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174results about How to "Expanded antimicrobial spectrum" patented technology

Slowly released type antibiotic medical catheter and preparation method thereof

The invention relates to the technical field of medical apparatus and instruments, which discloses a sustained release type antibacterial medical catheter and a preparation method thereof. A silver inorganic antimicrobial is characterized by high content of silver, safety and the like, and the silver inorganic antimicrobial which adopts zirconium phosphate as a carrier is selected and mixed into catheter material to prepare the sustained release type antibacterial medical catheter that is most widely applied to clinic, such as an antibacterial catheter, an antibacterial central venous catheter, an antibacterial trachea cannula and the like. The catheter has high use safety, wide antibacterial spectrum, good antibacterial effects, antimicrobial constituent sustained release and long duration of antibacterial effects, and can reduce the frequency of replacing medical catheters so as to have safe and convenient clinical use, effectively reduce nosocomial infections related to catheters due to the use of the medical catheters, greatly reduce medical expenses related to anti-infection, and the like, and save medical resources.
Owner:HUADONG HOSPITAL +1

Veterinary suspension containing amoxicillin, colistin sulfate and prednisolone and preparation method thereof

The invention discloses a veterinary suspension containing amoxicillin, colistin sulfate and prednisolone and a preparation method thereof. The veterinary suspension adopts the amoxicillin, the colistin sulfate and the prednisolone as active ingredients. The preparation method of the veterinary suspension containing the amoxicillin, the colistin sulfate and the prednisolone comprises the following steps of: (1) dissolving or dispersing a suspending agent, an antioxidant and a preservative in a hot dispersion medium to obtain a solution (A); (2) adding 40-80 percent of dispersion medium in a formula ratio in a colloid mill, starting the colloid mill, then slowly adding the solution (A) and adding a wetting agent while stirring after the solution (A) is fully added; (3) sequentially adding the amoxicillin, the colistin sulfate and the prednisolone after fully adding all the accessories, and grinding by adopting two alternate modes, i.e. an endless grinding mode and a non-endless grinding mode; and (4) detecting the grain fineness, stopping grinding when the grain fineness accords with the requirement, adding the dispersion medium to the formula ratio, mixing, canning, sealing and sterilizing to obtain the veterinary suspension containing the amoxicillin, the colistin sulfate and the prednisolone.
Owner:CHINA AGRI UNIV +1

Biological-source nutritional preservative for seafood

The invention relates to a biological-source nutritional preservative for seafood. The biological-source nutritional preservative is characterized in that each liter of the distilled water of the biological-source nutritional preservative contains 0.4-0.6g of lysozyme, 2.5-3.5g of tea polyphenols, 20-28g of carboxymethyl chitosan, 10-14g of nisin, 17-23g of sodium alginate, 20-30g of lactobacillus, 1.5-2.5g of propolis extract and 10-14g of spice extract, wherein the spice extract is made of rhizoma galangae, garlic, onion, cinnamon, clove and rosemary. The biological-source nutritional preservative has the advantages that the biological-source nutritional preservative is compound by biological preservatives and is safe, nontoxic, simple in preparation and application method, outstanding in microorganism inhibition effect, good in preservation effect, capable of greatly prolonging the shelf life of the seafood and high in industry value.
Owner:黎建波

Chitosan gel dropping pill for gynaecologic bacteriostasis and preparation method thereof

The invention relates to a chitosan gel dropping pill for gynaecologic bacteriostasis and a preparation method thereof. The gel dropping pill comprises the following constituents: compound chitosan with different molecular weights and deacetylation degrees, gelatinizer, acidifier, sodium chloride, purified water and dropping pill matrix. The method comprises the steps of mixing the compound chitosan and aqueous solution of sodium chloride with certain concentration, so as to form suspension, then feeding a proper amount of gelatinizer to the suspension, adjusting the pH value of the suspension through the acidifier, feeding compound chitosan gel obtained into matrix melt, uniformly mixing the compound chitosan gel and the matrix melt, and feeding the compound chitosan gel and the matrix melt into a pill dropping machine to prepare dropping pills, so as to obtain the chitosan gel dropping pill. The chitosan gel dropping pill is good in roundness, rapid in drug dissolution and high in bioavailability, the antibacterial ability of the chitosan gel dropping pill for gram-positive bacteria and gram-negative bacteria reaches greater than 99 percent, and the chitosan gel dropping pill is applied to the curing of monilial vaginitis, bacterial vaginitis, trichomonas vaginitis or cervicitis in gynecology, has good curative effect, high safety and good biocompatibility. The invention also relates to a preparation method and the medical application of the chitosan gel dropping pill.
Owner:武汉品瑞医学科技有限公司

Pleuromutilin derivatives with antibacterial activity as well as preparation method and application thereof

The invention discloses pleuromutilin derivatives with the structure as shown in a formula (I) in the specification and the antibacterial activity, salts, solvates, optical isomers and polymorphism compounds thereof acceptable in pharmacy and / or veterinary medicines as well as a preparation method and an application of the pleuromutilin derivatives and the salts, solvates, optical isomers and polymorphism compounds thereof in antibacterial compositions. The preparation method has the beneficial effects that two different lead compounds are connected together by covalent bonds so as to generate a synergistic effect, an additive effect or new pharmacological activity in vivo; sulfonamides are spliced into side chains of pleuromutilin so as to generate new pleuromutilin derivatives, the antibacterial activity of the obtained new compounds can be enhanced, the obtained new compounds have obvious antibacterial activity for gram-positive bacterium, gram-negative bacterium and mycoplasma and an obvious inhibiting effect on drug-resistance bacteria such as MRSA, and the antibacterial spectrums of the obtained new compounds are effectively expanded.
Owner:SOUTH CHINA AGRI UNIV +1

Method for improving antibacterial performance of porcine lysozyme through N-terminal fusion with poly-hexapeptide

The invention discloses a method for improving antibacterial performance of porcine lysozyme through N-terminal fusion with poly-hexapeptide and belongs to the field of bioengineering. The method comprises steps as follows: design of a fusion porcine lysozyme gene, expression by an escherichia coli expression system as well as renaturation. Antimicrobial activity detection proves that the fusion porcine lysozyme not only has obvious resistance to Gram-positive bacteria, but also can kill various Gram-negative bacteria, and a good case is provided for improving the antibacterial activity of lysozyme. The preparation technology for the porcine lysozyme has the characteristics of being simple and efficient, a product can be electrophoretically pure, and the purity is 90% or higher.
Owner:JIANGNAN UNIV

Compound ivermectin sustained release tablet and preparation method thereof

The invention belongs to the technical field of pharmaceutic preparation and discloses a compound ivermectin sustained release tablet and a preparation method thereof. The compound ivermectin sustained release tablet is prepared by 1 to 15 parts by weight of ivermectin, 20 to 50 parts by weight of albendazole, 110 to 153 parts by weight of diluents, 20 to 30 parts by weight of sustained-release materials, 0.5 to 0.7 part by weight of lubricating agents and an appropriate quantity of adhesion agents. The ivermectin, the albendazole, the sustained-release materials and the diluents are fully and uniformly mixed in a mixing machine to obtain a mixture, the uniformly mixed mixture is placed in a one-step granulator, the adhesion agents are sprayed to form particles, the particles are dried, the lubricating agents are added in the particles to be fully and uniformly mixed, and the particles are prepared into tablets in a tablet machine. The compound ivermectin sustained release tablet and the preparation method thereof have the advantages that the antibacterial spectrum is wide, the action time is long, the drug resistance can not be easily generated, and the curative ratio is high; compared with common compound tablets, the tablet has better therapeutic effect; and compared with simple recipe drugs, the compound ivermectin sustained release tablet has the advantages that the curative effect is remarkable, simultaneously the dosage is reduced, and the treatment costs are lowered.
Owner:河南亚卫动物药业有限公司

Compound florfenicol preparation for aquatic products and preparation method and application thereof

The invention discloses a compound florfenicol preparation for aquatic products and a preparation method and application thereof. The compound florfenicol preparation for the aquatic products consists of the following components in percentage by mass: 5 to 20 percent of florfenicol, 1 to 25 percent of neomycin sulfate and the balance of glucose. The florfenicol and the neomycin sulfate are combined, so that the antibacterial effect of the compound florfenicol preparation for the aquatic products can be improved, the prevention and treatment effects of the compound florfenicol preparation on the bacterial diseases of the aquatic products are effectively improved, and medicine consumption and cost are reduced; and the preparation method of the compound florfenicol preparation for the aquatic products is simple and practicable and greatly improves bioavailability, and the preparation has high solubility.
Owner:清远海贝生物技术有限公司

Method for eliminating bacterial pollution of tissue culture seedlings

The invention discloses a method for eliminating bacterial pollution of tissue culture seedlings. The method comprises the following steps: step A, weighing the following raw materials in parts by weight: herba houttuyniae, aloes, small centipeda herb, folium artemisiae argyi, herba pogostemonis and garlic; mixing the raw materials and then pulping or mixing the raw materials, adding water for immersing for a period of time and pulping to obtain Chinese herbal medicine pulp; step B, adding the Chinese herbal medicine pulp into a certain amount of conventional culture medium in parts by weight; uniformly mixing and then carrying out high-pressure sterilization to obtain a pollution removing culture medium; step C, transferring polluted tissue culture seedlings into the pollution removing culture medium and culturing for 7 to 10 days; step D, repeating the step A to the step C until pollution of the polluted tissue culture seedlings is eliminated, so as to obtain pollution-removed culture medium seedlings; step E, transferring the pollution-removed culture medium seedlings into the conventional culture medium and continually culturing. The method disclosed by the invention has the advantages of good sterilization effect, small damages to the culture medium seedlings, low cost, and simplicity and convenience for operation, and is suitable for industrial popularization and the like.
Owner:GUANGXI BOTANICAL GARDEN OF MEDICINAL PLANTS
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