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148results about "Component separation" patented technology

Caustic stable chromatography ligands

ActiveUS20100221844A1Cost-effectiveComponent separationBiological material analysisImmunoglobulin bindingImmunoglobulin class
The present invention relates to chromatography ligands having improved caustic stability, e.g., ligands based on immunoglobulin-binding proteins such as, Staphylococcal protein A, as well as methods of making and using such ligands.
Owner:EMD MILLIPORE CORP

Serum specificity metabolite spectrum for patient with lung cancer, and building method thereof

ActiveCN103616450AEasy to handleStrong qualitative analysis abilityComponent separationGas phaseOriginal data
The invention discloses a serum specificity metabolite spectrum for a patient with a lung cancer and a building method thereof, and particularly discloses a method for carrying out liquid-phase/gas-phase chromatography mass spectrometry metabonomics analysis based on the patient suffering from the lung cancer. The method comprises the following steps: collecting fasting blood samples of a healthy and normal detected person and the patient suffering from the lung cancer 7 days before and after an operation, separating by a chromatogram column after processing; extracting and aligning original data of an instrument after adopting mass spectrometry analysis; building a mathematical model to analyze the metabolites spectrum by adopting multivariable data statistical software; comparing with the difference between an average person with the metabolites spectrum of the patient with the lung cancer, so as to determine the specificity metabolite spectrum. By adopting the method disclosed by the invention, the mutation status of the metabolite of the patient with the lung cancer can be generally and comprehensively reflected, and the serum specificity metabolite spectrum can be applied to early diagnosis of the lung cancer or a beneficial technical support is supplied for prognosis.
Owner:HUZHOU CENT HOSPITAL

CWB conductivity monitor

InactiveUS20120178175A1Low accuracyLow reliabilityComponent separationGeneral water supply conservationIon-exchange resinOrganic compound
This invention is a method and apparatus for monitoring the concentration of carbon dioxide dissolved in water by means of conductivity. It distinguishes between the conductivity resulting from carbon dioxide and the conductivity resulting from other constituents dissolved in water. It can be used to monitor the quality of demineralized water, boiler feedwater, steam, or condensate in electric power generation and other industrial facilities. It is constructed by adding a column containing weak base anion exchange resin and a conductivity instrument to a typical cation conductivity monitor. A sample of the water to be monitored flows first through a typical cation conductivity monitor, then through a weak base anion exchange column, and then through an additional conductivity instrument. Conductivity measured at the outlet of the weak base anion exchange column will be essentially due to whatever concentration of carbon dioxide is dissolved in the sample because other dissolved constituents that affect conductivity have been essentially removed by either the cation exchange resin that is part of a typical cation conductivity monitor, or by the weak base anion exchange resin. By subtracting the value of conductivity due to carbon dioxide (at the outlet of the weak base anion exchange column) from the value of cation conductivity (at the outlet of the cation exchange column), the value of degassed cation conductivity is obtained. In the title of the invention, CWB conductivity is an abbreviation for cation—weak base conductivity.In combination with existing methods for oxidizing organic compounds dissolved in water, this invention is also a method and apparatus for monitoring the concentration of dissolved or total organic carbon in water by means of conductivity. It distinguishes between the conductivity resulting from organic carbon and the conductivity resulting from inorganic constituents dissolved in water including carbon dioxide.
Owner:CROSMAN JAY CLIFFORD

Detection method and application of 2-methylimidazole and 4-methylimidazole in baked food

InactiveCN105510480AEasy to handleLow costComponent separationSolid phase extractionChloroacetic acid
The invention discloses a detection method of 2-methylimidazole and 4-methylimidazole in baked food. A mixed solution of trichloroacetic acid and methyl alcohol is added to a baked food sample to make protein, colloid and other impurities subside, supersonic extraction is conducted, a solution to be detected is obtained through centrifugation and filtering, a CAPCELL CR (1:4) chromatographic column (5 microns, 2.0 mm*150 mm) is adopted for separation, and the 2-methylimidazole and the 4-methylimidazole are subjected to qualitative and quantitative analysis through an isotope dilution ultra high performance liquid chromatography tandem mass spectrometry method. The method is free of solid phase extraction and other complex sample pre-processing procedures, three types of isomeride of the methylimidazole can be effectively separated, the ion inhibition effect is effectively lowered, sensitivity is improved, and the detection method has the advantages of being low in detection limit and good in accuracy.
Owner:FUJIAN INSPECTION & RES INST FOR PROD QUALITY +1

Purge and trap concentrator with sparge vessel

InactiveUS7803635B1Optimize volumeAnalysing fluids using sonic/ultrasonic/infrasonic wavesComponent separationEngineeringOptical transducers
A purge and trap concentrator system that includes a sparge vessel, and includes a variable gas flow valve for controlling the gas pressure in an analytic trap or the sparge vessel; a sensor that detects both a foaming sample state and a high liquid level in the sparge vessel, using one optical sensor; a control scheme that re-directs the purge gases to a second inlet of the sparge vessel during a foaming condition; a control scheme that uses a split flow to enhance the quantity of sample gases passed from an analytic trap; an electrically powered thermal energy source with a fan raising the sparge vessel temperature via thermal convection.
Owner:PROFESSIONAL TECHN SERVICES

Chlorogenic acid and galuteolin in honeysuckle flower superhigh pressure extraction method and HPLC quantitative analysis method

InactiveCN103257187AReduce consumptionNon-volatileComponent separationChlorogenic acidSolvent
The invention discloses a rapid and high efficiency chlorogenic acid and galuteolin in honeysuckle flower extraction method and a HPLC quantitative analysis method, and which comprise the following steps: superhigh pressure extraction and quantitative analysis. Superhigh pressure extraction comprises the steps as follows: firstly crushing dried honeysuckle flower and filtering by a sieve with 60-80 meshes, adding water or ethanol, methanol and n butanol organic solvent into the honeysuckle flower powder according to 1:10-1:100 solid liquid ratio, mixing and sealing, immersing at normal temperature, placing the mixture into a high pressure container, leaching with pressure at 20-60 DEG C. for 1-5 min, relieving pressure, carrying out centrifugation of extract product and obtaining the honeysuckle flower extract. Quantitative analysis: after centrifugation, diluting 2ml of the obtained supernatant to 10 ml with distilled water in a volumetric flask, refrigerating for standby. The chlorogenic acid and galuteolin in honeysuckle flower are extracted by a superhigh pressure technology and are carried out by a content determination, and the invention has the characteristics of high recovery rate, short extraction time, small solvent amount, simple operation, accuracy, good repeatability, no pollution, safety, low energy consumption, etc.
Owner:SUZHOU UNIV

PR-HPLC (phase reversing-high performance liquid chromatography) determination method for simultaneously determining contents of five amino acids in earthworm injection

InactiveCN104391053AComponent separationChromatographic columnChemistry
The invention discloses a PR-HPLC (phase reversing-high performance liquid chromatography) determination method for simultaneously determining contents of five amino acids in earthworm injection. The method is characterized by comprising the following steps: preparing chromatographic conditions: a C18 or C8 phase reversing chromatographic column, column temperature: 37 DEG C, a detection wavelength: 248nm, gradient elution with flow rate of 0.8ml/min, a flowing phase A is 0.7% trifluoroacetic acid aqueous solution of 5.0mmol/L heptafluorobutyric acid, a flowing phase B is a 60% acetonitrile aqueous solution, and the flow rate of elution solution is as follows: 0 min 100%A, 0.5 min 98.5%A, 10min 90%A, 15min 67%A, 20min 20%A and 25min 0%A; preparing a reference solution and a test solution; and respectively measuring 10 microliters of reference solution and 10 microliters of test solution, respectively injecting the reference solution and the test solution into a phase reversing liquid chromatography, and carrying out the phase reversing liquid chromatographic determination and analysis. The determination method is simple and rapid in operation, and no derivating agent is needed; moreover, the stability is high, the repeatability is good, and the active ingredients and quality of the earthworm injection can be better controlled.
Owner:广东新峰药业股份有限公司

Detection method of ultra-high performance liquid chromatography-tandem mass spectrometry of ipconazole residues in maize

ActiveCN107664670AEasy extractionImprove purification effectComponent separationEnvironmental behaviorSolvent
The invention discloses a detection method of ultra-high performance liquid chromatography-tandem mass spectrometry of ipconazole residues in maize. The detection method comprises the steps of: firstly extracting the ipconazole in the maize by utilizing an optimized QuEChERS method (purifying agents in extraction and purification steps are three kinds of PSA, C18 and GCB) with acetonitrile as an extraction solvent, and obtaining higher adding standard recovery rate; and then adopting the ultra performance liquid chromatography-tandem mass spectrometry (UPLC-ESI+-MS / MS) to detect the ipconazolein the maize. The detection method is simple, sensitive and selective, and can provide scientific techniques for safety monitoring and environmental behavior assessment of agricultural products.
Owner:INST OF QUALITY STANDARDS & TESTING TECH FOR AGRO PROD OF SHANDONG ACADEMY OF AGRI SCI

Method for preparing test solution for quality detection of safe stagnation removing preparation

InactiveCN102539588AEliminate distractionsGood for qualitative and quantitative analysisComponent separationSolventAlkaloid
The invention relates to a method for preparing a test solution for quality detection of a safe stagnation removing preparation. The method comprises the following steps of: (1), extracting solution preparation: weighting 0.5-10.0g of solid safe stagnation removing preparation or contents thereof, adding a universal solvent for extracting alkaloid, carrying out ultrasonic treatment or heating backflow, cooling down, and filtering to obtain a filter liquid as an extract liquid for later use; or weighting 4-80ml of liquid safe stagnation removing preparation, and filtering to obtain the filter liquid as the extract liquid for later use; and (2) extract liquid purification: taking out the extract liquid, drying through steaming, dissolving residues by adding 1-10ml of hydrochloric acid solution (1-5,000) to the residues, centrifuging a mixed solution, taking out supernatant to slowly pass through an octadecylsilane bonded silica gel column (50-500mg), eluting by water of 2-30ml, collecting an effluent liquid and an eluting liquid, drying by steaming, dissolving the residues by adding 1-10ml of methanol with the volume percent of 30-100% or alcohol with the volume percent of 50-95%, standing, and taking out supernatant which is the test solution for a leonurus indexity element stachydrine hydrochloride thin layer discriminating and/or content determining method in the safe stagnation removing preparation.
Owner:YUNNAN LIANGFANG PHARMA

Dense core permeability measuring device and method

ActiveCN110208164AEasy to operateAvoid the problem of inaccurate flow meteringComponent separationPermeability/surface area analysisVacuum pumpingLine tubing
The invention discloses a dense core permeability measuring device and method. The dense core permeability measuring device comprises a core holder, a standard gas mixture supply system, a confining pressure pump, a vacuum pump, a gas chromatograph and a thermostat, wherein an air inlet end of the core holder is connected with the standard gas mixture supply system through a pipeline. The method for measuring the dense core permeability of the dense core permeability measuring device comprises the following steps: S1, placing a rock sample to be measured with a length L into a rock sample cavity, and performing vacuum pumping on the rock sample and gas in the device by using the vacuum pump; and S2, starting the confining pressure pump, increasing the confining pressure of a confining pressure cavity to a required confining pressure value, and keeping the pressure constant. Through adoption of the dense core permeability measuring device and method, the problems of difficulty in measuring flow and no consideration of dispersion and slip in the process of measuring the permeability with the existing steady state method are solved.
Owner:SOUTHWEST PETROLEUM UNIV

Method for detecting biogenic amine in yellow wine by using chromatographic sheet

InactiveCN103983733AImprove linearityShorten detection timeComponent separationSolventThin layer chromatogram
The invention discloses a method for detecting biogenic amine in yellow wine by using a chromatographic sheet, belonging to the technical field of analysis and detection of components in the yellow wine. The method comprises the steps of carrying out derivation on a biogenic amine standard substance and a to-be-tested yellow wine sample by using a derivatization reagent, enriching the biogenic amine by using liquid-liquid extraction, carrying out sample application on a sheet plate, arranging the sheet plate in a saturate tank loaded with a certain proportion of developing solvent and unfolding; developing and observing under an ultraviolet lamp, and qualitatively detecting the target biogenic amine; and finally, quantitatively measuring the biogenic amine in the yellow wine by using a thin layer chromatograph. According to the method, the detection limit range of the biogenic amine is 0.5-5 mug / mL, the average adding standard recovery rate is 88.5-110.3 percent, the standard deviation is 3.8-12.5 percent, and at most 13 samples can be simultaneously detected on a 20*20 thin layer glass plate. Compared with other analysis methods, the method has the advantages that qualitative and quantitative analysis of the biogenic amine in the yellow wine can be realized, the operation is simple and convenient, the cost is low, and a plurality of samples can be simultaneously detected.
Owner:JIANGNAN UNIV

Medicine for treating cold grasserie and method of preparing the medicine

ActiveCN101584809ADrug effectEffectiveComponent separationSkeletal disorderMirabilis jalapaPharmaceutical drug
The invention discloses a medicine for treating cold grasserie, comprising the raw medicine by weight parts: 50 to 150 parts of Tibet pleurospermum, 50 to 150 parts of Himalayan four-o'clock root, 50 to 150 parts of caltrop, 50 to 150 parts of Polygonati Rhizoma and 50 to 150 parts of asparagus; grain diameter of the medicine is 0.1 to 100 microns. The medicine of the invention has higher effective dissolution of medicine, medicine penetration power and bioavailability, and better medicine effect. The invention further discloses a method of preparing the medicine for treating cold grasserie and special quality examination method thereof such that the quality examination method effectively controls the stability of the medicine, and also effectively identifies the specificity of pharmaceutical ingredients in medicine.
Owner:GANSU CHEEZHENG TIBETAN MEDICINE CO LTD

Methods and apparatus for improving the sensitivity of capillary zone electrophoresis

InactiveUS20070014699A1Analysis using chemical indicatorsComponent separationElectrophoresisAnalytical chemistry
The present invention relates to novel methods and apparatus for improving the sensitivity of capillary zone electrophoresis (CZE). The invention particularly concerns devices comprising a channel that contains an in-line sol-gel column to concentrate samples being subjected to capillary zone electrophoresis, and the use of such devices to enhance the sensitivity of capillary zone electrophoresis.
Owner:BECKMAN COULTER INC

Method for determining methamidophos in rice wine

InactiveCN102156177AFully extractedEasy to operateComponent separationAcetic acidPositive sample
The invention discloses a method for determining methamidophos in rice wine and particularly discloses a method for detecting the content of methamidophos in rice wine by utilizing gas chromatography and liquid chromatography-tandem mass spectrometry. The method comprises the following steps: (1) extraction and purification: utilizing a solid phase extraction column to extract the methamidophos in the rice wine and using ethyl acetate to elute the methamidophos adsorbed on the solid phase extraction column; (2) preparation of matrix matched standard working solution; (3) qualitative screening and quantification by utilizing gas chromatography; (4) qualitative confirmation of positive samples by using liquid chromatography-tandem mass spectrometry; (5) blank test; and (6) result calculation and representation. The method has the following beneficial effects: the pretreatment operation is simple and practical, and the recovery rate of the methamidophos is high; and by adopting the matrix matched standard working solution, the problem of matrix effect of the methamidophos on the gas chromatograph is solved, and accurate quantification is implemented.
Owner:SHAOXING ENTRY EXIT INSPECTION & QUARANTINE BUREAU OF THE PEOPLES REPUBLIC OF CHINA

Analysis device and method for detecting multiple anions simultaneously

InactiveCN105628854ASimple structureImprove performanceComponent separationAnalysis by electrical excitationIon chromatographyData treatment
The invention provides an analysis device for detecting multiple anions simultaneously. The analysis device comprises an ion chromatography separating system and a liquid cathode glow discharge atomic emission spectroscopy detecting system. The ion chromatography separating system comprises a chromatographic pump for conveying a mobile phase, a leacheate generator, a six-way injection valve, a guard column, a separation column, an ion suppressor and a cation exchange column. The liquid cathode glow discharge atomic emission spectroscopy detecting system comprises a sample injection unit, a light source generating part generating glow discharge, a light split unit for carrying out light splitting treatment on a glow discharge emission spectrum, a detecting unit for detecting the emission spectrum obtained after light splitting treatment, and a data processing unit for analyzing data generated by the detecting unit. The ion chromatography separating system and the liquid cathode glow discharge atomic emission spectroscopy detecting system are combined for use, the analyzing process comprises separation of anions, conductive background suppression and ion conversion, the overall structure is simple, the performance is stable, and the price is low.
Owner:SHANGHAI INST OF CERAMIC CHEM & TECH CHINESE ACAD OF SCI
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