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41results about How to "Easy to prepare materials in batches" patented technology

Separation process of natural free radical scavenger in Saxifraga tangutica and application of natural free radical scavenger

The invention relates to the technical field of separation of natural free radical scavengers in Saxifraga tangutica, in particular to a separation process of a natural free radical scavenger in Saxifraga tangutica and application of the natural free radical scavenger. The separation process comprises the following six steps: extraction, coarse separation via a microporous resin column, online free radical scavenger component screening, preparation via a reversed-phase preparative column, reversed-phase preparative liquid chromatographic purification of Fr1-1and hydrophilic / reversed-phase two-dimensional liquid chromatographic purification of Fr1-3. The method is low in cost, and product purity is greater than 95%; a technical means adopted by the invention can realize large-scale production: requirements on raw materials are not high, cost is low, and batch preparation is easy; room-temperature cold leaching extraction with methanol is adopted, so operation is easy; the microporous resin column is adopted for coarse separation, and a microporous resin separation material can be loaded in a medium-pressure column chromatography system, so large-scale production can be easily realized; and reversed-phase preparative liquid chromatography or hydrophilic preparative liquid chromatography used in separation and purification is a rapid isocratic method.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

A method for efficiently enriching diarylheptanes in Saxifrage tangutata

The present invention relates to a method for efficiently enriching diaryl heptane compounds in Saxifrage tangutica, the method comprising the following steps: (1) Extraction: crushing the medicinal material of Saxifraga tangutica and carrying out alcohol extraction, and obtaining Tanggu S. saxifrage extract; (2) alcohol-resistant film for impurity removal: the extract of saxifrage tangutica is treated with an alcohol-resistant film, and the permeate is collected, and the permeate is dried under reduced pressure to obtain saxfrage tangutata Grass diaryl heptane compound crude sample; (3) Reverse-phase solid phase extraction column enrichment: add water to dissolve in the described saxifrage diaryl heptane compound crude sample, then pass through the reverse phase solid phase extraction column Separation, and carry out step gradient elution, collect 50% ~ 70% methanol eluate; (4) described 50% ~ 70% methanol eluate is dried under reduced pressure to obtain Saxifrage tangutata diaryl heptane compound components. The invention has simple process, easy large-scale implementation and stable and controllable quality.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Method for preparing glycine betaine chemical reference substances from boxthorn leaves

The invention relates to a method for preparing glycine betaine chemical reference substances from boxthorn leaves. The method includes the following steps: (1), drying the boxthorn leaves in the shade, smashing the boxthorn leaves, adding analysis pure water to perform extraction, and filtering and drying the mixture under reduced pressure into paste to obtain brown black solid boxthorn leaf water extracts; (2), performing elution after subjecting the boxthorn leaf water extracts to silica gel column chromatography separation, collecting cut fractions according to 1000-2000mL / part, and combining the cut fractions with Rf values being 0.1-0.2 through thin-layer chromatography detection; drying the cut fractions with the Rf values being 0.1-0.2 under reduced pressure to obtain brown powdery glycine betaine crude products; (3), dissolving the glycine betaine crude products in ethanol solutions, performing filtering and hydrophilic liquid phase preparative chromatography separation to collect main chromatographic peak cut fractions in preparative chromatograms, and drying the chromatographic peak cut fractions under reduced pressure to obtain the white powdery reference substances with purity larger than 99%. The method has the advantages of simple technology and proneness to mass production.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Method for preparing calycosin-7-O-beta-D-glucoside and ononin chemical reference products synchronously

The invention relates to novel process for preparing calycosin-7-O-beta-D-glucoside and ononin chemical reference products synchronously. The calycosin-7-O-beta-D-glucoside and ononin chemical reference products with a purity of over 98 percent can be obtained by purifying alcohol extract of astragalus by silica gel column chromatography, resin column impurity removal and preparation of high performance liquid chromatography. In the invention, the process steps are simple, the purity is high, the color and luster are desirable, and large-scale production is easy.
Owner:DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI

Method for simultaneously preparing chemical reference substances of calycosin and formononetin

The invention relates to a novel process for simultaneously preparing chemical reference substances of calycosin and formononetin, comprising two steps of purifying astragalus root alcohol extracts by utilizing silicagel column chromatography and recrystallizing to obtain the two types of chemical reference substances of the calycosin and the formononetin with purities greater than 98%. The method has the advantages of simple process steps and high purity of obtained products, and is easy for scale production.
Owner:DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI

Method for preparing armillaria luteo-virens chewable tablets capable of improving sleep

The invention relates to a method for preparing armillaria luteo-virens chewable tablets capable of improving sleep. The method includes the following steps: (1) removing the root and base of the armillaria luteo-virens fruiting body, washing and removing impurities, drying, smashing, and sieving to obtain armillaria luteo-virens powder; (2) curing the armillaria luteo-virens powder, and drying and cooling to obtain cured armillaria luteo-virens powder; (3) mixing the cured armillaria luteo-virens powder with a filling agent and a corrigent uniformly, carrying out superfine grinding to obtain superfine powder; (4) spraying edible alcohol on the ultrafine powder, and stirring uniformly to prepare a soft material with moderate hardness; pressing and sieving the soft material to obtain the granular product; (5) drying the granular product and then adding a lubricant; after mixing uniformly, pressing to obtain circular tablets with the thickness of 0.7 cm and the radius of 1.5 cm; (6) drying the circular tablets, sterilizing and packaging, so as to obtain the chewable tablet finished product. According to the invention, the technology is simple and facilitates scale production.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Novel diaryl nonane II free radical inhibitor in Saxifraga sinomontana as well as separation and preparation process and application of novel diaryl nonane II free radical inhibitor

The invention discloses a novel diaryl nonane II free radical inhibitor in Saxifraga sinomontana as well as a separation preparation process and application of the diaryl nonane II free radical inhibitor. The specific preparation process comprises the following five steps: extraction, on-line free radical inhibitor component screening, medium-pressure chromatography coarse separation in a microporous resin column, on-line free radical inhibitor screening and reversed-phase preparative column preparation. The novel diaryl nonane Saximonsin B free radical inhibitor in the Saxifraga sinomontana prepared by the method can be applied to preparation of free radical inhibition medicines or health foods, and is specifically used as an effective component to be prepared into various medicinal preparations or health foods according to any pharmaceutically or food science acceptable carrier. An extraction solvent, a microporous resin column, a reversed-phase chromatographic column separation solvent and materials for reversed-phase chromatographic separation in the preparation process can be recycled; and the raw material source is wide, large-scale operation can be realized in the process steps such as methanol room-temperature cold leaching extraction, and high-pressure preparative chromatographic separation can ensure that the purity of the product is greater than 95%.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Sample pretreatment method and application of flavonoid component of dracocephalum heterophyllum benth

The invention relates to a sample pretreatment method of flavonoid component of dracocephalum heterophyllum benth. The sample pretreatment method comprises the following steps: (1) carrying out liquid-liquid partitioning enrichment, namely, carrying out dispersion, extraction and vacuum drying on pohytol extract of dracocephalum heterophyllum benth to obtain medium polar component part of dracocephalum heterophyllum benth; (2) removing purities by adopting micro-reticular resin, namely, dissolving the medium polar component part of dracocephalum heterophyllum benth, filtering, separating by a micro-reticular resin column, eluting, collecting the eluate, and carrying out vacuum drying on the eluate to obtain the yellow flavonoid component of dracocephalum heterophyllum benth; (3) and carrying out chromatography isolation by adopting a silicagel column, namely, separating the flavonoid component crude product of dracocephalum heterophyllum benth by adopting the silicagel column chromatography, eluting, detecting by adopting thin-layer chromatography, mixing, and collecting fraction with the Rf value being 0.1-0.8, and carrying out vacuum drying on the fraction, thus obtaining the flavonoid component of dracocephalum heterophyllum benth, which is in the form of yellow powder. The technology is simple, and easy in realizing scale production. The invention further discloses an application of the flavonoid component of dracocephalum heterophyllum benth in preparing a drug or health food for resisting hepatitis virus.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Method for preparing rutin and quercetin chemical reference substances simultaneously from lycium barbarum leaves

The invention relates to a method for preparing rutin and quercetin chemical reference substances simultaneously from lycium barbarum leaves. The method comprises the following steps: (1) carrying out impurity removal with microporous resin: dissolving a lycium barbarum leaf alcohol extract with a methanol solution, filtrating the solution, loading the filtrate to a microporous resin column for separation, then, carrying out stepped gradient elution sequentially with water, a 20-35% methanol solution and a 70% methanol solution, collecting 70% methanol water eluate, and enabling the methanol water eluate to be subjected to reduced-pressure drying, thereby obtaining rutin and quercetin crude products; (2) enabling the rutin and quercetin crude products to be subjected to silicagel-column chromatographic separation, eluting, and combining fractions with the Rf value of 0.3-0.5; enabling the fractions to be subjected to reduced-pressure drying, thereby obtaining brown-yellow powdered rutin and quercetin components; and (3) refining with reversed phase liquid preparative chromatography: dissolving the rutin and quercetin components with a methanol solution, filtrating the solution, separating the filtrate with an efficient reversed phase liquid preparative chromatographic column, collecting two major chromatographic peak fractions from a preparative chromatogram, and enabling the chromatographic peak fractions to be subjected to reduced-pressure drying, thereby obtaining yellow powdered rutin and quercetin reference substances. The method is simple in process and facilitates large-scale production.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Novel diaryl nonane I free radical inhibitor in Saxifraga sinomontana as well as separation and preparation process and application of the novel diaryl nonane I free radical inhibitor

The invention discloses a novel diaryl nonane I free radical inhibitor in Saxifraga sinomontana as well as a separation and preparation process and application of the diaryl nonane I free radical inhibitor. The specific preparation process comprises the following five steps: extraction, on-line free radical inhibitor component screening, medium-pressure chromatography coarse separation in a microporous resin column, on-line free radical inhibitor screening and reversed-phase preparative column preparation. The novel diaryl nonane Saximonsin A free radical inhibitor in the Saxifraga sinomontana, prepared by the method, can be applied to preparation of free radical inhibition medicines or health foods, and is specifically used as an effective component to be prepared into various medicinal preparations or health foods according to any pharmaceutically or food science acceptable carrier. An extraction solvent, a microporous resin column, a reversed-phase chromatographic column separation solvent and materials for reversed-phase chromatographic separation in the preparation process can be recycled; the raw material source is wide, large-scale operation can be realized in the process steps such as methanol room-temperature cold leaching extraction, and high-pressure reversed-phase preparative chromatography separation can ensure that the purity of the product is greater than 95%.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Method for preparing calycosin-7-O-beta-D-glucoside and ononin chemical reference products synchronously

The invention relates to novel process for preparing calycosin-7-O-beta-D-glucoside and ononin chemical reference products synchronously. The calycosin-7-O-beta-D-glucoside and ononin chemical reference products with a purity of over 98 percent can be obtained by purifying alcohol extract of astragalus by silica gel column chromatography, resin column impurity removal and preparation of high performance liquid chromatography. In the invention, the process steps are simple, the purity is high, the color and luster are desirable, and large-scale production is easy.
Owner:DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI

Method for preparing colon cancer resistance notopterygium extract powder in scale mode

The invention relates to a method for preparing colon cancer resistance notopterygium extract powder in a scale mode, which comprises steps: 1 exaction: notopterygium medical materials are extracted by alcohol and filtered after being smashed, and is decompress and dried to be a paste state, thereby obtaining notopterygium alcohol extract; 2 liquid-liquid distribution enrichment: the notopterygium alcohol extract is smashed, extracted, decompressed and dried to obtain a notopterygium ethyl acetate position; 3 resin column chromatography edulcoration: the notopterygium ethyl acetate position is separated through a resin column after being dissolved, is eluted in a gradient mode, 90% methanol contents are collected, the 90% methanol contents are decompressed and dried to obtain notopterygium extract coarse powder; 4 silica gel column chromatography separation: the notopterygium extract coarse powder is separated and eluted through a silica gel column chromatography after being dissolved, and is detected through a thin-layer chromatography, and fractions which are 0.1-0.8 in radio frequency (Rf) values are collected, id decompressed and dried to obtain yellow powder-shaped notopterygium extract powder. The method for preparing the colon cancer resistance notopterygium extract powder in the scale mode is simple in process, easy to carry out in a scale mode and is steady and controllable in quality.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

A kind of preparation method and application of hard acyl glycerol in black wolfberry

The invention relates to a preparation method for stearylglycerol in Lycium ruthenicum Murr. The method comprises the following steps: (1) impurity removal with microporous resin: a step of dissolving extract of Lycium ruthenicum Murr with an ethanol solution, separating the obtained solution by using a microporous resin column, carrying out step gradient elution and subjecting eluate to pressure-reduced drying so as to obtain a crude product of stearylglycerol; and (2) silica gel column chromatography separation: a step of subjecting the crude product of stearylglycerol to silica gel column chromatography separation, carrying out elution, collecting fraction, detecting and collecting fraction with an Rf value of 0.1 to 0.2 by using thin-layer chromatography and subjecting the collected fraction to pressure-reduced drying so as to obtain colorless oily 1-[(12E,16E)-12,16-eicosadienoyl]-2-[(E,E)-7,11-octadecadienoyl]-3-stearylglycerol with purity of greater than 95%. The preparation method is simple and has a high recovery rate; and the prepared 1-[(12E,16E)-12,16-eicosadienoyl]-2-[(E,E)-7,11-octadecadienoyl]-3-stearylglycerol has good blood fat-reducing effect.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Preparation method of corydalis incisa amine

The invention discloses a preparation method of corydalis incisa amine. The preparation method comprises the following steps of: (1) taking hypecoum leptocarpum, crushing the hypecoum leptocarpum, adding ethanol for extraction, filtering and concentrating the hypecoum leptocarpum into thick paste with the relative density of 1.1-1.3; (2) taking the thick paste in the step (1), loading the thick paste on a macroporous resin column, sequentially eluting with water and ethanol, collecting an ethanol elution part, concentrating and drying to obtain a hypecoum leptocarpum refined extract; and (3) dissolving the hypecoum leptocarpum refined extract obtained in the step (2) in methanol, filtering, separating filtrate by using preparative high performance liquid chromatography, collecting a chromatographic peak fraction with the highest response value in a preparative chromatogram, concentrating and drying the fraction to obtain the corydalis incisa amine. The purity of the corydalis incisa amine prepared by the preparation method disclosed by the invention is greater than 98%.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Method for preparing rosmarinic acid chemical reference substances from three kinds of alpine sage plants

The invention relates to a method for preparing a rosmarinic acid chemical reference substance from three types of high mountain salvias. The method comprises the following steps: (1) performing pore resin decontamination: dissolving an alcohol extract of one of salvia roborowskii, salvia przewalskii and salvia prattii with ethanol solution, filtering, separating on a pore resin column, eluting with water solution for decontaminating, then performing stepwise gradient elution with methanol solution, collecting 30% to 50% of methyl alcohol water eluate, and drying the methyl alcohol water eluate under reduced pressure to obtain a phenolic acid type component crude product; (2) performing silica gel column enrichment: performing silica gel column chromatography separation on the phenolic acid type component crude product, then eluting, and collecting a fraction with an Rf value of 0.18 to 0.22; drying the fraction under reduced pressure to obtain a faint yellow and powdery rosmarinic acid crude product; (3) performing preparative liquid chromatography purification: dissolving the rosmarinic acid crude product with methanol solution, filtering, performing preparative liquid chromatography separation, collecting a chromatography peak fraction, and drying the chromatography peak fraction under reduced pressure to obtain the white and powdery reference substance. The method is simple in process and easy for large scale.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Method for Separating and Preparing Rosmarinic Acid from Green Orchid Isophyllum and Its Application

The invention relates to a method for isolating and preparing rosmarinic acid from Dracocephalum heterophyllum, comprising the steps of (1) extracting, to be specific, soaking powder of Dracocephalum heterophyllum herb, and performing reflux extraction and vacuum concentration to obtain Dracocephalum heterophyllum extract; (2) cleaning by microporous resin, to be specific, dissolving the Dracocephalum heterophyllum extract, filtering, feeding to MCI microporous resin columns, eluting, collecting 50% ethanol solution eluent, and subjecting the 50% ethanol solution eluent to vacuum concentration to obtain rosmarinic acid crude extract; (3) isolating and purifying by hydrophilic liquid chromatography, to be specific, dissolving the rosmarinic acid crude extract, filtering with a microporous filter membrane, and isolating and purifying by using hydrophilic liquid chromatography to obtain rosmarinic acid having purity of higher than 98%. In addition, the invention also discloses application of the rosmarinic acid. The method is simple and is easy for large-scale production.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

A method for simultaneously preparing rutin and quercetin chemical reference substances from wolfberry leaves

The invention relates to a method for preparing rutin and quercetin chemical reference substances simultaneously from lycium barbarum leaves. The method comprises the following steps: (1) carrying out impurity removal with microporous resin: dissolving a lycium barbarum leaf alcohol extract with a methanol solution, filtrating the solution, loading the filtrate to a microporous resin column for separation, then, carrying out stepped gradient elution sequentially with water, a 20-35% methanol solution and a 70% methanol solution, collecting 70% methanol water eluate, and enabling the methanol water eluate to be subjected to reduced-pressure drying, thereby obtaining rutin and quercetin crude products; (2) enabling the rutin and quercetin crude products to be subjected to silicagel-column chromatographic separation, eluting, and combining fractions with the Rf value of 0.3-0.5; enabling the fractions to be subjected to reduced-pressure drying, thereby obtaining brown-yellow powdered rutin and quercetin components; and (3) refining with reversed phase liquid preparative chromatography: dissolving the rutin and quercetin components with a methanol solution, filtrating the solution, separating the filtrate with an efficient reversed phase liquid preparative chromatographic column, collecting two major chromatographic peak fractions from a preparative chromatogram, and enabling the chromatographic peak fractions to be subjected to reduced-pressure drying, thereby obtaining yellow powdered rutin and quercetin reference substances. The method is simple in process and facilitates large-scale production.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Separation process and application of natural free radical scavengers from Saxifrage tangutica

The invention relates to the technical field of separation of natural free radical scavenger in saxifrage tangutica, in particular to a separation process and application of the natural free radical scavenger in saxifrage tangutica. Its preparation method: extraction, microporous resin column rough separation, online free radical scavenger component screening, reversed-phase preparative column preparation, reversed-phase preparative liquid chromatography purification of Fr1-1 and hydrophilic / reversed-phase two of Fr1-3 Six steps of liquid chromatography purification. The present invention has low cost and product purity greater than 95%; the technical means adopted in the present invention can carry out large-scale production: raw material requirements are not high, the cost is low, and it is easy to prepare materials in batches; methanol is extracted by cold soaking at room temperature, and it is easy to operate; the separation adopts a microporous resin column For coarse separation, the microporous resin separation material can be installed in a medium-pressure column chromatography system, which is easy to scale; the reversed-phase preparative liquid chromatography or hydrophilic preparative liquid chromatography used in separation and purification is a fast isocratic method.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Novel diaryl nonane V, VI and VII free radical inhibitors in saxifraga tangutica as well as separation and preparation process and application thereof

ActiveCN113087608ALow average cost of separationTo achieve large-scale production needsAntinoxious agentsNatural extract food ingredientsPharmaceutical drugPharmaceutical medicine
The invention discloses novel diaryl nonane free radical inhibitors V, VI and VII in saxifraga tangutica as well as a separation and preparation process and application thereof. The specific preparation process comprises the following four steps: extraction, coarse separation with a microporous resin column, on-line free radical inhibitor component screening and high-pressure reversed-phase chromatographic column separation. The prepared diaryl nonane Saxitansin B, the prepared diaryl nonane Saxitansin C and the prepared diaryl nonane Saxitansin D can be applied to preparation of free radical inhibition drugs or health-care foods, and are specifically used as active ingredients to be prepared into various medicinal preparations or health-care foods according to any pharmaceutically or food science acceptable carrier. An extraction solvent, a microporous resin column, a solvent used for high-pressure reversed-phase chromatographic column separation and an analysis material in the preparation process can be recycled; the raw materials are wide in source, large-scale operation can be realized in the process steps of methanol room-temperature cold leaching extraction, microporous resin column coarse separation, high-pressure reversed-phase isocratic liquid chromatography preparation and the like, and the isocratic separation of high-pressure preparative chromatography can ensure that the purity of the product is greater than 95%.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Novel diaryl nonane II and I free-radical inhibitor in Saxifraga tangutica, separation and preparation process for novel diaryl nonane II and I free-radical inhibitor and application of novel diaryl nonane II and I free-radical inhibitor

The invention discloses a novel diaryl nonane II and I free-radical inhibitor in Saxifraga tangutica, a separation and preparation process for the novel diaryl nonane II and I free-radical inhibitor and application of the novel diaryl nonane II and I free-radical inhibitor. The specific process comprises the steps of extracting, microporous-resin-column rough separating, online free-radical inhibitor component screening, out-phase medium-pressure chromatographic column separating, online free-radical inhibitor screening, and high-pressure preparative column preparing. The prepared free-radical inhibitor can be applied to preparation of free-radical inhibiting drugs or health-care foods and is specifically prepared into all classes of pharmaceutical preparations or health-care foods as an effective ingredient according to any support acceptable in pharmacy or food science. In the process, an extraction solvent, a microporous resin column, and a solvent and a separating material which are employed by the out-phase medium-pressure chromatographic column separating all can be recycled; and the source of raw materials is wide, processing steps such as methanol room-temperature cold-soaking extraction, microporous-resin-column rough separating and the out-phase medium-pressure chromatographic column separating all can achieve formalized operation, and the condition that the purity of a product is higher than 95% can be guaranteed by high-pressure preparation chromatographic separation.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

A pretreatment method for nucleoside components of Armillaria chrysanthemum fruiting bodies

The present invention relates to a pretreatment method for the nucleoside components of Armillaria chrysanthemum fruiting bodies, the method comprising the following steps: (1) Extraction: After the Armillaria chrysanthemum fruiting bodies are crushed, analytical pure water is added for extraction, after filtration, decompression Dry to paste to obtain Armillaria chrysanthemum fruiting body aqueous extract; (2) Alcohol precipitation: Add water to the aqueous extract of Armillaria chrysanthemum fruiting body to dissolve, then carry out alcohol precipitation, filter, and dry under reduced pressure to obtain a brown-yellow extract (3) Resin column chromatography enrichment: add ethanol solution to the brownish yellow extract to dissolve, and separate through resin column, carry out gradient elution with aqueous solution and ethanol solution respectively, and each eluate obtains 20% ethanol solution respectively after drying under reduced pressure The eluate, 50% ethanol solution eluate, 75% ethanol solution eluate and 95% ethanol solution eluate can obtain nucleoside target components. The invention has the advantages of simple process, easy large-scale implementation, repeatability, stable and controllable quality.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

A method for preparing gentiopicroside chemical reference substance from Gentiana japonica

The present invention relates to a method for preparing gentiopicroside chemical reference substance from Gentiana gentipicroside, the method comprising the following steps: (1) extraction with 95% ethanol solution: drying the whole herb of gentipicroside in the shade, crushing, carrying out alcohol extraction, filtering, and drying to paste , to obtain the alcoholic extract of Gentiana japonica; (2) Resin column enrichment: dissolving the alcoholic extract of Gentiana kinkanii with methanol solution and separating it through a resin column, first eluting with aqueous solution to remove large polar impurities, and then using 30% methanol solution, Step gradient elution with 50% methanol solution, collect 50% of the eluate, and dry the 50% of the eluate under reduced pressure to obtain the crude product of Gentiana japonica; (3) Refined by reverse-phase liquid phase preparative chromatography: after the crude product of Gentiana genus twisted is dissolved in methanol solution , after filtration, reversed-phase liquid phase preparative chromatographic separation, the main chromatographic peak fraction in the preparative chromatogram was collected, and the chromatographic peak fraction was dried under reduced pressure to obtain a white powdery reference substance with a purity greater than 98%. The invention has short separation time, good separation effect and high product purity.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Separation and preparation method of lignan derivatives in thuja arborvitae

The invention relates to the technical field of natural medicinal chemistry, in particular to a method for separating and preparing lignan derivatives from cypress arborvitae. Its preparation method includes four steps: extraction, microporous resin enrichment, reversed-phase C18 liquid chromatography separation, and reversed-phase phenyl column liquid chromatography purification and separation. The technical means adopted in the present invention can carry out large-scale production: the raw materials are widely planted, the cost is low, and it is easy to prepare materials in batches; n-hexane room temperature percolation extraction is easy to operate; the separation adopts microporous resin rough separation, and the microporous resin separation material can be installed In the medium-pressure column chromatography system, it is easy to scale up; the reverse-phase high-pressure preparative liquid chromatography used in the separation and purification is a fast isocratic method and can ensure that the product purity is greater than 98%.
Owner:YANTAI UNIV

A method for the separation and preparation of petrogin chemical reference substance in black saxifrage

The invention relates to the technical field of natural medicine chemistry, in particular to a method for separating and preparing a chemical reference substance of petracenin in saxifrage. Its preparation method includes three steps: extraction, polyamide column enrichment and microporous resin column separation. The present invention has low cost and product purity greater than 98%; the technical means adopted in the present invention can be used for large-scale production: the requirements for raw materials are not high, the cost is low, and it is easy to prepare materials in batches; the methanol is extracted by cold soaking at room temperature, and it is easy to operate; the polyamide column is used for enrichment , the separation material can be installed in a medium-pressure column system and connected to the preparative liquid chromatography, which is easy to scale; the microporous resin column used in the separation is a rapid isocratic method.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

A method for large-scale preparation of wedelolide chemical reference substance

InactiveCN104045648BFacilitate streamlined productionImprove separation efficiencyOrganic chemistryWedelolactoneWedelia
The invention relates to a new technology for large-scale preparation of a wedelolactone chemical reference substance. Through wedelolactone stability and preparation process streamlining optimization, a self-made large medium-pressure or pressure reduced silica gel column is employed for chromatography purification to obtain the wedelolactone chemical reference substance with purity greater than 98% in batches, and the scale is up to the 10g grade.
Owner:DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI

Method for large-scale preparation of adenosine chemical reference substance from fruiting bodies of Armillaria chrysogenum

The present invention relates to a method for large-scale preparation of adenosine chemical reference substance from Armillaria chrysanthemum fruiting bodies, the method comprising the following steps: (1) Alcohol precipitation and impurity removal: the aqueous extract of Armillaria chrysanthemum fruiting bodies is dissolved in water, then alcoholic precipitation, After filtering and drying under reduced pressure, a brownish-yellow extract is obtained; (2) microporous resin column enrichment: the brownish-yellow extract is dissolved in ethanol solution, filtered, and separated on a microporous resin column, followed by step gradient elution with water and ethanol solution , collect 50% ethanol water eluate, and dry the eluate under reduced pressure to obtain crude adenosine; (3) Reverse-phase liquid phase preparation chromatography purification: the crude adenosine is dissolved in methanol solution, filtered, and prepared by high-efficiency reverse-phase liquid phase The chromatographic column is separated, and the main chromatographic peak fraction in the preparation chromatogram is collected. The chromatographic peak fraction can be dried under reduced pressure to obtain the white powder adenosine reference substance. The process of the invention is simple and easy to scale.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

A method for preparing salidroside chemical reference substance from Rhodiola angustifolia root

The invention relates to a method for preparing a salidroside chemical reference substance from Rhodiola kirilowii root, which comprises the following steps: (1) silica gel column chromatography enrichment: carrying out silica gel column chromatography separation and elution on a Rhodiola kirilowii root alcohol extract, carrying out thin-layer chromatography detection, and drying under reduced pressure to obtain a brown yellow powdered salidroside crude product; (2) microporous resin impurity removal: dissolving the salidroside crude product, separating through a microporous resin column, eluting, and drying under reduced pressure to obtain a salidroside component; and (3) reversed liquid-phase preparative chromatography refinement: dissolving the salidroside component, filtering through a microporous filter membrane, separating through a high-performance reversed liquid-phase preparative chromatography column, collecting the target chromatogram peak fraction in the preparative chromatogram, and drying the target chromatogram peak fraction under reduced pressure to obtain the white powdered salidroside reference substance. The method is simple in technique and can easily implement scale-up production.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST

Method for simultaneously preparing chemical reference substances of calycosin and formononetin

The invention relates to a novel process for simultaneously preparing chemical reference substances of calycosin and formononetin, comprising two steps of purifying astragalus root alcohol extracts by utilizing silicagel column chromatography and recrystallizing to obtain the two types of chemical reference substances of the calycosin and the formononetin with purities greater than 98%. The method has the advantages of simple process steps and high purity of obtained products, and is easy for scale production.
Owner:DALIAN INST OF CHEM PHYSICS CHINESE ACAD OF SCI

A kind of preparation method and application of the flavonoid components of isoflavone

The invention relates to a sample pretreatment method of flavonoid component of dracocephalum heterophyllum benth. The sample pretreatment method comprises the following steps: (1) carrying out liquid-liquid partitioning enrichment, namely, carrying out dispersion, extraction and vacuum drying on pohytol extract of dracocephalum heterophyllum benth to obtain medium polar component part of dracocephalum heterophyllum benth; (2) removing purities by adopting micro-reticular resin, namely, dissolving the medium polar component part of dracocephalum heterophyllum benth, filtering, separating by a micro-reticular resin column, eluting, collecting the eluate, and carrying out vacuum drying on the eluate to obtain the yellow flavonoid component of dracocephalum heterophyllum benth; (3) and carrying out chromatography isolation by adopting a silicagel column, namely, separating the flavonoid component crude product of dracocephalum heterophyllum benth by adopting the silicagel column chromatography, eluting, detecting by adopting thin-layer chromatography, mixing, and collecting fraction with the Rf value being 0.1-0.8, and carrying out vacuum drying on the fraction, thus obtaining the flavonoid component of dracocephalum heterophyllum benth, which is in the form of yellow powder. The technology is simple, and easy in realizing scale production. The invention further discloses an application of the flavonoid component of dracocephalum heterophyllum benth in preparing a drug or health food for resisting hepatitis virus.
Owner:CHINA ACAD OF SCI NORTHWEST HIGHLAND BIOLOGY INST
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