US20090317341A1 - Compositions for Lightening Skin Color - Google Patents

Compositions for Lightening Skin Color Download PDF

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US20090317341A1
US20090317341A1 US12/141,561 US14156108A US2009317341A1 US 20090317341 A1 US20090317341 A1 US 20090317341A1 US 14156108 A US14156108 A US 14156108A US 2009317341 A1 US2009317341 A1 US 2009317341A1
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acid
cosmetic composition
heterosubstituted
integer
mixture
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US12/141,561
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Stephen Alan Madison
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Conopco Inc
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Conopco Inc
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Priority to US12/141,561 priority Critical patent/US20090317341A1/en
Assigned to CONOPCO, INC., D/B/A UNILEVER reassignment CONOPCO, INC., D/B/A UNILEVER ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: MADISON, STEPHEN ALAN
Priority to EP09765749.8A priority patent/EP2285342B9/en
Priority to CA2728978A priority patent/CA2728978C/en
Priority to CN201711095416.6A priority patent/CN108158836A/en
Priority to EP14163576.3A priority patent/EP2752184B1/en
Priority to AU2009259483A priority patent/AU2009259483B2/en
Priority to EA201300756A priority patent/EA026945B1/en
Priority to PL14163576T priority patent/PL2752184T3/en
Priority to EP16177361.9A priority patent/EP3103434B1/en
Priority to EA201170042A priority patent/EA018806B1/en
Priority to CN200980122854.4A priority patent/CN102065829B/en
Priority to ES14163576.3T priority patent/ES2611791T3/en
Priority to CN201410170094.7A priority patent/CN103976889B/en
Priority to BRPI0914843-4A priority patent/BRPI0914843B1/en
Priority to KR1020167010797A priority patent/KR101788998B1/en
Priority to PL09765749T priority patent/PL2285342T3/en
Priority to MX2010014098A priority patent/MX2010014098A/en
Priority to KR1020107028407A priority patent/KR101617478B1/en
Priority to ES09765749.8T priority patent/ES2511916T3/en
Priority to PCT/EP2009/056886 priority patent/WO2009153169A1/en
Priority to JP2011513979A priority patent/JP5620908B2/en
Priority to SA109300373A priority patent/SA109300373B1/en
Priority to TW098119831A priority patent/TWI442943B/en
Priority to ARP090102190A priority patent/AR072165A1/en
Publication of US20090317341A1 publication Critical patent/US20090317341A1/en
Priority to US12/908,248 priority patent/US9227090B2/en
Priority to ZA2010/08792A priority patent/ZA201008792B/en
Priority to CL2010001461A priority patent/CL2010001461A1/en
Priority to HK11108430.8A priority patent/HK1153954A1/en
Priority to HK15101435.4A priority patent/HK1200737A1/en
Priority to US14/948,461 priority patent/US20160074295A1/en
Priority to US16/380,657 priority patent/US20190336424A1/en
Abandoned legal-status Critical Current

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    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/365Hydroxycarboxylic acids; Ketocarboxylic acids
    • 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
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/27Zinc; Compounds thereof
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/347Phenols
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35Ketones, e.g. benzophenone
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/362Polycarboxylic acids
    • 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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • 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
    • A61K8/58Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • 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
    • A61K8/67Vitamins
    • A61K8/671Vitamin A; Derivatives thereof, e.g. ester of vitamin A acid, ester of retinol, retinol, retinal
    • 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
    • A61K8/67Vitamins
    • A61K8/673Vitamin B group
    • A61K8/675Vitamin B3 or vitamin B3 active, e.g. nicotinamide, nicotinic acid, nicotinyl aldehyde
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/02Preparations for care of the skin for chemically bleaching or whitening the skin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/04Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations

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  • Life Sciences & Earth Sciences (AREA)
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  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Cosmetics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)

Abstract

Skin lightening additives and skin lightening compositions having at least one of a heterosubstituted, saturated or unsaturated aliphatic acid are described. The compositions are suitable for topical application and may comprise 12-hydroxystearic acid, ricinoleic acid or both.

Description

    FIELD OF THE INVENTION
  • The present invention is directed to a skin lightening additive as well as compositions comprising the same. More particularly, the present invention is directed to a cosmetic composition comprising a skin lightening additive whereby the skin lightening additive comprises a heterosubstituted, saturated or unsaturated aliphatic acid, or a mixture thereof. The skin lightening additive, when used, results in a cosmetic composition that can provide moisturizing benefits. Moreover, it has been unexpectedly discovered that such aliphatic acids have skin lightening benefits when topically applied.
  • BACKGROUND OF THE INVENTION
  • Many consumers are concerned with the characteristics of their skin. For example, consumers are concerned with the degree of pigmentation of their skin, freckles and/or age spots. Other consumers wish to reduce skin darkening caused by exposure to sunlight. To meet the needs of consumers, many attempts have been made to develop products that improve skin characteristics. The products developed thus far, however, often tend to have low efficacy, undesirable side effects or both. Furthermore, such products can be expensive and are often not an alternative for lower income consumers.
  • There is an increasing interest to develop a cosmetic composition that comprises new skin lightening additives. This invention, therefore, is directed to cosmetic compositions that comprise new skin lightening additives. The cosmetic compositions of the present invention preferably comprise, as a lightening additive, compounds like 12-hydroxystearic acid, ricinoleic acid or both. The cosmetic compositions of this invention result in a decrease in melanin content which is at least about 8% lower (preferably, at least about 11% lower) when comparing MelanoDerm™ cultures treated with the same to MelanoDerm cultures that have not been subjected to a composition with the newly discovered skin lightening additives of this invention.
  • ADDITIONAL INFORMATION
  • Efforts have been disclosed for making skin care cosmetic compositions. In U.S. Pat. No. 6,875,425, skin lightening agents with 4-substituted resorcinol derivative compounds are described.
  • Other efforts have been disclosed for making skin treatment compositions. In U.S. Pat. Nos. 7,250,158 and 7,247,294, methods for treating with skin lightening agents are described.
  • Still other efforts have been disclosed for treating skin. In U.S. Pat. No. 5,998,423, compositions with polycyclic nitrogen heterocycles are described.
  • None of the additional information above describes skin lightening compositions that comprise, as a lightening additive, a heterosubstituted, saturated or unsaturated aliphatic acid, or mixture thereof.
  • SUMMARY OF THE INVENTION
  • In a first aspect, the present invention is directed to a skin lightening additive, the skin lightening additive comprising a heterosubstituted, saturated or unsaturated aliphatic acid, or both.
  • In a second aspect, the present invention is directed to a cosmetic composition for skin lightening, the cosmetic composition comprising a skin lightening agent comprising the skin lightening additive of the first aspect of this invention.
  • In a third aspect, the present invention is directed to a method for lightening skin with the cosmetic composition of the second aspect of this invention.
  • All other aspects of the present invention will more readily become apparent upon considering the detailed description and examples which follow.
  • As used herein, a decrease in melanin content means a melanin content decrease when comparing two (2), three week old MatTek MelanoDerm cultures that have not been treated with a composition comprising the skin lightening additive of this invention to two (2), three week old MatTek MelanoDerm cultures that have been treated with a composition comprising the skin lightening additive of this invention wherein treated means:
      • (a) placing the MelanoDerm culture within a six (6) well tissue culture dish and set about 0.3 cm off of the tissue culture dish;
      • (b) subjecting the MelanoDerm culture to 0.1 and 5 micromolar compositions having the skin lightening additive of this invention, the composition being one prepared from a 10 millimolar solution of skin lightening additive and carrier (e.g., dimethyl sulfoxide) having been diluted with Dulbecco's Modified Eagle Media; and
      • (c) comparing the treated and untreated cultures by obtaining average melanin content (expressed in micrograms) by extracting melanin from MelanoDerm and obtaining absorbance readings at 490 nm (OD490) using a commercially available spectrophotometer like a Hach Spectrophotometer.
  • Cosmetic composition, as used herein, is meant to include a composition for topical application to skin of mammals, especially humans. Such a composition may be generally classified as leave-on or rinse off, and is meant to include conditioners or tonics, lipsticks, color cosmetics, and general topical compositions that in some fashion and at the very least, reduce the effect of melanin on keratinocytes. Lightening and whitening as used herein are meant to mean the same and they include the lightening of skin directly as well as the lightening of spots on the skin, like age spots and freckles. Dulbecco's Modified Eagle Media means the nutrient solution sold by MatTek Corporation and treated and used according to instructions supplied with the product commercially identified as MEL3001OBBLLMM. Skin lightening additive means a component suitable to result in physical, but especially biological whitening (i.e., a reduction in melanin production) whereby the skin lightening additive can comprise, consist essentially of or consist of the skin lightening additive. MelanoDerm means the product having normal, human-derived epidermal keratinocytes and melanocytes which have been cultured to form a multilayered, highly differentiated model of the human epidermis, all of which is made commercially available by MatTek Corporation. Unsaturated, as used herein, means having at least one bond that is not sp3 hybridized. Comprising, as used herein, is meant to include consisting essentially of and consisting of.
  • The cosmetic composition of the present invention can be in the form of a liquid, lotion, cream, serum, gel, soap bar or toner, or applied via a face mask or patch. The composition of this invention is one that at the very least, lightens skin when skin is meant to include skin on the face, neck, chest, back, arms, hands, legs and scalp. All ranges identified herein are meant to implicitly include all ranges subsumed therein, if, for example, reference to the same is not explicitly made.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • The only limitation with respect to the skin lightening additive that may be used in this invention is that the same may be used in a topical composition suitable for use on humans. The preferred additive is a heterosubstituted, saturated or unsaturated aliphatic acid or a mixture thereof.
  • In a most preferred embodiment, the skin lightening additive employed in the present invention comprises a compound having the formulae:
  • Figure US20090317341A1-20091224-C00001
  • or a mixture thereof,
    wherein each R is independently hydrogen, hydroxyl, C1-6 alkoxy, C1-6 alkyl, arylalkyl or an amine, with the proviso that at least one R group comprises a heteroatom; each R1 is independently hydrogen, C1-6 alkoxy, C1-6 alkyl, arylalkyl or an amine; n is an integer from about 7 to about 19; and s and e are each independently an integer from about 0 to about 8, where s+e≧6 ; q is an integer from about 6 to about 11; each r is independently an integer from 0 to 1, with the proviso that each r is not 1 when x is 1; x is an integer from 0 to 1 with the proviso that x is 0 when at least one r is 1; and each t is independently an integer from 1 to 7.
  • The preferred compounds suitable for use in this invention (either alone or in a mixture) are aleuritic acid; phloionolic acid; 9,10,13-trihydroxy-11-octadecenoic acid; 9,13-dihydroxy-12-ethoxy-10-octadecenoic acid; 9-hydroxy-10,12-octadecadienoic acid; 4,14-dihydroxy-octadecanoic acid; 12-hydroxystearic acid(12-hydroxyoctadecanoic acid); lesquerolic acid; ricinelaidic acid; ambrettolic acid, and rincinoleic acid (12-hydroxy-9-cis-octadecanoic acid) as represented by either formula I or II. Other preferred compounds suitable for use in this invention include beta-dimorphecolic acid; densipolic acid; 8-methoxy-13-hydroxy-9,11-octadecadienoic acid; 7-oxo-octadecanoic acid; 9-oxo-octadecanoic acid; 12-oxo-octadecanoic acid and 10-oxo-14-methyl-pentadecanoic acid as represented by formula III. Furthermore it is within the scope of the present invention to include any derivative (like an ester derivative) and/or salt of the acid represented by formulae I-III, and especially, Mg, Na and/or Ca salts thereof. Such compounds are commercially available from suppliers like Vertellus Specialties, Inc., Welch, Home & Clark Co., Inc., as well as Croda Chemicals.
  • The cosmetic compositions of the present invention typically comprise from about 0.001 to about 15% by weight, and preferably, from about 0.1 to about 12%, and most preferably, from about 1 to about 10% by weight skin lightening additive, based on total weight of the cosmetic composition and including all ranges subsumed therein.
  • While it is within the scope of this invention for the skin lightening additive to consist essentially of and to consist of heterosubstituted, saturated or unsaturated aliphatic acid or a mixture thereof, in an often desired embodiment, the skin lightening additive of this invention comprises from about 0.2 to about 95%, and preferably, from about 10 to about 85%, and most preferably, from about 30 to about 65% by weight heterosubstituted saturated or unsaturated aliphatic acid, or a mixture thereof, based on total weight of skin lightening additive and including all ranges subsumed therein.
  • In yet another desired embodiment, the cosmetic composition of this invention comprises from about 2 to about 9%, and preferably, from about 3 to 8%, and most preferably, from about 3 to about 6% by weight heterosubstituted, saturated or unsaturated aliphatic acid, or a mixture thereof, based on total weight of the cosmetic composition and including all ranges subsumed therein.
  • When used in combination, the weight ratio of heterosubstituted, saturated or unsaturated aliphatic acid to heterosubstituted, saturated aliphatic acid is from about 5:95 to about 95:5, and preferably, from about 20:80 to about 80:20, and most preferably, from about 40:60 to about 60:40, including all ratios subsumed therein.
  • It should be known that commercially acceptable and conventional vehicles may be used, acting as diluents, dispersants and/or carriers for the skin lightening agents and additives described herein and for any other optional but often preferred additives. Therefore, the cosmetically acceptable vehicle suitable for use in this invention may be aqueous-based, anhydrous or an emulsion whereby a water-in-oil or oil-in-water emulsion is generally preferred. If the use of water is desired, water typically makes up the balance of the cosmetic composition, and preferably, makes up from about 5 to about 99%, and most preferably, from about 40 to about 80% by weight of the cosmetic composition, including all ranges subsumed therein.
  • In addition to water, organic solvents may be optionally included to act as carriers or to assist carriers within the compositions of the present invention. Illustrative and non-limiting examples of the types of organic solvents suitable for use in the present invention include alkanols like ethyl and isopropyl alcohol, mixtures thereof or the like.
  • Other optional additives suitable for use include ester oils like isopropyl myristate, cetyl myristate, 2-octyldodecyl myristate, avocado oil, almond oil, olive oil, neopentylglycol dicaprate, mixtures thereof or the like. Typically, such ester oils assist in emulsifying the cosmetic composition of this invention, and an effective amount is often used to yield a stable, and most preferably, water-in-oil emulsion.
  • Emollients may also be used, if desired, as carriers within the cosmetic composition of the present invention. Alcohols like 1-hexadecanol (i.e., cetyl alcohol) and phenoxyethanol are often desired as are the emollients generally classified as silicone oils and synthetic esters. Silicone oils suitable for use include cyclic or linear polydimethylsiloxanes containing from 3 to 9, preferably from 4 to 5, silicon atoms. Nonvolatile silicone oils useful as an emollient material in the inventive cosmetic composition described herein include polyalkyl siloxanes, polyalkylaryl siloxanes and polyether siloxane copolymers. The essentially non-volatile polyalkyl siloxanes useful herein include, for example, polydimethylsiloxanes.
  • The ester emollients that may optionally be used are:
      • (1) Alkenyl or alkyl esters of fatty acids having 10 to 20 carbon atoms.
  • Examples thereof include isoarachidyl neopentanoate, isononyl isonanonoate, oleyl myristate, oleyl stearate, and oleyl oleate.
      • (2) Ether-esters such as fatty acid esters of ethoxylated fatty alcohols.
      • (3) Polyhydric alcohol esters. Ethylene glycol mono and di-fatty acid esters, diethylene glycol mono-and di-fatty acid esters, polyethylene glycol (200-6000) mono- and di-fatty acid esters, propylene glycol mono- and di-fatty acid esters, polypropylene glycol 2000 monooleate, polypropylene glycol 2000 monostearate, ethoxylated propylene glycol monostearate, glyceryl mono- and di-fatty acid esters, polyglycerol poly-fatty esters, ethoxylated glyceryl mono-stearate, 1,3-butylene glycol monostearate, 1,3-butylene glycol distearate, polyoxyethylene polyol fatty acid ester, sorbitan fatty acid esters, and polyoxyethylene sorbitan fatty acid esters are satisfactory polyhydric alcohol esters.
      • (4) Wax esters such as beeswax, spermaceti, stearyl stearate and arachidyl behenate.
      • (5) Sterols esters, of which cholesterol fatty acid esters are examples.
  • Emollients when used, typically make up from about 0.1 to about 50% by weight of the cosmetic composition, including all ranges subsumed therein.
  • Fatty acids having from 10 to 30 carbon atoms may also be included as cosmetically acceptable carriers within the composition of the present invention. Illustrative examples of such fatty acids include pelargonic, lauric, myristic, palmitic, stearic, isostearic, oleic, linoleic, arachidic, behenic or erucic acid, and mixtures thereof. Compounds that are believed to enhance skin penetration, like dimethyl sulfoxide, may also be used as an optional carrier.
  • Humectants of the polyhydric alcohol type may also be employed in the cosmetic compositions of this invention. The humectant often aids in increasing the effectiveness of the emollient, reduces scaling, stimulates removal of built-up scale and improves skin feel. Typical polyhydric alcohols include glycerol, polyalkylene glycols and more preferably alkylene polyols and their derivatives, including propylene glycol, dipropylene glycol, polypropylene glycol, polyethylene glycol and derivatives thereof, sorbitol, hydroxypropyl sorbitol, hexylene glycol, 1,3-butylene glycol, 1,2,6-hexanetriol, ethoxylated glycerol, propoxylated glycerol and mixtures thereof. For best results the humectant is preferably propylene glycol or sodium hyaluronate. The amount of humectant may range anywhere from 0.2 to 25%, and preferably, from about 0.5 to about 15% by weight of the cosmetic composition, based on total weight of the cosmetic composition and including all ranges subsumed therein.
  • Thickeners may also be utilized as part of the cosmetically acceptable carrier in the cosmetic compositions of the present invention. Typical thickeners include cross-linked acrylates (e.g. Carbopol 982), hydrophobically-modified acrylates (e.g. Carbopol 1382), cellulosic derivatives and natural gums. Among useful cellulosic derivatives are sodium carboxymethylcellulose, hydroxypropyl methylcellulose, hydroxypropyl cellulose, hydroxyethyl cellulose, ethyl cellulose and hydroxymethyl cellulose. Natural gums suitable for the present invention include guar, xanthan, sclerotium, carrageenan, pectin and combinations of these gums. Amounts of the thickener may range from 0.0 to 5%, usually from 0.001 to 1%, optimally from 0.01 to 0.5% by weight.
  • Collectively, the water, solvents, silicones, esters, fatty acids, humectants and/or thickeners will constitute the cosmetically acceptable carrier in amounts from 1 to 99.9%, preferably from 80 to 99% by weight.
  • Surfactants may also be present in cosmetic compositions of the present invention. Total concentration of the surfactant will range from about 0 to about 40%, and preferably, from about 0 to about 20%, optimally from about 0 to about 5% by weight of the composition. The surfactant may be selected from the group consisting of anionic, nonionic, cationic and amphoteric actives. Particularly preferred nonionic surfactants are those with a C10-C20 fatty alcohol or acid hydrophobe condensed with from 2 to 100 moles of ethylene oxide or propylene oxide per mole of hydrophobe; C2-C10 alkyl phenols condensed with from 2 to 20 moles of alkylene oxide; mono- and di- fatty acid esters of ethylene glycol; fatty acid monoglyceride; sorbitan, mono- and di- C8-C20 fatty acids; block copolymers (ethylene oxide/propylene oxide); and polyoxyethylene sorbitan as well as combinations thereof. Alkyl polyglycosides and saccharide fatty amides (e.g. methyl gluconamides) are also suitable nonionic surfactants.
  • Preferred anionic surfactants include soap, alkyl ether sulfate and sulfonates, alkyl sulfates and sulfonates, alkylbenzene sulfonates, alkyl and dialkyl sulfosuccinates, C8-C20 acyl isothionates, acyl glutamates, C8-C20 alkyl ether phosphates and combinations thereof.
  • Perfumes may be used in the cosmetic composition of this invention. Illustrative non-limiting examples of the types of perfumes that may be used include those comprising terpenes and terpene derivatives like those described in Bauer, K., et al., Common Fragrance and Flavor Materials, VCH Publishers (1990).
  • Illustrative yet non-limiting examples of the types of fragrances that may be used in this invention include myrcene, dihydromyrenol, citral, tagetone, cis-geranic acid, citronellic acid, or cis-geranic acid nitrile, mixtures thereof or the like.
  • Preferably, the amount of fragrance employed in the cosmetic composition of this invention is in the range from about 0.0% to about 10%, more preferably, about 0.00001% to about 5 wt %, most preferably, about 0.0001% to about 2%.
  • Various types of optional additional active ingredients may be used in the cosmetic compositions of the present invention. Actives are defined as skin benefit agents other than emollients and other than ingredients that merely improve the physical characteristics of the composition. Although not limited to this category, general examples include talcs and silicas, as well as alpha-hydroxy acids, beta-hydroxy acids, peroxides, zinc salts, and sunscreens.
  • Beta-hydroxy acids include salicylic acid, for example. Zinc pyrithione is an example of the zinc salts useful in the cosmetic composition of the present invention.
  • Sunscreens include those materials commonly employed to block ultraviolet light. Illustrative compounds are the derivatives of PABA, cinnamate and salicylate. For example, avobenzophenone (Parsol 1789®) octyl methoxycinnamate and 2-hydroxy-4-methoxyl benzophenone (also known as oxybenzone) can be used. Octyl methoxycinnamate and 2-hydroxy-4-methoxy benzophenone are commercially available under the trademarks, Parsol MCX and Benzophenone-e, respectively. The exact amount of sunscreen employed in the compositions can vary depending upon the degree of protection desired from the sun's UV radiation. Additives that reflect or scatter the suns rays may also be employed. These additives include oxides like zinc oxide and titanium dioxide.
  • Many cosmetic compositions, especially those containing water, should be protected against the growth of potentially harmful microorganisms. Anti-microbial compounds, such as triclosan, and preservatives are, therefore, typically necessary. Suitable preservatives include alkyl esters of p-hydroxybenzoic acid, hydantoin derivatives, propionate salts, and a variety of quaternary ammonium compounds. Particularly preferred preservatives of this invention are methyl paraben, propyl paraben, phenoxyethanol and benzyl alcohol. Preservatives will usually be employed in amounts ranging from about 0.1% to 2% by weight of the composition.
  • Still other optional ingredients that may be used with the cosmetic composition of this invention include dioic acids (e.g., malonic acid, sebacic acid), antioxidants like vitamin E, vitamins, like niacinamide and vitamin C and its derivatives, recorcinols and its derivatives (including those esterified with, for example, ferulic acid, vanillic acid or the like) and retinoids, including retinoic acid, retinal, retinol and retinyl esters, conjugated linoleic acid, petroselinic acid and mixtures thereof, as well as any other conventional ingredients well known for wrinkle-reducing, skin whitening, anti-acne effects and reducing the impact of sebum.
  • The cosmetic compositions of the present invention are intended for use primarily as a product for topical application to human skin, especially and at least as a product for lightening the skin. Thus, the inventor has discovered that the described aliphatic acids have excellent skin lightening capabilities whereby the same may be employed as skin lightening additives in topical cosmetic compositions that are applied topically to areas of the skin where lightening or whitening is desired. Other benefits may include skin moisturizing, decreasing the effect of sebum on the skin and skin wrinkle reducing. Often, the cosmetic composition of the present invention has a melting point from about 30° C. to about 45° C., including all ranges subsumed therein. In an especially preferred embodiment, the cosmetic composition of the present invention has a pH from about 4.5 to about 7.5, including all ranges subsumed therein.
  • When making the cosmetic composition of the present invention, the desired ingredients are mixed in no particular order and usually at temperatures from about 70 to about 80° C. and under atmospheric pressure.
  • The packaging for the composition of this invention can be a patch, bottle, tube, roll-ball applicator, propellant driven aerosol device, squeeze container or lidded jar.
  • The examples which follow are provided to illustrate and facilitate an understanding of the invention. The examples are not intended to limit the scope of the claims.
  • EXAMPLES
  • Commercially available human skin equivalents (MelanoDerm™ from MatTek) were obtained for testing the impact of heterosubstituted, saturated or unsaturated aliphatic acid on melanogenesis. Solutions having a final concentration of 0.1 to 5 micromolar were prepared from a 10 millimolar dimethyl sulfoxide stock solution and dosed ten (10) times in a three (3) week period into the media of the MelanoDerm cultures. The media consisted of commercially available basal Dulbecco's Modified Eagles media, prepared and treated in the manner set forth in the manufacturer's instructions. For long term maintenance of the MelanoDerms, the basal media was supplemented with bFGF and alpha MSH to stimulate melanocyte growth and melanogenesis. Each treatment condition was done in duplicate and three (3) sets were made for each treatment, as well as for a control (culture not treated with the aliphatic acid). The cultures were maintained at a temperature of about 37° C. and incubated in a humidified, 5% CO2 incubator during the dosing period, but removed while being dosed.
  • After a three (3) week period, the MelanoDerm cultures were removed and solubilized in a centrifuge tube containing 250 microliters of Solvable reagent (GNE9100, Packard) for sixteen (16) hours (overnight) in a 60° C. oven. Following solubilization, the centrifuge tube containing the sample was spun at 12,000 g for five (5) minutes. Two hundred (200) microliters of supernatant were removed and placed in a ninety-six (96) well plate. A spectrophotometer was used to measure the absorbance of the supernatant at 490 nm. A standard curve using synthetic melanin was set up in parallel to allow quantitation of melanin, in micrograms, of the samples. The results are provided below:
  • TABLES
    Active Average MC ΔMC
    MC* Value Range
    Control 76.0-78.4 77.2
    Aliphatic acidi 67.9-69.2 68.6 8.6
    MC Value Range
    Control 76.0-78.4 77.2
    Aliphatic acidii 69.9-67.6 68.8 8.4
    i= ricinoleic acid (0.1 uM)
    ii= 12-hydroxystearic acid (5 uM)
    *MC = melanin content
  • The results, as they relate to MelanoDerm cultures, show that cosmetic compositions with the aliphatic acids of this invention unexpectedly result in skin lightening.

Claims (19)

1. A skin lightening additive comprising a heterosubstituted, saturated or unsaturated aliphatic acid, or a mixture thereof.
2. The skin lightening additive according to claim 1 wherein aliphatic acid is
Figure US20090317341A1-20091224-C00002
or a mixture thereof
wherein each R is independently hydrogen, hydroxyl, C1-6 alkoxy, C1-6 alkyl, arylalkyl or an amine, with the proviso that at least one R group comprises a heteroatom; each R1 is independently hydrogen, C1-6 alkoxy, C1-6 alkyl, arylalkyl or an amine; n is an integer from about 7 to about 19; and s and e are each independently an integer from about 0 to about 8, where s+e≧6; q is an integer from about 6 to about 11; each r is independently an integer from 0 to 1, with the proviso that each r is not 1 when x is 1; x is an integer from 0 to 1 with the proviso that x is 0 when at least one r is 1; and each t is independently an integer from 1 to 7.
3. The skin lightening additive according to claim 1 wherein the heterosubstituted, saturated aliphatic acid is at least one of aleuritic acid; phloionolic acid, 9,10,13-trihydroxy-11-octadecenoic acid; 9,13-dihydroxy-12-ethoxy-10-octadecenoic acid; 9-hydroxy-10,12-octadecadienoic acid; 4,14-dihydroxy-octadecanoic acid; 12-hydroxystearic acid or a mixture thereof and the heterosubstituted, unsaturated aliphatic acid is at least one of lesquerolic acid; ricinelaidic acid; ambrettolic acid; ricinoleic acid; beta-dimorphecolic acid; densipolic acid; 8-methoxy-13-hydroxy-9,11-octadecadienoic acid; 7-oxo-octadecanoic acid; 9-oxo-octadecanoic acid; 12-oxo-octadecanoic acid; 10-oxo-14-methyl-pentadecanoic acid or a mixture thereof.
4. The skin lightening additive according to claim 1 wherein the skin lightening additive comprises the heterosubstituted, saturated aliphatic acid and heterosubstituted, unsaturated aliphatic acid at a weight ratio from about 10:90 to about 90:10.
5. The skin lightening additive according to claim 1 wherein the skin lightening additive consists essentially of heterosubstituted, saturated aliphatic acid, heterosubstituted, unsaturated aliphatic acid, or both.
6. A cosmetic composition comprising
a. a skin lightening additive comprising a heterosubstituted, saturated or unsaturated aliphatic acid, or a mixture thereof; and
b. a cosmetic carrier.
7. The cosmetic composition according to claim 6 wherein aliphatic acid is represented as formula I, formula II and/or formula III
Figure US20090317341A1-20091224-C00003
or a mixture thereof
wherein each R is independently hydrogen, hydroxyl, C1-6 alkoxy, C1-6 alkyl, arylalkyl or an amine, with the proviso that at least one R group comprises a heteroatom; each R1 is independently hydrogen, C1-6 alkoxy, C1-6 alkyl, arylalkyl or an amine; n is an integer from about 7 to about 19; and s and e are each independently an integer from about 0 to about 8, where s+e≧6; q is an integer from about 6 to about 11; each r is independently an integer from 0 to 1, with the proviso that each r is not 1 when x is 1; x is an integer from 0 to 1 with the proviso that x is 0 when at least one r is 1; and each t is independently an integer from 1 to 7.
8. The cosmetic composition according to claim 7 wherein the heterosubstituted, saturated aliphatic acid is at least one of aleuritic acid; phloionolic acid; 9,10,13-trihydroxy-11-octadecenoic acid; 9,13-dihydroxy-12-ethoxy-10-octadecenoic acid; 9-hydroxy-10,12-octadecadienoic acid; 4,14-dihydroxy-octadecanoic acid; 12-hydroxystearic acid or a mixture thereof and the heterosubstituted, unsaturated aliphatic acid is at least one of lesquerolic acid; ricinelaidic acid, ambrettolic acid; ricinoleic acid; beta-dimorphecolic acid; densipolic acid; 8-methoxy-13-hydroxy-9,11-octadecadienoic acid; 7-oxo-octadecanoic acid; 9-oxo-octadecanoic acid; 12-oxo-octadecanoic acid; 10-oxo-14-methyl-pentadecanoic acid or a mixture thereof.
9. The cosmetic composition according to claim 6 wherein the skin lightening additive comprises the heterosubstituted, saturated aliphatic acid and heterosubstituted, unsaturated aliphatic acid at a weight ratio from about 90:10 to about 10:90.
10. The cosmetic composition according to claim 6 wherein the skin lightening additive consists essentially of heterosubstituted, saturated aliphatic acid, heterosubstituted, unsaturated aliphatic acid, or a mixture thereof.
11. The cosmetic composition according to claim 6 wherein the cosmetic composition further comprises an alpha-hydroxy, beta-hydroxy acid, sunscreen or a mixture thereof.
12. The cosmetic composition according to claim 6 wherein the cosmetic composition further comprises a vitamin.
13. The cosmetic composition according to claim 12 wherein the vitamin is niacinamide.
14. The cosmetic composition according to claim 7 wherein the cosmetic composition further comprises niacinamide.
15. The cosmetic composition according to claim 6 wherein the composition further comprises conjugated linoleic acid, petroselinic acid or both.
16. The cosmetic composition according to claim 6 wherein the composition further comprises antioxidant.
17. The cosmetic composition according to claim 7 whereby a salt or derivative of the aliphatic acid represented by formula I, II and/or III is used.
18. A method for lightening skin color comprising the steps of:
a. contacting skin with the composition of claim 6; and
b. suppressing melanin production.
19. The method for lightening skin color according to claim 17 wherein the skin composition further comprise niacinamide, conjugated linoleic acid, petroselinic acid, sunscreen, alpha-hydroxy acid, beta-hydroxy acid or a mixture thereof.
US12/141,561 2008-06-18 2008-06-18 Compositions for Lightening Skin Color Abandoned US20090317341A1 (en)

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US12/141,561 US20090317341A1 (en) 2008-06-18 2008-06-18 Compositions for Lightening Skin Color
JP2011513979A JP5620908B2 (en) 2008-06-18 2009-06-04 Composition for whitening skin color
KR1020167010797A KR101788998B1 (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
MX2010014098A MX2010014098A (en) 2008-06-18 2009-06-04 Compositions for lightening skin color.
CN201711095416.6A CN108158836A (en) 2008-06-18 2009-06-04 For the method for blast skin
EP14163576.3A EP2752184B1 (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
AU2009259483A AU2009259483B2 (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
EA201300756A EA026945B1 (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
KR1020107028407A KR101617478B1 (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
EP16177361.9A EP3103434B1 (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
EA201170042A EA018806B1 (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
CN200980122854.4A CN102065829B (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
ES14163576.3T ES2611791T3 (en) 2008-06-18 2009-06-04 Compositions to lighten skin color
CA2728978A CA2728978C (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
BRPI0914843-4A BRPI0914843B1 (en) 2008-06-18 2009-06-04 COSMETIC COMPOSITION AND METHOD FOR LIGHTENING SKIN COLOR
EP09765749.8A EP2285342B9 (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
PL09765749T PL2285342T3 (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
CN201410170094.7A CN103976889B (en) 2008-06-18 2009-06-04 Method for blast skin
PL14163576T PL2752184T3 (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
ES09765749.8T ES2511916T3 (en) 2008-06-18 2009-06-04 Skin color lightening compositions
PCT/EP2009/056886 WO2009153169A1 (en) 2008-06-18 2009-06-04 Compositions for lightening skin color
SA109300373A SA109300373B1 (en) 2008-06-18 2009-06-10 Compositions for Lightening Skin Color
TW098119831A TWI442943B (en) 2008-06-18 2009-06-12 Compositions for lightening skin color
ARP090102190A AR072165A1 (en) 2008-06-18 2009-06-17 COMPOSITIONS TO CLEAR UP THE COLOR OF THE SKIN. SKIN CLEARING ADDITIVE. METHOD.
US12/908,248 US9227090B2 (en) 2008-06-18 2010-10-20 Method for lightening skin
ZA2010/08792A ZA201008792B (en) 2008-06-18 2010-12-07 Compositions for lightening skin color
CL2010001461A CL2010001461A1 (en) 2008-06-18 2010-12-17 Cosmetic composition comprising a skin lightening additive that is 12-hydroxystearic acid and / or a salt, a cosmetic carrier and niacinamide; and a method to clarify skin color.
HK11108430.8A HK1153954A1 (en) 2008-06-18 2011-08-11 Compositions for lightening skin color
HK15101435.4A HK1200737A1 (en) 2008-06-18 2015-02-10 A method for lightening skin
US14/948,461 US20160074295A1 (en) 2008-06-18 2015-11-23 Method for lightening skin with ricinoleic acid
US16/380,657 US20190336424A1 (en) 2008-06-18 2019-04-10 Method for lightening skin with ricinoleic acid

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012062554A2 (en) 2010-11-11 2012-05-18 Unilever Plc Leave-on non-solid skin conditioning compositions containing 12-[(12-hydroxyoctadecanoyl)oxy] octadecanoic acid
WO2012061991A1 (en) 2010-11-11 2012-05-18 Unilever Plc Leave-on nonsolid skin conditioning compositions containing 12-hydroxystearic acid
WO2012080272A2 (en) 2010-12-15 2012-06-21 Unilever Plc Leave-on non-solid skin conditioning compositions containing 12-hydroxystearic acid and ethoxylated hydrogenated castor oil
WO2012110276A1 (en) 2011-02-17 2012-08-23 Unilever Plc Leave -on non- solid skin conditioning composition which has a continuous phase and contains 12 - hydroxystearic acid
WO2013068345A2 (en) 2011-11-11 2013-05-16 Unilever Plc Organogel structured with 12-hsa and a selected copolymer
WO2014095257A1 (en) * 2012-12-20 2014-06-26 Unilever N.V. Eutectic mixtures in personal care compositions
US9539190B2 (en) 2010-05-07 2017-01-10 Conopco, Inc. Skin conditioning compositions containing 12-hydroxystearic acid
US9597271B2 (en) 2013-10-24 2017-03-21 The Procter & Gamble Company Cosmetic compositions and methods
US9956257B2 (en) 2005-10-27 2018-05-01 KGK Science, Inc. Canola extracts containing high levels of phenolic acids
US10172772B2 (en) * 2013-01-31 2019-01-08 KGK Science, Inc. Methods of skin whitening by use of canola extracts
US10660836B2 (en) 2015-12-22 2020-05-26 Conopco, Inc. Hydroxy functionalized solvent based skin benefit composition
US20220202670A1 (en) * 2020-12-30 2022-06-30 Galaxy Surfactants Ltd. Personal and home care compositions comprising fatty acids from tung seed oil as antimicrobial preservative
CN116056684A (en) * 2020-07-30 2023-05-02 联合利华知识产权控股有限公司 Personal care compositions comprising atractylenolide-I or a source of atractylenolide-I

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090317341A1 (en) * 2008-06-18 2009-12-24 Conopco, Inc., D/B/A Unilever Compositions for Lightening Skin Color
DE102010056550A1 (en) 2010-12-30 2012-07-05 Evonik Goldschmidt Gmbh Use of 13-hydroxy-9,11-octadecadienoic acid for tanning human skin
EP2604248B1 (en) 2011-12-13 2017-10-25 Unilever PLC Oil-in-water cosmetic composition
EP3334403B1 (en) 2015-08-10 2021-03-31 Mary Kay, Inc. Topical compositions
JP6880011B2 (en) * 2015-10-05 2021-06-02 ユニリーバー・ナームローゼ・ベンノートシヤープ Skin whitening composition
CN109069384B (en) * 2016-04-13 2022-10-18 帝斯曼知识产权资产管理有限公司 10-hydroxystearic acid composition
BR112018077141B1 (en) * 2016-07-27 2022-02-01 Unilever Ip Holdings B.V. Personal care composition and uses of a skin care composition
WO2018113637A1 (en) * 2016-12-21 2018-06-28 Unilever Plc Personal care compositions with glutathione precursor comprising nicotinamide and amino acids
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US11260005B2 (en) 2016-12-21 2022-03-01 Conopco, Inc. Personal care compositions with glutathione precursor comprising 4-substituted resorcinols and amino acids
WO2019183494A1 (en) 2018-03-23 2019-09-26 Mary Kay Inc. Topical compositions and methods
CN111110607B (en) * 2020-02-26 2020-12-15 李应坤 Mild moisturizing type foam facial cleanser and preparation method thereof
WO2022226209A1 (en) * 2021-04-22 2022-10-27 Glo Pharma, Inc. Skin peel compositions
WO2023061962A1 (en) 2021-10-13 2023-04-20 Unilever Ip Holdings B.V. A personal care composition comprising vitamin k2 and hydroxystearic acid
WO2023151986A1 (en) 2022-02-09 2023-08-17 Unilever Ip Holdings B.V. A skin brightening composition

Citations (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4096240A (en) * 1975-04-10 1978-06-20 Lever Brothers Company Skin lightening composition and method
JPH05201847A (en) * 1992-01-28 1993-08-10 Sunstar Inc Skin-beautifying cosmetic
US5262153A (en) * 1989-09-20 1993-11-16 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkujo Skin-whitening agent
US5399785A (en) * 1992-08-05 1995-03-21 Nippon Paint Co., Ltd. Tyrosinase activity inhibitor
US5429816A (en) * 1992-05-12 1995-07-04 Procter & Gamble Antiperspirant gel stick compositions
US5516511A (en) * 1994-05-06 1996-05-14 The Procter & Gamble Company Antiperspirant gel compositions comprising chelators
US5591424A (en) * 1993-06-30 1997-01-07 The Procter & Gamble Company Antiperspirant gel stick compositions
US5744130A (en) * 1996-12-20 1998-04-28 The Procter & Gamble Company Antiperspirant gel-solid stick compositions substantially free of select polar solvents
US5776494A (en) * 1996-12-20 1998-07-07 The Procter & Gamble Company Pharmaceuticals compositions containing gellants in the form of alkyl amides of di-and tri-carboxylic acids
US5863546A (en) * 1997-03-02 1999-01-26 Swinehart; James M Cosmetic composition
US5965113A (en) * 1997-06-23 1999-10-12 Procter & Gamble Company Low residue antiperspirant gel-solid stick compositions containing volatile nonpolar hydrocarbon solvents
US5968489A (en) * 1998-05-01 1999-10-19 The Procter & Gamble Company Antiperspirant composition containing 1,2-hexanediol
US5998423A (en) * 1996-10-08 1999-12-07 Therasys, Inc. Methods for modulating melanin production
US6033651A (en) * 1998-06-10 2000-03-07 Revlon Consumer Products Corporation Gel cosmetic compositions
US6090369A (en) * 1997-06-04 2000-07-18 Stewart; Ernest Glading Sunscreen formulation with avobenzone and method for stabilizing sunscreen formulation which contains avobenzone
US6153177A (en) * 1997-12-15 2000-11-28 Chesebrough-Ponds's Usa, Co., Division Of Conopco, Inc. Skin lightening composition
US6171581B1 (en) * 1998-12-18 2001-01-09 Revlon Consumer Products Corporation Water and oil emulsion solid antiperspirant/deodorant compositions
US6171601B1 (en) * 1996-12-20 2001-01-09 The Procter & Gamble Company Low residue antiperspirant gel-solid stick compositions
US6183730B1 (en) * 1999-05-18 2001-02-06 The Procter & Gamble Company Antiperspirant and deodorant compositions containing cyclohexasiloxane
US6197343B1 (en) * 1996-04-01 2001-03-06 Kao Corporation Skin color improver
US6280764B1 (en) * 1995-06-20 2001-08-28 Lavipharm Laboratories Inc. Device for topical treatment of acne and its method of manufacture
US6352688B1 (en) * 2000-05-17 2002-03-05 The Procter & Gamble Company High efficacy, low residue antiperspirant stick compositions
US6365137B1 (en) * 1999-04-06 2002-04-02 Collaborative Laboratories, Inc. Skin whitening agents
US6423325B1 (en) * 1999-07-30 2002-07-23 Conopco, Inc. Skin care composition
US20020106384A1 (en) * 1999-12-10 2002-08-08 Zhang Kelly Hua Cosmetic compositions and methods for lightening the skin
US20020192243A1 (en) * 1999-12-16 2002-12-19 Tsung-Min Hsu Transdermal and topical administration of drugs for the treatment of Alzheimer's disease using basic enhancers
US6680285B2 (en) * 2000-12-21 2004-01-20 Unilever Home & Personal Care Usa A Division Of Conopco, Inc. Skin cleansing bar with high levels of liquid emollient
US20040044078A1 (en) * 2000-11-29 2004-03-04 Rolf Kawa Cosmetic and/or pharmaceutical emulsions
US20040043044A1 (en) * 2000-06-30 2004-03-04 Granger Stewart Paton Skin conditioning compositions containing compounds for mimicking the effect on skin of retinoic acid
US6713051B2 (en) * 2001-06-18 2004-03-30 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Antiperspirant or deodorant compositions
US20040081672A1 (en) * 2002-10-25 2004-04-29 Gupta Shyam K. Niacinamide, niacin, and niacin esters based delivery systems for treating topical disorders of skin and skin aging
US20040208902A1 (en) * 2003-04-18 2004-10-21 Gupta Shyam K. Controlled-release nano-diffusion delivery systems for cosmetic and pharmaceutical compositions
US20040253275A1 (en) * 2000-01-10 2004-12-16 Meir Eini Pharmaceutical and cosmetic carrier or composition for topical application
US6835373B2 (en) * 2002-07-12 2004-12-28 The Procter & Gamble Company Non-irritating antiperspirant compositions containing acidic antiperspirant active
US6849251B2 (en) * 2000-04-28 2005-02-01 Henkel Kommanditgesellschaft Auf Aktien Anhydrous antiperspirant composition containing polysaccharides
US6875425B2 (en) * 2002-12-12 2005-04-05 Unilever Home & Personal Care Usa Skin lightening agents, compositions and methods
US20050120917A1 (en) * 2003-12-09 2005-06-09 Reinhold Ruger Coloured microstructured effect pigments
US6932984B1 (en) * 1999-11-17 2005-08-23 Tagra Biotechnologies Ltd. Method of microencapsulation
US6936242B2 (en) * 2002-11-15 2005-08-30 The Gillette Company Multi-portion antiperspirant composition
US20050220726A1 (en) * 2002-03-01 2005-10-06 Gilles Pauly Use of sugar esters in cosmetic and/or pharmaceutical preparations
US20060067960A1 (en) * 2004-09-30 2006-03-30 Russ Julio G Color cosmetic compositions
US20060115441A1 (en) * 2004-11-26 2006-06-01 Conopco Inc, D/B/A Unilever Underarm cosmetic method and compositions
US7247294B1 (en) * 2006-03-30 2007-07-24 Conopco, Inc. Skin lightening agents, compositions and methods
US7250158B1 (en) * 2006-03-30 2007-07-31 Conopco, Inc. Skin lightening agents, compositions and methods
US20070253911A1 (en) * 2002-10-25 2007-11-01 Foamix Ltd. Foamable compositions, kits and methods for hyperhidrosis
US20080193393A1 (en) * 2004-09-24 2008-08-14 Lipo Chemicals Inc. Delivery System for Topically Applied Compounds

Family Cites Families (56)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63115809A (en) * 1986-10-31 1988-05-20 Kanebo Ltd Skin cosmetic
US5389677B1 (en) * 1986-12-23 1997-07-15 Tristrata Inc Method of treating wrinkles using glycalic acid
IN169917B (en) 1989-03-21 1992-01-11 Lever Hindustan Ltd
JPH05345705A (en) 1992-02-03 1993-12-27 Nippon Shinyaku Co Ltd Skin-beautifying cosmetic composition
JPH05306231A (en) 1992-04-24 1993-11-19 Pola Chem Ind Inc Skin external preparation
JP3480952B2 (en) 1992-08-17 2003-12-22 株式会社コーセー External preparation for skin
JPH06227939A (en) * 1993-02-05 1994-08-16 Yuka Sangyo Kk Cosmetic
JPH0725742A (en) 1993-07-15 1995-01-27 Kao Corp Fair-skinning cosmetic
JP3025605B2 (en) 1993-07-21 2000-03-27 花王株式会社 Whitening cosmetics
JPH07238010A (en) * 1994-02-24 1995-09-12 Kanebo Ltd Skin cosmetic
JP3696271B2 (en) 1994-09-22 2005-09-14 花王株式会社 Whitening cosmetics
JPH0892055A (en) 1994-09-22 1996-04-09 Kao Corp Whitening cosmetic
FR2735688B1 (en) * 1995-06-26 1997-08-14 Oreal USE IN COMBINATION OF AN ALPHA-HYDROXYACID AND A TITANIUM OXIDE FOR SKIN WHITENING
JPH0987135A (en) 1995-07-13 1997-03-31 Shiseido Co Ltd Dermal preparation for external use
JPH0952817A (en) 1995-08-09 1997-02-25 Kao Corp Beautifying and whitening cosmetic
JP3645633B2 (en) 1995-12-13 2005-05-11 花王株式会社 Whitening cosmetics
JPH10203921A (en) 1997-01-20 1998-08-04 Shiseido Co Ltd Skin preparation for external use
JPH10265322A (en) 1997-03-19 1998-10-06 Shiseido Co Ltd Skin preparation for external use
JPH10265321A (en) 1997-03-19 1998-10-06 Shiseido Co Ltd Skin preparation for external use
JP3592918B2 (en) 1997-05-14 2004-11-24 花王株式会社 Cosmetics
RO118174B1 (en) * 1997-08-21 2003-03-28 Aventis Pharma Deutschland Gmbh Nail polish and use thereof
JPH11124308A (en) 1997-10-22 1999-05-11 Kao Corp Cosmetic
JPH11246343A (en) 1998-02-27 1999-09-14 Shiseido Co Ltd Preparation for external use for skin bleaching
JP2000143479A (en) 1998-11-05 2000-05-23 Kao Corp Skin-bleaching cosmetic
JP2000302661A (en) 1999-04-21 2000-10-31 Kao Corp Cosmetic
JP2001163755A (en) 1999-12-07 2001-06-19 Shiseido Co Ltd Preparation for external use for skin
JP2001181173A (en) 1999-12-27 2001-07-03 Kose Corp Bleaching preparation for external use
JP2001206833A (en) 2000-01-25 2001-07-31 Kao Corp Cosmetic
GB0006867D0 (en) * 2000-03-21 2000-05-10 Unilever Plc Method and composition for skin lightening
US6881414B2 (en) * 2000-11-22 2005-04-19 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Mild cosmetic composition with stabilized retinoids
JP2002179516A (en) 2000-12-13 2002-06-26 Pola Chem Ind Inc Skin-whitening composition
JP2002265387A (en) 2001-03-06 2002-09-18 Kose Corp Skin care preparation
JP2002284664A (en) 2001-03-29 2002-10-03 Shiseido Co Ltd External skin preparation for whitening
GB0119583D0 (en) 2001-08-10 2001-10-03 Unilever Plc Cosmetic composition and method of treating skin
JP3934371B2 (en) 2001-08-15 2007-06-20 玲子 渡久地 Beauty soap
JP2003128521A (en) 2001-10-16 2003-05-08 Rohto Pharmaceut Co Ltd External preparation
JP2003306419A (en) 2002-04-16 2003-10-28 Nikko Chemical Co Ltd Cosmetic
WO2004010960A1 (en) 2002-07-25 2004-02-05 Amcol International Corporation Viscous compositions containing hydrophobic liquids
JP2004075645A (en) 2002-08-22 2004-03-11 Kanebo Ltd Cosmetic
DE10238449A1 (en) 2002-08-22 2004-03-04 Beiersdorf Ag Cosmetic and / or dermatological preparation
JP2004115381A (en) 2002-09-24 2004-04-15 Shiseido Co Ltd External preparation for skin
JP2004238394A (en) 2003-01-17 2004-08-26 Kose Corp Rebound inhibitor and skin care preparation for external use containing the same
JP2004262853A (en) 2003-03-03 2004-09-24 Kanebo Ltd Cosmetic
JP2005002050A (en) 2003-06-12 2005-01-06 Shiseido Co Ltd Bleaching agent and skin care preparation for external use formulated therewith
TW200607529A (en) 2004-07-28 2006-03-01 Cream Holdings Pty Ltd Natural sunscreen composition
JP2006219423A (en) 2005-02-10 2006-08-24 Kao Corp Skin cosmetic
JP5137256B2 (en) * 2005-03-31 2013-02-06 ユニリーバー・ナームローゼ・ベンノートシヤープ Enhanced delivery of skin benefit agents
CN101146509B (en) * 2005-03-31 2012-10-10 荷兰联合利华有限公司 Enhanced delivery of skin benefit agents
EP1888015A1 (en) 2005-05-03 2008-02-20 Unilever Plc Skin lightening composition comprising a conjugated linoleic acid and niacinamide
JP2009508895A (en) 2005-09-23 2009-03-05 ディーエスエム アイピー アセッツ ビー.ブイ. Use of opioid receptor antagonists
ITBA20060049A1 (en) 2006-08-02 2008-02-03 Pierre S R L FOOD SUPPLEMENT BASED ON BIOLOGICAL LYCOPENE AND PROCEDURE FOR OBTAINING BIOLOGICAL LICOPENE.
JP2008150314A (en) 2006-12-18 2008-07-03 Shiseido Co Ltd Bleaching agent
TWI454261B (en) 2007-01-09 2014-10-01 Unigen Inc Chromones as therapeutic agents
KR100823533B1 (en) 2007-02-27 2008-04-30 바이오스펙트럼 주식회사 COMPOSITIONS FOR IMPROVING SKIN CONDITIONS COMPRISING alpha;-BISABOLOL AS AN ACTIVE INGREDIENT
US20090317341A1 (en) * 2008-06-18 2009-12-24 Conopco, Inc., D/B/A Unilever Compositions for Lightening Skin Color
US8247405B2 (en) * 2008-12-10 2012-08-21 Conopco, Inc. Skin lightening compositions with acetylcholinesterase inhibitors

Patent Citations (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4096240A (en) * 1975-04-10 1978-06-20 Lever Brothers Company Skin lightening composition and method
US5262153A (en) * 1989-09-20 1993-11-16 Kabushiki Kaisha Hayashibara Seibutsu Kagaku Kenkujo Skin-whitening agent
JPH05201847A (en) * 1992-01-28 1993-08-10 Sunstar Inc Skin-beautifying cosmetic
US5429816A (en) * 1992-05-12 1995-07-04 Procter & Gamble Antiperspirant gel stick compositions
US5399785A (en) * 1992-08-05 1995-03-21 Nippon Paint Co., Ltd. Tyrosinase activity inhibitor
US5591424A (en) * 1993-06-30 1997-01-07 The Procter & Gamble Company Antiperspirant gel stick compositions
US5650144A (en) * 1993-06-30 1997-07-22 The Procter & Gamble Co. Antiperspirant gel stick compositions
US5516511A (en) * 1994-05-06 1996-05-14 The Procter & Gamble Company Antiperspirant gel compositions comprising chelators
US6280764B1 (en) * 1995-06-20 2001-08-28 Lavipharm Laboratories Inc. Device for topical treatment of acne and its method of manufacture
US6197343B1 (en) * 1996-04-01 2001-03-06 Kao Corporation Skin color improver
US5998423A (en) * 1996-10-08 1999-12-07 Therasys, Inc. Methods for modulating melanin production
US6171601B1 (en) * 1996-12-20 2001-01-09 The Procter & Gamble Company Low residue antiperspirant gel-solid stick compositions
US5744130A (en) * 1996-12-20 1998-04-28 The Procter & Gamble Company Antiperspirant gel-solid stick compositions substantially free of select polar solvents
US5776494A (en) * 1996-12-20 1998-07-07 The Procter & Gamble Company Pharmaceuticals compositions containing gellants in the form of alkyl amides of di-and tri-carboxylic acids
US5863546A (en) * 1997-03-02 1999-01-26 Swinehart; James M Cosmetic composition
US6090369A (en) * 1997-06-04 2000-07-18 Stewart; Ernest Glading Sunscreen formulation with avobenzone and method for stabilizing sunscreen formulation which contains avobenzone
US5965113A (en) * 1997-06-23 1999-10-12 Procter & Gamble Company Low residue antiperspirant gel-solid stick compositions containing volatile nonpolar hydrocarbon solvents
US6153177A (en) * 1997-12-15 2000-11-28 Chesebrough-Ponds's Usa, Co., Division Of Conopco, Inc. Skin lightening composition
US5968489A (en) * 1998-05-01 1999-10-19 The Procter & Gamble Company Antiperspirant composition containing 1,2-hexanediol
US6139880A (en) * 1998-06-10 2000-10-31 Revlon Consumer Products Corporation Gel cosmetic compositions
US6033651A (en) * 1998-06-10 2000-03-07 Revlon Consumer Products Corporation Gel cosmetic compositions
US6171581B1 (en) * 1998-12-18 2001-01-09 Revlon Consumer Products Corporation Water and oil emulsion solid antiperspirant/deodorant compositions
US6365137B1 (en) * 1999-04-06 2002-04-02 Collaborative Laboratories, Inc. Skin whitening agents
US6183730B1 (en) * 1999-05-18 2001-02-06 The Procter & Gamble Company Antiperspirant and deodorant compositions containing cyclohexasiloxane
US6423325B1 (en) * 1999-07-30 2002-07-23 Conopco, Inc. Skin care composition
US6932984B1 (en) * 1999-11-17 2005-08-23 Tagra Biotechnologies Ltd. Method of microencapsulation
US20020106384A1 (en) * 1999-12-10 2002-08-08 Zhang Kelly Hua Cosmetic compositions and methods for lightening the skin
US20020192243A1 (en) * 1999-12-16 2002-12-19 Tsung-Min Hsu Transdermal and topical administration of drugs for the treatment of Alzheimer's disease using basic enhancers
US20040253275A1 (en) * 2000-01-10 2004-12-16 Meir Eini Pharmaceutical and cosmetic carrier or composition for topical application
US6849251B2 (en) * 2000-04-28 2005-02-01 Henkel Kommanditgesellschaft Auf Aktien Anhydrous antiperspirant composition containing polysaccharides
US6352688B1 (en) * 2000-05-17 2002-03-05 The Procter & Gamble Company High efficacy, low residue antiperspirant stick compositions
US20040043044A1 (en) * 2000-06-30 2004-03-04 Granger Stewart Paton Skin conditioning compositions containing compounds for mimicking the effect on skin of retinoic acid
US20040044078A1 (en) * 2000-11-29 2004-03-04 Rolf Kawa Cosmetic and/or pharmaceutical emulsions
US6680285B2 (en) * 2000-12-21 2004-01-20 Unilever Home & Personal Care Usa A Division Of Conopco, Inc. Skin cleansing bar with high levels of liquid emollient
US6713051B2 (en) * 2001-06-18 2004-03-30 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Antiperspirant or deodorant compositions
US20050220726A1 (en) * 2002-03-01 2005-10-06 Gilles Pauly Use of sugar esters in cosmetic and/or pharmaceutical preparations
US6835373B2 (en) * 2002-07-12 2004-12-28 The Procter & Gamble Company Non-irritating antiperspirant compositions containing acidic antiperspirant active
US20040081672A1 (en) * 2002-10-25 2004-04-29 Gupta Shyam K. Niacinamide, niacin, and niacin esters based delivery systems for treating topical disorders of skin and skin aging
US20070253911A1 (en) * 2002-10-25 2007-11-01 Foamix Ltd. Foamable compositions, kits and methods for hyperhidrosis
US6936242B2 (en) * 2002-11-15 2005-08-30 The Gillette Company Multi-portion antiperspirant composition
US6875425B2 (en) * 2002-12-12 2005-04-05 Unilever Home & Personal Care Usa Skin lightening agents, compositions and methods
US20040208902A1 (en) * 2003-04-18 2004-10-21 Gupta Shyam K. Controlled-release nano-diffusion delivery systems for cosmetic and pharmaceutical compositions
US20050120917A1 (en) * 2003-12-09 2005-06-09 Reinhold Ruger Coloured microstructured effect pigments
US20080193393A1 (en) * 2004-09-24 2008-08-14 Lipo Chemicals Inc. Delivery System for Topically Applied Compounds
US20060067960A1 (en) * 2004-09-30 2006-03-30 Russ Julio G Color cosmetic compositions
US20060115441A1 (en) * 2004-11-26 2006-06-01 Conopco Inc, D/B/A Unilever Underarm cosmetic method and compositions
US7247294B1 (en) * 2006-03-30 2007-07-24 Conopco, Inc. Skin lightening agents, compositions and methods
US7250158B1 (en) * 2006-03-30 2007-07-31 Conopco, Inc. Skin lightening agents, compositions and methods

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Wineski et al. 1989. Phenoxyethanol as a nontoxic preservative in the dissection laboratory. Acta Anat (Basel); 136(2): (abstract). *

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9956257B2 (en) 2005-10-27 2018-05-01 KGK Science, Inc. Canola extracts containing high levels of phenolic acids
US9539190B2 (en) 2010-05-07 2017-01-10 Conopco, Inc. Skin conditioning compositions containing 12-hydroxystearic acid
WO2012061991A1 (en) 2010-11-11 2012-05-18 Unilever Plc Leave-on nonsolid skin conditioning compositions containing 12-hydroxystearic acid
WO2012062554A2 (en) 2010-11-11 2012-05-18 Unilever Plc Leave-on non-solid skin conditioning compositions containing 12-[(12-hydroxyoctadecanoyl)oxy] octadecanoic acid
CN103189109A (en) * 2010-11-11 2013-07-03 荷兰联合利华有限公司 Leave-on non-solid skin conditioning compositions containing 12-[(12-hydroxyoctadecanoyl)oxy] octadecanoic acid
WO2012080272A2 (en) 2010-12-15 2012-06-21 Unilever Plc Leave-on non-solid skin conditioning compositions containing 12-hydroxystearic acid and ethoxylated hydrogenated castor oil
US8613939B2 (en) 2010-12-15 2013-12-24 Conopco, Inc. Leave-on nonsolid skin conditioning compositions containing 12-hydroxystearic acid and ethoxylated hydrogenated castor oil
EA025588B1 (en) * 2011-02-17 2017-01-30 Унилевер Н.В. Leave-on non-solid skin conditioning composition which has a continuous oil phase and contains 12-hydroxystearic acid
WO2012110276A1 (en) 2011-02-17 2012-08-23 Unilever Plc Leave -on non- solid skin conditioning composition which has a continuous phase and contains 12 - hydroxystearic acid
WO2013068345A2 (en) 2011-11-11 2013-05-16 Unilever Plc Organogel structured with 12-hsa and a selected copolymer
US9744109B2 (en) 2012-12-20 2017-08-29 Conopco. Inc. Eutectic mixtures in personal care compositions
EA028959B1 (en) * 2012-12-20 2018-01-31 Юнилевер Н.В. Eutectic mixtures in personal care compositions
WO2014095257A1 (en) * 2012-12-20 2014-06-26 Unilever N.V. Eutectic mixtures in personal care compositions
US10172772B2 (en) * 2013-01-31 2019-01-08 KGK Science, Inc. Methods of skin whitening by use of canola extracts
US11896696B2 (en) 2013-01-31 2024-02-13 1242753 Ontario Inc. Methods of skin whitening by use of canola extracts
US9597271B2 (en) 2013-10-24 2017-03-21 The Procter & Gamble Company Cosmetic compositions and methods
US10660836B2 (en) 2015-12-22 2020-05-26 Conopco, Inc. Hydroxy functionalized solvent based skin benefit composition
CN116056684A (en) * 2020-07-30 2023-05-02 联合利华知识产权控股有限公司 Personal care compositions comprising atractylenolide-I or a source of atractylenolide-I
US20220202670A1 (en) * 2020-12-30 2022-06-30 Galaxy Surfactants Ltd. Personal and home care compositions comprising fatty acids from tung seed oil as antimicrobial preservative

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