119results about How to "Relieve nausea" patented technology

Active cooling of a person, such as to induce mild / moderate hypothermia, is accomplished by transferring heat from the persons body. Heat transfer and patient comfort are aided by administration of an anti-shivering drug and an anti-emetic drug.

The invention discloses an alcohol-alleviating anti-fatigue beverage, which is prepared by the following raw materials: 0.1-0.7% of corn oligopeptide, 0.1-0.9% of Hyriopsis cumingii polysaccharide, 0.02-0.3% of Maca powder, 0.05-1.2% of Paullinia cupana extractive, 0.01-0.04% of kudzu vine root, 0.1-0.3% of Turnjujube, 0.1-0.5% of liquorice, 0.01-1.0% of chrysanthemum, 0.02-1.0% of medlar, 0.04-0.06% of taurine, 3.0-6.0% of fructose and / or 3.0-6.0% of honey, 0.1-1.0% of isomaltitol and the balance of water. The beverage is used for alleviating alcohol and obviously improving the alcohol decomposition efficiency, can rapidly reduce the alcohol concentration in blood and has protection effects on livers and stomachs; and the beverage is good for eliminating uncomfortable drunkenness symptoms and has the advantages of anti-fatigue performance, capability of rapidly replenishing energy, refection and the like.

Disclosed is a production process of electuary for relieving effects of alcohol, wherein the constituents include (by weight ratio) kudzu vine root 19-22%, flower of kudzuvine 19-22%, hovenia dulcis thunb 19-22%, poria cocos wolf 6-12%, dried orange peel 6-12% and white hyacinth bean 19-22%.

The invention provides a method for preparing an enhanced DC-CIK cell induced by traditional Chinese medicines. The method comprises the step of adding extracts of radix astragali and radix codonopsitis into a DC or CIK cell culture fluid or DC-CIK cell culture fluid or DC, CIK and DC-CIK cell culture fluids, wherein the extracts of radix astragali and radix codonopsitis are radix astragali polysaccharide and radix codonopsitis polysaccharide. According to the method disclosed by the invention, the activity and the functions of the DC or CIK cell can be activated, and the specificity of the DC-CIK cell is improved so that the DC-CIK cell can resist tumor in the body for long time; a large amount of DC-CIK cells can be obtained according to the method, and the cell culture time is reduced; the enhanced DC-CIK cells obtained according to the method disclosed by the invention can be used for cell treatment of tumor diseases, and can directly kill tumor cells and adjust the immunity of the body when re-infused into the body.

The invention provides an anti-dizziness chair capable of being automatically balanced which is installed on a vehicle. The anti-dizziness chair capable of being automatically balanced comprises a seat, a stable platform and a vibration absorber. The anti-dizziness chair has the characteristics that: the vibration absorber comprises a base which can be fixed with the vehicle, a semicircular ring which is fixed with the stable platform, horizontal and vertical gyro stabilizers which are installed under the stable platform, an outer circular ring which is connected with the base through a magnet vibration absorber, and inner circular rings which are provided with two pairs of concentric holes with mutually vertical axes along ring centers, wherein the outer circular ring which is out of the inner circular rings is hinged with the inner circular rings in one pair of the concentric holes and the semicircular ring which is under the inner circular rings is hinged with the inner circular rings in the other pair of the concentric holes. With the adoption of the anti-dizziness chair provided by the invention, gestures can be automatically adjusted when the vehicle sways from left to right and from front to back and the balance can be kept; when the vehicle bumps or fluctuates, the anti-dizziness chair also can be freely moved to carry out amplitude decreasing or amplitude increasing, so that the conditions that passengers feel sick, vomit, feel uncomfortable and the like can be relieved, and carsickness, seasickness and airsickness can be reduced.

The invention provides entecavir fatty acid derivatives and pharmaceutical composition thereof and further relates to preparation methods of the entecavir fatty acid derivatives. The entecavir fatty acid derivatives had higher bioavailability and smaller toxic and side effects, and the pharmaceutical composition of the entecavir fatty acid derivatives is safer and more efficient when used for treating hepatitis B virus infection.

The invention discloses a method for producing raisin tree seed sobering tea. The raisin tree seed sobering tea comprises the following components: 35 to 45 percent of raisin tree seeds, 25 to 35 percent of kudzuvine root, 15 to 25 percent of raisin tree leaves and 10 to 15 percent of bud tea. The raisin tree seed sobering tea solves the problems that the traditional water, tea and vinegar drinking modes for sobering are slow and the natural sobering medicaments such as kudzuvine root and kudzuvine flower have weak effect of conditioning the spleen and stomach and have no pure enough medicinal properties, and is suitable for wine drinkers and drunk people to drink.

The invention discloses a synbiotic composition as well as a preparation and application thereof. The synbiotic composition comprises prebiotics and probiotics in the weight ratio of the prebiotics tothe probiotics being (1-10) to (1-10). The synbiotic composition can exert the physiological and pathological bacterial activity of the probiotics, and through cooperation with the prebiotics, can selectively and quickly increase the quantity of the probiotics, so that the action speed of the probiotics is high, the effect is durable, and the physiological function of the probiotics and the prebiotics can be exerted at the same time. The synbiotic composition can effectively promote the repair of damage caused by antibiotics and damage caused by chemotherapy, and can particularly promote therepair of damage for a digestive system. Through scientific selection of combination of the probiotics and the prebiotics, and through an appropriate compounding ratio of the components, the synbioticcomposition is clear and notable in efficacy, the components are safe and effective, and the raw materials are reasonable in collocation. The synbiotic composition disclosed by the invention also hasthe advantages of being notable in effects, taking effect quickly, and being high in safety.

The invention relates to the technical field of a dairy product, particularly to stomach-protecting yoghurt powder. The stomach-protecting yoghurt powder comprises components, by mass part: 90-100 parts of milk powder, 10-20 parts of lactalbumin powder, 1-10 parts of phosphatide, 3-5 parts of corn oligopeptide, 0.5-2 parts of yam flour, 0.01-0.05 part of dahurian angelica roots, 0.1-0.5 part of flos puerariae, 0.1-0.5 part of ginseng, 1-15 parts of fucoidin, 1-15 parts of soybean oligosaccharide, 0.01-2 parts of lactobacillus powder, 3-8 parts of soluble dietary fiber, 0.001-0.003 part of vitamin B, and 0.001-0.003 part of vitamin C. A customer can ferment the yoghurt powder by himself or herself according to his or her requirements, and the manufacture process is simple. The yoghurt powder contains yam and flos puerariae, can make a protective membrane formed on the gastric wall, reduces alcohol irritation to the gastric mucosa, and reduces the absorption rate of the stomach to alcohol. The yoghurt powder contains corn oligopeptide and ginseng, improves the function of detoxifying the liver, prevents interference of alcohol to metabolism of a human body, and relieves symptoms of headache, nausea and hangover due to drunkenness.

The invention discloses a weakly-alkaline anti-alcoholism and hepatoprotective hovenia and mesona tea and a preparation method thereof, solving the problems of dizziness, headache, stomach pain and liver pain caused by drinking too much or for a long time. The weakly-alkaline anti-alcoholism and hepatoprotective hovenia and mesona tea is prepared by hovenia, mesona, kudzuvine flower, kudzuvine root, dark plum, tangerine peel, licorice, sodium bicarbonate and white sugar in a certain weight ratio. The anti-alcoholism and hepatoprotective health-care heat-removing tea is convenient to drink in daily life, can be drunk in the drinking process or after drinking too much, has the effects of avoiding drunkenness and helping to recover from the drunkenness, and has the effects of removing heat and detoxifying, nourishing Yin and blood, relaxing bowel, nourishing the lung and promoting the secretion of saliva or body fluid; when being used for relieving the alcoholism, the anti-alcoholism and hepatoprotective health-care heat-removing tea is quick to take effect and good in effect; the anti-alcoholism and hepatoprotective health-care heat-removing tea is simple in components, comprehensive in functions, mild in efficacy and free of toxic side effects and has a variety of health-care effects; the shapes of the selected raw materials are in accordance with customary understanding of the heat-removing tea; and the anti-alcoholism and hepatoprotective health-care heat-removing tea has a pure and mild taste after drinking.

The invention discloses a gastrointestinal contrast agent containing a traditional Chinese medicine extract. The gastrointestinal contrast agent is prepared from the following components in parts by weight: 55-75 parts of barium sulfate, 5-15 parts of the traditional Chinese medicine extract and 20 parts of mannitol, wherein the traditional Chinese medicine extract is prepared by the following steps: taking 25 parts of tuber fleeceflower stems, 15 parts of polygala tenuifolia, 10 parts of rhizoma acori graminei, 8 parts of cynanchum auriculatum, 25 parts of seville orange flowers, 15 parts of emblic leafflower fruits, 25 parts of hawthorn, 10 parts of white hyacinth beans, 10 parts of edestan, 15 parts of radix curcumae, 25 parts of astragalus membranaceus, 15 parts of codonopsis pilosula, 15 parts of sedum sarmentosum, 15 parts of pseudo-ginseng and 25 parts of liquorice; mixing; soaking with water; decocting; filtering to obtain a filtrate; and drying the filtrate to obtain the gastrointestinal contrast agent. The gastrointestinal contrast agent disclosed by the invention has the beneficial effects of shortening the inspection time, relieving the side effects brought by X-ray inspection, has a maintaining or health-care effect on stomach, liver and the like and is good in using effect.

The invention discloses a glipizide enteric sustained-release preparation combination and a preparation method thereof. The glipizide enteric sustained-release preparation combination is mainly prepared from glipizide bulk drugs, sustained-release materials, enteric materials and other appropriate auxiliary materials. The glipizide enteric sustained-release preparation provided by the invention can not only prevent glipizide from disintegrating in the stomach and causing irritation to gastric mucosa and avoid the adverse reactions caused by the administration, such as nausea, abdominal pain, diarrhea and the like, but also deaccelerate the release rate of drugs, reduce the frequency of administration and improve the patient compliance. The invention provides a novel form of drug featuring higher safety and better patient compliance and having the advantages of high quality controllability and stability of the preparation process.

The invention discloses a gastrointestinal contrast agent containing traditional Chinese medicine ingredients. The gastrointestinal contrast agent consists of the following components in parts by weight: 55-75 parts of barium sulfate, 5-15 parts of a traditional Chinese medicine extract and 20 parts of mannitol, wherein the traditional Chinese medicine extract is prepared by a method comprising the following steps: mixing the following materials in parts by weight: 20-30 parts of bark of Chinese corktree, 10-20 parts of dried tangerine peel, 10-20 parts of coix seed, 5-10 parts of all-grass of hirsute gonostegia, 10-20 parts of tuckahoe, 20-30 parts of hawthorn, 5-15 parts of herb of christensen ceropegia, 20-30 parts of officinal magnolia bark, 10-20 parts of immature bitter orange, 20-30 parts of dwarf lilyturf tuber, 10-20 parts of Chinese angelica, 10-20 parts of turmeric root-tuber, 5-15 parts of Chinese caterpillar fungus and 10-20 parts of licorice; mixing; immerging by adding water; decocting; filtering; and drying. The gastrointestinal contrast agent disclosed by the invention can achieve beneficial effects of shortening the examination time, relieving side effects (nausea, emesis, inappetence and fatigue) caused by X-ray examination and the like, can also achieve an effect of nourishing or taking good care of stomach, liver and the like, and has a better using effect.

The invention provides a traditional Chinese medicine health-care cervical vertebra pillow. The cervical vertebra pillow comprises a pillow sleeve 1 and a pillow inner 2 located in the pillow sleeve 1. The pillow inner 2 comprises, by weight, 20 parts to 25 parts of agastache, 21 parts to 26 parts of mints, 10 parts to 12 parts of schisandra chinensis, 85 parts to 110 pars of semen cassiae and 90 parts to 120 parts of tartary buckwheat. The clinic use proves that according to the clinical symptoms and signs of cervical spondylosis and the corresponding physical examination result, after the traditional Chinese medicine health-care cervical vertebra pillow is used, the corresponding clinical symptoms are obviously relieved, the specialized examination result which is originally positive is converted to be weakly positive or negative, and the average service life is 19.64 days.

An herbal preparation for relief of sleep apnea contains lobelia and / or lobelia extract material acting as a respiratory stimulant in combination with meadowsweet to reduce nausea. Optional but preferred materials also include thyme to increase pleural activity, together with chamomile and cramp bark to facilitate relaxation.

The invention relates to a traditional Chinese medicine preparation used for alleviating nausea of pregnant women. It is well known that pregnant women are prone to nausea of pregnancy reaction during pregnancy and especially within the first three months after conception, which makes pregnant women suffer. Also, because of the unborn child, the pregnant women shouldn't take any western medicine containing chemical component during pregnancy. There is currently no solution to the situation, such that the majority of pregnant women are in pain.

The invention discloses a liquid feed bag which comprises a bag body made of a flexible material, wherein a liquid orifice used for allowing liquid to flow in and out of the bag body and an air orifice used for allowing air to flow in and out of the bag body are formed in the bag body; a liquid tube is inserted into the liquid orifice and connected with the bag body in a sealed manner; the tail end of the liquid tube stretches into the bottom of the interior of the bag body; concentrated liquor or dried powder of a corresponding amount is filled in the bag body according to the volume of the bag body and the concentration of the needed solution; the interior of the bag body is vacuumized, and when the preparation needs to be prepared, reverse osmosis water is injected into the bag body through the liquid tube. The invention further provides a displacement liquid preparation system which comprises the liquid feed bag, and a blood circuit, a blood filter, a displacement liquid circuit, a dialysate supply switch circuit and a waste liquid discharging circuit. The invention has the beneficial effects of being automatic in adjustment, high in control precision, wide in usage range, convenient to use, low in cost, stable and reliable.

The present invention provides a trospium chloride slow-release composition and a preparation method thereof. According to the trospium chloride slow-release composition, an active drug component trospium chloride, an enteric material and a slow-release material are directly mixed according to a specific ratio so as to be adopted as a slow-release coating layer, such that rapid-release, slow-release and enteric delayed-release can be integrated, the drug release behavior and the blood drug level are stable, the toxic-side effect is reduced, and the treatment effect is good. The trospium chloride slow-release composition comprises, by weight, 40-60 parts of a blank pill core, 20-30 parts of a drug loading layer wrapped on the blank pill core, 1-5 parts of a separation layer wrapped on the drug loading layer, and 20-30 parts of a slow-release coating layer wrapped outside the separation layer, wherein the active drug of the drug loading layer is trospium chloride, and the slow-release coating layer comprises, by weight, 19-26 parts of a slow-release material, 0.8-1.8 parts of an enteric material and 0.2-1.2 parts of trospium chloride.

The present invention provides a dispersible tablet dosage form of doxifluridine, which is characterized by its speedy decentralization and dissolution when being in vitro. Through clinical applications, it is found that compared to common doxifluridine capsules, the clinical curative effect is considerably improved, at the same time the adverse reaction is remarkably reduced and unexpected effects are acquired. In accordance with the present invention, for extensive cancer patients executing chemotherapy by adopting doxifluridine, the pains of chemotherapy are considerably alleviated, the neoplastic chemotherapy effect is improved, and said medicine has prodigious clinical use values; 5-FU is a specific anti-metabolizing medicine during the S period, and the unexpected effects obtained in accordance with the present invention are of good enlightening significance for researching pharmacodynamics features and mechanism of action of doxifluridine. In addition, it is convenient for aged and children to take the medicine in accordance with the present invention, with stable formulation, fast absorption, high bioavailability and few adverse reaction, which can be used as medicine for treating breast carcinoma, cancer of stomach, carcinoma of colon, restocarcinoma, nasopharyngeal carcinoma and the like.

The invention relates to a combination therapy for the treatment of tumors and tumor metastases comprising administration of integrin ligands, preferably integrin antagonists, together with co-therapeutic agents or therapy forms that have synergistic efficacy when administered consecutively with said ligands, such as chemotherapeutic agents and or radiation therapy. The therapy results in a synergistic potential increase of the inhibition effect of each individual therapeutic on tumor cell proliferation, yielding more effective treatment than found by administering an individual component alone, concurrently or not in the dosage regime of the present invention.

The invention discloses a double-cavity balance fluid supply system with fluid preparation functions for purifying blood. The double-cavity balance fluid supply system comprises a blood circuit, a blood filter, a substitution fluid circuit, a dialysis fluid supply switching circuit and a waste fluid drain circuit. A first inlet of the blood filter is communicated with an outlet of the dialysis fluid supply switching circuit and the arteries of a human body via the blood circuit, and a first outlet of the blood filter is communicated with the veins of the human body via the blood circuit; a second inlet of the blood filter is communicated with an outlet of the substitution fluid circuit via the dialysis fluid supply switching circuit, and fluid can be outwardly drained from a second outlet of the blood filter via the dialysis fluid supply switching circuit and the waste fluid drain circuit; the dialysis fluid supply switching circuit comprises at least two supply circuits, and the various supply circuits are alternately communicated with the second inlet of the blood filter or closed to the second inlet of the blood filter and can be alternately communicated with the second outlet of the blood filter or closed to the second outlet of the blood filter, so that continuous supply structures can be switched over. The double-cavity balance fluid supply system has the advantages of automatic adjustment, high control precision, convenience in use, stability and reliability.

The invention relates to a traditional Chinese medicine preparation for treating peptic ulcer. The preparation is composed of the following traditional Chinese herbals: cuttlefish bone, banksia rose, dittany bark, rhizoma corydalis, pseudo-ginseng powder, dark plum, rheum officinale, bletilla striata, Korean pine bark charcoal, chorion ovi, curcuma tuber, indigo naturalis, borneol, pomegranate rind, scorched bighead atractylodes rhizome, radix bupleuri, and adenophora root, and has the functions of neutralizing acid, astringing ulcer, activating blood, removing stasis, promoting tissue generation, regulating qi, relieving pains, soothing the liver, invigorating the stomach, warming the middle, and dissipating cold. The drug directly acts on the internal organs after being orally taken, is capable of reducing the acid concentration in stomach and improving the pH value of the stomach, can reduce the pepsin activity, promote the repairing of gastric mucosa, and strengthen the defensive performance of gastric mucosa, can also promote the proliferation of mucosa cells, and maintain the integrity of mucosa, moreover, is capable of inhibiting the activity of gastric wall cells and acid secretion caused by various irritants, promotes the gastric dynamic to recover the self-adjusting performance of the digestive system, can radically eliminate the symptoms such as nausea, emesis, abdominal distention, and the like, and finally radically cures the peptic ulcer.

A scent-releasing strip includes a release liner and a plurality of tab units coupled to the liner. Each of the plurality of tab units includes a sealed pouch having a pad dosed with at least one scent-emitting substance. The scent may induce a physiological effect. The sealed pouch is disposed on a base label. The pad may be an aroma-containing pad that includes at least one of an oil or other substance that emits a desired fragrance.

The present invention is directed to the treatment of chronic pain that occurs in chronic disease such as chronic pancreatitis by the application, of the drug, resiniferatoxin, to a visceral organ, such as the stomach, which then reduces the pain present in a second visceral organ, such as the pancreas. The reduction of said pain associated with the chronic disease occurs through the drug-induced desensitization of primary pain-sensing neurons that are shared between the two visceral organs. Additionally, application of the drug resiniferatoxin into the first organ, reduces the inflammation that occurs in the second diseased organ. This modulation of shared nerve activity by application of resiniferatoxin, may also be directed to modulate the pain and inflammation in any two visceral organs that share a common spinal or vagal nerve. Finally, application of the drug resiniferatoxin to either the stomach or the jejunum may be used to treat disease and disorders that involve gastroparesis. The resiniferatoxin improves gastric emptying and reduces nausea, thus may be effective therapy for these conditions.

The invention discloses a functional drink for decreasing internal heat, invigorating stomach and protecting liver and a preparation technology thereof. The functional drink for decreasing internal heat, invigorating stomach and protecting liver is prepared from the following materials: 1-5 parts of mung beans, 1-5 pats of root of kudzuvine, 1-5 parts of chrysanthemum flower, 1-5 parts of hawthorn, 1-5 parts of malt, 1-5 parts of flower of kudzuvine, 1-5 parts of fruit of Japanses raisintree, 1-5 parts of honey or white sugar, and 100-150 parts of purified water. The functional drink for decreasing internal heat, invigorating stomach and protecting liver contains various plant ingredients, and main raw materials of the functional drink come from natural plants with homology of medicine and food. The functional drink has certain effects of decreasing internal heat, invigorating stomach, protecting liver, increasing physical strength and the like, can alleviate the damages of liver, stomach and kidney caused by long-time drinking, and can improve the immunity of a human body.

The invention discloses a solute clearing monitoring system of blood purification equipment. The solute clearing monitoring system comprises a blood loop, a blood filter, a displacement liquid loop, a dialysate supply switching loop and a waste liquid discharging loop, wherein a first electric conducting detection device is connected in series between a second inlet of the blood filter and the dialysate supply switching loop; a second electric conducting detection device is connected in series between a second outlet of the blood filter and the dialysate supply switching loop. The invention also provides a solute clearing monitoring method of the blood purification equipment; the method comprises the following steps of (1) respectively detecting the electrical conductivity of the second inlet and the second outlet of the blood filter through the first electric conducting detection device and the second electric conducting detection device every other set time; (2) obtaining the clearing rate of dialyzate ions according to an expression; (3) calculating a urea clearing kinetic model. The system and the method have the advantages that the monitoring on the concentration of the cleared solute in real time can be realized; the concentration of concentrated electrolyte A and B does not need to be changed in the real-time monitoring process.

The invention discloses a method for preparing a Rhodiola rosea traditional Chinese medicinal decoction piece. The method concretely comprises the following steps: cleaning Rhodiola rosea rhizomes byusing a medicine washing machine, immersing the cleaned Rhodiola rosea in ammonia water, performing ultraviolet irradiation to promote the generation of salidroside and salidroside aglycone in Rhodiola rosea, immersing the Rhodiola rosea in a prepared medicinal liquor to improve the medicinal property of the Rhodiola rosea to be mild, stirring the Rhodiola rosea with a ginger juice, stewing the Rhodiola rosea in a pressure cooker, stir-frying the Rhodiola rosea above weak fire, performing far-infrared radiation drying, and breaking the dried Rhodiola rosea to form slices. The method has the advantages of simplicity in preparation, effectiveness in improvement of the absorption of Rhodiola rosea by human bodies, and wide application prospect.

A scent-releasing strip includes a release liner and a plurality of tab units coupled to the liner. Each of the plurality of tab units includes a sealed pouch having a pad dosed with at least one scent-emitting substance. The scent may induce a physiological effect. The sealed pouch is disposed on a base label. The pad may be an aroma-containing pad that includes at least one of an oil or other substance that emits a desired fragrance.