97 results about "Bioanalysis" patented technology

The invention relates to the technical field of environmental and biological analysis and detection, in particular to a method for extracting perfluorinated / polyfluorinated compounds based on confinement fluid. The method comprises the following steps: providing a multi-dimensional reticular nanopore material; growing mutually staggered carbon nanofibers on the surface of a substrate through a chemical vapor deposition method; loading a confinement fluid in a pore channel of the multi-dimensional reticular nano-pore channel material; contacting the material with a to-be-detected sample, and extracting; desorbing the extracted material by using a desorption solvent to obtain a desorption solution; and detecting the perfluorinated / polyfluorinated compounds in the desorption solution. A multi-dimensional net-shaped nano pore channel formed by mutual staggering of the carbon nanofibers provides a stable multi-dimensional micro-nano confinement space for confinement fluid. According to the structure, mass transfer and distribution of a target analyte from a complex matrix to a confinement fluid are greatly promoted, so that efficient enrichment of various perfluoro / polyfluoro compounds is realized, and the recovery rate and the detection sensitivity of the method are improved.

A microneedle device comprises a device structure, insertable to a living body and being formed with an opened niche at least partially surrounded by walls of micrometric heights above a base of the niche for allowing the niche to be filled with a blood sample upon the insertion. The device also comprises a biosensor configured to sense a bioanalyte in the blood sample and having a sensing element formed on the base. The thickness of the sensing element is less than the micrometric heights of the walls.

The invention relates to the technical field of oral medicine and biological information analysis, in particular to an evaluation system for oral microbiological analysis and decayed tooth risk prediction. The system comprises a sample collection module, a microorganism detection module, a data preprocessing module, a microorganism population dynamic analysis module, a multi-dimensional feature extraction module, a decayed tooth risk assessment module and a personalized suggestion generation module. By constructing microbial population evolution analysis based on a Lotka-Volterra competitive model, diversity dynamic change analysis based on Shannon entropy and evolution trend prediction based on a Lyapunov stability theory, the system deeply reveals a dynamic evolution law of an oral micro-ecosystem, and a multi-dimensional feature adaptive weighting mechanism based on mutual information is adopted, so that the dynamic evolution law of the oral micro-ecosystem is improved. Personalized accurate risk assessment is realized, a causal reasoning theory is introduced to generate personalized intervention suggestions with causal support, and the accuracy and the prevention effect of dental caries risk prediction are remarkably improved.

This invention provides a simple synthesis method for Fe-Ag / CMP nanopolymers with catalase-like activity and their application in hydrogen peroxide detection, belonging to the field of bioanalytical technology. The method of this invention includes the following steps: (1) preparing a 4-hydroxyethylpiperazine thiosulfonic acid (HEPES) standard buffer solution; (2) adding cytidine monophosphate (CMP) to the solution obtained in step (1) and stirring until the CMP is fully dissolved. Then, under vigorous stirring, ferric nitrate aqueous solution and silver nitrate aqueous solution are added sequentially, at which point the colorless solution turns pale yellow; (3) transferring the mixed solution obtained in step (2) to a centrifuge tube, centrifuging at 12000 rpm for 8 min to collect the precipitate, washing it three times with distilled water, and finally adding 4 mL of distilled water to obtain a 1 mg / mL Fe-Ag / CMP suspension. This invention utilizes CMP as a biological ligand and Ag... + Fe 3+ Simultaneous coordination, and the reducing amino groups on CMP can directly transfer Ag... + In situ reduction to silver nanoparticles (AgNPs) led to the one-step synthesis of a bimetallic Fe-Ag / CMP nanopolymer with hydrogen peroxide-like nanozyme activity, enabling the detection of hydrogen peroxide.

The invention discloses a cascade seven-core optical fiber sensor applied to folic acid detection and a preparation method of the cascade seven-core optical fiber sensor, and belongs to the technical field of optical fiber sensing and biological analysis detection. The sensor comprises a first single-mode optical fiber, a seven-core optical fiber section and a second single-mode optical fiber, a double-microsphere-cavity structure is arranged at the optical fiber connecting position to form a cascade interference optical path, and tapering is conducted on the middle portion of the seven-core optical fiber section to form a sensing area. According to the invention, mode matching is improved through the microsphere cavity, an evanescent field is enhanced through tapering, and high-sensitivity specific detection of folic acid is realized in cooperation with the folic acid binding protein biological functional layer fixed on the surface; the sensor obtains stable linear response to a folic acid standard solution in the range of 0-50 ng / mL, a clinical serum sample verifies that the detection result of the sensor is highly consistent with that of a chemiluminescence method, the sensor has good reusability, and the sensor has the advantages of being easy to prepare in structure, rapid in response, high in sensitivity, capable of being matched with a complex matrix and the like, and has good application prospects. The method has huge potential in clinical folic acid quantitative detection.

The invention relates to the technical field of biological analysis and detection, and particularly discloses a streptococcus mutans detection kit based on an anchored CRISPR-Cas12a enhanced paper-based micro-fluidic chip and a detection method. The detection kit comprises an RAA solution or RAA freeze-dried powder, magnesium acetate or a magnesium acetate solution, TMB or a TMB solution, an RAA forward primer, an RAA reverse primer, a cell lysis buffer, a buffer system and a paper-based micro-fluidic chip. The detection method comprises the following steps: establishing a standard curve and detecting a sample. The detection kit is used for detecting the content of streptococcus mutans and has the characteristics of high efficiency, rapidness, specificity, sensitivity, portability and the like, and the method is simple and convenient to operate, low in detection cost and capable of being applied to on-site detection of streptococcus mutans.

The application belongs to the field of biological analysis, and provides a method for precise metabolic flow analysis of TCA cycle based on isotope tracing technology combined with high-resolution mass spectrometry. By optimizing mass spectrometry parameters and liquid chromatography method, one injection within 6 min is realized, and high-throughput, high-sensitivity and high-resolution detection is realized on 11 biomarkers related to TCA cycle metabolic pathways. At the same time, the application innovatively uses LC-MS / MS to decipher 13 C the stepwise position-specific transfer from glucose to subsequent metabolites by glycolysis and TCA cycle, thereby calculating 13 C the integrated steady-state analysis of key metabolic rates of position-specific transfer from sequential precursors to their products (pyruvate dehydrogenase, beta-oxidation, pyruvate carboxylase, isocitrate dehydrogenase and pyruvate cycle). This technology has wide applicability and can potentially characterize mitochondrial metabolism of any tissue or cell.

The invention discloses construction and application of a biosensor for triggering controlled release based on adjacent induced DNA strand displacement, and belongs to the technical fields of electrochemical luminescence, biological analysis and nano science. According to the invention, by integrating adjacent induced DNA strand displacement and controlled release strategies, the ultra-sensitive self-closing dual-mode biosensor taking the Au-Ag nanocluster as a luminous body is developed, and the ultra-sensitive self-closing dual-mode biosensor is used for trace detection of neuron-specific enolase. Due to the synergistic characteristic between the double metals, the Au-Ag nanocluster has high electrochemical luminescence (ECL) efficiency. Meanwhile, the reduction of S2O8 < 2-> is catalyzed by cyclic conversion between Fe < 2 + > / Mn < 3 + > and Fe < 3 + > / Mn < 4 + >, and a large amount of SO4 <-> is generated for ECL emission. The specific binding between the target antigen and the antibody can drive DNA strand displacement to open a blocked hole, so that the electrochemical probe falls off and the probe is quenched to release, the self-closing of an electrochemical signal and an ECL signal is realized, the detection sensitivity and accuracy of the sensor are effectively improved, and the sensor is suitable for immunoassay of various biomarkers.

The invention relates to the technical field of bioanalytical chemistry, in particular to a gold nanoparticle detection method for realizing multi-microorganism detection. The preparation method comprises the following steps: synthesizing gold nanostars with rich tip structures by adopting a surfactant-free reduction method, taking the gold nanostars as a high-activity SERS substrate, coding by utilizing different Raman reporter molecules, and coupling a specific antibody through a heterobifunctional PEG (Polyethylene Glycol) connecting arm to prepare the multiple SERS immune nano-label; meanwhile, functional immunomagnetic nanoparticles are constructed and are used for capturing and enriching target bacteria from a complex sample. The detection process adopts a magnetic enrichment-compounding-SERS spectrum reading mode to form a magnetic bead-bacteria-SERS label compound, and a portable Raman spectrometer is used for collecting signals and combining a deconvolution algorithm to realize synchronous qualitative and quantitative analysis of various pathogens. The method disclosed by the invention has the advantages of high detection sensitivity, high detection speed, strong matrix interference resistance, no spectral crosstalk due to multiple detection and the like.

The application belongs to the technical field of nanomaterials, and provides ascorbic acid oxidation mimetic enzyme and preparation thereof. The application adopts a methanol solution of zinc nitrate, copper acetylacetonate and 2-methyl imidazole to perform a hydrothermal reaction, and obtains the ascorbic acid oxidation mimetic enzyme by oxygen isolation calcination of a hydrothermal product. The copper-nitrogen-carbon nanomaterial obtained by the application has a rhombohedron structure, can specifically oxidize ascorbic acid, and can be applied to ascorbic acid content detection, oxidized ascorbic acid preparation and dehydroascorbic acid preparation as ascorbic acid oxidation enzyme mimetic enzyme. The nanomaterial can maintain ascorbic acid oxidation mimetic enzyme activity under acid, alkaline and high temperature conditions; the steady-state kinetic parameter (Michaelis constant is 0.012 mM) is better than that of natural ascorbic acid oxidation enzyme, and the ascorbic acid oxidation mimetic enzyme activity of the material has a broad application prospect in the fields of nanozyme, nanotechnology and biological analysis detection.

The invention discloses an amino acid L / D type enantiomer separation and quantitative detection method based on LC-MS, and belongs to the technical field of biological analysis. Aiming at the problems of difficulty in separation of amino acid L / D type enantiomers in human serum, low detection sensitivity, complex analysis process and the like, the method disclosed by the invention is simple in pretreatment, short in instrument collection time, high in chiral enantiomer separation degree, small in matrix effect, high in sensitivity, low in cost and convenient for large-scale clinical sample detection in a laboratory; the method not only can make up the limitation that only the L type is detected at present, but also can provide a key analysis method for early warning of diseases, drug effect and toxicokinetics research and precise medical evaluation.

The invention discloses a probe BBM for anchoring OPA1 protein and application of the probe BBM, and belongs to the technical field of biological analysis. Based on the characteristic that the OPA1 protein is rich in hydrophobic amino acid residues and polar amino acids, the probe BBM capable of generating multiple interaction forces with the OPA1 protein is designed by reasonably introducing hydrophobic groups and polar groups. Theoretical calculation and experimental results (including OPA1 knock-down and overexpression) show that the probe realizes efficient enrichment in a mitochondrial inner membrane region. By using the unique probe, the hydrogen peroxide induced mitochondrial inner membrane viscosity change is systematically researched, and the myocardial cell oxidative damage is further confirmed to be realized by a p53 protein mediated apoptosis pathway. The method provides a reliable means for accurately evaluating the oxidative stress of the mitochondrial inner membrane, and has important promotion significance for the development of the cardiovascular research field.

This document describes medical systems for detecting biological analytes. For example, this document describes sensors for the continuous monitoring of biological analytes, such as glucose and / or lactate, in aqueous solutions and body fluids (e.g., blood) based on a readout of fluorescence or luminescence signals.WO

The invention provides a fluorescent probe as well as a preparation method and application thereof, and belongs to the technical field of biological analysis and detection. The fluorescent probe disclosed by the invention has a structure as shown in a formula I; the invention also provides a preparation method of the fluorescent probe and application of the fluorescent probe in cell activity detection or preparation of a cell activity detection kit. The fluorescent probe provided by the invention can reflect the cell state by migrating organelles, realizes dual-channel imaging, and can meet the actual requirements of cell activity detection.

The invention relates to a method for quantitatively determining biological analytes in an aqueous solution in the presence of one or more functionalised surfaces, wherein the aqueous solution comprises at least one type of biological analyte and at least one type of fluorescene marker, characterised in that the quantity and / or concentration of the biological analyte or analytes is determined by measuring the florescence emission of the unbound fluorescence markers, as well as to a device for carrying out said method.

The present invention relates to a method for bioanalysis, in particular, to a method for generating electrochemiluminescence signal at low voltage to achieve high signal-to-noise ratio and improved concentration-signal response relationship, thereby improving electrochemiluminescence (ECL) immunoassay performance.

The invention belongs to the technical field of biological analysis, and relates to a method for performing mass spectrum imaging analysis on lung tissues and application. In order to solve the problem that the structural integrity is difficult to maintain in the lung tissue freezing and slicing process, a liquid shaping agent is adopted to conduct internal perfusion on fresh lung tissue, the airway and the pulmonary alveoli are filled, and the shaping agent supports the lung tissue to maintain the natural state in the subsequent operation after being solidified at low temperature. The prepared lung tissue frozen section can be used for mass spectrum imaging analysis and research.

The application belongs to the field of sensing detection, and relates to a method for rapidly detecting sulfur ions in a double channel, which uses tin telluride nanometer enzyme as a double channel colorimetric probe, detects sulfur ions through two channels, one channel is a specific brown change caused by the binding energy between tin ions and sulfur ions, and is used for detecting sulfur ions with a concentration of greater than or equal to 100 muM; the other channel is a TMB colorimetric method for detecting sulfur ions with a concentration of less than 100 muM; it is found for the first time that the double channel colorimetric probe tin telluride nanometer enzyme can be used for detecting sulfur ions, has high selectivity for sulfur ions, has super-high sensitivity, and is not easily disturbed by other ions; specific brown changes caused by the binding between tin ions and sulfur ions can realize the visualization of sulfur ions in a solution and the rapid, accurate and wide-range concentration determination of photoelectrochemistry; therefore, the method provides a new idea for a 'one platform and multiple channels' detection method of chemical and biological analysis.

The application discloses an immunological analysis method based on high-molecular amplification signal amplification and belongs to the technical field of biological medicines. The application combines protein-high-molecular conjugates with biological analysis together, and successfully develops a method for protein quantitative analysis. On the basis of taking silica microspheres as a solid-phase carrier material, target analysis antigen protein molecules are coated in advance, specific recognition reaction of antigen and antibody is utilized, antibody IgG-I macromolecules grafted with a photo initiator in advance are indirectly fixed on the surface of the microspheres, and a "competition" immunological detection method is constructed. The method is a rapid, simple, inexpensive and enzyme-free cascade amplification detection technology, and has a wide application prospect.

The invention pertains to the technical fields of bioanalytics and agriculture, and relates to a method and to an assembly for in-ovo sexing of bird eggs. The aim of the present invention is to provide a method and an assembly by means of which in-ovo sexing of bird eggs is achieved with a stable predictive accuracy of the sex and which are simple and cost-effective. The aim is achieved using a method and an assembly in which a fertilised bird egg incubated for 3 to 9 days is irradiated with at least two light-emitting laser beam sources with different excitation waves after the shell is opened, the captured and processed fluorescence scattering spectra and Raman scattering spectra being used, as complementary spectra associated with the different excitation wavelengths, to determine a classification value, and the sex being determined by comparing the determined classification value with an intrinsically determined threshold value. The method and the assembly can be used for sexing farm poultry.

The invention belongs to the field of biomedical technology analysis, and particularly relates to a high-sensitivity oligonucleotide pharmacokinetic analysis method. The high-sensitivity oligonucleotide pharmacokinetic analysis method comprises the following steps: (1) establishing an LC-MS / MS analysis method for quantifying target oligonucleotide in a biological sample; (2) performing full verification on the LC-MS / MS analysis method established in the step (1) according to a biological analysis guidance principle; (3) detecting a biological sample by using the LC-MS / MS analysis method verified in the step (2) to obtain concentration data; and (4) performing pharmacokinetic parameter calculation based on a detection result in the step (3). Optionally, the oligonucleotide to be detected can be subjected to GalNAc conjugate coupling modification. The LC-MS / MS method may also be replaced by an RT-qPCR, LC-FL, or LC-HRMS method as a paratactic regimen. The invention provides a reliable and compliant analysis means for accurate pharmacokinetic evaluation of oligonucleotide drugs.

The invention discloses a fluorescent substrate 7-HC-P-E, a preparation method thereof and application of the fluorescent substrate 7-HC-P-E in detection of the active concentration of alkaline phosphatase (ALP). The fluorescent substrate can be catalytically hydrolyzed by ALP under an alkaline condition to release 7-hydroxycoumarin (7HC) with a strong fluorescent signal, so that high-sensitivity and high-specificity detection on the enzyme activity is realized. The invention further provides a synthesis route and an optimization process of the fluorescent substrate, the operation is simple and convenient, the product purity is high, and the fluorescent substrate is suitable for multiple fields such as biological analysis, medical diagnosis and environmental monitoring.

A lighting system and a bioanalytical instrument comprising the same are disclosed. The lighting system comprises two or more interleaved mirrors configured to split an incoming light beam into at least two sub-beams, and a guiding module configured to guide the sub-beams to provide oblique illumination to an area. Compared to conventional lighting systems for bioanalytical instruments, the lighting system is capable of improving illumination efficiency, reducing background signal and improving image uniformity.

The invention provides a fusion method of pore protein and a membrane, a pore protein jack buffer solution and application. The fusion method comprises the following steps: distributing a first solution on the first side of the membrane, and distributing a second solution on the second side of the membrane; applying voltage to two sides of the membrane, fusing the pore protein and the membrane, and detecting current in the solution; when the current is increased, the pore protein is inserted into the membrane, the voltage is adjusted to 0V, and the fusion of the pore protein and the membrane is completed; the first solution comprises a first buffer solution containing pore protein, and the second solution comprises a second buffer solution without pore protein; the osmotic pressure of the first solution is greater than that of the second solution. The porous protein and membrane fusion single porosity problem in the prior art can be solved, and the method is suitable for the field of biological analysis and detection.

This invention relates to the fields of environmental and bioanalytical technology, and particularly to a method for simultaneous pretreatment and detection of bisphenol S and bisphenol AF in biological tissues. The technical solution includes a framework process for simultaneous pretreatment and detection of bisphenol S and bisphenol AF in biological tissues. This invention establishes a dual-solvent secondary extraction system composed of n-hexane and methyl tert-butyl ether, achieving differentiated adaptation to different tissue matrices. By combining the advantages of non-polar and moderately polar solvents, it can simultaneously handle the relatively highly polar bisphenol S and the relatively non-polar bisphenol AF in a single extraction process. Furthermore, this method sets key physical parameters during the extraction process according to the histological characteristics of each organ. For heart and lung tissues, specific ultrasonic power is used to ensure thorough cell disruption; while for liver and spleen with high lipid content, different power and time are used to ensure the full release of lipid-bound target substances.

The present invention generally relates to a system and method for detecting multiple analytes in a blood sample. The present invention relates to an advanced cartridge specially designed for detecting multiple analytes in a blood sample. The cartridge integrates a series of components to process blood samples, encompassing the overall process from sample reception to plasma separation. Subsequently, the plasma is precisely metered and guided to an incubation process, so that the plasma is mixed with a reagent under controlled conditions and incubated. And after incubation is completed, analyzing the plasma by using a lateral flow test strip so as to detect and quantify various target analytes. The card box system is particularly suitable for instant detection, a simple and automatic scheme is provided for executing complex detection including immunoassay and electrochemical analysis, and the accuracy and efficiency of detection are remarkably improved.

The invention discloses a constructed wetland pollution reduction and carbon reduction synergistic effect analysis system and method, and relates to the technical field of water pollution control and greenhouse gas emission reduction. Comprising a simulated wetland reaction unit, a multi-parameter monitoring module, an operation regulation and control module, a microbiological analysis module and a synergistic effect evaluation module. The simulated wetland reaction unit is filled with a FeC composite matrix to realize subsurface flow constructed wetland environment simulation; the multi-parameter monitoring module acquires water quality and greenhouse gas emission data in real time; the operation regulation and control module realizes accurate regulation and control of water inlet parameters; the microbiological analysis module analyzes microflora and functional gene information; and the synergistic effect evaluation module integrates multi-module data to construct a correlation model, calculates a synergistic effect index and outputs an optimization parameter. Through five stages of matrix optimization, operation regulation and control, microbial mechanism revealing, collaborative evaluation optimization and feedback application, evaluation and optimization of the constructed wetland pollution reduction and carbon reduction collaborative efficiency are realized, and a scientific basis is provided for actual constructed wetland engineering design and operation.

The application belongs to the technical field of nanomaterials and biological analysis, and particularly relates to a ratio type photoelectrochemical analysis method based on multifunctional CeO2 / CdS and interface etching. First, a multifunctional CeO2 / CdS nanocomposite is synthesized by an in-situ growth method, and the nanocomposite has photoelectric properties of CdS and CeO2 peroxidase activity; second, a beacon antibody labeled with nanogold and glucose oxidase is prepared by an electrostatic adsorption method, a target protein, the beacon antibody and an antibody coated on an enzyme-labeled microplate are mixed and incubated to form an immune complex, and after glucose is added, H2O2 is generated by catalysis of the glucose oxidase on the beacon antibody; the generated H2O2 is catalyzed by CeO2 in the CeO2 / CdS nanocomposite to generate hydroxyl radicals, and in-situ etching of CdS in the electrode interface reduces the photocurrent, and a photocurrent intensity ratio (Iw / Ic) of a double-channel electrode has a linear relationship with the concentration of the target protein, so that quantitative analysis can be realized. The application has a sensitive response to the detection of proteins and has a fast detection speed.

A biological analysis system can include an excitation module and an emission module. The excitation module can include a collimator element to receive excitation light from the excitation light source and transmit collimated excitation light in a first direction, and a plurality of excitation mirrors arranged along an excitation light path, each excitation mirror disposed at an acute angle relative to the first direction and configured to reflect collimated excitation light in a second direction. The emission module can be positioned to receive excitation light transmitted in the second direction and can include a sample block containing a plurality of sample receptacles positioned to receive collimated excitation light beams, and a plurality of photodetectors configured to receive emission light transmitted from a respective sample receptacle in a direction transverse to the second direction of the excitation light path.