Stabilisierungsverfahren
1,162,452. Stabilized compositions. F. HOFFMANN-LA ROCHE & CO. A.G. 1 March, 1968 [2 March, 1967], No. 10141/68. Heading ASB. Stabilized therapeutic compositions for the treatment 'of inflammatory skin disorders and arteriosclerosis comprise licosatetrayn-(5, 8, 11, 14)-oic (1) acid or an a...
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description | 1,162,452. Stabilized compositions. F. HOFFMANN-LA ROCHE & CO. A.G. 1 March, 1968 [2 March, 1967], No. 10141/68. Heading ASB. Stabilized therapeutic compositions for the treatment 'of inflammatory skin disorders and arteriosclerosis comprise licosatetrayn-(5, 8, 11, 14)-oic (1) acid or an alkyl ester containing 1 to 7 carbon atoms in the alkyl group or pharmaceutically acceptable salt thereof in admixture with an edible oil, edible fat or edible wax or a mixture thereof. The oils Imay be the glycerides of fatty acids such as the mono-, di- or tri-glyceride of saturated or unsaturated fatty acids containing from 6 'to 24 carbon atoms, e.g. coconut, sasame, peanut. corn, cottonseed or soy bean oil or modified fractions c,f these oils, lard and butter oil; and the wax may comprise beeswax, cetyl alcohol, montan wax or Japan wax. The composition may contain alipid-soluble antioxidant. Suitable salts of the acid include alkali-metal salts (e.g. Na and K), ammonium, alkaline-earthmetal (e.g. Ca) and organic arnine salts (e.g. ethylamine, diethylamine, triethylamine, ethylenediamine, mono-, di- or tri-ethianolamine, ethyldiethanolamine, butylmonocthanolamine, p-(tertiary amyl)-phenyldiethanolamine, galactamine, N-methyl-glutamine, glucosamine and guaridine salts). The compositions may be administered orally in the form of solutions, suspensions or capsules (e.g. gelatin capsules) containing conventional excipients. |
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Stabilized therapeutic compositions for the treatment 'of inflammatory skin disorders and arteriosclerosis comprise licosatetrayn-(5, 8, 11, 14)-oic (1) acid or an alkyl ester containing 1 to 7 carbon atoms in the alkyl group or pharmaceutically acceptable salt thereof in admixture with an edible oil, edible fat or edible wax or a mixture thereof. The oils Imay be the glycerides of fatty acids such as the mono-, di- or tri-glyceride of saturated or unsaturated fatty acids containing from 6 'to 24 carbon atoms, e.g. coconut, sasame, peanut. corn, cottonseed or soy bean oil or modified fractions c,f these oils, lard and butter oil; and the wax may comprise beeswax, cetyl alcohol, montan wax or Japan wax. The composition may contain alipid-soluble antioxidant. Suitable salts of the acid include alkali-metal salts (e.g. Na and K), ammonium, alkaline-earthmetal (e.g. Ca) and organic arnine salts (e.g. ethylamine, diethylamine, triethylamine, ethylenediamine, mono-, di- or tri-ethianolamine, ethyldiethanolamine, butylmonocthanolamine, p-(tertiary amyl)-phenyldiethanolamine, galactamine, N-methyl-glutamine, glucosamine and guaridine salts). 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Stabilized compositions. F. HOFFMANN-LA ROCHE & CO. A.G. 1 March, 1968 [2 March, 1967], No. 10141/68. Heading ASB. Stabilized therapeutic compositions for the treatment 'of inflammatory skin disorders and arteriosclerosis comprise licosatetrayn-(5, 8, 11, 14)-oic (1) acid or an alkyl ester containing 1 to 7 carbon atoms in the alkyl group or pharmaceutically acceptable salt thereof in admixture with an edible oil, edible fat or edible wax or a mixture thereof. The oils Imay be the glycerides of fatty acids such as the mono-, di- or tri-glyceride of saturated or unsaturated fatty acids containing from 6 'to 24 carbon atoms, e.g. coconut, sasame, peanut. corn, cottonseed or soy bean oil or modified fractions c,f these oils, lard and butter oil; and the wax may comprise beeswax, cetyl alcohol, montan wax or Japan wax. The composition may contain alipid-soluble antioxidant. Suitable salts of the acid include alkali-metal salts (e.g. Na and K), ammonium, alkaline-earthmetal (e.g. Ca) and organic arnine salts (e.g. ethylamine, diethylamine, triethylamine, ethylenediamine, mono-, di- or tri-ethianolamine, ethyldiethanolamine, butylmonocthanolamine, p-(tertiary amyl)-phenyldiethanolamine, galactamine, N-methyl-glutamine, glucosamine and guaridine salts). The compositions may be administered orally in the form of solutions, suspensions or capsules (e.g. gelatin capsules) containing conventional excipients.</description><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1971</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZJAILklMyszJLM5MLSrNSy8uSy1KS8woSs3jYWBNS8wpTuWF0twMCm6uIc4euqkF-fGpxQWJyal5qSXxLq6GZmYWRsYWjobGRCgBAPggIow</recordid><startdate>19711125</startdate><enddate>19711125</enddate><creator>LEON NEWMARK,HAROLD</creator><creator>THUROE CARSTENSEN,JENS</creator><creator>JAMES VANCE,JOHN</creator><scope>EVB</scope></search><sort><creationdate>19711125</creationdate><title>Stabilisierungsverfahren</title><author>LEON NEWMARK,HAROLD ; THUROE CARSTENSEN,JENS ; JAMES VANCE,JOHN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE1668238A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1971</creationdate><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><toplevel>online_resources</toplevel><creatorcontrib>LEON NEWMARK,HAROLD</creatorcontrib><creatorcontrib>THUROE CARSTENSEN,JENS</creatorcontrib><creatorcontrib>JAMES VANCE,JOHN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>LEON NEWMARK,HAROLD</au><au>THUROE CARSTENSEN,JENS</au><au>JAMES VANCE,JOHN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Stabilisierungsverfahren</title><date>1971-11-25</date><risdate>1971</risdate><abstract>1,162,452. Stabilized compositions. F. HOFFMANN-LA ROCHE & CO. A.G. 1 March, 1968 [2 March, 1967], No. 10141/68. Heading ASB. Stabilized therapeutic compositions for the treatment 'of inflammatory skin disorders and arteriosclerosis comprise licosatetrayn-(5, 8, 11, 14)-oic (1) acid or an alkyl ester containing 1 to 7 carbon atoms in the alkyl group or pharmaceutically acceptable salt thereof in admixture with an edible oil, edible fat or edible wax or a mixture thereof. The oils Imay be the glycerides of fatty acids such as the mono-, di- or tri-glyceride of saturated or unsaturated fatty acids containing from 6 'to 24 carbon atoms, e.g. coconut, sasame, peanut. corn, cottonseed or soy bean oil or modified fractions c,f these oils, lard and butter oil; and the wax may comprise beeswax, cetyl alcohol, montan wax or Japan wax. The composition may contain alipid-soluble antioxidant. Suitable salts of the acid include alkali-metal salts (e.g. Na and K), ammonium, alkaline-earthmetal (e.g. Ca) and organic arnine salts (e.g. ethylamine, diethylamine, triethylamine, ethylenediamine, mono-, di- or tri-ethianolamine, ethyldiethanolamine, butylmonocthanolamine, p-(tertiary amyl)-phenyldiethanolamine, galactamine, N-methyl-glutamine, glucosamine and guaridine salts). The compositions may be administered orally in the form of solutions, suspensions or capsules (e.g. gelatin capsules) containing conventional excipients.</abstract><oa>free_for_read</oa></addata></record> |
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title | Stabilisierungsverfahren |
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