Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q19/00—Preparations for care of the skin
  • A61Q19/04—Preparations for care of the skin for chemically tanning the skin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
  • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
  • A61K8/35—Ketones, e.g. benzophenone

Definitions

• individuals who tan without difiiculty may desire to extend the normal life of a naturally acquired tan, without reexposure to the sun.
• a skin tan may be desired when weather or other conditions do not permit the usual exposure to the sun in order to acquire the conventional sun tan.
• sun lamps are used extensively to produce a tan on the human skin; such lamps are expensive and must be used for extended periods of time to attain the desired intensity of coloration. The inherent inconvenience and expense, has limited the use of sun lamps for the purpose indicated.
• one object of this invention is to provide a cosmetic preparation applicable to the human skin Which is effective to produce a simulated tan eifect thereon.
• Another object of this invention is to provide an improved composition which may be applied to the human skin to produce a simulated tan effect of regulated intensity; the resultant tan being resistant to removal by water or detergents.
• Still another object of this invention is to provide a composition containing an active agent which is effective to produce a tan coloration on the human skin which is substantially indistinguishable from a tan accruing from exposure to the sun; such agent being physiologically inert and without adverse elfects on the skin or organs of the human body.
• Yet another object of this invention is to provide a composition applicable to the human body for producing a skin tan within a relatively short time after such application; the tan effect being maintained for from 4 to 6 days.
• dihydroxyacetone may be applied to the human skin by way of a suitable vehicle or base; with a resultant modification of the normal appearance of the skin to give a simulated tan.
• the darkening of the human epidermis takes place within approximately 2 to 24 hours after application of a suitable composition containing the dihydroxyacetone as the active agent, the actual time varying with the individual and the extent of the application.
• the intensity of the simulated tan achieved may be regulated by the concentration of the active agent in a single application; or may be achieved by repeated apl Patented Aug. 16, 1960 2 V lications of the composition at clo'sely spaced time intervals.
• the maximum intensity of the colorant elfect is achieved within 2 to 24 hours after application; the intensity of the color thereafter progressively decreasing, in a manner similar to that of a'hatural, sun inducedtan. It has been found that the use of the cosmetic preparation of the instant invention'will provide 'a tan coloration for the skin which may last from 4 to 6 days and will be proof against removal by theapplication or water or detergents during such period. The epidermis will be unharmed during the period of tan and will be unaffected after the tan period.
• the active agent dihydroxyaceto'ne maybe carried or suspended in various cosmetic bases suitable for-external application directly to the human skin.
• such base may take the form of liquid or cream lotions, ointments, dusting .powders and the like.
• the active agent may housed in varying proportions rang--' ing from about 0.05 to about 90.0 by weight of the composition, with'a preferred range or" from about 0.1,
• the acetone has the eifect of substantially reducing the normal tackiness of the lotion-
• the dihydroxyacetone may be admixed with other vehicles to provide lotions and creams, including glycerine, vegetable oils such as castor or almond oil and the like, mineral oil, petrolatum and other cosmetic bases known in the art.
• the dihydroxyacetone may also be incorporated in an ointment base, as by mixing, by weight, 10.0 parts of glycerol monostearate, 10.0 .parts of cetyl alcohol, 30 parts of spermacetti, 10.0 parts of Span 20 (sorbitan monolaurate), 10.0 parts of Tween 20 (polyoxyalkylene derivative of sorbitan monolaurate); 12.5 parts of glycerin and 100 parts of water.
• the resultant ointment base was compounded with 0.5% by weight of the base of dihydroxyacetone, on an anhydrous basis. A thin coating of the ointment was applied to the skin and within 3 hours a uniform tan developed. A second application of the same ointment, approximately 1 hour after the first application, had the effect of increasing the intensity of the final tan.
• a dusting powder was prepared from equal amounts by weight of talc and chalk, with minor additions of colorant. About 1.0% by weight of dihydroxyacetone was added to the powder. Application of the dusting powder to the skin produced a tan within several hours after application.
• a skin cream was prepared by melting together g. stearin, 5 g. lanolin and 10 g. cetyl alcohol. A mixture of 36 g. glycerine, 5 cc. triethanolamine and 250 cc. water, with a small amount of perfume, was slowly added to the molten mass with stirring until cold. Dihydroxyacetone in amounts ranging from 0.2 to 4.0% was added to several portions of the cream, respectively, followed by thorough admixture of the active agent with the cream base.
• sun screening agents may be compounded with the dihydroxyacetone, in a selected cosmetic base, including homomenthyl salicylate; butyl benzal acetone oxalate; acetanilide; benzyl salicylate; oxymaphthoic acid; dimethyl aminobenzoic acid; phenyl salicylate and the like, all of which function to filter out the actinic rays from the sun. 7
• cosmetic base in lotion, cream, ointment or powder form, may be variously compounded in accordance with the knowledge of the pertinent art, to provide a suitable carrier or vehicle for the active agent d-ihydroxyacetone.
• composition applicable to the human epidermis for imparting a tan thereto comprising a cosmetic base and dihydroxyacetone distributed through said base, said base comprising an oleaginous material.
• a method of tanning the human epidermis comprising applying to the epidermis a composition comprising a cosmetic base and dihydroxyacetone distributed through said base.
• a method of tanning the human epidermis comprising applying to the epidermis a composition comprising a liquid cosmetic base and dihydroxyacetone distributed through said base.
• a cosmetic composition for imparting a tan efiect to the human epidermis comprising a cosmetic powdered inert base and dihydroxy'acetone distributed through said base.
• a cosmetic preparation applicable to the human epidermis for imparting a tan effect thereto within 2 to 24 hours after application thereto, said composition comprising by weight about 50% ethyl alcohol, about water, about 4% dihydroxyacetone, and about 1% acetone.
• said preparation comprising a cosmetic base and a mixture of dihydroxyacetone and a. sun screening agent distributed through said base.
• a cosmetic preparation applicable to the human epidermis for imparting a tan effect thereto comprising a cosmetic base and a mixture of dihydroxyacetone and an anti-tackiness agent comprising acetone distributed through said base.
• compositions applicable to the human epidermis for imparting a tan thereto comprising a cosmetic base, dihydroxyacetone and acetone distributed through said base, said base comprising a mixture of ethyl alcohol and water, and said dihydroxyacetone amounts to from about 0.1 to about 25.0% by weight of said composition.

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• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Dermatology (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Emergency Medicine (AREA)
• Birds (AREA)
• Epidemiology (AREA)
• Cosmetics (AREA)

Priority Applications (8)

Applications Claiming Priority (3)

Publications (1)

Family

ID=27245420

Family Applications (1)

Country Status (6)

Cited By (54)

Families Citing this family (4)

Family Cites Families (1)

• 0
  • BE BE588291D patent/BE588291A/xx unknown
  • NL NL249148D patent/NL249148A/xx unknown
• 1960
  • 1960-02-09 US US7510A patent/US2949403A/en not_active Expired - Lifetime
  • 1960-02-20 DE DEA34028A patent/DE1103521B/de active Pending
  • 1960-02-25 GB GB6595/60A patent/GB881336A/en not_active Expired
  • 1960-03-03 FR FR820315A patent/FR1250196A/fr not_active Expired

Non-Patent Citations (1)

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