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39 results about "Succus entericus" patented technology

Succus entericus An antiquated, nonspecific term for the sum total of intestinal secretions. succus (suk'kus) plural.succi [L. succus, juice]

Production method of enteric-coated kitasamycin for feed

The invention discloses a production method of enteric-coated kitasamycin for feed, which comprises the following process steps: step one, the preparation of drug-loaded pellets; step two, inner layer sustained-release coating of the drug-loaded pellets, which prolongs the release and acting time of kitasamycin; and steps three, outer layer enteric coating of the drug-loaded pellets, which ensures the release in succus entericus and small or no release in gastric juice. The method has the advantages that the kitasamycin is subjected to pellets pelletizing and 99 percent of the prepared granulums can pass through 24 meshes, so the dust is greatly reduced and the fluidity is increased; the coating of the inner layer sustained-release agent (HPMC) prolongs the release and acting time of the kitasamycin, reduces medication times and reduces the medication cost; and a layer of enteric substance, namely acrylic resin-III is sprayed and coated on the outer layer of particles. The substance protects the kitasamycin which is a weakly alkaline antibiotic from being damaged by gastroc acid in stomach, quickly disintegrates after entering enteric canal and releases the kitasamycin; and then the kitasamycin is absorbed by gastrointestinal mucosa into blood drug to play a role of restraining the reproduction of pathogenic microorganism and preventing diarrhea. Insoluble in the stomach, kitasamycin coating formulations have no pessimal stimulation on the stomach, and cannot result in regurgitation and vomiting. In addition, the sustained-release formulation, namely the kitasamycin prolongs the acting time so the medication times is reduced, the medication cost of farmers is reduced, and the economic benefit is improved.
Owner:WUXI ZHENGDA POULTRY

Application of fucoidin and hydrolyzed oligosaccharide thereof in preparing probiotic protection agent and method

The invention discloses application of fucoidin and hydrolyzed oligosaccharide thereof in preparing a probiotic protection agent and a method. According to the application and the method, the fucoidinand the hydrolyzed oligosaccharide thereof embed probiotics for the first time, the survival conditions in gastric acid and small intestinal fluid are simulated, it is shown through a result that thesurvival time of the probiotics embedded by the fucoidin and the hydrolyzed oligosaccharide is prolonged, the embedding effect of the hydrolyzed oligosaccharide is better than that of the fucoidin, and a foundation is laid for prolonging the high activity of the probiotics in the gastrointestinal environment.
Owner:SOUTHWEST UNIVERSITY +1

Lactobacillus plantarum GL-5 with oxidation resisting activity and application thereof

The invention belongs to the technical field of microbes and particularly relates to lactobacillus plantarum GL-5 with oxidation resisting activity and application thereof. The lactobacillus plantarumGL-5 with oxidation resisting activity disclosed by the invention is screened out from a home-made fermented dairy product of a herdsman's house of a Qinghai Guoluo region with an altitude of 4,000mor more, is collected in China General Microbiological Culture Collection Center of China Committee for Culture Collection of Microorganisms on November, 21, 2019 and has an accession number of CGMCCNo. 18988. The lactobacillus plantarum GL-5 has a 16S rRNA sequence shown in SEQ ID NO: 1. The lactobacillus plantarum GL-5 provided by the invention has relatively good bacteriostatic activity, and activity of enteropathogenic bacteria, i.e., staphylococcus aureus and escherichia coli can be remarkably inhibited; the lactobacillus plantarum GL-5 provided by the invention has relatively high oxidation resisting activity and can remarkably tolerate catalase; and the lactobacillus plantarum GL-5 provided by the invention has relatively high gastrointestinal fluid tolerance and cholate tolerance,and the survival rate of the lactobacillus plantarum GL-5 after culture in simulated gastric fluid and intestinal fluid is remarkably higher than that of lactobacillus rhamnosus LGG.
Owner:LANZHOU UNIVERSITY

Lactobacillus capable of adsorbing or degrading enterotoxin and application thereof

The invention discloses a lactobacillus capable of adsorbing or degrading enterotoxin and an application thereof. The preservation number of the lactobacillus is CCTCC No: M2015128. The lactobacillus can adsorb or degrade enterotoxin and has the good effects of resisting acid, cholate, artificial gastric juice and artificial intestinal juice. The lactobacillus is specifically characterized in that the enterotoxin can be adsorbed or degraded, and good enterotoxin removal capacity is achieved; growth of common pathogenic bacteria can be restrained; the lactobacillus can resist acid and cholate and can survive in the digestive tract. In specific application, a method includes the step that freeze-dried bacterial powder is dissolved in water at normal temperature to be taken orally or is directly added according to a certain proportion to make functional food or healthcare products. The lactobacillus is screened from multiple lactobacilli, has the high enterotoxin removal capacity and good performance, and can be used for human body healthcare.
Owner:山东凤凰生物科技股份有限公司

Novel salmonella bacteriophage microencapsulated microspheres and preparation method thereof

The invention provides a preparation method of novel salmonella bacteriophage microencapsulated microspheres. The method comprises the following steps of mixing a cationic etherified starch solution and a bacteriophage suspension, and uniformly stirring to obtain a first mixed solution; uniformly stirring and mixing the first mixed solution, a sodium alginate solution, a xanthan gum solution and a nano TiO2 solution to obtain a second mixed solution; and dropwise adding the second mixed solution into a calcium chloride solution to form calcium alginate gel, filtering and collecting bacteriophage microspheres, putting the bacteriophage microspheres into a cationic chitosan oligosaccharide solution, coating for 30 minutes, and filtering and collecting the bacteriophage microencapsulated microspheres. In actual use, after the bacteriophage microspheres enter gastric juice, the bacteriophage surface coated material can effectively resist erosion of gastric acid and prolong the survival time of bacteriophage, and after the bacteriophage microspheres enter intestinal juice, the bacteriophage surface coated material can react with the intestinal juice and is cracked to release the bacteriophage in the material so as to achieve the sterilization effect. The method has the advantages that microencapsulation preparation is carried out at room temperature, the process is simple, the application range is wide, and the cost is low; and the raw materials are wide in source, cheap and easy to obtain, and the bacteriophage in the product is high in activity and encapsulation efficiency and can be directly applied to feed addition.
Owner:HEBEI UNIV OF ENG

Millimeter-level polykaryon capsules for transporting nutrient substances/medicines to small intestines and realizing slow release and preparation method and application of millimeter-level polykaryon capsules

ActiveCN111450077AWith particle size uniformityEvenly distributedAntipyreticMetabolism disorderFormularyActive agent
The invention provides millimeter-level polykaryon capsules for transporting nutrient substances / medicines to small intestines and realizing slow release and a preparation method and application of the millimeter-level polykaryon capsules. The millimeter-level polykaryon capsules comprise a wall material and oil substances, wherein the oil substances are evenly or unevenly distributed on the innerwall of the wall material in the manner of uniform or ununiform oil droplets, so that the millimeter-level polykaryon capsules are obtained. Bulges are formed on the surfaces of the millimeter-levelpolykaryon capsules, and the oil droplets are placed in the ridges. The wall material is calcium ion cross-linking alginate or calcium cross-linking alginate and a surfactant. The entire preparation method is simple and easy to operate, complex polymer modification and formulas are not added, and the prepared millimeter-level polykaryon capsules are mainly released during simulation of small intestinal juice and are not released in simulation of gastric juice. The millimeter-level polykaryon capsules are particularly suitable for medication through mouths to specially transport fish oil to thesmall intestines and realize slow release of the fish oil / medicines in the small intestines, and can be used for transporting nutrient substances and medicines as specific carriers.
Owner:SHANGHAI OCEAN UNIV

Production method of enteric-coated kitasamycin for feed

The invention discloses a production method of enteric-coated kitasamycin for feed, which comprises the following process steps: step one, the preparation of drug-loaded pellets; step two, inner layer sustained-release coating of the drug-loaded pellets, which prolongs the release and acting time of kitasamycin; and steps three, outer layer enteric coating of the drug-loaded pellets, which ensures the release in succus entericus and small or no release in gastric juice. The method has the advantages that the kitasamycin is subjected to pellets pelletizing and 99 percent of the prepared granulums can pass through 24 meshes, so the dust is greatly reduced and the fluidity is increased; the coating of the inner layer sustained-release agent (HPMC) prolongs the release and acting time of the kitasamycin, reduces medication times and reduces the medication cost; and a layer of enteric substance, namely acrylic resin-III is sprayed and coated on the outer layer of particles. The substance protects the kitasamycin which is a weakly alkaline antibiotic from being damaged by gastroc acid in stomach, quickly disintegrates after entering enteric canal and releases the kitasamycin; and then the kitasamycin is absorbed by gastrointestinal mucosa into blood drug to play a role of restraining the reproduction of pathogenic microorganism and preventing diarrhea. Insoluble in the stomach, kitasamycin coating formulations have no pessimal stimulation on the stomach, and cannot result in regurgitation and vomiting. In addition, the sustained-release formulation, namely the kitasamycin prolongs the acting time so the medication times is reduced, the medication cost of farmers is reduced, and the economic benefit is improved.
Owner:WUXI ZHENGDA POULTRY

Development of Lipid Matrix Granules with Incorporation of Polysaccharides for Effective Delivery of an Antimicrobial Essential Oil

Antibiotics have long been used at sub-therapeutic levels to control incidences of post-weaning diarrhea and to improve growth performance in pigs. However, the current trend world-wide is to eliminate the use of in-feed antibiotics due to increased public concerns over the spread of antibiotic resistance in bacterial pathogens, which poses a threat to public health. Alternatives to in-feed antibiotics are needed. Thymol essential oil exhibits strong in vitro antibacterial activity; however; direct inclusion of essential oils to pig feeds has limited efficacy due to their high volatility, low stability during feed processing, interactions with other feed components and poor availability in lower gut. To solve these problems, we developed lipid matrix beads using thymol and a fatty acid with incorporation of 2% polysaccharides via a melt-granulation technique. Laurie acid was identified as a suitable carrier for thymol. In vitro release of thymol from lipid matrix granules was determined using simulated salivary fluid (SSF), simulated gastric fluid (SGF) and simulated intestinal fluid (SIF), respectively. The lipid matrix granules with 2% polysaccharides exhibited a slow release rate (%) of essential oil and fatty acid in SSF (21.2±2.3; 36±1.1), SGF (73.7±6.9; 54.8±1.7) and SIF (99.1±1.2; 99.1±0.6), respectively. However, the lipid matrix granules without polysaccharides had quick release (%) of essential oil and fatty acid from the SSF (79.9±11.8; 84.9±9.4), SGF (92.5±3.5; 75.8±5.9) and SIF (93.3±9.4; 93.3±4.6), respectively.
Owner:UNIVERSITY OF MANITOBA

Preparing method of radix scutellariae-gypsum oral preparation capable of relieving sore throat

The invention belongs to the technical field of traditional Chinese medicine compound preparation and particularly relates to a preparing method of radix scutellariae-gypsum oral preparation capable of relieving sore throat. The method includes the steps of firstly, extracting volatile oil of gypsum, fructus forsythiae, mint and perilla leaf in a microwave manner; secondly, adding buffalo horn grinding fluid into artificial gastric juice extract and artificial intestinal juice extract; thirdly, jointly decocting fructus forsythiae, mint, perilla leaf and gypsum residues with radix scutellariae, rhizoma anemarrhenae, radix rehmanniae, red peony root, spina gleditsiae, dandelion and liquorice; fourthly, welling mixing the volatile oil clathrate compound and the extract obtained in the first step and the third step, adding the buffalo horn extract in the second step, adding 0.1% of agar and 0.2% of sorbic acid, well mixing, immediately filtering, cooling, adding the volatile oil clathrate compound obtained in the first step, 1% of apple essence and 1.5% of sodium cyclamate, adding distilled water to reach 1000ml, split charging into glass ampoules of 10ml, and sterilizing. The method is simple and easy to operate and stable in experiment results.
Owner:TONGHUA GOLDEN-HORSE PHARM IND CO LTD

Fish feed additive containing traditional Chinese medicine ingredients

The invention discloses a fish feed additive containing traditional Chinese medicine ingredients, and relates to the field of fish culture, and the fish feed additive comprises the following components in parts by weight: 10-16 parts of tartaric acid, 8-10 parts of betaine, 7-9 parts of a phagostimulant, 7-10 parts of Toxicodendron vernicifluum leaves, 12-15 parts of zanthoxylum ailanthus, 5-10 parts of licorice, 2.5-4 parts of purslane, 1.5-2 parts of medicated leaven, 3-5 parts of polygonum multiflorum, 2-4 parts of gynostemma pentaphyllum and 20-30 parts of bile acid. The tartaric acid, the phagostimulant, the medicated leaven and the purslane are added into the additive disclosed by the invention, so that the feeding frequency of fishes in sultry weather can be increased, the effect of increasing appetite can be achieved, secretion of gastric juice and intestinal juice is promoted, nutrient absorption of organisms is promoted, nutrient substances are promoted to enter the organisms more quickly, and the food intake of the fishes is increased; the fish feed additive solves the problem that fishes are unwilling to ingest or have a slow ingestion speed in sultry weather, uses Chinese herbal medicines for compatibility, is derived from natural components of plants, is green and environment-friendly, has no toxic effects, and has high social and economic benefits.
Owner:深圳市沙利文生物科技有限公司

An improved nano-suspension freeze-dried preparation based on Guanxinning and its preparation method

The invention belongs to the field of medicine, and relates to an improved nano-suspension freeze-dried preparation based on Guanxinning and a preparation method thereof. The technical problem solved by the present invention is to provide an oral preparation containing both insoluble and water-soluble components of Chuanxiong and Salvia miltiorrhiza, which solves the technical problems of improving the dissolution of the insoluble components and improving their oral bioavailability. The oral preparation of the present invention is an oral freeze-dried preparation made from the extracts of Chinese medicinal materials Chuanxiong and Salvia miltiorrhiza as raw materials: the weight ratio of Salvia miltiorrhiza extract and Chuanxiong extract is 8-12:6-10; the preparation method is as follows: A 2. Preparation of nanosuspension: the salvia miltiorrhiza extract and the chuanxiong extract are made into a nanosuspension of 100-1000 nm; B. the nanosuspension obtained in step A is freeze-dried to make a freeze-dried powder. The apparent solubility of the poorly soluble components is significantly higher than that of the extract, the release rate in simulated gastric juice and simulated intestinal fluid in vitro is accelerated, and the cumulative release rate is also significantly increased, which provides a new technical idea for clinical application of Chuanxiong and Salvia miltiorrhiza.
Owner:SOUTHWEST UNIV
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