37results about How to "Give full play to the medicinal effect" patented technology

The invention discloses lucid ganoderma tea, lucid ganoderma teabag and a processing technology thereof. The lucid ganoderma tea comprises the following four components in parts by weight: 50-60 parts of inonotus obliquus powder, 10-20 parts of phellinus igniarius powder, 10-20 parts of phellinus linteus powder and 5-30 parts of lucid ganoderma extract. Thus, the lucid ganoderma tea disclosed by the embodiment of the invention has perfect mouthfeel, can give full play to the medicinal effect and healthcare effect of lucid ganoderma, improves the body immunity, and realizes an effect of adjusting and protecting the central nervous system, digestive system, endocrine system and respiratory system and the organs such as liver, prostate and the like.

The invention relates to an immunity enhancing Dendrobium officinale jelly and a production method thereof. The jelly is produced from a Dendrobium officinale normal juice, Ligustri Lucidi Fructus powder and Polygonatum sibiricum paste. The jelly has good immunity enhancing and nutrition and health functions, the Polygonatum sibiricum paste and the Ligustri Lucidi Fructus powder are used as auxiliary materials to produce the jelly with unique flavor, and the jelly becomes people's favorite nutrition and health instant food; and the jelly has the health functions of Dendrobium officinale, has extremely good mouthfeel, is suitable for all people to eat, and fully performs the medicinal efficacy of the Dendrobium officinale.

The invention provides a herbal modified material based on PU foam as well as a preparation method and an application of the herb modified material. The material is prepared from the following raw materials in parts by weight: 80 parts of traditional Chinese medicines, 320 parts of sponge, 14-23 parts of a diluent, 42.8-51.5 parts of gum and 0.6-1 part of a catalyst. The herbal modified material has the advantages that secondary pollution is avoided, the production efficiency is high, long-term bacteriostat and deodorant effects can be realized, the bacteriostat and deodorant properties can be significantly improved when the material is applied to shoe soles or insoles, foot odor is prevented, and accordingly, the life quality of people is improved.

The invention relates to a white gourd beverage for clearing away heat and toxic substances and increasing urine excretion and a preparation method thereof. The white gourd beverage is prepared from the following components according to parts by weight: 100-150 parts of white gourd, 6-10 parts of mung bean, 1-3 parts of lotus seed and 100-360 parts of water. The preparation method of the white gourd beverage sequentially comprises the steps of water treatment; preparation of white gourd pulp; preparation of mung bean juice and lotus seed juice; and preparation of composite white gourd juice. The white gourd beverage for clearing away heat and toxic substances and increasing urine excretion disclosed by the invention is convenient to make, low in cost and good in mouth feel, and the white gourd beverage has the effects of clearing away heat, increasing urine excretion, dissolving phlegm, clearing away toxic substances, and the like so as to bring medicinal efficacy of white gourd into full play. Moreover, the composite white gourd juice is mixed with pulp, so that various requirements of vast consumers are met, and the implementation effect is good.

The invention relates to cefixime liposome and preparation method therefore as well as dry suspension containing the cefixime liposome. The dry suspension is composed of the cefixime liposome and pharmaceutically acceptable carriers, wherein the cefixime liposome comprises the following components in parts by weight: 1 part of cefixime, 1.25-5 parts of hydrogenated soybean lecithin, 1.25-5 parts of hydrogenated yolk lecithin, 2.5-10 parts of cholesterol and 0.1-5 parts of polysorbate 80. The dry suspension not only accords with the requirements of Chinese pharmacopoeia, but also has the advantages of better storage stability in normal temperature, faster effect exertion and obviously improved bioavailability in comparison with the common cefixime medicaments.

The invention discloses a cynanchum otophyllum dispersible tablet and a preparation method thereof, relating to medicines. The cynanchum otophyllum dispersible tablet is made of the following raw materials by weight portions: 50-200 portions of an extract of cynanchum otophyllum total glucoside, 20-100 portions of an disintegrating agent, 1-10 portions of a lubricant and 1-20 portions of a surfactant, wherein, the disintegrating agent is CMS-Na, CCNa, PVPP, L-HPC and dry starch, the lubricant is magnesium stearate or talcum powder or superfine silica gel powder, the surfactant is SDS, sodium hexadecyl sulfate and sodium stearyl sulfate. The preparation method consists of the following steps: 20-200 portions of total glucoside of the cynanchum otophyllum by weight is taken out and sieved with a 100-mesh sieve; 20-100 portions of the disintegrating agent by weight and 1-10 portions of the lubricant by weight are taken out and respectively sieved with the 100-mesh sieve; 1-20 portions of the surfactant by weight is taken out and sieved with a 80-mesh sieve; then the sieved extract, the sieved disintegrating agent, the sieved lubricant and the sieved surfactant are ground and evenly mixed, and then the mixture is sieved with the 80-mesh sieve, and direct compression and sieving are carried out on the sieved mixture to obtain the dispersible tablet. The dispersible tablet has high dissolution and high bioavailability, can fully exert the drug action of the cynanchum otophyllum, and the preparation method is simple and feasible while suitable for industrialized production.

The present invention discloses a transdermal delivery based pharmaceutical composition. The composition comprises a compound as shown in a formula (I) or pharmaceutically acceptable salt thereof, a macromolecular dispersing carrier material, a hot melting protecting agent and an optional fluxing agent. A preparation method of the transdermal delivery based pharmaceutical composition comprises thesteps of micronizing the compound as shown in the formula (I) or the pharmaceutically acceptable salt thereof, the macromolecular dispersing carrier material and the hot melting protecting agent, optionally adding the fluxing agent, mixing the components uniformly, and performing hot melting extrusion and micronizing to obtain microparticles of the compound as shown in the formula (I) or the pharmaceutically acceptable salt thereof. In addition, the invention provides an application of the pharmaceutical composition. The transdermal delivery based pharmaceutical composition can enable the compound as shown in the formula (I) to be quickly absorbed, so that the purpose of calming before anesthesia is achieved, breathing is not affected, and the adverse psychological effects on children dueto intramuscular injection or intravenous injection are avoided. Meanwhile, the pharmaceutical composition also can be used for preventing and/or treating hyperactivity.

The invention relates to a preparation method for medicinal liquor. The preparation method includes the following steps: A. traditional Chinese medicine in a formula is taken and crushed; B. the crushed traditional Chinese medicine is put into a bag and is placed in a distiller for distilling and curing together with fermented liquor grain till the baking of the liquor is finished so as to obtain distilled liquor with medicine scent, and then the traditional Chinese medicine bag is taken out for stand-by use; C. the distilled liquor obtained in the step B is blended to 38 to 50 DEG; D. the traditional Chinese medicine bag taken out in the step B is soaked in blended liquor obtained in the step C for 60 to 90 days in a sealed manner; E. the traditional Chinese medicine bag is taken out and filtered to obtain the traditional Chinese medicinal liquor in the invention. The medicinal liquor prepared by the method in the invention can lead effective ingredients of the traditional Chinese medicine to be dissolved in the liquor to the maximum degree. Moreover, the medicinal liquor has the advantages of being mellow as well as palatable and has good taste.

The invention relates to a cefprozi liposome, a preparation method thereof and a tablet containing the cefprozi liposome. The cefprozi liposome comprises cefprozi, hydrogenated soybean phosphatidylcholine, hydrogenated egg yolk lecithin and cholesterol, wherein the weight ratio of the cefprozi, the hydrogenated soybean phosphatidylcholine, the hydrogenated egg yolk lecithin and the cholesterol is 1:1.25-5:1.25-5:2.5-10. The cefprozi tablet meets the requirements of Chinese Pharmacopoeia and also has the advantages of higher dissolution rate, faster effect and greatly enhanced bioavailability compared with the ordinary cefprozi drug composite.

The invention relates to a cefprozil liposome and a preparation method thereof as well as a capsule containing the cefprozil liposome. The cefprozil liposome comprises cefprozil, hydrogenated yolk lecithin, soyabean lecithin, cholesterol and vitamin E, wherein the weight ratio of the cefprozil to the hydrogenated yolk lecithin to the soyabean lecithin to the cholesterol and to the vitamin E is 1:(1.25-5):(1.25-5):(2.5-10):(0.1-3). The cefprozil capsule not only meets the Chinese pharmacopoeia requirement but also has the advantages of higher dissolution rate, faster action of medicament effect and obvious improvement of bioavailability compared with those of a common cefprozil pharmaceutical composition.

The present invention discloses one kind of gastrodia tuber food additive and its preparation process. The gastrodia tuber food additive is prepared with gastrodia tuber starch gastrodia tuber dregs and gastrodia tuber, and through washing, crushing, grinding, centrifugal separating and drying. The present invention features the comprehensive gastrodia tuber utilizing process including separating fresh gastrodia tuber juice in a centrifuge to obtain fresh gastrodia tuber juice, fresh gastrodia tuber starch and gastrodia tuber dregs; producing gastrodia tuber beverage with the fresh gastrodia tuber juice; and producing food additive with gastrodia tuber starch, gastrodia tuber dregs and partial gastrodia tuber juice. The gastrodia tuber food additive has high medicinal value, low cost and simple production process.

The invention discloses a pharmaceutical composition for transdermal administration. The pharmaceutical composition contains tapentadol or a pharmaceutically acceptable salt thereof, a polymer dispersion carrier material, a hot-melt protective agent and an optional solubilizer. A preparation method of the pharmaceutical composition includes the following steps: mixing the tapentadol or the pharmaceutically acceptable salt thereof, the polymer dispersion carrier material, the hot-melt protective agent and the optional solubilizer, performing hot-melt extrusion, and performing micronization to obtain the microparticles of the tapentadol or the pharmaceutically acceptable salt thereof. The pharmaceutical composition for the transdermal administration can make the tapentadol or the pharmaceutically acceptable salt thereof rapidly absorbed, and achieve the purpose of sedation before anesthesia without affecting breathing, thereby avoiding the adverse psychological effects of intramuscular injection or intravenous injection acupuncture on children; and at the same time, the pharmaceutical composition can also be used to prevent and/or treat and delay the development of Parkinson disease.

The invention discloses a pharmaceutical composition for transdermal administration. The pharmaceutical composition comprises sufentanil or a pharmaceutically acceptable salt thereof, a polymer dispersion carrier material, a hot-melt protective agent and an optional solubilizer. The pharmaceutical composition for transdermal administration is obtained by the following steps: mixing the sufentanilor the pharmaceutically acceptable salt thereof, the polymer dispersion carrier material, the hot-melt protective agent and the optional solubilizer, performing hot-melt extrusion and micronization toobtain microparticles of the sufentanil or the pharmaceutically acceptable salt of the sufentanil. In addition, the invention provides a preparation method and application of the above pharmaceuticalcomposition. According to the pharmaceutical composition for transdermal administration, the sufentanil can be quickly absorbed, the purpose of treating postoperative pain without affecting breathingcan be achieved, and adverse psychological effects of intramuscular injection or intravenous injection acupuncture on patients can be avoided; and at the same time, the pharmaceutical composition canbe used to prevent and/or treat postherpetic neuralgia.

The invention provides a health-care product preparation capable of relaxing bowel. The health-care product preparation has the effects of relaxing bowel, and nourishing yin and generating body fluid. The formula is prepared from dendrobium officinale, mulberry fruits, radix polygoni multiflori, semen platycladi, fructus cannabis and Chinese angelica. Research results of traditional Chinese medicine theory and modern pharmacology, and experimental study on pharmacodynamics and clinical practice treatment application prove that the health-care product preparation has an accurate curative effect in the aspect of relaxing bowel and has no untoward effect; and the health-care product preparation has the effects of nourishing yin and generating body fluid, relaxing bowel and purging heat and removing stagnancy, is accurate in curative effect, rapid in effect and high in healing rate, can be used for treating both symptoms and root causes, and is safe and has no toxic or side effect.

The present invention relates to a Chinese medicine for curing anal diseases and its preparation method. The described medicine is made up by using 11 Chinese medicinal materials of clematis root, dahurian angelica root, chrysanthemum, flower, wolfberry bark, rubia root and others through the processes of pulverizing and mixing.