50 results about "Dihydroxyaluminium aminoacetate" patented technology

The invention provides a medical cold compress plaster. The medical cold compress plaster is composed of a support layer, a gel layer and an isolating layer, and has the special shape according with the physiological curve of the applied part. An oil phase and a water phase forming the hydrophilic gel layer respectively comprise the following components in percentage by weight: the oil phase: 20-35% of a dispersing agent, 5-7% of macromolecule resin, 0.05-0.15% of dihydroxyaluminium aminoacetate, 0.01-0.15% of ethylene diamine tetraacetic acid, 0.15% of absolute ethyl alcohol, 0.04-0.1% of menthol, 0.1-1% of vitamin E, and 0.05-0.1% of triclosan; the water phase: 0.2-0.8% of tartaric acid, 1.2-2% of carbomer, 0.5-1% of sodium carboxymethylcellulose, 0.01-0.1% of vitamin C, the balance of medical purified water, and the total weight percentage is 100%. A preparation process comprises the following steps: dispersing all the components of the oil phase into the dispersing agent, and uniformly stirring the components; dissolving all the components of the water phase into water, and uniformly stirring the components; mixing the water phase and the oil phase, uniformly stirring the water phase and the oil phase in a vacuum mixing pot, thus obtaining the hydrophilic gel substrate of the medical cold compress plaster, coating the support layer with the hydrophilic gel substrate, meanwhile covering with the isolating layer, and carrying out cutting, solidifying and packaging to obtain the needed medical cold compress plaster product.

The invention aims at disclosing a chitin gel band-aid and a preparation method thereof. The band-aid comprises a carrier, wherein the carrier is provided with hydrogel hemostasis surgical dressing, the hydrogel hemostasis surgical dressing comprises the following components by weight percentage: 0.5-5% of chitin, 1.5-5% of sodium polyacrylate, 5-10% of sodium carboxymethylcellulose, 0.5-1% of povidone, 0.5-2% of gelatin, 0.05-0.5% of dihydroxyaluminium aminoacetate, 20-40% of glycerinum, 36-71.9% of purified water, and 0.05-0.5% of glacial acetic acid. Compared with the prior art, the chitin gel band-aid has anti-inflammatory and sterilizing functions due to the combination of the wet environment and the effect of the chitin added into the gel, so that the wound can be healed quickly, the pain of a patient is reduced, and the purpose of the chitin gel band-aid is reached.

The invention discloses a gel plaster base, which comprises the following components in parts by mass: 4.0-6.0 parts of partially neutralized sodium polyacrylate, 0.2-2.5 parts of pullulan, and 0.12-2 parts of glyoxate 0.30 parts, 20-30 parts of glycerin, 0.08-0.20 parts of disodium edetate, 0.20-0.60 parts of tartaric acid, 0.3-0.5 parts of galadan, 60-75 parts of water. The gel plaster matrix of the present invention has the advantages of high initial adhesion, good formability, good skin followability, and no irritation to the skin, and is very suitable for preparing gel plasters; meanwhile, the gel plaster of the present invention The preparation method of the ointment base is simple, easy to operate, short in time, low in energy consumption and low in cost, and is very suitable for industrial production.

The invention discloses a patch capable of calming nerves and helping sleep. The patch capable of calming nerves and helping sleep comprises a backing layer, a polymer gel layer and an anti-sticking layer, wherein the anti-sticking layer is formed by a polyethylene film and is arranged on the upper layer of the polymer gel layer; the backing layer is arranged on the lower layer of the polymer gel layer; the polymer gel layer comprises the following components in percentage by weight: 30-32% of a polymer gel material, 0.07-0.08% of dihydroxyaluminium aminoacetate, 0.5-1.5% of lavender essential oil, 0.5-1.5% of rose essential oil and purified water which is added until the percentage by weight is 100%; the polymer gel material comprises a dispersing agent, a wetting agent, a cross-linking agent, an adhesive and a thickening agent; the preparation method of the patch capable of calming nerves and helping sleep comprises the following steps: adding 24.5-25% of glycerol and 0.07-0.08% of dihydroxyaluminium aminoacetate into 2.7-3.1% of sodium polyacrylate and stirring for 20 minutes; adding 0.2-0.4% of polyvinylpolypyrrolidone, 2.3-3% of polyvinylpyrrolidone, 0.3-0.5% of sorbitol and purified water, and vacuum stirring for 5-8 minutes; adding active materials comprising 0.5-1.5% of rose essential oil and 0.5-1.5% of lavender essential oil, and vacuum stirring for 5 minutes. The preparation method of the patch capable of calming nerves and helping sleep is convenient in process; the prepared patch is convenient to use; the requirements of daily life are met.

The invention relates to a method for preparing a compound aspirin double-layer tablet. The method is characterized in that aspirin, tartaric acid, low-substituted hydroxypropyl cellulose, starch and talcum powder are prepared into a first layer, and while heavy magnesium carbonate, dihydroxyaluminium aminoacetate, starch, lemon yellow and talcum powder are prepared into a second layer, and then the first layer and the second layer are pressed into the tablet. The compound aspirin tablet prepared by the method is smooth in surface, free of layering, and high in stability.

Provided is cataplasma for treating body surface infectious diseases applied to the technical field of medicines. The product prescription comprises cortex phellodendri chinensis, calcined gypsum, sodium polyacrylate, peach gum, polyvinylpyrrolidone, sodium carboxymethylcellulose, kaolin, glycerol, dihydroxyaluminium aminoacetate, tartaric acid, azone, diethylamine tetraacetic acid disodium and water. The preparation method includes solving the polyvinylpyrrolidone in water completely, adding the sodium carboxymethylcellulose and the peach gum into the mixture, mixing the mixture evenly, continuously adding the tartaric acid to obtain mixing liquid 1, namely water phase, placing the sodium polyacrylate, the diethylamine tetraacetic acid disodium, the dihydroxyaluminium aminoacetate, the azone and the kaolin in the glycerin, stirring the mixture to enable the mixture to be completely swelled, then adding the cortex phellodendri chinensis and the calcined gypsum, evenly stirring the mixture to obtain mixing liquid, namely oil phase 2, adding the water phase into the oil phase, completely stirring the mixture till the mixture is even, coating paste on medical non-woven fabric through a compression molding method, conducting film bonding and slice cutting, and placing the mixture to conduct complete crosslinking to obtain the cataplasma. The cataplasma is simple in using method, suitable for being applied in summer, free of side effects, good in air permeability, free of pollution to clothes and free of residual. Users do not have uncomfortable feeling if using the cataplasma, and the cataplasma has no stimulation and anaphylaxis on skins.

The invention provides a traditional Chinese medicine cataplasma for treating arthralgia and myalgia. The traditional Chinese medicine cataplasma is composed of non-woven fabrics, an antiadherent filmand a medicine containing ointment. The medicine containing ointment comprises Chinese angelica, banksia rose, polyghace seche, Radix Astragali, Radix Codonopsis, Rhizoma Paridis, gentrin knotweed, cassia twig, wolfberry, bark of ash, radix aconiti preparata, wild aconite root, Himalayan teasel root, cinnamon, safflower, polyisobutylene, dihydroxyaluminium aminoacetate, EDTA-2Na, sodium polyacrylate, carbomer, glycerin, Arabic gum, polyvinylpyrrolidone, borneol, menthol, purified water and ethanol. A preparation method of the traditional Chinese medicine cataplasma comprises the following steps: firstly extracting volatile oil and an extract respectively; then preparing a matrix; adding borneol and menthol and the extract and volatile oil into the matrix; uniformly stirring; coating; slicing; and packaging to obtain the cataplasma. The cataplasma of the invention has remarkable curative effects on arthralgia and myalgia, numbness of limbs and rheumatic arthritis, is not easy to causeirritability, has a simple production method, and is suitable for industrial mass production.

The invention relates to a medicament matrix composition and a preparation method. PVPK90 (polyvinylpyrrolidone K90), PAAS700 (sodium polyacrylate 700), dihydroxyaluminium aminoacetate, tartaric acid, glycerol and purified water are taken as raw materials and are mixed, stirred and formed into the medicament matrix composition. The matrix has the characteristics of primary viscous force, keeping viscous force, peel strength, adhesive force balancing, and the like; the matrix is mixed with the raw material drugs; the materials are uniformly stirred and mixed, coated, dried, checked and packaged, thereby acquiring the gel plaster used for treating the related diseases.

The invention discloses a pain relieving cataplasma for relaxing tendon and activation collaterals. The pain relieving cataplasma comprises 1-5 weight parts of active pharmaceutical ingredient and 30-300 weight parts of matrix, wherein the matrix is prepared from the following raw materials in parts by weight: 5-60 parts of Carbopol, 10-90 parts of partial neutrolization sodium polyacrylate, 0.1-2 parts of ethylenediamine tetraacetic acid, 5-80 parts of povidone K30, 10-120 parts of gelatin, 60-180 parts of glycerinum, 1-5 parts of ethylparaben, 0.1-2 parts of dihydroxyaluminium aminoacetate, 0.05-1 part of citric acid, 1-8 parts of ethyl alcohol and 150-300 parts of water. The invention further discloses a preparation method for the pain relieving cataplasmata, the pain relieving cataplasmat for relaxing tendon and activation collaterals prepared by the method is simple in process and safe in production, has no pollution to the environment, the efficacy of the pain relieving cataplasma is obvious, and the pain relieving cataplasmat generates little irritation and allergy to the skin.

A medicine contains aspirin, red koji extrat, liver-protecting medicine, dihydroxyaluminium aminoacetate, heavy magnesium carbonate and/or magnesium aluminate carbonate. A packing box is also disclosed, which contains 60 tablets of red koji extract and 60 tablets of aspirin.

The invention discloses a hydrogel emergency tobacco control patch formula and a method for preparing a tobacco control patch. The method for preparing the tobacco control patch comprises the steps that hydrogel is prepared by mixing 0.1%-2.0% of natural tobacco extracts, 1%-15% of nicotine clathrate compound, 0.5%-3.0% of mint extracts, 5.0%-10.0% of sodium polyacrylate, 0.5%-3.0% of sodium carboxymethylcellulose, 0.1%-2.0% of dihydroxyaluminium aminoacetate, 0.2%-1.0% of dihydroxysuccinic acid, 4.0%-8.0% of ethyl alcohol, 20.0%-30.0% of glycerinum and 45.0%-60.0% of purified water, and then the hydrogel is smeared on base cloth. The tobacco control patch prepared through the method is low in nicotine content, long in stipulated use time, good in even slow-release effect, safe, controllable, high in skin friendliness, good in adhering performance and convenient to carry and use, the preparation technique is simple, secondary pollution to the environment is avoided, and the tobacco addiction can be released and controlled.

The invention discloses physique cold compress gel and a preparation method thereof. The physique cold compress gel is prepared from a raw material drug and an accessory drug; the raw material drug isprepared from the following medicinal materials, in parts by weight: 72-78 parts of resina draconis, 72-78 parts of radix notoginseng, 47-53 parts of frankincense, 56-62 parts of myrrh, 46-52 parts of flos carthami, 8-12 parts of calcined native copper, 14-17 parts of velvet antler, 48-52 parts of rhizoma cibotii, 48-50 parts of cortex acanthopanacis, 48-52 parts of radix dipsaci and 3-6 parts ofborneol; the accessory drug is prepared from, in parts by weight: 1-10 parts of carbomer, 5-15 parts of triethanolamine, 1-10 parts of azone, 5-15 parts of twain-80, 400-500 parts of glycerinum, 20-100 parts of sodium polyacrylate, 20-100 parts of kaolin, 1-10 parts of dihydroxyaluminium aminoacetate, 0.5-20 parts of ethylene diamine tetraacetic acid and 0.5-20 parts of tartaric acid. The prepared gel has no irritation and allergenicity to the skin, does not pollute the clothes, has no residual, has the good drug releasing performance, and can continuously release the drug; and compared withthe prior art, the gel has the characteristics that the curative effects are precise, the safety is good, no side effects exists, application is convenient, the cost is low, the effect is superior tothe prior art.

The invention discloses a preparation method and application of PAMs (natural plant antimicrobial solution) hydrogel patch. The hydrogel patch is prepared from 15-45 parts by weight of glycerol, 2-6 parts by weight of NP-700, 0.2-0.6 parts by weight of dihydroxyaluminium aminoacetate, 13.6-40.7 parts by weight of distilled water, 0.1-0.3 parts by weight of tartaric acid, 1.5-4.5 parts by weight ofazone, 1.5-4.5 parts by weight of propylene glycol, 0.25-0.75 parts by weight of SDS (sodium dodecyl sulfate), and 15.85-47.55 parts by weight of PAMs. The hydrogel patch provided by the invention has the beneficial effects of good moldability, viscoelasticity, gas permeability, good peeling property from skin and good therapeutic effect on skin burns, and can prevent skin ulceration, and has good antimicrobial and anti-inflammatory effects on wounds and good repairing effects on wound surface to slow down the problem of scar residue. The hydrogel patch is obtained by one-time heat preservation crosslinking, and the operation is convenient and advantageous for large-scale production.

The invention belongs to the technical field of pharmacy, and particularly relates to an aluminum, magnesium and aspirin tablet (II) and a preparing method thereof. The aluminum, magnesium and aspirin tablet (II) is made by tableting an aspirin layer and a buffering layer, and the aspirin layer is prepared from aspirin, mannitol, corn starch, tartaric acid, gelatin, tartrazine aluminum lake and silicon dioxide; the buffering layer is prepared from dihydroxyaluminium aminoacetate, heavy magnesium carbonate, mannitol, corn starch, gelatin and silicon dioxide. The aluminum, magnesium and aspirin tablet (II) prepared from the preparing technology has a better dissolution rate, and the impurities are obviously lowered compared with an impurity index in an existing product.

A compound aspirin-tatin medicnie contains proportionally aspirin, the medicine in tatin kind, hypolipemic medicine, dihydroxyaluminium aminoacetate, heavy magnesium carbonate or magnesium aluminate carbonate, skeleton and medical auxiliary. Its application is also disclosed.

The invention discloses novel plaster and a preparation method of the novel plaster. The plaster comprises, by weight percentage, 75 percent of purified water, 0.18 percent of citric acid, 1.03 percent of carbomer, 0.03 percent of ethylenediamine tetraacetic acid disodium, 3.65 percent of sodium polyacrylate, 0.4 percent of dihydroxyaluminium aminoacetate, 0.1 percent of methylparaben, 0.1 percent of ethylparaben, 18.5 percent of glycerin, 0.7 percent of ethyl alcohol, 0.3 percent of menthol and 0.01 percent of erioglaucine. The novel plaster is convenient to prepare, comfortable and long-acting.

The invention relates to the technical field of pharmaceutical preparations, and discloses an oxybutynin transdermal plaster and a preparation method thereof. The oxybutynin transdermal plaster comprises a backing layer and an ointment-containing body, wherein the ointment-containing body comprises the following raw materials in percentage by mass: 3-5% of oxybutynin and/or pharmaceutically acceptable salt thereof, 10-15% of sodium polyacrylate, 5-8% of pre-crosslinked pectin, 1-2% of hydroxypropyl methylcellulose, 0.5-1% of dihydroxyaluminium aminoacetate, 1.5-3.5% of pectinase @ ethyl cellulose/chitosan microcapsule, 10-15% of sorbitol, 1-2% of laurinol azone, 10-15% of ethanol and the balance water; and the pH value of the ointment-containing body is controlled to be 5.0-6.0 by a pH regulator. The oxybutynin transdermal plaster disclosed by the invention has relatively high air permeability, and can promote the release of oxybutynin by slowly releasing pectinase in the later period of application, thereby prolonging the drug effect duration and application time of the plaster.

The invention discloses an anti-inflammatory and analgesic gold bone patch which comprises a backing layer, a hydrogel paste layer and an anti-sticking layer. Paste in the hydrogel paste layer comprises the components in weight of 100g: 65-80g of traditional Chinese medicine extract, 3-8g of sodium polyacrylate, 1-5g of polyacrylic acid, 0.01-0.2g of dihydroxyaluminium aminoacetate, 0.5-3g of carbomer, 1-5g of polyvinyl alcohol, 0.1-1g of medical urea, 1-5g of propylene glycol, 10-20g of glycerinum, 0.01-0.3g of organic acid and 0.1-0.6g of preservative. The traditional Chinese medicine extract is prepared from eight traditional Chinese medicinal materials including radix clematidis, caulis spatholobi, caulis sinomenii, rhizoma dioscoreae nipponicae, radix et caulis flemingiae, all-grass of nippon dinquefoil, herba epimedii and radix achyranthis bidentatae, and is used in the hydrogel paste layer of the gold bone patch, the traditional Chinese medicinal materials supplement one another, adhesion and edema of damaged muscle groups are eliminated by promoting blood circulation to remove blood stasis, dispelling wind and eliminating dampness through targeted drug therapy for lesion sites, normal controllable functions of damaged nerves and damaged muscle groups are recovered, intervertebral disc degenerative changes are reversed, and normal activities of vertebral bodies and bonejoints are recovered.