112 results about "Luminol" patented technology

The invention discloses a method for detecting glufosinate-ammonium residues in coffee in dual modes of colorimetry and chemiluminescence, and belongs to the technical field of chemical analysis and detection.The method comprises the steps that Schiff base formed by 4-aminoantipyrine and glutaraldehyde serves as a complexing agent of Cu < 2 + >, and then a copper-doped carbon dot Cu-CDs nano-enzyme is prepared through microwave digestion; according to the present invention, the Cu-CDs nano-enzyme has excellent peroxidase-like activity, can oxidize the colorless 2, 2 '-biazo-bis-3-ethylbenzothiazoline-6-sulfonic acid into the blue-green oxidized ABTS, and can improve the chemiluminescence intensity of the reaction of N-(4-aminobutyl)-N-ethylisoluminol and H2O2 by nearly 100 times when the Cu-CDs nano-enzyme is used as the chemiluminescence catalyst; based on the inhibition effect of glufosinate-ammonium on the activity of Cu-CDs POD, a sensitive and rapid colorimetric and chemiluminescence two-channel GM detection technology is developed, and the method has potential application value in the aspect of coffee safety monitoring.

The invention discloses an immunosensor for detecting cytokine interferon gamma through electrochemiluminescence as well as a preparation method and application of the immunosensor. The immunosensor comprises a three-electrode system consisting of an immunoelectrode, a reference electrode and a counter electrode, the immunoelectrode is a VMSF modified electrode confined to cerium dioxide nano enzyme and platinum nano particles, and is obtained by covalently immobilizing an IFN-gamma antibody and closing a non-specific site; when the immunosensor is used for detection, a solution containing luminol is used as an electrolyte. The CeO2 and the PtNPs which are confined in the nano channel show a remarkable synergistic catalysis effect. Compared with direct modification on a plate electrode, CeO2-PtNPs has higher catalytic activity and stability. The sensor provided by the invention is used for INF-gamma detection, has the advantages of high sensitivity, low detection limit and wide detection range, does not need complex pretreatment and separation processes during detection, reduces the detection cost, is simple to operate, and is suitable for large-scale application.

The application discloses an electrochemiluminescence immunosensor for detecting interleukin-1 beta and a preparation method and application thereof, and comprises a three-electrode system of a working electrode, a reference electrode and a counter electrode; the working electrode is a modified electrode of CoAl layered double hydroxide, is loaded with platinum nanoparticles after being etched by alkali, and is obtained by fixing interleukin-1 beta antibodies and blocking non-specific sites; and a solution containing luminol is used as an electrolyte during detection of the immunosensor. The working electrode of the immunosensor takes oxygen-rich vacancy CoAl layered double hydroxide as a substrate, combines with platinum nanoparticles to realize EMSI effect, significantly enhances the electrochemiluminescence signal of a luminol-dissolved oxygen system, realizes quantitative detection of IL-1 beta by combining with specific antigen-antibody recognition, and has the characteristics of strong anti-interference ability, fast detection speed and good stability.

The invention discloses a confinement composite nano-enzyme enhanced electrochemiluminescence immunosensor for detecting tumor necrosis factors and a construction method and application of the immunosensor. The immunosensor is a three-electrode system, and liquid to be detected contains luminol; wherein the working electrode is obtained by covalently immobilizing a tumor necrosis factor specific antibody after an SNF epoxy modified electrode is subjected to confinement of Ni (OH) 2-CeO2 composite nano-enzyme and then closing a non-specific site. The Ni (OH) 2-CeO2 composite nano-enzyme is confined in a nano-channel, the Ni (OH) 2-CeO2 composite nano-enzyme and the nano-channel can synergistically accelerate the process of an oxygen reduction reaction, the modification stability of the nano-enzyme is effectively improved, and a formed immune complex causes increase of interface resistance and steric hindrance of a sensing electrode to cause signal reduction; therefore, high-sensitivity detection of the tumor necrosis factor is realized, and the constructed sensor has the advantages of low detection limit, wide detection range and the like, and is very suitable for being widely applied to the fields of auxiliary clinical diagnosis, large-scale screening, health monitoring and the like.

The invention is suitable for the field of electrochemical luminescence detection equipment, and provides a dispersion device suitable for electrochemical luminescence detection, which comprises a monochromator body, the monochromator body is composed of a monochromator housing, a reflector assembly, a grating assembly, a collimating mirror assembly, a focus lens assembly, a slit, a flange snap ring and a flange; an M-shaped light path is arranged in the monochromator body, and a slit, a reflector assembly, a collimating mirror M1 in the collimating mirror assembly, a customized blazed grating G1 in the grating assembly and a focusing mirror M2 in the focusing mirror assembly are sequentially arranged in the light propagation direction. The customized blazed grating G1 is designed by adopting specific parameters including the scribed line density, the blazed wavelength, the notch groove depth and the groove width ratio, and primary light energy enhancement and secondary light intensity suppression can be realized; according to the invention, an optical filter is not needed, the diffraction efficiency of a monochromator is improved to 60-86%, the intensity ratio of luminol secondary light to primary light is less than or equal to 1.6%, the detection limit of ruthenium bipyridine is reduced from 100pmol / L to 50pmol / L, and the electrochemical luminescence detection device is suitable for various electrochemical luminescence detection scenes.

The invention discloses an electrochemical luminescence immunosensor for detecting interleukin-1 beta as well as a preparation method and application of the electrochemical luminescence immunosensor. The electrochemical luminescence immunosensor comprises a three-electrode system consisting of a working electrode, a reference electrode and a counter electrode, the working electrode is a modified electrode of CoAl layered double hydroxides, the modified electrode is subjected to alkali etching and then loaded with platinum nanoparticles, then an interleukin-1 beta antibody is fixed, and non-specific sites are closed, so that the working electrode is obtained; when the immunosensor is used for detection, a solution containing luminol is used as an electrolyte. The working electrode of the immunosensor takes oxygen vacancy-rich CoAl layered double hydroxide as a substrate, platinum nanoparticles are combined to realize an EMSI effect, an electrochemical luminescence signal of a luminol-dissolved oxygen system is remarkably enhanced, and antigen-antibody specific recognition is combined to realize quantitative detection of IL-1beta. The method has the characteristics of strong anti-interference capability, high detection speed and good stability.

The invention discloses an immunofluorescence imaging method for driving tyramine signal amplification based on chemiluminescence and application thereof, and relates to the technical field of biomedical imaging. The immunofluorescence imaging method comprises the following steps: carrying out first incubation on a to-be-detected sample and a peroxidase-labeled antibody; performing second incubation on the to-be-detected sample after the first incubation and a tyramine substrate containing a fluorophore under a dark condition; adding a chemiluminescent substrate solution into the to-be-detected sample after the second incubation, and carrying out image acquisition; wherein the antibody can be specifically bound with a target protein; the tyramine substrate can generate active free radicals under the catalysis of peroxidase, so that the active free radicals are covalently cross-linked with tyrosine residues; the chemiluminescent substrate solution comprises hydrogen peroxide and luminol. The immunofluorescence imaging method improves imaging signal and fluorescence stability, effectively reduces background interference and phototoxicity, is suitable for long-time stable fluorescence immunoimaging, and is especially suitable for high-sensitivity detection of low-expression protein markers.

The application relates to a method for enhancing electrochemiluminescence signals by ion-pi interaction, belonging to the fields of electrochemiluminescence and analytical chemistry. 2+ By modifying the working electrode with a conjugated pi system, cation-pi interaction is introduced into the Ru(bpy)3 / triethylamine (TEA) system, efficient enrichment of TEA protonated cations near the electrode is realized, thereby greatly enhancing the electrochemical reaction rate and ECL signal. Further, anion-pi interaction is utilized to realize ECL signal enhancement of the luminol ECL system. In addition, the conjugated pi system is exposed to the outermost boundary of the electrode, so as to provide effective ion-pi interaction for ECL; when the pi system is covered by an alkyl chain, the modified electrode can only exhibit hydrophobic interaction. The method disclosed by the application provides a new strategy for extending ion-pi interaction to all types of ECL systems and constructing a high-sensitivity ECL analysis platform.

This invention relates to a dual-potential electrochemiluminescence immunosensor based on enzymatic in-situ generation of a co-reactant, its preparation method, and its application. The sensor includes: a substrate electrode; a GOx@Au@MoS2 multifunctional sensing interface; a hybrid probe consisting of a cathode probe and an anode probe; the cathode probe is a Py-HOF-labeled AFB1 antibody, and the anode probe is a UiO66-NH2@luminol-labeled OTA antibody; glucose is added to the detection solution, and hydrogen peroxide is generated in situ through immobilized glucose oxidase, serving as the single co-reactant for both the cathode and anode. During detection, this invention generates H2O2 in situ through enzymatic generation, simultaneously exciting ECL signals at both the cathode and anode; it solves problems such as poor stability of the H2O2 co-reactant, inconvenient concentration control, multiple operation steps, and insufficient continuous supply; and it enables simultaneous quantitative detection of AFB1 and OTA with a single sample addition, without the need for external H2O2.

To provide methods and apparatus for simultaneously detecting a quantity and / or concentration within a large range of protein.SOLUTION: Some embodiments described herein relate to a method that includes separating an analyte-containing sample via electrophoresis in a capillary. The capillary is loaded with a chemiluminescence agent, such as luminol, that is configured to react with the analyte (e.g., HRP-conjugated proteins) to produce a signal indicative of a concentration and / or quantity of analyte at each location along the length of the capillary. A first image of the capillary containing the analytes and the chemiluminescence agent is captured over a first period of time. A second image of the capillary containing the analytes and the chemiluminescence agent is captured over a second, longer, period of time. A concentration and / or quantity of a first population of analytes at a first location is determined using the first image, and a concentration and / or quantity of a second population of analytes at a second location is determined using the second image.SELECTED DRAWING: None

The invention relates to the technical field of electrochemical luminescence sensing, and discloses an electrochemical luminescence immunosensor for detecting interleukin-1 beta, a preparation method and application thereof, the electrochemical luminescence immunosensor comprises a working electrode, a reference electrode and a counter electrode; the working electrode comprises a substrate electrode and an ordered mesoporous silica film (SNF) modified on the surface of the substrate electrode; a composite nano-enzyme containing cobaltosic oxide nanoparticles and nitrogen-doped graphene quantum dots is loaded in a nano-pore channel of the SNF, the outer surface of the SNF is modified with an epoxy group, and an anti-interleukin-1beta antibody is covalently immobilized through the epoxy group; a detection system of the electrochemical luminescence immunosensor is a luminol / dissolved oxygen system. According to the electrochemical luminescence immunosensor, a luminol / dissolved oxygen system signal can be remarkably enhanced, and high-sensitivity and accurate quantitative detection of interleukin-1 beta is realized under a neutral condition.

This invention belongs to the field of immunoassay and biosensing technology, and discloses a method for preparing a ratiometric ECL biosensor based on Eu / Tb-Lu MOGs. Using Eu / Tb-Lu MOGs as the luminescent material and H3-tctpy and luminol as ligands, a single-luminescent material with dual ECL emission is synthesized. Lanthanide ions provide the cathode ECL emission, enhanced by the antenna effect and Tb→Eu energy transfer; the anode emits light from luminol using dissolved oxygen in water, requiring only the addition of K2S2O8 as a single co-reactant, resulting in fewer side reactions and a stable signal. The dual-potential ratiometric sensing utilizes the dual ECL signal for self-calibration, improving anti-interference and reliability; the single-luminescent dual-potential system achieves synchronous anode / cathode luminescence, simplifying the system and improving detection accuracy. By detecting changes in the ECL signal of different concentrations of analytes, the detection of microRNA-126 is achieved.

This invention develops a pH-responsive controlled-release electrochemiluminescence sensor based on glucose oxidation and its application in the detection of CYFRA 21-1, belonging to the field of electrochemiluminescence sensor construction technology. The sensor constructed in this invention uses BSA / luminol-Ab2 / SiO2-PEI@Au NPs as the secondary antibody label and CeO2-Au as the substrate material. It utilizes the oxidation of glucose to gluconic acid under voltage, thereby lowering the pH. The sensor constructed in this invention has a wide detection range, high sensitivity, and low detection limit, providing a feasible solution for the detection of CYFRA 21-1.

The application belongs to the technical field of electroluminescence, and particularly relates to a preparation method of a high-entropy oxide material and application of the high-entropy oxide material in electrochemiluminescence detection of levofloxacin. The high-entropy oxide material is a kind of five-element high-entropy oxide HEO-800 material with simple raw materials, convenient synthesis, excellent electrochemiluminescence performance, which is synthesized by taking metal nitrate of Fe, Co, Cu, Zn and Ni as raw materials, and taking Na2CO3 and NaOH as raw materials. The HEO-800 material has excellent conductivity and chemical stability, and a multi-electron reaction potential accelerates the conversion of dissolved oxygen into reactive oxygen species (ROS), enhances the electroluminescence intensity, and based on the quenching effect of LVX, a method for detecting LVX by using a luminol / HEO-800 system is established. By fitting the change of ECL intensity with the concentration of LVX, a linear calibration curve is obtained, the correlation coefficient is 0.993, and the detection limit is 1.02*10 ‑5 μM (S / N=3). The material has good sensitivity, stability and reproducibility for electrochemiluminescence detection of LVX, and provides a new scheme for designing a new electrocatalyst for testing LVX.

The invention discloses a preparation and use method of a co-reactant-free anti-pollution electrochemical luminescence sensor for detecting cadmium ions in grains, which is characterized in that the oxygen evolution reaction activity of porphyrin, the anti-pollution capability and conductivity of poly (3, 4-ethyldioxythiophene)-polystyrene sulfonate chitosan hydrogel and the luminescence stability of luminol are utilized to detect the cadmium ions in the grains. According to the recognition effect of cadmium ions on aptamers and the signal amplification strategy of a DNA walker, a non-co-reactant anti-pollution electrochemical luminescence sensor for detecting the cadmium ions in the grains in an on-off mode is constructed. The sensor disclosed by the invention can be used for judging whether the detected grain contains target ions or not according to the change of the electrochemical luminescence peak value of the cadmium ions in a detection result. The method has the advantages that the sensor is low in cost, simple in detection operation, free of co-reactants and high in pollution resistance; the cadmium heavy metal can be qualitatively and quantitatively measured; the method has high sensitivity and low detection limit, and provides a thought for detection of other ions and small molecular substances.

The invention discloses an HRP chemiluminescent substrate system, a kit and a preparation method, the HRP chemiluminescent substrate system is composed of a liquid A and a liquid B which are physically isolated and stored; the solution A is an alkaline buffer system with the pH value of 9.0-9.6, and comprises isoluminol or a salt substrate thereof, a cationic surface active agent CTAC and a metal chelating agent diethylene triamine pentaacetic acid; and the solution B is an acidic solution with the pH value of 4.5-5.5, and comprises an oxidizing agent and a reinforcing agent N-(3-chloro-4-hydroxyphenyl) acetanilide. According to the invention, the reinforcing agent N-(3-chloro-4-hydroxyphenyl) acetanilide is placed in the acidic liquid B, when the acidic liquid B is mixed with the alkaline liquid A, the mixed system is maintained at a specific pH value of 8.3-8.6, and the reinforcing agent is rapidly dissociated into phenoxy anions; and carrying out in-situ capture and enrichment on a micelle interface by CTAC cationic micelles with positive charges, which exist in the solution A in advance, through electrostatic attraction. And in cooperation with a low-ion-strength environment brought by no buffer salt in the liquid B, the system ensures the high activity of the HRP enzyme, realizes directional interface catalysis of the enhancer, and significantly improves the luminous efficiency and stability.

The invention belongs to the field of antibiotic detection, and relates to detection of norfloxacin (NOR). The invention provides a Luminol-Eu-NCDs ratiometric fluorescent probe as well as a preparation method and application of the Luminol-Eu-NCDs ratiometric fluorescent probe. According to the application, a novel ratiometric fluorescence sensor is constructed through covalent linkage of Luminol-Eu self-assembled and synthesized by AIE and NCDs derived from Listeria monocytogenes. The Luminol-Eu NPs with the AIE effect overcomes the fluorescence quenching characteristic of a traditional fluorophore in a high concentration or aggregation state, so that the reference fluorescence brightness of fluorescence analysis is greatly improved. In addition, due to the introduction of the Luminol-Eu NPs, the sensitivity and the accuracy of NOR detection can also be improved. On the basis, a simple ratio fluorescence sensor with high selectivity is developed, and the ratio fluorescence sensor is used for detecting NOR residues in a milk sample.

The invention relates to the technical field of immunosensors, in particular to a double-ligand Cu-MOF composite material, an immunosensor, a preparation method and application. The preparation method of the double-ligand Cu-MOF composite material comprises the following steps: dissolving isoluminol and 2-aminoterephthalic acid in a first organic solvent, then adding glutaraldehyde, and stirring under a dark condition to obtain a solution A; dissolving polyether F127 in a mixed solvent, and then adding copper salt to obtain a solution B; and mixing the solution A and the solution B, and carrying out a first heating reaction to obtain Cu-ABEI. The invention also provides the double-ligand Cu-MOF composite material prepared by adopting the method, an antigen-combined illuminant, an immunosensor and a preparation method of the double-ligand Cu-MOF composite material. According to the invention, the problem that the ECL signal stability of isoluminol is poor is solved, and the problem that the sensitivity is low when an existing sensor is used for detecting DBP is also solved.

The invention discloses a method for identifying organic Wuchang rice and common Wuchang rice based on electrochemical luminescence, and belongs to the field of analysis and detection. On the basis of an electrochemical luminescence system of luminol and hydrogen peroxide, by means of different catalase contents in organic Wuchang rice and common Wuchang rice, supernate obtained after treatment of the two kinds of rice is added into the luminescence system of luminol and hydrogen peroxide, different inhibition effects are achieved, and then the reduction rates of the two kinds of rice are compared; the identification of the organic Wuchang rice and the common Wuchang rice is successfully realized. The method provided by the invention has the characteristics of safety, accuracy, effectiveness, simplicity and convenience, and determines that the rice is organic Wuchang rice with the reduction effect on the luminescence system within the range of 65 + / -4.9% and the rice is common Wuchang rice with the reduction effect on the luminescence system within the range of 55 + / -4.9%.

The application relates to a luminol-embedded iron-based metal organic framework composite material and a preparation method and application thereof, and belongs to the technical field. The application discloses a preparation method of a luminol-embedded iron-based metal organic framework composite material (luminol@Fe-DOBDC MOFs), mainly adopting 2,5-dihydroxyterephthalic acid (DOBDC) as an organic linking agent, and Fe in FeCl3.6H2O 3+ As a metal node, Fe-DOBDC MOFs (Fe 3+ And the electronic interaction between the carboxyl groups, the fluorescence of the ligand is significantly quenched, and the stirring reaction with luminol can obtain a fluorescent double-emission composite material, that is, the luminol-embedded iron-based metal organic framework composite material (luminol@Fe-DOBDC MOFs).

The invention discloses an application of an improved isoluminol luminescent substrate in a MaglumiX8 chemiluminescence immunoassay system, and belongs to the technical field of in vitro diagnostic reagents. The luminescent substrate comprises an alkaline solution containing a metal leaf line complex and a derivative thereof, and a piperazine phenol derivative, and a peroxide solution containing urea and stannate. According to the invention, a metal leaf line substance is added into an alkaline solution, an active structure is stabilized through coordination modification, a reaction with hydrogen peroxide is promoted, a chemiluminescence signal is enhanced, and the luminous efficiency and the detection sensitivity are improved; by adding the piperazine phenol derivative, lasting glow of isoluminol is realized, signal stability is ensured, and result reliability is improved. In a hydrogen peroxide system, a urea / stannate stabilizer is added, so that the stability of a substrate is improved. Experimental verification shows that the substrate has high accuracy correlation with an original reagent, excellent precision and stable performance after being stored at room temperature for 24 months, and is suitable for the detection fields of hormones, tumor markers and the like.

According to the light-induced photoelectrochemical integrated device provided by the invention, electrochemical luminescence and PEC signal simultaneous output are realized in a single sensing system for the first time, and dual-mode simultaneous quantification of markers in serum is realized. The preparation method comprises the following steps: preparing and screening an ECL / PEC material pair with matched wavelength: luminol-Au / Bi2WO6, and successively assembling Bi2WO6 and luminol-Au labeled probes on an indium tin oxide electrode by utilizing a layer-by-layer self-assembly mode; when a voltage is applied, the luminol-Au emits a strong ECL signal and triggers the Bi2WO6 to generate an obvious light current. A marker miRNA-21 is taken as a model, recognition molecules with a hairpin structure are introduced into a system, and sensitive and accurate dual-mode analysis of the miRNA-21 is realized by adopting an enzyme-assisted amplification method. The detection method provided by the invention not only can realize ECL-PEC dual-mode simultaneous detection of the target object, but also has relatively high universality, and a new example can be provided for precise biological analysis by replacing and recognizing molecules through the sensor.

This invention relates to the field of microfluidic sensing and detection technology, and more particularly to a photoelectric / fluorescence dual-mode self-calibrating microfluidic sensor for the detection of various mycotoxins, its fabrication method, and its application. The microfluidic sensor comprises a three-channel microfluidic chip and a substrate. In its fabrication, the three independent working electrodes and an integrated reference-counter electrode system are integrated into the microfluidic chip, utilizing oxygen-rich vacancy Io. 0.2~0.4 S 0.3~0.5 Using BiOBr (ISBO-OVs)@Au composite material as the sensing substrate, an internal secondary light source is formed by the chemiluminescence reaction of luminol-superoxide radicals, which can cascade and amplify the photocurrent signal. At the same time, combined with the specific recognition function of 7DCCA labeled aptamers, the sensitivity and specificity of microfluidic sensors for detecting trace fungal toxins are greatly improved.

A system and method for in-situ quantitative assessment of Bovine Mastitis (BM) in collected milk samples using optical imaging is disclosed. A bio-functionalized assay tray contains multiple wells, each having a gel with a specially prepared mixture of hemoglobin (Hb) and metal ions. At least one of the wells is filled with a reference milk sample which is characteristic of milk with no BM disease. Other wells are filled with collected milk samples. After waiting an interaction time, luminol and hydrogen peroxide solutions are added to the wells, causing chemiluminescent (CL) light emission. The intensity of CL light emitted by wells containing haptoglobin (Hp) is inhibited due to Hb-Hp binding. After waiting a CL light stabilization time, the tray is placed in a dark box, and a camera and image processor are used to analyze the CL light intensities. A calibration curve yields the Hp concentration in each well.

The embodiment of the invention discloses a method for screening a tumor immune checkpoint inhibitor based on electrochemical luminescence sensing. According to the invention, an electrochemiluminescence sensor is established, and resonance energy transfer between luminol (an electrochemiluminescence donor) and a PD-L1-targeting metal cluster (an electrochemiluminescence receptor) is utilized; the electrochemical luminescence sensor capable of rapidly, sensitively, simply, conveniently and quantitatively analyzing the equilibrium dissociation constant between the non-antibody immune checkpoint inhibitor and the PD-L1 expressed on the tumor cell membrane at low cost is established. The efficiency of blocking the PD-1 / PD-L1 by the inhibitor is evaluated through quantitative analysis of the constant, so that the potential non-antibody immune checkpoint inhibitor is effectively screened.

The present application belongs to the field of biosensors, and relates to a dual-mode sensor for detecting BACE1, in particular to a dual-mode sensor for detecting BACE1 and a preparation method and application thereof. The present application first uses silver nanoparticles co-modified by luminol and short peptides as an electrochemiluminescence and electrochemical dual-mode signal unit, uses a three-dimensional aggregate formed by CB[8] induced aggregation of silver nanoparticles co-modified by luminol and short peptides P2 as a signal probe, carries out signal labeling and signal amplification, and thus improves the sensitivity of BACE1 activity detection. It is worth noting that the dual-mode sensor provides diversified analysis data for the detection of BACE1 activity, and shows high selectivity and repeatability. Compared with a single-mode sensor, the dual-mode sensor can significantly improve the analysis efficiency and accuracy, and has important scientific significance and application value.

The present invention discloses a method for dual-mode detection of glufosinate residues in coffee by colorimetry and chemiluminescence, belonging to the technical field of chemical analysis and detection. In this method, the Schiff base formed by 4-aminoantipyrine and glutaraldehyde is used as a complexing agent for Cu 2+ . Then, microwave digestion is used to prepare copper-doped carbon dots Cu-CDs nanozyme. The Cu-CDs nanozyme has excellent peroxidase-like activity, oxidizes colorless 2,2'-azino-bis-(3-ethylbenzothiazoline-6-sulfonic acid) into blue-green oxidized ABTS, and is used as a catalyst for chemiluminescence, which can increase the chemiluminescence intensity of the reaction between N-(4-aminobutyl)-N-ethylisoluminol and H2O2 by nearly 100 times. Based on the inhibitory effect of glufosinate on the POD-like activity of Cu-CDs, a sensitive and rapid dual-channel GM detection technology by colorimetry and chemiluminescence has been developed. The method of the present invention has potential application value in coffee safety monitoring.

The invention belongs to the technical field of biomedical nano materials, and particularly relates to a phosphazene-based amphiphilic conjugate, an anti-inflammatory nano-micelle as well as a preparation method and application of the phosphazene-based amphiphilic conjugate and the anti-inflammatory nano-micelle. The structural formula of the phosphazene-based amphiphilic conjugate is shown in the specification. The anti-inflammatory nano-micelle based on the phosphazene-based amphiphilic conjugate can spontaneously form a micelle-shaped nano-structure with uniform particle size and high stability in an aqueous solution, and the solubility and the dispersity of insoluble active ingredients such as luminol and the like are remarkably improved; and the anti-inflammatory nano-micelle has the synergistic active oxygen scavenging ability of luminol and Tempol, can effectively regulate the oxidative stress microenvironment of an inflammatory site and relieve inflammatory response, and can be used as an inflammatory response carrier to realize targeted delivery of anti-inflammatory drugs.

This invention belongs to the field of electroluminescence technology, specifically relating to a method for preparing a high-entropy MOF material and its application in the electrochemiluminescence detection of rifampicin. The high-entropy MOF material is a pentagonal high-entropy MOF material (HE-ATA) synthesized from metal nitrates of Fe, Co, Cu, Cr, and Zn and ATA as raw materials. This invention yields a HE-ATA catalyst with simple raw materials, convenient synthesis, and excellent electrochemiluminescence performance. It exhibits chemical stability and a multi-electron reaction potential that accelerates the conversion of dissolved oxygen to reactive oxygen species (ROS), enhancing the electroluminescence intensity. Based on the quenching effect of RIF, a method for detecting RIF using a luminol / HE-ATA system was established. By fitting the change in ECL intensity with RIF concentration, a linear calibration curve with a correlation coefficient of 0.996 and a detection limit of 3.3 × 10⁻⁶ was obtained. ‑6 µM (S / N=3). This material exhibits good sensitivity, stability, and reproducibility in the electrochemiluminescence detection of RIFs, providing a new approach for designing novel electrocatalysts for RIF detection.

The application discloses a construction method and application of an electrochemiluminescence (ECL) antifouling sensor based on a zwitterionic hydrogel, and belongs to the fields of photoelectric sensing analysis, interface antifouling and environmental science and technology. In the application, a hydrogel based on a methacrylic acid sulfobetaine zwitterion and bovine serum albumin is used as an antifouling coating, so that the adsorption of biological proteins and bacteria is effectively hindered, and the service life of the sensor is prolonged. Meanwhile, an internal standard Au luminol is encapsulated in the antifouling hydrogel, so that the integration of interface antifouling and ratio detection is realized, the detection accuracy is improved, and the construction process of the ECL sensor is simplified. The constructed ECL antifouling sensor has high sensitivity for chloramphenicol detection, and the detection limit is 0.39 pM, so that the ECL antifouling sensor is suitable for trace detection of antibiotics in seawater.