Patents
Literature
Hiro is an intelligent assistant for R&D personnel, combined with Patent DNA, to facilitate innovative research.
Hiro

661results about How to "Clear ingredients" patented technology

Agrobacterium ZX09, water-soluble beta-glucan prepared from Agrobacterium ZX09 and preparation method thereof and application on reducing blood sugar

The invention discloses Agrobacterium ZX09, water-soluble beta-glucan prepared from the Agrobacterium ZX09 and the preparation method thereof and the application on reducing blood sugar, wherein the bacterial strain of the Agrobacterium ZX09 is obtained by separating saline soil from Dongying city in Shandong province; the bacterial strain is Agrobacterium sp. and is collected in China Center for Type Culture Collection (CCTCC) on January 21st, 2010; and the collection number is CCTCC NO:M2010020. The structure general formula of the water-soluble beta-glucan prepared from the Agrobacterium ZX09 is as follows: ->(3)-beta-D-Glup-(1->3)-[beta-D-Glup-(1->3)-beta-D-Glup-]3-alpha-D-Glup-(1->3)-alpha-D-Glup-(1)n->, and n in the structural formula is from 100 to 200. The bacterial strain has the advantages of novelty, special properties, salt resistant growth, no pigment secretion in the process of growth, simple and convenient cultivation operation, simple technology, total synthetic media, definite components and low cost, and is suitable for industrial production.
Owner:SICHUAN HETAI SYNLIGHT BIOTECH LTD

Serum-free medium for umbilical cord mesenchymal stem cells

The invention provides a serum-free medium for umbilical cord mesenchymal stem cells and belongs to the technical field of cell culture. The serum-free medium for umbilical cord mesenchymal stem cells comprises a basal culture medium body and added ingredients, wherein the basal culture medium body is a DMEM culture medium; the added ingredients include a basic fibroblast growth factor hFGF, a epidermal growth factor hEGF, insulin hI, a leukaemia inhibitory factor hLIF and astragalus polysaccharide. The umbilical cord mesenchymal stem cells are subjected to subculture and amplification in the medium, and the surfaces of the cultured cells are marked and analyzed. The serum-free medium for umbilical cord mesenchymal stem cells overcomes the defect of exogenous pollution of serum and solves the problem of contradiction between the cell expansion number and cost reduction. The medium is free of serum, thereby preventing influence of animal-derived serum ingredients on cell culture. The medium can be used for studying the differentiation and proliferation adjusting mechanism of the umbilical cord mesenchymal stem cells.
Owner:SHANDONG JINGYUAN BIOTECH CO LTD

Epigallo-catechin gallate (EGCG) with high purity and preparation method thereof

The invention provides an epigallo-catechin gallate (EGCG) with high purity and a preparation method thereof. The EGCG content is 98.0 percent to 99.9 percent. The preparation method mainly comprisesthe working procedures of extracting, separating by a chromatography and crystallizing. The invention has favorable reproducibility of preparation process, high acquired EGCG content, low cost and stable and controllable quality and is suitable for industrialized production.
Owner:JIANGSU TIANSHENG PHARMA

Amplifying, freezing and storing and recovering method of activated lymphocyte with CD3+CD8+as major

InactiveCN102839153ASolve the problem of multiple blood collectionHigh purityDead animal preservationBlood/immune system cellsPatient needT lymphocyte
The invention discloses culturing, freezing and recovering methods of an activated lymphocyte with CD3+CD8+as major, which can solve problems that a patient needs carrying out blood sampling for many times caused by continuously utilizing the activated lymphocyte with CD3+CD8+as major. The method comprises the following steps of: (1) contacting the extracted lymphocyte of the peripheral blood with IL-2, IL-15, an anti-CD3 antibody and an anti-CD28 antibody, so as to amplify the activated lymphocyte with CD3+CD8+as major; (2) freezing and storing the activated lymphocyte; and (3) recovering the activated lymphocyte. The activated lymphocyte cultured via the method disclosed by the invention has clear components, and comprises few CD4+CD25+Treg cells and more CD8+T lymphocyte; feedback time and frequency of the activated lymphocyte can be adjusted according to other treatments for a patient, such as a radiotherapy or a chemotherapy, so that diseases, such as tumor, infectious diseases and immunodeficiency can be treated well.
Owner:JINAN TAISHENG BIOLOGICAL TECH CO LTD

Umbilical cord mesenchymal stem cell injection as well as preparation method and application thereof

The invention provides umbilical cord mesenchymal stem cell injection as well as a preparation method and application thereof. The umbilical cord mesenchymal stem cell injection comprises mesenchymal stem cells and a frozen stock solution, wherein the frozen stock solution comprises the following components: a balanced electrolyte solution with the volume percentage of 25-70 percent, hydroxyethyl starch 130 / 0.4 with the mass / volume percentage (g / ml) of 1-10 percent, triphosadenine disodium magnesium chloride with the volume percentage of 5-20 percent, clinical-grade DMSO with the volume percentage of 5-20% and 20% human albumin with the volume percentage of 1-50 percent. The prepared umbilical cord mesenchymal stem cell injection is free of animal serum, safe, high in cell viability after cryopreservation resuscitation, can be used for treating inflammatory bowel disease, has a good effect and has no toxic or side effects.
Owner:北京青藤谷禧干细胞科技研究院有限公司

MSC (mesenchymal stem cell) injection as well as preparation and application thereof

The invention relates to the field of biology, in particular to MSC (mesenchymal stem cell) injection as well as a preparation and an application thereof. The injection comprises MSCs and a cell cryopreservation solution, wherein the cryopreservation solution comprises components in percentage by volume as follows: 25%-70% of an electrolyte balance solution, 5%-20% of clinical-grade DMSO (dimethyl sulfoxide), 1%-50% of 20% human serum albumin, 1%-10% of hydroxyethyl starch 130 / 0.4 and 5%-20% of triphosadenine-disodium magnesium chloride freeze-drying powder. The injection is free of animal serum, has clear ingredients and good cell cryopreservation effect and is safe and controllable, long-term storage and long-distance transport are facilitated, the survival rate of cells after recovery is higher than 95%, the vitality is high, and the injection can effectively relieve injury and inflammation symptoms of lesion tissue of lungs and promote tissue regeneration of the lungs, so that acute lung injury can be fundamentally and comprehensively treated.
Owner:北京青藤谷禧干细胞科技研究院有限公司

Stem cell freezing and storing medium and preparation method and freezing and storing method thereof

ActiveCN110050782AReduces freeze damageHigh activityDead animal preservationCvd riskExcipient
The invention discloses a stem cell freezing and storing medium and a preparation method and freezing and storing method thereof. The stem cell freezing and storing medium comprises, by weight, 3-10 parts of dimethyl sulfoxide, 2-7 parts of human serum albumin, 0.5-3 parts of mycose, 0.2-2 parts of dextran 40 and 2-6 parts of hetastarch. Cells can be frozen for a long time by the stem cell freezing and storing medium, freezing damage of the cells can be remarkably reduced, the resuscitated cells have a high degree of survival rate and adherent property, and freezing and storing effect of the cells is improved; meanwhile, the compositions of the stem cell freezing and storing medium are clear and are medical compendial injection-grade excipients without containing serum, the risk of contamination and allergen introduced by the use of heterogeneous serum is effectively prevented, the content of DMSO (dimethylsulfoxide) is low, the negative effect of the DMSO on the cells is lowered, highsecurity and good stability are achieved, requirements of CFDA (China food and drug administration) and FDA (food and drug administration) are met, and the stem cell freezing and storing medium can be directly used in human infusion and is suitable for clinical research and treatment.
Owner:广州赛隽生物科技有限公司

Preparation method for efficiently extracting separating high-purity flavone components from ginkgo leaf

InactiveCN103110670AIncrease contentThe ingredients and content are clearNervous disorderGinkgophyta medical ingredientsChemistryKaempferol-3-O-rutinoside
The invention provides a preparation method for efficiently extracting separating high-purity flavone components from ginkgo leaf. The main components are kaempferol-3-O-2'', 6''-dirhamnosylglucoside, rutin, quercetin glucosyl rhamnoside, kaempferol-3-O-rutinoside, isorhamnetin-3-O-rutinoside, quercetin p-coumaroyl glucose rhamnoside and kaempferol p-oumaroyl glucose rhamnoside. The preparation method comprises the following steps: pulverizing the medicinal material ginkgo leaf, adding an alcohol water solution to carry out extraction, concentrating, carrying out nonpolar macroporous adsorbent resin column chromatography on the filtrate, carrying out two-dimensional separation with a novel silica gel substrate bonded material, eluting with a methanol solution, collecting the eluate, concentrating, and drying to obtain the gingko flavone components. The invention enhances the target component content, and obtains the flavone components with definite content. The extraction and separation process has the advantages of high repetitiveness and favorable operability, and is suitable for large-scale preparation of flavone components by separation from ginkgo leaf. The flavone components can be used as a raw material for Shuxuening injections.
Owner:北京华润高科天然药物有限公司

Undifferentiated anti-aging amplification culture medium for human umbilical cord/adipose tissue-derived stem cells

The invention provides an undifferentiated anti-aging amplification culture medium for human umbilical cord / adipose tissue-derived stem cells. The problem in the prior art that a serum-free medium used for culturing mesenchymal stem cells is easy to differentiate and easily causes aging and apoptosis of adult stem cells is solved. The undifferentiated anti-aging amplification culture medium for human umbilical cord / adipose tissue-derived stem cells comprises cell factors, vitamins and chemical small molecules, and the culture system comprises multiple chemical small molecules and biomacromolecules and has the effects of improving physiological metabolism and proliferation and growth potential of cells, resisting oxidative stress response, scavenging free radicals, preventing DNA mutation, protecting mitochondria, reducing molecular wastes in the cells and activating longevity genes and telomerase.
Owner:北京殷氏细胞生物科技集团有限公司

Phellinus igniarius mycelium culture medium and process for fermenting phellinus igniarius using same

The invention discloses a phellinus igniarius mycelium culture medium and a process for fermenting phellinus igniarius using the same. The phellinus igniarius culture medium comprises the following components per liter: 25-35 g of maltose, 18-25 g of yeast powder, 2.4-4.2 g of mineral elements, 5-10 mg of vitamin B1, 3-5 mg of vitamin B2, 0.5-1 mg of vitamin B6, 20-30 mg of niacinamide, 2-3 mg of calcium pantothenate, 3-10 g of aqueous extract of ramulus mori and the balance of water. The phellinus igniarius is cultured in a culture solution for 4-6 days, wherein the inoculation amount is 10-20%, the culture temperature is 22-29 DEG C, the liquid amount in a shake flask is 50-70%, the rotation speed of a reciprocating shaker is 100-150 rpm and the fermentation time is 5-10 days. The invention has the advantages that: the components are clear, the quality is stable, a special nutrition source for phellinus igniarius is provided, and the invention can be used for the large-scale culture of phellinus igniarius mycelium with medicinal activity.
Owner:ZHEJIANG ACADEMY OF AGRICULTURE SCIENCES

Serum-free adipose tissue-derived mesenchymal stem cell culture medium

ActiveCN103255103AAvoid exogenous contaminationAvoid the influence of cultivationSkeletal/connective tissue cellsPenicillinCuticle
The invention relates to a serum-free adipose tissue-derived mesenchymal stem cell culture medium, which consists of a basic culture medium and added ingredients, wherein the basic culture medium is DMEM-LG, and the added ingredients and the content of each added ingredient are shown as follows: 5 to 20ng / mL of alkaline fiberblast growth factors, 5 to 20ng / mL of epidermal growth factors, 100U / mL of penicillin, 100 micrograms / mL of streptomycin, 50 to 200 micrograms / mL of heparin, 2 to 8mM of L-glutamine, 100 to 300 microM of 2-mercaptoethanol, 500 to 2000U / mL of leukaemia inhibitory factors and 0.5 to 2mM of sodium pyruvate. The serum-free adipose tissue-derived mesenchymal stem cell culture medium does not contain the serum, so that the inter-batch difference and the influence of the serum component on the cell culture can be avoided; the exogenous pollution of the serum and the toxicity of the serum on the cells can be avoided; and the ingredients are clear, so that the research of the psychological regulation mechanism of the cells can be facilitated.
Owner:冯文峰

High safety battery electrolyte solution

The invention discloses a high safety battery electrolyte solution, which includes an electrolyte and a solvent. The solvent is a mixed solvent of carbonic ester and a fluoro-ether solvent. The electrolyte solution provided by the invention can significantly improve the safety performance of batteries, and effectively prevent electrolyte solution combustion or even explosion due to overheat of batteries.
Owner:NINGBO INST OF MATERIALS TECH & ENG CHINESE ACADEMY OF SCI

Preparation method of NK (Natural Killer) cells

The invention discloses a preparation method of NK (Natural Killer) cells. The preparation of the NK cells is prepared through the steps of coating a culture bottle, collecting peripheral blood, separating mononuclear cells, inoculating, amplifying and harvesting the cells. A serum free culture medium provided by the invention has clear components and high safety; after the mononuclear cells are cultured and activated by the culture medium, the amplification capability is strong; after being cultured for 15 to 18 days, the mononuclear cells are amplified for 160 to 200 times; after the cells are detected by a flow cytometer, the content of the NK cells of CD3<->CD56<+> is 65 to 70 percent and the content of T cells of an NK sample of CD3<+>CD56<+> is 5 to 15 percent; the content of NK andNKT cells exceeds 75 percent and the killing activity on K526 reaches 85 percent or above when the multiplicity of infection is 20 to 1; furthermore, an amplification method is simple and efficient and large-scale production is facilitated.
Owner:GENESIS STEMCELL REGENERATIVE MEDICINE ENG CO LTD

Production method of beta-glucan

The invention discloses a production method of beta-glucan. The production method comprises the following steps of (1) schizophyllum commune activation; (2) seed activation; (3) fermentation culture; (4) coarse extraction; (5) purification. A colorless liquid culture medium prepared from 25 to 30g / L of glucose, 10 to 15g / L of sorbitol, 0.2 to 0.8g / L of monopotassium phosphate, 3 to 5g / L of epsom salt, 0.5 to 1g / L of ammonium sulphate, 0.1 to 0.5g / L of triethylamine hydrochloride, 1 to 2.2ml / L of trace element mixed solution and water is used as a fermentation culture medium for performing deep layer liquid fermentation culture on strains to obtain the colorless fermentation liquid. No pigment exists in the whole process; a decoloring step is not needed; loss due to adsorption is reduced; the problem of beta-glucan separation purification is overcome; high-purity white beta-glucan is obtained; the production method is suitable for mass industrial production.
Owner:NINGBO XINUOYA MARINE BIOTECH CO LTD

Novel electrolysis system applicable to lithium titanate battery

InactiveCN103682437AInhibit flatulenceFit closelySecondary cellsElectrolytic agentPower battery
The invention discloses a novel electrolysis system applicable to a lithium titanate battery. The novel electrolysis system comprises electrolyte and a solvent, wherein the solvent is a mixed solvent of an ether solvent and an carbonic ester solvent comprising cyclic carbonate and the mass ratio of the ether solvent to the carbonic ester solvent is (1-x):x, wherein x is larger than 0 and less than or equal to 0.9. The electrolysis system provided by the invention well accords with an existing lithium titanate battery, has no need of replacing a film, an anode material and a shell, can effectively inhibit the flatulence phenomenon of the lithium titanate battery, and has a wide application prospect in the fields of power batteries and energy storage batteries.
Owner:NINGBO INST OF MATERIALS TECH & ENG CHINESE ACADEMY OF SCI

Serum-free culture fluid for culture of salivary gland epidermal cell and salivary gland stem cell of mammals

The invention provides serum-free culture fluid for culture of salivary gland epidermal cells and salivary gland stem cells of mammals, which is prepared by using MCDB153HAA as basic culture medium and adding amino acid, vitamins, salts, lipid, trace elements, buffer fluid, hormone-like compounds, transgenic metalloprotein, antioxidants, seralbumin, glucide, purine, pyrimidine base substances and pH value indicators. The serum-free culture fluid has the advantages that salivary gland epidermal cells of the mammals can vigorously grow, good cell activity and physiological properties are maintained, in addition, the serum-free culture fluid is also suitable for the salivary gland epidermal cell culture, is particularly suitable for the field of study relevant to biological tissue engineering and belongs to the commercial cell culture fluid.
Owner:INST OF DONGGUAN SUN YAT SEN UNIV

Diphenyl ethylene glycosides derivatives

The invention relates to a new type 2, 3, 5, 4'- tetra-hydroxyl diphenyl ethylene-2-O-beta-D-glucoside crystal, a method for making same, and pharmaceutical compositions containing the crystal. The content of the crystal is 90-99. 9tested by high performance liquid chromatography, and the stilbene glucoside crystal of high-purity is obtained by abstracting fleece-flower root, extracting with an organic solvent, separating by column chromatography and crystallizing in appropriate dissolvent. The preparing process provides high yield, low cost, and is suitable for industrial production.
Owner:NANJING CHIA TAI TIANQING PHARMA

Serum-free culture medium for human umbilical cord MSCs (mesenchymal stem cells)

The invention discloses a serum-free culture medium for human umbilical cord MSCs (mesenchymal stem cells). The serum-free culture medium comprises the major ingredients of amino acid, inorganic salt ingredients, growth factors and albumin ingredients. The serum-free culture medium for human umbilical cord MSCs does not contain any serum ingredients; in addition, the ingredients are clear; the foreign protein pollution and pathogenic microorganism risks are avoided; the biosecurity problem of the MSCs clinic application is solved. When the serum-free culture medium provided by the invention is used for culturing the human umbilical cord MSCs, the high-quantity high-purity safe and high-quality umbilical cord MSCs can be obtained in vitro; meanwhile, the cell survival rate can be improved; the stem cell characteristics are maintained. The problem of insufficient cell quantity can be solved; the cell number, the survival rate and the immunophenotyping in each batch are more stable; the relevant index requirements are met.
Owner:王晓柯

Antioxidant and anti-aging medicinal and health-care product

The present invention relates to an antioxidant and anti-aging astaxanthin health-care composition and preparation method thereof. The composition comprises the following components in parts by weight: astaxanthin 120-160 parts, lycopene 83-133 parts, and grape seed extracts 67-89 parts. The composition can be processed into hard capsules, soft capsules and oral liquid by adding accessories accepted by the pharmaceutical technology. By using astaxanthin, lycopene, and grape seed extracts as raw materials, aiming at the physical signs and food culture features of Chinese people, and scientifically quantifying and blending the raw materials, the composition maximally exerts the synergistic effect of anti-oxidation, and makes the functional features of these three varieties complement each other, thus leading to comprehensive antioxidant effect and remarkable anti-aging effect.
Owner:李燕铭 +1

Stem cell culture medium

The invention discloses a stem cell culture medium. The stem cell culture medium comprises an improved DMEM (Dulbecco's Modified Eagle Medium) / F12 basal culture medium and an additive, wherein the additive comprises sodium bicarbonate, selenium amino acid chelate, recombinant human insulin growth factors, recombinant human basic fibroblast growth factors, recombinant human lactoferrin, ascorbic acid, recombinant human platelet-derived growth factors, recombinant human vascular endothelial cell growth factors, octacosanol, polyvinyl alcohol, polyvinylpyrrolidone and recombinant human epidermal growth factors. According to the stem cell culture medium, the potential of stem cells is not influenced while the stem cells can be proliferated rapidly, the proliferation speed of the stem cells is increased by 3-5 times compared with a common culture medium, and further, the stem cell culture medium can be used for culturing the stem cells of various kinds of tissue and has excellent applicability; the cultured stem cells have high differentiation capability, can be differentiated into multiple functional cells and have very high scientific research and medical application values, culture medium components are exact, the quality is stable, and accordingly, the cultured stem cells are not likely to generate human body rejection reaction after transplanting.
Owner:XINXIANG MEDICAL UNIV

Serum-free and DMSO-free cell cryopreservation solution and preparation method thereof

InactiveCN110934132AHigh biosecurityHigh clinical application prospectsDead animal preservationHydroxyethyl starchCytokine
The invention discloses a serum-free and DMSO-free cell cryopreservation solution, which comprises a 16.762-16.825 g / L DMEM / F-12 basal culture medium, 32-34 mg / L cytokines, 0.2-0.8 mg / L hydroxyethyl starch, 1-3 mg / L vitamins, 0.15-0.16 g / L antibiotics, 5-6 mg / L protein polypeptide, 1-4 mg / L lipids and a 0.1-0.41 g / L intracellular and extracellular cryoprotectant. According to the technical scheme,the obtained cell cryopreservation solution does not contain serum or DMSO components, the components of the formula are determined, the cell cryopreservation solution has high biological safety andclinical application prospects, and the cell cryopreservation liquid has a cell recovery survival rate of more than 85%, can maintain good cell activity and good physiological characteristics, and issuitable for the related research fields of primary cells and stem cells.
Owner:苏州君欣生物科技有限公司

Non protein culture medium adapted to large-scale culture of NSO cell and production of antibody

The invention relates to a protein-free medium suitable for large-scale cultivation and antibody production of NSO cells, which is a protein-free medium provided with clear chemical compositions. The compositions of the protein-free medium comprises 21 types of amino acid, 13 types of vitamin, 8 types of salt, 4 types of fat, 6 types of microelement, progesterone, sodium bicarbonate, Hepes, glucose, a citric acid, taurine, thymidine, adenine, hypoxanthine, phenol red, mercaptoethanol and Pluronic F-68. The protein-free medium has the advantages that the protein-free medium can support long-term subculture of the NSO cells without the necessity of adaptation, can well support normal growth and antibody expression of the NSO cells, does not contain proteins, various hydrolysate and animal origin compositions, has clear chemical compositions, is favorable for separation and purification of products, improves the quality of medical and biological products, and is convenient to prepare and suitable for mass production and application.
Owner:EAST CHINA UNIV OF SCI & TECH

Earthworm protein polypeptide preparation

The invention discloses an earthworm protein polypeptide preparation, its preparation method and application. The protein polypeptide preparation is prepared by hydrolyzing the earthworm homogenate coarse extract or hydrolyzing the earthworm homogenate coarse extract to obtain the hydrolyzed protein polypeptide, separating by a hyperfiltration membrane with different hole diameter to obtain the protein polypeptide ingredients with different hole diameter. Test proves that the earthworm protein polypeptide preparation has good angiotensin converting enzyme after enzyme hydrolysis and can effectively prevent the high blood pressure. The invention provides a preparation method for the earthworm protein polypeptide preparation with strong operability, high efficiency and realizes an industrialization big production.
Owner:NANJING UNIVERSITY OF TRADITIONAL CHINESE MEDICINE

Serum-free culture medium and stem cell culture method

The invention relates to a serum-free culture medium which comprises a basal culture medium, insulin, iron-containing food additive, sodium arsenite, fibronectin, glucagon, hepatocyte growth factor and myllicin. In addition, the invention further discloses a stem cell culture method. The stem cell culture method includes the following steps: acquiring stem cells; adopting the serum-free culture medium for in vitro culture. By the serum-free culture medium, the problem of difficulty in cell purifying due to pollution of pathogens carried by a serum culture medium can be avoided, stability of cell production can be improved, cell proliferation amount can be increased, and cell activity can be enhanced.
Owner:SHEN ZHEN ISTEM REGENERATIVE MEDICINE SCI TECH CO LTD

Chlorogenic acid injection, its preparing method and use

The present invention relates to a chlorogenic acid power injection. It is characterized by that it is made up by using purified effective component chlorogenic acid extracted from lonicera flower and medicinal auxiliary material for injection through a certain preparation process. Said chlorogenic acid powder injection mainly is used for curing angiocardiopathy and cerebrovascular disease. Besides, said invention also provides its preparation method and concretes steps.
Owner:广东仁泰药业有限公司

Traditional Chinese medicine extract capable of improving CIK cell proliferation rate as well as preparation method and application of same

The invention relates to a traditional Chinese medicine extract capable of obviously improving CIK (Cytokine-Induced Killer) cell proliferation rate. The extract is prepared from the raw materials of red ginseng, radix ophiopogonis and milk vetch according to a certain weight ratio. A formula of the extract comprises the steps as follows: the red ginseng, the radix ophiopogonis and the milk vetchare added with water and decocted, and are subjected to ethanol precipitation and filtered; ethanol is recovered; the extract liquid is enriched with macroporous resin columns, eluted to be colorlesswith distilled water and eluted with ethanol; the eluant is collected; the extract liquid is filtered with a microporous filtration film; and the filter liquor is condensed, the pH value is adjusted,the filter liquor is filtered again with the microporous filtration film, sterilized, and subpackaged, and then the traditional Chinese medicine extract is obtained. Pharmacological experiments show that the traditional Chinese medicine extract can remarkably improve the proliferation rate of CIK cells.
Owner:CHINA JILIANG UNIV

Purification method applicable to manufacturing food-grade ovalbumin on large scale

The invention discloses a purification method applicable to manufacturing food-grade ovalbumin on a large scale. The purification method includes steps of collecting egg white at the room temperature, diluting the egg white according to a volume ratio of the egg white to fresh deionized water being 1:2 without adjusting pH (potential of hydrogen) of the egg white, uniformly stirring the egg white and then centrifuging the egg white to obtain supernatant; adding polyethylene glycol with the molecular weight ranging from 200 to 20000 into the supernatant obtained by means of centrifuging, uniformly stirring the supernatant and the polyethylene glycol and then centrifuging the supernatant and the polyethylene glycol to obtain high-purity ovalbumin liquor with the polyethylene glycol; carrying out ultra-filtration treatment on the high-purity ovalbumin liquor with the polyethylene glycol to manufacture high-purity ovalbumin without the polyethylene glycol. The purification method has the advantages that the purification method is simple, convenient and speedy and is low in cost and applicable to large-scale industrial production, and the food-grade ovalbumin can be manufactured under mild and safe conditions, are extremely high in quality and can be conveniently directly processed to obtain various foods, healthcare products and medical products in follow-up procedures.
Owner:JIANGSU UNIV

Preparation method of effective part of radix bupleuri and application thereof

The invention relates to a preparation method for extracting an effective part from traditional Chinese medicine radix bupleuri and an application of the effective part obtained by utilizing the method and a preparation thereof in medicines for preventing and treating liver fibrosis, hepatocirrhosis, chronic hepatitis and the like. The preparation of the effective part of the radix bupleuri can be granules, soft capsules, capsules, dripping pills, tablets, dispersing tablets, effervescence tablets, injection and the like. The invention has simple operation method and utilizes a modern medicine effect sieving technology, an extracting and purifying technology, a preparation technology and a quality control technology to carry out deep development on the radix bupleuri preparation; the effective part of the radix bupleuri and the preparation thereof obtained by utilizing the technological method of the invention are rich in active components, have definite effective components, obvious pharmacological action, obviously enhanced medicine effect, stable performance, controllable quality, safety, reliability and small dose and are beneficial to the transportation and storage of the medicine and the taking of a patient.
Owner:JIANGXI HERBFINE HI TECH

Active ingredients of camptosorus sibiricus, and extraction method and use of same

The invention belongs to the technical field of medicaments and provides active ingredients of Chinese herbal medicine camptosorus sibiricus and an extraction method and use of the same. The extraction method comprises a water extraction method, an alcohol extraction method, a macroporous resin purification method and a solvent extraction method. The main active ingredients of an extract obtained by the method are total flavonoids, total momordica saponins and total organic acids, wherein the content of the total flavonoids is 1 to 35 percent, the content of the total momordica saponins is 1 to 25 percent and the content of the total organic acids is 1 to 3 percent. The invention also provides a method for preparing the camptosorus sibiricus into a proper formulation directly or by mixing with solid or liquid commonly used for preparations of the type in pharmaceutics. The active ingredients of the camptosorus sibiricus and the preparation thereof have functions of treating thromboangiitis obliterans, nephritis, traumatism and bleeding, metrorrhagia, neurodermitis, hemiplegia caused by cerebral embolism and diabetes-related complications. The extraction method is simple, easy to implement and low in cost. And the extract obtained is free from toxic and side effects.
Owner:SHENYANG PHARMA UNIVERSITY
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products