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

The invention provides kitasamycin microcapsule and a preparation method and application thereof, which pertains to a feed drug additive field, in particular relates to novel kitasamycin preparation and a preparation technique thereof, and the application thereof in the preparation of livestock and poultry antibiotic growth promoter. The kitasamycin microcapsule of the invention comprises the kitasamycin and medical auxiliary materials; the weight of the medical auxiliary materials is 2-16 times of that of the kitasamycin material; the microcapsule is prepared through mixing the kitasamycin with heated and melted medical auxiliary materials and spray cooling. The kitasamycin microcapsule eliminates the bitterness of kitasamycin, intensifies the delayed release function of kitasamycin, reduces the stimulation of the kitasamycin to the stomach and the damage and decomposition degree thereof in the stomach, and enhances the effective intestines concentration and the functioning time of kitasamycin; the method for preparing the kitasamycin microcapsule is a wholly close manufacturing process and a wholly close material conveying system, thus decreasing flying of dust and material loss with has high yield of the products.

The invention discloses a compound acetylisovalery tylosin tartrate pellet. The compound acetylisovalery tylosin tartrate pellet is made by wrapping a drug-loading pellet core by adopting a coating material, wherein the drug-loading pellet core comprises the following components in percentage by weight: 1-30% of acetylisovalery tylosin tartrate, 1-30% of sulfadimidine, 5-20% of lactose, 5-25% of corncob powder, 10-60% of starch, 15-35% of microcrystalline cellulose and 0.5-12% of pelletizing binding agent; and weight of the coating material is not more than 8% of the total weight of the compound acetylisovalery tylosin tartrate pellet. The compound acetylisovalery tylosin tartrate pellet has a better clinical treatment effect, application amount of acetylisovalery tylosin tartrate can be reduced, and production cost can be saved; and drug release can be delayed, drug action time can be prolonged, and long-acting effect can be achieved, so that administration frequency is reduced and labour intensity can be alleviated.

The invention relates to compound enrofloxacin pellets and a preparation method of the compound enrofloxacin pellets, wherein the enrofloxacin pellets comprise coatings and medicine-carrying pill cores; the coatings wrap the medicine-carrying pill cores; the medicine-carrying pill cores are prepared by the following steps that: amoxicillin and enrofloxacin are mixed with starch, microcrystalline cellulose, carboxymethyl starch and the like uniformly; an appropriate amount of pelleting adhesive is added in the mixture to prepare the soft material, the soft material is added into an extrusion pelleter to be extruded out, the extruded material is placed in a shot blasting machine to prepare the medicine-carrying pill cores. Then, the pill cores are placed into a fluidized bed to be dried andthen sieved; finally the sieved pill cores are placed into the fluidized bed, coating liquid is injected for coating, fluidized drying is then carried out after the coating, and then the finished product is obtained. According to the invention, both the amoxicillin and enrofloxacin are used, so that double effects are achieved, the medicine administration frequency and dose are reduced, and the pellets are easy to take only by stirring, and feed intake of animals is not influenced. In addition, the preparation method of the compound enrofloxacin pellets has simple process steps and low energyconsumption, is safe to produce and easy to implement, and the prepared pellets have uniform granularity.

The invention relates to a self-help-feeding drug carrier for sheep and a preparation method thereof. The product is composed of the following components in percentage by mass: 10-30% of Chinese yam, 12-25% of corn flour, 0.4-8% of carrageenin, 5-12% of albumen powder, 5-10% of molasses, 0.3-0.5% of table salt, 0.1-2% of vitamin complex, 0.1-2% of composite mineral, 0.02-0.05% of potassium sorbate and 37-65% of water. The product is suitable for directly feeding, and is used for preventing and treating common clinical diseases of sheep 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 discloses a compound acidifier for improving digestive ability of piglet feed and the piglet feed obtained by the compound acidifier. The compound acidifier is prepared from the following components in parts by weight: 5-10 parts of lactic acid, 40-60 parts of fumaric acid, 20-40 parts of anhydrous citric acid and 10-20 parts of a carrier. The compound acidifier is obtained through redesign according to the effective total acid content, and the compound acidifier can release more hydrogen ions when the pH value is 3.5, so that gastric acid can be effectively supplemented, the effects of activating proteogen and promoting protein digestion are achieved, and the defect that the proteogen cannot be activated effectively due to the fact that the hydrogen ions released by a traditional acidifying agent are too few under the pH value is overcome; and meanwhile, fumaric acid, citric acid and lactic acid are compounded, so that the purpose of better activating the proteogen can be achieved, and the obtained compound acidifier is good in palatability, does not affect feed intake, has a component proportion which is simple and easy to control, and is high in comprehensive cost performance and very suitable for being used as an additive of the piglet feed.

The invention discloses a sustained release type tylosin phosphate microcapsule preparation. The preparation comprises the following components in weight percentage: 2.2-22% of tylosin phosphate, and78-97.8% of excipients, wherein the sum of the weight percentages of the components is 100%. The sustained release type tylosin phosphate microcapsule preparation provided by the invention has the advantages of uniform distribution of the effective drug tylosin phosphate, round particles, good fluidity and dispersibility, and easy mixing with the feed; and effective drug components are isolated from the outside to achieve odor mask, moisture prevention, and improvement of drug stability and drug bioavailability. The invention also discloses a preparation method of the sustained release type tylosin phosphate microcapsule preparation; and the method has the advantages of simple process and high production efficiency, and can meet assembly line production.

The invention belongs to a production method for adding brewer grain fattening pannage, which belongs to the technical field of the feed processing. The production method comprises the following steps that: the brewer grain is undertaken the steam explosion pretreatment and is added with mixed bacteria and / or complex enzyme to be undertaken the solid anaerobic fermentation so as to degrade the fiber content in the brewer grain and to improve the soluble nitrogen content of the brewer grain, so the quality is better, and the nutrition is more balanced; then the fermented brewer grain, waste yeast powder, corn meal, soybean meal and pre-mixed material are uniformly mixed to obtain the fattening pannage being added with brewer grain. The source of the brewer grain and the waste yeast is abundant, the nutrition for matching the brewer grain and the waste yeast is balanced, and the cost of the feed can be reduced; and the brewer grain is processed with the steam explosion pre-treatment technology, the enzymolysis technology and the biological fermentation technology, so the fiber content is reduced, the protein quality is improved, and the type of the aminoacid is more abundant; and the production method can reduce the grain ratio, improves the daily gain, reduces the feed compositions, and is free from influencing the feed intake and the growth of the fatty pigs.

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.

An enrofloxacin immediate-release pellet relates to the field of veterinary medicine. The pellet core is composed of the following components by weight percentage: 10%-45% of enrofloxacin, 18%-86% of excipient, disintegrating 1% to 5% of disintegrating agent, 1% to 2% of binder; the coating solution has a weight gain of 2% to 30%. In addition, it also relates to the preparation method of the enrofloxacin immediate-release pellets. The invention can cover up the bitter taste of enrofloxacin, ensure the rapid disintegration and release of the preparation in the gastrointestinal tract, and simplifies the prescription compared with the commercially available preparations. There are few types of auxiliary materials, which reduces the preparation quality problem caused by uneven mixing of raw and auxiliary materials in the preparation process, and the preparation process is simple, the quality is stable and reliable, and the bioavailability of the drug in the animal body is significantly improved.

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 sheep and a preparation method thereof. The product is composed of the following components in percentage by mass: 10-30% of Chinese yam, 12-25% of corn flour, 0.4-8% of carrageenin, 5-12% of albumen powder, 5-10% of molasses, 0.3-0.5% of table salt, 0.1-2% of vitamin complex, 0.1-2% of composite mineral, 0.02-0.05% of potassium sorbate and 37-65% of water. The product is suitable for directly feeding, and is used for preventing and treating common clinical diseases of sheep 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 cats and a preparation method thereof. The drug carrier is composed of the following components in percentage by mass: 15-30% of cod leftover, 0.2-1.2% of carrageenin, 0.2-0.8% of composite phosphate, 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 69-84% of water. The product is suitable for directly feeding, and is used for preventing and treating common clinical diseases of cats 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 pig self feeding type drug carrier and a preparation method thereof. The drug carrier comprises the following components by weight percent: 12%-25% of hawthorns, 3%-9% of bee honey, 0.4%-8% of carrageenan, 0.8%-1.2% of calcium hydrogen phosphate, 0.01%-2% of compound vitamins, 0.01%-0.5% of compound mineral substances, 0.02%-0.05% of potassium sorbate, and 58%-82% of moisture. The drug carrier is suitable for direct feeding, is used for treating and preventing the common clinical diseases of pigs, and achieves the double effects of treating and preventing the diseases and enhancing physique, meanwhile, the drug carrier has the advantages of good palatability, convenience in use, and the like, and the pigs eat the drug carrier independently. The problems of time and effort consumption during operation, animal stress response, pain and the like caused by feeding and injecting the drugs, are solved. In addition, the drug carrier has the advantages that the production technology is simple, the source of raw materials is wide, the production cost is low, and the drug carrier is suitable for large scale production.

The invention relates to a self-ingestion type plant source composite pharmaceutical effect nutriment for a horse and a preparation method of the self-ingestion type plant source composite pharmaceutical effect nutriment. The self-ingestion type plant source composite pharmaceutical effect nutriment consists of the following components in percentage by mass: 10-25 percent of corn flour, 4-10 percent of groundnut meal, 0.01-2.6 percent of plant source composite pharmaceutical effect nutrient substance in which the ratio of astragalus polysaccharide extract to acanthopanax senticosus extract to asarum sieboldi extract is equal to (1-28):(1-10):(1-12), 0.4-4 percent of carrageenan, 4-10 percent of molasses, 0.5-5 percent of salt, 0.1-2 percent of composite vitamin, 0.1-2 percent of composite mineral substance, 0.02-0.05 percent of potassium sorbate and 59-80 percent of water. The self-ingestion type plant source composite pharmaceutical effect nutriment is suitable for direct feeding, the organism immunity of the horse is improved, and the occurrence of diseases is reduced; meanwhile, the composite pharmaceutical effect nutriment is good in palatability, can be applied to self-ingestion of the horse, and is convenient to use. In addition, the composite pharmaceutical effect nutriment is simple in production process, wide in source of raw materials, low in production cost and suitable for large-scale production.

The invention relates to a self-help-feeding plant-source composite-drug-effect nutrient for cattle and a preparation method thereof. The product is composed of the following components in percentage by mass: 12-28% of peanut straw, 5-15% of barley flour, 0.01-2.2% of plant-source composite-drug-effect nutrient substance (radix astragali polysaccharide extract, acanthopanax extract and asarum extract in a ratio of (1-28):(1-15):(1-10)), 0.4-4% of carrageenin, 2-6% of sesame oil, 1-5% of rice bran, 0.3-5% of table salt, 0.1-4% of vitamin complex, 0.1-4% of composite mineral, 0.02-0.05% of potassium sorbate and 51-79% of water. The product is suitable for direct feeding, and can strengthen the organism immunity of cattle 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.