunosorbent assay (BNLISA) based on MIPs and nanozyme labels was first proposed. For nanozyme labels, platinum nanoparticles (PtNPs) acted as peroxidase by catalyzing the oxidation of colorless 3,3′,5,5′-tetramethylbenzidine (TMB) into an ideal surface-enhanced Raman scattering (SERS) marker. Blue TMB2+ and bovine serum albumin (BSA)–hapten showed superior selectivity when competing with targets for binding sites on MIPs, named the Pt@BSA–hapten probe. The BNLISA method was employed to detect triazophos with a limit of detection of 1 ng mL–1 via colorimetric and SERS methods. Replacing traditional enzymes with nanozymes for combination with MIPs may bring about a new prospect for other compound analyses.

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Herein, a molecularly imprinted membrane chromatography strip using a combination of electrospinning, molecular imprinting, and fluorescent lateral flow test strips (LFTS) was developed for specific recognition of triazophos residues in tap water.

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In this study, a direct competitive biomimetic enzyme-linked immune-sorbent assay (BELISA) based on a molecularly imprinted nanomembrane as an artificial antibody was developed for the determination of triazophos in real samples. The imprinted film was directly synthesized on the well surface of a 96-well plate using a dummy molecular template under the conditions of thermal polymerization. The developed BELISA using a hapten of triazophos as an enzyme-labeled probe is much more sensitive, simple, quick, steady and inexpensive than the other instrumental and immuno assay methods. Under optimal conditions, the linear range of the method was 0.001-10 000 mg L À1 with a good regression coefficient of 0.977. The sensitivity (IC 50 ) and the limit of detection (LOD) of BELISA were 428 mg L À1 and 0.001 mg L À1, respectively. This method was performed to detect triazophos in cabbage and apple samples, and showed excellent recovery and relative standard deviations (RSDs) ranging from 70.5 to 119.8% and from 5.2 to 19.7%, respectively. The results correlated well with those obtained using high performance liquid chromatography-tandem mass spectrometry.

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