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

35results about How to "The preparation technology is simple" patented technology

Nitrogen and sulfur co-doped hierarchical porous carbon composite material, and preparation method and application thereof

The invention discloses a nitrogen and sulfur co-doped hierarchical porous carbon composite material, and a preparation method and an application thereof, and belongs to the technical field of supercapacitor electrode materials. A natural polymer material which is abundant in the nature, low in price and easy to obtain is used as a carbon source, graphene oxide is added to improve the conductivity, an activator and a doping agent are added in advance, and a general two-step technology (high-temperature carbonization and chemical activation) for preparing a carbon material is simplified into one-step high-temperature annealing, so that the carbon material with a high specific surface area and a hierarchical porous three-dimensional structure is obtained; and nitrogen and sulfur doping improves the electrochemical performances of the material. The composite carbon material has the advantages of high mass specific capacitance, excellent high-current rate capability, ultra-long cycle life,high mass energy density and high power density when used as a high-performance electrode material for a supercapacitor. The preparation method has the advantages of simplicity, feasibility, low requirements on reaction deices, environmental friendliness, and suitableness for industrial production.
Owner:WUHAN UNIV

Preparation method of amycin controlled-release chitosan nano particles with pH/oxido-reduction dual response

The invention relates to a preparation method of amycin controlled-release chitosan nano particles with pH / oxido-reduction dual response. Thiolated chitosan, carboxymethyl chitosan, sodium tripolyphosphate, doxorubicin hydrochloride and hydrogen peroxide are taken as raw materials. The preparation method comprises the following steps: mixing a thiolated chitosans solution with a doxorubicin hydrochloride solution so as to obtain a solution I; mixing a carboxymethyl chitosan solution with a sodium tripolyphosphate solution so as to obtain a mixed solution II; dropwise adding the mixed solution I into the mixed solution II while stirring, controlling the dosage of carboxymethyl chitosan and thiolated chitosan, regulating the ph value of the solution to 6-8, performing ultrasonic blending, performing ion crosslinking and polymer condensing, then dropwise adding hydrogen peroxide into the system so as to finish oxidization crosslinking, performing room-temperature stirring reaction, separating products, and drying the products to obtain the amycin controlled-release chitosan nano particles with pH / oxido-reduction dual response. The amycin controlled-release chitosan nano particles with pH / oxido-reduction dual response is capable of escaping away from tumor cell endosome / lysosome, is capable of automatically regulating and controlling to realize cytoplast release based on unique microenvironments of tumor cells, improving the amycin medicine delivery efficiency and the medical effect, and has a favorable research and development application background in multiple aspects such as medicine and medical materials.
Owner:OCEAN UNIV OF CHINA

Slow-release pesticide for preventing and treating corn ear pests, and preparation method of slow-release pesticide

The invention discloses a slow-release pesticide for preventing and treating corn ear pests, wherein the slow-release pesticide is prepared by the following method: dissolving chitosan by using glacial acetic acid and / or sodium acetate aqueous solution, and uniformly stirring to obtain a chitosan solution; adding an emulsifier into the chitosan solution, and uniformly stirring to obtain a first mixed solution; dissolving a pesticide active agent into an organic solvent to obtain a pesticide dissolving solution, then dropwise and rapidly dripping the pesticide dissolving solution into the firstmixed solution under a stirring condition, and uniformly stirring to obtain a second mixed solution; dropwise adding a cross-linking agent into the second mixed solution, and uniformly stirring to obtain a third mixed solution; dropwise adding a carboxymethyl chitosan aqueous solution into the third mixed solution, and uniformly stirring to obtain a pesticide active agent entrapped micron dispersion body; and centrifugally removing the micron dispersion body to obtain the slow-release pesticide. The slow-release pesticide provided by the invention can effectively control the release time of the pesticide and reduce the risk of percutaneous poisoning during pesticide application.
Owner:SOUTH CHINA AGRI UNIV

Sodium alginate degradation method

InactiveCN106565852AAchieve degradationSolve not easy to separateViscous liquidThermal insulation
The invention belongs to the technical field of polysaccharide degradation, and relates to a sodium alginate degradation method, which is characterized by comprising: 1) dispersing sodium alginate in an alcohol solution, adding an acid solution under a stirring condition, carrying out a reflux reaction under a thermal insulation state, stirring, and controlling the degradation time so as to complete the degradation reaction; 2) filtering the reaction system obtained in the step 1), washing the solid sequentially with deionized water and 75% ethanol to achieve a neutral state, dispersing in 75% ethanol, adding a sodium hydroxide solution under stirring, and adjusting the pH value of the system to more than or equal to 7; and 3) filtering the reaction system obtained in the step 2), washing the solid with 75% ethanol to achieve a neutral state, washing sequentially with 75% ethanol, 95% ethanol and dehydrated alcohol, dewatering, and carrying out vacuum drying to obtain the degraded sodium alginate product. According to the present invention, the method has advantages of convenient operation, simple preparation technology process, low manufacturing cost, and the like; the sodium alginate is dispersed in the blending liquid of the alcohol and the acid to carry out the heterogeneous degradation reaction so as to conveniently separate the product at the late stage; and the obtained degraded sodium alginate is the white or light yellow solid powder, and is dissolved in water to form the viscous liquid.
Owner:OCEAN UNIV OF CHINA

Method for preparing hulless oat blood sugar reducing polypeptide with hulless oat albumen powder

ActiveCN105713943APolysaccharide metabolism hypoglycemic health careSimple technical processHydrolysed protein ingredientsMetabolism disorderAlgluceraseChemistry
The invention provides a method for preparing hulless oat blood sugar reducing polypeptide with hulless oat albumen powder. The method comprises the steps that degreased hulless oat albumen powder is added into pure water at the material to liquid ratio of 1:(100-500), the pH value is regulated to be 1.0-3.0 with 1M hydrochloric acid, pepsin is added according to E/S of 1:(50-100), enzymolysis is carried out for 1-4 h at 37 DEG C, and primary enzymatic hydrolysate is obtained; the pH value of the primary enzymatic hydrolysate is regulated with 1M NaoH to be 7.0-8.0, then trypsin, alpha-chymotrypsin and elastase are added according to E/S of 1:(50-100), enzymolysis is carried out for 1-4 h at 37 DEG C, and secondary enzymatic hydrolysate is obtained; the secondary enzymatic hydrolysate is heated to 95 DEG C for enzyme denaturalixation for 15 min, spraying drying is carried out, and polypeptide containing alpha glucosidase inhibiting activity is obtained. The process is simple, the production cost is low, and the product is safe and free of toxic or side effects. The hulless oat blood sugar reducing polypeptide prepared through the method can be applied in preparing medicine or health-care products for preventing and treating diabetes.
Owner:内蒙古佟明阡禾食品有限责任公司

Method for preparing chitosan grafted cetirizine nano-micelles

The invention relates to a method for preparing chitosan grafted cetirizine nano-micelles in the field of biotechnologies. Chitosan and cetirizine hydrochloride are used as raw materials, chitosan and cetirizine grafted materials are synthesized by the aid of carbodiimide processes, and ultrasonic treatment is carried out on chitosan and cetirizine grafted material solution to obtain the chitosan grafted cetirizine nano-micelles. The method includes carrying out desalting treatment on the cetirizine hydrochloride; adding carboxyl activators into the cetirizine hydrochloride, activating carboxyl and then mixing the cetirizine hydrochloride with chitosan solution; carrying out continuous reaction to obtain reaction products; sufficiently dialyzing and drying the reaction products to obtain chitosan grafted cetirizine; carrying out ultrasonic treatment on chitosan grafted cetirizine solution to obtain the chitosan grafted cetirizine nano-micelles. The method has the advantages that the substitution degree of the chitosan grafted cetirizine nano-micelles is 2.8-5.6%, the chitosan grafted cetirizine nano-micelles are regularly spherical, the particle sizes of the chitosan grafted cetirizine nano-micelles are 80.6-320.1 nm, and the method has excellent research and development application prospects in the aspects of chronic rhinitis and asthma treatment and the like.
Owner:OCEAN UNIV OF CHINA

A preparation method of doxorubicin controlled-release chitosan nanoparticles with ph/redox double response

The invention relates to a preparation method of amycin controlled-release chitosan nano particles with pH / oxido-reduction dual response. Thiolated chitosan, carboxymethyl chitosan, sodium tripolyphosphate, doxorubicin hydrochloride and hydrogen peroxide are taken as raw materials. The preparation method comprises the following steps: mixing a thiolated chitosans solution with a doxorubicin hydrochloride solution so as to obtain a solution I; mixing a carboxymethyl chitosan solution with a sodium tripolyphosphate solution so as to obtain a mixed solution II; dropwise adding the mixed solution I into the mixed solution II while stirring, controlling the dosage of carboxymethyl chitosan and thiolated chitosan, regulating the ph value of the solution to 6-8, performing ultrasonic blending, performing ion crosslinking and polymer condensing, then dropwise adding hydrogen peroxide into the system so as to finish oxidization crosslinking, performing room-temperature stirring reaction, separating products, and drying the products to obtain the amycin controlled-release chitosan nano particles with pH / oxido-reduction dual response. The amycin controlled-release chitosan nano particles with pH / oxido-reduction dual response is capable of escaping away from tumor cell endosome / lysosome, is capable of automatically regulating and controlling to realize cytoplast release based on unique microenvironments of tumor cells, improving the amycin medicine delivery efficiency and the medical effect, and has a favorable research and development application background in multiple aspects such as medicine and medical materials.
Owner:OCEAN UNIV OF CHINA

A method for preparing oatmeal hypoglycemic polypeptide from oatmeal protein powder

ActiveCN105713943BGood hypoglycemic health functionInhibit hydrolytic activityHydrolysed protein ingredientsMetabolism disorderHydrolysateChymase
The invention provides a method for preparing hulless oat blood sugar reducing polypeptide with hulless oat albumen powder. The method comprises the steps that degreased hulless oat albumen powder is added into pure water at the material to liquid ratio of 1:(100-500), the pH value is regulated to be 1.0-3.0 with 1M hydrochloric acid, pepsin is added according to E / S of 1:(50-100), enzymolysis is carried out for 1-4 h at 37 DEG C, and primary enzymatic hydrolysate is obtained; the pH value of the primary enzymatic hydrolysate is regulated with 1M NaoH to be 7.0-8.0, then trypsin, alpha-chymotrypsin and elastase are added according to E / S of 1:(50-100), enzymolysis is carried out for 1-4 h at 37 DEG C, and secondary enzymatic hydrolysate is obtained; the secondary enzymatic hydrolysate is heated to 95 DEG C for enzyme denaturalixation for 15 min, spraying drying is carried out, and polypeptide containing alpha glucosidase inhibiting activity is obtained. The process is simple, the production cost is low, and the product is safe and free of toxic or side effects. The hulless oat blood sugar reducing polypeptide prepared through the method can be applied in preparing medicine or health-care products for preventing and treating diabetes.
Owner:内蒙古佟明阡禾食品有限责任公司

A kind of preparation method of chitosan grafted cetirizine nano-micelle

The invention relates to a method for preparing chitosan grafted cetirizine nano-micelles in the field of biotechnologies. Chitosan and cetirizine hydrochloride are used as raw materials, chitosan and cetirizine grafted materials are synthesized by the aid of carbodiimide processes, and ultrasonic treatment is carried out on chitosan and cetirizine grafted material solution to obtain the chitosan grafted cetirizine nano-micelles. The method includes carrying out desalting treatment on the cetirizine hydrochloride; adding carboxyl activators into the cetirizine hydrochloride, activating carboxyl and then mixing the cetirizine hydrochloride with chitosan solution; carrying out continuous reaction to obtain reaction products; sufficiently dialyzing and drying the reaction products to obtain chitosan grafted cetirizine; carrying out ultrasonic treatment on chitosan grafted cetirizine solution to obtain the chitosan grafted cetirizine nano-micelles. The method has the advantages that the substitution degree of the chitosan grafted cetirizine nano-micelles is 2.8-5.6%, the chitosan grafted cetirizine nano-micelles are regularly spherical, the particle sizes of the chitosan grafted cetirizine nano-micelles are 80.6-320.1 nm, and the method has excellent research and development application prospects in the aspects of chronic rhinitis and asthma treatment and the like.
Owner:OCEAN UNIV OF CHINA

A kind of doxycycline controlled-release quaternary ammonium salt chitosan-liposome composite nanoparticle with pH responsiveness and preparation method thereof

The invention provides a doxycycline controlled-release quaternary-ammonium-salt chitosan-lipidosome composite nanoparticle with pH responsiveness and a preparation method thereof. The doxycycline controlled-release quaternary-ammonium-salt chitosan-lipidosome composite nanoparticle prepared by adopting chitosan, lecithin, doxycycline, iodomethane and the like as raw materials and adopting a thin-film dispersion method and a positive-negative charge adsorption method can be adsorbed on the surface of a pellicle by charge action, and when the composite nanoparticle is in a unique low-pH environment of the pellicle, free amino groups without being quaternized in the quaternary-ammonium-salt chitosan generate protonation reaction, so that a nanoparticle shell carries more positive charges, the stability of the original quaternary-ammonium-salt chitosan-lipidosome nanoparticle is destructed, the release of doxycycline at the pellicle is promoted and finally the effects of destructing the pellicle and killing germs are achieved. The doxycycline controlled-release quaternary-ammonium-salt chitosan-lipidosome composite nanoparticle with pH responsiveness and the preparation method provided by the invention have the advantages that the medicine delivery efficiency and the medical effect of the doxycycline are improved and the prospect of study, development and application in the aspects of medicines and medical materials and the like is good.
Owner:THE AFFILIATED HOSPITAL OF QINGDAO UNIV
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