100 results about "Oral glucose" patented technology

The invention provides a worm-disease-resisting compound niclosamide tablet for beasts and birds and a preparation method thereof. The worm-disease-resisting compound niclosamide tablet for beasts and birds respectively includes the following components by mass: 0.5-2 parts of tiandixiang (a flavoring agent), 0.5-2 parts of aspartame, 8-12 parts of starch, 20-40 parts of oral glucose or cane sugar, 0.5-2 parts of mannitol, 0.3-0.8 part of magnesium stearate, 40-60 parts of niclosamide and 2.5-5 parts of levamisole hydrochloride. The preparation method includes performing 17-mesh palletizing through a starch inside-outside addition and wet process mode, drying for 2-3 hours at the temperature of 65-75 DEG C, performing 17-mesh granulating straightening, additionally mixing the tiandixiang, the aspartame and the magnesium stearate, performing tabletting and the like to obtain the finished products. The worm-disease-resisting compound niclosamide tablet is bright and clean in appearance, fast in disintegration, good in desinsectization effect after being taken orally, simple in process, good in taste and suitable for industrial production, and various indexes of the tablet are optimized.

The invention discloses a moringa leaf extract with blood sugar lowering activity and a preparation method thereof. The preparation method comprises the following steps: crushing and sieving, performing alkali treatment, performing protease enzymolysis, performing cellulase enzymolysis, performing high-pressure homogenization, performing high-temperature extraction, performing low-temperature high-speed centrifugation, performing ultrafiltration separation and concentration, performing protease enzymolysis, performing low-temperature high-speed centrifugation, performing secondary ultrafiltration separation and concentration, performing freeze drying and the like to obtain the moringa leaf extract with the blood sugar lowering activity. The extract has the polysaccharide content of 30% orabove; an animal experimental model of a type-2 diabetic rat verifies that the extract has good blood sugar lowering activity and can effectively reduce the fasting blood glucose of the type-2 diabetic rat and enhance the oral glucose tolerance dosage thereof; the acting effect of the extract is similar to that of metformin with the same dosage. An extracting technology is simple, the whole technological process can meet a food-grade requirement, and the moringa leaf extract can be applied to the field of medicines, health-care products, food and the like.

The invention relates to an oral glucose liquid composition and a preparation method thereof. The composition is prepared from maltodextrin, fructose, citric acid, sodium citrate, potassium citrate, a sweetening agent, a food flavor and a proper amount of purified water, and is mainly used for being orally taken by a patient suffering from perioperative management before an operation. The oral glucose liquid composition is capable of changing the energy storage under a limosis condition of the patient and keeping the carbohydrate metabolism, reducing the postoperative insulin resistance, alleviating preoperative thirst, hunger and anxiety, improving the postoperation subjective symptom of the patient so as to improve consciousness, reducing the body weight loss of emaciated patients, and shortening the hospitalization time.

The invention discloses florfenicol and a preparation process for compound recipe soluble powder thereof. The preparation process mainly comprises the following steps: taking 5+-0.5 grams of florfenicol, evenly mixing the florfenicol with 5-10 grams of polyethylene glycol 6000, grinding or crushing the mixture, adding oral glucose or lido powder into the mixture till the total weight reaches 100+-3 grams, screening the mixture through a No.4 sieve, packaging the mixture and obtaining the compound recipe soluble powder. The process has the advantages that: the process is simpler and quicker than an enclosing technology or a fusion eutectic technology and also has cost lower than that of the enclosing technology or the fusion eutectic technology.

The invention discloses a use of lactobacillus plantarum ST-III in preparation of an alpha-glucosidase inhibitor or the preparation of a fermented bean product with alpha-glucosidase inhibition activity. The invention further discloses fermented soymilk or fermented beans with the alpha-glucosidase inhibition activity, which can be obtained by inoculating the lactobacillus plantarum ST-III into sterile soymilk or cooked soymilk and fermenting at the temperature of 25-40 DEG C. Water is added into the fermented beans for homogenizing, the pH value is regulated to 6.5-7.5, the boiling is performed for 10-60 minutes, cooling is performed, then solid-liquid separation is performed, and a liquid phase is taken so as to get a water-soluble extract of the fermented soymilk. The lactobacillus plantarum ST-III has high alpha-glucosidase inhibition activity and can be used in glucose-reducing foods, health care products or medicaments. As the oral glucose-reducing foods, the health care products or the medicaments, the high postprandial blood glucose of patients with diabetes can be reduced and the postprandial blood glucose fluctuation can be regulated.

The invention discloses a pyrantel pamoate chewable tablet used for dogs and cats. The invention overcomes the poor palatability defect of the existing tablet to promote the thorough chewing absorption by dogs and cats, so as to effectively guarantee the medicine-supply dose, to enhance the cure rate of diseases of dogs and cats and to reduce the medicine waste. The tablet of the invention comprises the following components represented by weight-percentage: 1 to 5 percent of aspartame; 20 to 30 percent of a mixture of oral dextrose and degreased milk powder; the ratio of 1:1 to 1:4 between the oral dextrose and degreased milk powder in the mixture; 40 to 60 percent of excipient; 0.5 to 1 percent of glidant and 30 to 50 percent of pyrantel pamoate.

The invention belongs to the field of traditional Chinese medicine manufacturing, and relates to application of leonurine to preparation of a medicament for treating 2-type diabetes. Animal experiments prove that the fasting blood glucose of a 2-type diabetes mouse, i.e., a db/db mouse, can be lowered by the leonurine, and the tolerance of oral glucose is improved; and meanwhile, fasting plasma insulin is increased, the plasma triglyceride is reduced and the content of the plasma high-density lipoprotein is increased. Experiment results also show that the expression of liver glucose metabolic enzymes such as glucokinase, glucose-6-phosphatase and phosphoenolpyruvate carboxyl enzyme is adjusted by the leonurine in an Akt dependent mode; and the biological response of an inflammatory mediator, such as generation of TNF (Tumor Necrosis Factor)-alpha, degradation of IkB-alpha and subsequent phosphorylation of NF-kBp65, is suppressed. Through the leonurine, the inflammatory state of the 2-type diabetes can be corrected, and the symptoms of the 2-type diabetes can be improved; and the leonurine can be used as a treatment medicament to be applied to the treatment of the 2-type diabetes.

The invention relates to veterinary compound apramycin sulfate soluble powder and application thereof. The veterinary compound apramycin sulfate soluble powder is characterized by being prepared by mixing the following components according to unit weight of 100g: 3-25g of apramycin sulfate, 5-10g of colistin sulfate, 0.1-0.2g of atropine sulfate, 2-5mg of epidermal growth factor, and the balance of medically applicable auxiliary materials. The components with optimal contents are as follows: 15g of apramycin sulfate, 5g of colistin sulfate, 0.15g of atropine sulfate, 3mg of epidermal growth factor, and the balance of medically applicable auxiliary materials, wherein the auxiliary materials comprise more than one of sucrose, anhydrous glucose and oral glucose. The invention also discloses the application of the veterinary compound apramycin sulfate soluble powder to treatment of piglet yellow-white scour. By adopting the compound preparation of antibiotics, anticholinergics and epidermal growth factors, the invention has effective treatment effect for piglet yellow-white scour, has the efficacy of treating both the symptoms and root cause and reduces the bacterial resistance probability with simple preparation, obvious effect and wide application.

The invention provides a method for constructing a related intestinal canal-pancreatic islet regulation axis function evaluation model. The method includes: allowing a subject to take different oral hypoglycemic drugs or blank control in different stages, then performing intravenous-oral dual hyperglycemic clamp tests on the subject in each stage, drawing an area under the curve for a serum insulin value, a C-peptide value, a plasma glucagon value and an active glucagon-like polypeptide-1 (GLP-1) value acquired through the dual hyperglycemic clamp tests in each stage, and applying Metlab to perform 3D (three-dimensional surface fitting on the areas under the curve in one-to-one correspondence to obtain the related intestine-pancreas axis function evaluation model. By the method, two-phase insulin secretion patterns in intravenous-oral glucose stimulation states can be evaluated and compared accurately, besides, intestinal canal hormone effect and insulin-glucagon secretion can be related quantitatively, and accordingly an accurate intestine-pancreas axis effect model evaluation system is obtained.

The invention discloses a praziquantel chewable tablet used for dogs and cats. The invention overcomes the poor palatability defect of the existing tablet to promote the thorough chewing absorption by dogs and cats, so as to effectively guarantee the medicine-supply dose, to enhance the cure rate of diseases of dogs and cats and to reduce the medicine waste. The tablet of the invention comprises the following components represented by weight-percentage: 1 to 5 percent of aspartame; 20 to 30 percent of a mixture of oral dextrose and degreased milk powder; the ratio of 1:1 to 1:4 between the oral dextrose and degreased milk powder in the mixture; 40 to 60 percent of excipient; 0.5 to 1 percent of glidant and 30 to 50 percent of praziquantel.

The invention discloses an application of trepang sulphated polysaccharide in preparation of drugs, health food or and functional food for preventing, improving or treating diabetes mellitus II. The trepang sulphated polysaccharide is one or two of trepang chondroitin sulfate and trepang fucus chitosan sulfate. The animal experiment shows that the trepang sulphated polysaccharide obviously reduces the fasting plasma glucose of diabetic mice, improves the tolerance dose of oral glucose, reduces the insulin resistance index, and obviously raises and activates the PI3K/PKB/Glut4 signal transduction pathway mediated by the insulin. The trepang sulphated polysaccharide further obviously coordinates the antidiabetic drugs thiazolidinediones, and eliminates the side effects of glucose-lowering medications at the same time. The trepang sulphated polysaccharide disclosed by the invention has good effects on reducing the blood sugar and improving the resistance of the insulin, so that the trepang sulphated polysaccharide can be applied to development of the drugs and products for preventing, improving or treating the diabetes mellitus II.

The invention discloses an insect protein containing protein powder for pets. The protein powder comprises the following raw materials in parts by weight: 22-32 parts of insect protein, 10-15 parts of soy isolate protein, 13-19 parts of whey protein, 17-22 parts of oral glucose and 0.1 part of aspartame. By adopting the insect protein, in particular with tenebrio molitor as main raw material, the tenebrio molitor dry product contains 30% of fat and 50% or more protein, and further contains major elements of phosphorus, potassium, iron, sodium, aluminium and the like and a plurality of microelements, the application value is high; the tenebrio molitor is rich in protein content, complete in variety of amino acids and reasonable in composition; the special nutrients of the tenebrio molitor are easy to digest and absorb; the prepared protein powder for pets has functions in improving body immunity, resisting fatigue, reducing blood lipid, preventing cancer, prompting metabolism and the like; the immunity of pets are enhanced, the harmony and health are realized, the nutrient content of the protein powder is high, and the drug residue is avoided.

The invention belongs to the technical field of veterinary medicines, and specifically relates to a preparation method for compound tilmicosin enteric-coated granules. The preparation method sequentially comprises the steps of: preparing materials, mixing the materials, granulating, preparing a coating solution, coating and the like, wherein the raw materials of the granules are tilmicosin, colistin, gatifloxacin, a sweetening agent, a flavouring agent, bromhexine hydrochloride, oral glucose, corn starch, saccharose powder, dextrin, talcum powder and starch slurry; the raw materials of the coating solution are HPMC, Tween-80, polyethylene glycol 6000, talcum powder and ethanol. The method disclosed by the invention enables the tilmicosin effective ingredient not to be broken in gastric acid, and to safely arrive at intestinal tracts to be absorbed; the obtained compound tilmicosin enteric-coated granules are capable of preventing and treating respiratory diseases such as mycoplasma diseases, pleuropneumonia and swine plague, capable of reducing the occurrences of bacterial diseases such as diarrhoea and salmonellosis, and capable of increasing the feed conversion.

The invention discloses a buccal tablet applicable to being taken for type II diabetes. The buccal tablet is prepared from the following components in parts by weight: 18-22 parts of island stichopus japonicas sea cucumber fucoidan chitosan sulfate, 17-19 parts of astragalus polysaccharide, 14-16 parts of rehmannia extract, 15-16 parts of tremella polysaccharide, 9-12 parts of microcrystalline cellulose, 7-9 parts of newtol, 7-9 parts of magnesium stearate, 4-5 parts of sodium citrate, and 0.3-0.5 part of peppermint essence. By adopting the buccal tablet disclosed by the invention, the fasting blood-glucose content of the mice with the type II diabetes can be obviously reduced; the tolerance dose of oral glucose is improved; C peptide and fasting insulin level in the blood are increased. Therefore, the buccal tablet has the advantages of being convenient to take, easy to store, high in bioavailability, convenient to carry, and suitable for living demands of fast-paced people.

The invention relates to a method for calculating insulin action factor based on non-invasive blood glucose detection model of energy metabolism conservation method. The method includes the step thatthrough oral glucose test combined with insulin release test, a BP neural network structure based on MATLAB platform is used to predict and train the four insulin evaluation indicators. By adjusting the number of nodes in different hidden layers, and selecting transfer functions with different hidden layers and output layers, the training results have the strongest generalization ability and the most reliable predicting results.

The invention relates to a plant nutrient solution, and concretely relates to a nutrient solution for improving the transplanting survival rate of Chinese torreya. The nutrient solution can be sprinkled to Chinese torreya trees. The nutrient solution comprises oral glucose, compound sodium nitrophenolate, Leffingwell, potassium dihydrogen phosphate and water. The nutrient solution can rise the transplanting forestation survival rate of Chinese torreya to above 90% from normal 70%, and realizes a highest rate of 96%, and has the advantages of no dropping and good growing of transplanted Chinese torreya nursery stocks, provision of support for a large-scale forestation technology, effective breaking of the bottleneck of difficult Chinese torreya plantation, solving of the problem of low survival rate of big seedlings of Chinese torreya, reduction of loss of foresters, reduction of soil balls in big seedling transplanting, convenient transportation and construction, and great reduction of forestation cost.

The invention discloses a method for producing marasmius androsaceus fermented powder by adopting an optimized solid culture medium, belonging to the field of biological fermentation, providing rich nutrient substances for strain culture and solving the problems of long culture time and low mycelium yield. The method for producing marasmius androsaceus fermented powder by adopting the optimized solid culture medium comprises the following steps of sterilizing a solid culture medium; inoculating, culturing; extracting; concentrating and powdering, wherein the solid culture medium is prepared from the following components in parts by weight: 50-80 parts of wheat bran, 20-30 parts of rice hull, 5-20 parts of oral glucose, 0.05-0.2 part of potassium dihydrogen phosphate, 0.025-0.1 part of magnesium sulfate and the balance of water, wherein various inorganic potassium salts, especially potassium phosphate can be used as a potassium source. The substances have the stimulation action on the growth of marasins so that short culture time, high mycelium yield and shortened production time are achieved. The solid culture medium of the invention has cheap and easily-obtainable raw material components and low cost and is suitable for industrialized production.

The invention discloses an enrofloxacin chewable tablet used for dogs and cats. The invention overcomes the poor palatability defect of the existing tablet to promote the thorough chewing absorption by dogs and cats, so as to effectively guarantee the medicine-supply dose, to enhance the cure rate of diseases of dogs and cats and to reduce the medicine waste. The tablet of the invention comprises the following components represented by weight-percentage: 1 to 5 percent of aspartame; 20 to 30 percent of a mixture of oral dextrose and degreased milk powder, and the ratio of 1:1 to 1:4 between the oral dextrose and degreased milk powder in the mixture; 40 to 60 percent of excipient; 0.5 to 1 percent of glidant and 5 to 20 percent of enrofloxacin.

The invention discloses a compound medicine for preventing and treating enteritis of poultry, which contains the following constituents by mass percent: 10-40% of antibiotics, 0.1-1% of obstruent, 2-12% of intestinal mucosa protector, and the balance of auxiliary material. The antibiotics constituent in the compound medicine is one or more of aminoglycosides, polymyxins and berberine hydrochloride. The obstruent is one of scopolamine methobr, atropine, diphenoxylate, loperamide and bismuth subnitrate, or combinations of more. The intestinal mucosa protector is one of vitamin K3, cimetidine and glutamine, or combination of more. The auxiliary material is one of oral glucose, anhydrous glucose, soluble starch, dextrin and cyclodextrin, or combination of more. The invention further discloses a preparation method of the compound medicine for preventing and treating enteritis of poultry.

The invention discloses a compound mequindox soluble powder for animals and a preparation method thereof, which aims to provide the compound mequindox soluble powder for the animals and the preparation method, wherein, the compound mequindox soluble powder for the animals can treat the complex infection of shigella shigae and colon bacillus of pigs, is quick to take effect, can solve the treatment failure phenomenon caused by feeding and drinking conditions of the pigs during the illness, and improve the rate of liveweight growth; and the preparation method has a simple process and is easy to realize. The powder comprises the compositions in percentage by weight: 2 to 10 percent of mequindox, 0.5 to 5 percent of colistin sulfate, 6 to 30 percent of sodium salicylate, and the balance being oral glucose. The soluble powder is a compound preparation formed by a double antimicrobial drug combined with a suspending agent, has quick effect on the complex infection of the shigella shigae and the colon bacillus of the pigs due to the fact that the mequindox and the colistin sulfate are jointly used, is effective and highly efficient, can solve the treatment failure phenomenon caused by feeding and drinking problems during the illness, accelerate the recovery of the pigs, and increase the weight of the pigs.

The invention discloses penetration powder essence for betel nuts and a preparation method of the penetration powder essence, and relates to the technical field of food additives. The essence is prepared from the following components in percentage by weight: 3 to 5 percent of vanillin, 2 to 4 percent of ethyl maltol, 0.1 to 0.5 percent of methyl cyclopentenolone, 0.5 to 1 percent of maltol, 1 to 2percent of ethyl vanillin, 0.5 to 1 percent of a red jujube extract, 0.2 to 0.5 percent of benzaldehyde, 2 to 3 percent of an oil phase solvent, 1 to 2 percent of essential oil, 0.02 to 0.05 percentof an acid group, 0.02 to 0.05 percent of a formyl group, 0.02 to 0.05 percent of sugar lactone, 0.05 to 0.1 percent of furanone and the balance of oral glucose, wherein the total weight percent is 100 percent. The vanillin, the ethyl maltol, the methyl cyclopentenolone, the maltol, the ethyl vanillin, the red jujube extract and the furanone achieve a synergistic effect, so that the fragrance fixing effect can be enhanced; the acid group and the formyl group has the effect of adjusting the fragrance, and also can cooperatively improve the permeability of all components in the essence; during the soaking of the betel nuts, the penetration powder essence penetrates into the betel nuts; during drying, the fragrance is not liable to volatilization, and lasts for a long time.

The invention relates to a frying cake with the sweet and spicy flavor and a preparation method thereof. The frying cake comprises following raw material: 4500-5500 parts by weight of wheat flour, 550-650 parts by weight of palm oil, 1100-1300 parts by weight of water, 30-70 parts by weight of edible salt, 280-340 parts by weight of maltose, 20-30 parts by weight of monosodium glutamate, 3-5 parts by weight of anise, 10-20 parts by weight of cassia, 2-6 parts by weight of myrcia, 1-2 parts by weight of netmeg, 20-40 parts by weight of beef powder and 40-50 parts by weight of oral glucose. The frying cake with the sweet and spicy flavor and the preparation method thereof have following beneficial effects: the frying cake can provide people with nutrition and simulate appetite of people due to the sweet and spicy flavor; inflammation is avoided; due to the lovely and compact shape of the spiral appearance, the requirement for a diversified drying cake can be satisfied; and the frying cake is convenient to eat and easy to store so that people can have meals in short time because of busy lives so that the frying cake brings convenience for livelihood.

The invention relates to a children nutrient soy sauce, in particular to a children nutrient soy sauce and a preparation method thereof. The children nutrient soy sauce is prepared by the reaction of non-genetically modified high-quality soybean, flour, refined salt and mountain water. The preparation method comprises the following steps of: carrying out high-temperature short-time quick-freezing stewing on the non-genetically modified high-quality soybean; preparing a strain by using high-quality Aspergillus oryzae as a thick-layer ventilating solid; keeping high-salt dilute state for one day; fermenting by adopting a sunlight airing method; brewing for 100 days by using a traditional solarization and night dew method; heating semi-finished products; adding oral glucose, Lys-MCL and calcium lactate in sequence and blending; and ultrafiltering at high temperature and entering an automatic package line for filling after being qualified by inspection. The invention has the advantages of enhancing glucose, nuclear amino acid and active calcium, not adding any soy sauce pigment or essence, having low-salt and sweetness of products, strong sauce flavor, rich nutrient and mediated five flavors and being especially suitable for the taste and nutrient complementation of junior Children.

The invention relates to a chicken sandwich puffed food and a preparation method thereof. The chicken sandwich puffed food is composed of the components in parts by weight: 4500-5500 parts of wheat flour, 4500-5500 parts of chicken, 6500-7500 parts of cooking wine, 550-650 parts of an egg white liquid, 450-550 parts of starch, 450-550 parts of white granulated sugar, 550-650 parts of palm oil, 750-950 parts of water, 30-70 parts of edible salt, 280-340 parts of maltose, 15-25 parts of monosodium glutamate, 50-90 parts of a chicken powder, 6-14 parts of a soy sauce powder, 0.5-1.5 parts of a monascus red pigment, 0.5-1.5 parts of stevioside, and 14-22 parts of oral glucose. The chicken sandwich puffed food is prepared by the steps of roasting chicken, carrying out pulp hanging, then putting in dough blanks prepared from the wheat flour, deep-frying together and carrying out syrup hanging after deep-frying, is unique in taste and rich in nutrition, makes people appetite greatly promoted, and is beneficial to human body health.

The invention discloses an analgin chewable tablet used for dogs and cats. The invention overcomes the poor palatability defect of the existing tablet to promote the thorough chewing absorption by dogs and cats, so as to effectively guarantee the medicine-supply dose, to enhance the cure rate of diseases of dogs and cats and to reduce the medicine waste. The tablet of the invention comprises the following components represented by weight-percentage: 1 to 5 percent of aspartame; 20 to 30 percent of a mixture of oral dextrose and degreased milk powder; the ratio of 1:1 to 1:4 between the oral dextrose and degreased milk powder in the mixture; 40 to 60 percent of excipient; 0.5 to 1 percent of glidant and 30 to 50 percent of analgin.