Electrochemiluminescence System Research Articles

Wireframe Orbit-Accelerated Bipedal DNA Walker for Electrochemiluminescence Detection of Methyltransferase Activity.

In spite of the DNA walkers executing the signal accumulation task in the process of moving along the predetermined paths, the enhancement of walking dynamics and walking path controllability are still challenging due to the unprogrammed arrangements of DNA orbits. Taking these dilemmas into account, a bipedal DNA walker was designed skillfully by the virtue of wireframe orbits assembled by DNA cubes in order, which improved the efficiency and the continuity of walking. It could be attributed to the fact that both the contact chance and the dynamic interaction between walking strands and designated orbits were beneficial to minimize the possibility of derailment and improve the accumulation of signal. In addition, the hollow titanium dioxide nanospheres coated with rubrene (Rub@TiO2 NSs) were prepared by the etching of inner silicon dioxide nanoparticles (SiO2 NPs) to regulate the distribution pattern of rubrene (Rub) molecules and expose more electrochemically active sites for high-efficient electrochemiluminescence (ECL). Benefiting by the pore confinement-enhanced ECL, the electron and mass transfer was significantly accelerated because of the hollow structure of Rub@TiO2 NSs. Subsequently, endogenous dissolved oxygen as the coreactant and palladium nanoparticles (Pd NPs) as the coreaction accelerator were employed to constitute a ternary ECL system with explosive signal response. Combining with this ECL platform, the bipedal walker activated by the target can autonomously and directionally move on the DNA wireframe orbits to release the quenching probes continuously. In this way, the biosensor displayed a low detection limit (2.30 × 10-8 U·mL-1) and a wide linear range (1.0 × 10-7 to 1.0 × 10-1 U·mL-1) for the sensitive detection of Dam methyltransferase (Dam MTase) activity. Therefore, a novel strategy for the accurate quantification of epigenetic targets was developed by virtue of improving the walking dynamics of DNA walker and amplifying the ECL of Rub molecules.

Electrochemical Generation of Hot Electrons in Fully Aqueous Solutions at Tetrahedral Amorphous Carbon Thin Film Electrodes and Electrochemiluminescence Immunoassay of Serum Amyloid A

AbstractElectrochemistry of hot electrons in fully aqueous solutions at tetrahedral amorphous carbon thin film electrodes is discussed. The generation of these highly reducing chemical species was confirmed by normal pulse voltammetry and several electrochemiluminescent systems. Electron transfer into pre‐existing solvent cavities was observed at approximately −2.65 V vs. Ag/AgCl (sat.). Electrogenerated hot electrons were utilized as chemiluminescent mediators in heterogeneous sandwich immunoassay of Serum Amyloid A. The calibration curve was linear over four orders of magnitude and the detection limit was 85 ng L−1 that demonstrates the efficiency of hot electron generation at this electrode material.

Highly Efficient PTCA/Co3O4/CuO/S2O82- Ternary Electrochemiluminescence System Combined with a Portable Chip for Bioanalysis.

Herein, we reported an efficient electrochemiluminescence (ECL) biosensor chip for sensitive detection of neuron-specific enolase (NSE). First, 3,4,9,10-perylenetetracarboxylic acid with good luminescence characteristics was used as a luminophore to obtain a stable ECL signal. Subsequently, hollow porous Co3O4/CuO concave polyhedron nanocages (CPNCs) were designed as co-reaction promoters to amplify the luminescence signals for highly sensitive trace detection of NSE. In brief, the rapid cyclic conversion of Co3+/Co2+ and Cu2+/Cu+ redox pairs could continuously catalyze the reduction of persulfate (S2O82-), thus providing a large number of essential active intermediates (SO4•-) for ECL emission. Meanwhile, the unique structure of Co3O4/CuO CPNCs possessed a large specific surface area, which greatly improved its catalytic efficiency. Third, NKFRGKYKC was developed as an affinity ligand for specific antibody fixation, which improved incubation efficiency and protected bioactivity of antibodies. Finally, we independently designed a microchip and applied it for ECL detection to improve the practical application ability of the sensor. The developed biosensor exhibited good sensitivity with a wide linear range (10 fg/mL to 100 ng/mL) and a low detection limit (3.42 fg/mL), which played an active role in the clinical application of sensing analysis.

A novel binary luminophore based high-efficient electrochemiluminescence biosensor for ultrasensitive detection of human epidermal growth factor receptor-2

For the first time, a high-efficient and low-cost electrochemiluminescence (ECL) biosensor was constructed for ultrasensitive detection of breast cancer related human epidermal growth factor receptor-2 (HER-2) using a novel binary luminophore and low concentration of coreactant. Firstly, Au nanoparticles decorated graphite-like carbon nitride (g-C3N4@Au) was designed as sensing platform, which can generate ECL signal in the potential range from −1.2 V to 0 V when peroxydisulfate (S2O82−) was used as the coreactant. Secondly, amino-modified capture probes (CP) were immobilized on the surface of g-C3N4@Au via Au-N bonds. In addition, Zr-based metal organic framework (Zr-MOF) modified bulk boron carbon oxynitride (BCNO), named ZMB, exhibited remarkable ECL intensity at the potential window of −2.0 V to 0 V with 0.8 mM S2O82−. ZMB possessed a large specific surface area and abundant amino groups to anchor Au@Pt nanoparticles (Au@PtNPs). Therefore, HER-2 binding aptamers (HBA) could be anchored on Au@PtNPs to form the tracer label. Under optimal conditions, the proposed ECL biosensor displayed a wide linear range from 10 fg mL−1 to 100 ng mL−1 with a limit of detection (LOD) as low as 0.2 fg mL−1. Importantly, this work utilized ZMB/S2O82− as new ECL system with satisfactory detection performances, which provided a potential approach to improve the sensitivity in clinical diagnosis.

Boron Carbon Nitride Nanosheets-Ru Nanocomposite Self-Enhancement Electrochemiluminescence Emitter with a Three-Dimensional DNA Network Structure as a Signal Amplifier for Ultrasensitive Detection of TK1 mRNA.

In this study, a neoteric self-enhanced nanocomposite boron carbon nitride nanosheets (BCN NSs)-Ru obtained by chemical crosslinking between boron carbon nitride nanosheets (BCN NSs) and tris (4,4'-dicarboxylicacid-2,2'-bipyridyl) ruthenium(II) dichloride (Ru(dcbpy)3Cl2) was used as an emitter to build an electrochemiluminescence (ECL) biosensor for ultrasensitive detection of the cancer marker human thymidine kinase 1 (TK1) mRNA. Importantly, the self-enhanced BCN NSs-Ru could exhibit strong ECL emission because boron radicals and amine groups derived from BCN NSs could significantly enhance the ECL response of Ru(dcbpy)3Cl2, which avoided the defects of the long electron transfer path and large energy loss between the emitter and coreactant in the traditional coreaction ECL system. Impressively, in the presence of target TK1 mRNA, three-dimensional DNA network structure-labeled numerous ferrocene probes could be assembled to quickly quench the ECL signal of BCN NSs-Ru, resulting in improved biosensor sensitivity. The obtained "on-off" biosensor showed excellent stability and high sensitivity with a detection limit of 32.3 aM. In general, the developed strategy provided a new biosensing way for ultrasensitive detection of biomolecules in early disease diagnosis.

The role of osteocalcin in regulation of glycolipid metabolism and muscle function in children with osteogenesis imperfecta.

ObjectiveOsteoblasts are discovered to secrete hormones with endocrine effects on metabolism, and osteocalcin (OC) is the most abundant non-collagenous protein in bone. We investigate the relationship between serum OC levels and glycolipid metabolism and muscle function in children with osteogenesis imperfecta (OI).MethodsA total of 225 children with OI and 80 healthy controls matched in age and gender were included in this single center study. Serum levels of fasting blood glucose (FBG), triglyceride (TG), total cholesterol (TC), low- and high-density lipoprotein cholesterol (LDL-C, HDL-C) were measured by automated analyzers. Serum levels of fasting insulin (FINS) were measured using an automated electrochemiluminescence system. Serum levels of OC and undercarboxylated osteocalcin (ucOC) were measured by enzyme-linked immunosorbent assay. Grip strength and timed-up-and-go (TUG) test were measured. Bone mineral density (BMD) and body composition were measured using dual-energy X-ray absorptiometry.ResultsOI patients had significantly higher body mass index (BMI), FBG, and HOMA-IR, but lower HDL-C levels, lower grip strength and longer TUG than control group (all P<0.05). Serum OC, ucOC levels, and ucOC/OC in OI type III patients were significantly lower than those in OI patients with type I and IV. Serum levels of OC, ucOC, and ucOC/OC were negatively correlated to BMI, FBG, insulin levels, and HOMA-IR (all P<0.05). The ratio of ucOC/OC was positively correlated to grip strength (r=0.512, P=0.036), lean mass percentage (%LM) of the total body and limbs, and negatively correlated to fat mass percentage (%FM) of the total body, %FM and fat mass index (FMI) of the trunk (all P<0.05).ConclusionsObesity, glucolipid metabolic abnormalities, and reduced grip strength were common in children with OI. Circulating osteocalcin and ucOC may play an important role in the regulation of glucose metabolism, as well as the muscle function of children with OI.

A convenient and economical strategy for multiple-target electrochemiluminescence detection using peroxydisulfate solution

As various aptasensors are adopted in clinical diagnosis, the development of convenient multiple-target determination is a field of ever-increasing interests. Herein, a label-free and amplified electrochemiluminescence (ECL) sensing platform was constructed to detect multiple targets of hemin, glucose and thrombin (TB) using peroxydisulfate (S2O82−) solution, which was one of the most convenient and economical ECL systems. It was worth mentioning that the target-induced bi-enzyme cascade catalysis reaction was developed to increase the ECL response strongly of S2O82− solution due to the production of (1O2)2* from the inter-reaction between reactive oxygen species (ROS) and sulfate radical (SO4•−). Specifically, with the layer-by-layer assembly of multi-walled carbon nanotubes (MWCNTs), glucose oxidase (GOx) and gold nanoparticles (AuNPs) as the interface, the guanine-rich (G-rich) thrombin aptamer (TBA) was anchored for hemin (target 1) detection, due to the electrocatalysis of hemin/G-quadruplex as a horseradish peroxidase mimicking DNAzyme (HRP-DNAzyme) towards dissolved oxygen for ROS generation. Second, in the presence of glucose (target 2), the ECL intensity was improved because glucose was the substrate of the bi-enzyme cascade catalysis reaction. Third, when TB (target 3) was sequentially incubated based on the above-mentioned aptasensor, the bi-enzyme catalysis was inhibited to decrease the ECL signal, due to the steric hindrance effect of the TB protein. As a result, the aptasensor achieved the nanomolar detection for hemin (3.33 nM), the micromolar detection for glucose (0.33 μM) and the femtomolar detection for TB (3.33 fM), respectively.

Poly(carbazole-co-1,4-dimethoxybenzene): Synthesis, Electrochemiluminescence Performance, and Application in Detection of Fe3+

In this study, four polycarbazole derivatives (PCMB-Ds) with different alkyl side chains were designed and synthesized via Wittig–Horner reaction. A novel solid-phase electrochemiluminescence (ECL) system was prepared by immobilizing PCMB-D on an indium tin oxide (ITO) electrode with polyvinylidene fluoride (PVDF) in the presence of tripropylamine (TPrA). It could be found that the increase in alkyl side chain length had little effect on the ECL signal of PCMB-D, while the increase in the degree of polymerization (DP) greatly enhanced the ECL signal. Furthermore, the P-3/ITO ECL sensor based on the polyoctylcarbazole derivative (P-3) with the best ECL performance was successfully constructed and detected Fe3+ under the optimal experimental conditions. The ECL signal steadily diminished with the increased concentration of Fe3+ because of the competition and complexation between Fe3+ and P-3 under the condition of pH 7.4. This P-3/ITO platform could realize a highly sensitive and selective detection of Fe3+ with a wide detection range (from 6 × 10−8 mol/L to 1 × 10−5 mol/L) and low detection limit of 2 × 10−8 mol/L, which could allow the detection of Fe3+ in multiple scenarios, and would have a great application prospect.

Recent Advances in Single Cell Analysis by Electrochemiluminescence.

Understanding biological mechanisms operating in cells is one of the major goals of biology. Since heterogeneity is the fundamental property of cellular systems, single cell measurements can provide more accurate information about the composition, dynamics, and regulatory circuits of cells than population-averaged assays. Electrochemiluminescence (ECL), the light emission triggered by electrochemical reactions, is an emerging approach for single cell analysis. Numerous analytes, ranging from small biomolecules such as glucose and cholesterol, proteins and nucleic acids to subcellular structures, have been determined in single cells by ECL, which yields new insights into cellular functions. This review aims to provide an overview of research progress on ECL principles and systems for single cell analysis in recent years. The ECL reaction mechanisms are briefly introduced, and then the advances and representative works in ECL single cell analysis are summarized. Finally, outlooks and challenges in this field are addressed.

A dual engine-triggered DNA walker based on luminous perylene-TiO2 nanospheres for efficient electrochemiluminescence bioassay

Despite the intrinsic programmability and flexible biological functions of DNA walkers, it remains challenging for traditional DNA walkers to precisely control mechanical running paths in nanoscale spaces. In this work, an elegant dual engine-triggered DNA walker was elaborated based on precise orientation protocol, applying the DNA cube as the scaffold for anchoring the dual swing arms as engines and tracks as signal switches. The order arrangement and dual engines enhanced the operating efficiency and controllability of the DNA walker markedly. Moreover, the electrochemiluminescence (ECL) molecule perylene doped-titanium dioxide (Pe-TiO2) organic–inorganic nanospheres with low cost and high reproducibility were synthesized as the ECL emitters by one-step sol–gel method. It was worth noting that TiO2 gel not only restricted the stacking mode of Pe molecules in vibration and rotation, but also enhanced the interfacial charge transfer ability in organic–inorganic hybrid mode, resulting in the improvement of ECL efficiency and structural stability. Based on the luminous Pe-TiO2 nanospheres, a ternary ECL system was proposed with S2O82− as coreactant, and silver nanoparticles (Ag NPs) as coreaction accelerator. Ultimately, by combing the dual engine-triggered DNA walker with the ternary ECL system, an efficient ECL bioassay platform was developed for microRNA let 7a (let-7a) detection with a wide linear range from 10 fmol/L to 100 nmol/L and a low detection limit of 7.0 fmol/L. Hence, this work offered a universal strategy to predesign walking paths and improve loading capacity in virtue of DNA nanostructures, as well as to expand the biology research of planar organic luminophores in an organic–inorganic hybrid manner.

Progress and Prospects of Electrochemiluminescence Biosensors Based on Porous Nanomaterials.

Porous nanomaterials have attracted much attention in the field of electrochemiluminescence (ECL) analysis research because of their large specific surface area, high porosity, possession of multiple functional groups, and ease of modification. Porous nanomaterials can not only serve as good carriers for loading ECL luminophores to prepare nanomaterials with excellent luminescence properties, but they also have a good electrical conductivity to facilitate charge transfer and substance exchange between electrode surfaces and solutions. In particular, some porous nanomaterials with special functional groups or centered on metals even possess excellent catalytic properties that can enhance the ECL response of the system. ECL composites prepared based on porous nanomaterials have a wide range of applications in the field of ECL biosensors due to their extraordinary ECL response. In this paper, we reviewed recent research advances in various porous nanomaterials commonly used to fabricate ECL biosensors, such as ordered mesoporous silica (OMS), metal–organic frameworks (MOFs), covalent organic frameworks (COFs) and metal–polydopamine frameworks (MPFs). Their applications in the detection of heavy metal ions, small molecules, proteins and nucleic acids are also summarized. The challenges and prospects of constructing ECL biosensors based on porous nanomaterials are further discussed. We hope that this review will provide the reader with a comprehensive understanding of the development of porous nanomaterial-based ECL systems in analytical biosensors and materials science.

High efficiency electrochemiluminescence of 3D porous g-C3N4 with dissolved O2 as co-reactant and its sensing application for ultrasensitive detection of microRNA in tumor cells

In this work, the electrochemiluminescence (ECL) phenomenon of three-dimensional graphitic carbon nitride (3D g-C3N4) was reported. Firstly, the proposed 3D g-C3N4 possessed 3D porous interconnected open-framework which enabled faster charge transport and efficient penetration of co-reactants due to “pore confinement effect”. Then, we found that the dissolved O2 could serve as an excellent co-reactant for cathodic ECL of 3D g-C3N4. And the high specific surface area was beneficial to better adsorbing and gathering of dissolved O2 and reactive oxygen species (ROSs), which made them full contact on the surface or inside of 3D g-C3N4, giving a more sufficient ECL reaction and higher ECL signal. Based on the proposed 3D g-C3N4-O2 ECL system, a sensitive biosensor was constructed for microRNA-21 (miRNA-21) detection with assistance of 3D spherical tracks assisted 3D DNA walking machine, which exhibited superior performance for miRNA-21 with detection limit of 0.22 fM. The proposed 3D g-C3N4-O2 ECL system with high ECL efficiency and the effective target conversion and amplification strategies were beneficial to construct ultra-sensitive ECL sensing platform, which would be better applied to clinical bioanalysis.

Plasmon-Boosted Fe, Co Dual Single-Atom Catalysts for Ultrasensitive Luminol-Dissolved O2 Electrochemiluminescence Detection of Prostate-Specific Antigen

Improving the sensitivity of electrochemiluminescence (ECL) systems is highly desired for in vitro ECL diagnosis and bio-detections due to the often-low content of biomarkers in diseases. And dissolved O2 (DO) as a co-reactant is considered superior to H2O2 in the most commonly used luminol ECL systems due to better stability and low biotoxicity, but it still suffers from low ECL performance due to the low reactivity of DO. In this study, an efficient luminol-DO ECL system was developed through the complexing of Fe, Co dual single-atom catalysts (D-SACs) supported by N-doped graphene with the luminol-capped Ag nanoparticles (AgNPs). Benefiting from the electronic interaction between Fe and Co metal sites in the relevant D-SACs and plasmon enhancement of AgNPs, the performance of the corresponding ECL system could be significantly boosted up to ≈677-fold under optimal testing conditions, comparable to the classic luminol-O2 system. Furthermore, the developed luminol-DO ECL system was successfully applied for the stable ultrasensitive detection of prostate-specific antigen (PSA) in a wide linear range of 1 fg/mL to 1 μg/mL, with a low limit of detection (0.98 fg/mL).

Single-Atom Iron Enables Strong Low-Triggering-Potential Luminol Cathodic Electrochemiluminescence.

The conventional cathodic electrochemiluminescence (ECL) always requires a more negative potential to trigger strong emission, which inevitably damages the bioactivity of targets and decreases the sensitivity and specificity. In this work, iron single-atom catalysts (Fe-N-C SACs) were employed as an efficient co-reaction accelerator for the first time to achieve the impressively cathodic emission of a luminol-H2O2 ECL system at an ultralow potential. Benefiting from the distinct electronic structure, Fe-N-C SACs exhibit remarkable properties for the activation of H2O2 to produce massive reactive oxygen species (ROS) under a negative scanning potential from 0 to -0.2 V. The ROS can oxidize the luminol anions into luminol anion radicals, avoiding the tedious electrochemical oxidation process of luminol. Then, the in situ-formed luminol anion radicals will directly react with ROS for the strong ECL emission. As a proof of concept, sensitive detection of the carcinoembryonic antigen was realized by glucose oxidase-mediated ECL immunoassay, shedding light on the superiority of SACs to construct efficient cathodic ECL systems with low triggering potential.

Wireless Anti-Stokes Photoinduced Electrochemiluminescence at Closed Semiconducting Bipolar Electrodes.

Wireless electrochemical systems constitute a rapidly developing field. Herein, photoinduced electrochemiluminescence (PECL) is studied at Si-based closed bipolar electrodes (BPEs) for designing anti-Stokes systems that can convert IR into visible photons, without direct electrical contact. We show that protection of the anodic emitting pole of the BPE allows the triggering of bright and longstanding emission under the synergetic actions of an external bias and IR illumination. Photoactive n- and p-type Si BPEs are studied with front-side and back-side illumination, respectively, and nonphotoactive n+-Si BPEs are studied in the dark. Two electrochemiluminescent (ECL) systems ([Ru(bpy)3]2+/TPrA and L-012) are tested, and we show that the onset bias and the anti-Stokes shift can be controlled by the ECL system that is employed. These advances, rationalized by simulations, will be useful for the design of original PECL systems for chemical sensing or photodetection.

A novel Cu:Al nanocluster-based electrochemiluminescence system with CeO2 NPs/polydopamine biomimetic film for BRCA detection

Herein, we have developed a novel kind of electrochemiluminescence (ECL) biosensor for BRCA detection. Based on the metal ion-induced enhancement mechanism, high luminous Cu:Al nanoclusters (Cu:Al NCs) was obtained as ECL nanoprobe. Moreover, the polydopamine (PDA) biomimetic film with CeO2 NPs was constructed as a sensing platform. The structure of the biomimetic film can provide a strong affinity to link biomolecules and functional nanoparticles. Meanwhile, the good ionic permeability of PDA film was in favor of the charge transfer in the ECL reaction on the electrode surface. In addition, CeO2 NPs on the biomimetic film further improved the ECL reaction efficiency. Therefore, this sensor was successfully applied in the detection of BRCA in the clinic serum sample. The current study has provided a feasible and reliable method for biochemical analysis and clinical detection.

Acidic pH and thiol-driven homogeneous cathodic electrochemiluminescence strategy for determining the residue of organophosphorus pesticide in Chinese cabbage

Electrochemiluminescent (ECL) sensors for organophosphorus pesticides (OPs) have received considerable attention, whereas complicated electrode’s immobilization, response to single hydrolysate and anodic emission correlated with ECL assays restrict their potential utilization. Herein, we developed a homogeneous dual-response cathodic ECL system for highly sensitive and reliable analysis of OP using CdTe QDs as emitters. CdTe QDs, emitting red light, were fabricated through a hydrothermal reaction and generated anodic and cathodic ECL emission upon stimulation of tripropyl amine and K2S2O8, respectively. Notably, CdTe QDs-K2S2O8 showed a simultaneous response to thiol and acidic pH, and were regarded as a ECL sensor for methidathion with limit of detection of 0.016 ng/mL based on hydrolysis of acetylthiocholine into thiocholine and CH3COOH by acetylcholinesterase (AChE) and OPs’ inhibition on AChE activity. This sensor also exhibited good practicability to detect methidathion in Chinese cabbage. Overall, the sensor will supply more useful information for ensuring OPs-related food safety.

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.

Electrochemiluminescence aptasensor for vascular endothelial growth factor 165 detection based on Ru(bpy)32+/Au nanoparticles film modified electrode and double signal amplification

Vascular endothelial growth factor (VEGF165) is a signal protein that plays a central role in the regulation of angiogenesis and can stimulate angiogenesis. The development of highly sensitive and selective detection method for VEGF165 is very important for disease diagnosis and follow-up treatment monitoring. In this study, an electrochemiluminescence (ECL) aptasensor for VEGF165 has been developed based on quench of H2O2 toward Ru(bpy)32+/TPrA ECL system and RecJf exonuclease induced target recovery and hybridization chain reaction (HCR) as amplification strategy. The presence of VEGF165 makes a large number of glucose oxidase (GOD) fixed on the electrode surface through the double signal amplification strategies. The present of GOD cause the production of a large amount of H2O2 near the electrode surface under excess amount of glucose, resulting in the inhibition of the ECL signal of Ru(bpy)32+/Au nanoparticles (Ru(bpy)32+/AuNPs) film fixed on the electrode surface. The ECL response of the designed biosensor has a good linear relationship with the logarithm of the concentration of VEGF165 in the range of 0.5 pg/mL to 500 ng/mL with a detection limit of 0.2 fg/mL. The VEGF165 in serum samples has been detected by the proposed aptasensor with satisfactory results.

Controllable Enhanced Ru(bpy)32+ Electrochemiluminescence Detection Systems Based on Eu@MOF253@AuNPs/GCE for the Sensitive Detection of Carbaryl in Food.

In this study, an electrochemiluminescence detection system for the sensitive detection of carbaryl was constructed based on the dual identification of Eu@MOF253, which has a recognition effect on carbaryl, and the electrochemiluminescence system of Ru(bpy)32+/S2O82-, which can react with carbaryl in a redox reaction. This method not only overcame the weakness of the electrochemiluminescence instability of the Ru(bpy)32+/S2O82- system but also changed the sensitivity of the sensing detection system to the target by adjusting the concentration of Ru(bpy)32+ and then proposed a detection strategy with a controllable detection range. After analyzing the electrochemiluminescence signal change mechanism of this system and optimizing the detection conditions, it was concluded that the strategy has good linear detection of carbaryl in the range of 1-1000 and 0.02-0.3 μg L-1, and the detection limits were 0.058 and 0.014 μg L-1. Finally, the strategy was also successfully applied to the detection of actual samples.