46results about How to "Does not affect the curative effect" patented technology

The invention relates to a compound preparation of an external use pharmaceutical composition for treating swelling and pain, which is a gel binder for treating swelling, and also provides its preparation method. The gel binder is prepared by 20-50% of swelling and pain medicine of the external use pharmaceutical composition for treating swelling and pain as well as proper pharmaceutical excipients. The gel binder for treating swelling is composed of a back lining layer, an ointment-containing body and a cover lining layer. The ointment-containing body, namely the kernel part, is prepared from the swelling and pain medicine, a basic polymer, a cross-linking agent, an organic acid, an excipient, a humectant, an adhesive and the like in certain ratio. The gel binder has the advantages of fast effect, good moisture preservation, high permeability and comfortable use. The product has merits of convenient usage, small irritation on skin and high compliance of patients.

The invention discloses a soup to treat burn, such as boiling water, molten steel slag, high-temperature steel board and flame, which comprises the following steps: dispensing the soup with camellia oil, calcium hydrate and water; adding 35-45g water into the container with 10-15g calcium hydrate; stirring until the water becomes clarified; fetching clear water in another container with 50-60g camellia oil; stirring evenly; obtaining light yellow emulsion-soup; using long feather on the duck wing to dip the dispensed soup to coat the burn everyday with good treating effect and short treating period without scar.

The invention relates to a hollow, ventilation and double-layer traditional Chinese medicine suppository for treating rhinitis and a production method of the traditional Chinese medicine suppository and belongs to the field of traditional Chinese medicine preparations. The production method includes applying a matrix plaster and an outer layer plaster to a suppository core outer wall formed by folding mulberry bark paper to prepare the hollow, ventilation and double-layer traditional Chinese medicine suppository for treating the rhinitis in twice. The matrix plaster and the outer layer plaster are separated for dispensing, are composed of traditional Chinese medicine ingredients and are capable of dispelling wind and ventilating lungs, clearing away heat and relieving exterior syndromes, resisting allergies and removing dampness, clearing livers and protecting brains, eliminating stagnation for resuscitation and removing necrotic tissue and promoting granulation. The hollow, ventilation and double-layer traditional Chinese medicine suppository for treating the rhinitis is effective in treatment of acute rhinitis and chronic rhinitis, and secretions of breath and nasal cavities of patients can be normally discharged when the traditional Chinese medicine suppository is used.

The invention discloses a pasty pharmaceutical composition and a preparation method thereof, and relates to a traditional Chinese medicine formula. The pasty pharmaceutical composition is characterized by comprising a fluid extract drug, a medicinal powder composition, drugs added later and minium. The preparation method comprises the following steps of heating a matrix to remove moisture of the matrix, putting a fluid extract drug into the matrix when green smoke is emitted, stirring uniformly, crushing valuable fine drugs into powder, orderly and slowly adding the powder, borneol, camphor, chlorpheniramine, piroxicam and laurocapram into the molten plaster, stirring, fast rolling up the uncooled mixed plaster by a bamboo chopstick, and spreading the uncooled mixed plaster on a paper cloth in a way that an end of the bamboo chopstick contacts the centre of the paper cloth and the bamboo chopstick turns clockwise a round on the paper cloth according to the size of the paper cloth so that the pasty pharmaceutical composition is obtained. Compared with the traditional pasty pharmaceutical composition, the pasty pharmaceutical composition provided by the invention adopts the fluid extract drug prepared from a crude drug by decoction to replace a fried crude drug so that large drug effect loss is avoided, has the characteristics of good drug effects, strong penetration, easiness of absorption and no production of skin allergy, realizes that a unit dose of the pasty pharmaceutical composition can be used for 7 to 10 days and the pasty pharmaceutical composition can be reused after being tore off without influences on treatment effects, and has a low price.

The invention discloses asthma moxibustion and a preparation method thereof. The asthma moxibustion comprises a heat-generating bag, and an ointment paste, the ointment paste comprises an ointment bagand an ointment body, and the ointment body is prepared from the following components in parts by weight: 10-15 parts of sinapis alba, 10-15 parts of herba asari, 10-15 parts of ginger juice, 20-25 parts of kansui root, 10-14 parts of rhizoma corydalis, 5-10 parts of folium artemisiae argyi, 4-6 parts of pubescent holly root, 4-6 parts of Chinese pyrola herb, 20-40 parts of glycerinum, and 5-10 parts of water. The heat-generating bag can locally heat the affected area, expand capillaries, speed up blood circulation and tissue metabolism, and relieve symptoms of non-breathing; a coupling agentis used for efficiently and evenly absorbing energy by the skin and tissue, and the coupling agent has the functions of coupling, conduction and penetration; the skin and subcutaneous tissue are affected, the molecular movement in cells is intensified, metabolism is accelerated, and damaged tissue is repaired; and according to the scheme, the ointment bag can inhibit vasoconstriction and relieveasthma symptoms.

The invention discloses a Chinese medicinal tincture for treating hemorrhoid, which is prepared from 31 kinds of Chinese medicinal herbs including astragalus root, red ginseng, broomrape, Chinese angelica root, eucommia bark, cortex acanthopanacis, dry human placenta, frankincense, buthus martensi karsch, centipede, and hog hoofs through white spirit immersion.

The invention discloses a nocardia rubra-cell wall skeleton solvent extraction method which is characterized by including the steps: (1) ethyl acetate extraction: adding ethyl acetate in nocardia rubra-cell wall skeleton fragments acquired after enzymolysis, stirring mixture for 5-18 hours at the indoor temperature, performing centrifuging treatment, abandoning liquid supernatant, and reserving sedimentation fragments; (2) absolute ethyl alcohol stirring and cleaning: adding the absolute ethyl alcohol into the sedimentation fragments acquired in the step (1) to uniformly stir mixture, performing centrifuging treatment, abandoning liquid supernatant, and reserving sedimentation fragments; (3) absolute ethyl alcohol extraction: adding the absolute ethyl alcohol into the sedimentation fragments acquired in the step (2), stirring mixture for 5-18 hours at the indoor temperature, performing centrifuging treatment, and abandoning liquid supernatant to obtain final sedimentation fragments. The proportion of the nocardia rubra-cell wall skeleton fragments and ethyl acetate is 1g: 5-8ml, and the proportion of the sedimentation fragments acquired in the step (2) and the absolute ethyl alcohol is 1g:5-8ml.

The invention discloses a method for improving a levodropropizine taste by cyclodextrin clathration. The method comprises that cyclodextrin or cyclodextrin derivatives as carriers are added into levodropropizine so that levodropropizine is included in the cavity of the cyclodextrin or cyclodextrin derivatives and thus a levodropropizine clathrate is obtained. In oral administration, levodropropizine does not contact with the oral cavity of a patient so that the patient does not feel a peculiar smell and a bitter taste of levodropropizine. Therefore, the method effectively improves a levodropropizine taste and patient compliance, can prepare the levodropropizine solid dispersoid of which levodropropizine effects are not influenced, and can effectively improve clinical application of levodropropizine.

The invention discloses a rhizoma acori graminei volatile oil fast-disintegrating oral tablet and a preparation method thereof. The rhizoma acori graminei volatile oil fast-disintegrating oral tablet is prepared by taking 1.2-3.5 percent of rhizoma acori graminei volatile oil by weight, 8-15 percent of a flavoring agent by weight, 55-75 percent of a filling agent by weight, 5-7 percent of a disintegrating agent by weight, 1-4 percent of a flow aid by weight and 0.15-0.8 percent of a lubricating agent by weight as materials, adopting a beta-cyclodextrin camplexation technique and a powder direct tabletting method or a wet process granulating and tabletting method and pressing by the utilization of a tabletting machine. Compared with the prior art, the rhizoma acori graminei volatile oil fast-disintegrating oral tablet and the preparation method thereof have the benefits that beta-cyclodextrin camplexation powder wrapped with the rhizoma acori graminei volatile oil and other auxiliary materials are mixed and directly tabletted into the fast-disintegrating oral tablet; after being placed in an oral cavity, the fast-disintegrating oral tablet is mixed with saliva to be swallowed by a patient, so that the objectionable odor of the rhizoma acori graminei volatile oil is masked, the stimulation to gastrointestinal tracts is also reduced, and meanwhile, the treatment effect of the rhizoma acori graminei volatile oil is also not affected; the swallowing is convenient for infants and middle and old aged patients, transportation and storage are facilitated, and the market prospect is wide.

The invention relates to the technical field of medicine preparation, in particular to slow release composition with cefaclor, which comprises materials by weight: 60% to 90% of the cefaclor, 5% to 20% of hydroxypropyl methylcellulose, 0.5% to 5% of a potential of hydrogen (pH) adjusting agent and 3% to 18% of a porogen. The slow release composition with the cefaclor can be completely released in 4 to 7 hours, thereby being good in release characteristics.

The invention discloses an eye drop for treating xerophthalmus and a preparation method. The eye drop is prepared from the following raw materials and auxiliary materials in parts by weight: 130-170 parts of an extract containing bear gall powder, 1.5-3.3 parts of borneol, 1-2 parts of a bacteriostatic agent, 6-10 parts of a solubilizer, 40 parts of sodium borate and 10 parts of boric acid. According to the physical and chemical properties of chemical components contained in the medicinal material in the formula, use of volatile oil is removed; the dosage of the borneol and the bear gall powder is adjusted; the borneol and the bear gall powder are added in different manners; muddy opalescence and the like caused by a conventional bear gall powder adding method are reduced; the medicinal composition is ensured; meanwhile, the preparation directly acts on the medication part; the dosage is greatly reduced; the onset time of the medicine is quickened; and the curative effect is improved.

The invention discloses a preparation method of a compound medicament for treating diarrhea. The compound medicament is a compound preparation prepared from zinc-containing medicinal raw materials and medicinal montmorillonite raw material, wherein the zinc-containing medicinal raw materials comprise zinc gluconate, zinc sulfate, zinc citrate, zinc acetate, zinc chloride, zinc lactate, zinc glycinate, L-lysine zinc and licorzinc; and the zinc-containing medicinal raw materials are mixed uniformly with montmorillonite and auxiliary materials by using an equivalent progressive increment method. The compound medicament plays a role in zinc complement and local treatment, and has good effect compared with interval administration of montmorillonite and zinc.

The invention discloses a diarrhea moxibustion patch and a preparation method thereof. The diarrhea moxibustion patch comprises a heating bag and an ointment patch, wherein one side of the heating bagis attached to the ointment patch which comprises an ointment bag and an ointment body, and the ointment body is prepared from, by weight, fructus evodiae, cortex cinnamomi, clove, myristica fragrans, pepper, folium artemisiae argyi, fresh ginger, herb of sweet basil, glycerinum and water. All the raw materials are combined to mainly treat stomach cold, abdominal pain, emesis and diarrhoea. The herb of sweet basil is neutral in nature and mild in drug effect, and the irritation effect of the sovereign drug is relieved without affecting the drug effect of the sovereign drug.

The invention relates to a cataplasm for curing acute injury of soft tissues and a preparation method thereof. The cataplasm is prepared by raw materials of angelica extract, saposhnikoviae radix extract, bitter orange extract, anemarrhena asphodeloides extract, rhizoma arisaematis (processed) extract, fructus trichosanthis extract, angelica dahurica extract, carthamus tinctorius extract, thunberg fritillary bulb extract and suitable accessories. The cataplasm consists of rear lining layers, ointments containing drugs, and cover lining layers. The cataplasm takes effect quickly, performances of moisture and air permeability are good, usage is comfortable and convenient, irritation on skins is small, and compliance of patients is high.

The invention discloses a traditional Chinese medicine formulation granule containing volatile oil composition and a preparation method thereof. In the preparing process of the traditional Chinese medicine formulation granule, a traditional Chinese medicine containing the volatile oil as an effective ingredient is selected to prepare the traditional Chinese formulation granule by immersing, quantitatively extracting the volatile oil, including by beta-cyclodextrin, extracting by water, decompressing and concentrating, spray drying and the other steps. The traditional Chinese medicine formulation granule not only sufficiently ensures drug effect, but also can avoid over violent drug property or adverse effect caused by over dosage of the volatile oil to ensure the safety of the granule; and by quantitatively collecting and adding the volatile oil, wherein the collecting amount of the volatile oil is equivalent to the dosage of the volatile oil in decoction. The preparation process improves the quality and stability of products, has high concentration of drug effective ingredient of the products, and is convenient for transportation, storage, portability and taking.

The invention discloses a method for preparing a medicine capsule for clearing away the heat and loosing the bowels and dispelling the rheumatism to relieve pain. The method comprises the following steps of: (1), an extraction process: 1, preparing materials and weighing, 2, extracting volatile oil, 3, preparing clear paste by taking cape jasmine fruits, licorice roots and chastetree fruits (fried), 4, percolating and 5, mixing; (2) a powder making process: 1, preparing the materials and weighing, 2, sterilizing, 3, drying and 4, pulverizing; and (3), a preparation process: 1, preparing the materials and weighing, 2, pelleting, 3, finishing granules, 4, totally blending, 5, filling and 6, polishing. When crude medicinal materials are extracted, the weight ratio of coptis chinensis to fructus forsythia to mint to inula flower to baical skullcap roots to schizonepeta to cape jasmine fruits to divaricate saposhnikovia roots to golden cypress to chrysanthemum to fructus viticis (fried) to licorice roots to szechuan lovage rhizome to rheum officinale to gypsum to platycodon grandiflorum to angelica root to dextrin to magnesium stearate is 5:40:20:10:40:40:40:20:20:80:40:20:20:160:20:40:40:30:2.8. The method has the advantage that the medicine capsule with good quality is produced.

The invention relates to a Chinese herbal medicine preparation for preventing and curing mycotic diseases infected by beasts and birds. The Chinese herbal medicine preparation is prepared from the following bulk drugs in parts by weight: 10-40 parts of baical skullcap roots, 10-20 parts of rheum officinale, 10-40 parts of hawthorns, 10-30 parts of medicated leaven, 10-30 parts of silybum marianum and 10-30 parts of pine needle meal. The Chinese herbal medicine preparation provided by the invention has a strong mycete restraining and killing capability, can resolve toxicant, is liver protective and cholagogue, and cardiotonic and diuretic, and has good preventing and curing effects.

The invention discloses a drug capsule for clearing away heat and loosing bowels and dispelling wind and relieving pain. The drug capsule is prepared from coptis root, weeping forsythia capsule, peppermint, inula flower, baical skullcap root, fineleaf schizonepeta herb, cape jasmine fruit, divaricate saposhnikovia root, amur corktree bark, chrysanthemum, fried shrub chastetree fruit, liquorice root, Sichuan lovage rhizome, rhubarb root and rhizome, gypsum, platycodon root, dahurian angelica root, fineleat schizonepeta oil, peppermint oil, forsythia suspansa oil, crude drug fine powder, dextrin and magnesium stearate, and is characterized in that when net drugs are extracted, the weight ratio of coptis root to weeping forsythia capsule to peppermint to inula flower to baical skullcap root to fineleaf schizonepeta herb to cape jasmine fruit to divaricate saposhnikovia root to amur corktree bark to chrysanthemum to fried shrub chastetree fruit to liquorice root to Sichuan lovage rhizome to rhubarb root and rhizome to gypsum to platycodon root to dahurian angelica root to dextrin to magnesium stearate is 5:40:20:10:40:40:40:20:20:80:40:20:20:160:20:40:40:30:2.8. The drug capsule has the advantage that a better medical treatment effect is achieved.

The invention relates to a freeze-dried powder injection for meglumine glycididazole, which contains the meglumine glycididazole, a pharmaceutical carrier and a pH value regulator. According to the property of the meglumine glycididazole compound, a freeze drying process is adopted to prepare the meglumine glycididazole compound into the freeze-dried powder injection, thereby providing the clinical application with the meglumine glycididazole freeze-dried powder injection with reliable stability, safety, effectiveness, and convenient use. And a method for preparing the meglumine glycididazole freeze-dried powder injection is provided.

The invention discloses orally disintegrating tablets for garlic oil and a preparation method of the orally disintegrating tablets. The preparation method comprises the following steps: by taking garlic oil, microcrystalline cellulose, sodium carboxymethyl starch, superfine silica powder, magnesium stearate, beta-cyclodextrin and lactose as materials, adopting a beta-cyclodextrin inclusion technology and a direct powder tabletting method or a wet granulation tabletting method, and preparing the orally disintegrating tablets by utilizing a tablet machine. Compared with the prior art, the orally disintegrating tablets and the preparation method thereof have the advantages that the medicines are put into the oral cavity and can be disintegrated within 25 seconds without drinking water, sense of foreign matters and gravel is avoided when the medicine is put into the mouth, the medicines enter the stomach by means of a natural deglutition effect and are in a high dispersion state, and bad odor and pungent smell of the garlic oil are completely covered. Therefore, the chemical stability of the garlic oil can be guaranteed, a specific curative effect can be achieved, and excessive stimulation to the gastrointestinal tract is avoided. Meanwhile, the orally disintegrating tablets can be produced in a large scale by using universal tabletting equipment.

The invention provides a traditional Chinese medicine composition for treating cardiac insufficiency and an application thereof, and belongs to the technical field of traditional Chinese medicines. The traditional Chinese medicine composition comprises the following components in parts by weight of 5-10 parts of codonopsis pilosula, 5-10 parts of raw astragalus membranaceus, 3-6 parts of radix ophiopogonis, 3-6 parts of schisandra chinensis, 2-4 parts of ramulus cinnamomi, 5-10 parts of radix paeoniae alba, 2-4 parts of rhodiola rosea, 5-10 parts of kudzuvine root, 2-4 parts of rhizoma cimicifugae, 5-10 parts of poria cocos, 3-6 parts of rhizoma atractylodis macrocephalae, 3-6 parts of rhizoma alismatis, 5-10 parts of herba leonuri, 5-10 parts of radix salviae miltiorrhizae, 3-6 parts of pericarpium citri reticulatae, 1-2 parts of rhizoma zingiberis and 1-2 parts of radix aconiti lateralis preparata. The traditional Chinese medicine composition provided by the invention can treat cardiac insufficiency.

The invention discloses a pharmaceutical composition with a synergistic effect and myofibroblast capable of resisting organ fibrosis and tumor stroma. The pharmaceutical composition is composed of tetrandrine, a tetrandrine derivative, baicalein and a baicalein derivative, has the synergistic effect and the myofibroblast capable of resisting organ fibrosis and tumor stroma, is capable of reducing expression of myofibroblast alpha-smooth muscle actin (alpha-SMA), enables the myofibroblast alpha-smooth muscle actin (alpha-SMA) to be restored to fibroblast in resting time, and is used for treating organ fibrosis and suppressing tumor growth, metastasis and infiltration. The pharmaceutical composition has no obvious toxic or side effects on fibroblast while obviously reducing expression of alpha-SMA.

The invention discloses a preparation process of a pain-relieving and stasis-removing hydrogel patch, which comprises the following steps: step 1, uniformly mixing powdery medicinal raw materials to obtain mixed powder; 2, carrying out alcohol extraction treatment on the mixed powder to obtain a mixed extracting solution; step 3, carrying out concentration treatment on the mixed extracting solution to obtain a concentrated solution; 4, uniformly mixing the concentrated solution with hydrogel to obtain mixed hydrogel; and 5, uniformly smearing the mixed hydrogel on the patch, pasting glass paper on the mixed hydrogel, and cutting themixed hydrogel into pieces to obtain a finished product. In the first step, the powdery medicinal raw materials comprise the following components in parts by weight: 95-105 parts of curcuma zedoary; 98-110 parts of turmeric; 95-105 parts of cortex phellodendri; 48-52 parts of frankincense; 45-55 parts of myrrh; 110-130 parts of radix angelicae dahuricae; 95-105 parts of garden balsam seed; 98-102 parts of semen momordicae; and 95-105 parts of muskroot-like semiaquilegia root. The preparation process has the advantages of being capable of improving use comfort and improving the treatment effect.