Abstract: Cosmetic agents for the control of head dandruff, containing customary cosmetic carrier substances and additives, and 1 to 5% by weight of salts of at least one biguanide derivative of the general formula ##STR1## wherein m is from 1 to 10 and n is from 1 to 6. Preferred salts include oligohexamethylene biguanide, oligotetramethylene biguanide and 1-methyl biguanide. Also preferred are the hydrochloride salts of biguanide derivatives. The agents may be in the form of shampoos, hair lotions, hair setting preparations, rinses, hair dressing gels and creams, hair oils, powders, or sprays. Customary carrier substances may be an ointment base, a powder, water, alcohol or water-alcohol mixtures. Customary cosmetic additives include resins, emulsifiers, thickeners, hair care substances, coloring agents, perfume oils, solid fillers, and propellants.
Abstract: This invention provides an extract from the plant Maytenus nemerosa (Eckl & Zeyh) Morais (Celastroceae) South Africa and a method of obtaining same. The extract is obtained by subjecting the plant to a series of extraction steps with a plurality of solvents having different polarities. In each extraction step, the solvent used has a polarity higher than that used in the preceding extraction step. All extraction steps are conducted at room temperature. The extracts have been found to possess biological activity.
Abstract: A process is described which consists, in a first stage, in applying a composition based on a substance of vegetable or animal origin, a synthetic organic substance or a mineral substance, in suspension or in solution in a solvent and having a viscosity suitable for application to the hair, or as a powder, and making it possible to prevent or substantially to limit the passage of the dyestuffs and/or of the dyestuff precursors as far as the scalp, and, in a second stage, in dyeing the hair using one or more compositions, at least one of which contains either an oxidizable dyestuff or a direct dyestuff, the dyeing being followed, after an interval sufficient for coloring the hair, by rinsing and optionally by shampooing.
Type:
Grant
Filed:
December 9, 1980
Date of Patent:
September 6, 1983
Assignee:
L'Oreal
Inventors:
Gregoire Kalopissis, Jacqueline Gallien, Bernard Jacquet, Daniel Bauer, Jean P. Chalaye
Abstract: Agents for the oxidative dyeing of hair, containing as coloring component 6-amino-3-methylphenol, also in the form of its salts or phenolates. The coloring component is contained in these agents in a quantity of about 0.01 to 2.0 percent by weight, alone or in a mixture with the customary developing and coupling substances. In the case of a mixture, the 6-amino-3-methylphenol is preferably used at a molar ratio below normal relative to these developing and coupling substances. The oxidative reaction of the 6-amino-3-methylphenol proceeding with an intensive yellow coloring is generally not influenced by the customary developing and coupling substances that may be present.
Abstract: Agents for the oxidative dyeing of hair, containing as coupling substance at least one derivative of 1,2-methylene dioxybenzene of the general formula ##STR1## in which R signifies an OH--, NH.sub.2 --, NHR.sup.1 -- or NR.sup.1 R.sup.2 -group, wherein R.sup.1 and R.sup.2 represent, independently of each other, an alkyl-, hydroalkyl-, or acyl group with 1 to 4 carbon atoms. The coupling substance is contained in these agents in a concentration of about 0.01 to 3.0 percent by weight, i.e. in a mixture with customary developing substances and, in given instances, also customary coupling substances. The particular possibility exists of producing dark natural tints by a mixture of 4-oxy-1,2-methylene dioxybenzene with the developing substance p-aminophenol.
Abstract: A method for decreasing urinary calcium content which comprises orally administering to a person whose urine contains insoluble calcium containing precipitates or has a propensity for forming calcium containing precipitates, an effective amount of an agent selected from water-soluble vinylbenzenesulfonic acid polymers and the nontoxic pharmaceutically acceptable salts thereof.
Abstract: Anticonvulsant, anxiolytic and hypnotic medicament containing, as active substance, 2-amino-6-trifluoromethoxy-benzothiazole or a salt of this compound with a pharmaceutically acceptable acid.
Abstract: Erythro-9,10-Dihydroxyoctadecan-1-ol acetate, a compound isolated in low yield from tung oil, was synthesized in high yield and found to have excellent potential as a boll weevil feeding deterrent when applied to cotton plants.
Type:
Grant
Filed:
January 28, 1981
Date of Patent:
June 29, 1982
Assignee:
The United States of America as represented by the Secretary of Agriculture
Abstract: Long chain fatty acid amides of styryl hexahydroindolinols in which the amido portions have ethyleneically unsaturated positions or cyclopropanyl rings, eg 1-(1-oxo-9-cis-octadecenyl)-(3aRS, 4RS, 7aRS)-4-(Z)-(3,4-dimethoxy)-styryl-hexahydro-4-indolinol, are useful as cholesterol ester-reducing agents and are obtainable by reacting corresponding long chain carboxylic acids (or derivatives thereof) with appropriate 4-styryl-4-hexahydroindolinols.
Abstract: Pharmaceutical compositions and methods of inhibiting phenylethanolamine N-methyltransferase using 2-indanamine compounds having 4 and/or 5 substituents.
Type:
Grant
Filed:
April 10, 1978
Date of Patent:
March 11, 1980
Assignee:
SmithKline Corporation
Inventors:
William E. Bondinell, Robert G. Pendleton
Abstract: An instillation composition, comprising an effective amount of at least one sparingly soluble active material suspended or partly dissolved in an aqueous emulsion containing a swelling agent. Advantageously the active substance is nitrofurantoin or a quinolone or pyridazine derivative, the active material has a particle size less than about 10 .mu.m and the swelling agent is a polysaccharide derivative present in about 0.3 to 3% by weight of the composition, the composition further containing at least one local anesthetic, antiphlogistic substance, emulsifier, buffer or stabilizer. With the invention, unit doses of only 50 ml. will contain sufficient active material.
Type:
Grant
Filed:
February 24, 1978
Date of Patent:
March 4, 1980
Assignee:
Boehringer Mannheim GmbH
Inventors:
Heinrich Woog, Werner Rothe, Werner Gruber
Abstract: Bromhexine derivatives corresponding to the following general formula ##STR1## and antitussive compositions therefrom, as well as a process for making same are described.
Abstract: A method of making a water-in-oil waterproof makeup comprising (a) a cosmetic emulsion oil, (b) a cosmetic pigment, and (c) an emulsifier combination comprising (i) a stearate and (ii) a polyhydric alcohol ester of a liquid fatty acid, and compositions therefrom.
Abstract: There is disclosed a pharmaceutical composition useful in stimulating blood circulation and healing of wounds. This composition comprises (a) albumin-freed calf blood extract, and (b) from about 0.001 to about 2.5 micrograms of at least one kinin per milligram of dry extracted substance. A method for treating patients in order to stimulate their blood circulation is also disclosed. This method comprises treating these patients with an effective amount of the pharmaceutical composition described above.
Type:
Grant
Filed:
December 30, 1977
Date of Patent:
December 4, 1979
Assignee:
Thera Gesellschaft fur Patentverwertung mbH
Abstract: Stable, aqueous or aqueous-alcoholic solutions of fat-soluble perfume oils or drugs, containing hydroxyalkyl ester- and/or N-(hydroxyalkyl)-amide-ethoxylates of the formula ##STR1## wherein R.sub.1 and/or R.sub.2 are an alkyl group having 1 to 18 carbon atoms or hydrogen, R.sub.3 is an alkyl group having 1 to 12 carbon atoms or an aryl group, X is an oxygen atom, the group >NH or the group >N--(C.sub.2 H.sub.4 O).sub.m H, and n and m are integers of from 0 to 40, with the proviso that the total of the carbon atoms of R.sub.1 +R.sub.2 is from 6 to 20 and the total of the numbers n+m is a value from 6 to 40.
Abstract: 1-Aryloxy-3-aminoalkylamino-2-propanol derivatives, processes for their manufacture, pharmaceutical compositions containing them and methods of using them in the treatment of heart diseases. The compounds possess .beta.-adrenergic blocking activity and some of them additionally possess cardiac stimulant activity. Representative of the compounds disclosed is 1-(2-cyanophenoxy)-3-.beta.(4-hydroxyphenylacetamido)ethylamino-2-propanol .
Abstract: A veterinary composition comprising 40 to 80% of an actively absorbed monosaccharide, 7.5 to 30% of an actively absorbed naturally occurring amino acid, and 0.5 to 10% of an agent which is citric acid or a salt thereof; except that when the agent is a salt of citric acid, then the amino acid represents no more than 13% of the composition; are useful in the treatment of diarrhoea in animals such as calves.