1057 results about "Officinal" patented technology

The invention relates to a quickly releasing oral solid medicinal composition containing rivaroxaban and a preparation method thereof. Proper medical auxiliaries are treated by a wet granulation process, and are mixed with active components of rivaroxaban to obtain the medicinal composition with remarkably improved dissolution. The preparation method has the characteristics of simple process and industrial production, and solves the problem of complicated preparation process in the prior art.

The invention provides thermoplastic elastomer materials used for a bottle cork for manufacturing medicines, a preparation method thereof and a method for applying the bottle cork for manufacturing medicines thereof. The materials are prepared by the following components: styrene copolymer or rubber materials as well as polyolefine matters. The styrene copolymer is PP or PE; besides, the materials also contain a plasticizer and a loading agent, contain or do not contain a compatibilizer, contain or do not contain an antioxidant, contain or do not contain an antistatic agent, contain or do not contain adhesion preventives. The preparation method thereof includes the steps of drying the materials, fusing a reaction kettle, using a plastic extruding machine to extrude the materials, using a cooling water slot to cool and shape the materials, using a hauling machine to haul and cut off the materials, and the like. The thermoplastic elastomer materials provided by the invention have the advantages of stable chemical property, no poison, low polarity and good rebound resilience.

This is a kind of baicalin total flavones glucoside distillation, baicalin monomer flavones glucoside and its preparation method and application, belonging to the Chinese native medicine drugs manufacturing technology field. The invention obtains the baical in total flavones glucoside distillation mainly containing biacalein, or baical in flavones glucoside monomer compound mainly containing biacalein or wogonoside or oroxylin; comminute baixcal, add water, have alcoholysis reaction at 41 -46 Deg. C, the baialinase and baicalin flavones glucoside naturally existing in baixcal directly have alcoholysis reaction without distillation and separation. The pharmacy preparation includes various pharmacy preparations comprised of officinal auxiliary materials with baicalin total flavones glucoside distillation or monomer flavones glucoside as pharmacy active components, and are used to prepare drugs for curing liver diseases and AIDS. The reaction condition of the invention is mild, and it has high distilling rate, good product quality, low energy waste simple craft, no pollution and low production cost.

The invention discloses a health-care growth-promoting fermented feed additive and a preparation method thereof. The fermented feed additive comprises, by weight, 10-40% of edible fungus chaff, 5-10% of traditional Chinese medicine residues, 10-30% of corncobs, 10-30% of bean pulp, 0.2-1% of fermentation strains and 20-30% of water. The fermented feed additive has the advantages that the edible fungus chaff and the traditional Chinese medicine residues are added into feed, so that the usage amount of cereal feed is reduced, and the feed cost is lowered; mycelia, saccharomycetes and other probiotics in the edible fungus chaff are utilized for performing solid fermentation treatment on the traditional Chinese medicine residues, so that both the medicinal value and the edible value of the medicine residues are brought into full play; crude protein, crude fat and crude fiber in the fungus chaff and medicinal ingredients not extracted from the medicine residues are fully degraded through a fermentation technology, so that the made fermented feed additive contains rich protein, saccharides, fat, microelements and other nutrient substances and also has the effects of improving immunity and promoting digestion.

The invention belongs to the technical field of medicines and relates to a puerarin nanocrystalline medical composition and a preparation method and application thereof. Specifically, the puerarin composition is a puerarin nanocrystalline composition. The puerarin composition provided by the invention remarkably improves the solubility and bioavailabilityof puerarin and reduces or eliminates the food effect of the medicine, and is good in stability and can be prepared into various common preparation forms easily, the stability and effect of the medicine are improved, so that the composition has good prospect.

The invention discloses an oil-in-water medicinal emulsion suitable for water-indissoluble medicaments which comprises, (1) 0.5-50 weight parts of active medicament, which contains water-indissoluble substance with a dissolvability of 0.001-10000mg/l of water at 25 deg. C, (2) 5-300 weight parts of emulsifying agent, (3) 0.5-200 weight parts of fatty oil, (4) 500-1500 weight parts of water. The disclosed medicinal emulsion has little side effect, and is especially suitable for extracts of traditional Chinese medicines.

The invention relates to an external composition, and a preparation and an application thereof and belongs to the field of medicines. The external composition provided by the invention is a medicine composition which contains chlorhexidine or officinal salt thereof, or benzalkonium bromide or officinal salt thereof and a recombinant human epidermal growth factor or a recombinant cattle alkali fibroblast growth factor. According to the invention, the medicine composition is also further prepared into gel, liniment, ointment or paste, and the gel further comprises chitosan or officinal salt thereof and hyaluronic acid or officinal salt thereof. When being used for treating vagina inflammation, the external composition disclosed by the invention can improve a vagina microenvironment, promote growth of granulation tissue and repair vagina micro damage; and when being used for skin wound atraumatic restorative treatment, the external composition also can speed up restoration and regeneration of a wound tissue, promote healing and reduce scar formation, so that the external composition has a wide medical application prospect.

The invention discloses a nicergoline pill and a preparation method thereof. Preparation comprises nicergoline, diluent, disintegrant, adhesive, lubricant and film coating premixing agent. The preparation method includes uniformly mixing the diluent with the internally added disintegrant; preparing blank particles in proper quantity by the adhesive, drying, pelleting and reserving; independently pelleting main drug by the proper adhesive, quickly drying, pelleting and reserving at lower temperature; uniformly mixing the main drug particles with the blank particles, adding externally added auxiliaries, mixing totally, pressing, coating a thin film and packaging. Accordingly, flowability of the particles is guaranteed, the drug can be dissolved beneficially, and more importantly, the problems that content of the main drug and the auxiliaries is lowered and relevant substances are increased due to the high drying temperature and long time in pelleting are avoided. Compared with the prior art, the nicergoline pill has the advantages of reasonable components, simplicity in process, unique preparation method, high dissolving degree, good stability of the preparation, low cost and the like.

The invention discloses a fabrication method of clothing dyed by medicinal plants with health efficacy. The method comprises the following steps: selecting the medicinal plants; extracting pigments of the medicinal plants to obtain a medicinal plant dye liquid; selecting the clothing materials and drying the cloth materials to obtain cloth dyed by the medicinal plants; and preparing the clothing from the cloth dyed by the medicinal plants by combining the acupuncture points of important parts of a human body. The medicinal plant dye for dyeing is a Chinese herbal medicine; the dyed fabric correspondingly has the medicinal efficacies of the medicinal plants; and the medicinal components are absorbed through the skin when directly contacting the human skin in the wearing process, so that the clothing has a good healthcare efficacy on the human body.

The invention relates to a traditional Chinese medicinal composition for improving human Qi and blood functions and improving the immunity and a detection method. Particularly, on one hand, the invention relates to the traditional Chinese medicinal composition. The traditional Chinese medicinal composition is prepared from the following components in parts by weight: 1200 parts of radix astragali,400-600 parts of radix angelicae sinensis, 300-500 parts of radix rehmanniae praeparata, 300-500 parts of radix codcnopsitis pilosulas, 100-300 parts of donkey-hide gelatin, 20-40 parts of ferrous gluconate and optional medicinal auxiliary materials. The invention further relates to a preparation method and a detection method of the traditional Chinese medicinal composition. The traditional Chinese medicinal composition can improve the human Qi and blood functions and improve the immunity, and shows excellent technical effects as described in a specification.

A medicinal white oil composition is prepared from an isomerized base oil. The isomerized base oil is filtered through a filter bed containing an acid activated clay having a surface area of at least 100 m²/g, for the base oil to be in compliant with at least one of European Pharmacopeia 3^rd Edition, US Pharmacopeia 23^rd edition (USP), FDA 21 CFR 172.878 and FDA 21 CFR 178.3620(a) for direct food contact, and FDA 21 CFR 178.3570 (USDA H-1). The medicinal white oil in one embodiment has a UV absorbance at 260 to 350 nm of less than 0.1.

The invention discloses medicinal application and an extracting method of shorthorned epimedium P.E, belonging to the field of medicines. The shorthorned epimedium P.E containing icariin, icariin A, icarisid II and epimedin B is applied to preparing medicines for treating chronic bacterial prostatitis, chronic nonbacterial prostatitis and hyperplasia of the prostate. The preparation method comprises the following steps: adding water or ethanol to epimedium for extraction; concentrating the extracting solution until the relative density is 1.01-1.10 at the temperature of 70 DEG C; and refining the filter liquor by a polyamide adsorption method, thus obtaining the shorthorned epimedium P.E. The invention has the following beneficial effects: by comparing data obtained in pharmacological tests with the data in related documents and patents, the medicines for treating chronic prostatitis and chronic hyperplasia of the prostate, which are prepared from the ehorthorned epimedium P.E, have definite curative effect, have no side effects and also have treatment effect superior to that of the prior art.

A freeze-dried powder of honokiol liposome for preparing the medicines to treat lung cancer and mammary cancer is proportionally prepared from honokiol, polyethanediol-phosphatidylethanolamine, lecithin and cholesterol. It has high synergistic and sensitizing action when it is applied in conjunction with chemicotherapeutic medicine.

The invention relates to a micro emulsion drug carrying system and a manufacturing method thereof, belonging to the field of pharmacy. The first technical problem the invention is intended to solve is to provide a micro emulsion drug carrying system without phase variation in the process of dilution. Proportioning by weight of the components of the system is medicated oil: emulsifier: assisting emulsifier; sodium chloride: water is equal to 1-25:5-20:5-25:1-20:50-85. The system features simple prescription, dosage of the emulsifier within the prescribed limit, the capacity to effectively prevent generation of toxicity, acrimony and hemolytic reaction; what is more, the system has good stability and no phase variation in the process of dilution, which is of great significance.

A Chinese medicine in the form of effervescent tablet is prepared from dandelion herb through extracting active components from it, mixing with auxiliary and tabletting.

The present invention relates to a plastic container which has a good biodegradability and a moisture permeability manufactured by using a novel polyester resin composition under a specific injection and extrusion molding conditions in the forms of a bottle, a blister pack, a medicated paper pouch and the like, which thus enables to preserve the contents of the container such as pharmaceutical drugs, food and beverages dry without the addition of desiccants and can be disposed of without causing environmental contamination.

The invention belongs to the technical field of medicines, and in particular relates to a medical composition which is high in stability, digestion and absorption and a preparation method thereof. The medical composition contains vilazodone or officinal salt of vilazodone and a solid matrix.

The invention relates to the field of Chinese medicines, in particular to a preparation method of total flavonoids in albizia julibrissin durazz and a medicinal composition thereof. The total flavonoids in albizia julibrissin durazz is prepared by using dry inflorescence or flower buds of albizia julibrissin durazz which is a plant of leguminous family as a raw material, extracting with water or aqueous solution of ethanol, concentrating the extract to a proper volume, and extracting the obtained extract with ethyl acetate, wherein the total flavonoid content accounts for over 50 weight percent of the total extract and the content of the main ingredient is measured. The extract and the medical composition containing the extract can be used for preparing medicines for preventing and treating nervous disorder diseases such as depression, dysphoria, Parkinson, senile dementia and the like. The preparation method has the advantages that: the medicinally active ingredients, namely total flavonoids, in albizia julibrissin durazz are obtained; and new medicinal resources are provided for preventing and treating nervous disorder diseases such as depression, dysphoria, Parkinson, senile dementia and the like.

The invention discloses a polypropylene transfusion soft bag which comprises a bag body and a filling port integrally formed with the bag body, wherein the bag body firstly inwards retracts and deforms from the direction of the middle of the bag body with continuous discharge of medicine liquid and respectively gradually extends towards the filling port and the bottom of the bag body. The polypropylene transfusion soft bag is characterized by being made from 10-30 percent by weight of a pharmaceutical grade ethylene and propylene copolymer or a pharmaceutical grade ethylene and propylene and butene copolymer or a pharmaceutical grade ethylene and propylene and styrene copolymer and 70-90 percent by weight of another polypropylene through mixing. The polypropylene transfusion soft bag has the characteristics of more transparency, more flexibility, low cost, high yield and more suitability for industrialized production in comparison with the traditional medical bag.