US3544684A - Cosmetic composition containing uracil-4-carboxylic acid - Google Patents

Cosmetic composition containing uracil-4-carboxylic acid Download PDF

Info

Publication number
US3544684A
US3544684A US693132A US3544684DA US3544684A US 3544684 A US3544684 A US 3544684A US 693132 A US693132 A US 693132A US 3544684D A US3544684D A US 3544684DA US 3544684 A US3544684 A US 3544684A
Authority
US
United States
Prior art keywords
carboxylic acid
uracil
composition containing
cosmetic composition
skin
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
US693132A
Inventor
Arthur Scherm
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
Application granted granted Critical
Publication of US3544684A publication Critical patent/US3544684A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/494Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
    • A61K8/4953Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom containing pyrimidine ring derivatives, e.g. minoxidil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/08Anti-ageing preparations

Definitions

  • Cosmetic preparations and devices for the treatment of ageing changes of the skin have the purpose of improving the water absorbing properties of the skin and reducing the formation of wrinkles by stimulating the metabolism.
  • the water absorption as well as the removal of wrinkles can be measured, the latter by determining the depth of the wrinkles.
  • a suitable method for measuring hydration changes of the skin is e.g. the determination of the resonance frequency.
  • the principle of this measuring method consists in converting electrical oscillations of a frequency generator to mechanical oscillations and applying said mechanical oscillations by means of a pin to the skin.
  • a second pin takes up said oscillations, converts them to electric oscillations, and transmits them to a recorder.
  • the measured resonance frequency measures the ratio of liquid to structured substance.
  • a decrease of tissue fluids, e.g., in atrophied skin increases the resonance frequency.
  • Juvenile skin with elevated turgor has a lower resonance frequency. When the water absorbency of the skin is improved by suitable cosmetic treatment, the resonance frequency shifts to lower frequencies.
  • the depth of wrinkles may be measured by combining an impression method with a relief recording method.
  • An impression is made on a suitable material and the impression is measured by means of a relief recorder which converts the unevenness of the impression or mold into electromagnetic oscillations and directly records the same.
  • uracil-4-carboxylic acid orotic acid
  • its organic and inorganic salts exert a favorable effect on the hydration as well as on the depth of the wrinkles. This is quite surprising because, heretofore, similar effects have been obtained only with placenta extracts and similar mixtures. The described effect was shown only by the uracil-4-carboxylic acid compounds themselves but not by the cosmetic base or additives used.
  • Suitable cosmetic bases for incorporation of the uracil- 4-carboxylic acid and its salts are conventional water-inoil emulsions, oil-in-water emulsions and/or gelatinous preparations, e.g., of mucilage, or synthetic thickening agents such as polyvinyl pyrrolidone, methyl cellulose, carboxymethyl cellulose.
  • Suitable water-in-oil emulsions are those on the basis of hydrocarbons, fats, lanolin and the like.
  • Oil-in-water emulsions are generally made from saponified fatty acid salts and esters, orthophosphoric acid esters, waxes, lanolin tetraglycol ethers, etc.
  • the proportion of uracil-4-carboxylic acid in cosmetic bases will be generally about 0.5 to 10 percent by weight.
  • the effect of the composition according to the invention on the hydration of the skin and the depth of the wrinkles depends on the frequency of application and is always observable after several days use. The effect is present still 24 hours after the last application; this shows that the composition penetrates into, and influences, also the deeper layers of the skin.
  • the novel cosmetic composition produces a long-term reduction of the wrinkle depth which is about 50% of the short-term reduction produced by preparations that have a purely physical tightening effect.
  • Such preparations e.g., those on the basis of chicken egg white, serum albumin and globulin, reduce, after drying of the applied solution, the depth of wrinkles by about 30 percent.
  • this effect remains only a short time and is removed by washing.
  • Uracil-4-carboxylic acid is found in milk as precursor of the pyrimidines and nuclei acid. It has particularly a growth stimulating effect, which is utilized therapeutically in oral and parenteral pharmaceutical compositions. Also in larger dosages, the compound is readily tolerated, and the skin is not affected even by prolonged and regular use.
  • the uracil-4-carboxylic acid is diflicultly soluble in water. Higher concentrations can be obtained by addition of a coupling agent, e.g., methyl glucamine.
  • EXAMPLE 5 Beeswax (bleached) 10.0 Peanut oil 30.0spermaceti 3.0 Lanolin 3.0 Glycerol 5.0 Uracil-4-carboxylic acid 4.0 Methylglucamine 5.0 p-Oxybenzoic acid ester (preservative) 0.2 Water ad 100.0.
  • compositionsncontaining uracilr-4-carboxylic acid or its salts are to be used for face masks, e.g., foam masks, they are used preferably as aerosols with addition of a foam stabilizer such as a salt 'of a condensation product of a saturatedfatty acid of medium chain length and sarcosine.
  • a cosmetic preparation for increasing hydration of the skin and producing along-lasting reduction of wrinkle depth consisting essentially of an aqueous cosmetic cream or lotionbase having incorporated therein about 0.5 to 10 percent .-by weight of a member of the solubility of the uracil-4-carboxylic -acid component in said aqueous cosmetic base.

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Dermatology (AREA)
  • Epidemiology (AREA)
  • Gerontology & Geriatric Medicine (AREA)
  • Birds (AREA)
  • Cosmetics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Description

United States Patent Oflice 3,544,684 Patented Dec. 1, 1970 Int. Cl. A61k 7/00, 27/00 US. Cl. 424-251 2 Claims ABSTRACT OF THE DISCLOSURE Uracil-4-carboxylic acid and its salts increase the softening effect of cosmetic bases.
Cosmetic preparations and devices for the treatment of ageing changes of the skin have the purpose of improving the water absorbing properties of the skin and reducing the formation of wrinkles by stimulating the metabolism. The water absorption as well as the removal of wrinkles can be measured, the latter by determining the depth of the wrinkles.
A suitable method for measuring hydration changes of the skin is e.g. the determination of the resonance frequency. The principle of this measuring method consists in converting electrical oscillations of a frequency generator to mechanical oscillations and applying said mechanical oscillations by means of a pin to the skin. A second pin takes up said oscillations, converts them to electric oscillations, and transmits them to a recorder. The measured resonance frequency measures the ratio of liquid to structured substance. A decrease of tissue fluids, e.g., in atrophied skin, increases the resonance frequency. Juvenile skin with elevated turgor has a lower resonance frequency. When the water absorbency of the skin is improved by suitable cosmetic treatment, the resonance frequency shifts to lower frequencies.
The depth of wrinkles may be measured by combining an impression method with a relief recording method. An impression is made on a suitable material and the impression is measured by means of a relief recorder which converts the unevenness of the impression or mold into electromagnetic oscillations and directly records the same.
It is known that an improved hydration of the skin does not necessarily or inherently smoothen the wrinkles. Numerous compositions which have been investigated influence neither the hydration nor the depth of the wrinkles. Others influence either the hydration or the depth of the wrinkles.
I have now found that uracil-4-carboxylic acid (orotic acid) and its organic and inorganic salts in conventional cream or lotion bases exert a favorable effect on the hydration as well as on the depth of the wrinkles. This is quite surprising because, heretofore, similar effects have been obtained only with placenta extracts and similar mixtures. The described effect was shown only by the uracil-4-carboxylic acid compounds themselves but not by the cosmetic base or additives used.
Suitable cosmetic bases for incorporation of the uracil- 4-carboxylic acid and its salts are conventional water-inoil emulsions, oil-in-water emulsions and/or gelatinous preparations, e.g., of mucilage, or synthetic thickening agents such as polyvinyl pyrrolidone, methyl cellulose, carboxymethyl cellulose. Suitable water-in-oil emulsions are those on the basis of hydrocarbons, fats, lanolin and the like. Oil-in-water emulsions are generally made from saponified fatty acid salts and esters, orthophosphoric acid esters, waxes, lanolin tetraglycol ethers, etc.
The proportion of uracil-4-carboxylic acid in cosmetic bases will be generally about 0.5 to 10 percent by weight.
The effect of the composition according to the invention on the hydration of the skin and the depth of the wrinkles depends on the frequency of application and is always observable after several days use. The effect is present still 24 hours after the last application; this shows that the composition penetrates into, and influences, also the deeper layers of the skin.
When determined as described hereinabove, the novel cosmetic composition produces a long-term reduction of the wrinkle depth which is about 50% of the short-term reduction produced by preparations that have a purely physical tightening effect. Such preparations, e.g., those on the basis of chicken egg white, serum albumin and globulin, reduce, after drying of the applied solution, the depth of wrinkles by about 30 percent. However, this effect remains only a short time and is removed by washing.
Uracil-4-carboxylic acid is found in milk as precursor of the pyrimidines and nuclei acid. It has particularly a growth stimulating effect, which is utilized therapeutically in oral and parenteral pharmaceutical compositions. Also in larger dosages, the compound is readily tolerated, and the skin is not affected even by prolonged and regular use.
The uracil-4-carboxylic acid is diflicultly soluble in water. Higher concentrations can be obtained by addition of a coupling agent, e.g., methyl glucamine.
Some cosmetic preparations according to the invention are given in the following examples. All parts are given by weight.
EXAMPLE 1 Water-containing lanolin alcohol ointment 90.0 Uracil-4-carboxylic acid 5.0 Liquid parafiin 5.0
EXAMPLE 2 Cety stearyl alcohol 6.0 Ointment bases of tert. ester of orthophosphoric acid and lanolin alcohol tetraglycol ether 10.0
Glycerol 5.0 Choline salt of uracil-4-carboxylic acid 6.0 Water ad 100.0.
EXAMPLE 3 Tragacanth 5.0 Glycerol 5.0 Uracil-4-carboxylic acid 3.0 Methyl glucamine 4.0 p-Oxybenzoic acid ester (preservative) 0.2 Water ad 100.0.
EXAMPLE 4 Stearic acid 18.0 Almond oil 2.0 Cetyl alcohol 0.6 Triethanolamine 3.0 Glycerol I 8.0 Uracil-4-carboxylic acid 3.0 p-Oxybenzoic acid ester (preservative) 0.2 Water ad 100.0.
EXAMPLE 5 Beeswax (bleached) 10.0 Peanut oil 30.0 Spermaceti 3.0 Lanolin 3.0 Glycerol 5.0 Uracil-4-carboxylic acid 4.0 Methylglucamine 5.0 p-Oxybenzoic acid ester (preservative) 0.2 Water ad 100.0.
r If .compositionsncontaining uracilr-4-carboxylic acid or its salts are to be used for face masks, e.g., foam masks, they are used preferably as aerosols with addition of a foam stabilizer such as a salt 'of a condensation product of a saturatedfatty acid of medium chain length and sarcosine.
I claim: a
1. A cosmetic preparation for increasing hydration of the skin and producing along-lasting reduction of wrinkle depth consisting essentially of an aqueous cosmetic cream or lotionbase having incorporated therein about 0.5 to 10 percent .-by weight of a member of the the solubility of the uracil-4-carboxylic -acid component in said aqueous cosmetic base.
group consistingof uracil-4-carboxylic acid and the choline salt of said acid.
2. The cosmetic preparation of claiml containing 15 also methyl glucamine in an amount sufiicient to increase References Cited UNITED STATES PATENTS 2/1944- Stambovsky 424310X 1/1964 Ferguson, Jr.-- 424351X OTHER REFERENCES I Us. c1; JR.
US693132A 1966-12-31 1967-12-26 Cosmetic composition containing uracil-4-carboxylic acid Expired - Lifetime US3544684A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEM0072266 1966-12-31

Publications (1)

Publication Number Publication Date
US3544684A true US3544684A (en) 1970-12-01

Family

ID=7314401

Family Applications (1)

Application Number Title Priority Date Filing Date
US693132A Expired - Lifetime US3544684A (en) 1966-12-31 1967-12-26 Cosmetic composition containing uracil-4-carboxylic acid

Country Status (5)

Country Link
US (1) US3544684A (en)
AT (1) AT275741B (en)
CH (1) CH507711A (en)
DE (1) DE1617631B1 (en)
GB (1) GB1142220A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4061741A (en) * 1974-04-01 1977-12-06 Firma Servomed Arzei Gmbh & Co. Pharma Kg Physiological substances for intensifying the pharmacological effect of drugs
WO1983002891A1 (en) * 1982-02-20 1983-09-01 Möller, Hinrich Uracil derivatives as anti-seborrheic additives for cosmetic products
US4606913A (en) * 1978-09-25 1986-08-19 Lever Brothers Company High internal phase emulsions
WO2001047479A2 (en) * 1999-12-28 2001-07-05 Colgate-Palmolive Company Skin moisturizing composition
WO2001080819A1 (en) * 2000-04-20 2001-11-01 Simo Rasi Cosmetic or dermatological cream composition, the preparation and the use thereof
WO2002072062A2 (en) * 2001-03-09 2002-09-19 Colgate-Palmolive Company Skin moisturizing composition

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2340776A (en) * 1940-07-25 1944-02-01 Gallowhur And Company Inc Topical epithelial anesthetic
US3118890A (en) * 1961-07-24 1964-01-21 William L Gould Procaine orotate

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2340776A (en) * 1940-07-25 1944-02-01 Gallowhur And Company Inc Topical epithelial anesthetic
US3118890A (en) * 1961-07-24 1964-01-21 William L Gould Procaine orotate

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4061741A (en) * 1974-04-01 1977-12-06 Firma Servomed Arzei Gmbh & Co. Pharma Kg Physiological substances for intensifying the pharmacological effect of drugs
US4606913A (en) * 1978-09-25 1986-08-19 Lever Brothers Company High internal phase emulsions
WO1983002891A1 (en) * 1982-02-20 1983-09-01 Möller, Hinrich Uracil derivatives as anti-seborrheic additives for cosmetic products
WO2001047479A2 (en) * 1999-12-28 2001-07-05 Colgate-Palmolive Company Skin moisturizing composition
WO2001047479A3 (en) * 1999-12-28 2002-02-21 Colgate Palmolive Co Skin moisturizing composition
US6475965B2 (en) 1999-12-28 2002-11-05 Colgate-Palmolive Company Skin moisturizing composition comprising a choline salt
WO2001080819A1 (en) * 2000-04-20 2001-11-01 Simo Rasi Cosmetic or dermatological cream composition, the preparation and the use thereof
JP2003531159A (en) * 2000-04-20 2003-10-21 シモ・ラシ Cosmetic or skin cream composition, its preparation and use
CN1304006C (en) * 2000-04-20 2007-03-14 西莫·拉西 Cosmetic or dermatological cream composition, the preparation and the use thereof
WO2002072062A2 (en) * 2001-03-09 2002-09-19 Colgate-Palmolive Company Skin moisturizing composition
WO2002072062A3 (en) * 2001-03-09 2003-05-08 Colgate Palmolive Co Skin moisturizing composition

Also Published As

Publication number Publication date
AT275741B (en) 1969-11-10
DE1617631B1 (en) 1971-12-23
GB1142220A (en) 1969-02-05
CH507711A (en) 1971-05-31

Similar Documents

Publication Publication Date Title
US4760096A (en) Moisturizing skin preparation
US4612331A (en) Skin treatment composition
KR930016085A (en) Cosmetic composition
GB1441424A (en) Surface-active compositions
US4518614A (en) Cosmetic preparation
JPS60214722A (en) Skin-protective novel cosmetics and dermatological composition
US6342486B1 (en) Polymer glucan ether derivatives, their manufacturing as well as their use
JPH0375523B2 (en)
US3544684A (en) Cosmetic composition containing uracil-4-carboxylic acid
US3689668A (en) Method of alleviating wrinkles on skin
EP1378224B1 (en) Sugar intake promoters
EP0342055A2 (en) Use of pyroglutamic acid alkyl esters for the manufacture of a medicament for the treatment of ichthyosis
JPH02180827A (en) Use of tocopherol, benzyl, chisantinol or hexyl nicotinate or tocopherol acetate
US4153726A (en) Skin protection agents containing polyethercarboxylic acids
RU2006144695A (en) ANTI-HEATING SKIN CARE COMPOSITION AND SKIN CARE PRODUCT
EP0244859A2 (en) Antiwrinkle cosmetic composition
JP4291177B2 (en) Cosmetic or dermatological pharmaceutical composition having a slimming effect and method of use thereof
JPS59501986A (en) cosmetic formulations
KR101605324B1 (en) Cosmetic composition for moisturizing skin which alleviates itchiness and dryness by removing keratin and increasing moisture
JPS62120308A (en) Cosmetic
WO2006122668A1 (en) Active ingredient combinations of glucosyl glycerides and creatine and/or creatinine
US3285818A (en) Hair and skin compositions containing pantethine
BR112012001920B1 (en) COSMETIC USE OF ISOLEUCIN N-HEXADECANOIL AND COSMETIC TREATMENT PROCESS FOR OBTAINING AN EFFECT OF ?? VOLUME ?? AND / OR "FILLING"? IN THE SKIN
JPH03275609A (en) Skin cosmetic
US4143160A (en) Process for moisturing the skin