US20100087548A1 - Dual Phase Cosmetic Composition - Google Patents

Dual Phase Cosmetic Composition Download PDF

Info

Publication number
US20100087548A1
US20100087548A1 US12/633,365 US63336509A US2010087548A1 US 20100087548 A1 US20100087548 A1 US 20100087548A1 US 63336509 A US63336509 A US 63336509A US 2010087548 A1 US2010087548 A1 US 2010087548A1
Authority
US
United States
Prior art keywords
volatile
weight
oil
total composition
amount
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.)
Abandoned
Application number
US12/633,365
Inventor
Linda Najdek
Derron T. Peck
Elena M. Ciriello
Ralph Vitale
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22117405&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=US20100087548(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Individual filed Critical Individual
Priority to US12/633,365 priority Critical patent/US20100087548A1/en
Publication of US20100087548A1 publication Critical patent/US20100087548A1/en
Abandoned legal-status Critical Current

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
    • A61K8/03Liquid compositions with two or more distinct layers
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8182Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/31Hydrocarbons
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/58Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585Organosilicon compounds
    • 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
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/891Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q1/00Make-up preparations; Body powders; Preparations for removing make-up
    • A61Q1/14Preparations for removing make-up

Definitions

  • the present invention relates to cosmetic compositions.
  • the invention relates to two-phase cleansing compositions which are particularly useful in makeup removal.
  • Dual phase skin cosmetic compositions are currently very popular, in that they provide a broad range of cleansing/conditioning potential within a single product, and are also aesthetically appealing to the consumer.
  • the dual phase product contains an aqueous phase and an oil phase, each adapted to removing a particular type of residue from the skin, or delivering a particular type of active.
  • the aqueous phase of a dual phase cleansing composition is designed to remove water-soluble material from the skin, while the oil phase is designed to remove oil-based, or “waterproof” material from the skin.
  • a number of factors must be considered in making a successful dual phase product.
  • the two phases must be vigorously mixed, providing a temporary apparently homogeneous single phase product which delivers both phases to the region to be treated simultaneously.
  • Surfactants are also frequently useful in the removal of waterproof makeup. Unfortunately, many such emulsifiers are drying to the skin and/or are irritating to users, and in particular cannot be routinely used in the eye area.
  • the two phases separate quickly after use, as the emulsified product has a cloudy appearance that is unappealing to consumers.
  • the time it takes for the phases to separate becomes longer and longer, and the product rapidly loses its initially attractive appearance.
  • oil soluble actives may be unstable if they remain in prolonged contact with the aqueous phase, and therefore, the amount of time spent in contact with the water phase should be minimized.
  • the dual phase product namely, the need for rapid and complete emulsification followed by rapid and complete separation, are at odds with each other, and to achieve both satisfactorily in a single product, in a way that is both cosmetically acceptable and attractive to the user, is often difficult.
  • the present invention provides a dual phase product in which the phases mix well and completely, and yet demixing is accomplished rapidly after use.
  • the product is non-irritating, and when used as a makeup remover, is highly successful in removing even the most difficult to remove oil-based cosmetics.
  • the present invention relates to a liquid dual phase cosmetic or dermatological composition
  • a liquid dual phase cosmetic or dermatological composition comprising an aqueous phase and an oil phase, at least one of the phases containing as a demixing agent, a film forming agent.
  • the demixing agent is a polyvinylpyrrolidone (hereinafter referred to as “PVP”) or a copolymer thereof.
  • PVP polyvinylpyrrolidone
  • the compositions of the invention are particularly useful when employed as a makeup remover, but may also be used for skin conditioning, or delivery of cosmetic or therapeutic active agents to the skin for the treatment and/or amelioration of various skin conditions.
  • demixing agents used in the present dual phase compositions are well-known in the art for being useful as film forming agents and for being useful in improving water resistance and wear of compositions. However, it has not been previously known that they can be used to facilitate rapid separation of phases in a two phase emulsion. In addition to this function, however, these demixing agents have the additional advantage of being extremely mild, and non-irritating. In particular, they do not appear to cause any irritation when in contact with the eye, which cannot be said of many other demixing agents.
  • any film-forming agent may be used in the compositions of the invention.
  • useful categories of demixing agents include acrylic acid polymers and copolymers, such as cyclo alkyl methacrylate copolymer; chitin or chitosan or derivatives thereof; or polyquaternium film formers, such as polyquaternium-11.
  • a preferred demixing agent is PVP or a copolymer thereof. Particularly preferred are PVP/hexadecene copolymer and/or PVP/polycarbamyl polyglycol ester. PVP/hexadecene copolymer is available commercially under the tradename Ganex V-216®, from ISP Sutton Labs of Chatham, N.J.
  • demixing agents include for example, PVP/dimethylaminoethylmethacrylate copolymer, PVP/eicosene copolymer, PVP/ethyl methacrylate/methacrylic acid copolymer, PVP/VA copolymer, PVP/1-triacontene, and listings of film formers in the CTFA Cosmetic Ingredient Handbook, incorporated herein by reference.
  • the demixing agent is added to either the oil phase or the water phase of the composition, usually in an amount of from about 0.001 to about 10 percent, preferably in an amount of about 0.01 to about 1 percent.
  • Dual phase compositions prepared with such a demixing agent emulsify rapidly and uniformly upon vigorous shaking, and demulsify completely upon resting within approximately 5 to 20 minutes.
  • the remainder of the composition is formulated depending on the nature of the desired end product.
  • the ratio of the oil phase to aqueous phase is not critical, and can be varied in accordance with the type of product, but will generally be between 30:70 to 70:30, more preferably between 40:60 to 60:40. Most preferably, the aqueous phase is present as a higher weight percent than the oil phase.
  • the aqueous phase may be any cosmetically acceptable water based material, such as deionized water, or floral water.
  • the oil phase may be any cosmetically or pharmaceutically acceptable oil, such an oil being defined for the present purpose as any pharmaceutically or cosmetically acceptable material which is substantially insoluble in water.
  • oils can perform different functions in the composition, the specific choice is dependent on the purpose for which it is intended.
  • the oils may be volatile or non-volatile, or a mixture of both.
  • suitable volatile oils include, but are not limited to, both cyclic and linear silicones, such as cyclomethicone, octamethylcyclotetrasiloxane, and decamethylcyclopentasiloxane; or straight or branched chain hydrocarbons having from 8-20 carbon atoms, such as decane, dodecane, tridecane, tetradecane, and C8-20 isoparaffins.
  • cyclic and linear silicones such as cyclomethicone, octamethylcyclotetrasiloxane, and decamethylcyclopentasiloxane
  • straight or branched chain hydrocarbons having from 8-20 carbon atoms such as decane, dodecane, tridecane, tetradecane, and C8-20 isoparaffins.
  • Non-volatile oils include, but are not limited to, vegetable oils, such as coconut oil, jojoba oil, corn oil, sunflower oil, palm oil, soybean oil; carboxylic acid esters such as isostearyl neopentanoate, cetyl octanoate, cetyl ricinoleate, octyl palmitate, dioctyl malate, coco-dicaprylate/caprate, decyl isostearate, myristyl myristate; animal oils such as lanolin and lanolin derivatives, tallow, mink oil or cholesterol; glyceryl esters, such as glyceryl stearate, glyceryl dioleate, glyceryl distearate, glyceryl linoleate, glyceryl myristate; non-volatile silicones, such as dimethicone, dimethiconol, dimethicone copolyol, phenyl
  • the composition also may contain other cosmetically or therapeutically useful components. It may, for example, be desirable to incorporate other surfactants into the formulation, again depending on the intended purpose of the formulation, for example, as cleansing agents to assist in wetting skin, emulsifying oils or solubilizing soil on skin or as foaming agents.
  • the surfactants employed may be any that are traditionally used for cosmetic or pharmaceutical purposes, and may be selected from nonionic, anionic, cationic or amphoteric surfactants, the identities of which are well known to those skilled in the art. Additional surfactants may be distributed in either or both of the phases of the formulation, and selection is limited only by a given surfactant's compatibility with the phase into which it is incorporated, and by the location to which the composition is to be applied.
  • emollients include emollients, humectants, fragrances, preservatives, and buffers.
  • humectants include emollients, humectants, fragrances, preservatives, and buffers.
  • buffers Such materials are routinely used in cosmetic products, and listings of appropriate materials can be found, for example in the International Cosmetic Ingredients Handbook, Third Edition, 1996 (CTFA).
  • the formulation can also be used for therapeutic or quasi-therapeutic purposes, and therefore may also comprise useful active ingredients, for the purposes of treating both the skin and hair.
  • useful active ingredients include, but are not limited to antioxidants, antimicrobials, sunscreens, analgesics, anesthetics, anti-acne agents, antidandruff agents, antidermatitis agents, antipruritic agents, anti-inflammatory agents, antihyperkeratolytic agents, anti-dry skin agents, antiperspirants, antipsoriatic agents, antiseborrheic agents, hair conditioners and hair treatment agents, antiaging agents, antiwrinkle agents, antihistamine agents, skin lightening agents, depigmenting agents, wound-healing agents, vitamins, corticosteroids, tanning agents, or hormones.
  • the location of the active in the formulation is determined by its solubility and/or stability in either oil or water.
  • the formulations of the present invention are useful for a variety of purposes, including skin or hair cleansers, skin or hair treatment products, sunscreen or suntanning products, and the like.
  • the composition is used for removing makeup.
  • the demixing agents because of their mildness, are eminently well-suited to being employed in a product which is usable around the eye.
  • the resulting makeup remover successfully cleans skin surfaces, particularly eyes and lips, of even the most transfer-resistant of currently used cosmetics, while remaining gentle and non-irritating to the user.
  • the oil phase contains a combination of both volatile and non-volatile oils.
  • the volatile oil portion is preferably a volatile hydrocarbon present in amounts of from about 30-70%, and more preferably 40-60%, and the non-volatile present at about 0.1-10%, preferably 0.2-5% by weight of the total composition.
  • the oil phase contains a blend of oils comprising isododecane at 25-40% by weight of the total composition, a volatile C 16 isoparaffin at 15-30% by weight of the total composition, and the non-volatile silicone at 0.1-1% by weight of the total composition.
  • the non-volatile portion of the oil phase is preferably a non-volatile silicone oil.
  • a preferred non-volatile silicone is dimethicone.
  • the amount of volatile oil used is considerably higher than that of the non-volatile oils; for example, the volatile oil will be present in an amount of about 30-70%, preferably about 40-60%, of the total composition, and the non-volatile oil in an amount of about 0.1-10%, preferably about 0.2-5% of the total composition.
  • the volatile oil portion contains a combination of a volatile silicone and a volatile hydrocarbon. More specifically, the oil phase contains a blend of oils comprising a low molecular weight cyclic silicone at 25-40% by weight of the total composition, a volatile C 16 isoparaffin at 15-30% by weight, and the non-volatile silicone at 0.1-1% by weight of the total composition.
  • the amount of surfactant added is preferably no more than 5%, and more preferably is in the range of 0.1-1%.
  • the surfactant may be of any type, i.e., anionic, nonionic, cationic or amphoteric; however, if the makeup remover is intended for use in the eye area, it is preferred that the surfactant should be a mild surfactant, such as LIPO-PEG-2 ⁇ L or disodium cocoaamphoidacetate (Miranol).
  • the components are combined as follows: the oil phase components, isododecane, isohexadecane, silicone and PEG-4 dilaurate are mixed with PVP/hexedecene copolymer (Ganex V-216®), and the water phase components, sodium chloride, potassium phosphate, hexylene glycol, fragrance, preservative and water are mixed together. First the oil phase is added to the selected container, then the water phase is added.

Abstract

The present invention relates to a method of formulating a liquid dual phase cosmetic or pharmaceutical composition in which the phases are separate before and after being mixed, the method comprising combining an aqueous phase and an oil phase, wherein one of the aqueous and oil phases has incorporated therein, as a demixing agent, an effective amount of a non-cationic film forming agent such as polyvinylpyrrolidone and copolymers thereof. The compositions of the invention are particularly useful as makeup removers.

Description

  • This application is a continuation of Ser. No. 11/926,671, filed Oct. 29, 2007, which is a divisional of application Ser. No. 10/618,803, filed on Jul. 14, 2003 (pending), which is a continuation of Ser. No. 09/074,051, filed Oct. 19, 2001 (granted), which is a CPA of 09/074,051, filed May 7, 1998 (now abandoned).
  • FIELD OF THE INVENTION
  • The present invention relates to cosmetic compositions. In particular, the invention relates to two-phase cleansing compositions which are particularly useful in makeup removal.
  • BACKGROUND OF THE INVENTION
  • Dual phase skin cosmetic compositions are currently very popular, in that they provide a broad range of cleansing/conditioning potential within a single product, and are also aesthetically appealing to the consumer. Typically, the dual phase product contains an aqueous phase and an oil phase, each adapted to removing a particular type of residue from the skin, or delivering a particular type of active. In a common use, for example, the aqueous phase of a dual phase cleansing composition is designed to remove water-soluble material from the skin, while the oil phase is designed to remove oil-based, or “waterproof” material from the skin.
  • A number of factors must be considered in making a successful dual phase product. For example, in order to function properly, the two phases must be vigorously mixed, providing a temporary apparently homogeneous single phase product which delivers both phases to the region to be treated simultaneously. This typically means that the product must contain one or more surfactants or emulsifiers, which will render the two phases at least temporarily compatible during the mixing and application stage. Surfactants are also frequently useful in the removal of waterproof makeup. Unfortunately, many such emulsifiers are drying to the skin and/or are irritating to users, and in particular cannot be routinely used in the eye area.
  • On the other hand, however, it is also desirable that the two phases separate quickly after use, as the emulsified product has a cloudy appearance that is unappealing to consumers. After prolonged, continuous mixing of the two phases during regular use, the time it takes for the phases to separate becomes longer and longer, and the product rapidly loses its initially attractive appearance. Moreover, oil soluble actives may be unstable if they remain in prolonged contact with the aqueous phase, and therefore, the amount of time spent in contact with the water phase should be minimized. As can readily be seen, these two aspects of the dual phase product, namely, the need for rapid and complete emulsification followed by rapid and complete separation, are at odds with each other, and to achieve both satisfactorily in a single product, in a way that is both cosmetically acceptable and attractive to the user, is often difficult. The present invention, however, provides a dual phase product in which the phases mix well and completely, and yet demixing is accomplished rapidly after use. Moreover, the product is non-irritating, and when used as a makeup remover, is highly successful in removing even the most difficult to remove oil-based cosmetics.
  • SUMMARY OF THE INVENTION
  • The present invention relates to a liquid dual phase cosmetic or dermatological composition comprising an aqueous phase and an oil phase, at least one of the phases containing as a demixing agent, a film forming agent. In a preferred embodiment, the demixing agent is a polyvinylpyrrolidone (hereinafter referred to as “PVP”) or a copolymer thereof. The compositions of the invention are particularly useful when employed as a makeup remover, but may also be used for skin conditioning, or delivery of cosmetic or therapeutic active agents to the skin for the treatment and/or amelioration of various skin conditions.
  • DETAILED DESCRIPTION OF THE INVENTION
  • The demixing agents used in the present dual phase compositions are well-known in the art for being useful as film forming agents and for being useful in improving water resistance and wear of compositions. However, it has not been previously known that they can be used to facilitate rapid separation of phases in a two phase emulsion. In addition to this function, however, these demixing agents have the additional advantage of being extremely mild, and non-irritating. In particular, they do not appear to cause any irritation when in contact with the eye, which cannot be said of many other demixing agents.
  • Any film-forming agent may be used in the compositions of the invention. Examples of useful categories of demixing agents include acrylic acid polymers and copolymers, such as cyclo alkyl methacrylate copolymer; chitin or chitosan or derivatives thereof; or polyquaternium film formers, such as polyquaternium-11. A preferred demixing agent is PVP or a copolymer thereof. Particularly preferred are PVP/hexadecene copolymer and/or PVP/polycarbamyl polyglycol ester. PVP/hexadecene copolymer is available commercially under the tradename Ganex V-216®, from ISP Sutton Labs of Chatham, N.J. Other demixing agents include for example, PVP/dimethylaminoethylmethacrylate copolymer, PVP/eicosene copolymer, PVP/ethyl methacrylate/methacrylic acid copolymer, PVP/VA copolymer, PVP/1-triacontene, and listings of film formers in the CTFA Cosmetic Ingredient Handbook, incorporated herein by reference.
  • The demixing agent is added to either the oil phase or the water phase of the composition, usually in an amount of from about 0.001 to about 10 percent, preferably in an amount of about 0.01 to about 1 percent. Dual phase compositions prepared with such a demixing agent emulsify rapidly and uniformly upon vigorous shaking, and demulsify completely upon resting within approximately 5 to 20 minutes. The remainder of the composition is formulated depending on the nature of the desired end product. The ratio of the oil phase to aqueous phase is not critical, and can be varied in accordance with the type of product, but will generally be between 30:70 to 70:30, more preferably between 40:60 to 60:40. Most preferably, the aqueous phase is present as a higher weight percent than the oil phase. The aqueous phase may be any cosmetically acceptable water based material, such as deionized water, or floral water.
  • The oil phase may be any cosmetically or pharmaceutically acceptable oil, such an oil being defined for the present purpose as any pharmaceutically or cosmetically acceptable material which is substantially insoluble in water. As the oils can perform different functions in the composition, the specific choice is dependent on the purpose for which it is intended. The oils may be volatile or non-volatile, or a mixture of both. For example, suitable volatile oils include, but are not limited to, both cyclic and linear silicones, such as cyclomethicone, octamethylcyclotetrasiloxane, and decamethylcyclopentasiloxane; or straight or branched chain hydrocarbons having from 8-20 carbon atoms, such as decane, dodecane, tridecane, tetradecane, and C8-20 isoparaffins.
  • Non-volatile oils include, but are not limited to, vegetable oils, such as coconut oil, jojoba oil, corn oil, sunflower oil, palm oil, soybean oil; carboxylic acid esters such as isostearyl neopentanoate, cetyl octanoate, cetyl ricinoleate, octyl palmitate, dioctyl malate, coco-dicaprylate/caprate, decyl isostearate, myristyl myristate; animal oils such as lanolin and lanolin derivatives, tallow, mink oil or cholesterol; glyceryl esters, such as glyceryl stearate, glyceryl dioleate, glyceryl distearate, glyceryl linoleate, glyceryl myristate; non-volatile silicones, such as dimethicone, dimethiconol, dimethicone copolyol, phenyl trimethicone, methicone, simethicone; and non-volatile hydrocarbons, such as isoparaffins, squalane, or petrolatum.
  • The composition also may contain other cosmetically or therapeutically useful components. It may, for example, be desirable to incorporate other surfactants into the formulation, again depending on the intended purpose of the formulation, for example, as cleansing agents to assist in wetting skin, emulsifying oils or solubilizing soil on skin or as foaming agents. The surfactants employed may be any that are traditionally used for cosmetic or pharmaceutical purposes, and may be selected from nonionic, anionic, cationic or amphoteric surfactants, the identities of which are well known to those skilled in the art. Additional surfactants may be distributed in either or both of the phases of the formulation, and selection is limited only by a given surfactant's compatibility with the phase into which it is incorporated, and by the location to which the composition is to be applied. Other potentially useful components of the formulation include emollients, humectants, fragrances, preservatives, and buffers. Such materials are routinely used in cosmetic products, and listings of appropriate materials can be found, for example in the International Cosmetic Ingredients Handbook, Third Edition, 1996 (CTFA).
  • As noted above, the formulation can also be used for therapeutic or quasi-therapeutic purposes, and therefore may also comprise useful active ingredients, for the purposes of treating both the skin and hair. Useful active ingredients include, but are not limited to antioxidants, antimicrobials, sunscreens, analgesics, anesthetics, anti-acne agents, antidandruff agents, antidermatitis agents, antipruritic agents, anti-inflammatory agents, antihyperkeratolytic agents, anti-dry skin agents, antiperspirants, antipsoriatic agents, antiseborrheic agents, hair conditioners and hair treatment agents, antiaging agents, antiwrinkle agents, antihistamine agents, skin lightening agents, depigmenting agents, wound-healing agents, vitamins, corticosteroids, tanning agents, or hormones. The location of the active in the formulation is determined by its solubility and/or stability in either oil or water.
  • The formulations of the present invention are useful for a variety of purposes, including skin or hair cleansers, skin or hair treatment products, sunscreen or suntanning products, and the like. In a particularly preferred embodiment, however, the composition is used for removing makeup. As already noted, the demixing agents, because of their mildness, are eminently well-suited to being employed in a product which is usable around the eye. When combined with an appropriate group of additional components, particularly in the oil phase, the resulting makeup remover successfully cleans skin surfaces, particularly eyes and lips, of even the most transfer-resistant of currently used cosmetics, while remaining gentle and non-irritating to the user.
  • In this preferred embodiment, the oil phase contains a combination of both volatile and non-volatile oils. The volatile oil portion is preferably a volatile hydrocarbon present in amounts of from about 30-70%, and more preferably 40-60%, and the non-volatile present at about 0.1-10%, preferably 0.2-5% by weight of the total composition. In a particularly preferred embodiment, the oil phase contains a blend of oils comprising isododecane at 25-40% by weight of the total composition, a volatile C16 isoparaffin at 15-30% by weight of the total composition, and the non-volatile silicone at 0.1-1% by weight of the total composition.
  • The non-volatile portion of the oil phase is preferably a non-volatile silicone oil. A preferred non-volatile silicone is dimethicone. In a particularly preferred embodiment, the amount of volatile oil used is considerably higher than that of the non-volatile oils; for example, the volatile oil will be present in an amount of about 30-70%, preferably about 40-60%, of the total composition, and the non-volatile oil in an amount of about 0.1-10%, preferably about 0.2-5% of the total composition.
  • In another embodiment, for example, the volatile oil portion contains a combination of a volatile silicone and a volatile hydrocarbon. More specifically, the oil phase contains a blend of oils comprising a low molecular weight cyclic silicone at 25-40% by weight of the total composition, a volatile C16 isoparaffin at 15-30% by weight, and the non-volatile silicone at 0.1-1% by weight of the total composition.
  • In this preferred embodiment, it may be desirable to provide an additional small amount of surfactant in the oil phase to facilitate removal of the cosmetic residue from the skin. The amount of surfactant added is preferably no more than 5%, and more preferably is in the range of 0.1-1%. The surfactant may be of any type, i.e., anionic, nonionic, cationic or amphoteric; however, if the makeup remover is intended for use in the eye area, it is preferred that the surfactant should be a mild surfactant, such as LIPO-PEG-2□L or disodium cocoaamphoidacetate (Miranol).
  • The invention is further illustrated in the following non-limiting examples:
  • EXAMPLES
  • The following illustrates a formulation of the present invention:
  • MATERIAL % BY WT
    Isododecane 30
    Isohexadecane 20
    Dimethicone 0.5
    PVP/hexadecene copolymer 0.1
    PEG-4 Dilaurate 0.4
    Purified water 45
    Sodium chloride 1
    Potassium phosphate 0.2
    Phenoxyethanol 0.5
    Glycerin 0.2
    Hexylene glycol 2
    Methylparaben 0.1
  • The components are combined as follows: the oil phase components, isododecane, isohexadecane, silicone and PEG-4 dilaurate are mixed with PVP/hexedecene copolymer (Ganex V-216®), and the water phase components, sodium chloride, potassium phosphate, hexylene glycol, fragrance, preservative and water are mixed together. First the oil phase is added to the selected container, then the water phase is added.

Claims (22)

1. A method of formulating a dual phase liquid cosmetic or pharmaceutical composition in which the phases are separate before and after being mixed, the method comprising combining an aqueous phase and an oil phase, wherein one of the aqueous and oil phases has incorporated therein, as a demixing agent, an effective amount of a non-cationic film forming agent.
2. The method of claim 1, in which, after being mixed, the phases separate completely upon resting within about 5 to 20 minutes.
3. The method of claim 1 in which the film forming agent is selected from the group consisting of polyvinylpyrrolidone and copolymers thereof.
4. The method of claim 3 wherein the film forming agent is selected from the group consisting of polyvinylpyrrolidone hexadecene copolymer, polyvinylpyrrolidone eicosene copolymer and polyvinylpyrrolidone 1-triacontene copolymer.
5. The method of claim 4 wherein the film forming agent is polyvinylpyrrolidone hexadecene copolymer.
6. The method of claim 1 in which the demixing agent is present in an amount of from about 0.001 to about 10 percent by weight of the total composition.
7. The method of claim 6 in which the demixing agent is present in an amount of from about 0.01 to about 1 percent by weight of the total composition.
8. The method of claim 1 in which the oil phase and aqueous phase are present in a ratio of from about 30:70 to about 70:30, by weight of the total composition.
9. The method of claim 8 in which the aqueous phase and oil phase are present in a ratio of from about 40:60 to about 60:40, by weight of the total composition.
10. The method of claim 1 in which the oil phase contains a combination of volatile and non-volatile oils.
11. The method of claim 10 in which the amount of volatile oil is about 30 to about 70 percent by weight of the total composition and the amount of non-volatile oil is about 0.1 to about 10 percent by weight of the total composition.
12. The method of claim 10 in which the volatile oil is a volatile hydrocarbon.
13. The method of claim 12 in which the volatile hydrocarbon is isododecane, isohexadecane, or a combination thereof.
14. The method of claim 11 in which the volatile oil comprises both a volatile silicone and a volatile isoparaffin.
15. The method of claim 14 in which the volatile silicone is cyclomethicone and the volatile isoparaffin is a C16 isoparaffin.
16. The method of claim 10 in which the non-volatile oil comprises a non-volatile silicone.
17. The method of claim 16 in which the non-volatile silicone is dimethicone.
18. The method of claim 16 which comprises a cyclic silicone present in an amount of about 25 to about 40 percent by weight of the total composition, a C16 isoparaffin present in an amount of about 15 to about 30 percent by weight of the total composition, and a non-volatile silicone present in an amount of about 0.1 to about 1 percent by weight of the total composition.
19. The method of claim 18 in which the cyclic silicone is cyclomethicone, the isoparaffin is isohexadecane, and the non-volatile silicone is dimethicone.
20. The method of claim 19 which comprises a surfactant in an amount of no greater than about 5 percent by weight of the total composition.
21. The method of claim 20 in which the surfactant is present in an amount of from about 0.1 to about 1 percent by weight of the total composition.
22. The method of claim 1 in which the composition is a makeup removal composition.
US12/633,365 1998-05-07 2009-12-08 Dual Phase Cosmetic Composition Abandoned US20100087548A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US12/633,365 US20100087548A1 (en) 1998-05-07 2009-12-08 Dual Phase Cosmetic Composition

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US09/074,051 US6649174B2 (en) 1998-05-07 1998-05-07 Dual phase cosmetic composition
US10/618,803 US9132078B2 (en) 1998-05-07 2003-07-14 Dual phase cosmetic composition
US11/926,671 US20080051468A1 (en) 1998-05-07 2007-10-29 Dual Phase Cosmetic Composition
US12/633,365 US20100087548A1 (en) 1998-05-07 2009-12-08 Dual Phase Cosmetic Composition

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US11/926,671 Continuation US20080051468A1 (en) 1998-05-07 2007-10-29 Dual Phase Cosmetic Composition

Publications (1)

Publication Number Publication Date
US20100087548A1 true US20100087548A1 (en) 2010-04-08

Family

ID=22117405

Family Applications (4)

Application Number Title Priority Date Filing Date
US09/074,051 Expired - Lifetime US6649174B2 (en) 1998-05-07 1998-05-07 Dual phase cosmetic composition
US10/618,803 Expired - Lifetime US9132078B2 (en) 1998-05-07 2003-07-14 Dual phase cosmetic composition
US11/926,671 Abandoned US20080051468A1 (en) 1998-05-07 2007-10-29 Dual Phase Cosmetic Composition
US12/633,365 Abandoned US20100087548A1 (en) 1998-05-07 2009-12-08 Dual Phase Cosmetic Composition

Family Applications Before (3)

Application Number Title Priority Date Filing Date
US09/074,051 Expired - Lifetime US6649174B2 (en) 1998-05-07 1998-05-07 Dual phase cosmetic composition
US10/618,803 Expired - Lifetime US9132078B2 (en) 1998-05-07 2003-07-14 Dual phase cosmetic composition
US11/926,671 Abandoned US20080051468A1 (en) 1998-05-07 2007-10-29 Dual Phase Cosmetic Composition

Country Status (10)

Country Link
US (4) US6649174B2 (en)
EP (1) EP0996408B1 (en)
JP (1) JP4355034B2 (en)
KR (1) KR20010014003A (en)
AT (1) ATE331497T1 (en)
AU (1) AU725334B2 (en)
CA (1) CA2293295C (en)
DE (1) DE69932133T2 (en)
ES (1) ES2262314T3 (en)
WO (1) WO1999056704A1 (en)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6649174B2 (en) * 1998-05-07 2003-11-18 E-L Management Corp. Dual phase cosmetic composition
KR100377261B1 (en) * 2000-11-13 2003-03-26 애경산업(주) Polymer emulsifying type of oil-free and oil-in-water composition
US6756059B2 (en) * 2001-08-20 2004-06-29 Skinvisible Pharmaceuticals, Inc. Topical composition, topical composition precursor, and methods for manufacturing and using
BRPI0201235B1 (en) * 2002-04-12 2017-05-02 Natura Cosmeticos Sa multiphase cosmetic makeup
US7135165B2 (en) * 2002-11-20 2006-11-14 Alzo International, Inc. Multiphase sunscreen compositions
FR2847468B1 (en) * 2002-11-26 2006-02-24 Oreal TRANSPARENT BIPHASE COMPOSITION FOR TOPICAL APPLICATION AND COSMETIC USE THEREOF
DE10258827A1 (en) * 2002-12-17 2004-07-08 Henkel Kgaa Two-layer temporarily emulsifiable compositions
US20040126339A1 (en) * 2002-12-31 2004-07-01 Roszell James A. Sunscreen composition and methods for manufacturing and using a sunscreen composition
DE10321138A1 (en) * 2003-05-09 2004-11-25 Henkel Kgaa Two-phase liquid antiperspirant compositions
US7712319B2 (en) 2004-12-27 2010-05-11 Carrier Corporation Refrigerant charge adequacy gauge
FR2881650B1 (en) 2005-02-09 2008-12-26 Oreal COSMETIC DEMAQUILLAGE ARTICLE
US20070141008A1 (en) * 2005-12-16 2007-06-21 Jones Dennis R Cosmetic remover composition
US20090098077A1 (en) * 2007-10-15 2009-04-16 Kpss-Kao Professional Salon Services Gmbh Two-Phase Composition for Improving Curl Retention
US20100137333A1 (en) * 2006-10-20 2010-06-03 Roszell James A Antifungal composition and methods for using
US20080124293A1 (en) 2006-11-24 2008-05-29 Kpss-Kao Professional Salon Services Gmbh Composition for keratin fibres
EP2022466A1 (en) 2007-08-07 2009-02-11 KPSS-Kao Professional Salon Services GmbH Two or multi phase composition for conditioning hair
EP2022467A1 (en) * 2007-08-07 2009-02-11 KPSS-Kao Professional Salon Services GmbH Two-phase composition for conditioning hair
US8128913B1 (en) 2007-12-06 2012-03-06 Skinvisible Pharmaceuticals, Inc. Sunscreen composition with enhanced UV-A absorber stability and methods
US8274777B2 (en) 2008-04-08 2012-09-25 Micron Technology, Inc. High aspect ratio openings
US8299122B2 (en) * 2008-04-14 2012-10-30 Skinvisible Pharmaceuticals, Inc. Method for stabilizing retinoic acid, retinoic acid containing composition, and method of using a retinoic acid containing composition
FR2993177B1 (en) 2012-07-16 2014-07-11 Oreal BIPHASIC COMPOSITION CONTAINING ALKYLPOLYGLUCOSIDE AND A FUSION POINT ESTER LESS THAN 10 ° C
FR3007638B1 (en) * 2013-06-28 2015-08-07 Oreal BIPHASE COMPOSITION COMPRISING MAGNESIUM ACETATE
FR3012330B1 (en) 2013-10-29 2015-10-23 Oreal BIPHASE COMPOSITION COMPRISING AN ESTER OF FATTY ACID AND SUGAR OR A LIQUID ALKYLPOLYGLUCOSIDE OF HLB <8, AND A C8-C18 BRANCHED ALKANE
US9713582B2 (en) * 2015-04-13 2017-07-25 The Procter & Gamble Company Multi-layered cosmetic composition
DE102015218065A1 (en) * 2015-09-21 2017-03-23 Beiersdorf Ag Glycerol-containing cosmetic with vinylpyrrolidone / triaconten copolymer
KR102463232B1 (en) 2015-09-30 2022-11-04 (주)아모레퍼시픽 Oil-dispersed fluid type cosmetic composition for eye make-up
CA3074150A1 (en) 2020-02-18 2021-08-18 Ovation Science, Inc. Composition and method for transdermal delivery of cannabidiol (cbd) and delta9-tetrahydrocannabinol (thc)
FR3112076B1 (en) 2020-07-01 2022-12-16 Oreal Two-phase composition comprising an alkylpolyglycoside surfactant, a particular diol and an alkane, ester or ether compound comprising from 15 to 30 carbon atoms

Citations (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3577528A (en) * 1966-05-27 1971-05-04 Zotos Int Inc Two phase hair conditioner compositions
US4335103A (en) * 1977-03-28 1982-06-15 Almay, Inc. Multiphase cosmetic composition
US4810489A (en) * 1986-12-04 1989-03-07 Bristol-Myers Company High oil phase pharmaceutical vehicles and sunscreen compositions having waterproof sun protection factors
US4980155A (en) * 1989-09-11 1990-12-25 Revlon, Inc. Two phase cosmetic composition
US5026540A (en) * 1987-06-04 1991-06-25 Chesebrough-Pond's Usa Co. Sunscreen composition
US5138043A (en) * 1989-12-07 1992-08-11 Union Carbide Chemicals & Plastics Technology Corporation Alkoxylated alkyl glucoside ether quaternaries useful in personal care
US5165917A (en) * 1988-11-09 1992-11-24 Societe Anonyme Dite: L'oreal Eye makeup remover with two separate phases
US5405878A (en) * 1993-06-18 1995-04-11 Wilmington Partners L.P. Contact lens solution containing cationic glycoside
US5468496A (en) * 1992-12-18 1995-11-21 L'oreal Two-phase cosmetic or dermatological composition
US5589177A (en) * 1994-12-06 1996-12-31 Helene Curtis, Inc. Rinse-off water-in-oil-in-water compositions
US5658559A (en) * 1992-12-16 1997-08-19 Creative Products Resource Associates, Ltd. Occlusive/semi-occlusive lotion for treatment of a skin disease or disorder
US5698211A (en) * 1992-11-13 1997-12-16 Isp Investments Inc. Stabilized agchemical concentrate and use thereof
US5871758A (en) * 1996-12-11 1999-02-16 E-L Management Corp. Dual phase cosmetic composition
US5993830A (en) * 1997-01-17 1999-11-30 Ponsus Ab Cosmetic skin preparation
US6019991A (en) * 1998-01-23 2000-02-01 Chesebrough-Pond's Usa Co., Two-phase cosmetic composition
US6649174B2 (en) * 1998-05-07 2003-11-18 E-L Management Corp. Dual phase cosmetic composition

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS554133B2 (en) 1972-07-27 1980-01-29
FR2478465A1 (en) 1980-03-18 1981-09-25 Oreal NEW COSMETIC COMPOSITIONS FOR HAIR, IN TWO LIQUID PHASES, AND THEIR APPLICATION
JPS6078907A (en) 1983-10-04 1985-05-04 Kobayashi Kooc:Kk Double-layered cosmetic
EP0289900A1 (en) 1987-04-30 1988-11-09 Abbott Laboratories Topical antibacterial compositions
GB9025711D0 (en) 1990-11-27 1991-01-09 Beecham Group Plc Topical composition
FR2670385B1 (en) 1990-12-12 1995-03-03 Oreal TWO PHASE LIQUID COSMETIC COMPOSITION CONTAINING AT LEAST ONE DIALKYLPHTHALATE, INSOLUBLE PARTICLES AND A DENSITY BALANCING AGENT.
DE9216886U1 (en) 1992-12-11 1994-04-14 Kao Corp Gmbh Cosmetic products
JP3591925B2 (en) 1995-08-22 2004-11-24 株式会社ダイゾー Non-foamable aerosol hair styling composition
GB2308063A (en) 1995-12-15 1997-06-18 Allbutt Garry Michael Two phase sun protection product
JPH09255523A (en) 1996-03-25 1997-09-30 Shiseido Co Ltd Cosmetic
DE19633012A1 (en) 1996-08-16 1998-02-19 Beiersdorf Ag Use of camphor derivatives to increase or increase the solubility of triazine derivatives in oil components
JPH11222415A (en) 1998-01-30 1999-08-17 Kose Corp Double layer type hair cosmetic
JPH11246348A (en) 1998-03-05 1999-09-14 Shiseido Co Ltd Facial cleansing agent composition

Patent Citations (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3577528A (en) * 1966-05-27 1971-05-04 Zotos Int Inc Two phase hair conditioner compositions
US4335103A (en) * 1977-03-28 1982-06-15 Almay, Inc. Multiphase cosmetic composition
US4810489A (en) * 1986-12-04 1989-03-07 Bristol-Myers Company High oil phase pharmaceutical vehicles and sunscreen compositions having waterproof sun protection factors
US5026540A (en) * 1987-06-04 1991-06-25 Chesebrough-Pond's Usa Co. Sunscreen composition
US5165917A (en) * 1988-11-09 1992-11-24 Societe Anonyme Dite: L'oreal Eye makeup remover with two separate phases
US5165917B1 (en) * 1988-11-09 2000-03-14 Oreal Eye makeup remover with two separate phases
US4980155A (en) * 1989-09-11 1990-12-25 Revlon, Inc. Two phase cosmetic composition
US5138043A (en) * 1989-12-07 1992-08-11 Union Carbide Chemicals & Plastics Technology Corporation Alkoxylated alkyl glucoside ether quaternaries useful in personal care
US5384334A (en) * 1989-12-07 1995-01-24 Amerchol Corporation Alkoxylated alkyl glucoside ether quaternaries useful in personal care
US5698211A (en) * 1992-11-13 1997-12-16 Isp Investments Inc. Stabilized agchemical concentrate and use thereof
US5658559A (en) * 1992-12-16 1997-08-19 Creative Products Resource Associates, Ltd. Occlusive/semi-occlusive lotion for treatment of a skin disease or disorder
US5468496A (en) * 1992-12-18 1995-11-21 L'oreal Two-phase cosmetic or dermatological composition
US5405878A (en) * 1993-06-18 1995-04-11 Wilmington Partners L.P. Contact lens solution containing cationic glycoside
US5589177A (en) * 1994-12-06 1996-12-31 Helene Curtis, Inc. Rinse-off water-in-oil-in-water compositions
US5871758A (en) * 1996-12-11 1999-02-16 E-L Management Corp. Dual phase cosmetic composition
US5993830A (en) * 1997-01-17 1999-11-30 Ponsus Ab Cosmetic skin preparation
US6019991A (en) * 1998-01-23 2000-02-01 Chesebrough-Pond's Usa Co., Two-phase cosmetic composition
US6649174B2 (en) * 1998-05-07 2003-11-18 E-L Management Corp. Dual phase cosmetic composition

Also Published As

Publication number Publication date
AU725334B2 (en) 2000-10-12
AU3100599A (en) 1999-11-23
JP4355034B2 (en) 2009-10-28
CA2293295C (en) 2002-12-10
DE69932133D1 (en) 2006-08-10
KR20010014003A (en) 2001-02-26
ES2262314T3 (en) 2006-11-16
JP2002509556A (en) 2002-03-26
US9132078B2 (en) 2015-09-15
US20080051468A1 (en) 2008-02-28
EP0996408A1 (en) 2000-05-03
DE69932133T2 (en) 2006-11-30
CA2293295A1 (en) 1999-11-11
US20050118214A1 (en) 2005-06-02
ATE331497T1 (en) 2006-07-15
WO1999056704A1 (en) 1999-11-11
EP0996408B1 (en) 2006-06-28
US6649174B2 (en) 2003-11-18
US20020098209A1 (en) 2002-07-25

Similar Documents

Publication Publication Date Title
US6649174B2 (en) Dual phase cosmetic composition
EP0847746B1 (en) Dual phase cosmetic composition
US7682620B2 (en) Gelled aqueous cosmetic compositions
JP2656225B2 (en) Oil-in-water cleansing emulsion
US6667044B1 (en) Cosmetic or dermatological gels based on microemulsions
KR100343412B1 (en) Stable o/w/o emulsion and its use as cosmetic and/or dermatological composition
AU737565B2 (en) Water containing wax-based product
US5449510A (en) Emulsion of the oil-in-water type based on silicone oil and its use in cosmetics and dermatology
JP2000119131A (en) Emulsion containing hydrophilic thickening compound and thickening copolymer and composition containing the same emulsion and its use
KR100356553B1 (en) Emulsion comprising a hydrophilic thickening compound and a polysaccharide alkyl ether, compositions comprising the said emulsion, and uses
EP0713381B1 (en) Cleansing composition containing hydroxy alkanoate derivatives
KR100245796B1 (en) A water-in-oil type cosmetic composition having low viscosity
KR100252518B1 (en) W1/o/w2 emulsion containing volatile silicon oil
WO2021110733A1 (en) A cosmetic composition and the use thereof and a method for improving sensory characteristics
JP3502702B2 (en) Water-in-oil emulsion cosmetics
JP2000302656A (en) Preparation for external use for skin

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION