45results about How to "Take fast" patented technology

A dispersing table of amlodipine benzosulfonate for treating hypertension is proportionally prepared from amlodipine benzosulfonate, microcrystalline cellulose, anhydrous lactose, carboxymethyl starch sodium, micropowdered silica gel, and magnesium stearate.

The invention discloses respiratory equipment for the respiration medicine department. The respiratory equipment comprises a respirator body, an atomizer, a drug mixing device, an oxygen tank and a mask, wherein the drug mixing device is arranged on one side of the respirator body; a stirring paddle is arranged in the drug mixing device; a rotary motor is arranged above the drug mixing device, and is connected with the stirring paddle; a water tank and the atomizer which is arranged on one side of the water tank are arranged on one side of the drug mixing device; and the oxygen tank is arranged on one side of the atomizer; and the mask is arranged on one side of the respirator body. The respiratory equipment is simple in structure, novel in design and convenient to use, is convenient for people to respire oxygen, can be used for heating oxygen, saving space and generating negative oxygen ions beneficial to human bodies, enables the atomized medicine to enter a human body along with the absorbed oxygen so as to quickly take the medicine, can be used for reminding people when the mask falls down or is loose, and is beneficial to large-scale popularization and application.

The invention provides a method of preparing a quick-acting jiuxin orally disintegrating tablet through 3D printing. The disintegrating tablet is formed by spraying a bonder through a nozzle of a 3D printer to bond medicinal powder, the medicinal powder comprises, by mass, 76-85% of, 12-18% of and 2-6% of, and 3D printing parameters include spraying radius of 2.5-10mm, spraying layer height of 0.1-0.5mm and spraying layer number of 10-50 layers. Heating is not needed in the preparation process, so that loss of active ingredients, such as borneol, which are unstable when being heated in conventional preparation methods is avoided; the disintegrating tablet prepared is high in medicine release speed, content of active ingredients meets requirements of the Chinese Pharmacopoeia, and the disintegrating tablet is especially suitable for acute diseases such as coronary heart disease and angina.

The invention discloses a medicinal composition containing sildenafil citrate and PD-1 type pregelatinized starch and a preparation method thereof. The medicinal preparation prepared from the medicinal composition containing the sildenafil citrate and the PD-1 type pregelatinized starch and the preparation method provided by the invention can be completely disintegrated in water at a degree of 37 DEG C within 15 to 30 seconds, and can pass through a screen in a size of 600 to 710 mu m.

The invention provides a phloroglucinol oral disintegrating tablet, which takes the phloroglucinol as the active ingredient, and disintegrating agents, fillers, lubricants, flavoring agents, binding agents and effervescent agents are added for preparation. The invention further provides a preparation method of the phloroglucinol oral disintegrating tablet. The phloroglucinol oral disintegrating tablet of the invention not only has the rapid disintegration, good taste and no sense of gravel, but can also can be taken under the condition of no water and have the rapid action and more convenient taking, so the invention can improve the compliance of the patients and the efficacy of the drug and other features of the orally disintegrating tablet, at the same time, the invention has light tablet weight, small volume, no powder falling, good brittleness and better dissolution effect than the freeze-dried orally disintegrating tablet. The production cost is low, the dissolution is faster, the invention is more beneficial to the absorption, and the invention can play the effect of pain reliving faster. The invention has the advantage that the invention can carry out the preparation by only adopting the ordinary pressing equipments and the simple technique without the need of special production equipments and conditions.

The present invention discloses unhatched-egg-extract-containing senile cardiovascular disease prevention instant powder, and relates to the technical field of health food products, and the unhatched-egg-extract--containing senile cardiovascular disease prevention instant powder is made from the following raw materials in parts by weight: 5-10 parts of a live-birth unhatched-egg-extract, 8-15 parts of live-birth unhatched-egg yolk powder, 20-25 parts of ginkgo biloba leaf, 15-20 parts of black fungus, 15-20 parts of spinach root, 15-20 parts of coconut powder, 13-16 parts of cattail pollen, 10-15 parts of maltodextrin, 10-15 parts of angelica, 10-15 parts of grape seed, 8-13 parts of cinnamon leaf, 7-11 parts of myotonin rice bran oil, 6-10 parts of cortex periplocae, 6-10 parts of wine residue, 5-8 parts bitter gourd seeds and 4-6 parts of kelp. The unhatched-egg-extract-containing senile cardiovascular disease prevention instant powder has rich nutritional value and good preventive effect, has no side effects after taking, is easy to take, can be quickly dissolved in water, can be easily absorbed and metabolized by human body after taking, and is an effective senile cardiovascular disease prevention product.

The invention discloses ferment with a function of loosening the bowel to relieve constipation and a preparation method and application thereof. The ferment is prepared from, by weight, 25-68 parts ofChinese herbal medicines, 32-76 parts of fruits, 5.8-7.9 parts of an ingredient and compound microorganisms through extracting and fermenting, wherein the adding amount of the compound microorganismsis 0.08-0.15 time of the total amount of the raw materials; the Chinese herbal medicines are one or more of fructus hippophae, herba houttuyniae, polygonatum kingianum, semen raphani and the root ofkudzu vine; the fruits are one or more of apples, blood oranges, blueberries, cranberries, red grapes, white grapes, pomegranate, pineapples and blackcurrant; the ingredient is a mixture of hydrolyzedcollagen powder, pumpkin seeds and fructo-oligose; the compound microorganisms are one or more of acetic bacteria, lactic acid bacteria and saccharomycetes. The ferment can improve intestinal flora,has the functions of relieve the constipation and improve the taste. The raw materials are easy to obtain, the required device is simple, the process can be controlled, and the practical popularization value is important.

The invention relates to a drug doser which is capable of dosing rapidly. An upper bottle body and a lower bottle body of the drug doser are designed independently, so that the drug doser can be assembled and disassembled conveniently, and operations such as sterilization and the like can be achieved according to different natures of substances held by the upper bottle body and the lower bottle body. By pressing a piston downwards, the piston punctures seal film, a first accommodation cavity is communicated with a second accommodation cavity through a guide groove, and accordingly, accommodation substances in the second accommodation cavity can enter the first accommodation cavity along the guide groove to be mixed with the accommodation substances in the first accommodation cavity. When mixing is completed, the lower bottle body is taken out directly, the mixed substances can be poured out from an opening end directly, drugs can be taken rapidly, and the drug doser is convenient to use.

The invention discloses a preparation method of calcium iron zinc selenium vitamin tablets. The preparation method of the calcium iron zinc selenium vitamin tablets comprises the following steps: mixing calcium carbonate, ferrous fumarate, zinc citrate, selenium-enriched yeast, vitamin A, vitamin D3, vitamin C, magnesium stearate, maltodextrin, stevioside and starch uniformly, and performing boiling pelletization to obtain a first prefabricated material; mixing microcrystalline cellulose and a gelatin compound uniformly to obtain a second prefabricated material; mixing the second prefabricated material, the first prefabricated material and talcum powder, pelletizing for the second time, and tabletting to obtain the calcium iron zinc selenium vitamin tablets. The calcium iron zinc selenium vitamin tablets obtained by the method have extremely high stability and long shelf life of effective components, and can be disintegrated quickly after entering intestines and stomach.

The present invention relates to functional food or health food, and more specifically discloses a composition for treating diarrhea and use thereof. The composition comprises the following components in parts by weight: 5 to 20 parts of ginseng, 5 to 20 parts of Gorgon fruit, 5 to 15 parts of tuckahoe, 20 to 30 parts of yam, 5 to 10 parts of white hyacinth Bean, 5 to 10 parts of fried lotus seeds, 10 to 20 parts of Coix seed, 5 to 10 parts of Amomum villosum, 5 to 10 parts of Platycodon grandiflorum and 5 to 10 parts of licorice. The components are combined and used for the purpose of treating the diarrhea by regulating of gastrointestinal function, invigorating the spleen and nourishing the stomach and dehumidifying and stopping diarrhea, and can be applied to people with the problems of diarrhea caused by irregular eating, quick meal and unhealthy outside food. Granules provided by the present invention are easy to carry, fast to take and good in taste and have a unique aroma. The composition applied to the treatment of diarrhea diseases has the characteristics of short taking period, good curative effect and no side effect and the like compared with conventional drugs for treating diarrhea.

The invention belongs to the field of food and particularly relates to lucid ganoderma effervescent tablets and a preparation method thereof. The lucid ganoderma essence effervescent tablets are prepared from ganoderma spore extract, NaHCO3, tartaric acid, lactose, tea polyphenol, cacao husk pigments, PEG6000, jasmine flower essence, green tea and absolute ethyl alcohol. According to the lucid ganoderma effervescent tablets and the preparation method thereof, the ganoderma spore extract serves as a main raw material of the lucid ganoderma healthcare products, the content of effective nutritional ingredients is increased, the bioavailability of the effective nutritional ingredients in the human body is improved, and the advantages of soothing the nerves of the human body, aiding sleep, improving immunity and the like of lucid ganoderma are enhanced. The tea polyphenol, the cacao husk pigments, the jasmine flower essence, green tea essence, lactose and other high-quality flavoring agents are added, and the taste of ganoderma spore powder is improved. The prepared lucid ganoderma essence effervescent tablets have the advantages of being rapid in disintegration, convenient to take and rapid in effect taking, high bioavailability is achieved, and healthcare benefits can be increased.

Disclosed is a device for closing in a tightening nut and a pipe joint module through an oil press. The device comprises a base, a closing low mold, a core rod, a mold core, a closing upper mold, a closing sleeve, an adjusting cushion and a limiting seat. The base is arranged on the workbench of the oil press; the mold core is threadedly arranged inside the core rod; the mold core and the core rod are arranged inside the base; the closing lower mold is arranged in transition fit inside the base; the limiting seat is arranged on the workbench of the oil press; the base is arranged inside the limiting seat; the adjusting cushion is arranged inside a shallow circular truncated cone at the upper end of the limiting base; the closing upper mold is arranged on the closing lower mold; the closing sleeve is arranged on a hydraulic press connecting seat. The device for closing in the tightening nut and the pipe joint module through the oil press is small in size, compact in structure, simple in operation, high in loading and unloading speed, accurate in axial and radial positioning of parts, high in consistency of closed portions of the closed parts, uniform and stable in experimental data and high in product percent of pass.

The invention discloses an ambroxol hydrochloride oally disintegrating tablet and a preparation method thereof. The orally disintegrating tablet consists of effective dose of ambroxol hydrochloride and pharmaceutical adjuvants, wherein the pharmaceutical adjuvants include a taste masking agent, a filler, a flavoring agent, a disintegrant, an adhesive and a lubricant; and the disintegrant is a combination of cross-linked povidone and other disintegrants. The ambroxol hydrochloride oally disintegrating tablet prepared by the invention has the characteristics of being convenient to take without the use of water, rapid in disintegrating, rapid in absorption, high in bioavailability and the like. The preparation method of the finished product (the ambroxol hydrochloride oally disintegrating tablet) provided by the invention is low in cost, simple in processing equipment, easy and controllable in implementation, low in operating cost, economic and convenient, and applicable to large-scale production.

A Chinese medicine for treating menalgia is prepared from cyperus tuber and Chinese angelica root through extracting by supercritical CO2 and dispensing. Its preparing process is also disclosed.

The invention discloses a common turnip composition with anti-hypoxia function and a preparation method and application thereof. Homologous materials of medicine and food-common turnip, root of silverweed cinquefoil and fructus hippophae are used as main materials and are extracted and refined to make a preparation, and the preparation can be used in medicine, health food, food, and the like. Theinvention has the advantages of unique and concise formula, high extraction rate of effective components, remarkable function, no toxic and side effects, rapid absorption, convenient taking, and the like. The composition integrates functions of anti-hypoxia and enhancing immunity and can be safely taken for a long time.

The invention discloses an oral disintegrating tablet for treating cough, whose medicinal active component is dextromethorphan hydrobromide, the weight portions for each component are, dextromethorphan Hydrobromide 1 part, filling agent 1-30 parts, crumbling agent 0.4-5 parts, flavoring agent 0.01-0.08 part. The tablet has the advantages of right hardness, good taste, quick action, facilitated administration and carrying. Its disintegration time is superior to the common tablets, its stability is higher than the solution agent. The tablet is recommended for children, the aged people, patients with deglutition obstacle or in field operations.

The invention discloses a medicament for treating seborrheic dermatitis. The medicament is prepared from the following raw material medicaments by weight: 15 to 20g of honeysuckle flower, 15 to 20g of scutellaria root, 15 to 18g of Chinese angelica, 10 to 15g of liquorice, 10 to 15g of Mongolian dandelion herb, 8 to 10g of selfheal spike, 7 to 10g of rehmannia root and 8 to 10g of folium artemisiae argyi. The medicament has the advantages of high recovery rate, simple using method, thorough treatment and no relapse after recovery.

A detection device which, when an arrhythmia occurs, can prompt rapid taking of a countermeasure against the arrhythmia, and an alarm system having the detection device are provided. A portable detection device 10 has: a measuring section which can measure an electrocardiogram in a state where the section is applied to the body surface of the user; an analyzing section which analyzes whether the electrocardiogram contains an abnormal waveform indicating an arrhythmia or not; and a transmitting section which, if the analyzing section detects the abnormal waveform, transmits a detection signal indicating that the abnormal waveform is detected, to a communication terminal 20 around the user.

The invention provides an entecavir granule formulation and a preparation method thereof. The raw materials of the granule formulation comprise the following components according to the part by weight: 0.001 to 0.5 of entecavir, 90 to 99.5 of a diluent and 0.5 to 5.0 of a binder. The granule formulation has a simple auxiliary composition and has a good palatability. no additional flavoring or essence or pigment is required. The granule formulation is well molded, and forms a clear solution with no chips or impurities after being dissolved in hot water.

The invention discloses a medicament for curing psoriasis, comprising the materials of black-tail snake, tuberfleeceflower, dendrobium, ledebouriella root, catmint, sophora flavescens ait, monkshood, scorpion, atractylodes, notopterygium, radix scrophulariae and liquorice. The invention has the advantages that firstly, 6-9g powder is taken and put into suitable boiled water to immerse for 15-20 minutes, and then can be taken orally, thereby the medicament is taken conveniently and the patient is easy to accept; secondly, the dose is small, and the medicament is only required to take three times each day after meals; thirdly, the side effect is little, and the invention doesn't have hormone and cytotoxic drugs; fourthly, the action is quick, each period of treatment is 7 to 15 days, and one period of treatment can do execution; fifthly, the curative effect is stable, and the common patient taking the medicament insistently can be cured through clinical trials for years; sixthly, the symptom is not easy to recur, the invention doesn't have toxic and side effects, the curing charge is low, and the medicament source is wide and the price is low; and seventhly, the invention for curing psoriasis has 90% effective rate and 85% cure rate.

The invention discloses a preparation method of compound fruit-vegetable-powder effervescent chewing tablets. The preparation method of the compound fruit-vegetable-powder effervescent chewing tablets comprises the following steps: (1) pre-treating fruits and vegetables; (2), blanching the pre-treated fruits and vegetables, and juicing the blanched fruits and vegetables; (3), blending the materials; (4), homogenizing and sterilizing the mixture; (5), carrying out freeze-drying; (6), carrying out granulation; and (7), compressing the granules into tablets. The invention relates to the technical fields of effervescent tablet preparation and chewing tablet preparation; more specifically, the invention relates to a preparation method of effervescent chewing tablets which utilizes freeze-dried fruit and vegetable powder as the main raw material, and added with a small amount of disintegrating agents and a small amount of sweeteners as the accessory ingredients. The structures of the effervescent chewing tablets prepared by the preparation method are similar to structures of common effervescent tablets and chewing tablets; however, the effervescent chewing tablets are unique in tastes as well as refreshing and tasty in flavors compared with the common effervescent tablets and chewing tablets.

The invention provides a medicine preparation for treating postmenopausal osteoporosis and belongs to the technical field of medicines. The medicine preparation contains alfacalcidol, tibolone and necessary pharmaceutical excipients. The medicine preparation for treating postmenopausal osteoporosis, provided by the invention, has the advantages of good disintegration, good absorbing degree, high bioavailability, quick curing effect and convenience for taking. Pharmacological actions of the alfacalcidol and the tibolone can be taken to a maximum extent, the defect of single preparation in efficacy is compensated, and the medicine preparation is an excellent medicine preparation for treating the postmenopausal osteoporosis.

The invention belongs to the field of pharmaceutical preparations, and particularly relates to effervescent tablets containing a stiripentol solid dispersion and a preparation method thereof. According to the effervescent tablets disclosed by the invention, in one aspect, an indissolvable drug is prepared into an amorphous solid dispersion, so that the defect that the permeability of gastrointestinal tracts is reduced by other solubilizing means is overcome while the water solubility and the dissolution rate are improved, and the effervescent tablets have relatively high encapsulation efficiency (16.67%-50%); in the other aspect, a common, easily available and safe enteric-coated material is selected as a solid dispersion carrier to ensure that the stiripentol is released in the small intestine in a positioned manner and cannot be dissociated in advance in a physiological solution to cause damage of gastric acid to medicine like other preparation means; and besides, compared with commercially available dosage forms (capsules and dry suspensions), the effervescent tablets overcome the problem that the content is easy to cake, and has the advantages of stable storage, convenience in taking, good taste, particular suitability for epilepsy children who cannot swallow solid preparations, and the like.

The invention discloses a pidotimod orally disintegrating tablet which includes, by mass, 50-90% of pidotimod main drug, 5-10% of a disintegrating agent, 5-30% of a filling agent, 1-5% of a corrigent and 0.05-2% of a lubricant. The invention also discloses a preparation method of the pidotimod orally disintegrating tablet. The method includes the steps of: 1) sieving a pidotimod raw material through a 60-mesh sieve; 2) uniformly mixing the sieved raw material with the filling agent, the disintegrating agent and the corrigent in a manner of increment by equal quantity; 3) adding the lubricant to the mixture, uniformly mixing the components, and tabletting the mixture, wherien each tablet is 500-600 mg in weight and is 20-40 N in hardness. The pidotimod orally disintegrating tablet is free of water for taking and can be disintegrated and dissolved in saliva. Through preparation technology, bad smell of medicine can be covered effectively. The tablet can be packaged by common aluminum plastic package and is convenient to use. The tablet improves compliance during long-time use of patients and is especially suitable for the elders and children.

The invention discloses a traditional Chinese medicine for treating appendicitis, which is prepared from the following raw material medicaments by weight: 30 grams of mongolian dandelion herb, 20 grams of hairyvein agrimonia herb and bud, 15 grams of peach seed, 10 grams of rhubarb, 15 grams of coix seed and 10 grams of Japanese honeysuckle stem. The invention has the advantages that: the traditional Chinese medicine treats the appendicitis fundamentally and avoids arousing pains in patients in the treatment process, the effectiveness is quick, the method is simple, and toxic and side effects are prevented.

The invention discloses a medicine for preventing and treating gall-stone. The medicine comprises the following components in parts by mass: 10-14 parts of rhizoma polygoni cuspidati, 12-16 parts of plantain herb, 5-10 parts of ligusticum chuanxiong hort, 8-12 parts of corn stigma, 8-15 parts of radix geutianae, 5-8 parts of achyranthes root, 5-7 parts of chicken's gizzard-membrane, 2-5 parts of herba houttuyniae, 12-14 parts of radix glycyrrhizae and 3-6 parts of mirabilite. The medicine is capable of effectively preventing and treating the gall-stone and fast in efficacy, can effectively alleviate pain of patients, does not cause any injury to human bodies, and can effectively fundamentally cure the gall-stone and avoid disease reoccurrence.

The invention discloses a medicament for treating skin diseases. The medicament is prepared from the following components by weight: 20-30 g of figwort, 10-15 g of Chinese violet, 8-10 g of gypsum, 5-8 g of China root, 6-8 g of angelica dahurica, 12-15 g of wild Chrysanthemum and 10-14 g of plantago seed. The medicament has the advantages of capability of treating a patient fundamentally without causing any pain in the treating process, quick response, simple method and no toxic or side effect.

A Chinese medicine in the form of dripping pill for treating gynopathy is prepared from balsamiferous blumea herb and matrix through mixing, stirring, dripping in cooling liquid, and drying. Its advantages are unique curative effect to gynopathic hemorrhage, and high stability.