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The establishment of a reliable and sensitive method for the detection of flavonoids, such as kaempferol (Kae) and quercetin (Que), is important and challenging in food chemistry and pharmacology because numerous structural analogues may interfere with the detection. Until now, designing an efficient switch-on fluorescence sensing strategy for Kae and Que was still in the unachievable stage. In this work, a switch-on near-infrared (NIR) luminescence sensing assay for Kae and Que was fabricated based on a metal-organic framework (MOF) called IQBA-Yb for the first time. The fluorescence enhancing mechanism was that analytes served as additional "antenna" of Yb

Background Spherical carbons have a porous structure and large surface area for adsorption of macromolecules in water-based adhesives. Supercritical fluid chromatography (SFC) can improve selectivity and obtain better separation for phthalate esters (PAEs). Objective The aim of this study was to develop a simple and green method for the simultaneous determination of 10 PAEs in water-based adhesives using SFC–tandem mass spectrometry with dispersion solid-phase extraction by spherical carbons. Method Separation of PAEs on a Viridis HSS C18 SB column and the parameters affecting the extraction were evaluated. Results Good accuracy and precision were obtained with the recoveries at 0.5, 2.0, and 10.0 mg/kg ranging from 82.9 to 99.5% and the intra- and inter-day precision less than 7%. The method had excellent sensitivity with limits of detection in the range of 0.015–0.029 mg/kg. In the 10–500 ng/mL concentration range, the linear correlation coefficients of all compounds were between 0.9975 and 0.9995. Conclusions The method was applied to the determination of 10 PAEs in actual samples. This method is simple and rapid with low solvent consumption and high extraction efficiency. When applied to the determination of PAEs in actual samples, the method is sensitive and accurate and can meet the batch processing requirements for trace PAEs in water-based adhesives. Highlights PAEs in water-based adhesives can be determined using inexpensive materials and simple procedures with SFC.

The schematic representation of the colorimetric sensors for glyphosate detection.

The morphology of nanomaterials (geometric shape and dimension) play a significant role in its various physical and chemical properties. Thus, it is essential to link morphology with performance in specific applications. For this purpose, the morphology of copper metal-organic polyhedra (Cu-MOP) can be modulated through distinct assembly process, which facilitates the exploration of the relationship between morphology and catalytic performance. In this work, the assemblies of Cu-MOP with three different morphologies (nanorods, nanofibers and nanosheets) were facilely prepared by the variation of solvent mixture of N, N-dimethylformamide (DMF) and methanol, revealed the important role of the interaction between the surface group and the solvent on the morphology of these assemblies. Cu-MOP nanofibers exhibited the highest mimetic peroxidase enzyme activity over the Cu-MOP nanosheets and nanorods, which have been utilized in the detection of glucose. Cu-MOPs assemblies with tunable morphology accompanied with adjustable mimic peroxidase activity, had great potential applications in the field of bioanalytical chemistry and biomedicals.

In this study, cetyltrimethylammonium bromide and zeolitic imidazolate framework-8 (ZIF-8) were first assembled via the chemical co-precipitation, and high-quality carbon-based metal-free nanomaterials were synthesized using a heat-treatment process. The internal and morphological characteristics of hexagonal Star ZIF-8 were investigated using scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The electrochemical sensor with a good response to Cd(II) was prepared via square-wave anodic stripping voltammetry (SWASV) with Star ZIF-8 nanomaterial-modified glassy carbon electrodes. The main parameters were adjusted to obtain the optimal stripping response and a wide linear range. Concurrently, under the calculation of SWASV, the sensitivity of Star ZIF-8-Nafion/GCE to Cd(II) was increased by five orders of magnitude (0.5-230 μg/L), and the determination level was even low to 0.48 μg/L. Based on the high anti-interference ability and stability of the sensor, the application potential of Star ZIF-8 carbon-based metal-free nanomaterials for the detection of trace Cd(II) in was confirmed.

This study had developed a rapid, simple, accurate, and efficient method for the qualitative and quantitative determination of thiram residues tobacco and tobacco products based on surface-enhanced Raman spectroscopy and differential Raman spectroscopy. Acetonitrile was used as the extractant and PSA and GCB as the scavengers to effectively reduce the matrix effect. At the same time, sodium chloride and hydrochloric acid were used to induce the agglomeration of the target molecule and the nano particles of enhanced colloid substrates. With this approach to improve the sensitivity of analysis, our results showed that the fine linear equations of thiram with the correlation coefficients equaled 0.9986. The detection of limits was 0.0084 mg/L and the recovery was within 85–117% and the RSD was less than 10%. The detection method of thiram had a good accuracy and precision, which was potentially suitable for other dithoicarbamate pesticide residues in tobacco and tobacco products.

In this study, a molecularly imprinted electrochemical sensor based on graphene/Au nanoparticles (G@AuNPs) compound materials and molecularly imprinted membrane (MIM) modified glassy carbon electrodes (GCEs) was developed for the sensitive detection of colchicine in pharmaceuticals and serum (MIM/G@AuNPs/GCE). The film was formed by the in situ polymerization of colchicine-imprinted membranes on the G@AuNPs-modified GCE using methacrylic acid as the functional monomer. The specific surface area, catalytic performance, and electrical conductivity of the electrode increased on account of the formation of G@AuNPs compound materials, thereby improving the sensitivity of the sensor. The MIM as a preconcentrator exhibited chemical selectivity. Under optimal conditions, the MIM/G@AuNPs/GCE sensor exhibited high selectivity and high anti-interference ability. Moreover, good linearity was obtained in the range of 1.2 × 10−8 to 1.2 × 10−6 mol L−1 and 1.2 × 10−6 to 1.0 × 10−4 mol L−1 of colchicine with a detection limit of 4.8 × 10−9 mol L−1. The sensor was successfully applied for the direct determination of colchicine in colchicine tablets and human serum samples, with a relative standard deviation of less than 3.1% (n = 5) and recoveries ranging from 97.5% to 110.0%.

The purpose of this study is to establish a novel, simple and rapid surface-enhanced Raman spectroscopy (SERS) detection technology for fenamidone. Fenamidone is a fungicide widely used with curative activity against oomycete diseases. Gold nanoparticles (AuNPs) were prepared by improved trisodium citrate reduction method of chloroauric acid. As a surface-enhanced Raman scattering (SERS) active colloid, the optimized product had the advantages of high sensitivity, reproducibility and chemical stability. The Results showed that the detection limit of fenamidone adsorbed on AuNPs was 0.01 mg/kg. The linear response between SERS intensity and logarithmic concentration was R2 = 0.9562. The method was preliminary applied in tobacco sample and showed its potential to serve as an alternative rapid quantification method of fenamidone residues with simplicity, efficiency, high accuracy and precision.

A rhodium (III) ion carbon paste electrode (CPE) based on an ion imprinted polymer (IIP) as a new modifying agent has been prepared and studied. Rh(III) ion imprinted polymer was synthesized by copolymerization of acrylamide-Rh(III) complex and ethylene glycol dimethacrylate according to the precipitation polymerization. Acrylamide acted as both functional monomer and complexing agent to create selective coordination sites in a cross-linked polymer. The ion imprinted carbon paste electrode (IIP-CPE) was prepared by mixing rhodium IIP-nanoparticles and graphite powder in n-eicosane as an adhesive and then embedding them in a Teflon tube. Amperometric i-t curve method was applied as the determination technique. Several parameters, including the functional monomer, molar ratio of template, monomer and cross-linking agent, the amounts of IIP, the applied potential, the buffer solution and pH have been studied. According to the results, IIP-CPE showed a considerably higher response in comparison with the electrode embedded with non-imprinted polymer (NIP), indicating the formation of suitable recognition sites in the IIP structure during the polymerization stage. The introduced electrode showed a linear range of 1.00×10-8~3.0×10-5 mol·L-1 and detection limit of 6.0 nmol L-1 (S/N = 3). The IIP-CPE was successfully applied for the trace rhodium determination in catalyst and plant samples with RSD of less than 3.3% (n = 5) and recoveries in the range of 95.5~102.5%.

An electrochemical sensor for podophyllotoxin (PPT) based on the molecular imprinting polymer (MIP) membranes was constructed. The sensor was prepared by electropolymerizing o-phenylenediamine (o-PD) on a glassy carbon electrode (GCE) in the presence of PPT as template, and then removing the template by immersing the modified GCE in ethanol. Experimental parameters such as the types of monomer, scan cycles, concentration of o-PD and extraction condition were optimized. Under optimal conditions, the sensor exhibits a good selectivity and high sensitivity. A good linearity was obtained in the range of 4 x 10-8 mol · L(-1) to 3.2 x 10(-5) mol · L(-1) with an estimated detection limit of 4.8 x 10(-9) mol · L(-1). The sensor was applied to the determination of PPT in podophyllum hexandrum and human serum samples with satisfactory results.

To develop a rapid and simple method for sensitive determination of artemisinin (ART) in complicated matrices, a novel electrochemical sensor was constructed by in-situ polymerization of ART-imprinted membranes (ART-MIMs) on the surface of graphene (G) modified glassy carbon electrode (GCE) using acrylamide (AM) as functional monomer, ethylene glycol dimethacrylate (EGDMA) as cross-linking agent after the experimental parameters for the preparation of ART-MIMs such as functional monomer, molar ratio of template, monomer and cross-linking agent together with extraction condition were optimized. Under the optimal conditions, the sensor named as ART-MIM/G/GCE exhibited a good selectivity, high sensitivity and considerably better resistance against some analogs of artemisinin such as dihydroartemisinin (DHA), artemether (ARM) and artesunate (ARTS). The calibration graph for the determination of artemisinin by the sensor was linear in the range of 1.0 × 10(-8)mol L(-1) to 4.0 × 10(-5)mol L(-1) with the detection limit of 2.0 × 10(-9)mol L(-1). Meanwhile, this sensor possessed of good regeneration, stability and practicability. It could retain more than 94% of its original response after used at least 80 times or stored in water at room temperature for 60 days. The obtained sensor was successfully applied to determine the contents of artemisinin in the extract of Artemisia annua L. with the relative standard deviation (RSD) of less than 3.5% (n=5).

To develop a convenient method for sensitive and selective determination of platinum in complicated matrices, an ion-imprinted electrode was studied by in situ polymerization of Pt(IV) ion-imprinted membranes (Pt(IV)-IIMs) on the surface of a glassy carbon electrode (GCE). After the experimental parameters for the preparation of Pt(IV)-IIMs such as functional monomer, molar ratio of template, monomer and cross-linking agent together with extraction condition were optimized, an electrode with good regeneration, high stability and specific recognition to Pt(IV) was obtained by modifying GCE with Pt(IV)-IIMs prepared in acetonitrile using allylurea (NAU) as functional monomer, ethylene glycol dimethacrylate (EGDMA) as cross-linking agent, azobisisobutyronitrile (AIBN) as initiator under the molar ratio of template (H2PtCl6), NAU and EGDMA as 1 : 4 : 40. The resulting electrode named as Pt(IV)-IIMs/GCE exhibits high response sensitivity to Pt(IV) in phosphate buffer (pH 5.29). The calibration graph for the determination of Pt(IV) by Pt(IV)-IIMs/GCE is linear in the range of 2.0 × 10−8 ∼ 2.5 × 10−4 mol L−1 with a detection limit of 4.0 × 10−9 mol L−1. No metal ions tested at a concentration 25 times higher than that of Pt(IV) interfered in the determination. The electrode was successfully applied to determine platinum in catalyst and plant samples with a relative standard deviation (RSD) of less than 3.0% (n = 5) and recoveries in the range of 97.8–103.6%.

A Novel Carbon Paste Electrode Based on Ion-Imprinted Polymer for Determination of Iridium To develop a convenient method for sensitive and selective determination of iridium in complicated matrices, a carbon paste electrode based on iridium ion imprinted polymer (IIP) was fabricated. Iridium ion selective cavities were created in the 2-(allylthiol) nicotinic acid based cross-linked polymer. In order to fabricate the sensor, carbon particles and polymer powder were mixed with melted n-eicosane. An explicit difference in the response was observed between the electrodes modified with ion imprinted polymer (IIP) and non imprinted polymer (NIP), indicating proper performance of the recognition sites of the IIP. Various factors, known to affect the response behavior of selective electrode, were investigated and optimized. The resulting sensor named as Ir(III) ion imprinted polymer carbon paste electrode (Ir(III)-IIP/CPE) exhibits high response sensitivity to Ir(III) in acetate buffer (pH 3.6). The calibration graph is linear in the range of 2.85×10-8∼2.31×10-5 mol L-1 with the detection limit of 7.84×10-9 mol L-1(S/N). The electrode showed high selectivity for iridium in the presence of common potential interferers was found to show satisfactory results, it was successfully applied to the determination of iridium in real samples.