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

50results about How to "No residual risk" patented technology

Environmentally-friendly and safe detergent with antibacterial function

The invention relates to an alga extract product with an antibacterial function, an antibacterial agent including the alga extract product, a composition, and a preparation method of the composition, and belongs to the technical field of antibacterial detergents. The composition contains the algal antibacterial agent, a surfactant, an antioxidant and water, and especially the algal antibacterial agent is selected from an alga extract product-anionic surfactant complex. The invention also discloses the preparation method and a use of the composition. Above detergents provided by the invention have the characteristics of no pollution to environment, safety and mildness to people, greenness and environmental protection, and facilitation of the safety of environment and human life.
Owner:深圳市海立方生物科技有限公司

Preparation method of high-efficiency cyhalothrin nano-pesticide

The invention discloses a preparation method of high-efficiency cyhalothrin nano-pesticide, belonging to the technical field of preparation of agricultural chemicals. The preparation method is characterized in that an amphiphilic copolymer is adopted and is self-assembled in an aqueous solution to form a nano-sized micelle with an obvious core-shell structure; the nano-pesticide is obtained by physical actions of an organic solvent and polyvinyl alcohol. The preparation method disclosed by the invention is simple and convenient; raw materials are easily obtained; a used solvent is water, so the pollution is small and the cost is low; the used amphiphilic copolymer has good environmental compatibility, biodegradation and no residual risks; in addition, a degraded product can be absorbed and utilized by crops; the nano-pesticide has the advantages of relatively small and relatively uniform particle size, relatively good permeability and certain slow release effect; the lasting period of pyrethroid pesticides is prolonged, and the using dose of the pesticide is reduced.
Owner:INST OF PLANT PROTECTION CHINESE ACAD OF AGRI SCI

Ganoderma spore powder refined polysaccharide with significant auxiliary anti-tumor activity and preparation method and application thereof

The invention relates to ganoderma spore powder refined polysaccharide with significant auxiliary anti-tumor activity and a preparation method and application thereof, and belongs to the field of medicinal-fungus extraction and separation and the field of drug and food application development. The refined polysaccharide is mainly prepared from heteropolysaccharide composed of mannose, glucose, galactose and fucose according to the molar ratio of 1: (40-50): (4-5.5): (1.5-2), the purity of the refined polysaccharide is greater than 80%, and the weight-average molecular weight is 160-200 KD. Thepreparation method of the ganoderma spore powder refined polysaccharide includes the steps of using hot water for dynamic extraction, removing residues by combining sedimentation and rough filtration, conducting refined filtration and clarification, removing impurities through ultrafiltration-membrane concentration, and drying through spray or airing through alcohol precipitation. The preparationmethod of the ganoderma spore powder refined polysaccharide is environmentally friendly and smart, saves energy, can solve industrialized difficulties and has significant scale advantages, prepared products meet the requirements, about the safety, availability, controllability and stability, in a drug and medicine quality controlling system. The ganoderma spore powder refined polysaccharide has significant functional activity at the auxiliary anti-tumor aspect and can be used for developing tumor prevention and treating drugs, and development of food and healthcare products in related fieldscan be carried out.
Owner:GUANGDONG YUEWEI EDIBLE FUNGI TECH

Preparation process for gout suppressant Lesinaurad intermediates

The invention discloses a preparation process for gout suppressant Lesinaurad intermediates, and particularly relates to the preparation process of cyclopropyl-naphthalene. The preparation process includes the steps of conducting cyclization on 3-(Dimethylamino)-1-(naphthalen-1-yl)propan-1-one hydrochloride and hydrazine hydrate under the alkaline condition to generate 1-(4,5)-pyrazoline-naphthalene, and conducting high-temperature pyrolysis on the 1-(4,5)-pyrazoline-naphthalene under the neutral condition or the alkali condition to generate the cyclopropyl-naphthalene. The preparation process is few in reaction step, raw materials are cheap and can be easily obtained, the production efficiency is high, the process is green and environmentally friendly, no precious metal is used, no heavy metal residuals are generated, and the industrial production is easy.
Owner:ASTATECH CHENGDU BIOPHARM CORP

Full-soluble edible mushroom protein and preparation method thereof

The invention discloses a full-soluble edible mushroom protein and a preparation method thereof. The full-soluble edible mushroom protein is prepared by the following steps: unmodified edible mushroom protein is expanded under an alkaline condition, and then acid is added to adjust the edible mushroom protein to be neutral. According to the preparation method, the primary structure of the protein is not changed, the nutritional value of the protein can be reserved to the maximum extent, the obtained edible mushroom protein is free of exogenous additive components, the acceptance degree of consumers is improved to the maximum extent, reasonable utilization of edible mushroom byproducts is achieved, and resource waste and environmental pollution are effectively avoided.
Owner:JIANGNAN UNIV

Making method of instant fresh stretched noodles

InactiveCN105249191AUnique tasteUnique toughnessFood scienceEdible oilFermentation
The invention relates to a making method of instant fresh stretched noodles, and belongs to the technical field of food making. A technical problem to be solved is providing the making method of the instant fresh stretched noodles. The method can guarantee unique mouthfeel and chewiness of present fresh stretched noodles, and also can meet people's fast easing demands, so the noodles can be immediately stretched and eaten without tedious dough kneading when people want to eat the stretched noodles. A technical scheme adopted in the invention to realize the above purposes is characterized in that the method comprises the following steps: uniformly mixing flour, edible salt, eggs and water, and kneading until smoothness to form dough; fermenting the dough, kneading once every 10-15min in the fermentation process, kneading the fermented dough to form circular elongated noodles, uniformly smearing the surfaces of the elongated noodles with edible oil, putting the elongated noodles in a dough holder, sealing, putting the sealed noodles in a refrigerator, refrigerating to obtain semi-finished fresh stretched noodles, taking the semi-finished fresh stretched noodles out of the refrigerator when people want to eat the noodles, unfreezing, and stretching the unfrozen semi-finished fresh stretched noodles to form the instant fresh stretched noodles.
Owner:刘建文

Crystal form of linagliptin and preparation method thereof

The invention discloses a crystal form of linagliptin and a preparation method thereof. For the crystal form, X-ray powder diffraction, expressed in 2 theta angle and using the alpha radiation of Cu-K(copper-potassium), has diffraction peaks at 23.1 plus or minus 0.2 degrees, 23.5 plus or minus 0.2 degrees, 24.6 plus or minus 0.2 degrees and 27.1 plus or minus 0.2 degrees. The preparation methodof the crystal form of the linagliptin includes the steps of preparing linagliptin solid into a suspension in a solvent and stirring, adding purified water therein after heating to 30-70 DEG C, cooling down to 0-20 DEG C and growing crystal at constant temperature for 0.5-2 hours, filtering crystal slurry, and drying to constant weight. The crystal form of the linagliptin has the advantages of good stability, high safety, and suitablility for industrial production.
Owner:SICHUAN KELUN PHARMA RES INST CO LTD

Scotogramma trifolii rottemberg attractant composition and preparation method of nano preparation thereof

The invention discloses scotogramma trifolii rottemberg attractant composition and a preparation method of a nano preparation thereof in the technical field of preparation of agricultural chemicals. According to the preparation method, an amphiphilic copolymer is adopted and subjected to self-assembly in an aqueous solution, nano-sized micelle with an obvious core-shell structure is formed, and anano-pesticide is prepared from the nano-sized micelle with an electrospinning technology. The preparation method is simple and convenient, the raw materials are easily available, the amphiphilic copolymer has quite good environmental compatibility, is biodegradable and is free of residual risk, and furthermore, a degradation product can be absorbed and used by crops; the prepared nano-pesticide is smaller and uniform in grain size and good in permeability and has certain slow-release effect, so that lasting period of scotogramma trifolii rottemberg sex pheromone and pyrethriods pesticides isprolonged, and the use dosage of the pesticide is reduced.
Owner:河北军星生物化工有限公司

Absorbable semi-flowing cross-linked polypeptide biological surgical bleeding-stopping substance

The present invention provides an absorbable semi-flowing cross-linked polypeptide biological surgical bleeding-stopping substance, which comprises a gelatin and a cross-linking agent, wherein a cross-linking agent is added to a gelatin solution to make high-reactivity amino acid side chains react with each other so as to form a cross-linking structure, and iron-calcium ions are added to increase the cross-linking degree so as to finally form the three-dimensional network cross-linked macromolecular polypeptide. According to the present invention, the absorbable semi-flowing cross-linked polypeptide biological surgical bleeding-stopping substance can be safely absorbed by human tissues, has characteristics of semi-fluidity, viscosity and adhesion, can promote the coagulation process of human body through physical and chemical principles, can rapidly stop bleeding, can treat surgical bleeding in the case of no damage on tissues so as to improve the convenience and the flexibility of surgical hemostasis and improve the safety and the effectiveness of surgical hemostasis, and can achieve the satisfactory bleeding-stopping effect in the cases of multi-point bleeding, large-area errhysis, bleeding in the narrow lacuna, hidden bleeding point or difficultly distinguished bleeding point, and bleeding difficultly operated and controlled by the existing bleeding-stopping methods.
Owner:北京纳什国际生物科技有限公司

Degradable meninx repairing material and preparing method thereof

The invention discloses a degradable meninx repairing material and a preparing method thereof. The degradable meninx repairing material is prepared from a bacterial cellulose film with gaps, and the bacterial cellulose film is oxidized bacterial cellulose with C6-site hydroxyl oxidized into carboxyl. The preparing method of the degradable meninx repairing material includes the following steps that 1, the gaps are formed in the bacterial cellulose film, and the bacterial cellulose film with the gaps are obtained; 2, a group oxidizing reaction is carried out on the bacterial cellulose film with the gaps obtained in the first step, and the degradable meninx repairing material can be obtained. The meninx repairing material has the synechia preventing function and the cerebrospinal fluid leakage preventing function, and can be gradually degraded while guiding auto-defect repairing of cerebral dura mater tissue.
Owner:YANTAI ZHENGHAI BIO TECH

Application of birch mushroom extract in preparing preparation for treating and/ or preventing intestinal flora disorder and related diseases

The invention relates to an application of an edible fungus extract in preparing a preparation for treating and / or preventing intestinal flora disorder and related diseases, in particular to an application of a birch mushroom extract in preparing a preparation for treating and / or preventing intestinal flora disorder and related diseases. The preparation method is simple and easy to implement, and low in operation cost; and an extraction solvent in the preparation method can be recycled, so that the residual risk of an organic reagent is avoided, the natural quality of the birch mushroom extract is ensured, and the method is environment-friendly, and belongs to a green manufacturing technology. According to the invention, the raw materials are completely extracted, the raw materials are fully utilized, and the utilization rate of the raw materials is high. The birch mushroom extract not only can obviously contribute to the recovery of the dominant flora structure in an intestinal tract and the diversity of a flora, but also has obvious treatment and / or prevention effects on diseases related to the flora structure of the intestinal tract, can be used in various fields such as medicines, health care products and the like, and has great economic and social values.
Owner:GUANGDONG INST OF MICROBIOLOGY GUANGDONG DETECTION CENT OF MICROBIOLOGY +1

A water-based polyester copolymer and preparation method and application thereof

ActiveCN112654658ABoth processabilityResistant to retortPolyester coatingsPolymer sciencePtru catalyst
The invention belongs to the technical field of coatings, and discloses awater-based polyester copolymer and a preparation method and application thereof.The water-based polyester copolymer is mainly prepared from the following components: polyol, polyacid and an environmentally friendly catalyst. The polyol includes spiro diols and diols with no less than 5 carbon atoms in the main chain. The polyacid includes aromatic polyacid, sulfonic acid group-containing dibasic acid (ester), fatty acid and alicyclic acid; the environmental protection catalyst is prepared by complexing reaction of titanate, silicate and amine compound; 70-100% of the total carboxyl end groups in the water-based polyester copolymer are derived from fatty acid and / or alicyclic acid end carboxyl groups. After the water-based polyester copolymer is used in the preparation of water-based coatings, the cured coating has excellent processability, boiling water resistance and stability.
Owner:GUANGZHOU KINTE IND

Primer-free blocking glue and its preparation method

The invention discloses a primer-free blocking glue and its preparation method. Through adding PVOH product with better blocking property in PVDC latex, the blocking property is improved (<=2cc / m2.24hr), and the polymerization technique is further adjusted; finally, the primer-free PVDC latex is prepared; on the basis of guaranteeing good blocking effect, the film primer coating process is reduced, generation of organic solvent in the production process is avoided; besides, there is no risk of solvent residue.
Owner:HAINAN BNK WATER BASED NEW MATERIAL CO LTD

Application of lentinula edodes dietary fiber extract in preparation of preparations for treating and/or preventing liver injury-related diseases caused by high fat diet

The invention relates to use of a lentinula edodes dietary fiber extract in the pharmaceutical field, in particular to application of the lentinula edodes dietary fiber extract in preparation of preparations for treating and / or preventing liver injury-related diseases caused by high fat diet. The lentinula edodes dietary fiber extract not only can obviously contribute to the recovery of the dominant flora structure in the intestinal tract and is beneficial to the diversification of the flora, but also shows obvious treatment and / or prevention effect on the liver injury-related diseases causedby high fat diet; the lentinula edodes dietary fiber extract can effectively inhibit the expression of inflammatory factors, effectively alleviates the deterioration of inflammation, improves variousphysiological and pathological indicators related to immunity, and can be used in various fields such as medicines and health care products, thus having great economic and social values.
Owner:GUANGDONG INST OF MICROBIOLOGY GUANGDONG DETECTION CENT OF MICROBIOLOGY +1

Hyaluronic acid composite gel for filling lacrimal duct and preparation method of hyaluronic acid composite gel

PendingCN114874468AExtend durationAvoid the Tyndall EffectPharmaceutical delivery mechanismTissue regenerationSodium hyaluronateLacrimal duct
The invention provides hyaluronic acid composite gel for filling lacrimal ducts and a preparation process of the hyaluronic acid composite gel. The composite gel is prepared by crosslinking medium-molecular-weight sodium hyaluronate, low-molecular-weight sodium hyaluronate and recombinant collagen, wherein the mass percent of the medium molecular weight sodium hyaluronate and the mass percent of the low molecular weight sodium hyaluronate in the composite gel are both 1.2-2.0%, the mass percent of the recombinant collagen in the composite gel is 0.4-0.7%, and the balance of the composite gel is the phosphate buffer solution. According to the preparation method, crosslinking is carried out through physical means of rapid heating, heat preservation and rapid cooling. According to the composite gel disclosed by the invention, the medium-molecular-weight sodium hyaluronate, the low-molecular-weight sodium hyaluronate and the recombinant collagen are matched, so that the filling effect can be ensured, the maintaining time of the filling effect can be prolonged, the Tyndall effect can be effectively avoided, the safety is high, and skin nutrition can be repaired and supplemented; the physical crosslinking method of rapid heating-heat preservation-rapid cooling does not need a crosslinking agent and has no residual risk.
Owner:HYAMED BIOTECHNOLOGY (ZHUHAI) CO LTD

Use of dietary fiber extract from oudemansiellara maflbes in preparation of preparations for treating and/or preventing liver injury-related diseases caused by high fat diet

The invention relates to use of a dietary fiber extract from oudemansiellara maflbes in the field of pharmacy, in particular to use of a dietary fiber extract from the oudemansiellara maflbes in preparation of preparations for treating and / or preventing liver injury-related diseases caused by high fat diet. The dietary fiber extract from the oudemansiellara maflbes not only can significantly contribute to the repair of liver injury caused by the high fat diet, but also shows obvious therapeutic and / or preventive effects on the liver injury-related diseases; for example, the dietary fiber extract from the oudemansiellara maflbes effectively inhibits the expression of inflammatory factors, effectively alleviates the deterioration of inflammation, improves various physiological and pathological indicators related to immunity, and can be used in various fields such as medicines and health care products, thus having great economic and social values.
Owner:GUANGDONG INST OF MICROBIOLOGY GUANGDONG DETECTION CENT OF MICROBIOLOGY +1

Application of cordyceps cicadae ethanol extract in preparation of preparations for treating and/or preventing alteration of intestinal flora and related diseases

The invention relates to application of an edible fungus extract in preparation of preparations for treating and / or preventing alteration of intestinal flora and related diseases, in particular to application of a cordyceps cicadae ethanol extract in preparation of preparations for treating and / or preventing alteration of intestinal flora and related diseases. The preparation method is simple andpracticable, the operation cost is low, only ethanol and water are used as the extraction solvents in the preparation method, the ethanol is recyclable, and no organic reagent residue risk exists. Thecordyceps cicadae ethanol extract is not only remarkable for helping recovering of the dominant bacterial community structure in the intestinal tract and diversifying the bacterial community but alsohas the remarkable curing and / or preventing effect to the diseases related to the dominant bacterial community structure, and the edible fungus extract can be used in various fields of drugs, healthcare products and the like and has great economic and social values.
Owner:GUANGDONG INST OF MICROBIOLOGY GUANGDONG DETECTION CENT OF MICROBIOLOGY +1

Preparing method of carotenoid preparation

The invention relates to a preparing method of a carotenoid preparation. The method comprises the following steps: 1) adding carotenoid and other raw materials into purified water, stirring, dissolving and emulsifying evenly; 2) transferring the materials prepared in the step 1) into a grinding device, grinding, sampling and measuring the particle size of 0.01-2 [mu]m; and 3) carrying out spray drying on the obtained material with the particle size of 0.01-2 [mu]m in the step 2), embedding with starch, and carrying out secondary granulation, to obtain carotenoid microcapsules. In the method, residues of an organic solvent on the microcapsules are effectively avoided, and no residual risk of the solvent exists; and preparation does not need to be carried out under conditions of high temperature and high pressure, the yield is improved, the process is simple, the preparation conditions are improved, the production process is optimized, and the industrialized production of the product isfacilitated.
Owner:GUANGZHOU WISDOM BIO TECH

Spotted cutworm isotropic nano-fiber preparation

The invention discloses a spotted cutworm isotropic nano-fiber preparation and a preparation method thereof and belongs to the technical field of agrochemical preparation. The spotted cutworm isotropic nano-fiber preparation is polymer nano-fiber containing spotted cutworm sex pheromone. The preparation method provided by the invention is simple and convenient and is available in raw material. According to the preparation method, a used polymer has good environmental compatibility, is bio-degradable and does not have a residue risk; the prepared nano-fibers are high in mechanical strength, relatively small and uniform in particle size and relatively high in drug loading capacity, has a certain sustained release effect, prevents sprayed fields from being scoured by air flows and rainstorms,reduces the dosage of the spotted cutworm sex pheromone, prolongs the sustained release persistent period of the spotted cutworm sex pheromone, and can perform effective isotropy on the spotted cutworm at the same time. Reference for comprehensively treating the spotted cutworm is provided.
Owner:INST OF PLANT PROTECTION CHINESE ACAD OF AGRI SCI

Jerusalem artichoke low-salt compound flavor pickle and preparation method thereof

The invention relates to a low-salt compound flavored pickle of jerusalem artichoke and a preparation method of the low-salt compound flavored pickle, belonging to the technical field of food processing. The method comprises the following steps: with certain quality of jerusalem artichoke, Chinese cabbage and cowpea as main raw materials, preparing a pickling liquid from water, salt, white sugar, chilli, pricklyash peels and ginger slices; adding a brittleness-keeping agent prepared from CaCl2, gelatin and pectinase, inoculating a leavening agent prepared from lactobacillus pentosus and lactobacillus plantarum, and producing the low-salt compound flavored pickle of the jerusalem artichoke; and packing, sterilizing, cooling to prepare the low-salt compound flavored pickle. According to the method, rapid production of the low-salt and high-quality flavored pickle of the jerusalem artichoke is realized; peeling is not needed; a color retention agent or a preservative is not added; the process is simple; the cost is low; the bioactive substances such as synanthrin and fructo-oligosaccharide are preserved to the maximal extent; meanwhile, new functional factors such as functional terpene compounds are generated by fermentation; the low-salt compound flavored pickle is bright in color and luster, sour, crisp and refreshing, and unique in flavor, and has the healthcare efficacies of appetizing, helping digestion, improving digestion, preventing decayed tooth, preventing obesity, lowering blood glucose and improving the immunity.
Owner:JIANGSU ACAD OF AGRI SCI

Dapoxetine hydrochloride monohydrate, preparation method and uses thereof

The invention discloses a dapoxetine hydrochloride monohydrate and a preparation method thereof, a composition containing the dapoxetine hydrochloride monohydrate, and uses of the composition in preparation of drugs for treatment of sexual dysfunction, wherein the dapoxetine hydrochloride monohydrate is represented by a formula I. According to the present invention, the dapoxetine hydrochloride monohydrate overcomes the disadvantages of easy moisture absorption, poor stability, high requirements on storage conditions and difficult long-term preservation of the existing crystal form or the amorphous form of dapoxetine hydrochloride, and is suitable for industrial scale-up and preparation production. The formula I is defined in the specification.
Owner:SUZHOU KELUN PHARMA RES CO LTD

Glycyrrhiza glabra extract and preparation method and application thereof

The invention discloses a glycyrrhiza glabra extract and a preparation method and application thereof. The preparation method comprises the following steps: S1, selecting roots and rhizomes of fresh glycyrrhiza glabra, then putting the selected roots and rhizomes of the fresh glycyrrhiza glabra into an ultrasonic cleaning machine, cleaning the roots and rhizomes of the fresh glycyrrhiza glabra through the ultrasonic cleaning machine, and cleaning impurities and pesticides on the surfaces of the roots and rhizomes of the fresh glycyrrhiza glabra; and S2, then taking out the cleaned roots and rhizomes of the fresh glycyrrhiza glabra, putting the roots and rhizomes into an electrothermal blowing drying box, and drying the cleaned roots and rhizomes of the fresh glycyrrhiza glabra through theelectrothermal blowing drying box. The process is simple to operate, industrial production is easy to realize, and the obtained product is clear in component, free of solvent residue risk, and safe and effective when being applied to series of cosmetic products.
Owner:薇娅(广州)药业有限公司

Method for preparing phosphatidylserine without organic solvent

The invention discloses a method for preparing phosphatidylserine without an organic solvent, which comprises the following steps: adding an enzyme-containing aqueous solution into soya bean lecithin and L-serine serving as raw materials, homogenizing and mixing for reaction, adding water into the reaction solution after the reaction is ended to dissolve the L-serine, centrifugally separating to obtain a water phase and a precipitate, washing the precipitate with water, centrifugally separating to obtain a water phase and a precipitate, and drying to obtain the phosphatidylserine. Combining water phases, concentrating through membrane filtration to recover L-serine, combining precipitates, and freeze-drying in vacuum to obtain a phosphatidylserine product. According to the method, phosphatidylserine is synthesized from soybean lecithin through an enzyme synthesis method, no organic solvent is used, the process is simple, energy consumption is low, and industrial production is easy to achieve.
Owner:WENGYUAN GUANGYE QINGYI FOOD TECH +1

Preparation for preventing and treating prawn enterocytozoon hepatopenaei disease as well as preparation method and application thereof

The invention discloses a preparation for preventing and treating prawn enterocytozoon hepatopenaei disease as well as a preparation method and application thereof. The preparation is prepared from the following raw materials: rosemary oil, anise oil, talcum powder and auxiliary materials. The preparation comprises following components in percentage by mass: 3.0 to 3.5 percent of rosemary oil, 1.0 to 2.0 percent of anise oil, 15.0 to 18.0 percent of talcum powder and 78.0 to 80.0 percent of auxiliary materials. The talcum powder is feed-grade talcum powder, and the auxiliary material is corn starch. The invention also provides a preparation method and application of the preparation. The preparation is added into a prawn feed for use, which is mixed with the feed and is orally taken for feeding, 2-3g of the preparation is added into per kilogram of the prawn feed, and the preparation is continuously used for 5-7 days. The compound preparation prepared by the invention is safe to target animals, can effectively inhibit the growth of the enterocytozoon hepatopenaei and kill the enterocytozoon hepatopenaei, and is simple in preparation process, convenient to use, non-toxic and free of drug residue risk.
Owner:上海联旺水产科技有限公司 +2

Lactobacillus fermentum PV22 with anti-virus capacity, and application of Lactobacillus fermentum PV22

The invention discloses a lactobacillus fermentum PV22 with an anti-virus capacity, and application of the lactobacillus fermentum PV22. The Lactobacillus fermentum PV22 is collected in the GuangdongMicrobial Culture Collection Center (GDMCC) on December 18th, 2020, the collection address is 5th floor, No.59 building, No.100, Xianlie Middle Road, Guangzhou, Guangdong Province, and the collectionnumber is GDMCC No.61376. The lactobacillus fermentum PV22 can obviously lower virus infectivity, obvious virus-antagonizing efficacy can be achieved in short time, in addition, an anti-virus effect is increased along with prolonging of action time, and a post-infection survival rate of a virus infection cell can be improved. Therefore, the lactobacillus fermentum (L.fermentum) PV22 can be appliedto preparation of products (such as foods, medicines, health care products and the like) used for preventing or treating virus infection, and has a huge application prospect.
Owner:GUANGDONG INST OF MICROBIOLOGY GUANGDONG DETECTION CENT OF MICROBIOLOGY +1

An absorbable semi-fluid cross-linked polypeptide biosurgical hemostat

The present invention provides an absorbable semi-flowing cross-linked polypeptide biological surgical bleeding-stopping substance, which comprises a gelatin and a cross-linking agent, wherein a cross-linking agent is added to a gelatin solution to make high-reactivity amino acid side chains react with each other so as to form a cross-linking structure, and iron-calcium ions are added to increase the cross-linking degree so as to finally form the three-dimensional network cross-linked macromolecular polypeptide. According to the present invention, the absorbable semi-flowing cross-linked polypeptide biological surgical bleeding-stopping substance can be safely absorbed by human tissues, has characteristics of semi-fluidity, viscosity and adhesion, can promote the coagulation process of human body through physical and chemical principles, can rapidly stop bleeding, can treat surgical bleeding in the case of no damage on tissues so as to improve the convenience and the flexibility of surgical hemostasis and improve the safety and the effectiveness of surgical hemostasis, and can achieve the satisfactory bleeding-stopping effect in the cases of multi-point bleeding, large-area errhysis, bleeding in the narrow lacuna, hidden bleeding point or difficultly distinguished bleeding point, and bleeding difficultly operated and controlled by the existing bleeding-stopping methods.
Owner:北京纳什国际生物科技有限公司

Indirect additive manufacturing equipment and additive manufacturing method thereof

The invention discloses indirect additive manufacturing equipment and an additive manufacturing method thereof. The indirect additive manufacturing equipment comprises an extrusion mechanism, a pre-degreasing system, a Z-axis mechanism, an industrial control computer and a movement guide rail driving the extrusion mechanism or the pre-degreasing system to move towards an X axis and a Y axis, wherein the extrusion mechanism is connected with a feeding system, a part supporting plate is arranged below the movement guide rail, and a grease collecting system is arranged on the part supporting plate; and the Z-axis mechanism is used for driving the part supporting plate to move along a Z axis. According to the indirect additive manufacturing equipment, part of a binder is removed in advance through layer-by-layer catalytic degreasing; uniformly distributed and communicated micropores are formed in a green body under the condition that the strength of the green body is not damaged, so that the difficulty of removing a binder degreasing product from the green body is reduced, the participation of a subsequent independent pre-degreasing process is avoided, the degreasing period can be shortened, the production cost is reduced, degreasing is more thorough, and the risk of binder component residues is avoided.
Owner:XIAN BRIGHT ADDTIVE TECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products