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US2520980A - Cosmetic creams - Google Patents

Cosmetic creams Download PDF

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Publication number
US2520980A
US2520980A US43344A US4334448A US2520980A US 2520980 A US2520980 A US 2520980A US 43344 A US43344 A US 43344A US 4334448 A US4334448 A US 4334448A US 2520980 A US2520980 A US 2520980A
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US
United States
Prior art keywords
ether
cosmetic
dicholesteryl
cosmetic creams
cholesteryl
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 - Lifetime
Application number
US43344A
Inventor
Terkel Maryan
Silberman Henryk
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.)
National Chemical Products Pty Ltd
Original Assignee
National Chemical Products Pty Ltd
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 National Chemical Products Pty Ltd filed Critical National Chemical Products Pty Ltd
Application granted granted Critical
Publication of US2520980A publication Critical patent/US2520980A/en
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Expired - Lifetime legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/63Steroids; Derivatives thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S516/00Colloid systems and wetting agents; subcombinations thereof; processes of
    • Y10S516/01Wetting, emulsifying, dispersing, or stabilizing agents

Definitions

  • Cosmetic creams usually comprise an aqueous emulsion of oleaginous material; such as fats, oils, waxes, fatty alcohols and the like. Various perfumes, antiseptics and medicinalagents are usually added to the emulsion. Cosmetic creams.
  • a cosmetic cream in accordance with this invention includes from 0.1% to 8% of a cholesteryl ether.
  • cholesteryl ethers appear to be particularly effective emulsifying agents for the oleaginous materials used in cosmetic creams.
  • cholesterol type compounds are found in the human body and it is possible that the close relationship which exists between the cholesterol type of compounds found in the human body and the cholesteryl ethers included in the cosmetic creams of this invention assists in the assimilation of the preparation into the secretions of the sebaceous glands.
  • the preferred cholesteryl ether is dicholesteryl ether, which may be obtained as a by-product of the production of cholesterol from animal tissue such as the nervous system of cattle.
  • the improvement in the cosmetic creams is noticeable with as little as 0.1% of dicholesteryl ether added to the cosmetic cream, and it is possible to add as much as 8% with advantage.
  • the economic range appears to be between 0.1% and 1% and normally the amount of dicholesteryl ether added rarely exceeds 1%.
  • dicholesteryl ether It is not necessary for the dicholesteryl ether to be pure; and actual practice 9 dicholesteryl ether obtained frompnimal tissue is usually-contaminated with other cholesterol derivativeswhich, however, donot detract from-theteifec tiveness of the; ether.
  • the mixture or stirring may be effected in any suitable apparatus, such as an emulsifier, homogeniser or colloid mill.
  • Dicholesteryl ether possesses numerous advantages. It is itself a very efficient emulsifying agent and is also capable of changing and. improving the properties of cholesterol as an emulsifying agent. Further, when both dicholesteryl ether and cholesterol are employed as emulsifying agents a smaller quantity is necessary than when cholesterol alone is employed. Cosmetic emulsions containing a cholesteryl ether improve the texture of the skin and induce smoothness thereof. When cosmetic creams made in accordance with this invention are rubbed into the skin they practically disappear leaving the skin soft and smooth.
  • Cosmetic cream comprising an emulsion of oleaginous and aqueous material, and from 0.1% to 8 of a cholesteryl ether.
  • Vanishing cream comprising an aqueous emulsion of steario acid and from 0.1% to 1% of dicholesteryl ether.
  • Cosmetic cream comprising an aqueous emulsion of Wax, fat and oil, and from 0.1 to 1% 0f dicholesteryl ether.

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

Description

Patented Sept. 5, 1950 Maryan Terkel, East, Sydney, New-South Wales, and Henry k Silberman, Meadowbank, neaiL Sydn y, N S u s. tralialassi nors. to National Chemical ProductsPty Limited, East Sydney, New. South; Wales, Australia, a company of New South Wales No Drawing. Application August-9, 1948, Serial- No. 43,344. In Australia ;Qctl?.1h39, 19 45 3-Clai ms. 1 This invention relates to-cosmetic creams of the emulsion type.
Cosmetic creams usually comprise an aqueous emulsion of oleaginous material; such as fats, oils, waxes, fatty alcohols and the like. Various perfumes, antiseptics and medicinalagents are usually added to the emulsion. Cosmetic creams.
arensed, among other things, for smoothingand' softening the skin and'also for relieving chapped skin.
We have now found that if a small amount of a cholesteryl ether is added to a cosmetic cream the properties of the cream, insofar as it affects the skin, are considerably improved. With continued use of such creams containing a cholesteryl ether the skin becomes much softer and smoother than when ordinary cosmetic creams are used. The effect is considerably more than that produced by ordinary cosmetic preparations.
Accordingly, a cosmetic cream in accordance with this invention includes from 0.1% to 8% of a cholesteryl ether.
It is believed that the marked improvement in the properties of a cosmetic cream containing a cholesteryl ether is due in part to the fact that the emulsifying action of the cholesteryl ether provides a particularly fine and effective dispersion of the droplets of oil and the like. Cholesteryl ethers appear to be particularly effective emulsifying agents for the oleaginous materials used in cosmetic creams. Furthermore, cholesterol type compounds are found in the human body and it is possible that the close relationship which exists between the cholesterol type of compounds found in the human body and the cholesteryl ethers included in the cosmetic creams of this invention assists in the assimilation of the preparation into the secretions of the sebaceous glands.
The preferred cholesteryl ether is dicholesteryl ether, which may be obtained as a by-product of the production of cholesterol from animal tissue such as the nervous system of cattle. The improvement in the cosmetic creams is noticeable with as little as 0.1% of dicholesteryl ether added to the cosmetic cream, and it is possible to add as much as 8% with advantage. However, due to the high cost of dicholesteryl ethers the economic range appears to be between 0.1% and 1% and normally the amount of dicholesteryl ether added rarely exceeds 1%.
It is not necessary for the dicholesteryl ether to be pure; and actual practice 9 dicholesteryl ether obtained frompnimal tissue is usually-contaminated with other cholesterol derivativeswhich, however, donot detract from-theteifec tiveness of the; ether.
illustrative-of the invention; the fats, oils: and waxes are heated--= and dicholesterylether, either"- alone; orwith 7 other emulsifying agents; such as lecithine orcholesterolis:added to the hot liquid mixture: Wateris heated t'crapproxisx mately the same temperature as the liquid oleaginous mixture, and the liquid of smaller volume is added to the liquid of larger volume with stirring. The mixture or stirring may be effected in any suitable apparatus, such as an emulsifier, homogeniser or colloid mill.
Examples of cosmetic creams in accordance.
with this invention are described below, but the application of the invention is not limited there- Mineral oil (to be substituted wholly or partly by vegetable oils) Petrolatum v 5 Dicholesterylether 4 Perfume 1 Water ad- 100 Example 2.Tzssue cream Parts Cocoa butter 4.5 Bees wax 12 Cetyl alcohol .4 Mineral oil Lecithine 1 Cholesterol 2 Dicholesteryl ether 8 Preservative 0.2 Perfume 0.8 Water ad Example 3.--Tissae cream Parts Lanolin 35 Petrolatum 43 Dicholesteryl ether 1 Spermacetti wax 5 Perfume 6 Water ad 100 In any of the above examples the dicholesteryl ether can be replaced either by ethyl cholesteryl ether or by methyl cholesteryl ether.
, Dicholesteryl ether possesses numerous advantages. It is itself a very efficient emulsifying agent and is also capable of changing and. improving the properties of cholesterol as an emulsifying agent. Further, when both dicholesteryl ether and cholesterol are employed as emulsifying agents a smaller quantity is necessary than when cholesterol alone is employed. Cosmetic emulsions containing a cholesteryl ether improve the texture of the skin and induce smoothness thereof. When cosmetic creams made in accordance with this invention are rubbed into the skin they practically disappear leaving the skin soft and smooth.
This application is a continuation-in-part of our application Serial No. 695,810, dated September 9, 1946, now abandoned.
We claim:
1. Cosmetic cream comprising an emulsion of oleaginous and aqueous material, and from 0.1% to 8 of a cholesteryl ether.
2. Vanishing cream comprising an aqueous emulsion of steario acid and from 0.1% to 1% of dicholesteryl ether.
3. Cosmetic cream comprising an aqueous emulsion of Wax, fat and oil, and from 0.1 to 1% 0f dicholesteryl ether.
MARYAN TERKEL. HENRYK SILBERMAN.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 1,985,747 Steindorfi Dec. 25, 1934 OTHER REFERENCES Levin: Journal of the Amer. Chem. $00.; Vol.
65, page 627 (Apr. 1943).
Industrial Chemist; Vol. 13, pages 264, 265 (1937).

Claims (1)

1. COSMETIC CREAM COMPRISING AN EMULSION OF OLEAGINOUS AND AQUEOUS MATERIAL, AND FROM 0.1% TO 8% OF A CHOLESTERYL ETHER.
US43344A 1945-10-30 1948-08-09 Cosmetic creams Expired - Lifetime US2520980A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
AU2520980X 1945-10-30

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US2520980A true US2520980A (en) 1950-09-05

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3002967A (en) * 1959-12-18 1961-10-03 Morey E Slodki Process for preparing phosphoric acid monoesters of mannose polymers
US4165385A (en) * 1973-05-29 1979-08-21 Dianis Creations, Inc. Water-in-oil emulsion for skin moisturizing
FR2520253A1 (en) * 1982-01-28 1983-07-29 Oreal NOVEL EMULSIFYING SYSTEM BASED ON PROTEIN CONDENSATION, POLYOXYETHYLENE STEROL AND PHOSPHATIDE AND USE THEREOF IN COSMETICS
WO2007006549A3 (en) * 2005-07-11 2007-03-29 Plt Patent & Licence Trading L Oligomers of cholesterol, cholesterol sulfate and cholesterol esters, and medicaments containing the same
US20190125656A1 (en) * 2017-10-30 2019-05-02 L'oreal Cosmetic compositions providing for a transformative texture

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1985747A (en) * 1934-12-25 Ether-like constituted compound

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1985747A (en) * 1934-12-25 Ether-like constituted compound

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3002967A (en) * 1959-12-18 1961-10-03 Morey E Slodki Process for preparing phosphoric acid monoesters of mannose polymers
US4165385A (en) * 1973-05-29 1979-08-21 Dianis Creations, Inc. Water-in-oil emulsion for skin moisturizing
FR2520253A1 (en) * 1982-01-28 1983-07-29 Oreal NOVEL EMULSIFYING SYSTEM BASED ON PROTEIN CONDENSATION, POLYOXYETHYLENE STEROL AND PHOSPHATIDE AND USE THEREOF IN COSMETICS
DE3302898A1 (en) * 1982-01-28 1983-09-01 L'Oreal, 75008 Paris EMULSIFYING SYSTEM
WO2007006549A3 (en) * 2005-07-11 2007-03-29 Plt Patent & Licence Trading L Oligomers of cholesterol, cholesterol sulfate and cholesterol esters, and medicaments containing the same
US20090105199A1 (en) * 2005-07-11 2009-04-23 Hans-Uwe Wolf Oligomers of cholesterol, cholesterol sulphate and cholesterol esters and also drugs containing these
US8318961B2 (en) 2005-07-11 2012-11-27 PLT Patent & Licensing Trading Ltd. Oligomers of cholesterol, cholesterol sulphate and cholesterol esters and also drugs containing these
US20190125656A1 (en) * 2017-10-30 2019-05-02 L'oreal Cosmetic compositions providing for a transformative texture
US11452685B2 (en) * 2017-10-30 2022-09-27 L'oreal Cosmetic compositions providing for a transformative texture

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