WO1999009936A1 - Procede de traitement des levres gercees - Google Patents

Procede de traitement des levres gercees Download PDF

Info

Publication number
WO1999009936A1
WO1999009936A1 PCT/US1998/017663 US9817663W WO9909936A1 WO 1999009936 A1 WO1999009936 A1 WO 1999009936A1 US 9817663 W US9817663 W US 9817663W WO 9909936 A1 WO9909936 A1 WO 9909936A1
Authority
WO
WIPO (PCT)
Prior art keywords
oil
lips
lipstick
wax
dimethicone
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.)
Ceased
Application number
PCT/US1998/017663
Other languages
English (en)
Inventor
Joseph F. Calello
Janet E. Opel
Renee J. Ordino
Robert W. Sandewicz
Natividad R. Jose
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.)
Revlon Consumer Products LLC
Original Assignee
Revlon Consumer Products LLC
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
Priority claimed from US08/980,431 external-priority patent/US6086859A/en
Application filed by Revlon Consumer Products LLC filed Critical Revlon Consumer Products LLC
Priority to AU89206/98A priority Critical patent/AU8920698A/en
Priority to CA002301810A priority patent/CA2301810A1/fr
Priority to EP98941061A priority patent/EP0998253A4/fr
Publication of WO1999009936A1 publication Critical patent/WO1999009936A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/02—Preparations containing skin colorants, e.g. pigments
    • A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
    • A61Q1/06—Lipsticks
    • 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
    • A61K8/37—Esters of carboxylic acids
    • 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
    • A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups

Definitions

  • lips to treat chapped, chafed, or windburned lips.
  • lip balms are generally very waxy, unpigmented or minimally pigmented sticks that
  • the invention comprises a method for preventing, retarding, arresting, or ameliorating
  • dimethicone dimethicone, glycerin, petrolatum, shark liver oil. and mixtures thereof,
  • an oil selected from the group consisting of nonvolatile oil, volatile oil, and
  • compositions used in the method of the invention are "full
  • color lipsticks which means that they are applied to the lips as a primary lip colorant
  • compositions used in the method of the invention comprise 0.1-30%, preferably 0.1-30%
  • a skin protectant selected from the group consisting of
  • the skin protectant used in the method of the invention is dimethicone having a viscosity of 5 to 1,000.000 centipoise at 25° C, more preferably a
  • compositions used in the method of the invention contain 1-25%, preferably 1.5-
  • pigments include various organic and inorganic pigments.
  • the organic pigments are
  • azo indigoid
  • triphenylmethane triphenylmethane
  • anthraquinone and xanthine dyes which are designated as D&C and FD&C blues, browns, greens, oranges,
  • Organic pigments generally consist of insoluble metallic salts of certified
  • Lakes Inorganic pigments include iron oxides, ultramarines, chromium, chromium hydroxide colors, and mixtures thereof.
  • compositions used in the method of the invention contain 5-85%. preferably 10-
  • nonvolatile oil volatile oil. and mixtures thereof.
  • volatile means that the oil or solvent has a vapor pressure of at least 2 mm. of mercury at 20° C.
  • the viscosity of the volatile solvent is
  • volatile solvents include volatile low viscosity
  • silicone fluids such as cyclic silicones having the formula:
  • Volatile linear polydimethylsiloxanes are also suitable and generally have from about 2 to 9 silicon atoms and are of the formula:
  • octamethylcyclotetrasiloxane decamethylcyclopentasiloxane, hexamethyldisiloxane, or mixtures thereof.
  • volatile solvent component straight or branched chain paraffinic hydrocarbons having 5-20 carbon atoms, more preferably 10-16 carbon atoms.
  • Suitable hydrocarbons are pentane. hexane, heptane, decane, dodecane, tetradecane.
  • tridecane. and C 8 . 20 isoparaffins as disclosed in U.S. patent nos. 3,439.088 and 3,818.105, both of which are hereby incorporated by reference.
  • Preferred volatile paraffinic hydrocarbons have a molecular weight of 70 to 190, more preferably 160-180, and a boiling
  • paraffinic hydrocarbons are available from EXXON under the ISOPAR trademark as ISOPAR A. B, C. D, E. G. H. K. L. and M. Similar paraffinic hydrocarbons
  • hydrocarbons are also available from Shell Oil under the Shellsol trademark, in particular
  • Shellsol 71 and from Phillips Petroleum under the tradename Soltrol 100. 130, and 220.
  • Soltrol 100. 130, and 220 In
  • paraffinic hydrocarbons may be purchased from Permethyl Corporation under
  • the volatile solvent may be a mixture of volatile silicone and paraffinic hydrocarbons
  • nonvolatile oil means that the oil has a vapor pressure of less than about 2 mm. of mercury at 20° C.
  • the nonvolatile oil generally
  • nonvolatile oil is a liquid to semi-solid at room temperature. Particularly preferred as the nonvolatile oil
  • the component is a C 12 . 22 fatty ester of citric acid.
  • the fatty ester of citric acid is formed by the reaction of a C 12 . 22 fatty alcohol with citric acid.
  • One, two, or three carboxylic acid groups of the citric acid may be esterified.
  • the fatty acid ester of citric acid generally
  • R,. R 2 . and R 3 are each independently H. or a C, 2 . 22 , preferably a C 16 . 22 alkyl, more
  • R,. R 2 . and R 3 are each a C 16 . 22 alkyl, preferably isostearyl and the compound is triisostearyl citrate.
  • nonvolatile oils that may be used include esters of the formula RCO-OR' wherein
  • R and R' are each independently a C,_ 25 . preferably a C 4 . 20 straight or branched chain alkyl, alkenyl
  • esters include isotridecyl
  • isononanoate PEG-4 diheptanoate. isostearyl neopentanoate, tridecyl neopentanoate. cetyl
  • octanoate cetyl palmitate. cetyl ricinoleate. cetyl stearate. cetyl myristate. coco- dicaprylate/caprate. decyl isostearate. isodecyl oleate. isodecyl neopentanoate, isohexyl neopentanoate, octyl palmitate, dioctyl malate, tridecyl octanoate, myristyl myristate, octododecanol, and fatty alcohols such as oleyl alcohol, isocetyl alcohol, and the like.
  • the oil may also comprise naturally occuring glyceryl esters of fatty acids, or
  • triglycerides Both vegetable and animal sources may be used. Examples of such oils include
  • castor oil castor oil, lanolin oil, triisocetyl citrate, C 10 _ 18 triglycerides, caprylic/capric/triglycerides. coconut
  • soybean oil sunflower seed oil, walnut oil, and the like.
  • glyceryl esters e.g. fatty acid
  • mono-, di-, and triglycerides which are natural fats or oils that have been modified, for example.
  • acetylated castor oil glyceryl stearate.
  • glyceryl dioleate glyceryl distearate.
  • glyceryl trioctanoate glyceryl trioctanoate.
  • glyceryl distearate glyceryl linoleate
  • glyceryl myristate glyceryl isostearate
  • PEG castor oils glyceryl distearate, glyceryl linoleate, glyceryl myristate.
  • glyceryl isostearate PEG castor oils.
  • PEG glyceryl oleates PEG glyceryl stearates, PEG glyceryl tallowates. and so on.
  • nonvolatile hydrocarbons such as isoparaffins, hydrogenated polyisobutene. mineral oil. squalene, petrolatum, and so on.
  • Straight or branched chain fatty alcohols having the formula R-OH. wherein R is a straight
  • Such fatty alcohols include cetyl alcohol, stearyl alcohol, cetearyl alcohol, and the like.
  • lanolin derivatives such as acetylated lanolin
  • nonvolatile oil examples include various fluorinated oils such as fluorinated
  • silicones fluorinated esters, or perfluropolyethers. Particularly suitable are fluorosilicones such as
  • silicones such as those disclosed in U.S. patent no. 5,118.496 which is hereby incorporated by
  • Guerbet esters are also suitable oils.
  • guerbet ester means an ester which is
  • R 1 and R 2 are each independently a C 4 . 20 alkyl and R 3 is a substituted or unsubstituted
  • fatty radical such as a C,. 50 straight or branched chain saturated or unsaturated alkyl or alkylene. or phenyl. wherein the substituents are halogen, hydroxyl, carboxyl. and alkylcarbonylhydroxy.
  • Particularly preferred is a carboxylic acid wherein the R group is such to provide an ingredient
  • the guerbet ester is a fluoro-guerbet ester which is
  • n is from 3 to 40.
  • suitable fluoro guerbet esters are set forth in U.S. patent no. 5,488,121which is hereby incorporated by reference. Suitable fluoro-guerbet esters are also set forth in U.S. patent no.
  • compositions used in the method of the invention comprise:
  • a volatile oil preferably cyclomethicone
  • a nonvolatile oil preferably a C )6 _ 22 fatty ester of citric acid.
  • the lipstick compositions used in the method of the invention may contain 3-40%, preferably 5-35%, more preferably 10-30%) by weight of the total composition of a wax
  • having a melting point of 30-135° C. generally includes animal waxes, plant waxes, mineral waxes, silicone waxes, synthetic waxes, and petroleum waxes.
  • waxes examples include bayberry, beeswax, candelilla, camauba,
  • jojoba wax lanolin wax. microcrystalline wax. mink wax, montan acid wax. montan wax.
  • dimethicone dimethicone behenate.
  • stearyl dimethicone and the like, as well synthetic
  • the waxes may also be fluorinated waxes, either alone or in addition to the above-
  • Patent No. 5,446,114 which is hereby incorporated by reference, having the general formula: wherein: p is an integer ranging from 1 to 2,000;
  • Me is methyl
  • R' is - ⁇ CH 2 )-O-(EO) a - ⁇ PO) b -(EO) c -H:
  • R is -(CH 2 MCF 2 ) S -(CF 3 );
  • s is an integer ranging from 1 to 13:
  • a. b. and c are each independently integers ranging from 0 to 20:
  • EO is -(CH 2 CH 2 - OW and PO is - ⁇ CH 2 CH(CH 3 )- O-.
  • fluorinated wax is dimethiconol fluoroalcohol dilinoleic acid, which
  • 135° C. will have a molecular weight ranging from about 100 and 2,000.
  • ethylene copolymers are comprised of ethylene monomer units in either repetitive or randon
  • R is a C,. 30 straight or branched chain saturated or unsaturated alkyl. aryl. or aralkyl,
  • the lipsticks used in the method of the invention contain 0.1-20%,
  • “sunscreen” is defined as an ingredient that absorbs at least 85% of the light in the
  • UV range at wavelengths from 290 to 320 nanometers, but transmits UV light at wavelengths
  • ingredients include PABA, cinoxide, DEA-
  • methoxycinnamate digalloyl trioleate, Benzophenone-8, ethyl dihydroxypropyl PABA, Octocrylene. octyl methoxycinnamate. octyl salicylate, glyceryl PABA. homosalate. menthyl
  • Particularly preferred lipsticks for use in the method of the invention comprise, by:
  • the lipsticks may be applied one. two, or more times a day as needed, in lieu of
  • Lipstick compositions were made according to the following formula:
  • Vitamin E acetate 0.10 0.10 0.10
  • Iron oxide/trioctyldodecyl citrate 60:40) 2.00 1.75 3.33 Iron oxide/trioctyldodecyl citrate (60:40) 0.30 1.95 1.33
  • Subjects selected based upon their perception that they had dry or chapped lips. Subjects chose from the three available lipstick shades, Mauve, Wine, and Nudity; which were 1, 2, and 3 respectively, from Example 1. Subjects were asked to apply the test lipstick a minimum of
  • EXAMPLE 4 A total of 18 subjects, after having refrained from using any lip products for 6 days, participated in the study. Dry lips were simulated by blowing a stream of dry air over the lips

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (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)

Abstract

L'invention concerne un procédé permettant de prévenir, de retarder, d'arrêter ou d'inverser les effets de l'irritation, des gerçures, des crevasses, ou du déssèchement des lèvres. Ce procédé consiste à appliquer aux lèvres une composition de rouge à lèvres pigmentée. Cette composition comprend, en pourcentage du poids total, 0,01 à 30 % d'un agent protecteur de la peau, sélectionné dans le groupe se composant d'allantoïne, de beurre de cacao, de diméthicone, de glycérine, de vaseline, d'huile de foie de requin et de mélanges de ces derniers; 1 à 25 % de pigment; 5 à 80 % d'une huile sélectionnée dans le groupe se composant d'huile non volatile, d'huile volatile et de mélanges de ces dernières; et 3 à 40 % d'une cire dont le point de fusion se situe entre 30 et 135 °C.
PCT/US1998/017663 1997-08-27 1998-08-26 Procede de traitement des levres gercees Ceased WO1999009936A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
AU89206/98A AU8920698A (en) 1997-08-27 1998-08-26 Method for treating chapped lips
CA002301810A CA2301810A1 (fr) 1997-08-27 1998-08-26 Procede de traitement des levres gercees
EP98941061A EP0998253A4 (fr) 1997-08-27 1998-08-26 Procede de traitement des levres gercees

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US91813497A 1997-08-27 1997-08-27
US08/918,134 1997-08-27
US08/980,431 1997-11-28
US08/980,431 US6086859A (en) 1997-08-27 1997-11-28 Method for treating chapped lips

Publications (1)

Publication Number Publication Date
WO1999009936A1 true WO1999009936A1 (fr) 1999-03-04

Family

ID=27129744

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1998/017663 Ceased WO1999009936A1 (fr) 1997-08-27 1998-08-26 Procede de traitement des levres gercees

Country Status (4)

Country Link
EP (1) EP0998253A4 (fr)
AU (1) AU8920698A (fr)
CA (1) CA2301810A1 (fr)
WO (1) WO1999009936A1 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1955692A1 (fr) * 2007-01-12 2008-08-13 L'oreal Utilisation d'actifs permettant d'augmenter la teneur en céramides dans les lèvres, à titre d'agent protecteur des lèvres fragiles
FR2918877A1 (fr) * 2007-07-16 2009-01-23 Oreal Utilisation de l'acide ascorbique ou de l'un de ses analogues a titre d'agent protecteur des levres fragiles
US20110224299A1 (en) * 2009-09-03 2011-09-15 Avon Products, Inc. Stabilized Wax Composition and Uses Thereof
US20220151911A1 (en) * 2014-07-11 2022-05-19 Mary Kay Inc. Cosmetic compositions
US20240269056A1 (en) * 2018-10-31 2024-08-15 Henkel Ag & Co. Kgaa Composition of active ingredients as booster for uv-filters

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5776441A (en) * 1996-08-30 1998-07-07 Avon Products, Inc. Lip treatment containing live yeast cell derivative

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1185173A (en) * 1967-04-24 1970-03-25 Richardson Merrell Ltd Formerl Application Sticks and Their Method of Manufacture
FR2237615A1 (en) * 1973-07-19 1975-02-14 Shiseido Co Ltd Water-in-oil cosmetic stick emulsion - contg. polyhydroxy cpd. and oleate or oleyl ether emulsifier gel

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5776441A (en) * 1996-08-30 1998-07-07 Avon Products, Inc. Lip treatment containing live yeast cell derivative

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
"BLISTEX, LIP TONE.", LIP TONE BROCHURE, XX, XX, 1 January 1996 (1996-01-01), XX, pages COMPLETE 02., XP002915144 *
See also references of EP0998253A4 *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1955692A1 (fr) * 2007-01-12 2008-08-13 L'oreal Utilisation d'actifs permettant d'augmenter la teneur en céramides dans les lèvres, à titre d'agent protecteur des lèvres fragiles
US8088399B2 (en) 2007-01-12 2012-01-03 L'oreal Use of active principles which are capable of enhancing the content of ceramides, as protective agent for delicate lips
EP3207920A1 (fr) * 2007-01-12 2017-08-23 L'oreal Utilisation d'actifs permettant d'augmenter la teneur en ceramides dans les levres, a titre d'agent protecteur des levres fragiles
FR2918877A1 (fr) * 2007-07-16 2009-01-23 Oreal Utilisation de l'acide ascorbique ou de l'un de ses analogues a titre d'agent protecteur des levres fragiles
US20110224299A1 (en) * 2009-09-03 2011-09-15 Avon Products, Inc. Stabilized Wax Composition and Uses Thereof
US20220151911A1 (en) * 2014-07-11 2022-05-19 Mary Kay Inc. Cosmetic compositions
US20240269056A1 (en) * 2018-10-31 2024-08-15 Henkel Ag & Co. Kgaa Composition of active ingredients as booster for uv-filters

Also Published As

Publication number Publication date
CA2301810A1 (fr) 1999-03-04
EP0998253A1 (fr) 2000-05-10
EP0998253A4 (fr) 2001-05-02
AU8920698A (en) 1999-03-16

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