45results about How to "Does not affect feed intake" patented technology

The invention relates to a tilmicosin enteric micro pellet. The tilmicosin enteric micro pellet is composed of tilmicosin, a high molecular carrier, a binder, and a coating liquid. Problems of tilmicosin, such as poor palatability and instability under acidic conditions, are solved, and clinical using amount is increased.

The invention discloses corn-dephenolized cottonseed protein type feeds for medium pigs (each pig is 35-60kg)and large pigs (each pig is 60-100kg), which use corns as main energy raw materials, use dephenolized cottonseed protein as main protein raw materials and comprise corns, soybean meal, the dephenolized cottonseed protein, defatted rice bran, salt, mountain flour, calcium hydrophosphate, lysine hydrochloride and premix. A novel protein resource for feeds is developed, the feeds containing the dephenolized cottonseed protein for medium and large pigs can accurately meet the requirements of the pigs to the protein and amino acid and are equivalent to conventional corn-soybean meal type feeds in growth performance, slaughter performance, blood biochemical indexes and meat quality performance.

The invention discloses an enrofloxacin quick-release pellet and relates to the field of veterinary medicines. The enrofloxacin quick-release pellet comprises the following components by weight percent: 10%-45% of enrofloxacin, 18%-86% of excipient, 1%-5% of disintegrating agent, 1%-2% of adhesive and 2%-30% of coating solution. The invention also relates to a preparation method for the enrofloxacin quick-release pellet. The enrofloxacin quick-release pellet is capable of covering the bitter taste of enrofloxacin and guaranteeing quick disintegration release of the preparation in gastrointestinal tracts. Compared with the preparation sold in the market, the enrofloxacin quick-release pellet has the advantages that the prescription is simplified, few sorts of ingredients are used, the quality problem of the preparation caused by uneven mixing of raw materials and ingredients in the preparation process is reduced, the preparation process is simple, the quality is stable and reliable andthe bioavailability of drugs in animal body is obviously increased.

The invention relates to a self-help-feeding plant-source composite-drug-effect nutrient for chickens and a preparation method thereof. The product is composed of the following components in percentage by mass: 15-20% of corn flour, 8-12% of bean pulp powder, 0.01-2% of plant-source composite-drug-effect nutrient substance (radix astragali polysaccharide extract, acanthopanax extract and asarum extract in a ratio of (1-30):(1-5):(1-15)), 0.4-4% of carrageenin, 3-7% of hawthorn, 2-8% of honey, 0.2-0.5% of table salt, 0.1-2% of vitamin complex, 0.1-2% of composite mineral, 0.02-0.05% of potassium sorbate and 62-71% of water. The product is suitable for direct feeding, and can strengthen the organism immunity of chickens and reduce the occurrence of diseases; and meanwhile, the composite-drug-effect nutrient has favorable palatability, can implement self-help feeding, and is convenient to use. Besides, the product has the advantages of simple production technique and low production cost, and is suitable for large-scale production.

The present invention relates to a cereal straw fermented compound micro-organism agent. The cereal straw fermented compound micro-organism agent comprises: 8-12 parts by weight of lactobacillus buchneri, 18-22 parts by weight of propionibacterium acidipropionici, 23-27 parts by weight of bacillus licheniformis, 13-17 parts by weight of bacillus subtilis, 13-17 parts by weight of candida utilis and 13-17 parts by weight of aspergillus niger. The present invention also includes a silage cereal straw feed prepared by the micro-organism agent and a preparation method thereof. The compound micro-organism agent can conduct processing and utilization of whole plant cereals, reduces the production costs and reduces the waste of the raw materials, does not affect the milk production of dairy cows, and also improves the milk quality of the dairy cows.

The invention discloses a microporous membrane-coated controlled-release trelagliptin succinate pellet and a preparation method thereof. The microporous membrane-coated controlled-release trelagliptin succinate pellet sequentially comprises a drug-containing pellet core and a controlled-release coating layer from inside to outside, wherein the drug-containing pellet core is prepared from a primary material and an auxiliary material at the ratio of (5%-20%):(80%-95%). According to the microporous membrane-coated controlled-release trelagliptin succinate pellet, a bitter taste can be coated, the effective ingredients can be dissolved out, constant long-acting plasma concentration is ensured, and the defect that a drug is discharged along with excrement before not completely released is avoided.

The invention discloses a feed supply device for a pig farm. The feed supply device comprises a first raising chamber, a second raising chamber, a sliding rail body and a pickup truck, wherein the second raising chamber is formed in one side of the first raising chamber, the sliding rail body is arranged above the first raising chamber and the second raising chamber, and the pickup truck is slidably arranged under the sliding rail body; the inner portion of the first raising chamber is provided with a first trough and a fourth trough, the fourth trough is formed in one side of the first trough, the inner portion of the second raising chamber is provided with a second trough and a third trough, and the third trough is formed in one side of the second trough; the pickup truck comprises a storage bin and a discharging box, wherein the outer surfaces of the two sides of the discharging box are in bolted connection with discharging motors respectively, and a spiral discharging shaft penetrates through the discharging box. The feed supply device for the pig farm can achieve the effect that single equipment performs feed putting on multiple raising chambers simultaneously, reduces the workload of workers, and can provide convenience for the workers to clear up blocked feed.

The invention relates to a self-help-feeding drug carrier for dogs and a preparation method thereof. The drug carrier is composed of the following components in percentage by mass: 15-30% of chicken, 0.5-3% of white granulated sugar, 0.2-1.2% of carrageenin, 0.05-0.3% of citric acid, 0.1-0.3% of sodium isoascorbate, 0.01-1% of vitamin complex, 0.1-2% of composite mineral, 0.02-0.05% of potassium sorbate and 66-84% of water. The product is suitable for directly feeding, and is used for preventing and treating common clinical diseases of dogs to achieve the dual effects of preventing and treating diseases and strengthening the constitution; and the drug carrier has the advantages of favorable palatability and the like, can implement self-help feeding, is convenient to use, and solves the problems of labor and time consuming, animal stress reaction, pains and the like caused by oral administration or injection administration. Besides, the product has the advantages of simple production technique, wide raw material sources and low production cost, and is suitable for large-scale production.

The invention relates to a preparation method of anionic salt having good palatability and used in the perinatal period of dairy cows. The anionic salt comprises the following components in parts by weight: 7-13 parts of magnesium sulphate, 0.075-5.575 parts of zinc sulphate, 0.01-5.3 parts of ferrous sulphate, 16-25 parts of calcium sulphate, 0.05-2.2 parts of manganese sulphate, 2-5.5 parts of ammonium chloride, 7.275-10.475 parts of magnesium chloride, 19-25 parts of rice hull powder, 1-5 parts of ammonium sulphate, and 25-35 parts of maltodextrin. The above raw materials are mixed and prepared into the anionic salt of the dairy cows. By means of the preparation method of the anionic salt having good palatability and used in the perinatal period of the dairy cows in the invention, the incidence rate of postpartum metabolic diseases, such as retained fetal membranes and parturient paresis of the dairy cows, can be obviously reduced; the incidence rate of postpartum hypocalcemia of the dairy cows can be reduced; the productivity effect of dairy cow breeding is increased; furthermore, the palatability is good; the food consumption of dry matters of the dairy cow in the perinatal period is not influenced.

The invention provides a production and preparation method of a calculus bovis factitius-venenum bufonis granule. According to the preparation method, blank liposome is coated with calculus bovis factitius and venenum bufonis, so the prepared calculus bovis factitius-venenum bufonis granule does not influence the feed intake of pigs at all, and meanwhile, calculus bovis factitius-venenum bufonis granule is beneficial to absorption of active pharmaceutical ingredients after being taken by animals, and curative effect is ensured.

The invention discloses a piglet antibiotic-free compound feed containing fermented mulberry leaf powder. The piglet antibiotic-free compound feed comprises the following raw materials in parts by weight: 5-20 parts of fermented mulberry leaf powder, 60-65 parts of corn, 10-15 parts of soybean meal, 1-2 parts of extruded soybeans, 1-1.5 parts of whey powder, 1-1.5 parts of odd feed powder, 2-4 parts of fish meal, 1-2 parts of glucose and 2-4 parts of antibiotic-free premix. Wherein the fermented mulberry leaf powder is obtained by cleaning mulberry leaves, airing, shredding, adding bran, uniformly mixing, bagging, fermenting, drying and crushing, the nutritional value can be effectively improved, the process is simple, the production cost is low, and production is facilitated. The piglet antibiotic-free compound feed containing the fermented mulberry leaf powder is of an antibiotic-free formula, is designed according to the characteristics of weaned piglets, can remarkably increase the number of lactobacillus in intestinal tracts and reduce the number of escherichia coli when being used for feeding the piglets, and is lower in feed conversion ratio and lower in diarrhea rate.

The invention relates to a self-help-feeding drug carrier for horses and a preparation method thereof. The product is composed of the following components in percentage by mass: 15-30% of apple, 10-25% of corn flour, 0.4-8% of carrageenin, 5-10% of peanut meal, 4-10% of molasses, 0.5-5% of table salt, 0.1-2% of vitamin complex, 0.1-2% of composite mineral, 0.02-0.05% of potassium sorbate and 37-74% of water. The product is suitable for directly feeding, and is used for preventing and treating common clinical diseases of horses to achieve the dual effects of preventing and treating diseases and strengthening the constitution; and the drug carrier has the advantages of favorable palatability and the like, can implement self-help feeding, is convenient to use, and solves the problems of labor and time consuming, animal stress reaction, pains and the like caused by oral administration or injection administration. Besides, the product has the advantages of simple production technique, wide raw material sources and low production cost, and is suitable for large-scale production.

The invention relates to a self-help-feeding drug carrier for chickens and a preparation method thereof. The drug carrier is composed of the following components in percentage by mass: 10-30% of pear, 12-25% of corn flour, 0.4-8% of carrageenin, 5-15% of bean pulp powder, 4-8% of honey, 0.2-0.5% of table salt, 0.1-2% of vitamin complex, 0.1-2% of composite mineral, 0.02-0.05% of potassium sorbate and 37-68% of water. The product is suitable for directly feeding, and is used for preventing and treating common clinical diseases of chickens to achieve the dual effects of preventing and treating diseases and strengthening the constitution; and the drug carrier has the advantages of favorable palatability and the like, can implement self-help feeding, is convenient to use, and solves the problems of labor and time consuming, animal stress reaction, pains and the like caused by oral administration or injection administration. Besides, the product has the advantages of simple production technique, wide raw material sources and low production cost, and is suitable for large-scale production.

The invention relates to A61K, in particular to a method for preparing an efficient tilmicosin premixing agent through adsorption crystallization and application of the efficient tilmicosin premixing agent. Comprising the following steps: adsorption crystallization: spraying a tilmicosin mixed solution into a porous material, and carrying out boiling drying at 50-100 DEG C for 10-15 minutes; by controlling the water content and the adsorption capacity of the porous material, adsorption of the tilmicosin mixed solution is promoted, and meanwhile, solvent water and the like in the tilmicosin mixed solution are controlled to be taken out by sucking and discharging boiling dry airflow at a certain temperature in a pore channel of the porous material with high adsorption capacity; therefore, the tilmicosin or the tilmicosin phosphate is promoted to rapidly crystallize in a short time and is adsorbed in the pore channels of the porous material to form adsorption crystals. Plant extract components can be further added after adsorption and crystallization, so that the effects of enhancing immunity, resisting inflammation, resisting oxidation, improving drug effects, reducing side effects of drugs and the like are achieved, or the taste of the preparation is improved, and the first-mouth selectivity and the long-term feed intake are improved.

The invention discloses a feed adhesive agent and a preparation method thereof. The feed adhesive agent per 100 g consists of, by weight, 10.0-40.0 g of modified polyvinylpyrrolidone K90, 5.0-15.0 g of potassium monododecyl phosphate, 10.0-20.0 g of poloxamer 407, and 4.0-20.0 g of hydroxypropyl-beta-cyclodextrin, with the balance being corn soft sugar. The feed adhesive agent can make drugs or additives adhered to the surfaces of feed particles and uneasy to fall off, so that uniform administration can be guaranteed, and the problems of uneven drug stirring of farms feeding complete pellet feed during feed stirring and administration can be solved; and the feed adhesive agent does not affect animal palatability and drug effects, is strong in stability and safe in clinical use, and does not chemically react with drugs. The preparation method is further disclosed. The preparation method is simple in technology, each in raw material purchasing, suitable for large-scale production and good in market prospects.