GB633062A - Improvements in or relating to ointment bases - Google Patents

Improvements in or relating to ointment bases

Info

Publication number
GB633062A
GB633062A GB2690/46A GB269046A GB633062A GB 633062 A GB633062 A GB 633062A GB 2690/46 A GB2690/46 A GB 2690/46A GB 269046 A GB269046 A GB 269046A GB 633062 A GB633062 A GB 633062A
Authority
GB
United Kingdom
Prior art keywords
cellulose
oil
glycol
alkylated
mixture
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB2690/46A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of GB633062A publication Critical patent/GB633062A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0014Skin, i.e. galenical aspects of topical compositions

Landscapes

  • Health & Medical Sciences (AREA)
  • Dermatology (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

An ointment base is prepared by heating a mixture including at least one normally liquid polyhydroxy alcohol, water, and a water-dispersible alkylated cellulose to produce a clear liquid, the amount of polyhydroxy alcohol exceeding the amount of alkylated cellulose, cooling the resulting mixture to form a gel structure, and incorporating a mineral oil and a dispersing agent for such oil into the mixture. The alkylated cellulose may be dispersed in water prior to mixing with the polyhydroxy alcohol. The mineral oil and the dispersing agent (preferably premixed) may be added to the mixture containing the alkylated cellulose and polyhydroxy alcohol while this mixture is, or has been heated to a temperature above that of gel formation. The preferred polyhydroxy alcohols are a triethylene glycol having a molecular weight of 150, tetra-ethylene glycol, pentaethylene glycol, hexaethylene or octa-ethylene glycols having molecular weights of 282 and 415 respectively, or other polyethylene glycols having molecular weights up to 900, propylene glycol, ethylene glycol and glycerine. Specified alkylated celluloses are hydroxyethyl cellulose, methyl cellulose and the glycollic acid ethers of cellulose and their sodium, aluminium or other metal salts. The mineral oil may be deodorized kerosene, light and heavy lubricating oils, petrolatums, solid paraffins, earth waxes and other paraffinic or naphthenic hydrocarbons or their admixtures. The dispersing agent may be an oil soluble phospholipoid such as corn oil, cotton-seed oil, or soya bean phosphatides, lecithins, cephalins, cholesterol, cholesteryl esters, glyceryl monostearate, sorbitol monolaurate, and nonaethylene glycol monostearate. These ointment bases are compatible with ichthyol, balsam tolu, lanolin, wood tar, iodine, weak and strong acids, alkalies, aluminium chloride, silver nitrate, silver iodide, silver oxide, sulphur, zinc oxide, zinc sulphide, alkaline polysulphides and bismuth hydroxide, and are solvents for sulphanilamide, sulphathiazole, sulphapyridine, gramicidin, tyrothricin, streptothricin, benzolaine, menthol, methyl salicylate, camphor, chorobutanol, phenothiazine, stilbestrol, estradiol, vitamins A and D, stropine, homatropine, methylene blue, phenol, tannic acid, isobornyl thio-cyanoacetate, and essential oils. The ointments are also compatible with insecticides or insect repellants such as D.D.T. and dimethyl phthalate.ALSO:An ointment base is prepared by heating a mixture including at least one normally liquid polyhydroxy alcohol, water, and a water-dispersible alkylated cellulose to produce a clear liquid, the amount of polyhydroxy alcohol exceeding the amount of alkylated cellulose, cooling the resulting mixture to form a gel structure, and incorporating a mineral oil and a dispersing agent for such oil into the mixture. The alkylated cellulose may be dispersed in water prior to mixing with the polyhydroxy alcohol. The mineral oil and the dispersing agent (preferably premixed) may be added to the mixture containing the alkylated cellulose and polyhydroxy alcohol while this mixture is, or has been heated to a temperature above that of gel formation. The preferred polyhydroxy alcohols are a triethylene glycol having a molecular weight of 150, tetraethylene glycol, pentaethylene glycol, hexaethylene or octaethylene-glycols having molecular weights of 282 and 415 respectively, or other polyethylene glycols having molecular weights up to 900, propylene glycol, ethylene glycol and glycerine. Specified alkylated celluloses are hydroxyethyl cellulose, methyl cellulose and the glycollic acid ethers of cellulose and their sodium aluminium or other metal salts. The mineral oil may be deodorized kerosene, light and heavy lubricating oils, petrolatums, solid paraffins, earth waxes and other paraffinic or napthenic hydrocarbons or their admixtures. The dispersing agent may be an oil soluble phospholiped such as corn oil, cotton seed oil, or soya bean phosphatides, lecithins, cephalins, cholesterol, cholesteryl esters, glyceryl monostearate, sorbitol monolaurate, and nonaethylene glycol monostearate. These ointment bases are compatible with ichthyol, balsam tolu, lanolin, wood tar, iodine, weak and strong acids, alkalies, aluminium chloride, silver nitrate, silver iodide, silver oxide, sulphur, zinc oxide, zinc sulphide, alkaline polysulphides and bismuth hydroxide and are solvents for sulphanilamide, sulphathiazole, sulphapyridine, gramicicdin, tyrothricin, streptothricin, benzocaine, menthol, methyl salicylate, camphor, chlorobutanol, phenothiazine, stilbestrol, estradiol, vitamins A and D, stropine, homatropine, methylene blue, phenol, tannic acid, isobornyl thio-cyano-acetate, and essential oils. The ointments are also compatible with insecticides or insect repellants such as D.D.T. and dimethyl phthalate.
GB2690/46A 1945-02-01 1946-01-28 Improvements in or relating to ointment bases Expired GB633062A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US633062XA 1945-02-01 1945-02-01

Publications (1)

Publication Number Publication Date
GB633062A true GB633062A (en) 1949-12-12

Family

ID=22048323

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2690/46A Expired GB633062A (en) 1945-02-01 1946-01-28 Improvements in or relating to ointment bases

Country Status (1)

Country Link
GB (1) GB633062A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2116423A (en) * 1982-01-13 1983-09-28 Quinoderm Ltd Dermatological compositions
GB2163956A (en) * 1984-09-08 1986-03-12 Ile De France Percutaneous anaesthetic composition for topical application
EP0716848A3 (en) * 1994-12-02 1999-12-22 Unilever Plc Cosmetic emulsions with a deposition triggering lipid system
FR2814075A1 (en) * 2000-09-18 2002-03-22 Phyt Immun Gmbh Nasal ointment for prophylaxis of inhalation-allergic reactions, especially hay fever, comprising mixture of saturated hydrocarbons and tannin(s)
CN110887720A (en) * 2019-12-11 2020-03-17 武汉原谷生物科技有限责任公司 Immunohistochemical pen semisolid pen paste and preparation method thereof

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2116423A (en) * 1982-01-13 1983-09-28 Quinoderm Ltd Dermatological compositions
GB2163956A (en) * 1984-09-08 1986-03-12 Ile De France Percutaneous anaesthetic composition for topical application
EP0716848A3 (en) * 1994-12-02 1999-12-22 Unilever Plc Cosmetic emulsions with a deposition triggering lipid system
FR2814075A1 (en) * 2000-09-18 2002-03-22 Phyt Immun Gmbh Nasal ointment for prophylaxis of inhalation-allergic reactions, especially hay fever, comprising mixture of saturated hydrocarbons and tannin(s)
CN110887720A (en) * 2019-12-11 2020-03-17 武汉原谷生物科技有限责任公司 Immunohistochemical pen semisolid pen paste and preparation method thereof

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