CA2589044A1 - Personal care compositions containing hydrophobically modified non-platelet particles - Google Patents

Personal care compositions containing hydrophobically modified non-platelet particles Download PDF

Info

Publication number
CA2589044A1
CA2589044A1 CA002589044A CA2589044A CA2589044A1 CA 2589044 A1 CA2589044 A1 CA 2589044A1 CA 002589044 A CA002589044 A CA 002589044A CA 2589044 A CA2589044 A CA 2589044A CA 2589044 A1 CA2589044 A1 CA 2589044A1
Authority
CA
Canada
Prior art keywords
skin
weight percent
composition according
composition
benefit agent
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.)
Granted
Application number
CA002589044A
Other languages
French (fr)
Other versions
CA2589044C (en
Inventor
Rebecca Ann Taylor
Mannie Lee Clapp
Ching Stella
John Christopher Wesner
Cynthia Ann Garza
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.)
Procter and Gamble Co
Original Assignee
The Procter & Gamble Company
Rebecca Ann Taylor
Mannie Lee Clapp
Ching Stella
John Christopher Wesner
Cynthia Ann Garza
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 The Procter & Gamble Company, Rebecca Ann Taylor, Mannie Lee Clapp, Ching Stella, John Christopher Wesner, Cynthia Ann Garza filed Critical The Procter & Gamble Company
Publication of CA2589044A1 publication Critical patent/CA2589044A1/en
Application granted granted Critical
Publication of CA2589044C publication Critical patent/CA2589044C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • 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
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/29Titanium; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations

Abstract

A rinsable personal care composition includes (a) 0 to 75 weight percent of a composition surfactant; (b) 0.01 to 99 weight percent of a skin benefit agent or emollient; (c) 0.01 to 20 weight percent of a hydrophobically modified non-platelet particle; and (d) 0 to 99 % water.

Description

PERSONAL CARE COMPOSITIONS CONTAINING HYDROPHOBICALLY
MODIFIED NON-PLATELET PARTICLES
FIELD OF THE INVENTION
The present invention relates to the field of personal care compositions for improving appearance and feel of keratinous surfaces. More specifically, the present invention relates to rinsable personal care compositions that provide excellent skin appearance, skin moisturization and conditioning.
BACKGROUND OF THE INVENTION
Personal care compositions are well known and widely used. These compositions have long been employed to cleanse and moisturize skin, deliver actives, hide imperfections and to reduce the oiliness/shine associated with sebum. Personal care compositions have also been used to alter the color and appearance of skin.

These compositions generally incorporate organic or inorganic particulate material to reduce the shine or redness of skin, to also cover over skin imperfections such as wrinkles, and even to provide cosmetic effects such as whitening or darkening.
For example, the use of TiO2 as a skin whitening agent has been known since ancient times, and the formulator's chemical library is replete with pigments which can be blended to produce an almost arbitrary range of colors to skin. Other particles, such as silicas and silicone resins can produce a mattifying effect on skin, reducing the appearance of fine lines and wrinkles.

Recently, advances have been disclosed in the art in depositing from rinse-off products a specific class of effect particles based on a platelet shape. When particles are present as platelets, they produce a higher degree of specular reflectance and tend to lend a shiny appearance to skin. While this may often be desired, it is also desirable to provide visual benefits to skin from particles that are non-platelet in shape, that do not have a shiny appearance on the skin surface.

While the compositions and disclosures of the prior art provide useful advances in the art of personal care compositions, there remains the need for improved rinse off compositions that deliver immediate improvements in appearance and skin feel that will effectively deposit on all parts of the body. The compositions also need to be non-greasy and easy to apply. Therefore, it is desirable to provide a topical rinse off composition comprising a select level and blend of non-platelet particles to provide a unique level of skin appearance change across all skin types. It is also desirable to provide personal care compositions that effectively provide skin moisturization. It is further desirable to deliver the above skin conditioning and appearance benefits via an in-the-shower or in-the-bath lotion. Unfortunately, in the shower/bath, moisturizers are often readily rinsed from the skin. This is particularly true when surfactant is present. Therefore a need still exists for compositions that can effectively deposit appearance and skin feel particles in a rinse-off environment.
SUMMARY OF THE INVENTION

The present invention relates to a rinsable personal care composition comprises (a) 0 to 75 weight percent of a composition surfactant; (b) 0.01 to 99 weight percent of a skin benefit agent or emollient;(c) 0.01 to 20 weight percent of a hydrophobically modified non-platelet particle; and (d) 0 to 99% water.

DETAILED DESCRIPTION OF THE INVENTION
All percentages and ratios used herein are by weight of the total composition and all measurements made are at 25 C, unless otherwise designated.
The term "amphoteric surfactant," as used herein, is also intended to encompass zwitterionic surfactants, which are well known to formulators skilled in the art as a subset of amphoteric surfactants.

The term "dermatologically-acceptable," as used herein, means that the compositions or components thereof so described are suitable for use in contact with human skin without undue toxicity, incompatibility, instability, allergic response, and the like.

The term "diameter" as used herein, means the largest distance across the major axis of the particulate material. Diameter can be determined by any suitable method known in the art, such as particle size analyzer Mastersizer 2000 manufactured by Malvern Instruments.

The term "gel-network" as used herein, means an emulsifying system comprised of fatty alcohol and a hydrophilic surfactant.
The term "hydrophobically modified interference pigment" or "HMIP", as used herein, means a portion of the interference pigment surface has been coated with a hydrophobic material.
The term "interference pigment", as used herein, means a pigment with pearl gloss prepared by coating the surface of a particle substrate material (generally platelet in shape) with a thin film. The thin film is a transparent or semitransparent material having a high refractive index. The higher refractive index material shows a pearl gloss resulting from mutual interfering action between reflection and incident light from the platelet substrate/coating layer interface and reflection of incident light from the surface of the coating layer.

As used, herein "Non-platelet particle," refers to any shape of a particle in the personal care composition differing from the platelet shape including configurations but not limited to spherical, cylindrical configuration, rectangular, triangular, trapezoidal, semi-circular, hourglass, or irregular shapes. The non-platlet particles may have an aspect ratio define by A/B = or >0.20, the length A and the width being B, more preferably greater than 0.25, even more preferably greater than 0.3 The term, "personal care composition" as used herein refers to unless otherwise specified, refers to the compositions of the present invention, wherein the compositions are intended to include compositions for topical application to the skin or hair.
The term "rinsable composition" as used herein, means a composition designed to be rinsed off by a liquid such as water. After the composition is rinsed off, pigments are deposited on the skin and the skin radiance is realized.

The term "safe and effective amount" as used herein means an amount of a compound, component, or composition sufficient to significantly induce a positive benefit, preferably a positive skin appearance or feel benefit, including independently the benefits disclosed herein, but low enough to avoid serious side effects, i.e., to provide a reasonable benefit to risk ratio, within the scope of sound medical judgment.
A "skin compatible oil" as defined herein, is an oil that is liquid or semi-solid at the temperature at which bathing is carried out that is deemed safe for use in cosmetics being either inert to the skin or actually beneficial.
The term "topical application", as used herein, means to apply or spread the compositions of the present invention onto the surface of the skin.
Active and other ingredients useful herein may be categorized or described herein by their cosmetic and/or therapeutic benefit or their postulated mode of action. However, it is to be understood that the active and other ingredients useful herein can in some instances provide more than one cosmetic and/or therapeutic benefit or operate via more than one mode of action. Therefore, classifications herein are made for the sake of convenience and are not intended to limit an ingredient to the particularly stated application or applications listed.

A. Composition surfactant The rinsable personal care composition of the present invention comprises 0 to weight percent of a composition surfactant. A wide variety of composition surfactants can be useful herein, both for emulsification of the dispersed phase as well as to provide acceptable spreading and in use properties for non-lathering systems. For cleansing applications, the surfactant phase also serves to clean the skin and provide an acceptable amount of lather for the user. The composition preferably contains no more than about 50 weight percent of a surfactant, more preferably no more than about 30 weight percent, still more preferably no more than about 15 weight percent, and even more preferably no more than about 5 weight percent of a surfactant. The composition preferably contains at least about 5 weight percent of a surfactant, more preferably at least about 3 weight percent, still more preferably at least about 1 weight percent, and even more preferably at least about 0.1 weight percent of a surfactant. For cleansing applications the personal care compositions preferably produces a Total Lather Volume of at least 300 ml, more preferably greater than 600ml as described in the Lathering Volume Test. The personal care compositions preferably produces a Flash Lather Volume of at least 100 ml, preferably greater than 200ml, more preferably greater than 300m1 as described in the Lathering Volume Test.

Preferable surfactants include those selected from the group consisting of anionic surfactants, nonionic surfactants, amphoteric surfactants, non-lathering surfactants, emulsifiers and mixtures thereof. Non-limiting examples of surfactants useful in the compositions of the present invention are disclosed in U.S. Pat. No.
6,280,757, to McAtee et al., issued Aug. 28, 2001.

a. Anionic Surfactants Non-limiting examples of anionic surfactants useful in the compositions of the 5 present invention are disclosed in McCutcheon's, Detergents and Emulsifiers, North American edition (1986), published by allured Publishing Corporation;
McCutcheon's, Functional Materials, North American Edition (1992); and U.S. Pat. No.
3,929,678, to Laughlin et al., issued Dec. 30, 1975.

A wide variety of anionic surfactants are useful herein. Non-limiting examples of anionic surfactants include those selected from the group consisting of sarcosinates, sulfates, isethionates, taurates, phosphates, lactylates, glutamates, and mixtures thereof.
Amongst the isethionates, the alkoyl isethionates are preferred, and amongst the sulfates, the alkyl and alkyl ether sulfates are preferred.

Other anionic materials useful herein are fatty acid soaps (i.e., alkali metal salts, e.g., sodium or potassium salts) typically having from a fatty acid having about 8 to about 24 carbon atoms, preferably from about 10 to about 20 carbon atoms. These fatty acids used in making the soaps can be obtained from natural sources such as, for instance, plant or animal-derived glycerides (e.g., palm oil, coconut oil, soybean oil, castor oil, tallow, lard, etc.) The fatty acids can also be synthetically prepared. Soaps and their preparation are described in detail in U.S. Pat. No. 4,557,853.

Other anionic materials include phosphates such as monoalkyl, dialkyl, and trialkylphosphate salts. Non-limiting examples of preferred anionic lathering surfactants useful herein include those selected from the group consisting of sodium lauryl sulfate, ammonium lauryl sulfate, ammonium laureth sulfate, sodium laureth sulfate, sodium trideceth sulfate, ammonium cetyl sulfate, sodium cetyl sulfate, ammonium cocoyl isethionate, sodium lauroyl isethionate, sodium lauroyl lactylate, triethanolamine lauroyl lactylate, sodium caproyl lactylate, sodium lauroyl sarcosinate, sodium myristoyl sarcosinate, sodium cocoyl sarcosinate, sodium lauroyl methyl taurate, sodium cocoyl methyl taurate, sodium lauroyl glutamate, sodium myristoyl glutamate, and sodium cocoyl glutamate and mixtures thereof.
Especially preferred for use herein is ammonium lauryl sulfate, ammonium laureth sulfate, sodium lauroyl sarcosinate, sodium cocoyl sarcosinate, sodium myristoyl sarcosinate, sodium lauroyl lactylate, and triethanolamine lauroyl lactylate.
b. Non-ionic Surfactants Non-limiting examples of nonionic surfactants for use in the compositions of the present invention are disclosed in McCutcheon's, Detergents and Emulsifiers, North American edition (1986), published by allured Publishing Corporation; and McCutcheon's, Functional Materials, North American Edition (1992).
Nonionic surfactants useful herein include those selected from the group consisting of alkyl glucosides, alkyl polyglucosides, polyhydroxy fatty acid amides, alkoxylated fatty acid esters, sucrose esters, amine oxides, and mixtures thereof.

Non-limiting examples of preferred nonionic surfactants for use herein are those selected form the group consisting of C8-C14 glucose amides, C8-C14 alkyl polyglucosides, sucrose cocoate, sucrose laurate, lauramine oxide, cocoamine oxide and mixtures thereof.
c. Amphoteric Surfactants A wide variety of amphoteric lathering surfactants can be used in the compositions of the present invention. Particularly useful are those which are broadly described as derivatives of aliphatic secondary and tertiary amines, preferably wherein the nitrogen is in a cationic state, in which the aliphatic radicals can be straight or branched chain and wherein one of the radicals contains an ionizable water solubilizing group, e.g., carboxy, sulfonate, sulfate, phosphate, or phosphonate.

Non-limiting examples of amphoteric surfactants useful in the compositions of the present invention are disclosed in McCutcheon's, Detergents and Emulsifiers, North American edition (1986), published by allured Publishing Corporation; and McCutcheon's, Functional Materials, North American Edition (1992).
Non-limiting examples zwitterionic surfactants are those selected from the group consisting of betaines, sultaines, hydroxysultaines, alkyliminoacetates, imninodialkanoates, aminoalkanoates, and mixtures thereof.

Preferred surfactants for use herein are the following, wherein the anionic surfactant is selected from the group consisting of ammonium lauroyl sarcosinate, sodium trideceth sulfate, sodium lauroyl sarcosinate, ammonium laureth sulfate, sodium laureth sulfate, ammonium lauryl sulfate, sodium lauryl sulfate, ammonium cocoyl isethionate, sodium cocoyl isethionate, sodium lauroyl isetlionate, sodium cetyl sulfate, sodium lauroyl lactylate, triethanolamine lauroyl lactylate, and mixtures thereof, wherein the non-ionic surfactant is selected from the group consisting of lauramine oxide, cocoamine oxide, decyl polyglucose, lauryl polyglucose, sucrose cocoate, C12_14 glucosamides, sucrose laurate, and mixtures thereof; and wherein the amphoteric surfactant is selected from the group consisting of disodium lauroamphodiacetate, sodium lauroamphoacetate, cetyl dimethyl betaine, cocoamidopropyl betaine, cocoamidopropyl hydroxy sultaine, and mixtures thereof.

d. Non-Lathering Surfactants A wide variety of non-lathering surfactants are useful herein. The composition of the present invention can comprise a sufficient amount of one or more non-lathering surfactants to emulsify the dispersed phase to yield an appropriate particle size and good application properties on wet skin.

Nonlimiting examples of these non-lathering compositions are: polyethylene glycol 20 sorbitan monolaurate (Polysorbate 20), polyethylene glycol 5 soya sterol, Steareth-20, Ceteareth-20, PPG-2 methyl glucose ether distearate, Ceteth-l0, Polysorbate 80, cetyl phosphate, potassium cetyl phosphate, diethanolamine cetyl phosphate, Polysorbate 60, glyceryl stearate, PEG-100 stearate, polyoxyethylene 20 sorbitan trioleate (Polysorbate 85), sorbitan monolaurate, polyoxyethylene 4 lauryl ether sodium stearate, polyglyceryl-4 isostearate, hexyl laurate, steareth-20, ceteareth-20, PPG-2 methyl glucose ether distearate, ceteth-10, diethanolamine cetyl phosphate, glyceryl stearate, PEG-100 stearate, and mixtures thereof.

e. Emulsifier systems In addition, there are several commercial emulsifier mixtures that are useful in some embodiments. Examples include but are not limited to PROLIPID 141 (glyceryl stearate, behenyl alcohol, palmitic acid, stearic acid, lecithin, lauryl alcohol, myristyl alcohol and cetyl alcohol) and 151 (Glyceryl stearate, cetearyl alcohol, stearic acid, 1-propanamium, 3-amino-N-(2-(hydroxyethyl)-N-N-Dimethyl,N-C(16-18) Acyl Derivatives, Chlorides) from ISP; POLAWAX NF (Emulsifying wax NF), INCROQUAT
BEHENYL TMS (behentrimonium sulfate and cetearyl alcohol) from Croda; and EMULLIUM DELTA (cetyl alcohol, glyceryl stearate, peg-75 stearate, ceteth-20 and steareth-20) from Gattefosse. The emulsifier systems used in conjunction with the present invention should not be limited to those disclosed in the specification, one skilled could use any emulsifier system know in the art keeping in mind the personal care composition of the present invention.

B. Skin benefit agent or emollient The compositions of the present invention comprise 0.01 to 99 weight percent of a skin benefit agent or emollient. The skin benefit agent or emollient comprises a skin compatible oil, gel, or wax, or mixtures thereof. By definition, the skin benefit agent or emollient will have negligible solubility in any aqueous phase and may be present as discrete particles in the composition. The skin benefit agent or emollient preferably comprises no more than about 99 weight percent of the composition, more preferably no more than about 70 weight percent, still more preferably no more than about 60 weight percent, and still more preferably no more than about 50 weight percent of the composition. The skin benefit agent or emollient preferably comprises at least about 0.01 weight percent, more preferably at least about 5 weight percent, even more preferably at least about 7 weight percent, and still more preferably at least 10% of the composition.
The shear index is a measure of how shear thinning the materials are as described in the Lipid Rheology method described herein. It is preferred that the skin compatible oil be shear thinning either by virtue of its composition or the structurants that may be added.
Preferably, the shear index of the skin benefit agent or emollient will preferably be less than 0.9, more preferably less than 0.75, even more preferably less than 0.6, even more preferably less than 0.5, and still more preferably less than 0.4.

The most useful skin compatible oils for the present invention include ester oils, hydrocarbon oils, and silicone oils.
Ester oils, as the name implies, have at least one ester group in the molecule. One type of common ester oil useful in the present invention are the fatty acid mono and polyesters such as cetyl octanoate, octyl isonanoanate, myristyl lactate, cetyl lactate, isopropyl myristate, myristyl myristate, diisopropyl sebacate, diisotearyl malate, isostearyl neopentanoate, isopropyl palmitate, isopropyl adipate, butyl stearate, decyl oleate, cholesterol isostearate, glycerol monostearate, glycerol distearate, glycerol tristearate, alkyl lactate, alkyl citrate and alkyl tartrate; sucrose ester and polyesters, sorbitol ester, and the like.

A second type of useful ester oil is predominantly comprised of triglycerides and modified triglycerides. These include vegetable oils such as jojoba, soybean, canola, sunflower, safflower, rice bran, avocado, almond, olive, sesame, persic, castor, coconut, and mink oils. Synthetic triglycerides can also be employed. Modified triglycerides include materials such as ethoxylated and maleated triglyceride derivatives provided they are liquids. Proprietary ester blends such as those sold by Finetex as Finsolv are also suitable, as is ethylhexanoic acid glyceride.

A third type of ester oil is liquid polyester formed from the reaction of a dicarboxylic acid and a diol. Examples of polyesters suitable for the present invention are the polyesters marketed by ExxonMobil under the trade name PURESYN ESTER®

A second class of skin compatible oils suitable for the present invention is liquid and semi-solid hydrocarbons. These include linear and branched oils such as liquid paraffin, squalene, squalane, mineral oil, low viscosity synthetic hydrocarbons such as polyalphaolefin sold by ExxonMobil under the trade name of PURESYN PAO and polybutene under the trade name PANALANE or INDOPOL. Light (low viscosity) highly branched hydrocarbon oils are also suitable.

Petrolatum is a unique hydrocarbon material and a useful component of the present invention. Its semi-solid nature can be controlled both in production and by the formulator through blending with other oils.
A third class of useful skin compatible oils is silicone based. They include linear and cyclic polydimethyl siloxane, organo functional silicones (alkyl and alkyl aryl), and amino silicones.

The personal care compositions of the present invention may optionally further comprise a skin benefit agent suitable for use on the skin, and which is otherwise compatible with the other selected ingredients in the composition. The skin benefit agent can be blended with the oils previously described and included as part of the main high internal phase emulsion. In this case the oil functions as a carrier for the skin benefit agent. The skin benefit agent may also be included as part of a separate high internal phase emulsion. The skin benefit agent may also be included as an add-on ingredient wherein it is not part of any of the high internal phase emulsion premixes.
Non-limiting examples of skin benefit agents suitable for use herein are described in The CTFA Cosmetic Ingredient Handbook, Second Edition (1992), which includes a 5 wide variety of cosmetic and pharniaceutical ingredients commonly used in the skin care industry, and which are suitable for use in the compositions of the present invention.
Non-limiting examples of such skin benefit agents include abrasives, absorbents, aesthetic components such as fragrances, pigments, colorings/colorants, essential oils, skin sensates, astringents, etc. (e.g., clove oil, menthol, camphor, eucalyptus oil, eugenol, 10 menthyl lactate, witch hazel distillate), anti-acne agents, anti-caking agents, antimicrobial agents (e.g., iodopropyl butylcarbamate), antioxidants, colorants, cosmetic astringents, cosmetic biocides, drug astringents, external analgesics, opacifying agents, pH adjusters, skin bleaching and lightening agents (e.g., hydroquinone, kojic acid, ascorbic acid, magnesium ascorbyl phosphate, ascorbyl glucosamine), skin-conditioning and/or moisturizing agents, i.e. glycerine and other humectants, skin soothing and/or healing agents (e.g., panthenol and derivatives (e.g., ethyl panthenol), aloe vera, pantothenic acid and its derivatives, allantoin, bisabolol, and dipotassium glycyrrhizinate), retinoids, (e.g.
retinol palmitate), tocopheryl nicotinate, skin treating agents, vitamins and derivatives thereof. In any embodiment of the present invention, however, the actives useful herein can be categorized by the benefit they provide or by their postulated mode of action.
However, it is to be understood that the actives useful herein can in some instances provide more than one benefit or operate via more than one mode of action.
Therefore, classifications herein are made for the sake of convenience and are not intended to limit the active to that particular application or applications listed. The skin benefit agents are furthered described hereinafter in details.
A) Desquamation Actives The skin benefit agent for use herein can include desquamation actives, preferred concentrations of which range from about 0.1% to about 10%, more preferably from about 0.2% to about 5%, even more preferably from about 0.5% to about 4%, by weight of the composition for non-surfactant containing actives and from about 0.1%
to about 3%, more preferably from about 0.2% to about 3%, even more preferably from about 0.5% to about 3% for surfactant containing actives. Desquamation actives enhance the skin appearance benefits of the present invention. For example, the desquamation actives tend to improve the texture of the skin (e.g., smoothness). One desquamation system that is suitable for use herein contains sulfhydryl compounds and zwitterionic surfactants and is described in U.S. Patent No. 5,681,852, to Bissett.

Another desquamation system that is suitable for use herein contains salicylic acid and zwitterionic surfactants and is described in U.S. Patent No. 5,652,228 to Bissett.
B) Anti-Acne Actives The skin benefit agent for use herein can also include anti-acne actives, preferred concentrations of which range from about 0.01 % to about 50%, more preferably from about 1% to about 20%, by weight of the composition. Non-limiting examples of anti-acne actives suitable for use herein include resorcinol, sulfur, salicylic acid, benzoyl peroxide, erythromycin, zinc, and other similar materials.

Other non-limiting examples of suitable anti-acne actives for use herein are described in U. S. Patent No. 5,607,980, issued to McAtee et al, which description is incorporated herein by reference.

C) Anti-Wrinkle Actives/Anti-Atrophy Actives The skin benefit agent for use herein can also include anti-wrinkle actives or anti-atrophy actives, including sulfur-containing D and L amino acids and their derivatives and salts, particularly the N-acetyl derivatives, a preferred example of which is N-acetyl-L-cysteine; thiols, e.g. ethane thiol; hydroxy acids (e.g., alpha-hydroxy acids such as lactic acid and glycolic acid or beta-hydroxy acids such as salicylic acid and salicylic acid derivatives such as the octanoyl derivative), phytic acid, lipoic acid;
lysophosphatidic acid, and skin peel agents (e.g., phenol and the like). Also suitable is niacinamide.

Hydroxy acids as skin benefit agents herein include salicylic acid and salicylic acid derivatives, preferred concentrations of which range from about 0.01 % to about 50%, more preferably from about 0.1% to about 10%, even more preferably from about 0.5% to about 2%, by weight of the composition.

Other non-limiting examples of suitable anti-wrinkle actives for use herein are described in U. S. Patent No. 6,217,888, issued to Oblong et al.
D) Anti-Oxidants/Radical Scavengers The skin benefit agent for use herein can also include anti-oxidants or radical scavengers, preferred concentrations of which range from about 0.1 % to about 10%, more preferably from about 1% to about 5%, by weight of the composition.

Non-limiting examples of anti-oxidants or radical scavengers for use herein include ascorbic acid and its salts, ascorbyl esters of fatty acids, ascorbic acid derivatives (e.g., magnesium ascorbyl phosphate, sodium ascorbyl phosphate, ascorbyl sorbate), tocopherol, tocopherol acetate, other esters of tocopherol, butylated hydroxy benzoic acids and their salts, 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (commercially available under the tradename Trolox ), gallic acid and its alkyl esters, especially propyl gallate, uric acid and its salts and alkyl esters, sorbic acid and its salts, lipoic acid, amines (e.g., N,N-diethylhydroxylamine, amino-guanidine), sulfhydryl compounds (e.g., glutathione), dihydroxy fumaric acid and its salts, lycine pidolate, arginine pilolate, nordihydroguaiaretic acid, bioflavonoids, curcumin, lysine, methionine, proline, superoxide dismutase, silymarin, tea extracts, grape skin/seed extracts, melanin, and rosemary extracts may be used.-E) Chelators The skin benefit agent for use herein can also include chelating agents. As used herein, the term "chelating agent" or "chelator" refers to those skin benefit agents capable of removing a metal ion from a system by forming a complex so that the metal ion cannot readily participate in or catalyze chemical reactions.

The chelating agents as skin benefit agents for use herein are preferably formulated at concentrations ranging from about 0.1 % to about 10%, more preferably from about 1% to about 5%, by weight of the composition. Non-limiting examples of suitable chelating agents are described in U.S. Patent No. 5,487,884, issued 1/30/96 to Bissett et al.; International Publication No. 91/16035, Bush et al., published 10/31/95; and International Publication No. 91/16034, Bush et al., published 10/31/95.

Preferred chelating agents for use in the active phase of the compositions of the present invention include furildioxime, furilmonoxime, and derivatives thereof.
F) Flavonoids The skin benefit agent for use herein includes flavonoid compounds suitable for use on the hair or skin, preferred concentrations of which range from about 0.01% to about 20%, more preferably from about 0.1% to about 10%, more preferably from about 0.5% to about 5%, by weight of the composition.
Non-limiting examples of flavonoids compounds suitable for use as skin benefit agents include flavanones such as unsubstituted flavanones, mono-substituted flavanones, and mixtures thereof; chalcones selected from unsubstituted chalcones, mono-substituted chalcones, di-substituted chalcones, tri-substituted chalcones, and mixtures thereof;
flavones selected from unsubstituted flavones, mono-substituted flavones, di-substituted flavones, and mixtures thereof; one or more isoflavones; coumarins selected from unsubstituted coumarins, mono-substituted coumarins, di-substituted coumarins, and mixtures thereof; chromones selected from unsubstituted chromones, mono-substituted chromones, di-substituted chromones, and mixtures thereof; one or more dicoumarols;
one or more chromanones; one or more chromaiiols; isomers (e.g., cis/trans isomers) thereof; and mixtures thereof. By the term "substituted" as used herein means flavonoids wherein one or more hydrogen atom of the flavonoid has been independently replaced with hydroxyl, C1-C8 alkyl, C1-C4 alkoxyl, 0-glycoside, and the like or a mixture of these substituents.

Examples of suitable flavonoids include, but are not limited to, unsubstituted flavanone, mono-hydroxy flavanones (e.g., 2'-hydroxy flavanone, 6-hydroxy flavanone, 7-hydroxy flavanone, etc.), mono-alkoxy flavanones (e.g., 5-methoxy flavanone, methoxy flavanone, 7-methoxy flavanone, 4'-methoxy flavanone, etc.), unsubstituted chalcone (especially unsubstituted trans-chalcone), mono-hydroxy chalcones (e.g., 2'-hydroxy chalcone, 4'-hydroxy chalcone, etc.), di-hydroxy chalcones (e.g., 2',4-dihydroxy chalcone, 2',4'-dihydroxy chalcone, 2,2'-dihydroxy chalcone, 2',3-dihydroxy chalcone, 2',5'-dihydroxy chalcone, etc.), and tri-hydroxy chalcones (e.g., 2',3',4'-trihydroxy chalcone, 4,2',4'-trihydroxy chalcone, 2,2',4'-trihydroxy chalcone, etc.), unsubstituted flavone, 7,2'-dihydroxy flavone, 3',4'-dihydroxy naphthoflavone, 4'-hydroxy flavone, 5,6-benzoflavone, and 7,8-benzoflavone, unsubstituted isoflavone, daidzein (7,4'-dihydroxy isoflavone), 5,7-dihydroxy-4'-methoxy isoflavone, soy isoflavones (a mixture extracted from soy), unsubstituted coumarin, 4-hydroxy coumarin, 7-hydroxy coumarin, 6-hydroxy-4-methyl coumarin, unsubstituted chromone, 3-formyl chromone, 3-formyl-6-isopropyl chromone, unsubstituted dicoumarol, unsubstituted chromanone, unsubstituted chromanol, and mixtures thereof.

Among these flavanoid compounds, preferred are unsubstituted flavanone, methoxy flavanones, unsubstituted chalcone, 2',4-dihydroxy chalcone, isoflavone, flavone, and mixtures thereof, more preferably soy isoflavones.

Other non-limiting examples of flavanoid compounds suitable for use as skin benefit agents herein are described in U.S. Patents 5,686,082 and 5,686,367.
G) Anti-Inflammatory Agents The skin benefit agent for use in the present composition can include anti-inflammatory agents, preferred concentrations of which range from about 0.1%
to about 10%, more preferably from about 0.5% to about 5%, by weight of the composition.
Non-limiting examples of steroidal anti-inflammatory agents suitable for use herein include corticosteroids such as hydrocortisone, hydroxyltriamcinolone, alpha-methyl dexamethasone, dexamethasone-phosphate, beclomethasone dipropionates, clobetasol valerate, desonide, desoxymethasone, desoxycorticosterone acetate, dexamethasone, dichlorisone, diflorasone diacetate, diflucortolone valerate, fluadrenolone, fluclorolone acetonide, fludrocortisone, flumethasone pivalate, fluosinolone acetonide, fluocinonide, flucortine butylesters, fluocortolone, fluprednidene (fluprednylidene) acetate, flurandrenolone, halcinonide, hydrocortisone acetate, hydrocortisone butyrate, methylprednisolone, triamcinolone acetonide, cortisone, cortodoxone, flucetonide, fludrocortisone, difluorosone diacetate, fluradrenolone, fludrocortisone, diflurosone diacetate, fluradrenolone acetonide, medrysone, amcinafel, amcinafide, betamethasone and the balance of its esters, chloroprednisone, chlorprednisone acetate, clocortelone, clescinolone, dichlorisone, diflurprednate, flucloronide, flunisolide, fluoromethalone, fluperolone, fluprednisolone, hydrocortisone valerate, hydrocortisone cyclopentylpropionate, hydrocortamate, meprednisone, paramethasone, prednisolone, prednisone, beclomethasone dipropionate, triamcinolone, and mixtures thereof may be used. The preferred steroidal anti-inflammatory for use is hydrocortisone.

Nonsteroidal anti-inflammatory agents are also suitable for use herein as skin benefit agents in the active phase of the compositions. Non-limiting examples of non-steroidal anti-inflammatory agents suitable for use herein include oxicams (e.g., piroxicam, isoxicam, tenoxicam, sudoxicam, CP-14,304); salicylates (e.g., aspirin, 5 disalcid, benorylate, trilisate, safapryn, solprin, diflunisal, fendosal);
acetic acid derivatives (e.g., diclofenac, fenclofenac, indomethacin, sulindac, tolmetin, isoxepac, furofenac, tiopinac, zidometacin, acematacin, fentiazac, zomepirac, clindanac, oxepinac, felbinac, ketorolac); fenamates (e.g., mefenamic, meclofenamic, flufenamic, niflumic, tolfenamic acids); propionic acid derivatives (e,g., ibuprofen, naproxen, benoxaprofen, 10 flurbiprofen, ketoprofen, fenoprofen, fenbufen, indopropfen, pirprofen, carprofen, oxaprozin, pranoprofen, miroprofen, tioxaprofen, suprofen, alminoprofen, tiaprofenic);
pyrazoles (e.g., phenylbutazone, oxyphenbutazone, feprazone, azapropazone, trimethazone); and combinations thereof as well as any dermatologically acceptable salts or esters of thereof.
15 Other non-limiting examples of suitable anti-inflammatory or similar other skin benefit agents include candelilla wax, bisabolol (e.g., alpha bisabolol), aloe vera, plant sterols (e.g., phytosterol), Manjistha (extracted from plants in the genus Rubia, particularly Rubia Cordifolia), and Guggal (extracted from plants in the genus Commiphora, particularly Commiphora Mukul), kola extract, chamomile, red clover extract, sea whip extract, and combinations thereof.
Other non-limiting examples of suitable anti-inflammatory or similar other skin benefit agents include compounds of the Licorice (the plant genus/species Glycyrrhiza glabra) family, including glycyrrhetic acid, glycyrrhizic acid, and derivatives thereof (e.g., salts and esters). Suitable salts of the foregoing compounds include metal and ammonium salts. Suitable esters include C2 - C24 saturated or unsaturated esters of the acids, preferably C 10 - C24, more preferably C 16 - C24. Specific non-limiting examples of the foregoing include oil soluble licorice extract, the glycyrrhizic and glycyrrhetic acids themselves, monoammonium glycyrrhizinate, monopotassium glycyrrhizinate, dipotassium glycyrrhizinate, 1-beta-glycyrrhetic acid, stearyl glycyrrhetinate, and 3-stearyloxy-glycyrrhetinic acid, disodium 3-succinyloxy-beta-glycyrrhetinate, and combinations thereof.

H) Anti-Cellulite Agents The skin benefit agent for use in the compositions of the present invention anti-cellulite agents, non-limiting examples of which include xanthine compounds such as caffeine, theophylline, theobromine, aminophylline, and combinations thereof.
I) Topical Anesthetics The skin benefit agent for use in the present invention include topical anesthetics, non-limiting exanlples of which include benzocaine, lidocaine, bupivacaine, chlorprocaine, dibucaine, etidocaine, mepivacaine, tetracaine, dyclonine, hexylcaine, procaine, ketamine, pramoxine, phenol, pharmaceutically acceptable salts thereof, and combinations thereof.

J) Tanning Actives The skin benefit agent for use in the present invention include tanning actives, preferred concentrations of which range from about 0.1 % to about 20% by weight of the composition. Non-limiting examples of such tanning agents include dihydroxyacetone, which is also known as DHA or 1,3-dihydroxy-2-propanone.
K) Skin Li hteningAgents The skin benefit agent for use in the present invention can include skin lightening agents, preferred concentrations of which range from about 0.1 % to about 10%, more preferably from about 0.2% to about 5%, more preferably from about 0.5% to about 2%, by weight of the composition. Non-limiting examples of skin lightening agents suitable for use herein include kojic acid, arbutin, ascorbic acid and derivatives thereof (e.g., magnesium ascorbyl phosphate or sodium ascorbyl phosphate), and extracts (e.g., mulberry extract, placental extract) as well as titanium dioxide and zinc oxide. Non-limiting examples of skin lightening agent~ suitable for use herein also include those described in WO 95/34280, WO 95/07432, and WO 95/23780.
L) Skin Soothing and Skin Healing Actives The skin benefit agent for use in the present invention include skin soothing and skin healing actives, preferred concentrations of which range from about 0.1 %
to about 30%, more preferably from about 0.5% to about 20%, still more preferably from about 0.5% to about 10 %, by weight of the composition. Non-limiting examples of skin soothing or skin healing actives suitable for use herein include panthenoic acid derivatives (e.g., panthenol, dexpanthenol, ethyl panthenol), aloe vera, allantoin, bisabolol, and dipotassiunl glycyrrhizinate.

M) Antimicrobial Actives The skin benefit agent for use in compositions of the present invention may include antimicrobial actives, preferred concentrations of which range from about 0.001%
to about 10%, more preferably from about 0.01% to about 5%, and still more preferably from about 0.05% to about 2%, by weight of the compositions.

Non-limiting examples of antimicrobial actives for use herein includes 13-lactam drugs, quinolone drugs, ciprofloxacin, norfloxacin, tetracycline, erythromycin, amikacin, 2,4,4'-trichloro-2'-hydroxy diphenyl ether, 3,4,4'-trichlorobanilide, phenoxyethanol, phenoxy propanol, phenoxyisopropanol, doxycycline, capreomycin, chlorhexidine, chlortetracycline, oxytetracycline, clindamycin, ethambutol, hexamidine isethionate, metronidazole, pentamidine, gentamicin, kanamycin, lineomycin, methacycline, methenamine, minocycline, neomycin, netilmicin, paromomycin, streptomycin, tobramycin, miconazole, tetracycline hydrochloride, erythromycin, zinc erythromycin, erythromycin estolate, erythromycin stearate, amikacin sulfate, doxycycline hydrochloride, capreomycin sulfate, chlorhexidine gluconate, chlorhexidine hydrochloride, chlortetracycline hydrochloride, oxytetracycline hydrochloride, clindamycin hydrochloride, ethambutol hydrochloride, metronidazole hydrochloride, pentamidine hydrochloride, gentamicin sulfate, kanamycin sulfate, lineomycin hydrochloride, methacycline hydrochloride, methenamine hippurate, methenamine mandelate, minocycline hydrochloride, neomycin sulfate, netilmicin sulfate, paromomycin sulfate, streptomycin sulfate, tobramycin sulfate, miconazole hydrochloride, ketaconazole, amanfadine hydrochloride, amanfadine sulfate, octopirox, parachlorometa xylenol, nystatin, tolnaftate, zinc pyrithione, clotrimazole, and combinations thereof.
N) Sunscreen Actives The skin benefit agent for use in the present invention may comprise a sunscreen active, either organic or inorganic sunscreen actives. Among the inorganic sunscreens useful hererin are metallic oxides such as titanium dioxide having an average primary particle size of from about 15 nm to about 100 nm, zinc oxide having an average primary particle size of from about 15 nm to about 150 nm, zirconium oxide having an average primary particle size of from about 15 nm to about 150 nm, iron oxide having an average primary particle size of from about 15 nm to about 500nm, and mixtures thereof.
The concentration of the sunscreen active for use in the composition preferably ranges from about 0.1% to about 20%, more typically from about 0.5% to about 10%, by weight of the composition. Exact amounts of such sunscreen actives will vary depending upon the sunscreen or sunscreens chosen and the desired Sun Protection Factor (SPF).
A wide variety of conventional organic sunscreen actives are also suitable for use herein, non-limiting examples of which include p-aminobenzoic acid, its salts and its derivatives (ethyl, isobutyl, glyceryl esters; p-dimethylaminobenzoic acid);
anthranilates (i.e., o-amino-benzoates; methyl, menthyl, phenyl, benzyl, phenylethyl, linalyl, terpinyl, and cyclohexenyl esters); salicylates (amyl, phenyl, octyl, benzyl, menthyl, glyceryl, and di-pro-pyleneglycol esters); cinnamic acid derivatives (menthyl and benzyl esters, a-phenyl cinnamonitrile; butyl cinnamoyl pyruvate); dihydroxycinnamic acid derivatives (umbelliferone, methylumbelliferone, methylaceto-umbelliferone); trihydroxy-cinnamic acid derivatives (esculetin, methylesculetin, daphnetin, and the glucosides, esculin and daphnin); hydrocarbons (diphenylbutadiene, stilbene); dibenzalacetone and benzalacetophenone; naphtholsulfonates (sodium salts of 2-naphthol-3,6-disulfonic and of 2-naphthol-6,8-disulfonic acids); di-hydroxynaphthoic acid and its salts; o-and p-hydroxybiphenyldisulfonates; coumarin derivatives (7-hydroxy, 7-methyl, 3-phenyl);
diazoles (2-acetyl-3-bromoindazole, phenyl benzoxazole, methyl naphthoxazole, various aryl benzothiazoles); quinine salts (bisulfate, sulfate, chloride, oleate, and tannate);
quinoline derivatives (8-hydroxyquinoline salts, 2-phenylquinoline); hydroxy-or methoxy-substituted benzophenones; uric and violuric acids; tannic acid and its derivatives (e.g., hexaethylether); (butyl carbotol) (6-propyl piperonyl) ether;
hydroquinone; benzophenones (oxybenzene, sulisobenzone, dioxybenzone, benzoresorcinol, 2,2',4,4'-tetrahydroxybenzophenone, 2,2'-dihydroxy-4,4'-dimethoxybenzophenone, octabenzone; 4-isopropyldibenzoylmethane;
butylmethoxydibenzoylmethane; etocrylene; octocrylene; [3-(4'-methylbenzylidene bornan-2-one), terephthalylidene dicamphor sulfonic acid and 4-isopropyl-di-benzoylmethane. Among these sunscreens, preferred are 2-ethylhexyl-p-methoxycinnamate (commercially available as PARSOL MCX), 4,4'-t-butyl methoxydibenzoyl-methane (commercially available as PARSOL 1789), 2-hydroxy-4-methoxybenzophenone, octyldimethyl-p-aminobenzoic acid, digalloyltrioleate, 2,2-dihydroxy-4-methoxybenzophenone, ethyl-4-(bis(hydroxy-propyl))aminobenzoate, 2-ethylhexyl-2-cyano-3,3-diphenylacrylate, 2-ethylhexyl-salicylate, glyceryl-p-aminobenzoate, 3,3,5-tri-methylcyclohexylsalicylate, methylanthranilate, p-dimethyl-aminobenzoic acid or aminobenzoate, 2-ethylhexyl-p-dimethyl-amino-benzoate, 2-phenylbenzimidazole-5-sulfonic acid, 2-(p-dimethylaminophenyl)-5-sulfonicbenzoxazoic acid, octocrylene and combinations thereof.

Non-limiting examples of other sunscreen actives suitable for use herein include those described in U.S. Patent No. 4,937,370 issued to Sabatelli on June 26, 1990, and U.S. Patent No. 4,999,186 issued to Sabatelli & Spirnak on March 12, 1991.
Among those sunscreen actives described, preferred are 4-N,N-(2-ethylhexyl)methyl-aminobenzoic acid ester of 2,4-dihydroxybenzophenone; N,N-di-(2-ethylhexyl)-4-aminobenzoic acid ester with 4-hydroxydibenzoylmethane; 4-N,N-(2-ethylhexyl)methyl-aminobenzoic acid ester with 4-hydroxydibenzoylmethane; 4-N,N-(2-ethylhexyl)methyl-aminobenzoic acid ester of 2-hydroxy-4-(2-hydroxyethoxy)benzophenone; 4-N,N-(2-ethylhexyl)-methylaminobenzoic acid ester of 4-(2-hydroxyethoxy)dibenzoylmethane;
N,N-di-(2-ethylhexyl)-4-aminobenzoic acid ester of 2-hydroxy-4-(2-hydroxyethoxy)benzophenone; and N,N-di-(2-ethylhexyl)-4-aminobenzoic acid ester of 4-(2-hydroxyethoxy)dibenzoylmethane and mixtures thereof. Especially preferred sunscreen actives include 4,4'-t-butylmethoxydibenzoylmethane, 2-ethylhexyl-p-methoxycinnamate, phenyl benzimidazole sulfonic acid, and octocrylene.
0) Visual Skin Enhancers The skin benefit agent for use in compositions of the present invention may include visual skin enhancement ingredients. These include ingredients that mask the appearance of any number of skin imperfections such as age spot, fine lines, wrinkles, blemishes etc., including but not limited to titanium dioxide, zinc oxide and iron oxides.
Also suitable for use herein are organic particulates that diffuse light when deposited on the skin. Preferred concentrations of these ingredients range from about 0.001% to about 10%, more preferably from about 0.01% to about 5%, and still more preferably from about 0.05% to about 2%, by weight of the compositions.

C. Hydrophobically modified non-platelet particle 5 The rinsable personal care composition of the present invention comprises from 0.01 to 20 weight percent of a hydrophobically modified non-platelet particle.
The non-platelet particles of the personal care compositions preferably comprises no more than about 20 weight percent of the composition, more preferably no more than about weight percent, even more preferably no more than about 7 weight percent, and still more 10 preferably no more than about 5 weight percent of the personal care composition. The non-platelet particles of the personal care composition preferably comprises at least about 0.01 weight percent of the personal care composition, more preferably at least about 0.05 weight percent, even more preferably at least about 0.1 weight percent, and still more preferably at least about 0.25 by weight of the composition.

15 Examples of particles which can be used in their hydrophobically modified state include but are not limited to those derived from a wide variety of materials including those derived from inorganic, organic, natural, and synthetic sources, provided that they meet the non-platelet shape requirement. Non-limiting examples of these materials include those selected from the group consisting of almond meal, alumina, aluminum 20 oxide, titanium dioxide, sodium stearate, stearic acid, zinc stearate, aluminum silicate, apricot seed powder, aftapulgite, barley flour, bismuth oxychloride, boron nitride, calcium carbonate, calcium phosphate, calcium pyrophosphate, calcium sulfate, cellulose, chalk, chitin, clay, corn cob meal, corn cob powder, corn flour, corn meal, corn starch, diatomaceous earth, dicalcium phosphate, dicalcium phosphate dihydrate, fullers earth, hydrated silica, hydroxyapatite, iron oxide, jojoba seed powder, kaolin, loofah, magnesium trisilicate, mica, microcrystalline cellulose, montmorillonite, oat bran, oat flour, oatmeal, peach pit powder, pecan shell powder, polybutylene, polyethylene, polyisobutylene, polymethylstyrene, polypropylene, polystyrene, polyurethane, nylon, teflon (i.e. polytetrafluoroethylene), polyhalogenated olefins, pumice rice bran, rye flour, sericite, silica, silk, sodium bicarbonate, sodium silicoaluminate, soy flour synthetic hectorite, talc, tin oxide, titanium dioxide, tricalcium phosphate, walnut shell powder, wheat bran, wheat flour, wheat starch, zirconium silicate, and mixtures thereof. Also useful are micronized particles made from mixed polymers (e.g., copolymers, terpolymers, etc.), such as polyethylene/polypropylene copolymer, polyethylene/propylene/isobutylene copolymer, polyethylene/styrene copolymer, and the like.
The particle size is determined by measuring the diameter thickness of the particulate material through traditional means such as light scattering. The non-platelet particle of the personal care compositions preferably have an average diameter not greater than about 200 m, more preferably not greater than 100 m, even more preferably not greater than about 80 m, still more preferably not greater than than about 60 m. The non-platelet particle of the personal care compositions preferably have a diameter of at least about 0.01 m, more preferably at least about 0.05 gm, even more preferably at least about 0.1 gm, and still more preferably at least about 0.2 m.
When particles are applied and rinsed as described in the Particle Deposition Tape Strip Method (below), the deposited particle on the skin is at least 0.5 g/cm2, more preferably at least 1 g/cm2, and most preferably at least 5 g/cm2.
In an embodiment of the present invention the non-platelet particle is either hydrophobic or has been hydrophobically modified. The Particle Contact Angle Test of the present invention is used to determine contact angle of non-platelet particles. The greater the contact angle, the greater the hydrophobicity of the non-platelet particle. The non-platelet particle of the present invention possess a contact angle of at least 60 , more preferably greater than 80 , even more preferably greater than 100 , still more preferably greater than 110 , even still more preferably greater than 120 , even still even more preferably greater than 130 , even still even more preferably greater than 135 . The hydrophobically modified non-platelet particle or HMNPP allows for the entrapment of the HMNPP within the dispersed phase and greater deposition of the HMNPP. In a preferred embodiment of the present invention, the invention contains both HMNPPs and a dispersed oil phase. Preferably the ratio of HMNPP to skin benefit agent or emollient is 1:1 to about 1:100 more preferably 1:2 to about 1:80, still more preferably 1:3 to about 1:70 and most preferably 1:7 to about 1:60.
The HMNPP of the present invention preferably has a hydrophobic coating comprising no more than about 20 weight percent of the total particle weight, more preferably no more than about 15 weight percent, even more preferably no more than about 10 weight percent, even more preferably no more than 5 weight percent and even more preferably no more than 2 weight percent. The HMNPP of the present invention preferably has a hydrophobic coating comprising at least about 0.1 weight percent of the total particle weight, more preferably at least about 0.5 weight percent, even more preferably at least about 1 weight percent. Nonlimiting examples of the hydrophobic surface treatment useful herein include silicones, acrylate silicone copolymers, acrylate polymers, alkyl silane, isopropyl titanium triisostearate, sodium stearate, magnesium myristate, perfluoroalcohol phosphate, perfluoropolymethyl isopropyl ether, lecithin, carnauba wax, polyethylene, chitosan, lauroyl lysine, plant lipid extracts and mixtures thereof, preferably, silicones, silanes and stearates.

When formulated into a product, the HMNPP's are preferably entrapped within the skin benefit agent or emollient. This necessitates that the oil phase particle size is generally larger than the HMNPP. In a preferred embodiment of the invention, the skin benefit agent or emollient contain only a small number of HMNPPs per oil particles.
Preferably this is less than 20, more preferably less than 10, most preferably less than 5.
These parameters, the relative size of the oil droplets to the HMNPP and the approximate number of HMNPP particles per dispersed oil particles, can be determined by using visual inspection with light microscopy.

The HMNPP and skin benefit agent or emollient can be mixed into the composition via a premix or separately. For the case of separate addition, the liydrophobic pigments partition into the skin benefit agent or emollient oil phase during the processing of the formulation. However, preferably the HMNPP may not be supplied dispersed in liquid prior to their incorporation into the personal care composition of the present invention.
D. Aqueous Phase The composition will preferably contain an aquouse phase. The aqueous phase will be composed of water and/or other hydroxyl containing solvents such as glycerine, propylene glycol and other water miscible solvents. The aqueous phase may be continuous or discontinuous depending on the formulation. Preferably, the composition will contain at least 10% water, more preferably at least 20%, even more preferably at least 30% and even more preferably 40% and most preferably at least 50%.
Preferably the aqueous phase will comprise no more than 90% of the composition, even more preferably no more than 80% of the composition, even more preferably less than 75% of the composition, and most preferably less than 70% of the composition.
E. Optional Ingredients The compositions of the present invention may contain one or more additional skin care components. In a preferred embodiment, where the composition is to be in contact with human keratinous tissue, the additional components should be suitable for application to keratinous tissue, that is, when incorporated into the composition they are suitable for use in contact with human keratinous tissue without undue toxicity, incompatibility, instability, allergic response, and the like within the scope of sound medical judgment.

The CTFA Cosmetic Ingredient Handbook, Second Edition (1992) describes a wide variety of nonlimiting cosmetic and pharmaceutical ingredients commonly used in the personal care industry, which are suitable for use in the compositions of the present invention.

In any embodiment of the present invention, however, the additional components useful herein can be categorized by the benefit they provide or by their postulated mode of action. However, it is to be understood that the additional components useful herein can in some instances provide more than one benefit or operate via more than one mode of action. Therefore, classifications herein are made for the sake of convenience and are not intended to limit the active to that particular application or applications listed.
a. Particles The present invention may optionally comprise particles having a wide range of shapes, surface characteristics, and hardness characteristics can be utilized to provide optical effect. These particles of the personal care compositions preferably have an average diameter not greater than about 200 m, more preferably not greater than 100 m, even more preferably not greater than about 80 m, still more preferably not greater than than about 60 m. The particles of the personal care compositions preferably have a diameter of at least about 0.01 gm, more preferably at least about 0.05 m, even more preferably at least about 0.1 m, and still more preferably at least about 0.2 m.

These particles may be used as is, without being hydrophobically modified (although some may in fact be 'naturally hydrophobic'), include but are not limited to those derived from a wide variety of materials including those derived from inorganic, organic, natural, and synthetic sources. Non-limiting examples of these materials include those selected from the group consisting of almond meal, alumina, aluminum oxide, titanium dioxide, mica, coated mica, sodium stearate, stearic acid, zinc stearate, aluminum silicate, apricot seed powder, aftapulgite, barley flour, bismuth oxychloride, boron nitride, calcium carbonate, calcium phosphate, calcium pyrophosphate, calcium sulfate, cellulose, chalk, chitin, clay, corn cob meal, corn cob powder, corn flour, corn meal, corn starch, diatomaceous earth, dicalciunl phosphate, dicalcium phosphate dihydrate, fullers earth, hydrated silica, hydroxyapatite, iron oxide, jojoba seed powder, kaolin, loofah, magnesium trisilicate, mica, microcrystalline cellulose, montmorillonite, oat bran, oat flour, oatmeal, peach pit powder, pecan shell powder, polybutylene, polyethylene, polyisobutylene, polymethylstyrene, polypropylene, polystyrene, polyurethane, nylon, teflon (i.e. polytetrafluoroethylene), polyhalogenated olefins, pumice rice bran, rye flour, sericite, silica, silk, sodium bicarbonate, sodium silicoaluminate, soy flour synthetic hectorite, talc, tin oxide, titanium dioxide, tricalcium phosphate, walnut shell powder, wheat bran, wheat flour, wheat starch, zirconium silicate, and mixtures thereof. Also useful are micronized particles made from mixed 'polymers (e.g., copolymers, terpolymers, etc.), such as polyethylene/polypropylene copolymer, polyethylene/propylene/isobutylene copolymer, polyethylene/styrene copolymer, and the like.

b. Interference Pigments ' The present invention may optionally comprise interference pigments, such as those disclosed in co-pending and commonly assigned under U.S. Patent Application Number 10/841,173 filed on May 7, 2004 by Clapp, et al.

The interference pigments of the present invention are platelet particulates.
The platelet particulates of the personal care compositions preferably have a thickness of no more than about 5 m, more preferably no more than about 2 m, still more preferably no more than about 1 gm. The platelet particulates of the personal care composition preferably have a thickness of at least about 0.02 m, more preferably at least about 0.05 m, even more preferably at least about 0.1 m, and still more preferably at least about 0.2 m.

5 The interference pigment of the personal care compositions preferably have an average diameter not greater than about 200gm, more preferably not greater than 100 m, even more preferably not greater than about 80 m, still more preferably not greater than than about 60 m. The interference pigment of the personal care compositions preferably have a diameter of at least about 0.1 m, more preferably at least about 1.0 m, even more 10 preferably at least about 2.0 m, and still more preferably at least about 5.0 m.

The interference pigment of the personal care compositions comprises a multilayer structure. The centre of the particulates is a flat substrate with a refractive index (RI) normally below 1.8. A wide variety of particle substrates are useful herein.
Nonlimiting examples are natural mica, synthetic mica, graphite, talc, kaolin, alumina flake, bismuth 15 oxychloride, silica flake, glass flake, ceramics, titanium dioxide, CaSO4, CaCO3, BaSO4, borosilicate and mixtures thereof, preferably mica, silica and alumina flakes.

A layer of thin film or a multiple layer of thin films are coated on the surface of a substrate described above. The thin films are made of highly refractive materials. The refractive index of these materials is normally above 1.8.

20 A wide variety of thin films are useful herein. Nonlimiting examples are Ti02, Fe203, Sn02, Cr203, ZnO, ZnS, ZnO, SnO, Zr02, CaF2, A1203, BiOCI, and mixtures thereof or in the form of separate layers, preferably Ti02, Fe203, Cr203 Sn02.
For the multiple layer structures, the thin films can be consisted of all high refractive index materials or alternation of tllin films with high and low RI materials with the high RI film 25 as the top layer.

The interference color is a function of the thickness of thin film, the thickness for a specific color may be different for different materials. For Ti02, a layer of 40nm to 60nm or a whole number multiple thereof gives silver color, 60nm to 80nm yellow color, 80nm to 100nm red color, 100nm to 130nm blue color, 130run to 160nm green color. In addition to the interference color, other transparent absorption pigments can be precipitated on top of or simultaneously with the TiO2 layer. Common materials are red or black iron oxide, ferric ferrocyanide, chromium oxide or carmine. It was found that the color of the interference pigment in addition to its brightness had a significant influence on human perception of skin tone. In general, preferred colors are silver, gold, red, green and mixtures thereof.

Nonlimiting examples of the interference pigments useful herein include those supplied by Persperse, Inc. under the trade name PRESTIGE , FLONAC ; supplied by EMD Chemicals, Inc. under the trade name TIMIRON , COLORONAO, DICHRONA
and XIRONA ; and supplied by Kobo Products, Inc. under the trade name Kobopearl ;
and supplied by Engelhard Co. under the trade name FLAMENCO , TIMICA , DUOCHROME .

c. Hydrophobically Modified Interference Pigments The present invention may optionally comprise Hydrophobically Modified Interference Pigments, such as those disclosed in co-pending and commonly assigned under U.S. Patent Application Number 10/841,173 filed on May 7, 2004 by Clapp, et al.

In an embodiment of the present invention the interference pigmeiit surface is either hydrophobic or has been hydrophobically modified. The Particle Contact Angle Test of the present invention is used to determine contact angle of interference pigments.
The greater the contact angle, the greater the hydrophobicity of the interference pigment.
The interference pigment of the present invention possess a contact angle of at least 60 , more preferably greater than 80 , even more preferably greater than 100 , still more preferably greater than 1100, even still more preferably greater than 120 , even still even more preferably greater than 130 , even still even more preferably greater than 140 . The hydrophobically modified interference pigment or HMIP allows for the entrapment of the HMIP within the skin benefit agent or emollient and greater deposition of the HMIP.
When formulated into a product, the HMIP's are preferably entrapped within the the skin benefit agent or emollient.

The HMIP and the oil can be mixed into the composition via a premix or separately. For the case of separate addition, the hydrophobic pigments partition into the oil phase during the processing of the formulation. Nonlimiting examples of the hydrophobic surface treatment useful herein include silicones, acrylate silicone copolymers, acrylate polymers, alkyl silane, isopropyl titanium triisostearate, sodium stearate, magnesium myristate, perfluoroalcohol phosphate, perfluoropolymethyl isopropyl ether, lecithin, carnauba wax, polyethylene, chitosan, lauroyl lysine, plant lipid extracts and mixtures thereof, preferably, silicones, silanes and stearates.
Surface treatment houses include US Cosmetics, KOBO Products Inc., and Cardre Inc.
d. Structurants The present invention may optionally comprise a structurant. The structurant can provide the dispersed phase with the correct rheological properties. This can aid in providing effective deposition and retention to the skin, the structured oil or oil phase should have a viscosity in the range of 100 to about 200,000 poise measured at 1 Sec-1, preferably 200 to about 100,000 poise, and most preferably 200 to about 50,000 poise as determined using the lipid rheology method described below. The amount of structurant required to produce this viscosity will vary depending on the oil and the structurant, but in general, the structurant will preferably be less than 75 weight percent of the dispersed oil phase, more preferably less than 50 weight percent, and still more preferably less than 35 weight percent of the dispersed oil phase.
Structurants meeting the above requirements with the selected skin compatible oil can form 3-dimensional network to build up the viscosity of the selected oils.
It has been found that such structured oil phases, i.e., built with the 3-dimensional network, are extremely desirable for use as wet-skin treatment compositions used in bathing. These structured oils can deposit and be retained very effectively on wet skin and retained after rinsing and drying to provide long-lasting after wash skin benefit without causing a too oily/greasy wet and dry feel. It is believed that the highly desirable in-use and after-use properties of such structured oils are due to their shear thinning rheological properties and the weak structure of the network. Due to its high low-shear viscosity, the 3-dimensional network structured oil can stick and retain well on the skin during application of the skin conditioner. After being deposited on the skin, the network yields easily during rubbing due to the weak structuring of the crystal network and its lower high-shear viscosity.
The structurant can be either an organic or inorganic structurant. Examples of organic thickeners suitable for the invention are solid fatty acid esters, natural or modified fats, fatty acid, fatty amine, fatty alcohol, natural and synthetic waxes, and petrolatum, and the block copolymers sold under the name KRATON by Shell. Inorganic structuring agents include hydrophobically modified silica or hydrophobically modified clay.
Nonlimiting examples of inorganic structurants are BENTONE 27V, BENTONE 38V or BENTONE GEL MIO V from Rheox; and CAB-O-SIL TS720 or CAB-O-SIL M5 from Cabot Corporation.

The structurant may be crystalline may be a natural or synthetic crystalline wax.
Mineral, animal or plant (vegetable) waxes are all described as natural waxes.
Synthetic waxes are described as those waxes that have been synthetically polymerized from raw materials or chemically modified natural waxes.

Among the natural crystalline waxes which may be used are petroleum based waxes such as paraffins and microcrystalline wax. Molecular weights of paraffin waxes generally range from 360 to 420 (26 to 30 carbon atoms), although versions with longer chains (molecular weights up to 600) are available. Typical melting points are F. (52-57 C.), the high molecular weight versions have melting points near 170 F. (77 C.). Paraffin waxes are brittle and the addition of oil weakens the structure (lowers the tensile strength).

Microcrystalline waxes (MC) melting points are 145 to 195 F. (63-91 C.). The crystals of MC wax are small and irregular and consist of several types:
plates, malcrystalline and needle. Animal waxes can be obtained from such things as bees, insects or whales. These waxes include but are not limited to beeswax, Chinese wax, shellac wax, spermaceti and wool wax. Plant waxes can be derived from beans, leaves and berries. Plant or vegetable waxes can include bayberry, candelilla, carnauba, cotton, esparto, fir, Japan, ouricury, palm, rice-oil, sugar cane, ucuhuba and cocoa butter.
Among synthetic ciystalline waxes which may be used are crystalline polymers such as polyethylene, Fischer-Tropsch waxes such as polymethylene, chemically modified waxes, polymerized alpha olefins and synthetic animal waxes. For example, siliconyl beeswax may be used which is beeswax that has been chemically modified.

Another structurant that may be optionally used in the present invention is the microcrystalline wax petrolatum (also known as petrolatum or mineral jelly), which typically comprises about 90% by wt. of a natural mixture of microcrystalline waxes plus minor amounts of other impurities In addition, structurant may be a natural or synthetic hydrogenated oil or fat.
Hydrogenated oils are also commonly referred to as fats. In addition some fatty acids and fatty alcohols can be used as structurant as well as salts of fatty acids, hydroxy fatty acids and fatty acid esters.

Hydrogenated oils can be hydrogenated vegetable oils, hydrogenated coconut oil, hydrogenated palm kernel oil, hydrogenated rapeseed oil and many others.
Another hydrogenated oil is castorwax.

Along with size and shape, a high concentration of particles is required so that the crystals interact in the dispersion. Above a certain critical volume fraction of crystals, these interactions will lead to a buildup of a network that extends throughout the whole volume. The crystal network creates a solid-like material having viscoelastic properties.
Thus, the ability of the fat crystals of the hydrogenated oils to form continuous networks that entrap the oil depends on the solid fat content in the fat/oil mixtures and also on crystal morphology. For example, when there is a high concentration of beta prime crystals, a continuous network of small crystals extends through the sample and the sample is solid and stable. Typically, at solid fat contents of 40-50%, the consistency is hard and brittle, at 20-30% the system is solid-like but yielding, at lower concentrations the consistency is more fluid often with a grainy texture and at very low concentrations the fat crystals separate from the liquid. However, the exact concentrations of crystals required to build desired structures varies depending on the fat and oil used.
In practice, the crystal formation is also dependent on processing conditions such as temperature, crystal formation rate and shearing.

Crystalline long chain fatty acids and long chain fatty alcohols can also be used to structure benefit agents. Examples of fatty acids are myristic acid, palmitic acid, stearic acid, arachidic acid and behenic acid. Examples of fatty alcohols are palmityl alcohol, stearyl alcohol, arachyl alcohol and behenyl alcohol. Some crystalline fatty acid esters and glyceride esters will also provide structuring benefit. -In addition, the crystalline materials can be combined with other structuring materials such as natural and synthetic waxes to form composite networks to structure benefit agents.

e. Thickeners The compositions of the present invention, in some embodiments, may further include one or more thickening/aqueous phase stability agents. Because different stability agents thicken with different efficiencies, it is difficult to provide an accurate 5 compositional range, however, when present, the composition preferably comprises no more than about 10 weight percent, more preferably no more than about 8 weight percent, and still more preferably no more than about 7 weight percent of the personal care composition. When present, the thickening/aqueous phase stability agent preferably comprises at least about 0.01 weight percent, more preferably at least about 0.05 weight 10 percent, and still more preferably at least about 0.1 weight percent of the personal care composition.

Nonlimiting examples of thickening agents useful herein include carboxylic acid polymers such as the carbomers (such as those commercially available under the tradename CARBOPOL 900 series from B.F. Goodrich; e.g., CARBOPOL 954).

15 Other suitable carboxylic acid polymeric agents include copolymers of C10-30 alkyl acrylates with one or more monomers of acrylic acid, methacrylic acid, or one of their short chain (i.e., C1-4 alcohol) esters, wherein the crosslinking agent is an allyl ether of sucrose or pentaerytritol. These copolymers are known as acrylates/Cio_3o alkyl acrylate crosspolymers and are commercially available as CARBOPOL 1342, CARBOPOL
20 1382, PEMULEN TR-1, and PEMULEN TR-2, from B.F. Goodrich.
Other nonlimiting examples of thickening agents include crosslinked polyacrylate polymers including both cationic and nonionic polymers.
Still other nonlimiting examples of thickening agents include the polyacrylamide polymers, especially nonionic polyacrylamide polymers including substituted branched or 25 unbranched polymers. More preferred among these polyacrylamide polymers is the nonionic polymer given the CTFA designation polyacrylamide and isoparaffin and laureth-7, available under the Tradename SEPIGEL 305 from Seppic Corporation (Fairfield, NJ). Other polyacrylamide polymers useful herein include multi-block copolymers of acrylamides and substituted acrylamides with acrylic acids and substituted 30 acrylic acids. Commercially available examples of these multi-block copolymers include HYPAN SR150H, SS500V, SS500W, SSSA100H, from Lipo Chemicals, Inc., (Patterson, NJ).
Another nonlimiting class of thickening agents useful herein are the polysaccharides. Nonlimiting examples of polysaccharide gelling agents include those selected from cellulose, and cellulose derivatives. Preferred among the alkyl hydroxyalkyl cellulose ethers is the material given the CTFA designation cetyl hydroxyethylcellulose, which is the ether of cetyl alcohol and hydroxyethylcellulose, sold under the tradename NATROSEL CS PLUS from Aqualon Corporation (Wilmington, DE). Other useful polysaccharides include scleroglucans which are a linear chain of (1-3) linked glucose units with a (1-6) linked glucose every three units, a commercially available example of which is CLEAROGELTM CS 11 from Michel Mercier Products Inc.
(Mountainside, NJ).
Another nonlimiting class of thickening agents useful herein are the gums.
Nonlimiting examples of gums useful herein include hectorite, hydrated silica, xantham gum, and mixtures thereof.
Yet another nonlimiting class of thickening agents useful herein are the modified starches. Acrylate modified starches such as WATERLOCKS from Grain Processing Corporation may be used. Hydroxypropyl starch phosphate, tradename STRUCTURE
XL
from National Starch is another example of a useful modified starch, and other useful examples include ARISTOFLEX HMB (Ammonium Acrylodimethyltaruate/Beheneth-25 Methacrylate Crosspolymer) from Clariant and cationic stabylens.
f. Cationic Polymers The present invention may also contain organic cationic deposition polymer Concentrations of the cationic deposition polymer preferably range from about 0.025% to about 3%, more preferably from about 0.05% to about 2%, even more preferably from about 0.1 % to about 1%, by weight of the personal care composition.
F. Analytical Methods:
a. Lipid Rheology Test Lipid rheology is measured on a TA Instruments AR2000 stress-controlled rheometer with a Peltier temperature controlled sample stage or an equivalent.
A parallel plate geometry is used with a 40mm plate and a lmm gap. The lower plate is heated to 85 C and the melted lipid and structurant (if present) is added onto the lower plate and allowed to equilibrate. The upper plate is then lowered to the 1 rnm gap while ensuring the lipid fills the gap fiully, [spinning the top plate and adding more lipid to promote wicking], and the sample is cooled quickly to 25 C and equilibrated at 25 C
for 5 minutes. Viscosity is then measured using a stress-ramp procedure common on these types of machines using a logarithmic stress ramp from 20 to 2000Pa at a rate of 60 seconds per decade (2 minute ramp test), with 20 measurements points per decade. The starting and ending stress is sufficient to induce flow and reach a shear rate of at least 10 sec-1. Viscosity is recorded and the data fitted to a power law model using Equation 1.
Only points between 0.001 sec-I and 40 seconds-1 are to be used in the power law fit.
The viscosity at 1.0 sec-1 is calculated from Equation 1. One should carefully watch the sample during the test so that when the material is ejected from under the plate, the method is stopped.
Viscosities are recorded and the data fit to a power law with the following Equation 1:
i1 = x=Y(dot)(") where rl= viscosity, x is the consistency and y(dot) is the shear rate, and n is the shearindex.

The viscosity at 1 sec-1 is then calculated using the calculated values of rl and n from the fitted data.

b. HMNPP Deposition Tape Strip Method The Pigment Deposition Tape Strip Method can be used to semi-quantitatively determine deposition of shiny particles onto keratinous surfaces. The method employs the use of a tape strip for removing particles from skin and imaging these particles for a quantitation of deposited particles.
The first step is to weigh 1 g of pigment that is the same as those in the product being tested in a vial. Next, 9g melted petrolatum is added and mixed well with a spatula.
Weigh out 994.17g purified water (Millipore or equivalent). While mixing @
-600-700 rpm using a Lightning Laboratory Stirrer or Heidolph 2051 mixer and appropriate blade, to the water slowly add 3.50g Pemulen TR-1 (BF Goodrich) so as to prevent clumping. Follow this with 30 minutes of stirring to ensure complete hydration of Pemulen. To the mixture, while still stirring slowly, add 2.33g TEA
(Triethanolamine 99%-Dow Chemical). Follow this by an additional 30 minutes of stirring to ensure homogeneity.
Evaluate product for separation after standing for 1 hour. Separation is not acceptable. Store in glass jars at room temperature. Now, mix lml of the pigment/petrolatum mixture with 19m1 of 0.35% Pemulen Gel mixture, using Cito Unguator on speed 8(-2050 rpm) for 4 minutes. This combination of the 1 ml of the pigment/petrolatum mixture with 19m1 of 0.35% Pemulen Gel mixture will be used to evaluate deposition of pigment on the skin.
Wash inner arms of subject with Olay Sensitive Skin bar and warm water, rinsing until all soap has been removed. Dry with clean paper towels. Mark inner arms of subject with three 4 x 6 cm sites per arm. Apply to site #1 (upper left, nearest elbow) 5 l of the mixture described previously, spreading evenly over site and rubbing in with gloved finger for - 20 seconds covering entire site. This application equals I
g pigment per cmZ. Apply to site #2 (middle left) 24 1 of mixture described previously, spreading evenly over site and rubbing in with gloved finger for - 20 seconds covering entire site.
This application equals 5 g pigment per cm2. Apply to site #3 (bottom left, nearest wrist) 48 1 of mixture described previously. This equals l0 g per cm2. Apply to site #4 (top right, nearest elbow) 96 1 of mixture described previously. This equals 20 g per cm2.
Let sites air dry for a minimum of 10 min. Apply to site #5 (middle right) 96 1 of the product being tested. Apply to site #6 (bottom right, nearest wrist) 96 l of the product being tested. Rinse each site #5 and #6 with warm tap water for 10 seconds each, not contaminating one site with the next while rinsing. Then pat each site dry gently with clean paper towels, again not contaminating one site with the next.
Take approximately 1" of Scotch Tape and apply to site #1. Rub over the top of the applied tape to pick up product below. Remove the tape and reapply same tape to very same previously stripped area, so as to pull product from area twice on the same tape. Then secure this stripping tape to a clean microscope slide, product side up, marking the slide as "1 g/cm2i. Repeat the application of Scotch Tape method described previously for sites #2 through #6 (in that order), niarking each slide appropriately.
Take microscope images of each tape strip that are made with a lOX objective and top lighting.
Visually compare the numbers of pigment particles in sites #5 and #6 images with those in the standard sites #1 through #4 images and give a deposition level, for example, 8 g/cm2. Take an average of the observations of sites #5 and #6 from at least 3 people.

c. Particle Contact Angle Test The Particle Contact Angle Test is used to determine hydrophobicity of shiny particles. The greater the contact angle the greater the hydrophobicity of the particle.
A Spectra-Tech Qwik Handi-Press (Thermo Nicolet, Madison, WI) is used to compress the powder into 7-mm diameter discs. After applying firm hand pressure, the compression is held for 1 min prior to releasing pressure and removing the disc. The disc is examined for smoothness and rejected unless the surface is smooth. First Ten Angstrom FTA 200 (First Ten Angstrom, Portsmouth, VA) contact angle analyzer is employed to determine advancing and receding contact angles. 7 microliters of water (Millipore, Milli Q deionized, distilled) is dangled from the needle and slowly placed on the middle of the disc. The needle is left inserted in the drop but not in contact with disc.
0.1 microliters/second of water is pumped into the drop. Contact angle images were captured every 0.1 sec. until the maximum contact angle is obtained. The process is reversed to determine the receding contact angle in that the needle is left in the drop and fluid is removed at 0.1 microliters/second until the minimum contact angle is obtained.
Images were obtained at 0.1 images/second, then calculate the contact angle.
To calculate the contact angle, a curve is fitted to the profile of the drop on both sides of the drop. The baseline is drawn across the drop. The intersection of the curves and baseline is determined on both sides of the drop. The tangent (slopes) of the curve at the intersection is determined on both sides of the drop. The contact angle is the angle between the baseline and the tangent interior to the drop. The average contact angle is determined from the contact angles from both sides of the drop.

d. Lather Volume Lather volume of a personal care composition can be measured using a graduated cylinder and a tumbling apparatus. A 1,000 ml graduated cylinder is chosen which is 5 marked in 10 ml increments and has a height of 14.5 inches at the 1,000 ml mark from the inside of its base (for example, Pyrex No. 2982). Distilled water (100 grams at 23 C) is added to the graduated cylinder. The cylinder is clamped in a rotating device, which clamps the cylinder with an axis of rotation that transects the center of the graduated cylinder. One gram of the total personal care composition is added into the graduated 10 cylinder and the cylinder is capped. The cylinder is rotated at a rate of 10 revolutions in about 20 seconds, and stopped in a vertical position to complete the first rotation sequence. A timer is set to allow 30 seconds for the lather thus generated to drain. After 30 seconds of such drainage, the first lather volume is measured to the nearest 10 ml mark by recording the lather height in ml up from the base (including any water that has drained 15 to the bottom on top of which the lather is floating).
If the top surface of the lather is uneven, the lowest height at which it is possible to see halfway across the graduated cylinder is the first lather volume (ml).
If the lather is so coarse that a single or only a few foam cells ("bubbles") reach across the entire cylinder, the height at which at least 10 foam cells are required to fill the space is the first 20 lather volume, also in ml up from the base. Foam cells larger than one inch in any dimension, no matter where they occur, are designated as unfilled air instead of lather.
Foam that collects on the top of the graduated cylinder but does not drain is also incorporated in the measurement if the foam on the top is in its own continuous layer, by adding the ml of foam collected there using a ruler to measure thickness of the layer, to 25 the ml of foam measured up from the base. The maximum foam height is 1,000 ml (even if the total foam height exceeds the 1,000 ml mark on the graduated cylinder).
One minute after the first rotation is completed, a second rotation sequence is commenced which is identical in speed and duration to the first rotation sequence. The second lather volume is recorded in the same manner as the first, after the same 30 seconds of drainage 30 time. A third sequence is completed and the third lather volume is measured in the same manner, with the same pause between each for drainage and taking the measurement.

The lather result after each sequence is added together and the Total Lather Volume determined as the sum of the three measurements, in ml. The Flash Lather Volume is the result after the first rotation sequence only, in ml, i.e., the first lather volume.
G. Examples The following examples further describe and demonstrate embodiments within the scope of the present invention. The examples are given solely for the purpose of illustration and are not to be construed as limitations of the present invention, as many variations thereof are possible without departing from the spirit and scope of the invention. All exemplified amounts are concentrations by weight of the total composition, i.e., wt/wt percentages, unless otherwise specified.

Ingredient Ex. Ex. Ex. Ex. Ex. Ex.

I. Aqueous Phase Composition wt% wt% wt% Wt% Wt% Wt%
Polymer Structure XL (Hydroxypropyl Starch Phosphate from National Starch) Pemulen TR2 (Acrylates/C 10-30 Alkyl 0.3 0.5 Acrylate Crosspolymer from Noveon, Inc.) Carbopol Ultrez 10 (Carbomer from 1.5 1.8 Noveon, Inc.) Xanthan Gum 0.1 Sepigel 305 (Polyacrylamide and C13-14 3.0 2.7 Isoparaffin and Laureth-7 from Seppic) Surfactant Polawax (Emulsifying Wax NF from 2.5 Croda) PEG-100 Stearate Tween 80 (Polysorbate 80 from Uniqema 2.1 0.25 0.3 Americas) Ammonium Lauryl Sulfate Incroquat Behenyl TMS (Behenetrimonium 2.0 2.5 methosulfate and cetearyl alcohole from Croda) Additional Ingredients NHance 3196 (Guar Hydroxypropyl 0.15 Trimonium Chloride from Aqualon) PEG 14M 0.1 AMP-95 (Amino Methyl Propanol from 0.1 0.14 0.1 0.18 Angus Chemical) Glycerine 0.6 0.5 0.7 Salicylic Acid Fragrance 1.0 1.0 1.0 1.0 1.0 1.0 Preservatives 0.8 0.8 0.8 0.8 0.8 0.8 Water Q.S. Q.S. Q.S. Q.S. Q.S. Q.S.
II. Lipid/HMIP phase Composition Superwhite Protopet (Petrolatum from 4 17.5 20 WITCO) Hydrobrite 1000 PO (Mineral Oil from 15 WITCO) Dow Corning 200 Fluid S0cst (Dimethicone 2 2 3 Fluid from Dow Corning) Isopropyl Palmitate 1 Soybean Oil 18 4 Puresyn 101LT (Polydecene from Exxon 3 Mobile) Lipovol Sun (Sunflower Seed Oil from 12 11 Lipo) SAT-T-CR50 (Titanium Dioxide/Siloxane 1.75 from US Cosmetics) Cardre LDP 1000 (Polymethyl methacrylate/titanium dioxide/triethoxycaprylylsilane from LCW) Cardre LDP 2000 (Polymethyl Methacrylate/Zinc Oxide/ Dimethicone from LCW) Cardre Titanium Dioxide AS (titanium 0.4 dioxide/alkyl silane from LCW) BTD-TTS2 (Titanium Dioxide/Isopropyl 0.8 Titanium Triisostearate/Triethoxycaprylylsilane) SAT-R-77491 (Red Iron 0.4 oxide/Dimethylpolysiloxane from US
Cosmetics) DHL -Y- 77492 (Yellow Iron 0.3 oxide/Diemthylpolysiloxane from US
Cosmetics) SAT -B- 77499 (Black Iron 0.14 oxide/Diemthylpolysiloxane from US
Cosmetics) 73044 Cardre Titanium Dioxide/PMMA
AQ (titanium dioxide/polymethylmethacrylate/dimethicon e copolyol from LCW) RBTD-11 S2 (titanium dioxide/triethoxy 5 caprylylsilane from Kobo Products Inc.) RBTD-12 (Titanium Dioxide/isopropyl 2.5 titanium triisostearate from Kobo Products Inc.) Kobopearl Stellar White-11 S2 (Mica/Titanium Dioxide/ Triethoxy caprylylsilane from Kobo Products Inc.) SAT-Timiron Splendid Red (Titanium 0.2 Dioxide/Mica/Silica/Dimethicone from US
Cosmetics) Kobopearl Fine White -11 S2 1 (Mica/Titanium Dioxide/ /Triethoxy caprylylsilane from Kobo Products Inc.) SAT-Timiron Super Green(Mica/Titanium Dioxide/Dimethicone from US Cosmetics) SA-M-M (Mica/Dimethicone from US 0.5 Cosmetics) SAT-Flamenco Ultra Silk 2500 (Mica/Titanium Dioxide/Dimethicone from US Cosmetics) TiPure R101-1 (Titanium dioxide from 2 0.5 Dupont) BTD-11 S2 (Titanium Dioxide/ Triethoxy caprylylsilane from Kobo Products, Inc.) Polyacrylate-4 (Helicone HC Maple from Kobo Products, Inc.) Examples 1-6 Premix the lipid phase and the hydrophobically modified particles and heat to 55C . If the formula contains a polymer, such as Nhance 3196 and PEG 14M from the above examples, add it to the water first, mix well. Add Polymer phase to the water in a stainless steel vessel using an overhead mixer, allow the polymer to fully incorporate. pH
adjust if needed. Add Surfactant phase, mix and heat to 80C . Add lipid premix mix well until batch is homogeneous in appearance. Allow batch to cool to 38C . If the formula contains the following: perfume, preservatives, salicylic acid, glycerine and non modified titanium dioxide, add it with additional mixing.

Ingredient Ex. Ex. Ex. Ex. Ex. Ex.

1. Aqueous Phase Composition wt% wt% wt% wt% wt% wt%
Polymer Structure XL (Hydroxypropyl Starch 3.5 3.5 3.5 4 3 Phosphate from National Starch) Pemulen TR2 (Acrylates/C 10-30 Alkyl Acrylate Crosspolymer from Noveon, Inc.) Carbopol Ultrez 10 (Carbomer from Noveon, Inc.) Xanthan Gum 0.8 Sepige1305 (Polyacglamide and C13-14 Isoparaffin and Laureth-7 from Seppic) Surfactant Polawax (Emulsifying Wax NF from 2.0 2.0 Croda) PEG-100 Stearate 2 1 Tween 80 (Polysorbate 80 from 0.1 Uniqema Americas) Ammonium Lauryl Sulfate 2.5 Incroquat Behenyl TMS 2.25 (Behenetrimonium methosulfate and cetearyl alcohole from Croda) Additional Ingredients NHance 3196 (Guar Hydroxypropyl Trimonium Chloride from Aqualon) AMP-95 (Amino Methyl Propanol from Angus Chemical) Glycerine 1 0.5 Salicylic Acid 0.1 Fragrance 1.0 1.0 1.0 1.0 1.0 1.0 Preservatives 0.8 0.8 0.8 0.8 0.8 0.8 Water Q.S. Q.S. Q.S. Q.S. Q.S. Q.S.
II. Lipid/HMIP phase Composition Superwhite Protopet (Petrolatum from 20 9 25 12 15 15 WITCO) Hydrobrite 1000 PO (Mineral Oil from 2 WITCO) Dow Coming 200 Fluid 50cst 2 2 (Dimethicone Fluid from Dow Coming) Isopropyl Palmitate 1 3 Soybean Oil 5 Puresyn 101 LT (Polydecene from 2 Exxon Mobile) Lipovol Sun (Sunflower Seed Oil from 4 Lipo) SAT-T-CR50 (Titanium Dioxide/Siloxane from US Cosmetics) Cardre LDP 1000 (Polymethyl 1.2 methacrylate/titanium dioxide/triethoxycaprylylsilane from LCW) Cardre LDP 2000 (Polymethyl 0.7 Methacrylate/Zinc Oxide/

Dimethicone from LCW) Cardre Titanium Dioxide AS (titanium 0.5 dioxide/alkyl silane from LCW) BTD-TTS2 (Titanium Dioxide/Isopropyl Titanium Triisostearate/Triethoxycaprylylsilane) SAT-R-77491 (Red Iron oxide/Dimethylpolysiloxane from US
Cosmetics) DHL -Y- 77492 (Yellow Iron oxide/Diemthylpolysiloxane from US
Cosmetics) SAT -B- 77499 (Black Iron oxide/Diemthylpolysiloxane from US
Cosmetics) 73044 Cardre Titanium Dioxide/PMMA AQ (titanium dioxide/polymethylmethacrylate/dimet hicone copolyol from LCW) RBTD-11S2 (titanium dioxide/triethoxy caprylylsilane from Kobo Products Inc.) RBTD-12 (Titanium Dioxide/isopropyl titanium triisostearate from Kobo Products Inc.) Kobopearl Stellar White-11S2 0.1 (Mica/Titanium Dioxide/ Triethoxy caprylylsilane from Kobo Products Inc.) SAT-Timiron Splendid Red (Titanium Dioxide/Mica/S ilica/Dimethicone from US Cosmetics) Kobopearl Fine White -11 S2 0.5 (Mica/Titanium Dioxide/ /Triethoxy caprylylsilane from Kobo Products Inc.) SAT-Timiron Super 0.2 Green(Mica/Titanium Dioxide/Dimethicone from US
Cosmetics) SA-M-M (Mica/Dimethicone from US
Cosmetics) SAT-Flamenco Ultra Silk 2500 0.1 (Mica/Titanium Dioxide/Dimethicone from US Cosmetics) TiPure R101-1 (Titanium dioxide from 1.5 Dupont) BTD-11S2 (Titanium Dioxide/ 1 0.4 Triethoxy caprylylsilane from Kobo Products, Inc.) Polyacrylate-4 (Helicone HC Maple 0.2 from Kobo Products, Inc.) Examples 7-12 In a stainless steel vessel add lipid (at 50 C) and hydrophobically modified particle and heat to 80 C with mixing. Add polymer and allow to mix well. Add surfactant, allow to incorporate fully. Separately, heat water to 75 C. Add 75 C water to lipid mixture and mix well until batch is homogeneous in appearance. Allow batch to cool to 38C . If the formula contains the following: perfume, preservatives, salicylic acid, glycerine and non modified titanium dioxide, add it with additional mixing.

Ingredient Ex. Ex. Ex. Ex. Ex.

1. Aqueous Phase Composition wt% wt% wt% wt% wt%
Ammonium Laureth Sulfate 9.4 12.5 Sodium Lauroamphoacetate 3.9 5.3 2 3.2 Ammoniuni Lauryl Sulfate 3.0 8.2 7.4 Sodium Laureth Sulfate 9 2.8 6.8 Lauric Acid 1.6 1 0.5 0.7 Mirataine CAB (Cocamidopropyl Betaine 1.6 5 3.2 from Rhodia Inc.) Trihydroxystearin 1 0.7 1.5 1 N-Hance 3196 (Guar Hydroxypropyl 0.7 Trimonium Chloride from Aqualon) PEG 14M 0.1 0.3 0.1 0.1 0.2 Sodium Chloride 0.7 2 3 1 Citric Acid 0.2 0.1 0.2 Salicylic Acid Fragrance 1.0 1.0 1.0 1.0 1.0 Preservatives 0.8 0.8 0.8 0.8 0.8 Water Q.S. Q.S. Q.S. Q.S. Q.S.
II. Lipid/HMIP phase Composition Superwhite Prototpet (Petrolatum from 17.5 20 15 WITCO) Hydrobrite 1000 PO (Mineral Oil from 15 WITCO) Dow Coming 200 Fluid 50cst (Dimethicone 2 3 Fluid from Dow Corning) Isopropyl Palmitate 3 Soybean Oil 4 Puresyn 101LT (Polydecene from Exxon 3 Mobile) Lipovol Sun (Sunflower Seed Oil from 11 Lipo) Cardre LDP 1000 (Polymethyl metliacrylate/titanium dioxide/triethoxycaprylylsilane from LCW) Cardre LDP 3000 (Polymethyl 1 methacrylate/silica/triethoxycaprylylsilane from LCW) Cardre Titanium Dioxide AS (titanium 1 dioxide/alkyl silane from LCW) SAT-Timiron MP 115 Starluster 0.5 (Mica/Titanium Dioxide/Dimethicone from US Cosmetics) BTD-401 (Titanium Dioxide/Isopropyl 2 Titanium Triisostearate from Kobo Products Inc.) Kobopearl Fine White-11 S 10 0.5 (Mica/Titanium Dioxide/ /Triethoxy caprylylsilane from Kobo Products Inc.) SAT-Timiron Super Green (Mica/Titanium 0.1 Dioxide/Dimethicone from US Cosmetics) SAT-Flamenco Ultra Silk (Mica/Titanium 0.3 Dioxide/Dimethicone from US Cosmetics) TiPure R101-01 (Titanium Dioxide from 2 1 1.5 Dupont) Examples 13-17 The compositions described above is prepared by conventional formulation and mixing techniques. The aqueous phase ingredients are mixed in a stainless steel vessel using an overhead mixer and heated to 95 C. Add the trihydroxystearin and allow to fully incorporate into the mixture, then add preservatives. Allow the phase to cool with mixing. Premix the lipid phase and the hydrophobically modified particles and heat to 55 C. Once the aqueous phase has cooled to 31 C, the lipid/particle premix is added and mixed well until batch is homogeneous in appearance. If the formula contains a non modified particle, such as TiPure R101-01 from the above example, add it at this point to the mixing batch. Then add perfume. Keep agitation until a homogenous solution forms.
All documents cited in the Detailed Description of the Invention are, in relevant part, incorporated herein by reference; the citation of any document is not to be construed as an admission that it is prior art with respect to the present invention.
While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention.
It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention.

Claims (15)

1. A rinsable personal care composition comprising:
a) from 0 to 75 weight percent of a surfactant;

b) from 0.01 to 99 weight percent of a skin benefit agent or emollient c) from 0.01 to 20 weight percent of a hydrophobically modified non-platelet particle; and d) from 0 to 99% water.
2. A composition according to claim 1, comprising preferably no more than 1 weight percent of said hydrophobically non-platelet particle, most preferably no more than weight percent of said hydrophobically non-platelet particle.
3. A composition according to claim 1 or 2, comprising no more than 80 weight percent of said skin benefit agent or emollient, preferably at least 1 weight percent of said skin benefit agent or emollient.
4. A composition according to any one of the preceding claims, wherein the ratio of said hydrophobically modified non-platelet particle to said skin benefit agent or emollient is from 1:1 to 1:100.
5. A composition according to any one of the preceding claims, wherein said skin benefit agent or emollient is selected from the group consisting of petrolatum, mineral oil, silicone, triglycerides, esters and mixtures thereof.
6. A composition according to any one of the preceding claims, further comprising a continuous aqueous phase.
7. A composition according to any one of the preceding claims, wherein said hydrophobically modified non platelet particle is entrapped within said skin benefit agent or emollient.
8. A composition according to any one of the preceding claims, wherein the composition comprises no more than 5 weight percent of said surfactant.
9. A composition according to any of the preceding claims, wherein said surfactant is present in a gel-network.
10. A composition according to any of claim 1 to 7, wherein the composition comprises at least 5 weight percent of said composition surfactant, preferably at least one anionic surfactant.
11. A composition according to any of the preceding claims, further comprising a polymer.
12. A composition according to any one of the preceding claims, comprising one or more benefit agents selected from the group consisting of skin moisturizing agents, humectants, vitamins, sunscreens, thickening agents, preservatives, anti-acne medicaments, antioxidants, skin soothing and healing agents, chelators and sequestrants, fragrances, essential oils, skin sensates, pigments, pearlescent agents, lakes, colorings and mixtures thereof.
13. A composition according to any one of the preceding claims, further comprising a structurant.
14. A composition according to any one of the preceding claims, further comprising a hydrophobically modified interference pigment.
15. A composition according to any one of the preceding claims, further comprising a non modified particle.
CA2589044A 2005-02-15 2006-02-03 Personal care compositions containing hydrophobically modified non-platelet particles Expired - Fee Related CA2589044C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US11/057,957 2005-02-15
US11/057,957 US8147853B2 (en) 2005-02-15 2005-02-15 Personal care compositions containing hydrophobically modified non-platelet particles
PCT/US2006/004000 WO2006088673A2 (en) 2005-02-15 2006-02-03 Personal care compositions containing hydrophobically modified non-platelet particles

Publications (2)

Publication Number Publication Date
CA2589044A1 true CA2589044A1 (en) 2006-08-24
CA2589044C CA2589044C (en) 2013-04-23

Family

ID=36815859

Family Applications (1)

Application Number Title Priority Date Filing Date
CA2589044A Expired - Fee Related CA2589044C (en) 2005-02-15 2006-02-03 Personal care compositions containing hydrophobically modified non-platelet particles

Country Status (7)

Country Link
US (1) US8147853B2 (en)
EP (1) EP1848508A2 (en)
JP (1) JP2008524263A (en)
CN (1) CN101090751A (en)
CA (1) CA2589044C (en)
MX (1) MX2007007149A (en)
WO (1) WO2006088673A2 (en)

Families Citing this family (61)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE493177T1 (en) * 2005-03-04 2011-01-15 Procter & Gamble WASHABLE OR WIPABLE SKIN CLEANING COMPOSITIONS
CA2603299A1 (en) * 2005-04-13 2006-10-26 The Procter & Gamble Company Structured multi-phased personal care composition comprising branched anionic surfactants
US7820609B2 (en) 2005-04-13 2010-10-26 The Procter & Gamble Company Mild, structured, multi-phase personal cleansing compositions comprising density modifiers
WO2007066310A2 (en) * 2005-12-08 2007-06-14 The Procter & Gamble Company A container comprising an in-mold label positioned proximate to a surface topography
US20070167338A1 (en) * 2006-01-09 2007-07-19 Mchugh Colin M Multiphase personal care compositions comprising beads
US8104616B2 (en) 2006-02-11 2012-01-31 The Procter & Gamble Company Clamshell package for holding and displaying consumer products
US8153144B2 (en) 2006-02-28 2012-04-10 The Proctor & Gamble Company Stable multiphase composition comprising alkylamphoacetate
US20090233825A1 (en) * 2006-11-08 2009-09-17 Colin Christopher David Giles Conditioning shampoo compositions
RU2466711C2 (en) * 2006-11-08 2012-11-20 Унилевер Н.В. Conditioning shampoo compositions
US20080317697A1 (en) * 2007-06-21 2008-12-25 Thomas Arthur Sturgis Shaving kit and method of shaving comprising a personal care composition and an in shower body lotion
US20090028809A1 (en) * 2007-07-27 2009-01-29 Jonathan Robert Cetti Personal care article for sequentially dispensing compositions with variable concentrations of hydrophobic benefit materials
US20090324521A1 (en) 2007-07-27 2009-12-31 Jonathan Robert Cetti Personal Care Article For Sequentially Dispensing Compositions With Variable Concentrations Of Hydrophobic Benefit Materials
US20090028808A1 (en) * 2007-07-27 2009-01-29 The Procter & Gamble Company Personal care article for sequentially dispensing compositions with variable concentrations of partitioned benefit or suspended benefit agents
US20110089196A1 (en) 2007-07-27 2011-04-21 Jonathan Robert Cetti Personal-care article for sequentially dispensing compositions with variable concentrations of hydrophobic benefit materials
CN104287977A (en) * 2008-07-28 2015-01-21 宝洁公司 Multiphase personal care composition with enhanced deposition
US8124064B2 (en) * 2008-07-28 2012-02-28 The Procter & Gamble Company In-vitro deposition evaluation method for identifying personal care compositions which provide improved deposition of benefit agents
CN102405035B (en) 2009-01-28 2014-07-16 宝洁公司 Methods for improving skin quality using rinse-off personal care compositions with variable amounts of hydrophobic benefit agents
WO2011015907A1 (en) * 2009-08-04 2011-02-10 Chanel Parfums Beaute Cosmetic composition based on substantially hemispherical particles
WO2011087525A1 (en) 2010-01-17 2011-07-21 The Procter & Gamble Company Biomarker-based methods for formulating compositions that improve skin quality and reduce the visible signs of aging in skin for individuals in a selected population
US9750674B2 (en) 2010-06-11 2017-09-05 The Procter & Gamble Company Compositions for treating skin
EP2694029A2 (en) 2011-04-04 2014-02-12 The Procter and Gamble Company Dissolvable, personal cleansing compositions
CN103458756B (en) 2011-04-04 2018-09-14 宝洁公司 Personal care product
EP2718413B1 (en) 2011-06-10 2017-11-15 The Procter and Gamble Company Personal care compositions
MX2014001896A (en) 2011-08-15 2014-05-27 Procter & Gamble Personal care methods.
WO2013025769A2 (en) 2011-08-15 2013-02-21 The Procter & Gamble Company Methods of enhancing skin hydration and improving non-diseased skin
WO2013086178A2 (en) 2011-12-09 2013-06-13 The Procter & Gamble Company Personal care compositions
US8895041B2 (en) 2012-03-23 2014-11-25 The Procter & Gamble Company Compositions for delivering perfume to the skin
US20140134217A1 (en) * 2012-11-09 2014-05-15 Johnson & Johnson Consumer Companies, Inc. Leave-on compositions containing cellulose materials
US20140134218A1 (en) 2012-11-09 2014-05-15 Johnson & Johnson Consumer Companies, Inc. Rinse-off skin care compositions containing cellulosic materials
US9370478B2 (en) 2012-11-09 2016-06-21 Johnson & Johnson Consumer Inc. Skin care compositions containing cotton and citrus-derived materials
US9056208B2 (en) * 2013-02-07 2015-06-16 Conopco Inc. Personal care compositions that include enrobed sugar
US9168394B2 (en) 2013-03-13 2015-10-27 Johnson & Johnson Consumer Inc. Pigmented skin-care compositions
US9168393B2 (en) 2013-03-13 2015-10-27 Johnson & Johnson Consumer Inc. Pigmented skin-care compositions
US9168209B2 (en) 2013-03-13 2015-10-27 Johnson & Johnson Consumer Inc. Pigmented skin-care compositions
US9320687B2 (en) 2013-03-13 2016-04-26 Johnson & Johnson Consumer Inc. Pigmented skin-care compositions
CA2916297C (en) 2013-06-27 2018-07-10 The Procter & Gamble Company Personal care compositions and articles
US20150098920A1 (en) 2013-10-09 2015-04-09 The Procter & Gamble Company Personal Cleansing Compositions and Methods
US9101551B2 (en) 2013-10-09 2015-08-11 The Procter & Gamble Company Personal cleansing compositions and methods
US20150210964A1 (en) 2014-01-24 2015-07-30 The Procter & Gamble Company Consumer Product Compositions
EP3113751A1 (en) 2014-03-07 2017-01-11 The Procter & Gamble Company Method of making personal care compositions comprising zinc compound and/or pyrithione
EP2960322B1 (en) * 2014-06-25 2021-01-13 The Procter and Gamble Company Structuring premixes comprising non-polymeric, crystalline, hydroxyl-containing structuring agents and a linear alkyl sulphate, and compositions comprising them
CN107148263B (en) 2014-11-10 2021-07-06 宝洁公司 Personal care compositions
CN106999417A (en) 2014-11-10 2017-08-01 宝洁公司 Personal cleaning compositions and method
EP3217949B1 (en) 2014-11-10 2020-06-17 The Procter and Gamble Company Personal care compositions with two benefit phases
US10966916B2 (en) 2014-11-10 2021-04-06 The Procter And Gamble Company Personal care compositions
MX2017006148A (en) 2014-11-10 2017-07-27 Procter & Gamble Personal care compositions with two benefit phases.
US20180185255A1 (en) 2017-01-05 2018-07-05 The Procter & Gamble Company Method of Selecting Mild Skin Cleansers
EP3697374B1 (en) 2017-10-20 2022-02-16 The Procter & Gamble Company Aerosol foam skin cleanser
EP3697375B1 (en) 2017-10-20 2021-12-01 The Procter & Gamble Company Aerosol foam skin cleanser
WO2019094913A2 (en) 2017-11-13 2019-05-16 The Procter & Gamble Company Personal care composition
EP3720568B1 (en) 2017-12-08 2022-01-12 The Procter & Gamble Company Methods of screening for mild skin cleanser
EP3801443A1 (en) * 2018-06-05 2021-04-14 The Procter & Gamble Company Clear cleansing composition
CN113015904A (en) 2018-11-29 2021-06-22 宝洁公司 Method for screening personal care products
CN113164787B (en) 2018-12-14 2023-11-03 宝洁公司 Shampoo composition comprising lamellar microcapsules
US11896689B2 (en) 2019-06-28 2024-02-13 The Procter & Gamble Company Method of making a clear personal care comprising microcapsules
EP4000725A1 (en) 2020-11-19 2022-05-25 The Procter & Gamble Company Consumer product comprising poly acrylate and poly(beta-amino ester) delivery capsules with enhanced degradability
WO2022109079A1 (en) 2020-11-19 2022-05-27 The Procter & Gamble Company Consumer product comprising biodegradable delivery particles
US20220152572A1 (en) 2020-11-19 2022-05-19 The Procter & Gamble Company Consumer product comprising biodegradable delivery particles
EP4247539A1 (en) 2020-11-19 2023-09-27 The Procter & Gamble Company Consumer product comprising biodegradable delivery particles
US11633072B2 (en) 2021-02-12 2023-04-25 The Procter & Gamble Company Multi-phase shampoo composition with an aesthetic design
US20230320949A1 (en) 2022-04-12 2023-10-12 The Procter & Gamble Company Compositions Having Capsules

Family Cites Families (248)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1985424A (en) 1933-03-23 1934-12-25 Ici Ltd Alkylene-oxide derivatives of polyhydroxyalkyl-alkylamides
US2438091A (en) * 1943-09-06 1948-03-16 American Cyanamid Co Aspartic acid esters and their preparation
US2528378A (en) 1947-09-20 1950-10-31 John J Mccabe Jr Metal salts of substituted quaternary hydroxy cycloimidinic acid metal alcoholates and process for preparation of same
US2703798A (en) * 1950-05-25 1955-03-08 Commercial Solvents Corp Detergents from nu-monoalkyl-glucamines
US2658072A (en) 1951-05-17 1953-11-03 Monsanto Chemicals Process of preparing amine sulfonates and products obtained thereof
BE557103A (en) 1956-05-14
US3123490A (en) * 1961-05-04 1964-03-03 Nacreous pigment and method for preparing same
US3087829A (en) * 1961-06-28 1963-04-30 Du Pont Micaceous pigment composition
US3892881A (en) 1968-12-18 1975-07-01 Petrolite Corp Non-Newtonian nutritive compositions
NL7307675A (en) * 1972-06-16 1973-12-18
US4606913A (en) 1978-09-25 1986-08-19 Lever Brothers Company High internal phase emulsions
US4389418A (en) 1981-02-25 1983-06-21 S. C. Johnson & Son, Inc. Skin care composition
NZ202128A (en) 1981-10-24 1985-02-28 Beecham Group Plc Detergent composition containing translucent gels
US5002680A (en) * 1985-03-01 1991-03-26 The Procter & Gamble Company Mild skin cleansing aerosol mousse with skin feel and moisturization benefits
US4999186A (en) * 1986-06-27 1991-03-12 The Procter & Gamble Company Novel sunscreen agents, sunscreen compositions and methods for preventing sunburn
US5004598A (en) * 1986-11-10 1991-04-02 The B. F. Goodrich Company Stable and quick-breaking topical skin compositions
US4832858A (en) * 1987-02-19 1989-05-23 Chesebrough-Pond's Inc. Water dispersible petroleum jelly compositions
US4981677A (en) * 1987-09-23 1991-01-01 L'oreal Petrolatum-containing aerosol foam concentrate
DE3856315T2 (en) * 1987-10-22 1999-10-14 Procter & Gamble Sunscreen containing chelating agents
JPH0660286B2 (en) 1989-02-15 1994-08-10 信越化学工業株式会社 Oily paste composition
US5035890A (en) 1989-04-10 1991-07-30 Dow Corning Corporation Emulsifier-free hand and body lotion
US5234619A (en) * 1989-05-05 1993-08-10 Lever Brothers Company, Division Of Conopco, Inc. Aqueous based personal washing cleanser
EP0398409B1 (en) 1989-05-16 1993-07-14 Unilever N.V. Fatty composition
US4956170A (en) 1989-06-28 1990-09-11 S. C. Johnson & Son, Inc. Skin moisturizing/conditioning antimicrobial alcoholic gels
US4980155A (en) 1989-09-11 1990-12-25 Revlon, Inc. Two phase cosmetic composition
ES2199214T3 (en) 1990-04-26 2004-02-16 THE PROCTER & GAMBLE COMPANY CHELATING COMPOSITIONS THAT INCLUDE OXIMATE COMPOUNDS.
WO1991016035A1 (en) 1990-04-26 1991-10-31 The Procter & Gamble Company Chelator compositions comprising alpha-diamine compounds
US5635171A (en) 1990-12-21 1997-06-03 L'oreal Cosmetic or pharmaceutical composition in the form of a rigid gel, particularly for containing inclusions therein
US5176665A (en) * 1991-01-18 1993-01-05 Alza Corporation Antimicrobial device for urine drainage container
FR2673372B1 (en) 1991-02-28 1993-10-01 Oreal COSMETIC COMPOSITION CAPABLE OF REDUCING SKIN DEFECTS.
AU658608B2 (en) 1991-03-25 1995-04-27 Astellas Pharma Europe B.V. Topical preparation containing a suspension of solid lipid particles
DE4207722A1 (en) 1991-05-28 1992-12-03 Merck Patent Gmbh SURFACE-MODIFIED PLAIN-SHAPED PIGMENTS WITH IMPROVED REALLY BEHAVIOR
US5387417A (en) * 1991-08-22 1995-02-07 Dow Corning Corporation Non-greasy petrolatum emulsion
US5304334A (en) * 1992-04-28 1994-04-19 Estee Lauder, Inc. Method of preparing a multiphase composition
JP2589932B2 (en) * 1992-06-15 1997-03-12 インターナショナル・ビジネス・マシーンズ・コーポレイション Global optimization method and system for device allocation
FR2694494B1 (en) 1992-08-05 1994-09-30 Rhone Poulenc Chimie Cosmetic composition containing non-water-soluble particles in suspension.
US5687779A (en) 1992-09-17 1997-11-18 Tetra Laval Holdings & Finance S.A. Packaging machine system for filling primary and secondary products into a container
US5490995A (en) * 1992-10-30 1996-02-13 The Procter & Gamble Company Solid nondigestible polyol polyesters containing esterified hydroxy fatty acids such as esterified ricinoleic acid
GB9223603D0 (en) 1992-11-11 1992-12-23 Unilever Plc Cosmetic composition
FR2699818B1 (en) 1992-12-24 1995-02-03 Oreal Cosmetic or pharmaceutical composition containing in combination a polyphenol and an extract of gingko.
US5989536A (en) 1993-07-03 1999-11-23 The Procter & Gamble Company Personal cleansing compositions containing alkoxylated ether and cationic ammonium salt for deposition of active agent upon the skin
AU691205B2 (en) * 1993-10-02 1998-05-14 Procter & Gamble Company, The Cosmetic make-up compositions
WO1995013048A1 (en) 1993-11-12 1995-05-18 The Procter & Gamble Company Desquamation compositions containing salicylic acid and zwitterionic compounds
US5681852A (en) 1993-11-12 1997-10-28 The Procter & Gamble Company Desquamation compositions
DE4341794C1 (en) 1993-12-08 1995-01-19 Henkel Kgaa Cosmetic and/or pharmaceutical compositions with improved skin feel
US6068834A (en) * 1994-03-04 2000-05-30 The Procter & Gamble Company Skin lightening compositions
US5472728A (en) 1994-04-22 1995-12-05 Kraft Foods, Inc. Edible fat-containing margarine type products and process for preparing same
GB9414572D0 (en) 1994-07-19 1994-09-07 Unilever Plc Soap composition
GB9414573D0 (en) * 1994-07-19 1994-09-07 Unilever Plc Detergent composition
GB9414574D0 (en) 1994-07-19 1994-09-07 Unilever Plc Detergent composition
US5534265A (en) 1994-08-26 1996-07-09 The Procter & Gamble Company Thickened nonabrasive personal cleansing compositions
US5578299A (en) 1994-10-20 1996-11-26 The Andrew Jergens Company Rinse-off skin conditioner
US5540853A (en) 1994-10-20 1996-07-30 The Procter & Gamble Company Personal treatment compositions and/or cosmetic compositions containing enduring perfume
GB9423573D0 (en) * 1994-11-22 1995-01-11 Rhone Poulenc Chemicals Process for the preparation of amphoacetate surfactants
EP0796084B1 (en) 1994-12-06 1999-05-06 The Procter & Gamble Company Shelf stable skin cleansing liquid with gel forming polymer, lipid and crystalline ethylene glycol fatty acid ester
US5948417A (en) * 1994-12-09 1999-09-07 The Proctor & Gamble Company Solid cosmetic composition
US5618522A (en) * 1995-01-20 1997-04-08 The Procter & Gamble Company Emulsion compositions
CN1097453C (en) * 1995-02-15 2003-01-01 普罗克特和甘保尔公司 Crystalline hydroxy waxes as oil in water stabilizers for skin cleansing lqiuid composition
US5607980A (en) * 1995-07-24 1997-03-04 The Procter & Gamble Company Topical compositions having improved skin feel
EP0839023B1 (en) 1995-08-07 2003-04-09 Unilever Plc Liquid cleansing composition comprising soluble, lamellar phase inducing structurant
FR2740334B1 (en) 1995-10-25 1997-12-05 Oreal COSMETIC COMPOSITION CONTAINING A MONOESTER OF C4-C10 ACID AND C16-C18 ALCOHOL AND HOLLOW PARTICLES
US5939082A (en) * 1995-11-06 1999-08-17 The Procter & Gamble Company Methods of regulating skin appearance with vitamin B3 compound
US5654362A (en) 1996-03-20 1997-08-05 Dow Corning Corporation Silicone oils and solvents thickened by silicone elastomers
AU3692097A (en) * 1996-08-02 1998-02-25 Plum Kemi Produktion A/S An oil-in-water emulsion for use on human skin for cleansing, preserving or improving the condition of the skin
US5760116A (en) 1996-09-05 1998-06-02 General Electric Company Elastomer gels containing volatile, low molecular weight silicones
US6132873A (en) 1996-09-21 2000-10-17 Merck Patent Gesellschaft Mit Beschrankter Haftung Multilayered interference pigments
US5716920A (en) * 1996-09-23 1998-02-10 The Procter & Gamble Company Method for preparing moisturizing liquid personal cleansing compostions
US6194364B1 (en) * 1996-09-23 2001-02-27 The Procter & Gamble Company Liquid personal cleansing compositions which contain soluble oils and soluble synthetic surfactants
US5972361A (en) 1996-10-25 1999-10-26 The Procter & Gamble Company Cleansing products
US5869071A (en) * 1996-11-07 1999-02-09 B & G Labs, Inc. One-step skin cleaning composition and skin treatment method for incontinent dermatitis
US5849281A (en) 1996-11-12 1998-12-15 S. C. Johnson & Son, Inc. Method of soap-free shaving
US5747011A (en) * 1996-11-25 1998-05-05 Schering-Plough Healthcare Products, Inc. Sunscreen with disappering color indicator
US6261541B1 (en) 1996-11-25 2001-07-17 Schering-Plough Healthcare Products, Inc. Sunless tanning emulsions with disappearing color indicator
US6290936B1 (en) 1996-11-25 2001-09-18 Schering-Plough Healthcare Products, Inc. Sunscreen with disappearing color indicator
DE19650952A1 (en) 1996-12-07 1998-06-10 Henkel Kgaa Two-phase skin care products
US5811487A (en) 1996-12-16 1998-09-22 Dow Corning Corporation Thickening silicones with elastomeric silicone polyethers
WO1998027193A1 (en) 1996-12-16 1998-06-25 The Procter & Gamble Company Personal cleansing bar composition containing sodium lauroyl lactylate
AU5898598A (en) 1996-12-19 1998-07-15 Rhodia Inc. Liquid delivery systems
US5954213A (en) 1996-12-27 1999-09-21 Lever Brothers Company Dual container and individual chamber therefor
US5817609A (en) 1997-01-08 1998-10-06 Lever Brothers Company, Division Of Conopco, Inc. Bar composition comprising low viscosity oils pre-thickened by non-antifoaming hydrophobic polymers
US5929019A (en) 1997-01-30 1999-07-27 Lever Brothers Company, Division Of Conopco, Inc. Cleansing composition with separately dispensed cleansing base and benefit base wherein benefit base also comprises surfactant
US6440399B1 (en) * 1997-03-25 2002-08-27 Beiersdorf Ag Emulsifier-free finely dispersed systems of the water-in-oil type
US5965501A (en) 1997-03-28 1999-10-12 Lever Brothers Company, Division Of Conopco, Inc. Personal washing bar compositions comprising emollient rich phase/stripe
US5885342A (en) * 1997-05-09 1999-03-23 Engelhard Corporation Blended nacreous pigments, colorants and adjuvants
US5888492A (en) * 1997-05-21 1999-03-30 The Andrew Jergens Company Rinse-off skin conditioner
US6280757B1 (en) 1997-05-22 2001-08-28 The Procter & Gamble Company Cleansing articles for skin or hair
US6174533B1 (en) * 1997-05-23 2001-01-16 The Procter & Gamble Company Skin care compositions and method of improving skin appearance
TW505521B (en) * 1997-06-25 2002-10-11 Kao Corp Hair cosmetics
US5965500A (en) 1997-07-24 1999-10-12 Levers Brothers Company, Division Of Conopco, Inc. Stable liquid composition comprising high levels of emollients
US5914177A (en) 1997-08-11 1999-06-22 The Procter & Gamble Company Wipes having a substrate with a discontinuous pattern of a high internal phase inverse emulsion disposed thereon and process of making
US5873494A (en) * 1997-09-05 1999-02-23 Aptargroup, Inc. Dual stream liquid dispensing structure
US5928632A (en) 1997-09-19 1999-07-27 The Andrew Jergens Company Surfactant free rinse-off skin conditioning formulation
JP2001519376A (en) * 1997-10-14 2001-10-23 ザ、プロクター、エンド、ギャンブル、カンパニー Personal cleansing composition comprising a mid-chain branched surfactant
US6150403A (en) 1997-10-14 2000-11-21 The Procter & Gamble Company Topical compositions for regulating the oily/shiny appearance of skin
US5997887A (en) 1997-11-10 1999-12-07 The Procter & Gamble Company Skin care compositions and method of improving skin appearance
EP0917870A1 (en) 1997-11-21 1999-05-26 Unilever Plc Crosslinked elastomeric silicones in aqueous emulsion cosmetic compositions
JPH11158026A (en) 1997-12-01 1999-06-15 Shiseido Co Ltd Moisturizing agent and skin lotion
CN1291883A (en) 1998-01-28 2001-04-18 宝洁公司 Liquid personal cleansing emulsion compositions with containing weighting oil
CN1291885A (en) 1998-01-28 2001-04-18 宝洁公司 Moisturizing personal cleansing compositions with improved lipid deposition
FR2780644B1 (en) * 1998-07-03 2001-07-20 Oreal COSMETIC OR DERMATOLOGICAL COMPOSITION IN THE FORM OF A DISPERSION OF AN OIL PHASE AND AN AQUEOUS PHASE, STABILIZED USING CUBIC GEL PARTICLES
US6419783B1 (en) 1999-04-16 2002-07-16 Unilever Home & Personal Care Usa Container and closure
DE19834821A1 (en) * 1998-08-01 2000-02-03 Beiersdorf Ag Emulsifier-free finely dispersed systems of the oil-in-water and water-in-oil type
FR2783159B1 (en) * 1998-09-16 2000-11-17 Oreal EMULSION CONSISTING OF A HYDROPHILIC THICKENING COMPOUND AND A THICKNING COPOLYMER, COMPOSITIONS CONSISTING OF THE SAID EMULSION, AND USES
DE19842744B4 (en) * 1998-09-18 2006-12-21 Beiersdorf Ag Emulsifier-free finely disperse oil-in-water and water-in-oil systems and their use
DE19842767A1 (en) 1998-09-18 2000-03-23 Beiersdorf Ag Emulsifier-free finely dispersed systems of the oil-in-water and water-in-oil type
DE19842732A1 (en) * 1998-09-18 2000-03-23 Beiersdorf Ag Emulsifier-free finely dispersed systems of the oil-in-water and water-in-oil type
DE19855767A1 (en) 1998-12-03 1999-12-23 Wella Ag Manually and reversibly emulsifiable hair- or scalp-treatment composition free of organic emulsifiers
JP2000229817A (en) 1999-02-09 2000-08-22 Nippon Shikizai Kogyo Kenkyusho:Kk Production of multi-colored solid cosmetic and apparatus for the same
US6183766B1 (en) * 1999-02-12 2001-02-06 The Procter & Gamble Company Skin sanitizing compositions
US6495498B2 (en) 1999-05-27 2002-12-17 Johnson & Johnson Consumer Companies, Inc. Detergent compositions with enhanced depositing, conditioning and softness capabilities
FR2794765B1 (en) 1999-06-09 2005-03-11 Oreal INTERFERENTIAL PIGMENT AND COSMETIC COMPOSITION COMPRISING SUCH A PIGMENT
JP3665844B2 (en) 1999-06-11 2005-06-29 株式会社コーセー Creamy detergent composition
FR2795317B1 (en) 1999-06-25 2001-08-24 Oreal HAIR COSMETIC PROCESS USING METALLIC-LIKE PARTICLES TO GIVE SHINE HAIR
DE19934943B4 (en) 1999-07-26 2007-08-02 Beiersdorf Ag Cosmetic and dermatological preparations based on O / W emulsions
US6516838B2 (en) * 1999-07-28 2003-02-11 Patrick Thibiant Apparatus and process for forming novel spiral compositions
CA2379651A1 (en) 1999-07-29 2001-02-08 The Procter & Gamble Company Hair conditioning composition comprising hydrophobically modified cellulose ether
JP3724988B2 (en) 1999-07-30 2005-12-07 信越化学工業株式会社 Novel silicone compound and cosmetic comprising the same
US6394323B2 (en) * 1999-08-24 2002-05-28 Owens-Brockway Plastic Products Inc. Dispenser package for fluent products and method of manufacture
US6797742B2 (en) 1999-08-25 2004-09-28 General Electric Company Polar solvent compatible polyethersiloxane elastomers
US6346583B1 (en) * 1999-08-25 2002-02-12 General Electric Company Polar solvent compatible polyethersiloxane elastomers
US6517939B1 (en) * 1999-09-03 2003-02-11 Engelhard Corporation Noble metal coated substrate pigments
FR2798062B1 (en) 1999-09-07 2001-10-26 Oreal COMPOSITION AND METHOD FOR MAKING UP KERATINIC MATERIALS
US6426326B1 (en) 1999-09-16 2002-07-30 Unilever Home & Person Care Usa, A Division Of Conopco, Inc. Liquid cleansing composition comprising lamellar phase inducing structurant with low salt content and enhanced low temperature stability
US6723688B1 (en) * 1999-09-27 2004-04-20 Shaklee Corporation Cleanser that is gentle to human skin
JP4557193B2 (en) * 1999-10-05 2010-10-06 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング Highly oriented flaky pigment and process for producing the same
WO2001026985A1 (en) 1999-10-08 2001-04-19 Lloyd James J Portable beverage delivery system
FR2800605B1 (en) 1999-11-08 2002-08-16 Oreal COMPOSITION CONTAINING AN AQUEOUS SUSPENSION OF ELASTOMERIC ORGANOPOLYSILOXANE PARTICLES, AND ITS COSMETIC USES
US6521216B1 (en) * 1999-11-12 2003-02-18 The Procter & Gamble Company Dual phase stannous oral compositions
GB9929969D0 (en) 1999-12-17 2000-02-09 Unilever Plc Packaged liquid cleansing composition
US6213166B1 (en) * 2000-01-12 2001-04-10 Patrick Thibiant Apparatus and process for forming novel spiral compositions
DE60119693T2 (en) 2000-01-31 2007-04-26 Engelhard Corp. TENSID-FREE TOPICAL COMPOSITIONS AND METHOD FOR THE FAST MANUFACTURE THEREOF
DE10008896A1 (en) * 2000-02-25 2001-08-30 Beiersdorf Ag Improving the solubility and compatibility of benzotriazole UV filters in oils, e.g. in cosmetics or dermatological compositions, by addition of dialkylnaphthalates
DE10008895A1 (en) 2000-02-25 2001-08-30 Beiersdorf Ag Stabilization of active substances that are sensitive to oxidation and / or UV
CA2300227C (en) 2000-03-08 2010-08-10 George's Cream Inc. Skin cream
US6534457B2 (en) * 2000-03-20 2003-03-18 Unilever Home And Personal Care Usa, Division Of Conopco, Inc. Extrudable multiphase composition comprising lamellar phase inducing structurant in each phase
US6534456B2 (en) * 2000-03-20 2003-03-18 Unilever Home And Personal Care Usa, Division Of Conopco, Inc. Extrudable multiphase composition comprising a lamellar phase and an isotropic phase
AU4594601A (en) 2000-03-23 2001-10-03 Collaborative Technologies Inc Base compositions for preparing surfactant free topical compositions
JP4530468B2 (en) 2000-03-30 2010-08-25 株式会社コーセー Cosmetics
DE10015992A1 (en) 2000-03-31 2001-10-18 Rwe Dea Ag Aqueous pearly luster concentrate comprises anionic surfactant component comprising anionic gemini surfactant(s) and poorly foaming anionic detergent component, nonionic surfactant and pearl luster component
AU2000240719A1 (en) 2000-04-05 2001-10-23 The Procter And Gamble Company Hair conditioning composition comprising a thickening system
US20010047039A1 (en) 2000-04-12 2001-11-29 Mcmanus Richard L. Cationic emulsifier-enhanced liquid crystal gel network based skin care moisturizing compositions
MXPA02010256A (en) 2000-04-17 2003-04-25 Procter & Gamble Phase separated rinse off hair coloring cleansing products.
US6245323B1 (en) 2000-05-26 2001-06-12 Engelhard Corporation Bonded metal hydroxide-organic composite polymer films on particulate substrates
US6695510B1 (en) * 2000-05-31 2004-02-24 Wyeth Multi-composition stick product and a process and system for manufacturing the same
EP1164171A3 (en) 2000-06-12 2002-04-24 General Electric Company Silicone compositions
US6310019B1 (en) * 2000-07-05 2001-10-30 Wako Pure Chemical Industries, Ltd. Cleaning agent for a semi-conductor substrate
DE10033414B4 (en) 2000-07-08 2004-02-19 Wella Aktiengesellschaft Clear, two-phase, foam-forming aerosol hair care product
US20020022040A1 (en) * 2000-07-10 2002-02-21 The Proctor & Gamble Company Methods of enhancing delivery of oil-soluble skin care actives
US6385992B1 (en) * 2000-08-21 2002-05-14 Joseph Frank Flore, Jr. Beverage bottle container
US6574985B2 (en) 2000-08-21 2003-06-10 Joseph F. Fiore, Jr. Beverage bottle container
US6429177B1 (en) 2000-08-22 2002-08-06 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Separating multi-phase personal wash composition in a transparent or translucent package
US6471762B1 (en) 2000-08-23 2002-10-29 Engelhard Corp. Bonded metal-hydroxide-organic composite polymer films on lamellar pigments
FR2814677B1 (en) 2000-10-03 2003-04-18 Oreal HYDROPHILIC CONTINUOUS PHASE COSMETIC COMPOSITION COMPRISING A MULTI-LAYER GONIOCHROMATIC PIGMENT AND USE THEREOF
EP1322280A1 (en) 2000-10-03 2003-07-02 Unilever Plc Cosmetic and personal care compositions
US6547063B1 (en) * 2000-10-10 2003-04-15 The Procter & Gamble Company Article for the delivery of foam products
JP2002128639A (en) 2000-10-26 2002-05-09 Kose Corp Cosmetic
GB0026473D0 (en) * 2000-10-30 2000-12-13 Unilever Plc Shear gel compositions
JP2002138010A (en) 2000-10-31 2002-05-14 Nippon Sheet Glass Co Ltd Cosmetic
DE10065047A1 (en) 2000-12-23 2002-07-04 Beiersdorf Ag Gelcèmes in the form of O / W emulsions containing one or more ammonium aryldimethyltaurate / vinylpyrrolidone copolymers
US6555509B2 (en) * 2001-01-29 2003-04-29 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Multi-phase toilet articles and methods for their manufacture
US6691394B1 (en) * 2001-02-12 2004-02-17 Owens-Brockway Plastic Products Inc. Disk-top fluid dispensing package
US6564978B1 (en) * 2001-02-12 2003-05-20 Owens-Brockway Plastic Products Inc. Disk-top fluid dispensing package
US6395690B1 (en) * 2001-02-28 2002-05-28 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Process for making mild moisturizing liquids containing large oil droplet
US6395691B1 (en) 2001-02-28 2002-05-28 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Personal wash compositions containing particle-in-oil dispersion
JP4693260B2 (en) 2001-03-15 2011-06-01 株式会社コーセー Cosmetics
US20030003069A1 (en) * 2001-04-04 2003-01-02 Carson John C. Multiple phase foaming personal cleansing products
US7192598B2 (en) * 2001-05-17 2007-03-20 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Wet-skin treatment compositions
US6923975B2 (en) * 2001-05-17 2005-08-02 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Method of enhanced moisture or reduced drying using wet-skin treatment compositions
CA2448822A1 (en) * 2001-06-01 2002-12-12 Lipo Chemicals, Inc. Method of using optically-activated particles in cosmetic preparations
WO2002100358A1 (en) 2001-06-11 2002-12-19 Patrick Thibiant Two-phase composition having a visible pattern
EP1418886A1 (en) 2001-08-10 2004-05-19 Beiersdorf AG Cosmetic cleansing formulations, based on a combination of sodium laureth sulphate and alkyl polyamphopolycarboxy glycinates
DE10141473A1 (en) * 2001-08-29 2003-03-20 Beiersdorf Ag Photoprotective cosmetic or dermatological composition, useful for moisturizing the skin and protecting it against light-induced aging, comprise a particulate UV filter and a dialkyl naphthalate
US20040234477A1 (en) 2001-09-14 2004-11-25 Koji Sakuta Composition and cosmetic preparation containing the same
EP1297821A1 (en) * 2001-10-01 2003-04-02 Hive of Beauty (Europe) BVBA Skin treatment compositions
MXPA04003015A (en) * 2001-10-03 2004-07-15 Procter & Gamble Shampoo containing particles and a deposition aid.
US20040005285A1 (en) * 2001-10-03 2004-01-08 The Procter & Gamble Company Conditioner containing particles
US20030161805A1 (en) 2001-11-16 2003-08-28 Kobo Products, Inc. Organosilicon treated cosmetic powders, their production and use
MXPA04006002A (en) 2001-12-21 2004-09-27 Rhodia Stable surfactant compositions for suspending components.
DE10200724A1 (en) 2002-01-11 2003-07-24 Clariant Gmbh Three-phase systems
US6645511B2 (en) * 2002-01-16 2003-11-11 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Wet-skin treatment compositions
US6673755B2 (en) * 2002-01-16 2004-01-06 The Procter & Gamble Company Personal cleansing compositions containing cleansing and skin active phases separated by one or more packaging barriers
EP1471880A1 (en) 2002-02-08 2004-11-03 The Procter & Gamble Company Rinse-off skin conditioning compositions
US6648176B1 (en) 2002-02-12 2003-11-18 James A. Donovan Safety toothpaste containers
US20030190336A1 (en) 2002-03-18 2003-10-09 Adams Christine Helga Personal care compositions comprising solid particles enterapped in a gel network
ES2193875B2 (en) 2002-04-09 2005-03-01 Laboratorios Del Dr. Esteve, S.A. DERIVATIVES OF BENZOXAZINONA, ITS PREPARATION AND ITS APPLICATION AS MEDICATIONS.
BRPI0201235B1 (en) 2002-04-12 2017-05-02 Natura Cosmeticos Sa multiphase cosmetic makeup
GB0209510D0 (en) 2002-04-26 2002-06-05 Procter & Gamble Containers comprising at least one label made of an elastomeric material adhered to a squeezable resilient wall
US20030211069A1 (en) * 2002-05-09 2003-11-13 The Procter & Gamble Company Rinsable skin conditioning compositions
DE10220867A1 (en) 2002-05-10 2003-11-20 Henkel Kgaa Cosmetic compositions with a silicone elastomer and a thickening polymer latex
JP4145681B2 (en) * 2002-05-27 2008-09-03 三好化成株式会社 Powder surface-treated with specific acid ester oil and cosmetic composition containing the same
US6752982B2 (en) 2002-06-12 2004-06-22 The Gillette Company Personal care product
US6673280B1 (en) * 2002-06-20 2004-01-06 Certainteed Corporation Process for making a board product from scrap materials
US6664217B1 (en) 2002-07-18 2003-12-16 Unilever Home & Personal Care, Usa Division Of Conopco, Inc. Toilet bar having simultaneous exfoliating and moisturizing properties
US6727209B2 (en) * 2002-08-14 2004-04-27 Unilever Home & Personal Care, Usa, Division Of Conopco, Inc. Biphasic composition induced by polydextrose and sucrose
US6759376B2 (en) * 2002-09-11 2004-07-06 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Oil-containing personal wash liquid compositions or emulsions comprising particles of high refractive index and defined thickness, geometry and size
JP4280237B2 (en) * 2002-09-11 2009-06-17 ユニリーバー・ナームローゼ・ベンノートシヤープ Oil-containing body wash composition or emulsion comprising particles of high refractive index
US6780826B2 (en) * 2002-09-11 2004-08-24 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Oil-containing personal wash compositions or emulsions comprising particles of high refractive index and defined thickness, geometry and size
FR2844707B1 (en) * 2002-09-19 2006-05-12 Oreal WIPES AND USES WITHOUT THE COSMETIC DOMAIN
JP4276181B2 (en) * 2002-09-20 2009-06-10 ザ プロクター アンド ギャンブル カンパニー Striped liquid personal cleansing composition containing cleansing phase and separated efficacy phase
US20040091445A1 (en) * 2002-11-01 2004-05-13 The Procter & Gamble Company Rinse-off personal care compositions comprising cationic perfume polymeric particles
US7524807B2 (en) * 2002-11-01 2009-04-28 The Procter & Gamble Company Rinse-off personal care compositions comprising anionic and/or nonionic perfume polymeric particles
EP1558718B1 (en) 2002-11-04 2007-09-12 The Procter & Gamble Company Liquid laundry detergent
EP1558208A1 (en) * 2002-11-04 2005-08-03 The Procter & Gamble Company Striped liquid personal cleansing compositions containing a cleansing phase and a separate benefit phase with improved stability
FR2843541A1 (en) 2002-11-06 2004-02-20 Oreal Transparent make-up removal composition comprises a vegetable oil, a volatile hydrocarbon and a non-ionic surfactant, useful for cleansing and removal of make-up from the skin
FR2843540A1 (en) 2002-11-06 2004-02-20 Oreal Transparent composition for external application comprising a volatile hydrocarbon, non-ionic surfactant and hexylene glycol, useful for skin cleansing or make-up removal
US6924256B2 (en) 2002-11-08 2005-08-02 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Liquid cleansing composition having simultaneous exfoliating and moisturizing properties
DE10301704A1 (en) 2003-01-17 2004-07-29 Basf Ag Mixture of alkoxylated alkyl (di)glycols and alkyl sulfates, ether sulfates and/or sulfonates useful in cosmetic compositions and washing-up liquids
US20040146475A1 (en) 2003-01-17 2004-07-29 Peffly Marjorie Mossman Personal care composition containing a cationic cellulose polymer and an anionic surfactant system
US20040180020A1 (en) 2003-03-15 2004-09-16 Manelski Jean Marie Cosmetic compositions
US7229486B2 (en) 2003-04-17 2007-06-12 Saralee/De N.V. Shoe and leather care product
WO2004098545A2 (en) 2003-05-01 2004-11-18 The Procter & Gamble Company Visually distinctive multiple liquid phase compositions
CN100558338C (en) * 2003-05-01 2009-11-11 宝洁公司 By cleansing phase and the striped liquid personal cleansing compositions that comprises the separate benefit phase composition of High Internal Phase Emulsion
CA2522826C (en) 2003-05-01 2011-09-20 The Procter & Gamble Company Striped liquid personal cleansing compositions containing a cleansing phase and a separate benefit phase comprising a water in oil emulsion
US20040234478A1 (en) 2003-05-08 2004-11-25 The Procter & Gamble Company Personal care compositions containing a silicone elastomer
US20050100570A1 (en) * 2003-05-08 2005-05-12 The Procter & Gamble Company Multi-phase personal care composition
US20040234565A1 (en) * 2003-05-08 2004-11-25 The Procter & Gamble Company Method for using personal care compositions containing shiny particles
US20040223991A1 (en) * 2003-05-08 2004-11-11 The Procter & Gamble Company Multi-phase personal care composition
US8790668B2 (en) 2003-05-08 2014-07-29 The Procter & Gamble Company Personal care compositions that deposit shiny particles
US20040223929A1 (en) * 2003-05-08 2004-11-11 The Procter & Gamble Company Personal care compositions containing hydrophobically modified interference pigments
US20040223992A1 (en) 2003-05-09 2004-11-11 The Procter & Gamble Company Wet skin treatment compositions comprising gel-networks
US20040232023A1 (en) 2003-05-21 2004-11-25 Unilever Bestfoods North America Asymmetric package for market appeal
US8092787B2 (en) 2003-05-22 2012-01-10 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Personal product compositions comprising structured benefit agent premix or delivery vehicle and providing enhanced effect of optical modifier separate from structured benefit agent
US20040234469A1 (en) 2003-05-22 2004-11-25 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Personal product bar compositions comprising crystalline wax structured premix or delivery vehicle
US7776346B2 (en) 2003-05-22 2010-08-17 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Personal product compositions comprising structured benefit agent premix or delivery vehicle
US7560125B2 (en) 2003-05-22 2009-07-14 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Personal product compositions comprising structured benefit agent premix or delivery vehicle and providing enhanced deposition of hydrophilic benefit agent
US7875582B2 (en) * 2003-05-22 2011-01-25 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Nonbar personal product compositions comprising crystalline wax structured benefit agent premix or delivery vehicle
US7776347B2 (en) 2003-05-22 2010-08-17 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Personal product compositions comprising structured benefit agent premix or delivery vehicle and providing enhanced effect of hydrophobic material separate from the structured benefit agent
US7838479B2 (en) 2003-06-09 2010-11-23 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Packaged product containing an extrudable multiphase composition of a free fatty acid phase and a soap phase
US20050003975A1 (en) * 2003-06-18 2005-01-06 Browne Yvonne Bridget Blooming soap bars
AU2004259004B2 (en) * 2003-07-22 2010-04-22 Rhodia Inc. New branched sulfates for use in personal care formulations
FR2863873A1 (en) 2003-12-18 2005-06-24 Oreal Anhydrous cosmetic composition useful for skin cleansing or exfoliation comprises an oil and a nonionic surfactant system comprising an ethoxylated fatty acid glyceride and an ethoxylated hydrogenated oil
US20050143269A1 (en) 2003-12-24 2005-06-30 Wei Karl S. Multi-phase personal cleansing compositions comprising a lathering cleansing phase and a non-lathering structured aqueous phase
US8951947B2 (en) * 2003-12-24 2015-02-10 The Procter & Gamble Company Multi-phase personal cleansing compositions comprising a lathering cleansing phase and a non-lathering structured aqueous phase
US7268104B2 (en) 2003-12-31 2007-09-11 Kimberly-Clark Worldwide, Inc. Color changing liquid cleansing products
WO2005084616A1 (en) 2004-02-27 2005-09-15 The Procter & Gamble Company A mild multi-phased personal care composition
AU2005219395A1 (en) 2004-02-27 2005-09-15 The Procter & Gamble Company A mild body wash
US20050238680A1 (en) 2004-04-21 2005-10-27 Qing Stella Personal care compositions that deposit hydrophilic benefit agents
US20050250658A1 (en) 2004-05-07 2005-11-10 Putman Christopher D Methods of conditioning the skin and articles of commerce
US20050276768A1 (en) 2004-06-14 2005-12-15 Karl Shiqing Wei Multi-phased personal care composition
US8623341B2 (en) * 2004-07-02 2014-01-07 The Procter & Gamble Company Personal care compositions containing cationically modified starch and an anionic surfactant system
WO2006010090A1 (en) * 2004-07-09 2006-01-26 The Procter & Gamble Company Multi-phased personal care composition
DE102004041573A1 (en) 2004-08-26 2006-03-02 Henkel Kgaa New agent for the treatment of keratinic fibers
DE102004045253A1 (en) 2004-09-17 2006-04-13 Henkel Kgaa New cationic diagonally cross linked copolymer useful for improving physical characteristics of keratinic fibers (preferably human hair) and for styling and conditioning hairs
US20060079420A1 (en) * 2004-10-08 2006-04-13 Wagner Julie A Multi-phase personal cleansing composition
US20060079421A1 (en) * 2004-10-08 2006-04-13 Wagner Julie A Stable multi-phased personal care composition
US7666825B2 (en) * 2004-10-08 2010-02-23 The Procter & Gamble Company Stable, patterned multi-phased personal care composition
ATE493177T1 (en) 2005-03-04 2011-01-15 Procter & Gamble WASHABLE OR WIPABLE SKIN CLEANING COMPOSITIONS
WO2006102113A2 (en) 2005-03-21 2006-09-28 The Procter & Gamble Company Multi-phase personal care composition comprising visually distinct phases

Also Published As

Publication number Publication date
EP1848508A2 (en) 2007-10-31
US20060182699A1 (en) 2006-08-17
CN101090751A (en) 2007-12-19
WO2006088673A3 (en) 2007-01-18
CA2589044C (en) 2013-04-23
JP2008524263A (en) 2008-07-10
US8147853B2 (en) 2012-04-03
MX2007007149A (en) 2007-08-14
WO2006088673A2 (en) 2006-08-24

Similar Documents

Publication Publication Date Title
CA2589044C (en) Personal care compositions containing hydrophobically modified non-platelet particles
CA2590348C (en) Rinse-off or wipe-off skin cleansing compositions
EP1633442B1 (en) Method for depositing shiny particles on keratinous surfaces from rinse-off compositions
US8790668B2 (en) Personal care compositions that deposit shiny particles
EP1633443B1 (en) Personal care compositions containing hydrophobically modified interference pigments
US20030152540A1 (en) Rinse-off skin conditioning compositions
JP2006506444A (en) Striped liquid personal cleansing composition containing cleansing phase and separated efficacy phase
JP4880078B1 (en) Powder cosmetics
CN101090752A (en) Rinse-off or wipe-off skin cleansing compositions

Legal Events

Date Code Title Description
EEER Examination request
MKLA Lapsed

Effective date: 20190204