217results about How to "Fast onset" patented technology

A Chinese medicine in the form of tablet, capsule, particle, or oral liquid for treating cardiovascular and cerebrovascular diseases is prepared from 16 Chinese-medicinal materials including Chuan-xiong rhizome, Chinese angelica root, red peony root, astragalus root, etc. Its preparing process is also disclosed.

The present invention relates to Chinese medicine and its extracting and processing technology, and is especially the effective part extracted from American ginseng leaf and ginseng leaf and its preparation process. The extracted effective part contains six kinds of ginsenoside substances, including ginsenoside Re, ginsenoside Rb1, ginsenoside Rb2, ginsenoside Rb3, ginsenoside Rc and ginsenoside Rd. Its preparation process includes water extracting American ginseng leaf and ginseng leaf in the weight ratio of 1 to 0.3, macroporous resin adsorption of the water extract liquid, water eluting to eliminate impurity, further eluting with two kinds of elutents, collecting the eluted liquid, and refining the total solid matter to reach purity up to 63.45 %. The extracted effective part has less side effects, and may be used widely in compound medicine preparation and functional food and for separating ginsenoside substance.

The invention belongs to the technical field of microbial insecticides, and specifically relates to the screening for a bacillus thuringiensis strain with high virulence for ditylenchus destructors and the application for the prevention and treatment of ditylenchus destructors. The invention screens a bacterial strain YBT-008 with high virulence from the bacillus thuringiensis for the ditylenchus destructors. The bacterial strain is stored in China Center for Type Culture Collection, and the collection number is CCTCC NO: M2011039. The invention also includes the application effects of a microbial agent prepared by the YBT-008 on controlling the ditylenchus destructors, the types of insecticidal crystal proteins generated by the YBT-008, the verification of Cyt2Ba, Cry11Aa, Cry4Aa and Cry4Ba, and the verification of that the microbe and the microbial agent of the invention belong to a novel microbe for killing the ditylenchus destructors.

The invention discloses a long-acting slow-release pharmaceutical preparation. The pharmaceutical preparation contains the following components in percentage by weight: 25%-60% of a water-insoluble or sparingly-soluble drug and 40%-75% of a high-molecular polymer. After the pharmaceutical preparation is subjected to one time of intramuscular injection administration, the rate of a maximum plasma concentration to a minimum plasma concentration in a main release period is less than 5; the slope of a linear trend line of a cumulative release curve is less than 8 under an in-vitro simulated release condition; the daily release amount is less than 8.5%; and the simulated release condition is a buffer solution with the temperature of 37+/-0.5 DEG C and the pH of 6.8-8.4. The prepared long-acting slow-release pharmaceutical preparation has the beneficial effects that an obvious release delay period or a burst release phenomenon are avoided after the administration, the steady state plasma concentration can be rapidly achieved, the plasma concentration with a relatively small fluctuation range can be maintained in several weeks or longer through once administration, and the pharmaceutical preparation can take effect rapidly and has good compliance with a patient.

The invention provides a zolmitriptan sublingual tablet, which is characterized in that it contains the main drug zolmitriptan, a disintegrating agent and a filler. In every 1000 sublingual tablets, the content of zolmitriptan is 1 -50g, the content of disintegrating agent is 2-20g, the content of filler is 40-200g; it also contains 0-20g of corrective agent, 10-60g of binder and 0.5-5g of lubricant. The present invention utilizes the characteristics of non-keratinized sublingual mucosa, rich capillaries, and fast blood flow, aiming at the absorption of zolmitriptan ordinary tablets through the gastrointestinal tract, slow onset of action, first-pass effect, and low bioavailability. The deficiencies of advanced prior art, zolmitriptan is made into sublingual tablet, can make it absorb through sublingual mucosa, directly enter blood circulation through jugular vein and superior vena cava, take effect rapidly; Avoid oral administration The first-pass effect improves bioavailability and ensures curative effect. Moreover, water is not needed when taking the medicine, and it is placed under the tongue to contain it, so it is convenient to take and has a good taste. With the characteristics of rapid onset of action, convenient administration and high bioavailability, it can provide patients with a new treatment option and fill the gap in the market.

The invention discloses a Nakedflower Beautyberry Leaf liquid capsule and the preparing and quality control methods thereof, characterized by that: the contents of it is prepared of the following raw materials in weight shares: dry Nakedflower Beautyberry Leaf extract powder 1, dispersant 1.2-1.6, and auxiliary suspending agent 0.04-0.07. and the preparing method: mixing the raw materials in proportion, uniformly grinding the mixture by colloid mill to make medical liquid uniform and fine, and finally making into capsules on a liquid capsule machine. It belongs to a hard capsule, and its contents are liquid, and as compared with original tablets, it has advantages of short disintegrating time, fast taking effect, high biological utilization ratio, etc.

The invention discloses wet chamber glasses and a control method thereof. The wet chamber glasses comprise a glasses frame, glasses legs, an inner frame, a microprocessor and lenses arranged on the glasses frame; a fence is arranged between the inner side of the glasses frame and the inner frame fitting the face of a wearer, and heating modules in a series connection round are distributed on the inner side of the glasses frame; at least one water storage chamber and mist passages are formed in the glasses legs, the mist passages are used for being connected with the top ends of the water storage chambers and the inner side of the fence; the microprocessor is connected with the heating modules, when the glasses are worn, the glasses frame, the lenses, the inner frame, the fence and the faceof the wearer can form a sealing cavity, and the microprocessor controls the heating modules to quickly emit heat, so that water in the water storage chambers is heated and evaporated to obtain vapor, the vapor flows to the eyes of the wearer through the mist passages. The wet chamber glasses have the advantages that the speed of taking effect is high, the dry eye symptom can be quickly relieved,and a hot compress effect is achieved.

A high-efficiency mothproofing agent at least contains two effective mixed matters playing the role of mothproofing under room temperature, and also contains an effective matter with a mildew-proof function. The mixture with the mothproofing function is prepared by mixing camphor, santochlor and other mothproofing agents with pyrethrin. The high-efficiency mothproofing agent also contains an additive convenient for producing a forming agent, namely micromolecule inorganic silicon substance, and can belongs to the powder type, the granulated type, the sheet type, the ball type or the massive agent type. The mothproofing agent is arranged in a bag or a box made of air-permeability paper with air permeability, non-woven fabrics and thin films. The pyrethrin is quick in taking effect, has obvious effect on killing moths, not only remedies the defects of a camphor mothproofing agent, but also greatly reduces input, and is safer and more effective. The camphor and the pyrethrin do not have the mildew-proof effect, so that a mildew-proof agent is added in the mixture of the camphor and the pyrethrin, therefore, the mothproofing agent has the effects of moth and mildew prevention.

A dripping pill of Chniese medicnie 'Huoxiang Zhengq pill' for treating cold, emesis, diarrhea, heat sroke and cholera is disclosed. Its advantages are high safety and lower toxic by-effect.

The invention provides a medicament which has the functions of antineoplastic, oxidation resistance, anti viral hepatitis and antiphlogistic. The invention particularly relates to a dripping pill which contains ursone and a process for preparation. The invention overcomes the shortcomings of the prior dripping pills that pure natural degrees of findings which are used by the prior dripping pills are not high, and chemosynthesis findings which are commonly used are not in food additives catalogs of some countries, and tastes of the dripping pills are worse. The invention is a pharmaceutical preparation whose natural degree is higher, safety is stronger, and side effect is lower.

A dripping pill of cucurbitacin for treating chronic metastatic hepatitis features high natural level and safety and low toxic by-effect. Its preparing process is also disclosed.

The invention belongs to the technical field of medicinal preparations, and relates to a formula and a preparation process of an oryzanol nanocrystal capsule preparation. The preparation is composed of oryzanol and stabilizers, nano-suspension is prepared, then spray dispersing agents are added into the nano-suspension, spray drying is performed to obtain oryzanol nanocrystals, and a capsule is filled to obtain an oryzanol nanocrystal capsule. The nanocrystals prepared by vortex blending are uniform in grain diameter, and solubility and dissolution rate are remarkably increased. The preparation has the remarkable advantages that the solubility of the oryzanol can be increased by the nanocrystals, bioavailability of the oral preparation is improved and is less affected by the eating condition of a patient, clinical curative effects are further enhanced, and individual difference is decreased.

The invention discloses a composition and a soft capsule for alleviating cough. The composition for alleviating cough comprises the following compositions in percent by weight: 30-100% of benzonatate, 0-60% of polyethylene glycol and 0-50% of polyol. The soft capsule comprises a soft-capsule shell and a contained substance cladded by the soft-capsule gelatin shell. The contained substance comprises the following compositions: benzonatate, polyethylene glycol and polyol. The soft-capsule gelatin shell is composed of gelatin, a plasticizer, purified water and a coloring agent. The composition for alleviating cough is simple in compositions, stable, effective, and rapid in dissolving and absorption. The soft capsule containing the above composition for alleviating cough is also provided. The soft capsule is applicable to irritable cough, paroxysmal cough and the like caused by acute bronchitis, bronchitis asthma, pneumonia and lung cancer, and is applied to prevent cough when fiberoptic bronchoscopy and laryngoscopy are performed.

The invention particularly relates to a method for producing ultra-micro ginger powder from ginger processing by-products, belonging to the agricultural product processing field. The method comprises the following steps: the ginger processing by-products are washed, desalted and deacidified by clear water, and are dried in the sun or dried at the temperature of 40-60 DEG C till the moisture content of the by-products is less than 8% to obtain dry ginger slag blocks, dry ginger slag blocks are then crushed to 100+/-20 mesh coarse ginger slag powder, and coarse ginger slag powder is crushed superfinely at the temperature of 0-5 DEG C to form 500-800-mesh fine powder, so as to obtain the ultra-micro ginger powder. The ultra-micro ginger powder prepared by the method can replace part of fresh ginger powder and is directly used for preparing ginger powder seasoning, ginger beverage, nutritional supplement, Chinese patent drug and the like. On the premise that active ingredients are not reduced, the cost of the raw material of the fresh ginger powder is greatly lowered, and the problem of environmental protection treatment for the discharge of leftovers during ginger processing is completely solved.

The invention discloses a wet tissue with the effects of activating blood circulation, dispersing stasis and relieving swellings and pain and relates to technical field of wet tissue production. The wet tissue consists of a wet tissue matrix and a base solution attached to the matrix, wherein the base solution is prepared from the following raw materials in parts by mass: 50-65 parts of pseudo-ginseng, 30-40 parts of curculigo sinensis, 30-35 parts of dipsacus asper, 20-30 parts of murraya, 20-25 parts of pink reineckea herb, 15-20 parts of claoxylon polot merr, 15-20 parts of sappanwood, 10-15 parts of semen vaccariae, 15-25 parts of gendarussa vulgaris, 10-15 parts of garden balsam stem, 5-10 parts of notopterygium root, 10-15 parts of magnoliae officinalis, 5-10 parts of scarlet kadsura root and 5-10 parts of cortex periplocae. The wet tissue with the effects of activating blood circulation, dispersing stasis and relieving swellings and pain is prepared by using natural Chinese herbal medicines as raw materials, and the medicinal ingredients enter the body from the skin, and can perform a local therapeutic effect and achieve the purpose of treating the whole body. The wet tissue rapidly takes effect, does not have adverse reaction, and is convenient to carry and use.

The invention relates to a preparation method of an inorganic and organic composite coagulant. Dimethyl diallyl ammonium chloride and water are mixed, ferric chloride and an initiator are sequentially added, the mixture is reacted at 85 DEG C-95 DEG C, and then the inorganic and organic composite coagulant is obtained. By means of the preparation method, the uniformity, stability and use effect of the composite coagulant can be improved, the prepared composite coagulant is not prone to layering, has good dispersion performance in use, takes effect fast and is high in sedimentation and clarification speed and good in treatment effect, and solid floc particles can be formed. The inorganic and organic composite coagulant is high in charge density and suitable for treating biological pharmacy wastewater and fermentation wastewater.

The present invention discloses a preparation made up by using artemisinin or its derivative and amodiaquine or its derivative and its preparation method. Said preparation is formed from active component and pharmaceutically-acceptable solid additive, the described active component is the mixture formed from artemisinin or its derivative and amodiaquine or its derivative. Said preparation can high-effectively and durably kill plasmodia.

A dripping pill for treating diabetes features high natural level and safety and low toxic by-effect. Its preparing process is also disclosed.

The invention relates to a holographic circulation repair pain-relieving external medicinal liquor for treating internal and external injury pain and a preparation method thereof, and belongs to the technical field of preparation of traditional Chinese medicines. The external medicinal liquor comprises liquor and Chinese herbal medicines, wherein the Chinese herbal medicines comprise, by weight, 10-30 parts of raw radix aconite, 10-30 parts of raw radix aconiti agrestis, 10-30 parts of resina draconis, 10-30 parts of scorpions, 10-30 parts of centipedes, 10-30 parts of earthworms, 10-30 partsof ground beetles, 10-60 parts of notopterygium root, 10-50 parts of cassia twigs, 10-50 parts of divaricate saposhnikovia root, 10-50 parts of rhizoma cyperi, 20-60 parts of suberect spatholobus stems, 20-60 parts of common clubmoss herb, 20-80 parts of phryma leptostachya, 20-60 parts of caulis pipers futokadsurae, 20-60 parts of caulis sinomenii, 20-80 parts of radix cyathulae, 20-80 parts of dipsacus asperoids, 20-80 parts of rhizoma cibotii, 20-60 parts of radix curcuma, 30-100 parts of raw radix astragali, 20-60 parts of white peony root, 20-60 parts of polygonum cuspidatum, 20-60 partsof safflower and 20-60 parts of radix angelicae pubescentis. The addition amount of the liquor is 8-15 times of the total weight of the Chinese herbal medicines. The external medicinal liquor can be used for treating various kinds of arthralgia and myalgia, and also can be used for conditioning and treating diseases of digestive systems, heart and brain systems and the like.

A dripping pill of haw flavone for treating cardiovascular and cerebrovascular diseases features high natural level and safety and low toxic by-effect. Its preparing process is also disclosed.

The invention provides a medicament which can enhance immune function. The invention overcomes the shortcomings of the prior dripping pills that pure natural degrees of findings which are used by the prior dripping pills are not high, and chemosynthesis findings which are commonly used are not in food additives catalogs of some countries, and tastes of the dripping pills are worse. The invention is a pharmaceutical preparation whose natural degree is higher, safety is stronger, and side effect is lower.