41results about How to "Detox fast" patented technology

Nicotine dependency is treated by administration of an opioid antagonist. In some embodiments, rapid or ultra rapid detoxification techniques include using a combination of an effective amount of an opioid antagonist such as nalmefene, naloxone or naltrexone or a mixture of any one of these, and either clonidine or related compounds either while awake, or while under sedation or anesthesia, followed by continued administration of an effective amount of an opioid antagonist with or without agents that enhance nicotine dependency treatment. Persons are also treated for nicotine dependency with more gradual detoxification methods using administration of a combination of an effective amount of an opioid antagonist such as nalmefene, naloxone, naltrexone, or a mixture of any of these, and an effective amount of agents used to treat nicotine withdrawal including nicotine, such as that delivered by a nicotine patch, nicotine chewing gum, nicotine inhaler or other methods for delivering nicotine, antidepressants and antianxiety agents, and / or clonidine and related compounds. Administration of an effective amount of an opioid antagonist to prevent relapse, attenuate craving, and reduce weight gain during and after treatment for nicotine dependency is continued in some embodiments.

The present invention provides a flowable composition suitable for use as a controlled release implant. The composition includes: (a) a biodegradable, biocompatible thermoplastic polymer that is at least substantially insoluble in aqueous medium, water or body fluid; (b) a cell-cycle dependent biological agent, a schedule-dependent biological agent, a metabolite thereof, a pharmaceutically acceptable salt thereof, or a prodrug thereof; and (c) a biocompatible organic liquid, at standard temperature and pressure, in which the thermoplastic polymer is soluble. The present invention also provides a method of treating cancer in a mammal. The present invention also provides a method of blocking, impeding, or otherwise interfering with cell cycle progression at the G1-phase, G1 / S interphase, S-phase, G2 / M interface or M-phase of the cell cycle in a mammal. The methods includes administering to a mammal an effective amount of a flowable composition of the present invention.

Biodegradable neurotoxin implants and methods of making and using such implants are provided. Biodegradable neurotoxin implants include a neurotoxin, a biodegradable polymer component, and an acidity regulating component. The biodegradable polymer component is effective in controlling the release of the neurotoxin from the implant when the implant is located in a patient's body. The acidity regulating component is effective in maintaining a pH of the implant in a desired range that may be effective in stabilizing the neurotoxin as the implant biodegrades when the implant is located in a patient's body. In one embodiment, an implant includes a botulinum toxin, a biodegradable polymer, and either monomers from which a biodegradable polymer is derived or oligomers including monomeric units substantially identical to a monomer from which a biodegradable polymer is derived, or a combination of such monomers and oligomers. The oligomers and biodegradable polymer may be derived from a single type of monomer. The implants disclosed herein may be administered to a human or animal patient in which a therapeutic effect is desired for prolonged periods of time.

A two-component, water based micro encapsulation composition and method for the cleanup of hydrocarbon spills or contaminates on various surfaces and media. The two-part formulation includes a first solution including water in a predetermined ratio of a water soluble alkaline silicate solution having at least one alkali metal and a predetermined ratio of at least one water soluble surfactant; and a second solution including water, a predetermined ratio of water soluble acid, a predetermined ratio of water dispersible polymer, a predetermined ratio of water soluble hydrotrope, and a predetermined ratio of at least one water soluble flocculating agent. A method of using the two-part formulation includes preparing the two-part formulation, allowing the first solution to contact the hydrocarbon or chemical contaminate; allowing the second solution to contact the first solution and contaminate to form a homogeneous mixture; and removing the homogeneous mixture.

Conversion of an untreated liquid to a clean harmless treated liquid through microbe removal, characterized in that a mechanical treatment for damaging microbes present in a liquid to thereby effect extinction thereof and sterilization, combined with a chlorination in which a chlorine-containing substance is formed from a liquid and injected into a liquid to thereby effect microbe extinction and sterilization, is applied to a liquid. There is further provided an electrolytic circulation system comprising applying a detoxification treatment for extinction of microbes in seawater and sterilization by means of detoxification facilities on land or on the sea to seawater introduced through a seawater introduction channel and accommodating the seawater having been thus treated in a ballast water tank. As a result, facility and operating costs can be reduced. Extinction of microbes of unlimited size and sterilization can be securely achieved without any strength drop on the side of treated liquid accommodation body. Further, the space for installation of detoxification apparatus for ballast water in ships can be reduced to thereby enable increasing of loading space for cargo, etc. Still further, on existing ships, the hull rework cost for installation of detoxification apparatus can be minimized.

The invention discloses a biological detoxification method of cottonseed meal, comprising: adding ferrous sulfate heptahydrate, 40,000-60,000 U / g of neutral xylanase, microorganism strains and the like into smashed cottonseed meal; after being evenly stirred, jointly acting for 4-5 days by microorganism and neutral xylanase at the temperature of 45-55 DEG C; and drying and smashing to obtain the product. The free gossypol content of the obtained product is lowered than the safety index specified by feed, the nutritional value thereof is higher than that of unleavened cottonseed meal, product protein content reaches 45-50%, free amino acid content is above 15%, and the cottonseed meal can be directly used as protein feed. The invention better solves the problems of incomplete detoxification of cottonseed meal, protein denaturation and secondary feed pollution due to adopting the chemical detoxification method in the prior art, and provides a non-toxic cottonseed meal production method which has favorable detoxification effect and low technical energy consumption and can reach feed standard requirements.

The invention discloses a method for breeding aphidius gifuensis within a short cycle. The method comprises the steps of: host plant cultivation, pest species breeding, and aphidius gifuensis large-scale breeding. A breeding cycle of the whole process is 29-40 days. Each dish of brassica chinensis can breed more than 12000 of aphidius gifuensis, a parasitism rate of the aphidius gifuensis is 95%, a formation rate of stiff aphids is 60%, and stiff aphids of the aphidius gifuensis in each dish can be used for controlling 10-15 mu of aphid-damaged farmland. Brassica chinensis of a vegetable variety is adopted as a host plant with high strong adaptability and fast growth; and the brassica chinensis a host plant variety with a shortest cultivation cycle in current breeding technology of sphidius gifuensis, thereby reducing a breeding cycle of the aphidius gifuensis, and improving breeding efficiency of the aphidius gifuensis. The method adopts a flotation breeding method for cultivating the host plant, is simple in process step and solves the problems such as high breeding energy consumption, a tedious technical process, poor activity of the aphidius gifuensis, and irregular formation of the stiff aphids of the aphidius gifuensis, and can increases a utilization rate of the aphidius gifuensis for wide application in agriculture and forestry industry, thereby enabling the aphidius gifuensis to have better feasibility of production, promotion, and application.

The invention discloses low-yanide semen armeniacae amarum and a preparation method thereof and belongs to the technical field of primary processing of semen armeniacae amarum. The preparation method comprises the following steps: semen armeniacae amarum is adopted as the raw material and subjected to peeling, debittering and detoxification to obtain almond carpel; the almond carpel is subjected to microwave drying to obtain dry almond carpel; semen armeniacae amarum skin is collected, frozen and crushed, and the crushed semen armeniacae amarum skin is uniformly mixed with a debittering liquid; the mixture is subjected to enzymolysis and twice distillation to obtain a semen armeniacae amarum skin extract; the semen armeniacae amarum skin extract is decolored and then mixed with the dry almond carpel at a certain proportion; the obtained mixture is stir-fried to obtain the semen armeniacae amarum which has the natural flavor of semen armeniacae amarum, is smooth and tidy, high in debittering ratio (98.5-99.8 percent), remarkable in detoxification effect (the cyanide residual quantity is 0.04-0.06 mg / kg) and long in guarantee period (24-36 months). The preparation method is simple in process, short in period, high in efficiency and energy-saving, can realize mass production, achieves the purpose of zero emission of toxic substances in the technical field of primary processing of semen armeniacae amarum, is environmental-friendly and explores a novel shortcut for deep processing of semen armeniacae amarum.

A process for extracting the scorpion venom and cleaning it includes such steps as cleaning the living scorpion, stimulating it at a temp higher than 30 deg.C in aseptic environment by electric pulses (8-10 v) at 139 Hz for a time less than 1 s, collecting scorpion venom by a container at -2-2 deg.C, filtering and freeze-drying. Its advantages are high quality and content of toxic protein, and low damage to scorpion.

The invention discloses an anti-wrinkle skin-tendering emulsion containing natural component extracts and a preparation method thereof. The emulsion is prepared from the following substances: grape seed oil, wheat-germ oil, broccoli juice, pea shoot juice, nicotinamide, vitamin C, synthetic squalane, sodium alginate, carbomer, poloxamer, a self-emulsified compound emulsifier, glycerol, triethanolamine, a 10% ethylenediamine tetraacetic acid disodium solution, a 20% methylparaben alcoholic solution and distilled water. Compared with the prior art, the emulsion has the characteristics of mild property and high safety, O / W type emulsion with uniform and fine texture, freshness without greasy feeling can be prepared by adopting a method of combining natural component extracts and plant essential oil. The emulsion is capable of firming skin and smoothing wrinkles, and exerting certain effects of removing spots, whitening and nourishing, so that the tender and moistened activity of skin can be rejuvenized.

The present invention provides one kind of Chinese medicine composition, and its suppository and application in preparing opioid drug-relieving medicine and, especially, opioid analgesic. The Chinese medicine composition contains the main active components including tea, cassia twig, borneol and freeze dried snake venom of Agkistrodon halys Pallas. The Chinese medicine composition and its suppository is superior to commonly used Western non-opium excitant, and has fast detoxification, high safety, no toxic side effect and no addiction, and is suitable for use in household.

The invention discloses environment-friendly bitter apricot kernels and a preparation method thereof, belonging to the technical field of bitter apricot kernel primary processing. The preparation method has the beneficial effects that bitter apricot kernels are taken as raw materials and are peeled, debitterized and detoxified to obtain apricot kernel segments, then the apricot kernel segments are subjected to microwave drying to obtain dry apricot kernel segments, bitter apricot kernel skins are collected, frozen and broken, are uniformly mixed with a debitterizing liquid and are subjected to enzymolysis and two-time distillation to obtain an apricot kernel skin extract, the apricot kernel skin extract is mixed with the dry apricot kernel segments according to a certain proportion after being decolorized, and the mixture is stir-fried, thus obtaining the bright, clean and tidy low-cost bitter apricot kernels with natural flavors of bitter apricot kernels, high debitterizing rate (98.5-99.8%), obvious detoxification effects (the residual quantity of cyanides is 0.04-0.06mg / kg) and long shelf life (24-36 months); the preparation method is simple in process, short in cycle and high in efficiency, has the effect of saving energy, can be used for large-scale production, achieves zero discharge of toxic substances in the technical field of bitter apricot kernel primary processing, is environment-friendly and has the effect of exploring a new shortcut for deep processing of bitter apricot kernels.

The invention provides a capsule for drug addiction treatment and a preparation method thereof. The capsule comprises the following components in parts by weight: 3 to 10 parts of campsis grandiflora, 3 to 10 parts of berba aristolochiae mollissima, 3 to 10 parts of stasis blocking medicine, 20 to 30 parts of hedyotis diffusa, 8 to 10 parts of sculellaria barbata, 10 to 15 parts of phryma leptostachya, 3 to 6 parts of celastrus orbiculatus, 20 to 30 parts of herba pteridis multifidae, 10 to 30 parts of zuobanteng (traditional Chinese medicine), 10 to 20 parts of selfheal, 2 to 6 parts of baizhongzhi (traditional Chinese medicine), 10 to 12 parts of blackberry lily, 10 to 15 parts of oldenlandia chrysotricha chun, 8 to 15 parts of herba violae, 8 to 15 parts of dandelion, and 6 to 8 parts of wikstroemia indica, amounting to 16 medicines. The preparation method of the capsule for drug addiction treatment comprises the steps of processing, concentrating, extracting and refining. The capsule for drug addiction treatment is mainly used for detoxicating, cleaning, eliminating and de-addicting a person taking heroin, amphetamin chloride, marihuana, dancing outreach and various addiction drugs, and is safe and convenient.

The invention relates to the technical field of traditional Chinese medicine formulas and preparation methods thereof, and particularly relates to a traditional Chinese medicine formula for stopping novel drug addiction and carrying out rehabilitation treatment on sequelae and a preparation method thereof. The traditional Chinese medicine formula comprises the following components in parts by weight: 20-45 parts of carambola flowers, 30-35 parts of salvia miltiorrhiza, 20-35 parts of polygala amflra, 30-45 parts of rhizoma acori graminei, 9-18 parts of gardenia jasminoides, 15-30 parts of fructus schizandrae, 25-50 parts of dried tangerine or orange peel, 40-50 parts of herba violae, 30-35 parts of radix semiaquilegiae, 40-50 parts of dandelion roots, 30-35 parts of Chinese milkwort, 20-30 parts of semen ziziphi spinosae, 20-30 parts of feather cockscomb seeds, 25-30 parts of mother-of-pearl, 30-35 parts of snakegourd seeds, 20-30 parts of pinellia ternate, and 10-20 parts of fritillaria cirrhosa. The traditional Chinese medicine formula disclosed by the invention is good in curative effect, and fills up a gap in stopping domestic novel drug addiction and carrying out rehabilitation treatment on sequelae.

The invention discloses a medicament for treating lymphoid tuberculosis and a preparation method thereof. The medicament comprises the following components in part by weight: 1 to 6 parts of kelp, 1 to 6 parts of seaweed, 1 to 6 parts of oyster shell, 1 to 6 parts of rhizoma smilacis glabrae, 1 to 6 parts of subprostrate sophora, 1 to 6 parts of wild buckwheat, 1 to 6 parts of perfoliate knotweed herb, 1 to 6 parts of bubble tree, 1 to 6 parts of nine rings, 1 to 6 parts of wild polygonum and 1 to 6 parts of citron day-lily. The medicament also comprises of wild buckwheat, schisandra propinqua leaf,chaulmoogratree, perfoliate knotweed herb, radix aconite and kusnezoff monkshood, and semen momordicae. The medicament is prepared by the following steps of: A, respectively taking 1 part of kelp, seaweed, oyster shell, rhizoma smilacis glabrae, subprostrate sophora, wild buckwheat, perfoliate knotweed herb, bubble tree, nine rings, wild polygonum and citron day-lily, and cutting into segments respectively; B, decocting the segments in a container for three times and merging into 60 milliliters of 100 percent decoction; C, taking the wild buckwheat and schisandra propinqua leaf and grinding into powder; and D, putting the ground powdery medicaments into the container, and adding warm boiled water, stirring uniformly and sealing. The medicament is used in a way that the finished liquid medicine is orally taken in three days; meanwhile, the pasty finished medicament is externally applied to the wound. The Chinese herbal medicament can effectively and radically cure the lymphoid tuberculosis disease.

The invention discloses bright bitter apricot seeds and a preparation method thereof, and belongs to the technical field of primary processing of bitter apricot seeds. The preparation method comprises the following steps of peeling, debitterizing and detoxifying the bitter apricot seeds serving as raw materials so as to obtain apricot seed cloves; then performing microwave drying so as to obtain dried apricot seed cloves; collecting bitter apricot seed peel, refrigerating the collected bitter apricot seed peel, crushing the refrigerated bitter apricot seed peel, uniformly mixing the crushed bitter apricot seed peel with debitterizing liquid, and performing enzymolysis and distillation twice so as to obtain an apricot seed peel extract; and then performing decoloration, mixing the apricot seed peel extract after the decoloration with the dried apricot seed cloves according to a certain proportion so as to obtain a mixture, and then stir-frying the mixture so as to obtain the bitter apricot seeds with natural flavor of the bitter apricot seeds, high smoothness and tidiness, high debitterizing rate (98.5-99.8%), significant detoxifying effects (the quantity of cyanide residues is 0.04-0.06mg / kg), long quality guarantee period (24-36 months) and low cost. The preparation method disclosed by the invention is simple in technology, short in cycle and high in efficiency, energy resources are saved, the large-scale production can be realized, zero discharge of toxic substances in the technical field of the primary processing of the bitter apricot seeds is realized, the preparation method is environment-friendly, and a new shortcut is explored for the deep processing of the bitter apricot seeds.

The invention discloses a natural galenical preparation for promoting nutrition rehabilitation of a mucous membrane of an animal. The natural galenical preparation consists of the following materials according to the parts by weight: 1-3 parts of dendrobe extract, 1-2 parts o f wrinkled giant hyssop extract, 1-3 parts of Astragalus mongholicus extract, 2-4 parts of Hypericum Perforatum extract, 2-5 parts of Hericium erinaceus extract, 1-5 parts of pine extract and 2-6 parts of carriers. A preparation method of the natural vegetable preparation comprises: extracting dendrobe, wrinkled giant hyssop, Astragalus mongholicus, Hypericum Perforatum, Hericium erinaceus and the pine respectively by alcohol and water to obtain dry extract powder; mixing the dry extract powder by proportion; adding the carriers for stirring; finally obtaining the natural vegetable preparation for promoting the nutrition rehabilitation of the mucous membrane of the animal. The invention has the advantages that the natural vegetable preparation repairs various tissues and the mucous membranes of conduits of the organisms of sub-health or ill livestock and birds fast, improves the immunization function of the organisms, enhances the disease resisting and preventing abilities of the organisms, improves the vitality, reduces the stress, promotes the growing of livestock and birds, protects the mucous membranes of the gastrointestinal tracts effectively and resists the invasion of mycotoxin and the like.

The invention discloses semen armeniacae amarum with a long quality guarantee period and a preparation method of the semen armeniacae amarum, and belongs to the technical field of primary processing of semen armeniacae amarum. The preparation method comprises the following steps of using the semen armeniacae amarum as raw materials, and peeling, debitterizing and detoxifying the semen armeniacae amarum so as to obtain the embryo of semen armeniacae amarum; then performing microwave drying so as to obtain the dried embryo of semen armeniacae amarum; collecting the seedcoat of semen armeniacae amarum, refrigerating the collected seedcoat of semen armeniacae amarum, crushing the refrigerated seedcoat of semen armeniacae amarum, uniformly mixing the crushed seedcoat of semen armeniacae amarum and debitterizing liquid, and performing enzymolysis and two times of distillation so as to obtain an extract of the seedcoat of semen armeniacae amarum; and then performing decoloration, mixing the extract after the decoloration with the dried embryo of semen armeniacae amarum according to a certain proportion so as to obtain a mixture, and then stir-frying the mixture so as to obtain the semen armeniacae amarum with a natural flavor of the semen armeniacae amarum, high smoothness and tidiness, a high debitterizing rate (98.5-99.8%), significant detoxifying effects (the quantity of cyanide residues is 0.04-0.06mg / kg), a long quality guarantee period (24-36months) and a low cost. The preparation method disclosed by the invention is simple in technology, short in cycle, and high in efficiency, saves energy resources, can realize large-scale production, can realize zero discharge of toxic substances in the technical field of the primary processing of the semen armeniacae amarum, is environment-friendly, and provides a new shortcut for the deeply processing of the semen armeniacae amarum.

The invention discloses a preparation method of novel fermented golden flaxseed meal and particularly relates to the technical field of feeds. The method includes: 1) preparing a fermenting agent including 15% of lactobacillus acidophilus, 25% of bacillus natto, 15% of lactobacillus plantarum, 20% of enterococcus faecalis, 10% of EM bacteria, and 15% of saccharomycetes; 2) adding water to the fermenting agent and golden flaxseed meal for mixing fermentation under a sealed condition for 70-72 h, wherein the fermenting agent accounts for 0.5 mass% of the golden flaxseed meal. The preparation method is simple, is good in condition controllability, and is short in fermenting time, high in efficiency and low in cost. After fermentation, contents of small-molecular peptides, active probiotics and organic acids in the golden flaxseed meal are high. The fermented golden flaxseed meal is blended with complete pig feed for feeding pigs, thus increasing the content of alpha-linolenic acid and eicosapentaenoic acid (EPA). The product also can effectively increase intake of pigs and increase daily gain and can increase feed conversion ratio and improve the taste and quality of the pork.

The invention relates to a Wuqing Tongti oral liquid and a method for preparing the same. The liquid consists of an A liquid and a B liquid, wherein the A liquid consists of the following components of ginseng, kudzu root, fleeceflower root, cassia seed, folium ginkgo, lotus leaf, chrysanthemum and black sesame seed; and the B liquid consists of the following components of shaddock juice, red date juice and olive oil; the preparation method is as follows: the Chinese medicine materials of the A liquid are put in a medicinal herb boiling kettle to be added with water, extracted and filtered, and dregs are added with water, extracted and filtered, and both filter liquors are mixed together and have dregs removed by a centrifuge, and the concentrated solution is obtained; the concentrated solution is added with quanta resonance magnetic water and stirred, volume-fixed and subpackaged, and an A oral liquid is obtained; the materials of the B liquid are mixed to prepare the material mixture, and the material mixture is added with quanta resonance magnetic water and stirred, volume-fixed and subpackaged, and a B oral liquid is obtained. The invention realizes the entire and complete expulsion of toxin, and the toxin expulsion process is simple and fast without pain and toxic and side effects; so that the invention has functions of reducing the blood fat and protecting the chemical liver injury.

The invention discloses a drug addiction treatment method for synthetic drugs, which comprises rapid detoxification, promotion of cerebral nerve cell function recovery, control of psychiatric symptoms, psychological treatment and treatment for relapse prevention. The drug addiction treatment method is an MDT (Multidisciplinary Team) multidisciplinary synthetic therapy which has the advantages of rapid detoxification, thorough detoxification, comprehensive treatment and definite therapeutic effect; through a unique Zexu secret recipe, in combination with infusion, urine acidification and traditional Chinese medicine fumigation methods, the drug addiction treatment method for the synthetic drugs can rapidly expel toxin in the body of a patient, and can repair cerebral nerve cells injured bydrug intake at the same time, and moreover, supplemented by psychological treatment, the drug addiction treatment method for the synthetic drugs can effectively get rid of psychological addition, helping drug addicts to get better rehabilitation later and increasing the rate of relapse prevention.

The invention discloses a fumigation agent for weight-losing and skin whitening and a preparation and using method thereof; the weight percentage of raw materials is as follows: 0.5-0.8% of saffron crocus, 0.5-0.8% of glossy ganoderma, 0.5-1% of Jinluohan (a kind of Tibetan medicines) , 8-10% of sarmentose pepper herb, 10-12% of passiflora perpera mast., 10-12% black bark maple, 10-12% of large bark maple, 3-8% of mahonia ganpinensis, 3-8% of watermelon pilea, 3-5% of polygonum cuspidate, 5-10% of mucuna macrocarpa and 40-45% of stone needle. The medicinal materials are soaked, boiled under high pressure and concentrated to obtain the fumigation agent which is put in a vapor generating vessel, then the generated vapor is conducted into a container, and the temperature is adjusted to 45-60% for use. The fumigation agent can facilitate weight losing and skin whitening; in addition, the fumigation agent also has excellent effect for preventing and treating rheumatism, rheumatoid arthritis, cervical spondylosis, scapulohumeral periarthritis, hyperosteogeny, talalgia, exogenous wind-cold, stiff neck, insomnia, air conditioning diseases, etc.

The present invention provides a substituted imidazopyridine derivative, a prodrug, an oxide, a salt, a metal complex or a stereochemical isomer having the structure of Formula I and a pharmaceutical composition containing the same, and a method of using the composition for the treatment of RSV viral infections. The compound provided by the invention has the advantages of high metabolic stability, high solubility, high oral absorbability, good bioavailability, fast detoxification, good antiviral activity, high therapeutic index, low cardiotoxicity and the like.

The invention discloses edible bitter apricot kernels and a preparation method thereof, belonging to the technical field of bitter apricot kernel primary processing. The preparation method has the beneficial effects that bitter apricot kernels are taken as raw materials and are peeled, debitterized and detoxified to obtain apricot kernel segments, then the apricot kernel segments are subjected to microwave drying to obtain dry apricot kernel segments, bitter apricot kernel skins are collected, frozen and broken, are uniformly mixed with a debitterizing liquid and are subjected to enzymolysis and two-time distillation to obtain an apricot kernel skin extract, the apricot kernel skin extract is mixed with the dry apricot kernel segments according to a certain proportion after being decolorized, and the mixture is stir-fried, thus obtaining the bright, clean and tidy low-cost bitter apricot kernels with natural flavors of bitter apricot kernels, high debitterizing rate (98.5-99.8%), obvious detoxification effects (the residual quantity of cyanides is 0.04-0.06mg / kg) and long shelf life (24-36 months); the preparation method is simple in process, short in cycle and high in efficiency, has the effect of saving energy, can be used for large-scale production, achieves zero discharge of toxic substances in the technical field of bitter apricot kernel primary processing, is environment-friendly and has the effect of exploring a new shortcut for deep processing of bitter apricot kernels.