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Antibacterial gel |
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IPC classes for russian patent Antibacterial gel (RU 2247555):
8-cyano-1-cyclopropyl-7-(1s,6s)-2,8-diazabicyclo- [4.3.0]-nonane-8-yl)-6- fl uoro-1,4-dihydro-4-oxo-3-quinoline carboxylic acid with crystalline modification a and drug eliciting effect against pathogenic microorganisms / 2247122
Invention describes 8-cyano-1-cyclopropyl-7-(1S,6S)-2,8-diazabicyclo-[4.3.0]-nonane-8-yl)-6-fluoro-1,4-dihydro-4-oxo-3-quinoline carboxylic acid of the formula (I): with the crystalline modification A and a drug eliciting effect against pathogenic microorganisms. The prepared crystalline modification shows stability and doesn't transform to another crystalline modification or amorphous form being even at prolonged storage.
Antibacterial agents / 2246941
Invention relates to applying compounds of the formula (I) for preparing an antibacterial composition and veterinary composition eliciting with the enhanced activity.
Synthetic phenolic compounds and vegetable extracts obtained from plants that are effective in treatment and prophylaxis of chlamydium infections / 2246939
Invention relates to compositions used for treatment and/or prophylaxis of chlamydium infections caused by C. pheumoniae. Pharmaceutical composition used for treatment and/or prophylaxis of chlamydium infection caused by C. pneumoniae comprises the taken phenolic compound, or extract, or fraction, or incomplete fraction comprising the taken phenolic compound or corresponding synthetic compound, or mixture of indicated compounds obtained from plants. An anti-chlamydium effect of phenolic compound or extract, or fraction, or incomplete fraction obtained from plants and comprising indicated compound or corresponding synthetic compound on C. pneumoniae represents the definite percent of inhibition for formation of inclusions. The composition useful for health eliciting an anti-chlamydium effect with respect to C. pneumoniae comprises the taken phenolic compound or extract, or fraction, or incomplete fraction containing indicated compound or corresponding synthetic compound, or mixture of indicated compounds obtained from plants. An anti-chlamydium effect of phenolic compound or extract, or fraction, or incomplete fraction comprising indicated compound or corresponding synthetic compound obtained from plants on C. pneumoniae represents the definite percent for inhibition in formation of inclusions. Also, invention relates to applying the composition useful for health in preparing foodstuffs or as supplements for nutrition for every day. Also, invention relates to applying phenolic compound or extract, or fraction, or incomplete fraction comprising indicated compound or corresponding synthetic compound or mixture of indicated compounds obtained from plants in manufacturing a medicinal agent used for treatment and/or prophylaxis of chlamydium infections caused by C. pneumoniae. An anti-chlamydium effect of phenolic compound or extract, or fraction, or incomplete fraction comprising indicated compound or corresponding synthetic compound obtained from plants on C. pneumoniae represents the definite percent in inhibition in formation of inclusions. Compositions promote to effective prophylaxis and treatment of chlamydium infections caused by C. pneumoniae.
Mixed inactivated aluminum hydroxide-containing vaccine against infectious pneumonia and salmonellosis in pigs and method for it preparing / 2246316
Vaccine comprises bacterial mass of Pasteurella multocida of serovariants A, B and D, Haemophilus pleuropneumonia of serogroups 1 and 2, and streptococcus of serogroups C and R, and also lysate-anigens of salmonellae Salmonella cholerae - suis, strain № 370 and Salmonella typhimurium № 415 mixed in the definite concentration. Vaccine elicits the high immunogenicity and provides the protection of pigs against infectious pneumonia of bacterial etiology and salmonellosis.
Method for treating chlamydiosis in calves / 2246298
The method deals with injecting oxylate once daily for 3 d at the dosage of 1 ml/30 kg body weight at repeated therapy course in 5 d at the background of antibioticotherapy. The method enables to normalize biochemical and morphological blood values and increase average daily body weight gain in sick animals.
7-acylaminocephalosporins substituted in position 3 with cyclic aminoguanidine groups / 2245884
Invention provides substituted 7-acylaminocephalosporins of formula I:
Thymol-containing composition useful in treatment of patients suffering from drug-resistant bacterial infections / 2245719
Composition is constituted by effective amount of thymol obtained from plant Trychyspermum ammi, mint oil combination of mint oil containing required amounts of monoterpenes and isolated from Mentha spicata and Mentha arvensis, and typical additives. Invention also relates to preparation of the composition by mixing above ingredients and to method of treating patients by administering therapeutically effective amount of the composition.
Ofloxacine composition for injections / 2245134
Claimed composition contains therapeutically acceptable amount of ofloxacine and trilon-B, sodium chloride, water for injections as additives.
Composition for treatment or prophylaxis of infection caused by microorganism neisseria / 2244749
Invention relates to a composition designated for treatment and prophylaxis of infections caused by Neisseria microorganism that comprises the following components: (a) protein with amino acid sequence similar by 65% and above with the natural Neisseria protein of a single species (the first group of amino acid sequences is given in the text) and/or its fragment consisting of 10 and more amino acids and eliciting antigen properties; (b) the second protein with amino acid sequence similar by 65% and above with the natural Neisseria protein of another species (the second group of amino acid sequences with even numbers is given in the text), and/or its fragment consisting of 10 or more amino acids and eliciting antigen properties; in particular, the second protein represents NspA. The composition comprises additionally adjuvant. The composition is used both a medicinal agent and for manufacturing the medicinal agent. Applying the invention provides enhancing the effectiveness of prophylaxis or treatment due to the universal effect of the composition (vaccine). Invention can be used in medicine for treatment of infections.
Cosmetic compositions including human serum albumin obtained out of transgenic animals, not out of men / 2247554
Human serum albumin (HAS) should be obtained out of transgenic animals, not out of men, to be mixed with corresponding carrier and/or adjuvant. HAS should be obtained out of cattle, sheep, swine, horse, rodents or goat. HAS should be obtained either out of milk or blood of transgenic animals, not out of men. HAS should be obtained out of an egg of transgenic poultry. Cosmetic composition should be obtained due to similar technique. Cosmetic composition is either lotion, cream, gel or oil to be applied in case of cosmetic treating wrinkles, scars and burn wounds. The present innovation enables to cheapen the product at keeping its high activity.
Cosmetic compositions / 2247553
The present innovation deals with either antiperspirant or deodorizing composition either in solid or soften-solid form including either antiperspirant or deodorizing active substance and a continuous phase that contains a liquid water-unmixed carrier and, also, it contains a structurizing agent being either completely or partially esterifying cellobiose of formula (I), in which every Z independently represents either hydrogen or acyl group of formula (II)
Cream for facial skin / 2246933
The suggested facial cream contains acetylated lanolin, olive oil, cacao oil, ethanol, glycerol, honey, germaben, triethanolamine, flavoring, bee wax, zinc stearate, stearin, methylcellulose, albumin fraction of caprine milk whey, fucoidan hydrolyzate, distilled water. Components should be taken at certain quantitative content. Cream favors wounds healing, improves metabolic processes in skin cells and prevents skin aging and its dryness and desquamation, as well.
Wet napkins favorably treating skin / 2246319
Device has emulsion composition of oil-in-water type containing natural fat or oil, sterol or sterol derivatives, moisture trap, emulsifying surfactant and water.
External agent for prophylaxis of skin infectious disease and method for prophylaxis / 2246292
Invention proposes a cosmetic agent for prophylaxis of skin infectious diseases that comprises an active substance and a conducting agent - multilamellar liposomes additionally. As an active substance dioxydin is used in the amount 0.00001-0.02 wt.-% to the external agent mass. Method for prophylaxis of skin infectious diseases involves using a cosmetic agent in the form of spoon or shampoo, or gel, or cream in the dose depending on selection of the composition and properties of cosmetic agent. Applying the agent results to reducing injurious effect on skin normal microflora, reducing danger from penetration of preparation in blood and providing high protection of skin against all species of infection. Invention can be used for prophylaxis of skin diseases in humans.
Cosmetic gel for facial skin / 2245707
The suggested cosmetic gel for facial skin contains a gel-forming component as acrylic acid copolymer - carbopol, a pH regulator as triethanolamine, a conservant, a flavoring, a biologically active additive and water, moreover, as a biologically active additive one should apply either fullerens or schungite water, oil of wheat sprouts, tocopherol acetate (vitamin E), vitamin A, vitamin F: components should be taken at a certain quantitative ratio. The suggested cosmetic gel for facial skin is of antiphlogistic, moisturizing and antioxidant action at simultaneous nourishing patient's skin with oxygen. The gel tones, softens and nourishes facial skin, improves cutaneous respiration. It is nontoxic and causes no allergic reactions.
Product designed as cosmetic wipes / 2245706
The present method deals with a product designed as disposable cosmetic wipes that contain soft water-insoluble substrate such as tissue impregnated with either alpha- or beta-hydroxycarbonic acid in cosmetically acceptable carrier-foundation. Impregnating cosmetic compositions will have pH of not above 6.8 in water. Silicone microemulsion is available to minimize stickiness being the result of applying hydroxycarbonic acid upon skin with the above-suggested wipes. In the presence of surface-active substances that contain groups of fatty acid, silicone microemulsion prevents the appearance of unpleasant odors which could be produced by surface-active substance in the course of hydrolysis at low pH.
Method for production of oil enriched in fatty hydroxyoctadecadienic acids (hode) or esters thereof from oil mixture containing linoleic acid or esters thereof / 2245358
Target oil, enriched in HODE, or esters thereof is obtained by controlled oxidation of linoleic acid and/or linolenic acid or esters thereof in presence of oxidation catalyst. Oxidation is stopped when total HODE or ester content is more than 5 %, and/or content of isomeric 9-hydroxy-10,12-octadecadienic acid (9-HODE) or esters thereof is more than 1,5 %; and hydroperoxides formed in oxidation process are reduced with reducing agent in presence of antioxidant. Invention is also relates to oil enriched in 9-HODE or esters or salts thereof having an lipolytic action; to drug or food additive for obesity treatment; cosmetic for local treatment of cellulite. Compound for controlling of adipocyte lipolytic activity and hydrolysis of triglycerides accumulated in adipocytes is also disclosed.
Method for correcting cosmetic skin defects / 2245131
One should carry out multiple desquamation by applying a preparation containing alpha-hydroacids, moreover, before desquamation one should purify skin against contamination and sebum with a preparation containing alpha-hydroacids and urea, moisten with a preparation at pH being 4.5-6.5 and then conduct desquamation with a preparation at pH being 1.6-2.2 by applying glycolic acid at 30-70% concentration as alpha-hydroacid, then one should activate reparative skin properties with a preparation containing isoflavones and soybean lecithin and restore functional properties of epidermal lipid barrier and protect skin against negative impact with a phospholipid-containing preparation upon lamellar basis. Moreover, moistening should be carried out with a preparation containing ascorbic acid or its derivatives, hydrolyzates of hyaluronic acid and collagen and polysiloxanes, and desquamation should be carried out with a preparation containing, additionally, hydrolyzates of mucoplysaccharides and proteins. Moreover, as alpha-hydroacids one should apply the mixture of glycolic and lactic acids, activation of reparative capacity of skin cells should be performed with a preparation containing the complex of vitamins A, E, F and C, and restoration of functional properties of epidermal lipid barrier and skin protection against negative impacts - with compositions upon lamellar basis with the complex of vitamins and hydrophobic film-forming substances. Moreover, to create lamellar basis it is necessary to apply the mixture of soybean lecithin, jojoba oil and unsaturated fatty acids.
Method for activating restorative skin processes / 2245130
One should carry out purification, desquamation and regeneration of skin, moreover, problematic skin should be desquamated before regeneration, and regeneration should be conducted by stages, moreover, at the first stage skin should be moistened, at the second stage it should be nourished and at the third stage one should restore its barrier function and protect the skin against environmental factors, and nutrition and restoration of skin epidermal barrier should be carried out with a preparation based upon soybean isoflavones, phytic acid, extracts of Iceland moss and bioactive preparations of maritime genesis. As for moistening it should be carried out with a preparation based upon vitamin C, hydrolyzates of collagen, elastin and hyaluronic acid; before desquamation one should additionally moisten the skin; nutrition and restoration of skin epidermal barrier should be fulfilled with a preparation based upon lamellar composition containing soybean isoflavones, phytic acid, extract of Iceland moss and bioactive preparations of maritime genesis. Moreover, additionally after moistening one should carry out antiphlogistic treatment of skin by applying gelatinous preparations containing plant extracts, allantoin, d-pantenol and amino acids, and as a preparation to restore skin barrier function and its protection against environmental unfavorable factors one should apply composition containing essential oils, plant extracts, vitamins K, A, C, E, F and microelements, as well.
Composition of nail vanish / 2245715
The present innovation deals with, a) at least, one fungicide substance and b) at least, one water-soluble film-forming substance, where b)-component is chitosan derivative chosen out of hydroxyalkyl chitosans and carboxyalkyl chitosans; nail vanish that includes the above-mentioned composition, and nail vanish that includes, at least, one water-soluble film-forming substance chosen out of hydroxyalkyl chitosans and carboxyalkyl chitosans. The suggested nail vanish is of high fungicide action and is free of multiple dermatological and esthetic disadvantages.
Antiseptic ointment for udder / 2245133
Antiseptic ointment comprises cationic surface-active substance, lower glycols, polyethylene glycols, water and ethylene glycol monophenolic ester and higher polyethylene glycols taken in the definite ratio of components. As cationic surface-active substance ointment comprises N-alkyl-N-alkoxycarbonylmethylhexahydroazipinium chloride or alkyldimethylbenzylammonium chloride, or cetylpyridinium bromide, or cetylpyridinium chloride, or 1,2-ethylenebis-(N-methylcarbdecyloxymethyl)ammonium dichloride, or ethylhexadecyldimethylammonium chloride, or chlorhexidine; as lower glycol ointment comprises 1,2-propylene glycol or polyethylene glycol-300, or polyethylene glycol-400; as higher polyethylene glycol ointment comprises polyethylene glycol-1500 or polyethylene glycol-3000, or polyethylene glycol-4000, or polyethylene glycol-6000. Ointment elicits the high antibacterial activity, broad spectrum of bactericidal effect and low irritating effect with respect to udder skin. Invention can be used for sanitary-hygienic treatment of udder of lactating cows for prophylaxis and rapid healing external damages of udder and nipples (arising cracks), prophylaxis of mastitis, enhancing milk purity by microbiological indices.
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FIELD: cosmetology. SUBSTANCE: the present innovation deals with cosmetic preparation for taking care of skin, in particular. The suggested antibacterial gel consists of either hydroxypropylcellulose or hydroxyethylcellulose, propylene glycol or diethylene glycol compound, polyguanidine or its synergistic mixture with quaternary ammonium compound, chitosan, oxyethylated ether of sorbitane, polyvinyl pyrrolidone at molecular weight ranged 10000 - 40000 or copolymer of polyvinylpyrrolidone, trilon-B - sodium salt of ethylene diamintetraacetic acid, perfumery composition, vitamin constituent and water. The present innovation provides increased regenerating formula of skin and its enhanced barrier function, improves homogeneity of the composition mentioned and its stability. EFFECT: higher efficiency of application. 5 cl, 4 ex, 3 tbl
The invention relates to the field of cosmetology, in particular to the means for skin care, and can be used for skin care of the face, hands, feet and other body parts. Known gel for antiseptic treatment of skin, containing in its composition modified cellulose derivative, antiseptic - Miramistin and water (U.S. Pat. Of the Russian Federation No. 2185157, class a 61 K 31/14, 2000). However, used Miramistin not have a prolonged effect and is effective for a narrow field of use. The closest solution to the present invention is a hygienic gel of the following composition, wt.%: the carbopol - 0,1-10,0; triethanolamine - 0,1-10,0; liposomal drug “Witch-2” (protivougrevoe) is 1-30; glycerin distilled PC-94 - 1-15; ethyl alcohol of the highest clean - 0,1-5,0; water-spiropiranovye burdock extract - 0,1-5,0; water-spiropiranovye the horsetail extract - 0,1-5,0; triclosan - 0,1-1,0; camphor synthetic - 0,01-1,0; dye C1 42090 - 0,1-1,0; fragrance composition is 0.1 to 1.5; drinking water - the rest (U.S. Pat. Of the Russian Federation No. 2150264, CLA 61 K 7/00, 1999). The disadvantages of this gel is that applied triclosan is deklarirovannoe derived bis-phenol, similar in structure to extremely dangerous substance dioxin. It is known that triclosan may contain a mixture of dioxin - extremely Tox is knogo and hazardous substances. In addition, it is known that chlorinated phenols by simply heating easily turn into dioxins. At the same time, the antibacterial activity of triclosan is extremely low. The technical problem solved by this invention is to reduce the toxicity of the gel through the use of low-toxic disinfectants with improved dermatological action and prolonged effect, enhancing the regenerative functions of the skin and strengthen its barrier function. In addition, improving the homogeneity of the composition and its stability. To solve the technical problem in the antibacterial gel, including alkylhydroxylamines connection, disinfectant, perfume composition, and water, as alkylhydroxylamines connections use propylene glycol or diethylene glycol, as a disinfectant is used as a compound of polyguanidine or synergistic mixture of Quaternary ammonium compounds and optionally enter a hydroxyethyl cellulose or hydroxypropylcellulose, chitosan, ethoxylated ether sorbitan, polyvinylpyrrolidone with a molecular weight of from 10000 to 40000 or copolymer of polyvinylpyrrolidone, Trilon B - sodium salt of ethylenediaminetetraacetic acid, a vitamin component, and water in the following ratio of components, wt.%: - hydroxyprop cellulose or hydroxyethylcellulose 0,3-3,0 - propylene glycol or diethylene glycol and 0.2 to 15.0 connection of polyguanidine or synergistic a mixture of Quaternary ammonium compounds in a 1:1 ratio 0,5-3,0 - chitosan 0,1-2,0 - polyoxyethylene ether sorbitan 0,01-1,0 - polyvinylpyrrolidone with a molecular weight of from 10,000 up to 40,000 or copolymer of polyvinylpyrrolidone 0,01-0,5 - Trilon B - sodium salt ethylenediaminetetraacetic acid of 0.1-2.0 - perfume 0,2-0,5 vitamin component of 0.1-2.0 - water the rest The antibacterial gel as polyguanidine use phosphate poly-(4,9-dioxadodecane-1,12-guanidine), or citrate/formate, guanidine, or gluconate/benzoate, guanidine, or chloride, guanidine. The antibacterial gel as a Quaternary ammonium compound used dimethylbenzylamine-sulfate, as well as ethoxylated ether sorbitan use tween-20 or tween-40 or tween-60, or tween-80. The antibacterial gel as a vitamin component use vitamin a, or vitamin E, or vitamin In5or their mixture in equal parts. Used as the gel is a highly active compound of polyguanidine or synergistic mixture of Quaternary ammonium is soedinenie - dimethylbenzylamine-sulfate has a broad spectrum of biocidal activity: antibacterial, fungicidal, virucidal. It allatoxin, does not penetrate intact skin (IY hazard class), is stored on it for a long time, protecting against attacks of microorganisms. Dimethylbenzylamine-sulfate is synthesized in two stages, based on benzylamine, dodecylamide and dimethylsulfate. First heated at a temperature of 60-80°With an alcohol solution of 97 g (1 mol) of benzylamine with 205 g (1 mol) of dodecylamine and 40 g (1 mol) sodium hydroxide before the termination of the precipitated NaCl. The solution benzyldimethylamine filtered off from the precipitate of NaCl and quaternized added 126 g (1 mol) of dimethylsulfate and 20 g (0.5 mol) of caustic soda. The resulting dimethylbenzylamine-sulfate dried at a temperature not above 60°C to constant weight. Its antimicrobial activity of the drug exceeds katamin AB and benzalconi-chloride. Used in the proposed composition as a gel-forming component hydroxypropylcellulose or hydroxyethylcellulose refers to the non-ionic cellulose ethers and is a powdery white material with a main component content not less than 97 wt.%, the degree of polymerization of not less than 500 (THE 6-05-1857-87). Noted the haunted esters of lower alcohols - propylene glycol (TU 6-09-2434-81) and diethylene glycol (GOST 10136-77) have preservative, antiseptic and bactericidal properties. The absorption of propylene glycol allows you to keep the gel to the desired consistency. Introduction in the gel propylene glycol increases the permeability through the skin. Used in the proposed composition of the chitosan - poly,4-2-amino-2 deoxy-D-glucans (THE No. 9289-002-11418234-99) is a cationic polysaccharide, a structural analogue of cellulose, obtained by deacetylation of chitin, a natural biopolymer, which is part of the shells of crustaceans and insects, forms the cellular structure of most fungi and some algae. Chitosan stimulates the body's cells involved in immunological protection against pathogenic microorganisms, accelerates the healing of wounds. Chitosan is introduced into the gel as an immunomodulator, a viscosity regulator, an antiseptic and a modifier. In addition, it enhances the action of the main antibacterial component polyguanidine or synergistic mixture of Quaternary ammonium compounds. Ethoxylated esters sorbitan (sorbital, twins) are nonionic surfactants. They are distinguished by a member of the molecule acid (stearic, oleic, lauric, palmitic) and the degree of oksietilirovannye (5 or 20). They races is Vratsa in water, ethanol, benzene, but insoluble in petroleum ether, mineral oil. Tween-80 (sorbitan O-20)-serviceorienteret is a light yellow oily liquid with a basic substance content of 98% (FS 42-2540-88). Tween-60 (sorbitan C-20)-serviceprocessinstaller is a light yellow oily liquid with a basic substance content of 96% (THE 6-14-1050-81). Twin room-40 (TL-N) and tween-20 (TL-W) - products company Cao Chemical, Japan. Ethoxylated esters sorbitan introduced to improve the penetrating power of the gel and improve the stability of the composition. Polyvinylpyrrolidone (molecular weight of from 10000 to 40000) is a white powder, easily soluble in water and most organic solvents (FS 42-2238-98). Polyvinylpyrrolidone (PVP) tells the gel prolonged action and is a known detoxifier (gemodez). In combination with polyguanidine forms complexes with reduced toxicity. In addition, PVP in gel alters the structure of water in which is dissolved GHG that contributes to the stability and homogeneity of the gel. Used copolymers of polyvinylpyrrolidone with acrylates, substituted alkylamines followed, are the products of the company ISP VAN DYK (USA): poly(vinyl pyrrolidone/dimethylaminoethylmethacrylate) - COPOLIMER845; and COPOLIMER - 937; poly(vinyl pyrrolidone and metallicametallicametall) - POLIQUTENIUM-28 and poly (vinyl pyrrolidone/dimethylaminoethyl methacrylate) - POLIQUTENIUM - N. Trilon B (GOST 10652) is a sodium salt of ethylenediaminetetraacetic acid, complexone III is an organic chelate forming compound, crystalline, soluble in water, ethanol and most organic solvents. Used as a titrant in complexometry, for division and separation of metal ions to dissolve and prevent the formation of various sediments, caused, for example, water hardness, for excretion from the body of toxic metals, stabilization of food, water softener, as components of detergents. Fragrance composition is an oily liquid with a characteristic smell and is introduced into the gel to give it a pleasant odor. Use perfume composition with the following scent: Apple, peach, apricot, banana, vanilla, cherry, grapefruit, Jasmine, honeysuckle, cocoa, cinnamon, kiwi, lavender, Lily of the valley, lemon, lime blossom, mango, chamomile, calendula, green tea, fruity floral and fruit-herbal (mint, burdock, St. John's wort, rosemary, tarragon, eucalyptus, sage, thyme, hops, violet, series). Manufacturers can be: FF (Italy), “Bell flowers and fragrances (Germany) or the company's Phytotechnology” (St. Petersburg). Vitamin a affects the metabolic processes of the skin, has a healing effect. Provitamin5(panthenol) stimulates the renewal of skin. Vitamin E has a regenerative effect, protects the immune system, is an effective antioxidant that stabilizes the composition. The quantitative content of the components of the gel is optimal and selected on the basis of numerous experiments. In table 1 presents data confirming the optimality of the declared limits. The process of preparation of antibacterial gel has the following stages. The first is the preparation of raw materials and equipment - includes checking the purity of the reactor mixing and weighing ingredients. The second stage is the dispersion of non-ionic cellulose ethers (hydroxyethyl cellulose or hydroxypropylcellulose) in diethylene glycol or propylene glycol for 30 minutes at a temperature of 35-40°with periodic mixing. The mixing mode and the design features of the reactor is supposed to prevent foaming. The third stage - sequential introduction with stirring the resulting dispersion weighted amount of water, ethoxylated ether sorbitan, trylon B, chitosan, polyvinylpyrrolidone or with whom alimera. Next, the mixture is heated to a temperature of 35-40°C for 2-4 hours until a homogeneous viscous solution. The fourth stage is the preparation of aqueous disinfectants in the mixer at a temperature of 30-40°C for 1.5-2 hours. The fifth stage is the mixing of the components in the reactor-mixer, which is a cylindrical vessel with cooled jacketed stainless steel with a ratio of diameter and height of 1-1,5:1-2, provided with a removable cover, intake fittings and anchor stirrer or turbine type. In the reactor pour the prepared homogeneous viscous solution obtained in the third stage of the process, an aqueous solution of disinfectant, perfume composition and a vitamin component. In the resulting mass of water is added and continuously stirred at a temperature of 25-30°C for 1 hour. Examples of specific performance of a gel. Example No. 1. Gel antibacterial hand contains the following components, wt%: - hydroxypropylcellulose 1,5 - propylene glycol 7,0 - phosphate poly(4.9 dioxadodecane 1,12-guanidine) 1,5 - chitosan 1,0 twin 20 0,5 - PVP 0,3 - Trilon B 1,0 - perfume 0,3 - provitamin51,0 - water the rest Used for protection of the skin against the penetration of germs and bacteria. After application of the gel is and the skin is formed thin film, which doesn't dry the skin and disrupts the pH balance. Example No. 2. The antibacterial gel for face contains the following components in wt.%: - hydroxypropylcellulose 0,3 - diethylene glycol 15,0 - citrate/formate pgmg 0,5 - chitosan 2,0 twin 60 0,01 - PVP 0,01 - Trilon B 0,1 - perfume 0,1 the mixture of vitamins E and a in the ratio of 1:1 to 2.0 - water the rest Used for problem skin, irritating and allergic action. Example No. 3. The antibacterial gel for feet contains the following components in wt.%: - hydroxyethylcellulose 3,0 - propylene glycol 0,2 - synergistic mixture of chloride pgmg and dimethylbenzylamine sulfate 3,0 - chitosan 0,1 twin 60 1,0 - PVP copolymer with molecular weight of 10000 0,5 - Trilon B 2,0 - perfume 0,5 - provitamin5, vitamin E, vitamin a in the ratio of 1:1:1 0,1 - water the rest Eliminates the smell of sweat, protects from infection by fungus and other skin diseases, kills pathogens. Example No. 4 - hydroxypropylcellulose 2,5 - propylene glycol 12,0 - gluconate/benzoate pgmg 2,5 - chitosan 1,5 twin 80 0,05 - PVP 0,3 - Trilon B 0,5 - perfume 0,4 - vitamin And 1.5 - water the rest Eliminates the smell of sweat, the sight is preserved from contamination by fungus and other skin diseases, kills pathogens. Testing of antimicrobial activity developed antibacterial gel was determined by zone of inhibition of microorganisms by diffusion of the analyte in a dense nutrient medium (Fedorov Y.A., Root NR. “Microbiological research methods in dental hygiene products” in the book. “Basics of oral hygiene”. L., “Medicine”, 1973, p.3-215). The Petri dish was filled with 20 ml of a dense nutrient medium. Prepared 24 hours a microbial suspension of test microorganism with a concentration of 5·105CFU/ml and applied to 1 ml of the suspension on the surface of the medium. Was dried for 30 min, and then in a nutrient medium made holes with a diameter of 6 mm, which was applied to the samples developed disinfectant gel. The number of holes should not exceed 6 per Petri dish. For 30 min in Petri dishes kept at room temperature (20°C), then they were placed in the incubator for 24-48 hours at a temperature of 37°and upon expiration of that period took into account the zone of inhibition of microbial growth, including the diameter of the hole. The size of zones of inhibition of growth of test microorganisms was judged on the antimicrobial activity of the test substance, although it should be considered that the diffusion rate of the polymeric disinfectants lower rate of diffusion belongs to low-polymeric who disinfectants. To obtain reliable test results for each analyte should be done in 2-3 series of replications. Determining the minimum time required for complete suppression of the growth and development of test organisms, were developed for antibacterial gel as follows. In the test substance was added to a suspension of the test organisms in the amount of 105CFU/ml in a test tube pour 1 ml of the test substance. The tubes were shaken and intervals 2-5-10 and 30 minutes did the crops in the dense medium. Petri dishes were placed in 24 to 48 hours in a thermostat at 37°C. After the expiration of that period were counting the number of grown colonies and this indicator was judged on the bactericidal activity of the test substance. The results of these studies are presented in table 2. From the presented data in table 2 it follows that a more sensitive test means were gram-positive organisms (S. aureus). All test tools formed a zone of stunted growth from 19 to 24 mm, which corresponds to a relatively high activity. Draws attention to the high activity of the preparation according to example 3 to gram-negative microorganisms of the species E. coli and Ps.aeruginosa. When determining the speed of the manifestations of antimicrob the activity to experience funds were obtained, presented in table 3. From the presented data in table 3 it follows that the antibacterial effect of the developed formulations is developing very quickly. After 2 minutes of contact in any case not found living microflora after contamination by Escherichia coli. Testing of disinfectant gel was carried out on 100 volunteers without burdened allergological anamnesis within 30 days. According to a patchwork of samples and sample application shows that the gel is harmless, irritating and allergenic action. 1. The antibacterial gel, including alkylhydroxylamines connection, disinfectant, perfume composition, and water, characterized in that as alkylhydroxylamines connections use propylene glycol or diethylene glycol, as a disinfectant is used as a compound of polyguanidine or synergistic mixture of Quaternary ammonium compounds and further comprises hydroxyethyl cellulose or hydroxypropylcellulose, chitosan, ethoxylated ether sorbitan, polyvinylpyrrolidone with a molecular mass of capabilities from 10,000 to 40,000 or copolymer of polyvinylpyrrolidone, Trilon B is the sodium salt of ethylendiaminetetraacetic the th acid, vitamin component, and water in the following ratios, wt.%: hydroxypropylcellulose or hydroxyethylcellulose 0,3-3,0 propylene glycol or diethylene glycol and 0.2 to 15.0 the connection of polyguanidine or synergistic mixture of Quaternary ammonium compound in the ratio 1:1 0,5-3,0 chitosan 0,1-2,0 ethoxylated ether sorbitan 0,01-1,0 polyvinylpyrrolidone with a molecular mass capabilities from 10,000 to 40,000 or copolymer polyvinylpyrrolidone 0,01-0,5 Trilon B-sodium salt ethylenediaminetetraacetic acid of 0.1-2.0 fragrance composition of 0.2-0.5 vitamin component of 0.1-2.0 water the rest 2. The antibacterial gel according to claim 1, characterized in that compounds of polyguanidine use phosphate poly-(4,9-dioxadodecane-1,12-guanidine), or citrate/formate, guanidine, or gluconate/benzoate, guanidine, or chloride, guanidine. 3. The antibacterial gel according to claim 1, characterized in that the Quaternary ammonium compound used dimethylbenzylamine-sulfate. 4. The antibacterial gel according to claim 1, characterized in that as a polyoxyethylene ether sorbitan use tween-20, is whether the twin 40, or tween 60 or tween 80. 5. The antibacterial gel according to claim 1, characterized in that as a vitamin component use vitamin a, or vitamin E, or vitamin In5or their mixture in equal parts.
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