57 results about "Pain killers" patented technology

An aerosol container 190a provided with an outer container 11, a collapsible inner bag 12 inserted in the outer container, and a valve 13. The inner bag 12 comprises an upper and lower chamber 27, 26 and the chambers are divided at a constriction part formed in the middle of the inner bag by a partitioning member 72. The valve 13 has communicating holes that communicates valve 13 with the upper chamber 27 and the lower chamber 26 through a dip tube 28. An inner bag type aerosol product may be obtained by charging different kind of contents A and B into the container. Two-liquid reaction type agents, such as hair dye. enzyme hair dye, hair dress agent or setting agent for hair, reduction of inflammation pain killer, anti-heat flushes, coolants, pack agents, cleansing agents, shaving foams, moisturizers, antipersipirants. vitamin preparations, emollients and etc. may be preferably used for the combination of the contents for aerosol product.

Compositions and related methods for treating IBS and other gastrointestinal disorders and conditions (e.g., gastrointestinal motility disorders, functional gastrointestinal disorders, gastroesophageal reflux disease (GERD), duodenogastric reflux, Crohn's disease, ulcerative colitis, inflammatory bowel disease, functional heartburn, dyspepsia (including functional dyspepsia or nonulcer dyspepsia), gastroparesis, chronic intestinal pseudo-obstruction (or colonic pseudoobstruction), and disorders and conditions associated with constipation, e.g., constipation associated with use of opiate pain killers, post-surgical constipation, and constipation associated with neuropathic disorders as well as other conditions and disorders are described. The compositions feature peptides that activate the guanylate cyclase C (GC-C) receptor.

Compositions and related methods for treating IBS and other gastrointestinal disorders and conditions (e.g., gastrointestinal motility disorders, functional gastrointestinal disorders, gastroesophageal reflux disease (GERD), duodenogastric reflux, Crohn's disease, ulcerative colitis, inflammatory bowel disease, functional heartburn, dyspepsia (including functional dyspepsia or nonulcer dyspepsia), gastroparesis, chronic intestinal pseudo-obstruction (or colonic pseudoobstruction), and disorders and conditions associated with constipation, e.g., constipation associated with use of opiate pain killers, post-surgical constipation, and constipation associated with neuropathic disorders as well as other conditions and disorders are described. The compositions feature peptides that activate the guanylate cyclase C (GC-C) receptor.

Compositions and related methods for treating IBS and other gastrointestinal disorders and conditions (e.g., gastrointestinal motility disorders, functional gastrointestinal disorders, gastroesophageal reflux disease (GERD), duodenogastric reflux, Crohn's disease, ulcerative colitis, inflammatory bowel disease, functional heartburn, dyspepsia (including functional dyspepsia or nonulcer dyspepsia), gastroparesis, chronic intestinal pseudo-obstruction (or colonic pseudoobstruction), and disorders and conditions associated with constipation, e.g., constipation associated with use of opiate pain killers, post-surgical constipation, and constipation associated with neuropathic disorders as well as other conditions and disorders are described. The compositions feature peptides that activate the guanylate cyclase C (GC-C) receptor.

The invention discloses an extraction method for high-purity tetrodotoxin, which is mainly used for extracting tetrodotoxin from animal feed puffer fish seeds and livers by jointly utilizing the methods of ultrasonic fast dissolving out, organic solvent derosination, plate frame multi-level filtration, positive ion exchange resin, small film filtration, high-performance liquid preparation and the like and obtaining high-purity high-stability tetrodotoxin crystals. Tetrodotoxin has the effect of blocking a sodium ion channel is obvious in analgesic effect and free of dependency and is widely used in advanced cancer, postoperative pain relieving, de-addiction curing of drug abuse and the like. Extraction and preparation of high-purity tetrodotoxin can provide the possibility of developing a novel high-efficiency pain killer free of dependency.

The invention belongs to the technical field of traditional Chinese medicines, and particularly relates to topical medicinal liquor for treating a rheumatoid bone disease. The topical medicinal liquor is prepared from prepared monkshood, prepared radix aconiti agrestis, eucommia ulmoides, flowers carthami, cinnamon, radix cyathulae, scorpio, long-noded pit viper, radices sileris, angelica sinensis, homalomena occulta, schizonepeta, radix clematidis, as arum, dipsacus root, pseudo-ginseng and white spirit. The prescription disclosed by the invention is appropriate and rigorous in compatibility of medicines, and unique in preparation method, can rapidly cure hyperostosis by the topical medicinal liquor disclosed by the invention, and is rapid to become effective, short in treatment course, high in recovery rate and low in expense. The drug has unique curative effects for rheumatism, rheumatoid arthritis, pain in waist and lower extremities, scapulohumeral periarthritis, limbs anesthesia, ischioneuralgia, hyperostosis, lumbar disc herniation, cervical spondylosis, ankylosing spondylitis, hyperplasia of mammary glands, various pain killer diseases, fracture sequelae and femoral head necrosis.

The invention belonging to the field of aquaculture technology relates to a method of anesthesia for tilapia. The invention is characterized in that, infuse warm water into the container, the water temperature is 18 DEG C-30 DEG C; infuse narcotic clove oil into container to prepare for the clove oil solution; put the tilapia into the clove oil solution, the anesthesia time is: 2-5 minutes, then move the anaesthetic anesthesia into the pool for recovery of 3-8 minutes, the tilapia is recovered to swim normally. The invention applies the clove oil on the market as the anesthesia to anaesthetize the tilapia, the anesthesia effect is good; the clove oil can be used as tooth pain killer for human, so the anaesthetic anesthesia is safe to eat; the price is low, and the applied range is wide.

The invention relates to a blood withdrawal device (10) having an active liquid (12) containing a platelet aggregation inhibitor, a microneedle patch (14) having a plurality of microneedles (20), wherein a plurality of microneedles (20) is configured for dispensing the active liquid (12) into the skin (34) of a patient, and comprising a negative pressure generating device (16) connected to a plurality of microneedles (20) such that blood (46) can be drawn from the skin (34) by means of the microneedles (20). According to the invention the active liquid (12) contains a pain killer, the active liquid (12) is arranged in the blood reservoir (18), and the negative pressure generating device (16) is connected to the blood reservoir (18) such that by generating an excess pressure in the blood reservoir (18), the active liquid (12) can be dispensed by way of microneedles (20), and by generating a negative pressure, blood (46) can be drawn into the blood reservoir (18).

A clamp and handle is designed exclusively for holding purchased containers of rub on and roll on pain killers, deodorants and any other substance that is in a container with a built in applicator. The handle is for applying these substances to hard or impossible places to reach due to anatomy or injury. The clamp, handle and knob are constructed from PVC that has a smooth glossy finish for the purpose of not causing any injury. The PVC can move smoothly over skin. The knob is flower shaped to make it easier to grip. The knob and clamp body prevent the stainless steel screw from scratching any skin. The screw will never rust.

A light guide type pain reliever includes a handle including a barrel accommodating a battery, a rear end cap and a front end cap respectively capped on two opposite ends of the barrel, a pushbutton mounted in the rear end cap and a switching connector mounted in the rear end cap and electrically connected to the battery and drivable by the pushbutton to switching on / off the battery, a holder shell connected to the front end cap and electrically coupled to the battery and having electrically connected thereto a vibrator and a light-emitting device, an adapter connected to the holder shell, and a light guide plate connected to adapter guiding out light rays emitted by the light-emitting device.

The present invention relates to a high-frequency thermotherapy device. More specifically, when a detection signal related to normal muscularity and abnormal muscularity, inputted through a sensor module, is received, the high-frequency thermotherapy device automatically changes the detection signal to have a frequency of 2 to 5 MHz in a frequency adjustment oscillation module of an impedance detection unit, and generates a high frequency in a high-frequency generation unit according to an impedance value, so as to provide the changed frequency to the location of the abnormal muscularity or skin, thereby enabling a treatment effect for deformation or various inflammations of the abnormal muscularity without damaging the normal muscularity and a reduction in the amount of a pain-killer used by alleviating pain, selectively adjusting an output from among three stages of strong, intermediate and weak according to a state of an affected part in a control panel unit of a display, adjusting voltage settings, and receiving power from a second power source unit and control a ceramic member to sequentially generate deep heat according to a set time of a timer in a control unit.

The invention provides a pain-killer plaster. The pain-killer plaster comprises a heating layer, a fabric layer, a far-infrared ceramic powder layer, a drug layer, a magnet layer and vent holes. The fabric layer is located on the upper layer of the heating layer, and a plurality of vent holes are arranged on the fabric layer; the far-infrared ceramic powder layer is located inside the fabric layer; the drug layer and the magnet layer are located on the fabric layer, and the drug layer surrounds the magnet layer. The far-infrared ceramic powder layer, the drug layer and the magnet layer in thepain-killer plaster of the invention can interact with each other to achieve a better therapeutic effect, wherein infrared rays emitted from the far-infrared ceramic powder layer help skins to betterabsorb drugs. The magnet layer has calming and soothing effects.

The invention discloses a coupling compound or salt or a stereoisomer or prodrug molecules, which are pharmaceutically acceptable. The coupling compound of the structure shown in the formula I or II or III is formed by connecting NSAID anti-inflammatory pain killers and an EGFR kinase inhibitor through ester bonds, wherein the R is the NSAID anti-inflammatory pain killers. The coupling compound obtained by coupling the NSAID anti-inflammatory pain killers and the EGFR kinase inhibitor has the good cancer treatment effect, and the new drug is provided for clinic treatment choices.

The present invention features compositions and related methods for treating IBS and other gastrointestinal disorders and conditions (e.g., gastrointestinal motility disorders, functional gastrointestinal disorders, gastroesophageal reflux disease (GERD), Crohn's disease, ulcerative colitis, Inflammatory bowel disease, functional heartburn, dyspepsia (including functional dyspepsia or nonulcer dyspepsia), gastroparesis, chronic intestinal pseudo-obstruction (or colonic pseudo-obstruction), and disorders and conditions associated with constipation, e.g., constipation associated with use of opiate pain killers, post-surgical constipation (post-operative ileus), and constipation associated with neuropathic disorders as well as other conditions and disorders using peptides and other agents that activate the guanylate cyclase C (GC-C) receptor.

The invention belongs to the technical field of medicines, and particularly discloses an anesthetic. According to the anesthetic, propofol is used as a basic medicament, and a chamomile extract, astragalus powder, mentholum, radix notoginseng powder and a flos daturae extract are used as auxiliary medicaments. The invention further provides a preparation method and a use method of the anesthetic. By adoption of a western and traditional Chinese medicine combined technology, under the condition of keeping the original propofol medicament effect, the pain easing function is enhanced; furthermore, a more serious circulation suppression and breathing suppression effect caused by the propofol is effectively improved; during use, the use amount of a cooperatively used pain killer is reduced, the side effect of the medicament is reduced, and the clinical safety is improved.

The invention discloses compound oxytetracycline injection and a preparation method, particularly relates to compound injection applied to animals. Every 100ml of injection comprises the following components: 5-23g of oxytetracycline, 1-5g of ketoprofen, 30-80ml of an organic slvent, 0.2-2g of an antioxidant, 1.8-8g of a complexing agent, 0.2-1g of a pain killer, 1-7ml of a pH regulator and the balance of injection water. The oxytetracycline and the ketoprofen are prepared into the compound preparation, wherein the oxytetracycline is wide-spectrum antibiotics, and the ketoprofen is an antipyretic-analgesic anti-inflammatory agent, so that the matched using effect is good. The oxytetracycline and the ketoprofen are injection dosage forms; in the past, when the drug is used on a pig, oxytetracycline is injected once on the pig and then the ketoprofen is injected once, however, at present, the compound injection only needs to inject once, so that the pains of the pig are reduced, the site injection work of veterinarians is performed in a more facilitated manner, and the working efficiency of the veterinarians is improved. Due to the use of the compound injection, the cost of packaging, transporting and the like of a medicament bottle are reduced, and the cost is reduced.

The invention discloses a tylosin injection liquid as well as a preparation method and application thereof. The tylosin injection liquid comprises the following components in content: 1.0-30.0% of alkali tylosin, 1.0-15.0% of a medicine slow-release agent, 1.0-10.0% of a surfactant, 1.0-5.0% of a pain killer, 1.0-30.0% of a solution medium and the balance of injection water. As an injection is directly prepared from the alkali tylosin, the treatment effect of a medicine can be greatly improved, and drinking times can be reduced; meanwhile, due to adoption of the high-performance medicine slow-release agent, the medicinal effect lasting time can be prolonged; in addition, by adopting the injection disclosed by the invention, the medicine viscosity can be effectively reduced, and irritationto animal bodies can be reduced.

The invention relates to a medicinal bioculture feeding and culturing device and particularly relates to a meridian-dredging pain-relieving medicinal bioculture device. The meridian-dredging pain-relieving medicinal bioculture device comprises an outer ring component, an inner ring component and a lounge component, wherein the inner ring component is arranged in the outer ring component; a livingarea is formed between the outer ring component and the inner ring component; and the lounge component is arranged in the inner ring component. The device is favorable to quality stability and yield increase of centipedes by imitating wild breeding, can be used for gradually separating big and small centipedes and avoiding occurrence of mutual biting of centipedes and eating off small centipedes by big centipedes due to synergized coordination of the outer ring component, the inner ring component and the lounge component, the lounge component provides a stable resting and producing environmentto spawning centipedes, and can improve the incubation efficiency of centipedes.

The invention belongs to the technical field of medicine, and provides a Tibetan pharmaceutical, lamiophlomis rotata total flavone extractive as well as an extracting method and the application thereof. The method uses Tibetan pharmaceutical lamiophlomis rotata as raw material, uses ethanol prepared by alkalescence solution with different pH values as solvent, and adopts a backflow method for extracting. After two steps of decontamination and the separation and enrichment of macropore resin, the total flavone extractive with the purity being 50 to 95 percent can be obtained from extracting solution. In the process of separation and enrichment, after the two steps of decontamination and the separation and enrichment of macropore resin, a sample with high purity can be obtained and the purity of the total flavone in the sample can be 95 percent at most, wherein, the percentage is higher than the number reported in documents. The invention also provides the application of the total flavone as pain killer medicine and stanch medicine. The paper optimizes and improves the extracting method so as to increase the transfer rate of effective ingredient, improve the utilization rate of medicinal materials and save a great amount of cost effectively, thus having high economical benefit.

The invention relates to a medicinal preparation for promoting healing of body surface injury and a method for preparing the medicinal preparation. Silver sulfadiazine (a), pain killers (b), asiaticoside (c) and other pharmaceutically acceptable carriers (d) are compatible with one another according to suitable proportions to obtain the medicinal preparation. The medicinal preparation and the method have the advantages that the medicinal preparation has double synergistic antibacterial and pain alleviating functions, accordingly, healing of wound surfaces can be promoted, epidermis hyperpigmentation due to the silver sulfadiazine can be prevented, and scar can be reduced; the shortcomings of poor hydrophilicity after existing pain killers and existing silver sulfadiazine are directly compatible with one another and easiness in volatilizing moisture in wound surfaces can be overcome.

The invention discloses a preparation method of a composite inactivated vaccine for an IBD (infection bursal disease) and belongs to the technical field of animal biological products. The preparation method comprises technological steps as follows: 1), virus reproduction; 2), preparation of the composite inactivated vaccine for the IBD: 1-2 parts of an immunopotentiator is added to each 1,000 ml of an IBDV (infection bursal disease virus) antigen solution checked to be qualified in inactivation, the mixture is uniformly mixed, emulsification packaging is performed on the mixture and a summit livestock water-in-oil-in-water adjuvant in the volume ratio being 3:2, and the composite inactivated vaccine for the IBD is prepared. The novel vaccine adjuvant is adopted, and the prepared vaccine has double characteristics of water in oil and oil in water, combines the sustained release function of an ordinary vaccine and has advantages of joint actions of the water-soluble immunopotentiator, flavone of traditional Chinese medicines, a pain killer and the like. With the adoption of the effective immunopotentiator, the immunity of a body is greatly improved, the cellular immunity capability of the inactivated vaccine is improved, the body is stimulated to generate efficient neutralizing antibodies, and the disease prevention capability of the body is improved.

The invention relates to a piece of cloth, in particular to a piece of far infrared cloth containing moxa and a preparation method thereof. The far infrared cloth containing moxa of the invention is formed by four materials of far infrared polypropylene fiber, polyester fiber, mucilage glue fiber and moxa which are mixed, crashed, heated, filtered, condensed, net sprayed and finally conglutinated by heat pressing. The cloth has the advantages of good hand feeling, being warm and comfortable, no pilling, good ventilation property and having moisture absorption property. The cloth can also effectively play the roles of diminishing inflammation, antibacterium and antivirus, sterilizing and relieving itching, antianaphylaxis, enhancing immunity and reducing pressure. Simultaneously, the far infrared rays of the cloth can promote and improve partial and systemic blood circulation, enhance metabolism, improve immunologic function and have the effects of inflammation diminishing, detumescence and pain killer.

A system is provided comprising a columnar sleeve of stretchable fabric, the sleeve produced in various skin tone colors and configured to slip upon an individual toe or finger and an absorbent padding configured for attachment to an inside surface of the sleeve, the padding configured to cover about one half of an interior circumference of the inside surface, the padding optionally infused with at least one of pain killers, antiseptics, and soothing gels. The system also comprises wax paper covering the padding prior to use of the sleeve, an applicator shaped to facilitate slipping the sleeve upon the individual toe or finger, and convex-shaped flex bands placed lengthwise into the sleeve. The flex bands exert downward pressure on one of a toe and a finger and are placed in a U-shape, thus promoting the downward pressure.

The invention discloses a liquid pain killer for treating trauma and a preparation method thereof. The liquid pain killer is prepared by soaking bulk drugs including dandelion root, dragon's blood, radix paeoniae rubrathe, frankincense and borneol in sesame oil. The liquid pain killer provided by the invention has efficacies of heat clearing, detoxifying, subsiding swelling, removing stasis, dredging qi and blood, dispersing blood stasis, relieving pain and engendering flesh, mainly treats wounds, carbuncle, sore, lingering unhealed ulcer and burn, and has advantages of convenience for usage, fast wound healing, short cure time and good prognosis effect. After application, the pain is relieved fast, and general wounds can be cured after 1-2 times of application. The problem of wound sticking of a surgical dressing can be avoided, so as to avoid pains on patients; a cure rate of 98% can be reached; and as reduction of drugs dose, the treatment cost for patients is reduced.

The invention discloses Yuanhu Zhitong Tablet and a preparation method thereof. The Yuanhu Zhitong tablet is composed of vinegar Corydalis and Angelica dahurica; the preparation method of the Yuanhu Zhitong tablet of the present invention is to ultrafinely pulverize 1 / 2 amount of Corydalis Corydalis, extract the remaining Corydalis Corydalis with compound enzymes, and perform supercritical extraction of Angelica dahurica; The invention has the advantages of more complete extraction of active ingredients, higher content, fast drug dissolution rate, high bioavailability and good stability through the improved process.

The invention relates to the field of eye-drop preparations and particularly relates to a pre-operation cornea flushing fluid and a preparation method and application of the pre-operation cornea flushing fluid. The pre-operation cornea flushing fluid is mainly prepared from various raw materials by weight: 0.5-1 part of an electrolyte balance regulator, 0.3-0.7 part of a pH regulator, 0.1-0.4 partof a bactericide, 0.06-0.12 part of a mydriatic, and 0.01-0.03 part of a pain killer. The pre-operation cornea flushing fluid can flush the cornea well before the operation, the particulate matter possibly adhered to the surface of the cornea is cleared, a therapist captures the diseased region conveniently, meanwhile, the cornea is sterilized, the pupillary is dilated, the pain is alleviated, the operation effect of the eye operation is improved, the secondary postoperative infection is prevented, and the osmotic pressure and the pH of the flushing fluid are appropriate, so that the irritation of the flushing fluid on the eye is reduced.

Disclosed are natural compositions including at least five core ingredients that provide pain relief without the side effects of synthetic pain relievers. Further provided are methods of making the disclosed herbal formulations or compositions, and methods of treating mammals that include administering the herbal compositions to a mammal in need thereof.

I have invented a vitamin formula named as “OM VITAMIN FORMULA” that will alleviate the ill-health symptoms induced by Lead intoxication from tap water or by some other means. Ill-health symptoms are: pain, itching, burning, insomnia, depression, panic attacks, infections, elevated blood pressure, elevated cholesterol . . . . Also likely blood sugar level will be elevated. Lack of vitamins in presence of Lead in body will affect body growth and other body functions. As Lead increases the requirements of vitamins in body so body cells start becoming mega (bloated) and will result in obesity.I have BS in Science and MS in Mathematics from India. I have MS in Engineering from UT Austin Tex. Currently, I am working as an Engineer for Dept. of Defense. I sought medical help once I started having multitude of ill-health symptoms. I was prescribed pain killer, sleeping tablets, and depression medicine. My mathematical mind convinced me that something somewhere is wrong and worked overtime for resolution. After 15+ years of suffering and continual experimenting the vitamins supplement in varying dose, I came up with this vitamin formula. Nowadays when causes for many ill-health symptoms are unknown, this formula will be a blessing to all of us.

The current invention provides peptide nucleic acid derivatives targeting the 3' splice site of exon 4 in the human SCN9A pre-mRNA. The peptide nucleic acid derivatives potently induce SCN9A mRNA splice variant(s) lacking the SCN9A exon 4 in cells, and are useful to safely treat pains or conditions involving Nav1.7 activity.