92results about How to "Play an anti-inflammatory role" patented technology

The invention relates to the technical field of traditional Chinese patent medicine, in particular to an itch relieving and detoxifying liquid for mosquito and insect biting. The itch relieving and detoxifying liquid for mosquito and insect biting comprises the following raw materials in parts by weight: 0.1-8 parts of camphor, 0.5-20 parts of menthol, 0.01-2 parts of borneol and 75-99 parts of medical alcohol. The camphor has the functions of dispelling the pollution, killing insects, relieving itch, eliminating swelling and stopping pain; the menthol is used as an excitant and is acted on the skin or musosa and has the efficacies of cooling and relieving itch; the borneol has the functions of inhibiting bacteria and resisting inflammation; and the medical alcohol has the efficacies of disinfecting and sterilizing. The raw materials of the itch relieving and detoxifying liquid are selected from the common and easily-obtained raw materials in daily life, have low cost and unique curative effects for red and swelling and intense itching formed by the mosquito and insect biting and can be directly coated or sprayed on wounds formed by the mosquito and insect biting; and after a moment, the itch relieving and detoxifying liquid can eliminate the inflammation and remove the detoxified liquid and has the advantages of favorable curative effect, quick response, convenience for use, has no paint and adverse reaction on human body and damage to the skin as well as no toxic or side effects.

The invention relates to a scalp care solution. The scalp care solution comprises, by weight, 1-2% of salicylic acid, 5-10% of a slow-release dispersant, 1-3.5% of a sebum conditioner, 0.5-2% of a repairing agent, 1% of a plant extract and the balance water; preferably, a suitable quantity of a cooling agent such as menthol can be added. The scalp care solution does not contain an alcohol reagent,reduces scalp stimulation and further repairs the skin barrier; by proportioning the content of the components, a synergistic effect of the components is fully exerted, a patient feels comfortable during use and has no stimulation and adverse reactions, and the clinical curative effect is good.

The invention discloses a wet tissue for relieving hemorrhoid symptoms. The wet tissue consists of a conditioning liquid and non-woven fabric bearing the conditioning liquid, wherein the conditioning liquid is prepared from components in parts by weight as follows: 30-60 parts of a witch hazel extracting solution, 0.05-0.1 parts of glucose chlorhexidine, 0.01-0.05 parts of borneol, 2-5 parts of dealdehyding alcohol, 2-8 parts of propylene glycol, 0.3-1 part of a preservative, 0.05-0.3 parts of a pH regulator and 26-66 parts of deionized water. The wet tissue can effectively relieve the hemorrhoid symptoms, perform sterilization, disinfection and detumescence, reduce exudation and promote wound healing, is mild and safe, has no side or toxic effects and is convenient to use. The invention further discloses a preparation method of the wet tissue for relieving the hemorrhoid symptoms. The preparation method adopts a simple process and is convenient to operate, high in security coefficient, operability and efficiency and low in cost.

The invention discloses an acne-removal cosmetic composition containing a purslane herb extract and a preparation method thereof. The acne-removal cosmetic composition is prepared from the following raw materials of purslane herb extract, mulberry leaf extract, pine needle essential oil, betaine, liquorice root extract, loquat leaf extract, a moisturizer, an emulsifier, a pH (potential of hydrogen) regulator, a thickener and water. The acne-removal cosmetic composition has the advantages that under the cooperation function of the purslane herb extract, the mulberry leaf extract, the liquoriceroot extract, the loquat leaf extract and the pine needle essential oil, the high-efficiency and safe antibacterial effect is realized, and the propionibacterium acnes, mites and other skin parasiticbacteria colonies can be quickly killed; the inflammation and acne forming due to invasion by bacterial promoters can be prevented, and the function of diminishing inflammation is realized; the function of controlling oil is realized, the excretion of grease is inhibited, the hair follicle is dredged, the metabolism of keratinocytes is accelerated, the death cells at the skin surface are stripped,the acne scar is removed, the injured skin is repaired, and the unevenness at the surface of the lesion is eliminated.

The invention discloses a temperature sensitive injectable drug-loading controlled release system, which comprises a star-shaped poly-lactic-co-glycolic acid-methoxy polyethylene glycol segmented copolymer and a simulated body fluid, and the content of the copolymer accounts for 15-40 weight by percent. The drug-loading controlled release system exists in a state of liquid which can freely flow in or below room temperature, is rapidly changed into oyster white physical crosslinking hydrogel which cannot flow at a human body temperature, and expresses a reversible sol- gel conversion behavior; the drug-loading controlled release system can uniformly disperse a loaded drug, and exists in a state of liquid which can freely flow in or below room temperature and gel which cannot freely flow at the body temperature; as a vagina drug-loading controlled release system, the temperature sensitive injectable drug-loading controlled release system has the characteristics that contraceptive compound estrogen, progestogen and an anti-inflammation drug are loaded into a copolymer hydrogel carrier by adopting a solution blending method, and the prepared drug-loading system serves as a birth control spraying agent; the drug-loading system is sprayed into vagina after women menses, and is shaped into mesh gel and attached into a wall, and the drug is slowly and controllably released and have an effect of birth control.

The invention discloses a preparation method and application of a dexamethasone sodium phosphate-sodium alga acid composite slow-release coating. A high polymer material is soaked in a sulfuric acid solution of potassium permanganate to conduct acidizing; then the high polymer material is placed in a polymine solution to obtain an amination embellished surface; and oxidation treatment is carried out on the sodium alga acid by using periodic acid or sodium periodate to enable aldehyde groups to be exposed at the tail end of an alginic acid segment to obtain multi-aldehyde group oxidation sodium alga acid, the dexamethasone sodium phosphate solution is soluble in deionized water, and finally materials of the amination embellished surface is placed in a reaction liquid to obtain the composite coating. The technical scheme is that the dexamethasone sodium phosphate and the sodium alga acid can be fixed on the surface of an extracorporeal circulation pipeline in a surface coating mode and has anti-freezing and anti-inflammatory double activity, external medicines are durable and stable in slow-release performance, the dexamethasone sodium phosphate-sodium alga acid composite slow-release coating can replace vein heparinization in a short period, systemic inflammatory response can be lightened through slow release, and short-period operation requirements in department of cardiac surgery can be met.

The near-infrared therapeutic cupping structure is shown in figure 1, which includes a tank body 1 with elastic rubber, a small barrel 2 arranged in the tank body, two small holes 3 arranged at the bottom of the small barrel, a high-power LED near-infrared emitting diode 4 and two leading-out power lines of the near-infrared emitting diode, infuser mixed with resin glue and mineral powder for fixing the near-infrared emitting diode. The power supply device is shown in figure 2. The AC 220v/110v power supply, a K power switch, a BX safety tube and an L indicator light are connected. The cuppingalso includes a controllable voltage-regulating device 7 and a power supply transformer B. Because the near infrared rays in the tank can penetrate the subcutaneous of the human body for about 5cm, the nitric oxide in the blood vessel can be released, the blood can be softened and the blood flow can be promoted, the nerves can be nourished, and the treatment effect of the traditional cupping canbe greatly improved.

The invention provides a skin care product containing multiple honeycomb active ingredients and a preparing method thereof.The skin care product contains a honeycomb composition with the mass fraction of 1-3%.The honeycomb composition comprises, by mass, 10-40 parts of honey extract, 10-40 parts of royal jelly, 10-40 parts of honey and 10-40 parts of propolis extract.The skin care product has a good moistening effect, high safety and excellent skin feel.

The invention discloses a urinary catheter having anti-clogging and anti-inflammatory functions. The urinary catheter is mainly composed of a urinary catheter body, an air supply tube and a urinary catheterization head; a support frame is arranged inside the part, close to the urinary catheterization head, of the urinary catheter body, so as to prevent the urinary catheter body from getting clogged; a drug accommodating hole, in which drugs made from a photo-biotin composite medical material or other anti-inflammatory drugs are accommodated, is formed in the urinary catheterization head; a drug hole formed in the urinary catheterization head is communicated with the drug accommodating hole to enable urine to make contact with the drugs; and urine conveys the drugs to the inner wall of bladder and urethra, so that the drugs can be directly applied to focuses to achieve an anti-inflammatory effect.

The invention discloses a veterinary doxycycline hydrochloride freeze-dried preparation and a preparation method thereof, the veterinary doxycycline hydrochloride freeze-dried preparation consists of an active component of doxycycline hydrochloride and medical excipients, the medical excipients comprise lysine, sodium sulfite and polyvinyl pyrrolidone, the weight ratio of doxycycline hydrochloride to lysine is 1:0.8-1:1, the weight ratio of doxycycline hydrochloride to sodium sulfite is 1:0.01-1:0.05 and the weight ratio of doxycycline hydrochloride to polyvinyl pyrrolidone is 1:0.05-1:0.1. The preparation method comprises the steps of adding lysine, sodium sulfite and polyvinyl pyrrolidone in doxycycline hydrochloride according to the weight ratio, placing solution after the filtration in a tube antibiotics glass vial after sub-packaging treatment, carrying out semi-tamponade and vacuum freeze-drying, thereby obtaining the veterinary doxycycline hydrochloride freeze-dried preparation. The preparation can lead the pH value to achieve 8-8.33 after re-dissolution, thereby thoroughly solving the problem of lower pH value of the doxycycline hydrochloride veterinary drug; and the prepration is non-toxic and has the advantages of easy transportation, long storage time, no degeneration, good stability, very small intramuscular injection stimulation, low manufacturing cost and the like.

The invention provides moisturizing lotion and a preparation method thereof. The lotion takes and combines active polysaccharide as a long-acting humectant for locking skin for skin; and various special greases and various grease proportions are adopted, so that the moisturizing effect is achieved, and inflammation resistance and itching relieving further can be achieved; and the prepared productis excellent in skin feeling, is good in ductility, is liable to coat, selects a natural preservative, and is safe and free of stimulus on skin.

The invention provides new medical application of thiazolopyranone analogues, in particular relates to application of the thiazolopyranone analogues in preparation of anti-inflammatory medicines. Theinflammation is aseptic inflammation. A general structural formula of the thiazolopyranone analogues is described in the description; the thiazolopyranone analogues are free from significant cytotoxicity and can effectively inhibit the release of nitric oxide from macrophage RAW264.7 induced by LPS; an experiment for detecting nitric oxide (NO) release by using a Griess method, an ELISA assay of PGE2, a Western Blot experiment and Xylene-induced mouse ear swelling experiments prove that the thiazolopyranone analogues can inhibit the production of NO and PGE2, and reduces the expression of iNOSand COX-2 by inhibiting MAPK (ERK, JNK and p38) signaling pathways. Therefore, the thiazolopyranone compounds can be used as active substances for the preparation of the anti-inflammatory medicines.

The invention belongs to the technical field of cosmetics, and particularly relates to a high-permeability moisturizing mask and a preparation method thereof. The mask liquid contains hyaluronic acid,hydrolyzed oat protein, sodium polyglutamate, acetyl hexapeptide-1, palmitoyl pentapeptide-4, acetyl hexapeptide-8, chondrus crispus extract, a bifida yeast fermentation product lysate alcohol, phytosphingosine and other nourishing components, can effectively reach dermal tissues, quickly improve the phenomena of dryness and darkness, repair cells with damaged skin barrier function and lack of nutrients, prevent skin moisture loss, achieve the effect of continuous long-acting moisturizing, and does not generate the phenomenon of essence dripping in the use process.

The invention relates to the technical field of daily chemical products, and discloses a bath gel mainly composed of radix sophorae flavescentis extract. The body wash gel of the invention comprises an active component and a base component, and the active component is a root extract of radix sophorae flavescentis, a root extract of radix glycyrrhizae inflata and a root extract of scutellaria baicalensis. The bath gel of the invention has no irritation to skin and can make skin tender, sterilize, inhibit bacteria, reduce inflammation and relieve itching, and the preparation process of the bathgel of the invention is simple and the cost is low.

The invention relates to the field of medical correction instruments, in particular to an ingrowing nail correction device.The ingrowing nail correction device is characterized by comprising a groove-shaped hook and a bandage, the groove-shaped hook is composed of an upper curved surface and a lower curved surface, the bandage is arranged at an opening end of the upper curved surface of the groove-shaped hook, and a plurality of penetrating holes are formed in the bandage.The ingrowing nail correction device is reasonable in design, simple in structure, low in cost and comfortable to wear, has good correction effect, can be adjusted according to width of nails (toenails) of different patients and is suitable for treatment of one-side and double-side ingrowing nails.

The invention relates to the technical field of biomedicine, and particularly discloses an oligopeptide and an active peptide composition and application of the oligopeptide and the active peptide composition in preparation of a product with an anti-inflammatory effect. The oligopeptide has a structure as shown in a formula I which is described in the specification. The active peptide composition comprises the oligopeptide with the structure as shown in the formula I and active cyclic peptide with the structure as shown in a formula II; and experiments show that both the oligopeptide bifidobacterium oligopeptide-alpha and the active peptide saccharomyces cerevisiae cyclic peptide-beta can inhibit HaCaT cell inflammatory injury and apoptosis caused by LPS exposure. Therefore, the bifidobacterium oligopeptide-alpha, the saccharomyces cerevisiae cyclopeptide-beta and the composition of the bifidobacterium oligopeptide-alpha and the saccharomyces cerevisiae cyclopeptide-beta can be used as active substances in cosmetics, skin care products, foods, health care products or medicines to play an anti-inflammatory role.

The invention discloses an anti-bacterial pants-type sanitary towel comprising a pants body. An elastic band is arranged at the position of a waist opening of the pants body, elastic fastening strips are arranged at positions of leg openings of the pants body, a moisture-absorbing core layer is further arranged at the bottom of the pants body, and anti-bacterial gel is arranged inside the moisture-absorbing core layer. The anti-bacterial pants-type sanitary towel can achieve anti-bacterial and anti-inflammation effect, and can effectively and completely eradicate lateral leakage, back leakage and the like as being of a pants-type structure.

The invention belongs to the technical field of pharmaceutical preparations and nanomedicine, and relates to a bionic nano-drug for preventing and treating aortic dissection, in particular to a mononuclear/macrophage membrane bionic modified multidrug co-loaded anti-inflammatory liposome and a preparation method thereof. The liposome is composed of cationic phospholipid and neutral phospholipid, co-loading of multiple anti-inflammatory drugs can be achieved in the liposome, anti-inflammatory cell-penetrating peptide is covalently modified on the surface of the liposome, and then mononuclear/macrophage membrane protein is used for bionic modification. According to the bionic anti-inflammatory liposome, multiple receptors and adhesion molecular ligands mediated and chemotactic on the surface of a mononuclear/macrophage membrane are utilized to realize a natural targeting effect on an inflammatory site, and non-specific clearance of a reticuloendothelial system (RES) to the liposome is reduced by virtue of modification of leukocyte self-recognition molecules. The bionic anti-inflammatory lipidosome can effectively cross a vascular endothelial barrier, gather and release anti-inflammatory drugs at the early lesion part of the aortic dissection in a targeted manner, play a synergistic anti-inflammatory role, inhibit inflammation-related cells from chemotaxis and infiltration into the lesion part, and further prevent and treat the occurrence and development of the aortic dissection.

The invention discloses a preparation method of a compound deodorant capable of reducing odor of livestock manure. On one hand, catechin and other ingredients contained in tea polyphenol of tea residues have a strong chemical adsorption function on polar gas molecules such as ammonia gas, hydrogen sulfide and the like, and tea polyphenol has an inhibition function on growth and propagation of harmful bacteria; on the other hand, fiber of the tea residues has a physical adsorption function on odor substances and an adjustment function on microecological balance of the intestinal tract, essential oil extracted after pine needles, mint leaves and radix glycyrrhizae are mixed is mixed with montmorillonite, the mixture is effectively adsorbed on montmorillonite and mixed with a water extract and the tea residues, the functions of killing bacteria and eliminating inflammation are effectively realized, the compound deodorant has high odor decomposition and absorption functions, and the breeding working environment is improved. The preparation method has a good odor removal effect and is low in cost, the production efficiency is improved while the piggery environment is improved, and the breeding benefits can be improved.

The invention discloses a nano composition as well as a preparation method and application thereof. The nano composition comprises a biological surfactant, active ingredients, lipid and water. The biological surfactant is adopted in the nano composition, so that various high-concentration water-soluble active ingredients and/or non-water-soluble active ingredients can be effectively wrapped, so that the transdermal delivery of various active ingredients can be realized, multiple effects and/or synergistic interaction are realized, the transdermal absorption rate and bioavailability of the active ingredients are improved, the transdermal action time is shortened, the skin retention volume is increased, and the instant and long-acting effects are achieved.