A molecule-imprinted electrochemiluminescence sensor based on CdS@MWCNTs for ultrasensitive detection of fenpropathrin.

A molecularly-imprinted electrochemiluminescence sensor was constructed for the determination of fenpropathrin (FPT) by molecular imprinting technology. In this sensing platform, the introduction of CdS@MWCNTs significantly enhanced the initial ECL signal of the luminol-O2 system. Specifically, MWCNTs was used as a carrier to adsorb more CdS, in which CdS acted as a co-reaction promoter for luminescence. Molecularly imprinted polymer (MIP) containing specific recognition sites of FPT was used as the material for selective recognition. With increasing amount of FPT the ECL signal decreased. Under the optimum conditions, the ECL response was linearly related to the logarithm of FPT concentration. The developed ECL sensor allowed for sensitive determination of FPT and exhibited a wide linear range from 1.0 × 10- 10 mol L- 1 to 1.0 × 10- 6 mol L- 1. The limit of detection was 3.3 × 10- 11 mol L- 1 (S/N = 3). It can be used for the detection of FPT in vegetable samples.

Ultrasensitive solid-state electrochemiluminescence sensor based on lotus root shaped carbon fiber, CdSe QDs and Fe3O4 synergically amplify Ru(bpy)32+ luminophore signal for detection of cyfluthrin.

An efficient and innovative electrochemiluminescence (ECL) sensor was developed for trace detection of cyfluthrin. The sensor utilized materials such as lotus root shaped carbon fiber (Co CNFs), cadmium selenide quantum dots (CdSe QDs), and Fe3O4 to amplify Ru(bpy)32+ signals. Co CNFs, with its large specific surface area and porosity, served the purpose of not only enhancing the stability of the sensor by fixing CdSe QDs and Ru(bpy)32+ on the Co CNFs/GCE, but also facilitating electron transfer. CdSe QDs was involved in the luminescence reaction and collaborated with Ru(bpy)32+ to enhance the sensor's sensitivity, while Fe3O4 promoted electron transfer in the system due to its large surface area. The solid-state ECL sensor achieved satisfactory signal under the synergistic action of these components. The ECL signal of the sensor was quenched by cyfluthrin, and a favorable linear relationship was observed between the sensor and cyfluthrin in the concentration range 1 × 10-12 to 1 × 10-6 M. The detection limit of the sensor was 3.3 × 10-13 M (S/N = 3). The utilization of lotus root shaped carbon fiber, CdSe QDs, and Fe3O4 in the Ru(bpy)32+ system demonstrated a synergistic effect for cyfluthrin detection, presenting a new approach for the rapid determination analysis of pesticide residues in foods.

Electrochemiluminescent assay based on Co-MOF and TiO2 for determination of bisphenol A.

An electrochemiluminescence (ECL) sensor for determining bisphenol A (BPA) was prepared based on titanium dioxide (TiO2) and Co-MOF. TiO2 is a co-reaction promoter that amplifies the ECL signal in the Ru(bpy)32+-trinpropylamine (TPrA) system. When the electrode is modified with Co-MOF the ECL signal is significantly enhanced. This is because Co-MOF can not only be used as a co-reaction accelerator but also as a carrier to adsorb more luminescent substances. Possible mechanisms for amplifying the original signal through the synergistic action of the two substances are investigated. The ECL strength decreases with increasing concentrations of BPA, and the amount of BPA can be determined by the change in ECL signal strength (ΔI). Under optimal experimental conditions, the linear range of BPA was 2.0 × 10-10 to 2.0 × 10-5 M, with a determination limit of 6.7 × 10-11 M (3σ/m). The relative standard deviation (RSD) of the signal for ten consecutive measurements was 1.5%. The sensor can be used to detect BPA in bottled samples with recoveries of 96 to 105%.

Electrospun nanofibers containing CdTe@ZnNi-MOF for electrochemiluminescent determination of chlorpyrifos.

Electrospun nanofibers containing CdTe@ZnNi-metal-organic frameworks (CdTe@ZnNi-MOF NFs) were used for the first time in luminol-O2 electrochemiluminescence (ECL) system to construct ECL sensor for chlorpyrifos (CPF) detection. Firstly, CdTe@ZnNi-MOF NFs obtained by blending method was used to modify the surface of a glassy carbon electrode, and then, the proposed solid-state ECL sensor was constructed by dropping luminol onto the surface of nanofiber benefiting from chitosan (CTS) viscosity. CdTe@ZnNi-MOF NFs with its large surface area and porosity can be used not only as luminol carrier but also as co-reaction promoter of the ECL system. The ECL sensor obtained satisfactory results in weakly alkaline solution under the synergistic action of CdTe@ZnNi-MOF NFs and luminol. The constructed ECL sensor can effectively detect CPF in the range 1.0 × 10-14-1.0 × 10-9 M, and the detection limit was 6.23 × 10-17 M (3σ/m). The constructed sensor was simple and sensitive, and can be used for the determination of CPF in vegetable samples. It not only broadened the application of MOFs in the field of ECL but also provided a new idea for expanding the application of the luminol-O2 system.

An electrochemiluminescence sensor for sensitive detection of malathion based on g-C3N4-CdTe composite nanomaterials.

A self-enhanced electrochemical luminescence (ECL) composite material g-C3N4-CdTe QDs was prepared. The combination of g-C3N4 and CdTe QDs can amplify the ECL signal and improve the stability. Based on this discovery, g-C3N4-CdTe QDs and acetylcholine esterase (AChE) were used to construct an ECL sensor for organophosphorus pesticides (OP) detection. The sensor showed a strong initial ECL signal in PBS containing S2O82-. It is because that g-C3N4 not only acts as a co-reaction promoter to amplify the ECL signal of the CdTe QDs/S2O82- system but also acts as a carrier with large specific surface area to adsorb more CdTe QDs and improve the sensitivity of the sensor. The reaction of AChE and acetylthiocholine (ATCl) was hindered by organophosphorus pesticides (OPs). The ECL signal was enhanced by the addition of OPs, and a linear relationship was displayed between the increasing value and the concentration of malathion. A good linear range from 2.52 × 10-13 to 2.52 × 10-8 mol L-1 was obtained and the limit of detection was 8.4 × 10-14 mol L-1 under optimized experimental conditions. The results indicated that the sensor had promising applications for the detection of OPs in vegetable samples.

Solid-state electrochemiluminescence sensor based on zeolitic imidazolate framework-67 electrospinning nanofibers for chlorpyrifos detection.

A novel solid-state electrochemiluminescence (ECL) sensor for chlorpyrifos (CPF) detection was constructed based on zeolitic imidazolate framework-67 electrospinning nanofibers (ZIF-67 NFs). Silver nanoparticles (Ag NPs), ZIF-67 NFs, tris(2,2'-bipyridyl) ruthenium(II) [Ru(bpy)32+], and Nafion were successively deposited on the surface of the electrode. Ag NPs played a role in promoting electron transfer, and ZIF-67 NFs played a role in fixing Ru(bpy)32+ and promoting electron transfer due to its large specific surface area and porosity. Nafion formed a film on the outermost layer of the electrode to further improve the stability of the system. Therefore, the modified electrode showed stable and obvious ECL signal in PBS solution containing 10 µL 0.01 M TprA (pH 8.0). CPF quenched the ECL signal of the system, and the quenching value was linear with the logarithm of CPF concentration in the range 1.0 × 10-13 to 1.0 × 10-6 M. The detection limit was 3.3 × 10-14 M (S/N = 3). In this study, ZIF-67 NFs were used as an ECL promoter for the first time, broadening the application range of ZIF-67 NFs.

A molecule-imprinted electrochemiluminescence sensor based on self-accelerated Ru(bpy)32+@ZIF-7 for ultra-sensitive detection of procymidone.

A molecular-imprinted electrochemiluminescence sensor for procymidone (PCM) detection was reported based on Ru(bpy)32+@ZIF-7. A novel self-accelerated Ru(bpy)32+@ZIF-7 was prepared by one-step synthesis method, which exhibited high electrochemiluminescence (ECL) emission as a coreactant in the presence of tri-n-propylamine (TPrA). Concretely, ZIF-7 was not only the carrier of Ru(bpy)32+, but also the co-reaction promoter of Ru(bpy)32+/TPrA ECL system. The introduction of molecular imprint polymer (MIP) with PCM gave new characteristics of specific recognition of analyte PCM. The change value of ECL intensity (ΔI) was proportional to the logarithm of PCM concentration, with a wide linear range and a low detection limit of 1.0 × 10-10 to 1.0 × 10-6 mol L-1 and 2.0 × 10-11 mol L-1, respectively. The presented MIP-ECL sensor had high sensitivity, selectivity and stability, and had great potential in the field of food safety detection.

Electrospun nanofibers modified with zeolitic imidazolate framework-8 for electrochemiluminescent determination of terbutaline.

For the first time it is demonstrated that zeolitic imidazolate framework-8 electrospun nanofibers (ZIF-8 NF) could serve as electrochemiluminescence (ECL) accelerator for the facile detection of terbutaline residual. A novel ECL sensor for the determination of terbutaline was fabricated based on ZIF-8 NF. The ZIF-8 NF were successfully prepared according to electrospinning and in-situ growth method. First, chitosan was modified on the surface of the electrode, and then the ZIF-8 NF was modified onto the upper layer of the chitosan. Taking advantages of chitosan and ZIF-8 NF in conductivity and electrocatalysis, the modified electrode presents obvious ECL phenomenon in 0.2 M PBS solution (pH 10.0) containing 0.025 M luminol. After the addition of terbutaline, ECL intensity decreased significantly, and the decreasing value showed a linear relationship with the logarithm of terbutaline concentration. The linear range was from 2.0 × 10-10 to 2.0 × 10-5 M, and the detection limit was 1.41 × 10-11 M (3σ/m). The method had high sensitivity, good stability, and good applicability to actual pork samples.

Astragaloside IV inhibits palmitic acid-induced apoptosis through regulation of calcium homeostasis in mice podocytes.

Loss of podocytes is a hallmark of diabetic nephropathy, and a growing body of evidence indicates that podocytes are susceptible to palmitic acid (PA). We have previously shown that AS-IV inhibited PA-induced podocyte apoptosis by activating sarcoendoplasmic reticulum Ca2+ ATPase (SERCA), which indicate calcium regulation may involve in the process. Immunofluorescence staining, Western blot and flow cytometry were used to measure the protective efficacy of AS-IV to ameliorate PA-induced ER stress and podocyte apoptosis. Meanwhile, AS-IV inhibited cytochrome c release, decreased mitochondrial membrane potential, accompany with the depletion of endoplasmic reticulum Ca2+ and elevation of cytosolic and mitochondrial Ca2+. Sequestration of cytosolic calcium with BAPTA-AM limited the response of podocyte apoptosis, while during the process the effect of AS-IV was also restrained. In contrast, elevation of cytosolic calcium with calcium ionophore ionomycin was depressed by AS-IV addition. Furthermore, inhibiting TRPC6 expression with SKF96365 or TRPC6 siRNA counteracted the beneficial effect of AS-IV. Our study provides further evidence to conclude the inhibitory effect of AS-IV to podocyte apoptosis is Ca2+-dependent. And the efficacy correlates with inhibiting TRPC6-mediated Ca2+ influx, and then cellular Ca2+ disturbance was coordinated.