US3092555A - Relatively collapsible aerosol foam compositions - Google Patents

Relatively collapsible aerosol foam compositions Download PDF

Info

Publication number
US3092555A
US3092555A US729543A US72954358A US3092555A US 3092555 A US3092555 A US 3092555A US 729543 A US729543 A US 729543A US 72954358 A US72954358 A US 72954358A US 3092555 A US3092555 A US 3092555A
Authority
US
United States
Prior art keywords
foam
hair
composition
dye
alkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US729543A
Inventor
Roy H Horn
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US729543A priority Critical patent/US3092555A/en
Application granted granted Critical
Publication of US3092555A publication Critical patent/US3092555A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • A61K9/12Aerosols; Foams
    • A61K9/122Foams; Dry foams
    • 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
    • A61K8/04Dispersions; Emulsions
    • A61K8/046Aerosols; Foams
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • A61K8/416Quaternary ammonium 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
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/06Preparations for styling the hair, e.g. by temporary shaping or colouring
    • A61Q5/065Preparations for temporary colouring the hair, e.g. direct dyes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S424/00Drug, bio-affecting and body treating compositions
    • Y10S424/02Resin hair settings

Definitions

  • This invention relates to a composition capable of forming a relatively stable, shape-retaining mass of foam and more particularly to such a composition usable as a carrier substance for dyes, cosmetics, pharmaceuticals and other substances.
  • the present composition is particularly suited for use as a carrier for hair dyes, since it leaves little residue, can normally be used with no preconditioning of the hair and reduces the necessity for rinsing the hair following use.
  • Hair coloring dyes are customarily supplied either in the form of dye solutions where deep coloring of the hair is desired or in the form of rinses or the like where only slight or moderate coloring or tinting of the hair is intended. Such solutions are generally applied in the form of liquids or sprays. In either case, contact with the skin or scalp of the user is inevitable with resultant staining and possible toxic effects on individuals who may be sensitive to the particular organic dye used. Furthermore, application in this manner is inconvenient and often requires careful preparation before application, careful attention during the application of the dye or rinse, and subsequent clean up to remove the results of spillage, etc.
  • compositions capable of forming a foam when being worked into the hair have been used to diffuse a dye or tinting material through the hair.
  • These substances generally require a conditioning wash or rinse of the hair prior to the application of the dye in order that it will set and must contain rather substantial quantities of surface active agents, a soap or detergent base and additional thickening or foam stabilizing agents.
  • the present foamable composition may not only be used as a carrier for applying hair coloring compositions, but may also find use as a carrier for cosmetic, pharmaceuticals, lubricants, shampoos and other related materials, since it can be readily applied to a particular area of the body with minimum difficulty.
  • This method enables uniform application of material to the hair or body while reducing the difficulties encountered when other methods are used.
  • a pharmaceutical composition in a salve carrier such as petroleum jelly, may require special applicators or require the user to place the material on his hands or fingers to apply it to some other part of the body, whereas the foam carrier of the present invention can be directly applied and permitted to dry to deposit the pharmaceutical at the proper location.
  • Another object of this invention is to provide a foamable carrier composition using an amphoteric surface active agent which can be effectively used in combination with cationic, anionic, non-ionic, as well as other amphoteric substances.
  • a further object of this invention is to provide a foamable carrier composition for pharmaceuticals, lubricants, shampoos, hair dyes and the like which includes a surface active agent which also acts as a stabilizer preventing the composition from being harmed by excessive heat or freezing.
  • Coloring materials may be applied to the hair by dissolving or dispersing the coloring dye in a foamable solution and then generating a dense, relatively stable and compact mass of foam which is substantially shape retaining.
  • the dye solution is first formed into a mass or blob of an aqueous foam which is light in density and will remain stable without any substantial drainage of liquid therefrom.
  • the foam in effect is in the form of a puff or similar mass which may be applied to the hair by means of a brush or similar applicator.
  • the dye solution is handled and applied not as a liquid but as a light, dispersed gas-liquid foam mass which is in effect semi-solid in nature, thus avoiding the disadvantages of liquid application even though the dye solution remains in liquid form Within the foam mass.
  • This method of applying materials not only possesses the manipulative advantages referred to, but also has the advantage of avoiding contact of excessive liquid with the skin or scalp and is much cleaner and neater to use.
  • the gas-liquid foam permits uniform dispersion of the coloring dye and thereby obtains non-streaking application of the dye to the hair. This is probably due to the fact that dispersion of the foam mass through the hair avoids concentration of the dye in localized areas, while the large surface area present permits thorough and uniform contact of the coloring matter present in the liquid film of the foam through the hair mass and around each individual hair. Additionally, it has been found that foam application of dye enables coloring of the hair to take place with smaller quantities of dye so that the possibility of incurring toxic effects is materially reduced.
  • a suitable foam structure having the desired stability, density and self-sustaining properties, permitting application in the manner desired may be obtained by employing an aqueous solution of a foam forming composition containing surface active agents, coloring or dyeing materims, and a suitable propellant. These materials are combined in proper proportions in a container and released by means of a manually operable valve. Upon operation of the valve, the propellant is volatilized and carries with it a proportion of the water, dye and other ingredients to generate the desired foam mass.
  • This same general type of arrangement is commonly used for dispersing insecticides, shaving creams, deodorants, lacquers and the like under the general designation of aerosol products.
  • compositions of the invention should include water, a foaming agent such as a surface active material and other ingredients, when required, to modify the foam structure.
  • a foaming agent such as a surface active material
  • the surface active material, or surfactant may serve the additional function of acting as a foam stabilizing agent or as an emulsifying agent, so that a separate stabilizer or emulsifier need not be added.
  • the propellant must be incorporated with the foamable composition.
  • a suitable dye is incorporated either in solution or in suspension within the aqueous phase.
  • Other ingredients such as hair softening materials, perfumes, etc. may also be added as desired.
  • the present composition can be separated into two broad groups of substances, solids and non-solids, the non-solids referring to the volatile components and the solids referring to the non-volatile components. Since the purpose of the composition is to provide a means for carrying a particular material to some part of the body, it is desired that the solids part of the composition be kept as low as possible to elimi-
  • the solids content in the invention falls within the range of from 1.5% to about 4.5% by weight of the total weight of the composition, these percentages being lower than those of existing foam compositions.
  • the volatile components including Water will evaporate and leave the solids or non-volatiles deposited on the hair or body.
  • a composition which can operate with such low percentages of solids, without impairing the foaming characteristics has advantages over compositions which must use relatively greater amounts of solids.
  • the preferred type of foamable carrier composition generates foam only when used in conjunction with an aerosol arrangement or its equivalent, so that the foam will tend to disappear after having performed its function of carrying an active agent to the desired location.
  • foam characteristic will be referred to as relatively collapsible to indicate that the foam will disappear once it has performed its function as a carrier.
  • the basic material that is the material primarily responsible for the improved results, is an amphoteric quaternary surface active agent, which can be effectively used with other amphoteric, cationic, anionic or non-ionic substances such as the dyes, etc.
  • the amphoteric nature of the quaternary surfactants reduces the necessity for rinsing or otherwise pretreating the hair before using a dye carried in the composition.
  • the quaternary compound is the sodium alcoholate or the carboxylate and alcoholate of a cycloimido derivative such as might be obtained by reacting a fatty acid, as stearic or oleic or palmitic acid, with a diamine such as ethylene or propylene diamine, plus a poly-functional alcohol, such as ethylene glycol, or both a poly-functional alcohol and a hydroxy acid, such as lactic or glycollic acid.
  • the quaternary compounds are made by forming a condensation product of either sodium alcoholate or sodium carboxylate with one of the fatty acids mentioned and then further condensing this product with one of the hydrocarbon diamines. The bior poly-functional alcohol or the hydroxy acid is then added to complete formation of the amphoteric, quaternary surfacant.
  • Suitable surface active agents include, for example, ethylene cycloimido 1 alkyl bis (2 hydroxyethylene sodium alcoholate); alkyl dimethyl benzyl ammonium chloride; and ethylene cycloimido 1 alkyl 2 hydroxyethylene sodium alcoholate methylene sodium carboxylate. In certain situations it may be preferred to combine more than one of these quaternaries in a single carrier compound to regulate the amphoteric character of the material.
  • the carrier composition will consist of 1.5 to 4.5% by weight of surface active agents, as mentioned, minor additions of dye or other material to be carried, and water.
  • the dye stuffs selected will depend on the color desired and whether the foam is to be utilized on human hair or upon other materials such as fabrics or the like.
  • the dye may be selected from those which have been certified by the Government as non-toxic, or those, which generally considered as nontoxic, will be essentially non-toxic when applied in accordance with the present invention.
  • Such dyes should be water soluble or dispersible. These dyes include quinoline, monoazo, disazo, diphenolmethane, triphenolmethane, anthraqu-inone, xanthene, acridine and indigoid types.
  • the concentration of the dye utilized will vary with the dye, the color desired, whether the product is to be used as a tint or for deep coloring etc.
  • a concentration of 0.001 to 0.5% by weight would be selected depending on color and intensity.
  • Other organic dyes suitable for coloring hair include the aromatic amines such as paraphenylenediamine or the aminophenols and the like.
  • water insoluble dyes may first be dissolved in water soluble solvents such as glycols or alcohols, or may be dispersed in the water with dispersant agents. Buffers may be added to insure maintenance of the pH range of the solution at the desired level for any particular dye.
  • compositions are shown as including hair dye, the quarternaries being added as Water diluted solutions, as indicated.
  • Example I Parts by weight Ethylene cycloimido 1 alkyl bis (2 hydroxyethylene
  • Example III Ethylene cycloimido 1 alkyl 2 hydroxyethylene sodium alcoholate methylene sodium carboxylate -35% solution 9.0
  • Example IV Amphoteric surface active material containing two hydrophilic sites one of which is anionic sulfate structure (Duponol XL) 8.0 Ethylene cycloimido 1 alkyl bis(2 hydroxyethylene sodium alcoholate) 35% solution 4.0
  • Alkyl dimethyl benzyl ammonium chloride 28% solution 1.5 Water soluble color 0.5 Water, bal. to 155 parts.
  • amphoteric surface active material cited in Example IV is sold under the trade name of Duponol, by the E. I. du Pont de Nemours & Co. and represents a line of surface active agents of the alcohol sulfate type containing two hydrophilic sites, one of these sites being an anionic sulfate structure.
  • compositions of the preceding examples are to be dispersed from aerosol pressure containers, about 18 parts of the propellant would be added to each of the compositions.
  • Propellant materials having little or no solubility in water and no destructive effects upon the foam are used, the Freons being a class of compounds which are highly suitable for this purpose.
  • propellants are the chlorine and fluorine substituted lower aliphatic hydrocarbons particularly the methane and ethane derivatives.
  • Preferred propellants of this type are dichlordifiuormethane, monochlortrifluormethane, monofiuortrichlormethane, 1,2 dichlor, 1,1,2,2 tetrafluorethane, trichlortrifluorethane, and mixtures of these.
  • organic materials which are gases at room temperature and liquid at elevated pressure may be utilized where the foamable composition and propellant are to be packaged under pressure.
  • propellants which may be used include propane, butane, isobutane, methylchloride, nitrous oxide, and in general such other materials which will not adversely efiect the foaming properties of the composition.
  • the propellant is generally utilized in proportions of from 5 to about 25% of the weight by mixture.
  • the final composition is formed by preparing a mixture of the water with the appropriate surfactants and then applying heat until the water soluble portion of the molecules enters into a solution-like relation to the water.
  • the resultant system tends to undergo a transition at temperatures from 110 to 130 F., when its viscosity sharply increases on cooling, and thixotropy appears.
  • suitable surface active materials may be the fatty acid soaps, vegetable oil soaps, synthetic detergents, or wetting agents, including those of cationic, anionic or non-ionic character such as fatty alkyl sulfates, alkyl aromatic sulfonates, alkyl olamine soaps, sodium lauryl sulfate, triethanolamine lauryl sulfate, sulfated ethanolamine of cocoanut oil fatty acids, sodium dodecyl benzene sulfonate and others well known in the art.
  • cationic, anionic or non-ionic character such as fatty alkyl sulfates, alkyl aromatic sulfonates, alkyl olamine soaps, sodium lauryl sulfate, triethanolamine lauryl sulfate, sulfated ethanolamine of cocoanut oil fatty acids, sodium dodecyl benzene sulfonate and others well known in the art.
  • foam stabilizing materials such as glue, glycerin, albumin, thickening or viscosity increasing agents such as ethyl and methyl cellulose, hydroxyethylcellulose, carboxymethylcellulose, and so forth. These materials are also used in small proportions, generally less than 5%.
  • Foam structure modifying agents may be added to produce denser and smalled bubbled foams. These materials may also include small proportions of anti-foaming or modifying agents such as electrolytes or water soluble salts like sodium sulfate, silicon oil, hydrocarbon oils, ethyl or methyl alcohol, etc., which may be added in concentrations of 0.001% or the like.
  • anti-foaming or modifying agents such as electrolytes or water soluble salts like sodium sulfate, silicon oil, hydrocarbon oils, ethyl or methyl alcohol, etc., which may be added in concentrations of 0.001% or the like.
  • Example VI Parts by weight In utilizing the materials described in the preceding Examples V-VII to carry out the present invention, the foamable composition is first prepared by dissolving the ingredients thereof plus the dye in the water. Where an aerosol container is to be used, the solution is placed therein along with the propellant which is introduced under pressure in the liquid phase. The container is provided with a valve and a dispersing nozzle. Prior to use, the container is agitated and the contents mixed. On opening of the valve the propellant forces the foamable composition through the nozzle and simultaneously generates a thick creamy foam. The dispersion of the foamable material from the aerosol container is the same in each form of the invention.
  • the valve In the coloring of hair the valve is opened for a long enough period to generate the desired mass or blob of foam. This mass is then applied to a brush or other applicator or directly to the hair, and the foam, while still in the foam state, is brushed or otherwise manipulated through the hair. By applying the foam in this manner progressively to selected areas of the hair, complete and uniform coverage can be obtained.
  • the application of other materials to parts of the body other than the hair can be carried out in much the same manner so that upon evaporation or disintegration of the foam a uniform film or material is deposited at the proper location.
  • a composition for carrying a material including hair dyes, pharmaceuticals, lubricants and shampoo, and for forming relatively collapsible foam bubbles carrying said material and which foam bubbles will collapse upon application and will form a non-foam drying film carrying said material
  • a foam-producing agent selected from the group consisting of ethylene cycloimido 1 alkyl bis (2 hydroxyethylene sodium alcoholate), alkyl dimethyl benzyl ammonium chloride, and ethylene cycloimido 1 alkyl 2 hydroxyethylene sodium alcoholate methylene sodium carboxylate, and mixtures thereof, a volatile aqueous solvent for said composition and a volatile foamgenerating propellant, the non-volatile contents of said composition being between about 1.5% and 4.5% by weight.
  • a liquid hair dye composition adapted to form a mass of relatively collapsible foam bubbles carrying a hair dye, which bubbles collapse upon application to deposit a film of said dye on the hair, which comprises in combination a hair coloring dye, a volatile aqueous vehicle in which said dye is dissolved, a foam-producing amphoteric quaternary surface active agent, and a volatile compressed propellant for generating said foam, all said components being admixed and contained in a pressurized container in liquid form for generation of said collapsible foam bubbles by said propellant upon release of a portion of said composition from said container, and the non-volatile contents of said composition being between about 1.5% and 4.5% by weight.

Description

United States Patent 3,092,555 RELATIVELY COLLAPSIBLE AEROSOL FOAM COMPOSITIONS Roy H. Horn, 38 N. Jefferson St, Dayton 2 Ohio No Drawing. Filed Apr. 21, 1958, Ser. No. 729,543 3 Claims. (Cl. 16788) This invention relates to a composition capable of forming a relatively stable, shape-retaining mass of foam and more particularly to such a composition usable as a carrier substance for dyes, cosmetics, pharmaceuticals and other substances.
The present composition is particularly suited for use as a carrier for hair dyes, since it leaves little residue, can normally be used with no preconditioning of the hair and reduces the necessity for rinsing the hair following use. Hair coloring dyes are customarily supplied either in the form of dye solutions where deep coloring of the hair is desired or in the form of rinses or the like where only slight or moderate coloring or tinting of the hair is intended. Such solutions are generally applied in the form of liquids or sprays. In either case, contact with the skin or scalp of the user is inevitable with resultant staining and possible toxic effects on individuals who may be sensitive to the particular organic dye used. Furthermore, application in this manner is inconvenient and often requires careful preparation before application, careful attention during the application of the dye or rinse, and subsequent clean up to remove the results of spillage, etc.
In some instances compositions capable of forming a foam when being worked into the hair have been used to diffuse a dye or tinting material through the hair. These substances generally require a conditioning wash or rinse of the hair prior to the application of the dye in order that it will set and must contain rather substantial quantities of surface active agents, a soap or detergent base and additional thickening or foam stabilizing agents. Of course dispersion of the dye through the hair with foam generated by the fingers enables the dye to stain the fingers and may require substantial effort to remove it from the hands following treatment of the hair. Often, also, the hair must be rinsed following the dyeing opera tion, since the foam may deposit a relatively heavy residue on the hair which is not only unattractive but can also be potentially harmful to the hair.
The present foamable composition may not only be used as a carrier for applying hair coloring compositions, but may also find use as a carrier for cosmetic, pharmaceuticals, lubricants, shampoos and other related materials, since it can be readily applied to a particular area of the body with minimum difficulty. This method enables uniform application of material to the hair or body while reducing the difficulties encountered when other methods are used. For example, a pharmaceutical composition in a salve carrier such as petroleum jelly, may require special applicators or require the user to place the material on his hands or fingers to apply it to some other part of the body, whereas the foam carrier of the present invention can be directly applied and permitted to dry to deposit the pharmaceutical at the proper location.
It is therefore a principal object of this invention to provide a composition capable of forming a relatively dense, shape retaining mass of foam, to act as a carrier for various materials, which overcomes the risks and inconveniences of existing carrier compositions.
It is another object of this invention to provide a foamable carrier composition capable of forming a shape retaining mass of material having a relatively low content of nonvolatile or solid material.
Another object of this invention is to provide a foamable carrier composition using an amphoteric surface active agent which can be effectively used in combination with cationic, anionic, non-ionic, as well as other amphoteric substances.
It is an additional object of this invention to provide a carrier composition which can be formed into a shape retaining foam only with suitable liquid or gaseous propellants.
A further object of this invention is to provide a foamable carrier composition for pharmaceuticals, lubricants, shampoos, hair dyes and the like which includes a surface active agent which also acts as a stabilizer preventing the composition from being harmed by excessive heat or freezing.
Other objects and advantages of this invention will be apparent from the following description and the appended claims.
The present invention, as previously mentioned, makes possible the effective and simple application of various types of substances to the body, and is particularly adapt able for use in applying coloring materials to the hair. Therefore, the invention will be described principally with reference to the use of the material in conjunction with hair dyes and the like. Coloring materials may be applied to the hair by dissolving or dispersing the coloring dye in a foamable solution and then generating a dense, relatively stable and compact mass of foam which is substantially shape retaining. In other Words, the dye solution is first formed into a mass or blob of an aqueous foam which is light in density and will remain stable without any substantial drainage of liquid therefrom. Thus, the foam in effect is in the form of a puff or similar mass which may be applied to the hair by means of a brush or similar applicator. In this way the dye solution is handled and applied not as a liquid but as a light, dispersed gas-liquid foam mass which is in effect semi-solid in nature, thus avoiding the disadvantages of liquid application even though the dye solution remains in liquid form Within the foam mass.
This method of applying materials not only possesses the manipulative advantages referred to, but also has the advantage of avoiding contact of excessive liquid with the skin or scalp and is much cleaner and neater to use. Furthermore, the gas-liquid foam permits uniform dispersion of the coloring dye and thereby obtains non-streaking application of the dye to the hair. This is probably due to the fact that dispersion of the foam mass through the hair avoids concentration of the dye in localized areas, while the large surface area present permits thorough and uniform contact of the coloring matter present in the liquid film of the foam through the hair mass and around each individual hair. Additionally, it has been found that foam application of dye enables coloring of the hair to take place with smaller quantities of dye so that the possibility of incurring toxic effects is materially reduced.
A suitable foam structure having the desired stability, density and self-sustaining properties, permitting application in the manner desired, may be obtained by employing an aqueous solution of a foam forming composition containing surface active agents, coloring or dyeing materims, and a suitable propellant. These materials are combined in proper proportions in a container and released by means of a manually operable valve. Upon operation of the valve, the propellant is volatilized and carries with it a proportion of the water, dye and other ingredients to generate the desired foam mass. This same general type of arrangement is commonly used for dispersing insecticides, shaving creams, deodorants, lacquers and the like under the general designation of aerosol products.
' nate deposition of excessive residue.
The compositions of the invention should include water, a foaming agent such as a surface active material and other ingredients, when required, to modify the foam structure. Of course the surface active material, or surfactant, may serve the additional function of acting as a foam stabilizing agent or as an emulsifying agent, so that a separate stabilizer or emulsifier need not be added. In addition, where the aerosol foaming technique is used, the propellant must be incorporated with the foamable composition. When utilized for coloring hair in accordance with this invention, a suitable dye is incorporated either in solution or in suspension within the aqueous phase. Other ingredients, such as hair softening materials, perfumes, etc. may also be added as desired.
The present composition can be separated into two broad groups of substances, solids and non-solids, the non-solids referring to the volatile components and the solids referring to the non-volatile components. Since the purpose of the composition is to provide a means for carrying a particular material to some part of the body, it is desired that the solids part of the composition be kept as low as possible to elimi- The solids content in the invention falls within the range of from 1.5% to about 4.5% by weight of the total weight of the composition, these percentages being lower than those of existing foam compositions. Obviously after an application of the material the volatile components including Water will evaporate and leave the solids or non-volatiles deposited on the hair or body. Thus, a composition which can operate with such low percentages of solids, without impairing the foaming characteristics, has advantages over compositions which must use relatively greater amounts of solids.
The preferred type of foamable carrier composition generates foam only when used in conjunction with an aerosol arrangement or its equivalent, so that the foam will tend to disappear after having performed its function of carrying an active agent to the desired location. Hereinafter, such a foam characteristic will be referred to as relatively collapsible to indicate that the foam will disappear once it has performed its function as a carrier. This property permits elimination of any rinsing operation following dyeing. The basic material, that is the material primarily responsible for the improved results, is an amphoteric quaternary surface active agent, which can be effectively used with other amphoteric, cationic, anionic or non-ionic substances such as the dyes, etc. The amphoteric nature of the quaternary surfactants reduces the necessity for rinsing or otherwise pretreating the hair before using a dye carried in the composition.
The quaternary compound is the sodium alcoholate or the carboxylate and alcoholate of a cycloimido derivative such as might be obtained by reacting a fatty acid, as stearic or oleic or palmitic acid, with a diamine such as ethylene or propylene diamine, plus a poly-functional alcohol, such as ethylene glycol, or both a poly-functional alcohol and a hydroxy acid, such as lactic or glycollic acid.
The quaternary compounds are made by forming a condensation product of either sodium alcoholate or sodium carboxylate with one of the fatty acids mentioned and then further condensing this product with one of the hydrocarbon diamines. The bior poly-functional alcohol or the hydroxy acid is then added to complete formation of the amphoteric, quaternary surfacant.
Suitable surface active agents include, for example, ethylene cycloimido 1 alkyl bis (2 hydroxyethylene sodium alcoholate); alkyl dimethyl benzyl ammonium chloride; and ethylene cycloimido 1 alkyl 2 hydroxyethylene sodium alcoholate methylene sodium carboxylate. In certain situations it may be preferred to combine more than one of these quaternaries in a single carrier compound to regulate the amphoteric character of the material.
Generally, the carrier composition will consist of 1.5 to 4.5% by weight of surface active agents, as mentioned, minor additions of dye or other material to be carried, and water.
The dye stuffs selected will depend on the color desired and whether the foam is to be utilized on human hair or upon other materials such as fabrics or the like. For use on human hair the dye may be selected from those which have been certified by the Government as non-toxic, or those, which generally considered as nontoxic, will be essentially non-toxic when applied in accordance with the present invention. Such dyes should be water soluble or dispersible. These dyes include quinoline, monoazo, disazo, diphenolmethane, triphenolmethane, anthraqu-inone, xanthene, acridine and indigoid types. The concentration of the dye utilized will vary with the dye, the color desired, whether the product is to be used as a tint or for deep coloring etc. In general, a concentration of 0.001 to 0.5% by weight would be selected depending on color and intensity. Other organic dyes suitable for coloring hair include the aromatic amines such as paraphenylenediamine or the aminophenols and the like. Where water insoluble dyes are used, they may first be dissolved in water soluble solvents such as glycols or alcohols, or may be dispersed in the water with dispersant agents. Buffers may be added to insure maintenance of the pH range of the solution at the desired level for any particular dye.
The following examples are illustrative of acceptable compositions and are shown as including hair dye, the quarternaries being added as Water diluted solutions, as indicated.
Example I Parts by weight Ethylene cycloimido 1 alkyl bis (2 hydroxyethylene Example III Ethylene cycloimido 1 alkyl 2 hydroxyethylene sodium alcoholate methylene sodium carboxylate -35% solution 9.0 Ethylene cycloimido 1 alkyl bis(2 hydroxyethylene sodium alcoholate) 35% solution 4.0
Polyglycol polyoxyethylene ether ester of stearic acid 1.5 Water soluble color 0.5 Water, bal. to parts.
Example IV Amphoteric surface active material containing two hydrophilic sites one of which is anionic sulfate structure (Duponol XL) 8.0 Ethylene cycloimido 1 alkyl bis(2 hydroxyethylene sodium alcoholate) 35% solution 4.0
Alkyl dimethyl benzyl ammonium chloride 28% solution 1.5 Water soluble color 0.5 Water, bal. to 155 parts.
The amphoteric surface active material cited in Example IV is sold under the trade name of Duponol, by the E. I. du Pont de Nemours & Co. and represents a line of surface active agents of the alcohol sulfate type containing two hydrophilic sites, one of these sites being an anionic sulfate structure.
Additionally, if the compositions of the preceding examples are to be dispersed from aerosol pressure containers, about 18 parts of the propellant would be added to each of the compositions.
Propellant materials having little or no solubility in water and no destructive effects upon the foam are used, the Freons being a class of compounds which are highly suitable for this purpose. Examples of such propellants are the chlorine and fluorine substituted lower aliphatic hydrocarbons particularly the methane and ethane derivatives. Preferred propellants of this type are dichlordifiuormethane, monochlortrifluormethane, monofiuortrichlormethane, 1,2 dichlor, 1,1,2,2 tetrafluorethane, trichlortrifluorethane, and mixtures of these. In general, organic materials which are gases at room temperature and liquid at elevated pressure may be utilized where the foamable composition and propellant are to be packaged under pressure. Other propellants which may be used include propane, butane, isobutane, methylchloride, nitrous oxide, and in general such other materials which will not adversely efiect the foaming properties of the composition. The propellant is generally utilized in proportions of from 5 to about 25% of the weight by mixture.
The final composition is formed by preparing a mixture of the water with the appropriate surfactants and then applying heat until the water soluble portion of the molecules enters into a solution-like relation to the water. The resultant system tends to undergo a transition at temperatures from 110 to 130 F., when its viscosity sharply increases on cooling, and thixotropy appears.
In another form of the invention suitable surface active materials may be the fatty acid soaps, vegetable oil soaps, synthetic detergents, or wetting agents, including those of cationic, anionic or non-ionic character such as fatty alkyl sulfates, alkyl aromatic sulfonates, alkyl olamine soaps, sodium lauryl sulfate, triethanolamine lauryl sulfate, sulfated ethanolamine of cocoanut oil fatty acids, sodium dodecyl benzene sulfonate and others well known in the art. Mixtures of these may sometimes be advantageous, and in general, as mentioned, these agents are utilized in concentrations of from 0.5 to less than 5% When surface active materials such as those just described are used it is often desirable to add various foam stabilizing materials. For example such materials as glue, glycerin, albumin, thickening or viscosity increasing agents such as ethyl and methyl cellulose, hydroxyethylcellulose, carboxymethylcellulose, and so forth. These materials are also used in small proportions, generally less than 5%.
Foam structure modifying agents may be added to produce denser and smalled bubbled foams. These materials may also include small proportions of anti-foaming or modifying agents such as electrolytes or water soluble salts like sodium sulfate, silicon oil, hydrocarbon oils, ethyl or methyl alcohol, etc., which may be added in concentrations of 0.001% or the like.
Example V Parts by weight 6 Example VI Parts by weight In utilizing the materials described in the preceding Examples V-VII to carry out the present invention, the foamable composition is first prepared by dissolving the ingredients thereof plus the dye in the water. Where an aerosol container is to be used, the solution is placed therein along with the propellant which is introduced under pressure in the liquid phase. The container is provided with a valve and a dispersing nozzle. Prior to use, the container is agitated and the contents mixed. On opening of the valve the propellant forces the foamable composition through the nozzle and simultaneously generates a thick creamy foam. The dispersion of the foamable material from the aerosol container is the same in each form of the invention.
In the coloring of hair the valve is opened for a long enough period to generate the desired mass or blob of foam. This mass is then applied to a brush or other applicator or directly to the hair, and the foam, while still in the foam state, is brushed or otherwise manipulated through the hair. By applying the foam in this manner progressively to selected areas of the hair, complete and uniform coverage can be obtained. The application of other materials to parts of the body other than the hair can be carried out in much the same manner so that upon evaporation or disintegration of the foam a uniform film or material is deposited at the proper location.
This application is a continuation-in-part of applicants copending application Serial No. 553,188, filed December 15, 1955, now abandoned.
While the compositions herein described constitute preferred embodiments of the invention, it is to be understood that this invention is not limited to these precise compositions and that changes may be made therein without departing from the scope of the invention which is defined in the appended claims.
What is claimed is:
1. A composition for carrying a material, including hair dyes, pharmaceuticals, lubricants and shampoo, and for forming relatively collapsible foam bubbles carrying said material and which foam bubbles will collapse upon application and will form a non-foam drying film carrying said material, which composition comprises in liquid form for admixture with said material a foam-producing agent selected from the group consisting of ethylene cycloimido 1 alkyl bis (2 hydroxyethylene sodium alcoholate), alkyl dimethyl benzyl ammonium chloride, and ethylene cycloimido 1 alkyl 2 hydroxyethylene sodium alcoholate methylene sodium carboxylate, and mixtures thereof, a volatile aqueous solvent for said composition and a volatile foamgenerating propellant, the non-volatile contents of said composition being between about 1.5% and 4.5% by weight.
2. A liquid hair dye composition adapted to form a mass of relatively collapsible foam bubbles carrying a hair dye, which bubbles collapse upon application to deposit a film of said dye on the hair, which comprises in combination a hair coloring dye, a volatile aqueous vehicle in which said dye is dissolved, a foam-producing amphoteric quaternary surface active agent, and a volatile compressed propellant for generating said foam, all said components being admixed and contained in a pressurized container in liquid form for generation of said collapsible foam bubbles by said propellant upon release of a portion of said composition from said container, and the non-volatile contents of said composition being between about 1.5% and 4.5% by weight.
3. A composition as set forth in claim 2 in which said hair dye is a basic hair dye.
References Cited in the file of this patent UNITED STATES PATENTS 2,528,378 Mannheimer Oct. 31, 1950 8 2,655,480 Spitzer et al Oct. 13, 1953 2,719,129 Richardson Sept. 27, 1955 2,763,269 Den Beste Sept. 18, 1956 2,801,201 Kipnis July 30, 1957 OTHER REFERENCES Redgrove: Hair-Dyes and Hair-Dyeing, Chem. Publ.
10 Co., N.Y., (1939), pp. 159-167.
Soap and Sanitary Chemicals (Hair Dye and Shampoo), April 1950, p. 89.
Jannaway; D. and C. Industry, 66:4, April 1950, p. 452.
I-Iilfer: Drug and Cosmetic Industry, 68:5, May 1951,
15 pp. 590-1 and 667.

Claims (1)

1. A COMPOSITION FOR CARRYING A MATERIAL, INCLUDING HAIR DYES, PHARMACEUTICALS, LUBRICANTS AND SHAMPOO, AND FOR FORMING RELATIVELY COLLAPSIBLE FOAM BUBBLES CARRYING SAID MATERIAL AND WHICH FOAM BUBBLES WILL COLLAPSE UPON APPLICATION AND WILL FORM A NON-FORM DRYING FILM CARRYING SAID MATERIAL, WHICH COMPOSITION COMPRISES IN LIQUID FORM FOR ADMIXTURE WITH SAID MATERIAL A FOAM-PRODUCING AGENT SELECTED FROM THE GROUP CONSISTING OF ETHYLENE CYCLOIMIDO 1 ALKYL BIS (2 HYDROXYETHYLENE SODIUM ALCOHOLATE), ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE, AND ETHYLENE CYCLOIMIDO 1 ALKYL 2 HYDROXYETHYLENE SODIUM ALCOHOLATE METHYLENE SODIUM CARBOXYLATE, AND MIXTURES THEREOF, A VOLATILE AQUEOUS SOLVENT FOR SAID COMPOSITION AND A VOLATILE FOAMGENERATING PROPELLANT, THE NON-VOLATILE CONTENTS OF SAID COMPOSITION BEING BETWEEN ABOUT 1.5% AND 4.5% BY WEIGHT.
US729543A 1958-04-21 1958-04-21 Relatively collapsible aerosol foam compositions Expired - Lifetime US3092555A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US729543A US3092555A (en) 1958-04-21 1958-04-21 Relatively collapsible aerosol foam compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US729543A US3092555A (en) 1958-04-21 1958-04-21 Relatively collapsible aerosol foam compositions

Publications (1)

Publication Number Publication Date
US3092555A true US3092555A (en) 1963-06-04

Family

ID=24931520

Family Applications (1)

Application Number Title Priority Date Filing Date
US729543A Expired - Lifetime US3092555A (en) 1958-04-21 1958-04-21 Relatively collapsible aerosol foam compositions

Country Status (1)

Country Link
US (1) US3092555A (en)

Cited By (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3103468A (en) * 1958-10-30 1963-09-10 Procter & Gamble Pressurized hair waving compositions
US3131152A (en) * 1960-06-13 1964-04-28 Allied Chem Foam producing formulations
US3194735A (en) * 1964-02-04 1965-07-13 Warner Lambert Pharmaceutical Hair coloring comprising a basic dye, a glycol and an amphoteric surfactant
US3233791A (en) * 1963-07-09 1966-02-08 Colgate Palmolive Co Package for fluent materials with a propellant operated gel piston
US3330730A (en) * 1962-08-03 1967-07-11 Colgate Palmolive Co Pressurized emulsion quick breaking foam compositions
US3415607A (en) * 1965-03-01 1968-12-10 Warner Lambert Pharmaceutical Hair dye composition containing 2-hydroxy-1,4-naphthoquinone
US3900560A (en) * 1972-04-23 1975-08-19 Amnon Jacobson Solution comprising a lacrymator
US3929985A (en) * 1974-01-18 1975-12-30 Richardson Merrell Inc Anhydrous candicidin foam compositions
US3947568A (en) * 1970-08-03 1976-03-30 Phoenix Research Inc. Effervescent cosmetic compositions
US3947566A (en) * 1970-08-03 1976-03-30 Phoenix Research Inc. Effervescent medicaments
US3970584A (en) * 1973-02-14 1976-07-20 S. C. Johnson & Son, Inc. Aerosol package containing a foam-forming emulsion and propellent system
US4097305A (en) * 1975-03-14 1978-06-27 Bickmore, Inc. Method for removing bot eggs from animal hair
DE2932301A1 (en) * 1978-08-09 1980-02-21 Chemsico Inc AEROSOL COMPOSITION
JPS58124713A (en) * 1982-01-20 1983-07-25 Kashiwa Kagaku Kogyo:Kk Colored aerosol for application to hair
EP0172713A2 (en) * 1984-08-09 1986-02-26 Bristol-Myers Squibb Company Process for applying reflective particles to hair
US4915935A (en) * 1984-08-09 1990-04-10 Clairol Incorporated Process for applying reflective particles to hair
FR2677369A1 (en) * 1991-06-05 1992-12-11 Promotion Rech Innovation Tec Aerosol foam
US5773016A (en) * 1995-01-27 1998-06-30 S C. Johnson & Son, Inc. Insecticidally-active water-in oil-out emulsions and insecticidally active compositions derived therefrom
US20040068805A1 (en) * 2002-10-15 2004-04-15 Yoram Fishman Hair treatment systems and methods
DE19653496B4 (en) * 1995-12-23 2007-03-22 Kao Corp. Semipermanent, acidic hair dye composition for an aerosol and its use
US7704518B2 (en) 2003-08-04 2010-04-27 Foamix, Ltd. Foamable vehicle and pharmaceutical compositions thereof
US7820145B2 (en) 2003-08-04 2010-10-26 Foamix Ltd. Oleaginous pharmaceutical and cosmetic foam
US20110045037A1 (en) * 2007-11-30 2011-02-24 Foamix Ltd. Foam containing benzoyl peroxide
US20110178162A1 (en) * 2005-10-14 2011-07-21 Medical University Of South Carolina Targeting pax2 for the induction of defb1-mediated tumor immunity and cancer therapy
US8343945B2 (en) 2007-12-07 2013-01-01 Foamix Ltd. Carriers, formulations, methods for formulating unstable active agents for external application and uses thereof
US8435498B2 (en) 2002-10-25 2013-05-07 Foamix Ltd. Penetrating pharmaceutical foam
US8486376B2 (en) 2002-10-25 2013-07-16 Foamix Ltd. Moisturizing foam containing lanolin
US8486375B2 (en) 2003-04-28 2013-07-16 Foamix Ltd. Foamable compositions
US8486374B2 (en) 2003-08-04 2013-07-16 Foamix Ltd. Hydrophilic, non-aqueous pharmaceutical carriers and compositions and uses
US8512718B2 (en) 2000-07-03 2013-08-20 Foamix Ltd. Pharmaceutical composition for topical application
US8518376B2 (en) 2007-12-07 2013-08-27 Foamix Ltd. Oil-based foamable carriers and formulations
US8618081B2 (en) 2009-10-02 2013-12-31 Foamix Ltd. Compositions, gels and foams with rheology modulators and uses thereof
US8636982B2 (en) 2007-08-07 2014-01-28 Foamix Ltd. Wax foamable vehicle and pharmaceutical compositions thereof
US8709385B2 (en) 2008-01-14 2014-04-29 Foamix Ltd. Poloxamer foamable pharmaceutical compositions with active agents and/or therapeutic cells and uses
US8722021B2 (en) 2002-10-25 2014-05-13 Foamix Ltd. Foamable carriers
US8795693B2 (en) 2003-08-04 2014-08-05 Foamix Ltd. Compositions with modulating agents
US8795635B2 (en) 2006-11-14 2014-08-05 Foamix Ltd. Substantially non-aqueous foamable petrolatum based pharmaceutical and cosmetic compositions and their uses
US8900554B2 (en) 2002-10-25 2014-12-02 Foamix Pharmaceuticals Ltd. Foamable composition and uses thereof
US9072667B2 (en) 2009-07-29 2015-07-07 Foamix Pharmaceuticals Ltd. Non surface active agent non polymeric agent hydro-alcoholic foamable compositions, breakable foams and their uses
US9167813B2 (en) 2009-07-29 2015-10-27 Foamix Pharmaceuticals Ltd. Non surfactant hydro-alcoholic foamable compositions, breakable foams and their uses
US9211259B2 (en) 2002-11-29 2015-12-15 Foamix Pharmaceuticals Ltd. Antibiotic kit and composition and uses thereof
US9265725B2 (en) 2002-10-25 2016-02-23 Foamix Pharmaceuticals Ltd. Dicarboxylic acid foamable vehicle and pharmaceutical compositions thereof
US9320705B2 (en) 2002-10-25 2016-04-26 Foamix Pharmaceuticals Ltd. Sensation modifying topical composition foam
US9539208B2 (en) 2002-10-25 2017-01-10 Foamix Pharmaceuticals Ltd. Foam prepared from nanoemulsions and uses
US9622947B2 (en) 2002-10-25 2017-04-18 Foamix Pharmaceuticals Ltd. Foamable composition combining a polar solvent and a hydrophobic carrier
US9849142B2 (en) 2009-10-02 2017-12-26 Foamix Pharmaceuticals Ltd. Methods for accelerated return of skin integrity and for the treatment of impetigo
US9884017B2 (en) 2009-04-28 2018-02-06 Foamix Pharmaceuticals Ltd. Foamable vehicles and pharmaceutical compositions comprising aprotic polar solvents and uses thereof
US10398641B2 (en) 2016-09-08 2019-09-03 Foamix Pharmaceuticals Ltd. Compositions and methods for treating rosacea and acne

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US2655480A (en) * 1949-11-02 1953-10-13 Spitzer Lather producing composition
US2719129A (en) * 1951-06-30 1955-09-27 Colgate Palmolive Co Pressurized liquid room and air deodorant compositions
US2763269A (en) * 1952-02-01 1956-09-18 Rayette Inc Foaming hair coloring compositions comprising basic dyes, and method of use
US2801201A (en) * 1953-04-09 1957-07-30 Lincoln Lab Inc Burn treatment filling for pressure packaged dispenser

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US2655480A (en) * 1949-11-02 1953-10-13 Spitzer Lather producing composition
US2719129A (en) * 1951-06-30 1955-09-27 Colgate Palmolive Co Pressurized liquid room and air deodorant compositions
US2763269A (en) * 1952-02-01 1956-09-18 Rayette Inc Foaming hair coloring compositions comprising basic dyes, and method of use
US2801201A (en) * 1953-04-09 1957-07-30 Lincoln Lab Inc Burn treatment filling for pressure packaged dispenser

Cited By (105)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3103468A (en) * 1958-10-30 1963-09-10 Procter & Gamble Pressurized hair waving compositions
US3131152A (en) * 1960-06-13 1964-04-28 Allied Chem Foam producing formulations
US3330730A (en) * 1962-08-03 1967-07-11 Colgate Palmolive Co Pressurized emulsion quick breaking foam compositions
US3233791A (en) * 1963-07-09 1966-02-08 Colgate Palmolive Co Package for fluent materials with a propellant operated gel piston
US3194735A (en) * 1964-02-04 1965-07-13 Warner Lambert Pharmaceutical Hair coloring comprising a basic dye, a glycol and an amphoteric surfactant
US3415607A (en) * 1965-03-01 1968-12-10 Warner Lambert Pharmaceutical Hair dye composition containing 2-hydroxy-1,4-naphthoquinone
US3947566A (en) * 1970-08-03 1976-03-30 Phoenix Research Inc. Effervescent medicaments
US3947568A (en) * 1970-08-03 1976-03-30 Phoenix Research Inc. Effervescent cosmetic compositions
US3900560A (en) * 1972-04-23 1975-08-19 Amnon Jacobson Solution comprising a lacrymator
US3970584A (en) * 1973-02-14 1976-07-20 S. C. Johnson & Son, Inc. Aerosol package containing a foam-forming emulsion and propellent system
US3929985A (en) * 1974-01-18 1975-12-30 Richardson Merrell Inc Anhydrous candicidin foam compositions
US4097305A (en) * 1975-03-14 1978-06-27 Bickmore, Inc. Method for removing bot eggs from animal hair
DE2932301A1 (en) * 1978-08-09 1980-02-21 Chemsico Inc AEROSOL COMPOSITION
JPS58124713A (en) * 1982-01-20 1983-07-25 Kashiwa Kagaku Kogyo:Kk Colored aerosol for application to hair
JPS6317806B2 (en) * 1982-01-20 1988-04-15 Kashiwa Kagaku Kogyo Kk
EP0172713A2 (en) * 1984-08-09 1986-02-26 Bristol-Myers Squibb Company Process for applying reflective particles to hair
JPS6147412A (en) * 1984-08-09 1986-03-07 ブリストル―マイヤーズ スクイブ カンパニー Method of rendering reflective particles to hair
EP0172713A3 (en) * 1984-08-09 1987-04-29 Bristol-Myers Squibb Company Process for applying reflective particles to hair
US4915935A (en) * 1984-08-09 1990-04-10 Clairol Incorporated Process for applying reflective particles to hair
FR2677369A1 (en) * 1991-06-05 1992-12-11 Promotion Rech Innovation Tec Aerosol foam
US5773016A (en) * 1995-01-27 1998-06-30 S C. Johnson & Son, Inc. Insecticidally-active water-in oil-out emulsions and insecticidally active compositions derived therefrom
DE19653496B4 (en) * 1995-12-23 2007-03-22 Kao Corp. Semipermanent, acidic hair dye composition for an aerosol and its use
US8512718B2 (en) 2000-07-03 2013-08-20 Foamix Ltd. Pharmaceutical composition for topical application
US7829069B2 (en) * 2002-10-15 2010-11-09 Yoram Fishman Hair treatment systems and methods
US20040068805A1 (en) * 2002-10-15 2004-04-15 Yoram Fishman Hair treatment systems and methods
US8435498B2 (en) 2002-10-25 2013-05-07 Foamix Ltd. Penetrating pharmaceutical foam
US9265725B2 (en) 2002-10-25 2016-02-23 Foamix Pharmaceuticals Ltd. Dicarboxylic acid foamable vehicle and pharmaceutical compositions thereof
US10322085B2 (en) 2002-10-25 2019-06-18 Foamix Pharmaceuticals Ltd. Dicarboxylic acid foamable vehicle and pharmaceutical compositions thereof
US9539208B2 (en) 2002-10-25 2017-01-10 Foamix Pharmaceuticals Ltd. Foam prepared from nanoemulsions and uses
US9492412B2 (en) 2002-10-25 2016-11-15 Foamix Pharmaceuticals Ltd. Penetrating pharmaceutical foam
US9320705B2 (en) 2002-10-25 2016-04-26 Foamix Pharmaceuticals Ltd. Sensation modifying topical composition foam
US9713643B2 (en) 2002-10-25 2017-07-25 Foamix Pharmaceuticals Ltd. Foamable carriers
US8486376B2 (en) 2002-10-25 2013-07-16 Foamix Ltd. Moisturizing foam containing lanolin
US8722021B2 (en) 2002-10-25 2014-05-13 Foamix Ltd. Foamable carriers
US9622947B2 (en) 2002-10-25 2017-04-18 Foamix Pharmaceuticals Ltd. Foamable composition combining a polar solvent and a hydrophobic carrier
US10117812B2 (en) 2002-10-25 2018-11-06 Foamix Pharmaceuticals Ltd. Foamable composition combining a polar solvent and a hydrophobic carrier
US8741265B2 (en) 2002-10-25 2014-06-03 Foamix Ltd. Penetrating pharmaceutical foam
US8840869B2 (en) 2002-10-25 2014-09-23 Foamix Ltd. Body cavity foams
US10821077B2 (en) 2002-10-25 2020-11-03 Foamix Pharmaceuticals Ltd. Dicarboxylic acid foamable vehicle and pharmaceutical compositions thereof
US8900554B2 (en) 2002-10-25 2014-12-02 Foamix Pharmaceuticals Ltd. Foamable composition and uses thereof
US11033491B2 (en) 2002-10-25 2021-06-15 Vyne Therapeutics Inc. Dicarboxylic acid foamable vehicle and pharmaceutical compositions thereof
US9211259B2 (en) 2002-11-29 2015-12-15 Foamix Pharmaceuticals Ltd. Antibiotic kit and composition and uses thereof
US8486375B2 (en) 2003-04-28 2013-07-16 Foamix Ltd. Foamable compositions
US8518378B2 (en) 2003-08-04 2013-08-27 Foamix Ltd. Oleaginous pharmaceutical and cosmetic foam
US9101662B2 (en) 2003-08-04 2015-08-11 Foamix Pharmaceuticals Ltd. Compositions with modulating agents
US7704518B2 (en) 2003-08-04 2010-04-27 Foamix, Ltd. Foamable vehicle and pharmaceutical compositions thereof
US8362091B2 (en) 2003-08-04 2013-01-29 Foamix Ltd. Foamable vehicle and pharmaceutical compositions thereof
US8703105B2 (en) 2003-08-04 2014-04-22 Foamix Ltd. Oleaginous pharmaceutical and cosmetic foam
US8486374B2 (en) 2003-08-04 2013-07-16 Foamix Ltd. Hydrophilic, non-aqueous pharmaceutical carriers and compositions and uses
US7820145B2 (en) 2003-08-04 2010-10-26 Foamix Ltd. Oleaginous pharmaceutical and cosmetic foam
US8795693B2 (en) 2003-08-04 2014-08-05 Foamix Ltd. Compositions with modulating agents
US8114385B2 (en) 2003-08-04 2012-02-14 Foamix Ltd. Oleaginous pharmaceutical and cosmetic foam
US9050253B2 (en) 2003-08-04 2015-06-09 Foamix Pharmaceuticals Ltd. Oleaginous pharmaceutical and cosmetic foam
US9636405B2 (en) 2003-08-04 2017-05-02 Foamix Pharmaceuticals Ltd. Foamable vehicle and pharmaceutical compositions thereof
US20110178162A1 (en) * 2005-10-14 2011-07-21 Medical University Of South Carolina Targeting pax2 for the induction of defb1-mediated tumor immunity and cancer therapy
US9682021B2 (en) 2006-11-14 2017-06-20 Foamix Pharmaceuticals Ltd. Substantially non-aqueous foamable petrolatum based pharmaceutical and cosmetic compositions and their uses
US8795635B2 (en) 2006-11-14 2014-08-05 Foamix Ltd. Substantially non-aqueous foamable petrolatum based pharmaceutical and cosmetic compositions and their uses
US9662298B2 (en) 2007-08-07 2017-05-30 Foamix Pharmaceuticals Ltd. Wax foamable vehicle and pharmaceutical compositions thereof
US10369102B2 (en) 2007-08-07 2019-08-06 Foamix Pharmaceuticals Ltd. Wax foamable vehicle and pharmaceutical compositions thereof
US8636982B2 (en) 2007-08-07 2014-01-28 Foamix Ltd. Wax foamable vehicle and pharmaceutical compositions thereof
US11103454B2 (en) 2007-08-07 2021-08-31 Vyne Therapeutics Inc. Wax foamable vehicle and pharmaceutical compositions thereof
US20110045037A1 (en) * 2007-11-30 2011-02-24 Foamix Ltd. Foam containing benzoyl peroxide
US9439857B2 (en) 2007-11-30 2016-09-13 Foamix Pharmaceuticals Ltd. Foam containing benzoyl peroxide
US11433025B2 (en) 2007-12-07 2022-09-06 Vyne Therapeutics Inc. Oil foamable carriers and formulations
US9549898B2 (en) 2007-12-07 2017-01-24 Foamix Pharmaceuticals Ltd. Oil and liquid silicone foamable carriers and formulations
US8343945B2 (en) 2007-12-07 2013-01-01 Foamix Ltd. Carriers, formulations, methods for formulating unstable active agents for external application and uses thereof
US8518376B2 (en) 2007-12-07 2013-08-27 Foamix Ltd. Oil-based foamable carriers and formulations
US9161916B2 (en) 2007-12-07 2015-10-20 Foamix Pharmaceuticals Ltd. Carriers, formulations, methods for formulating unstable active agents for external application and uses thereof
US8900553B2 (en) 2007-12-07 2014-12-02 Foamix Pharmaceuticals Ltd. Oil and liquid silicone foamable carriers and formulations
US9795564B2 (en) 2007-12-07 2017-10-24 Foamix Pharmaceuticals Ltd. Oil-based foamable carriers and formulations
US8709385B2 (en) 2008-01-14 2014-04-29 Foamix Ltd. Poloxamer foamable pharmaceutical compositions with active agents and/or therapeutic cells and uses
US10363216B2 (en) 2009-04-28 2019-07-30 Foamix Pharmaceuticals Ltd. Foamable vehicles and pharmaceutical compositions comprising aprotic polar solvents and uses thereof
US10213384B2 (en) 2009-04-28 2019-02-26 Foamix Pharmaceuticals Ltd. Foamable vehicles and pharmaceutical compositions comprising aprotic polar solvents and uses thereof
US10588858B2 (en) 2009-04-28 2020-03-17 Foamix Pharmaceuticals Ltd. Foamable vehicles and pharmaceutical compositions comprising aprotic polar solvents and uses thereof
US9884017B2 (en) 2009-04-28 2018-02-06 Foamix Pharmaceuticals Ltd. Foamable vehicles and pharmaceutical compositions comprising aprotic polar solvents and uses thereof
US10092588B2 (en) 2009-07-29 2018-10-09 Foamix Pharmaceuticals Ltd. Foamable compositions, breakable foams and their uses
US9572775B2 (en) 2009-07-29 2017-02-21 Foamix Pharmaceuticals Ltd. Non surfactant hydro-alcoholic foamable compositions, breakable foams and their uses
US11219631B2 (en) 2009-07-29 2022-01-11 Vyne Pharmaceuticals Inc. Foamable compositions, breakable foams and their uses
US9072667B2 (en) 2009-07-29 2015-07-07 Foamix Pharmaceuticals Ltd. Non surface active agent non polymeric agent hydro-alcoholic foamable compositions, breakable foams and their uses
US9167813B2 (en) 2009-07-29 2015-10-27 Foamix Pharmaceuticals Ltd. Non surfactant hydro-alcoholic foamable compositions, breakable foams and their uses
US10350166B2 (en) 2009-07-29 2019-07-16 Foamix Pharmaceuticals Ltd. Non surface active agent non polymeric agent hydro-alcoholic foamable compositions, breakable foams and their uses
US10463742B2 (en) 2009-10-02 2019-11-05 Foamix Pharmaceuticals Ltd. Topical tetracycline compositions
US8992896B2 (en) 2009-10-02 2015-03-31 Foamix Pharmaceuticals Ltd. Topical tetracycline compositions
US10265404B2 (en) 2009-10-02 2019-04-23 Foamix Pharmaceuticals Ltd. Compositions, gels and foams with rheology modulators and uses thereof
US10322186B2 (en) 2009-10-02 2019-06-18 Foamix Pharmaceuticals Ltd. Topical tetracycline compositions
US10213512B2 (en) 2009-10-02 2019-02-26 Foamix Pharmaceuticals Ltd. Topical tetracycline compositions
US9675700B2 (en) 2009-10-02 2017-06-13 Foamix Pharmaceuticals Ltd. Topical tetracycline compositions
US10137200B2 (en) 2009-10-02 2018-11-27 Foamix Pharmaceuticals Ltd. Surfactant-free water-free foamable compositions, breakable foams and gels and their uses
US9849142B2 (en) 2009-10-02 2017-12-26 Foamix Pharmaceuticals Ltd. Methods for accelerated return of skin integrity and for the treatment of impetigo
US8618081B2 (en) 2009-10-02 2013-12-31 Foamix Ltd. Compositions, gels and foams with rheology modulators and uses thereof
US10086080B2 (en) 2009-10-02 2018-10-02 Foamix Pharmaceuticals Ltd. Topical tetracycline compositions
US10517882B2 (en) 2009-10-02 2019-12-31 Foamix Pharmaceuticals Ltd. Method for healing of an infected acne lesion without scarring
US10238746B2 (en) 2009-10-02 2019-03-26 Foamix Pharmaceuticals Ltd Surfactant-free water-free foamable compositions, breakable foams and gels and their uses
US10610599B2 (en) 2009-10-02 2020-04-07 Foamix Pharmaceuticals Ltd. Topical tetracycline compositions
US10821187B2 (en) 2009-10-02 2020-11-03 Foamix Pharmaceuticals Ltd. Compositions, gels and foams with rheology modulators and uses thereof
US8945516B2 (en) 2009-10-02 2015-02-03 Foamix Pharmaceuticals Ltd. Surfactant-free water-free foamable compositions, breakable foams and gels and their uses
US10835613B2 (en) 2009-10-02 2020-11-17 Foamix Pharmaceuticals Ltd. Compositions, gels and foams with rheology modulators and uses thereof
US10029013B2 (en) 2009-10-02 2018-07-24 Foamix Pharmaceuticals Ltd. Surfactant-free, water-free formable composition and breakable foams and their uses
US10946101B2 (en) 2009-10-02 2021-03-16 Vyne Therapeutics Inc. Surfactant-free water-free foamable compositions, breakable foams and gels and their uses
US10967063B2 (en) 2009-10-02 2021-04-06 Vyne Therapeutics Inc. Surfactant-free, water-free formable composition and breakable foams and their uses
US8871184B2 (en) 2009-10-02 2014-10-28 Foamix Ltd. Topical tetracycline compositions
US8865139B1 (en) 2009-10-02 2014-10-21 Foamix Pharmaceuticals Ltd. Topical tetracycline compositions
US10849847B2 (en) 2016-09-08 2020-12-01 Foamix Pharamaceuticals Ltd. Compositions and methods for treating rosacea and acne
US11324691B2 (en) 2016-09-08 2022-05-10 Journey Medical Corporation Compositions and methods for treating rosacea and acne
US10398641B2 (en) 2016-09-08 2019-09-03 Foamix Pharmaceuticals Ltd. Compositions and methods for treating rosacea and acne

Similar Documents

Publication Publication Date Title
US3092555A (en) Relatively collapsible aerosol foam compositions
AU628115B2 (en) Self-foaming oil compositions and process for making and using same
US3541581A (en) Package containing a post-foaming gel
US2879231A (en) Shampoo composition
CN100556395C (en) The non-pressurised back intumescent composition of using
AU2001288814B9 (en) Stable emulsions useful for skin care wipes
EP1181002B1 (en) Foamable shower oil composition
EP0521893A1 (en) Foaming personal cleansing product with foam enhancing polymer
WO1988003792A1 (en) Cosmetic material
EP1071399A1 (en) Water soluble dry foam personal care product
JPH06509319A (en) shaving composition
EP0247766A2 (en) Instant lathering shampoo
JPH01153624A (en) Post-foamable gel shower product
US4495169A (en) Aerosol gel shaving cream
JPH05220383A (en) Fluid composition containing micro dispersion product of wax and cationic surface active agent and its production and application
US7405242B2 (en) Aerosol delivery systems
TWI342888B (en) Aerosol biliquid foam
US4931204A (en) Self-foaming oil compositions and process for making and using same
US5826546A (en) Method for shampooing a pet using a foam-dispensed pet shampoo composition
JP2799362B2 (en) Post-foamable gel composition
TW200422367A (en) Biliquid foam furniture polish
JPH06305934A (en) Aerosol type cosmetic
US3728276A (en) Pressurized foam-producing composition and process therefor
US3370014A (en) Skin cleansing compositions
WO1990011343A1 (en) Self-foaming oil compositions and process for making and using same