US20100226948A1 - Methods and compositions for treating acne - Google Patents

Methods and compositions for treating acne Download PDF

Info

Publication number
US20100226948A1
US20100226948A1 US12/716,130 US71613010A US2010226948A1 US 20100226948 A1 US20100226948 A1 US 20100226948A1 US 71613010 A US71613010 A US 71613010A US 2010226948 A1 US2010226948 A1 US 2010226948A1
Authority
US
United States
Prior art keywords
composition
skin
yrs
carbopol
benzoyl peroxide
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
US12/716,130
Inventor
Waranush Jitpraphai
Eugene Gans
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.)
Medicis Pharmaceutical Corp
Original Assignee
Medicis Pharmaceutical Corp
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 Medicis Pharmaceutical Corp filed Critical Medicis Pharmaceutical Corp
Priority to US12/716,130 priority Critical patent/US20100226948A1/en
Assigned to MEDICIS PHARMACEUTICAL CORPORATION reassignment MEDICIS PHARMACEUTICAL CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: GANS, EUGENE, JITPRAPHAI, WARANUSH
Publication of US20100226948A1 publication Critical patent/US20100226948A1/en
Priority to US13/335,151 priority patent/US8263097B2/en
Assigned to GOLDMAN SACHS LENDING PARTNERS LLC reassignment GOLDMAN SACHS LENDING PARTNERS LLC SECURITY AGREEMENT Assignors: MEDICIS PHARMACEUTICAL CORPORATION
Assigned to BARCLAYS BANK PLC, AS SUCCESSOR AGENT reassignment BARCLAYS BANK PLC, AS SUCCESSOR AGENT NOTICE OF SUCCESSION OF AGENCY Assignors: GOLDMAN SACHS LENDING PARTNERS, LLC
Abandoned 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
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0014Skin, i.e. galenical aspects of topical compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/14Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/06Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/10Anti-acne agents

Definitions

  • the present invention relates to methods and compositions for preventing and/or treating acne on the skin.
  • Acne is a condition of the human skin characterized by an excess flow of sebum, or skin oil, from the sebaceous glands located in the pilosebaceous apparatus. Sebum reaches the skin surface through the duct of the hair follicle. The presence of excessive amounts of sebum and slouched follicle cells in the duct and on the skin acts to block or stagnate the continuous flow of sebum from the follicular duct, thus producing a thickening and a solidification of the sebum to form a solid plug known as a comedone. When this process occurs, hyperkeratinization of the follicular opening is stimulated, thus tending to partially or completely close the duct.
  • Topical therapeutic agents are employed in the treatment of acne and seborrhea to prevent the blocking of the follicular duct, to reopen the duct once it has become blocked, to act against the infecting bacteria or the thickened sebum and resulting inflammation, or to provide combinations of each of these actions.
  • the horny outer layer of the skin which is known as the stratum corneum, is formed of dead cells composed largely of keratin.
  • Therapeutic agents which act to prevent the blocking of the follicular duct by promoting the removal or sloughing off of excess keratin are known as keratolytic agents.
  • Benzoyl peroxide has been used as a very effective keratolytic and antibacterial agent in the treatment of acne.
  • the topical application of benzoyl peroxide for skin lesion therapy is well known.
  • U.S. Pat. Nos. 5,445,823; 5,545,407; 5,648,389; and 5,932,228 disclose compositions for treating acne and other skin lesions and also to methods of treatment utilizing these compositions.
  • These compositions and methods of treatment employ benzoyl peroxide plus compounds for reducing the skin irritation associated with benzoyl peroxide, and a topical carrier.
  • One form for advantageously administering anti-acne agents is application to the skin via impregnated small cloth towelettes, wipes, or applicator porous articles.
  • the cloths can be packaged in plural in a sealed pouch or individually. Examples of such cloths are disclosed in U.S. Pat. Nos. 5,242,433; 5,254,109; 5,368,581; 5,417,674; 5,460,620; 5,470,323; 5,538,732; 5,562,642; 6,001,380; and 6,740,330 as well as U.S. Published Patent Application Publication Nos. 2005/0025817, 2005/0100585, and 2005/0232978.
  • the invention described herein provides new methods for treating and/or preventing acne and new compositions useful in such respects.
  • the invention provides new methods for treating acne with benzoyl peroxide that improve user compliance and/or contact of the benzoyl peroxide with the skin.
  • a method for treating acne on the skin comprising: (a) providing an drapeable or flexible porous article impregnated with an aqueous cleansing composition comprising a carrier, benzoyl peroxide, and one or more cleansing agents; (b) contacting an area of the skin affected by acne with the porous article such that the skin is contacted by the composition; and (c) removing the composition from the skin wherein residual benzoyl peroxide remains on the skin in an anti-acne effective amount, preferably while surface dirt and/or irritants are removed.
  • an exemplary anti-acne composition has water, benzoyl peroxide, a salt of a fatty acid ester having from 12 to 20 carbon atoms, and a salt of a fatty acid isethionate having from 12 to 20 carbon atoms.
  • the fatty acid ester salt and the fatty acid isethionate salt are present in an amount sufficient to render the composition foamable and to maintain a substantially homogeneous dispersion of the benzoyl peroxide in the composition to cleanse and medicate the skin.
  • the composition comprises water, benzoyl peroxide, a cellulose ether, and a polyacrylic polymer.
  • the cellulose ether and the polyacrylic polymer are present in an amount sufficient to impart substantial stability to the composition (e.g., in terms of reduced phase separation).
  • the cellulose ether and the polyacrylic polymer also keep the benzoyl peroxide uniformly suspended within the impregnated cloth and minimize preferential binding to the cloth (and/or erratic or uneven binding to the skin) and enhance contact with and/or bioavailability to the skin.
  • Anti-acne compositions of the invention typically are impregnated in an absorbent porous article. Impregnation refers to the entrainment of the composition in the porous article and is deemed to include both absorption and adsorption.
  • the active agent, benzoyl peroxide is released from the porous article when the composition is transferred from the porous article to a user's skin. Depending on conditions of use, any useful portion or substantially all of the benzoyl peroxide may be released.
  • the term “acne” means a common inflammatory disease of the pilosebaceous glands characterized by comedones, erythema, general irritation, papules, pustules, inflamed nodules, superficial or greater pus-filled cysts, and (in extreme cases) canalizing and deep, inflamed, sometimes purulent sacs.
  • Types of acne within the scope of the present subject matter include acne vulgaris or topical acne.
  • “acne” is believed to be caused by an interaction among hormones, keratin, sebum, and bacteria.
  • One common bacterial causative agent is Propionibacterium acnes.
  • Benzoyl peroxide is used in the composition an anti-acne agent. Benzoyl peroxide has antimicrobial and antibacterial effect as well as a keratolyic and drying effect. Benzoyl peroxide is present in the composition at up to 15 wt %, preferably from about 1 wt % to about 15 wt %, and most preferably from about 3 wt % to about 9 wt % based on the total weight of the composition.
  • the composition has a surfactant system of one or more surfactants.
  • Benzoyl peroxide is relatively insoluble in water, so it can be desirable to form a suspension of the benzoyl peroxide in aqueous media in the impregnant composition and for the purpose of stabilization and entrainment therein.
  • the surfactant system is selected to provide for release of the benzoyl peroxide from the porous article upon contact with the skin and retention of a residue or portion of the benzoyl peroxide after the composition has been rinsed or otherwise substantially removed from the skin.
  • the surfactant system (one or more surfactants) is present in the impregnant composition in an amount of about 0.1 wt % to about 75 wt % of the total composition.
  • the surfactant system is present from about 4 wt % to about 40 wt % of the total composition. More preferably, the surfactant system is present from about 10 wt % to about 30 wt % of the total composition.
  • the surfactant system may have surfactants known in the art, such as anionic, nonionic, amphoteric, cationic, and zwitterionic surfactants.
  • Preferred systems have one or more anionic surfactants for the cleansing and lathering effects.
  • the surfactant system preferably has one or more anionic surfactants present in an amount of about 0.1 wt % to about 75 wt % and more preferably about 4 wt % to about 40 wt % based on the total weight of surfactants in the surfactant system.
  • anionic surfactants include carboxylates, amino acid derivatives, alkyl sulphates, alkyl ether sulfates, sulphonates, isethionates, taurates, sulfosuccinates, alkyl sulfoacetates, phosphates, alkyl phosphates, lauramine oxide, and any combination thereof.
  • Preferred anionic surfactants include salts of fatty acid esters having from 12 to 20 carbon atoms, such as sodium methyl cocoyl taurate; salts of fatty acid isethionates having from 12 to 20 carbon atoms, such as sodium cocoyl isethionate; salts of fatty acid sulfoacetates having from 12 to 20 carbons, such as sodium lauryl sulfoacetate; and disalts of fatty acid sulfosuccinates having from 12 to 20 carbons, such as disodium laureth sulfosuccinate.
  • salts of fatty acid esters having from 12 to 20 carbon atoms and salts of fatty acid isethionates having from 12 to 20 carbons are together present at a total of about 8 to about 30 wt %, such as about 8 to about 20 wt % active material (e.g., sodium cocoyl isethionate), typically about 9 to about 15 wt % active material (e.g., about 10 to about 12% active material), but alternatively about 12 to about 27 wt % based on the total weight of the composition.
  • the salt is sodium methyl cocoyl taurate.
  • a relatively lower concentration can be suitable (e.g., about 1 to about 15 wt %, such as about 2 to about 8 wt % active material).
  • salts of fatty acid sulfoacetates having from 12 to 20 carbons and disalts of fatty acid sulfosuccinates having from 12 to 20 carbons are together present at a total of about 1 to about 10 wt %, more preferably at a total of about 2 to about 8 wt %, and most preferably at a total of about 3 to about 6 wt % based on the total weight of the composition.
  • nonionic surfactants examples include alkanolamides, amine oxides, esterified carboxylic acids, ethoxylated alcohols, poloxamers, and any combination thereof.
  • amphoteric/zwitterionic surfactants examples include betaine surfactants, such as cocamidopropyl betaine and lauramidopropyl betaine.
  • Examples of useful cationic surfactants include alkylamines, alkylimidazolines, and quaternary ammonium compounds.
  • Examples of cationic surfactants include, benzethonium chloride, cetrimide, cetylpyridinium chloride, stearalkonium chloride and dicetyldimonium chloride.
  • the impregnant composition can be aqueous or nonaqueous or aqueous/nonaqueous, i.e., an emulsion.
  • water can be present as a carrier or solvent for suspending, dispersing, and/or dissolving composition ingredients.
  • the water is present in the composition at up to 90 wt %, preferably about 10 wt % to about 90 wt %, and more preferably from about 20 wt % to about 80 wt %, and most preferably from about 40 wt % to about 80 wt % based on the total weight of the composition.
  • Useful nonaqueous and/or hydrophilic solvents include monohydric alcohols, polyhydric alcohols, and C 12-15 alkyl benzoates and can be present in the composition in the percentages indicated above for water.
  • Viscosity is important to the storage stability of the liquid impregnant composition and the rheology or flow properties of the composition during impregnation of the porous article. Viscosity may also vary depending on the form of the composition employed, e.g., gel, dispersion, emulsion, or suspension. The gel form is preferred. Viscosity of the composition is preferably from about 500 cP to about 3,000,000 cP, more preferably about 30,000 cP to about 150,000 cP, and most preferably about 35,000 cP to about 65,000 cP.
  • the viscosity of the composition can be regulated with the presence of one or more gelling agents and/or a thickening agents as optional ingredient(s).
  • the gelling agent(s) and/or thickening agents are present in the composition at up to 30 wt %, preferably from about 0.1 wt % to about 10 wt % based on the total weight of the composition.
  • useful gelling agents include various cellulose agents, including cellulose ethers such as carboxymethylcellulose sodium, carboxymethylcellulose calcium, hydroxypropyl cellulose, hydroxyethylmethyl cellulose, ethylcellulose, hydroxyethylcellulose, methylcellulose, hydroxypropylcellulose, and hydroxypropylmethylcellulose.
  • a preferred cellulose ether is hydroxypropylmethylcellulose.
  • Other useful cellulose agents include cellulose gum, xanthan gum, gum arabic, gum tragacanth, locust bean gum, guar gum, derivatives thereof, and any combination thereof.
  • the gelling agent(s) (and other possible components of the composition) preferably do not stain or otherwise impair hair, skin, and/or clothing.
  • cellulose ethers When one or more cellulose ethers are present, it is preferably present from about 0.1 wt % to about 3 wt % and more preferably from about 0.45 wt % to about 1 wt % in the composition.
  • gelling agents useful include polyacrylic polymers, carboxy vinyl polymers such as carboxypolymethylene, derivatives thereof, and any combination thereof.
  • a preferred polyacrylic polymer is the carbomers, such as the Carbopol polymers available from Noveon Inc.
  • a preferred polyacrylic polymer is an acrylates/C 10-30 alkyl acrylate crosspolymer.
  • Preferred polyacrylic polymers are carbomers.
  • suitable carbomers are Carbopol 1342, Carbopol 940, Carbopol 941, Carbopol 980, Carbopol 981, Carbopol 1382, Carbopol 971P, Carbopol 974P, Carbopol 71G, Carbopol 910, Carbopol 934, Carbopol 934P, Carbopol 5984, Carbopol ETD, Carbopol Ultrez 10, Carbopol Ultrez 21, Pemulen TR-1, Pemulen TR-2, and any combination of the foregoing.
  • Carbopol 1342 is a preferred carbomer.
  • one or more polyacrylic polymers When one or more polyacrylic polymers are present, it is preferably present from about 0.1 wt % to about 3 wt % and more preferably from about 0.45 wt % to about 1 wt % in the composition.
  • useful thickening agents include fatty alcohols of 10 to 24 carbon atoms, such as cetyl alcohol, cetearyl alcohol, cetostearyl alcohol, stearyl alcohol, lauryl alcohol, myristyl alcohol, arachidyl alcohol, behenyl alcohol, oleyl alcohol, and erucyl alcohol; fatty acids of 10 to 24 carbon atoms, such as stearic acid, myristic acid, lauric acid, arachidic acid, behenic acid, oleic acid, and erucic acid; fatty esters of 10 to 24 carbon atoms, such as sodium stearate, glyceryl monostearate and glyceryl monooleate; magnesium aluminum silicate; xanthan gum; PEG-150 pentaerythrityl tetrastearate; derivatives thereof; and any combination thereof.
  • Preferred thickening agents are fatty alcohols, fatty acids, and fatty esters. More preferred thickening agents are fatty alcohols.
  • fatty alcohols, fatty acids, or fatty esters of 10 to 24 carbon atoms are present in the composition, it is preferably present from about 0.5 wt % to about 10 wt % and more preferably from about 0.5 wt % to about 3 wt %.
  • the thickening agent may also take the form of one or more organic waxes, such as emulsifying wax (nonionic emulsifying wax), anionic emulsifying wax, cetyl ester wax, microcrystalline wax, white wax, yellow wax, paraffin, synthetic waxes such as high molecular weight organic esters, and any combination of the foregoing.
  • emulsifying wax nonionic emulsifying wax
  • anionic emulsifying wax cetyl ester wax
  • microcrystalline wax white wax, yellow wax, paraffin
  • synthetic waxes such as high molecular weight organic esters
  • the thickening agent may also take the form of one or more of the following: chitosan, carrageenan, colloidal silicon dioxide, hydroxypropyl starch, kaolin, polycarbophil, propylene glycol alginate, sodium alginate, alginic acid, tragacanth, acacia, trehalose, and any combination of the foregoing.
  • compositions further have a moisturizer.
  • benzoyl peroxide can dry out areas of the body to which compositions having it are applied.
  • moisturizers examples include glycerin, pentylene glycol, butylene glycol, polyethylene glycol, sodium pyrrolidone carboxylate, alpha-hydroxy acids, beta-hydroxy acids, polyhydric alcohols, ethoxylated and propoxylated polyols, polyols, polysaccharides, panthenol, pantethine, hexylene glycol, propylene glycol, polypropylene glycol, octyldodecanol, dipropylene glycol, sorbitol, sodium hyaluronate, sodium pyrrolidone carboxylic acid (sodium PCA), derivatives thereof, and any combination thereof.
  • Preferred moisturizers are glycerin, sodium hyaluronate, and sodium PCA.
  • the composition may optionally further have a humectant.
  • useful humectants include sorbitol, glycerin, sorbitol syrup, E965 maltitol, maltitol, maltitol syrup, E1200 polydextrose, E1518 glyceryl triacetate, triacetin, glyceryl triacetate, 1,2,3-propanetriyl triacetate, 1,2,3-propanetriol triacetate, triacetylglycerol, E1520 propylene glycol, 1,2-propanediol, 1,2-dihydroxypropane, methylethylene glycol, propane-1,2-diol, E420 sorbitol, propylene glycol, polyethylene glycol (PEG) esters, PEG-20 stearate, PEG-40 stearate, PEG-150 stearate, PEG-150 distearate, PEG-100 stearate, laureth-12, cete
  • the composition optionally further has a pH modifier.
  • useful pH modifiers include inorganic hydroxides, inorganic oxides, inorganic salts of weak acids, inorganic acids, organic acids, inorganic oxides, derivatives thereof, and any combination thereof.
  • useful inorganic hydroxides include ammonium hydroxide, alkali metal hydroxide, alkaline earth metal hydroxides. Sodium hydroxide is a preferred pH modifier.
  • useful inorganic oxides include magnesium oxide, calcium oxide, derivatives thereof, and any combination thereof.
  • useful inorganic salts of weak acids useful herein include ammonium phosphate (dibasic), alkali metal salts of weak acids such as sodium acetate, sodium borate, sodium metaborate, sodium carbonate, sodium bicarbonate, sodium phosphate (tribasic), sodium phosphate (dibasic), potassium carbonate, potassium bicarbonate, potassium citrate, potassium acetate, potassium phosphate (dibasic), potassium phosphate (tribasic), alkaline earth metal salts of weak acids such as magnesium phosphate and calcium phosphate, derivatives thereof, and any combination thereof.
  • weak acids such as sodium acetate, sodium borate, sodium metaborate, sodium carbonate, sodium bicarbonate, sodium phosphate (tribasic), sodium phosphate (dibasic), potassium carbonate, potassium bicarbonate, potassium citrate, potassium acetate, potassium phosphate (dibasic), potassium phosphate (tribasic), alkaline earth metal salts of weak acids such as magnesium phosphate and calcium phosphate, derivative
  • useful inorganic acids include hydrochloric acid, hydrofluoric acid, hydrobromic acid, nitric acid, nitrous acid, hydrocyanic acid, perchloric acid, chlorous acid, sulfurous acid, hypochlorous acid, phosphoric acid, acetic acid, sulfuric acid, derivatives thereof, and any combination thereof.
  • Examples of useful organic acids include lactic acid, citric acid, glutamic acid, methanoic acid, ethanoic acid, maleic acid and salts, glycolic acid and salts, benzoic acid, phenol, monochloroethanoic acid, dichloroethanoic acid, trichloroethanoic acid, butanoic acid, salicylic acid, glycolic acid, salts thereof, and any suitable combination thereof.
  • the composition optionally further has a chelating agent.
  • useful chelating agents include citric acid, isopropyl (mono) citrate, stearyl citrate, lecithin citrate, gluconic acid, tartaric acid, oxalic acid, phosphoric acid, sodium tetrapyrophosphate, potassium monophosphate, sodium hexametaphosphate, calcium hexametaphosphate, sorbitol, glycine (aminoacetic acid), methyl glucamine, triethanolamine (trolamine), EDTA, DEG (dihydroxyethylglycine), DPTA (diethylene triamine pentaacetic acid), NTA (Nitrilotriacetic Acid), HEDTA (N-(hydroxyethyl)-ethylenetriaminetriacetic acid), aminocarboxylates, dimercaperol (BAL), larixinic acid (Maltol), unidentate ligands (fluoride and cyanide
  • the composition may further have one or more zinc compounds useful as an astringent.
  • the one or more zinc compounds is selected from the group consisting of water soluble, poorly water soluble and water insoluble zinc salts, compounds and complexes, such as zinc acetate, zinc bacitracin, zinc bromide, zinc caprylate, zinc chloride, zinc citrate, zinc fluoride, zinc formate, zinc glycolate, zinc glycinate, zinc iodate, zinc lactate, zinc nitrate, zinc nitrite, zinc oleate, zinc oxalate, zinc oxide, zinc permanganate, zinc peroxide, zinc phenolsulfonate, zinc phosphate, zinc propionate, zinc pyrophosphate, zinc ricinoleate, zinc salicylate, zinc selenate, zinc silicate, zinc selenide, zinc sulfate, zinc stearate, zinc sulfide, zinc tannate, zinc tartrate, zinc valerate, zinc peptides, and
  • composition optionally may have other ingredients and excipients known in the art as useful in dermatological compositions.
  • the method of the present invention employs a porous article impregnated with the anti-acne composition to deliver the composition to the skin of a user.
  • the porous article of the delivery system allows for easy application of the composition.
  • the porous article is preferably made of a material in which the composition is capable of being absorbed and/or adsorbed yet still allowing transmission to the skin to provide suitable contact/bioavailability after application.
  • the porous article can be made from a drapeable or flexible plastic foam, a sponge, a woven or nonwoven natural or synthetic fiber fabric or cloth, including that of gauze, felt, cotton, paper, or any other material capable of absorbing and/or adsorbing the composition.
  • the porous article is made of synthetic or natural material and woven or non-woven material.
  • the porous article is made of a non-woven synthetic material(s) in the form of a cloth article.
  • the porous article is flexible and can be easily manipulated by hand.
  • the porous article can be composed of a single layer or be formed of two or more layers. Different layers can be made of the same or different materials.
  • the porous articles are of discrete size and can be of various forms or shapes, for example, rectangular, circular, or oval.
  • the porous articles can also take the form of a pattern, such as a glove or mitten.
  • the impregnated porous articles are supplied to the user in the form of a package or container.
  • a plurality of porous articles may be supplied together in a single package or container, or porous articles may be supplied individually packaged.
  • the porous articles are supplied as individually packaged and hermetically sealed so as to better and more efficiently maintain the moisture content of the articles.
  • the porous articles are also packaged so as to not allow leakage of liquid composition from the container or package.
  • the package or container may be constructed of any material that provides a sufficient barrier to air and/or moisture permeation, such as foil, a plastic-lined foil, or a suitable plastic composition.
  • a plurality of individually packaged impregnated porous articles may be in turn packaged in a larger package or container, such as a box.
  • the container may take the form of a plastic, metal, or glass jar suitable for receiving and retaining a plurality of the porous articles.
  • the plastic, metal, or glass jar is made of a suitable plastic, metal, or glass material that does not react with the impregnant composition.
  • the porous articles are preferably supplied in a moistened state so at to facilitate immediate use by the end user.
  • the article is contacted with an area of the skin affected by acne by touching, dabbing, rubbing, wiping, or similar mechanical motion or action.
  • the contact may be carried out by hand or with by hand in conjunction with a mechanical implement, such as a trowel, brush, or other pad holder that permits a pad surface to contact skin.
  • Contact may be maintained for any period of time but is preferably maintained for a period of time sufficient to effect a desirable degree of cleansing action and deposition of benzoyl peroxide from the article to the skin.
  • the typical user will contact, e.g., rub the article on the surface of the skin for about five seconds or more and more typically about 10 seconds to 30 seconds.
  • the impregnant composition has a lathering surfactant(s)
  • the user will typically contact the affected area with the article so as to produce a lather simultaneous with the cleansing effect.
  • the impregnant composition imparted to the skin, together with any dirt, oils, or lather are removed by any practical means, such as rinsing off with water or contact with a wet or dry washcloth, towel, or other cloth.
  • the impregnant composition may be removed by wiping thoroughly with the composition itself.
  • the residual benzoyl peroxide may be similar to the originally applied amount. Residual amounts of benzoyl peroxide, an ingredient only sparingly soluble in water, remain on the skin to provide a residual anti-acne effect when the applied amount is removed by rinsing.
  • the amount of residual benzoyl peroxide can be up to about 50 wt % of the applied amount, typically up to 20 wt % and more typically from about 0.1 wt % to about 10 wt % of the benzoyl peroxide originally present in the impregnant composition in the porous article.
  • the proportion of residual benzoyl peroxide can be considerably less compared to the amount of benzoyl peroxide originally present in the impregnant composition in the porous article but still measurable (and therapeutically and/or prophylactically effective) on the skin.
  • the method of the present invention can be used to treat existing acne or to facilitate the prevention of acne. Any area of the skin can be treated, although the face and the back are the areas more commonly susceptible to the occurrence of acne.
  • the porous articles may be supplied substantially dry, i.e., the water in the impregnant composition (containing the benzoyl peroxide) has been partially or wholly reduced.
  • the end user must moisten the porous article with water or other liquid solvent prior to contacting the skin with the article.
  • the impregnant compositions are stable, i.e., the compositions substantially maintain phase stability and homogeneous dispersion of benzoyl peroxide therewithin at ambient temperature conditions.
  • the foaming cloth provides efficacious lathering and cleaning of the face.
  • the lather is desirably easily washed of and imparts a cosmetically elegant feel to the skin. After washing, a residual amount of benzoyl peroxide remains on the skin to reduce or diminish the incidence of acne.
  • Formulations for impregnant compositions were made. A goal was to provide products with good foaming characteristics and/or good skin application properties and good safety profile.
  • the active formulations are amenable to coating on a non-woven material to make impregnated cloth articles.
  • Formulations containing benzoyl peroxide as an active ingredient at a concentration of 3%, 6%, and 9% (w/w) were made. Since benzoyl peroxide is practically insoluble in water, the formulations were designed as aqueous gels, wherein the benzoyl peroxide was homogeneously suspended. However, solvents for some or all of the benzoyl peroxide also or alternatively can be used in similar formulations.
  • the gelling agent used in the formulations was Carbopol 1342.
  • Each of three foaming agents including sodium methyl cocoyl taurate, sodium cocoyl isethionate, and lauramidopropyl betaine were selected since they provided good foaming characteristics.
  • the pH of the formulations was targeted at 5.0-5.5 since it was found to be the most stable and appropriate pH range for benzoyl peroxide topical formulations.
  • the formulation compositions are provided in Table 1.
  • the gelling agent was changed from Carbopol 1342 to Carbopol 940.
  • 2 thickening agents methyl gluceth 20 and PEG-150 pentaerythrityl tetrastearate, were added.
  • Example 8 Hydroxypropyl Formulation was fluffy methylcellulose, Magnesium Aluminum Silicate, cetyl alcohol, and Carbopol
  • Example 9 Hydroxypropyl Formulation was fluffy methylcellulose, Veegum, PEG-150 Pentaerythrityl Tetrastearate, and Carbopol
  • Methyl gluceth 20 in Example 4 was replaced with cetyl alcohol and hydroxypropyl methylcellulose and magnesium aluminum silicate were removed. Additional moisturizers were added. These included 0.1% allantoin, 0.01% sodium hyaluronate, and 0.1% sodium PCA. Lauramidopropyl betaine was replaced with cocamidopropyl betaine.
  • Example 11 The formulation of Example 11 was made with a higher concentration of carbomer (0.8%). The viscosity of this formulation was 70,000 cP.
  • the formulations were prepared according to the following:
  • formulations were further modified to adjust viscosity according to the following:
  • Formulations having sodium lauryl sulfoacetate and disodium laureth sulfosuccinate had a higher viscosity than formulations without them.
  • Formulations having a higher concentration of glycerin had a lower viscosity than the formulations containing a lower concentration of glycerin.
  • the 3% and 6% formulations having adjusted HPMC and Carbopol levels were made.
  • the formulations had two different levels of glycerin (0.5% and 0.1%).
  • the formulations are set forth in Table 9.
  • Example 21 A Purified Water, USP 42.56 42.86 38.06 38.11 Sodium Hyaluronate 0.01 0.01 0.01 0.01 B Carbomer 1342, NF 0.80 0.90 0.70 0.90 C Hydroxypropyl 0.50 0.45 0.30 0.45 Methylcellulose (HPMC) D Allantoin 0.10 0.10 0.10 0.10 Glycerin, USP 0.50 0.10 0.50 0.10 E Sodium Methyl Cocoyl 7.00 7.00 7.00 7.00 Taurate Sodium Cocoyl Isethionate 11.25 11.25 11.25 11.25 Cetyl Alcohol, NF 1.00 1.50 1.00 1.00 F sodium lauryl 4.00 4.00 4.00 4.00 sulfoacetate and disodium laureth sulfosuccinate G Purified Water, USP 20.00
  • the formulations were prepared according to the following:
  • Example 18 and Example 20 Phase GH was added after the batch was cooled to 35-40° C. The temperature was kept in this range with to enhance the chemical stability of benzoyl peroxide in the formulations. At this temperature the batch was thick, so the temperature was changed to 55-60° C. for the formulations of Example 19 and Example 21.
  • Impregnated porous articles can be prepared using the formulations of the foregoing examples.
  • impregnated cloth articles can be prepared by exposing a non-woven fabric or cloth to an amount that is suitable to contact the acne-affected area of the skin.
  • a cloth article useful in the method of the present invention and two commercial anti-acne compositions were compared in a consumer/user study for efficacy and desirable product features.
  • a consumer research guidance test was conducted to evaluate the attributes of a facial cleansing cloth (BPO Foaming Cloth) useful in the method of the present invention.
  • the study was conducted at two separate testing facilities.
  • the following Table 11 is a summary of the number of subjects in each age group and gender that completed the study.
  • test material usage was also determined by the randomization design. All subjects were blinded to all three test materials.
  • Test Material Descriptions (A) Test material 0357-06CC/0125-07C identification number (TMIN): (B) Test material BPO Foaming Cloth (Benzoyl identification: Peroxide 6%) (C) Physical description: White, opaque, medication-coated cloth applicator (D) Test material 0358-06CC/0162-07C identification number (TMIN): (E) Test material BPO Cleanser (Benzoyl Peroxide identification: 6%) (F) Physical description: White, opaque cream (G) Test material 0359-06CC/0163-07C identification number (TMIN): (H) Test material BPO Wash (Benzoyl Peroxide 4%) identification: (I) Physical description: White, opaque cream
  • the BPO Cleanser (benzoyl peroxide 6%) used as a comparison composition in the consumer research guidance test had the following ingredients: benzoyl peroxide, glycerin USP, petrolatum USP, C 12-15 alkyl benzoate, sodium cocoyl isethionate, special petrolatum fraction, sodium C 14-16 olefin sulfonate, zinc lactate, carbomer, potassium metaphosphate NF, titanium dioxide USP, trolamine NF, glycolic acid, lavender extract, and menthol USP.
  • the BPO Wash (benzoyl peroxide 4%) used as a comparison composition in the consumer research guidance test had the following ingredients: benzoyl peroxide, alpha olefin sulfonate, cetosteryl alcohol NF, glycerin USP, glyceryl monostearate SE, methylparaben NF, phosphoric acid NF, propylene glycol USP, sodium PCA, and white soft paraffin USP.
  • BPO Foaming cloth At least five minutes after washing with the first cleanser, subjects used the second assigned cleanser (BPO Cleanser or BPO Wash) as instructed.
  • the first and second washes for subject 054 were separated by two (2) minutes instead of five (5) minutes. This deviation is not expected to have an impact on the outcome of the study.
  • Table 13 presents the results of the top 2 box (positive responses: score of 1 or 2)/bottom 2 box (negative responses: score of 4 or 5) analysis of the questionnaires regarding product attributes.
  • the number of subjects with the specific response is listed, followed by the percentage of the total subject population in parentheses.
  • An asterisk (*) indicates that the proportion of subjects responding positively for a given statement is statistically greater than the proportion of subjects responding negatively.
  • Table 14 presents the results of the top 2 box/bottom 2 box analysis of the questionnaires regarding product preference.
  • the number of subjects with the specific response is listed, followed by the percentage of the total subject population in parentheses.
  • An asterisk (*) indicates that the proportion of subjects who selected BPO Foaming Cloth for a given statement is statistically greater than the proportion of subjects who selected the other assigned cleanser (BPO Cleanser or BPO Wash).
  • Table 15 summarizes the results of the top 2 box/bottom 2 box analysis for the Product Attribute Questionnaire.
  • An asterisk (*) indicates that a statistically significant proportion of subjects responded positively (Strongly Agree/Agree—score of 1 or 2) than negatively (Disagree/Strongly Disagree—score of 4 or 5).
  • BPO Foaming Cloth vs. BPO Cleanser (Benzoyl Peroxide 6%) All Subjects Male Subjects Female Subjects All 17-22 yrs 23-30 yrs All 17-22 yrs 23-30 yrs All 17-22 yrs 23-30 yrs (17-30 yrs) old old (17-30 yrs) old old (17-30 yrs) old old 1. More convenient to use * * * * * * * * 2. Easier to use * * * * * * * 3. More portable * * * * * * * * * * * 4.
  • the BPO Foaming Cloth may provide a higher degree of lathering compared to the BPO Cleanser and the BPO Wash. Further, the BPO Foaming Cloth may impart a higher degree of cosmetically elegant feel to the skin compared to the BPO Cleanser and the BPO Wash. Further, the BPO Foaming Cloth may leave a higher degree of a residual benzoyl peroxide on the skin compared to the BPO Cleanser and the BPO Wash after wash-off.
  • the foaming tendency of the BPO Foaming Cloth was also tested and compared to that of the BPO Cleanser and the BPO Wash.
  • the test method employed was ASTM D-3519-88.
  • the test method was used to measure foaming tendency in aqueous media under high shear conditions (blender test). The testing was performed with deionized (DI) water and hard water (100 ppm) in triplicate.
  • the test samples were prepared by cutting two pads of BPO Foaming Cloths into small pieces and adding them to 190 mL of water.
  • the test samples for BPO Cleanser and BPO Wash were prepared by adding 10 mL of the test product into 190 mL of water.
  • the test samples were equilibrated for 1 hour in a 25 ⁇ 1° C. water bath.
  • the foam volume was determined after blending for 30 seconds using a blender with a glass jar agitating between 8000 and 9000 rpm.
  • the residual foam height was also determined after allowing the blender to stand undisturbed for 5 minutes.
  • the testing results of maximum foam height and residual foam height after 5 min are summarized in Table 18.
  • the maximum foam height generated by BPO Foaming Cloths was 7.4 ⁇ 0.3 cm.
  • the residual foam height after 5 minutes remained high at 5.6 ⁇ 0.3 cm for BPO Foaming Cloths.
  • the maximum foam height generated by BPO Cloths was 4 and 3 times of that by BPO Cleanser and BPO Wash, respectively.
  • the residual foam height after 5 minutes for BPO Foaming Cloths was 19 and 4 times of that for BPO Cleanser and BPO Wash, respectively.

Abstract

A method for treating acne on the skin. The method has the steps of (a) providing an drapeable or flexible porous article impregnated with an aqueous cleansing composition having a carrier, benzoyl peroxide, and one or more cleansing agents; (b) contacting an area of the skin affected by acne with the porous article such that the skin is contacted by the composition; and (c) removing the composition from the skin wherein residual benzoyl peroxide remains on the skin in an anti-acne effective amount. There are also anti-acne compositions.

Description

    CROSS-REFERENCE TO A RELATED APPLICATION
  • The present application claims priority based upon U.S. Provisional Application No. 61/306,808, filed Feb. 22, 2010, and U.S. Provisional Application No. 61/157,817, filed Mar. 5, 2009, both of which are incorporated herein by reference in their entireties.
  • BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The present invention relates to methods and compositions for preventing and/or treating acne on the skin.
  • 2. Description of the Related Art
  • Acne is a condition of the human skin characterized by an excess flow of sebum, or skin oil, from the sebaceous glands located in the pilosebaceous apparatus. Sebum reaches the skin surface through the duct of the hair follicle. The presence of excessive amounts of sebum and slouched follicle cells in the duct and on the skin acts to block or stagnate the continuous flow of sebum from the follicular duct, thus producing a thickening and a solidification of the sebum to form a solid plug known as a comedone. When this process occurs, hyperkeratinization of the follicular opening is stimulated, thus tending to partially or completely close the duct. The usual results are papules, pustules, or cysts, often contaminated with bacteria which cause secondary infections and inflammation. Acne is particularly characterized by the presence of comedones, inflammatory papules, pustules, or cysts. The effect of acne ranges from slight to substantial skin irritation and pitting to disfiguring scars.
  • Many topical therapeutic agents are employed in the treatment of acne and seborrhea to prevent the blocking of the follicular duct, to reopen the duct once it has become blocked, to act against the infecting bacteria or the thickened sebum and resulting inflammation, or to provide combinations of each of these actions. The horny outer layer of the skin, which is known as the stratum corneum, is formed of dead cells composed largely of keratin. Therapeutic agents which act to prevent the blocking of the follicular duct by promoting the removal or sloughing off of excess keratin are known as keratolytic agents.
  • Benzoyl peroxide has been used as a very effective keratolytic and antibacterial agent in the treatment of acne. The topical application of benzoyl peroxide for skin lesion therapy is well known. For example, U.S. Pat. Nos. 5,445,823; 5,545,407; 5,648,389; and 5,932,228 disclose compositions for treating acne and other skin lesions and also to methods of treatment utilizing these compositions. These compositions and methods of treatment employ benzoyl peroxide plus compounds for reducing the skin irritation associated with benzoyl peroxide, and a topical carrier.
  • One form for advantageously administering anti-acne agents is application to the skin via impregnated small cloth towelettes, wipes, or applicator porous articles. The cloths can be packaged in plural in a sealed pouch or individually. Examples of such cloths are disclosed in U.S. Pat. Nos. 5,242,433; 5,254,109; 5,368,581; 5,417,674; 5,460,620; 5,470,323; 5,538,732; 5,562,642; 6,001,380; and 6,740,330 as well as U.S. Published Patent Application Publication Nos. 2005/0025817, 2005/0100585, and 2005/0232978.
  • SUMMARY OF THE INVENTION
  • The invention described herein provides new methods for treating and/or preventing acne and new compositions useful in such respects.
  • In one aspect, the invention provides new methods for treating acne with benzoyl peroxide that improve user compliance and/or contact of the benzoyl peroxide with the skin.
  • According to the present invention, there is, in a particular exemplary aspect, provided a method for treating acne on the skin, comprising: (a) providing an drapeable or flexible porous article impregnated with an aqueous cleansing composition comprising a carrier, benzoyl peroxide, and one or more cleansing agents; (b) contacting an area of the skin affected by acne with the porous article such that the skin is contacted by the composition; and (c) removing the composition from the skin wherein residual benzoyl peroxide remains on the skin in an anti-acne effective amount, preferably while surface dirt and/or irritants are removed.
  • Further according to the present invention, there is provided an exemplary anti-acne composition. The composition has water, benzoyl peroxide, a salt of a fatty acid ester having from 12 to 20 carbon atoms, and a salt of a fatty acid isethionate having from 12 to 20 carbon atoms. The fatty acid ester salt and the fatty acid isethionate salt are present in an amount sufficient to render the composition foamable and to maintain a substantially homogeneous dispersion of the benzoyl peroxide in the composition to cleanse and medicate the skin.
  • Still further according to the present invention, anti-acne compositions are provided. In one aspect, the composition comprises water, benzoyl peroxide, a cellulose ether, and a polyacrylic polymer. The cellulose ether and the polyacrylic polymer are present in an amount sufficient to impart substantial stability to the composition (e.g., in terms of reduced phase separation). The cellulose ether and the polyacrylic polymer also keep the benzoyl peroxide uniformly suspended within the impregnated cloth and minimize preferential binding to the cloth (and/or erratic or uneven binding to the skin) and enhance contact with and/or bioavailability to the skin.
  • DETAILED DESCRIPTION OF THE INVENTION
  • Anti-acne compositions of the invention typically are impregnated in an absorbent porous article. Impregnation refers to the entrainment of the composition in the porous article and is deemed to include both absorption and adsorption. The active agent, benzoyl peroxide, is released from the porous article when the composition is transferred from the porous article to a user's skin. Depending on conditions of use, any useful portion or substantially all of the benzoyl peroxide may be released.
  • As used herein, the term “acne” means a common inflammatory disease of the pilosebaceous glands characterized by comedones, erythema, general irritation, papules, pustules, inflamed nodules, superficial or greater pus-filled cysts, and (in extreme cases) canalizing and deep, inflamed, sometimes purulent sacs. Types of acne within the scope of the present subject matter include acne vulgaris or topical acne. As described above, “acne” is believed to be caused by an interaction among hormones, keratin, sebum, and bacteria. One common bacterial causative agent is Propionibacterium acnes.
  • Benzoyl peroxide is used in the composition an anti-acne agent. Benzoyl peroxide has antimicrobial and antibacterial effect as well as a keratolyic and drying effect. Benzoyl peroxide is present in the composition at up to 15 wt %, preferably from about 1 wt % to about 15 wt %, and most preferably from about 3 wt % to about 9 wt % based on the total weight of the composition.
  • The composition has a surfactant system of one or more surfactants. Benzoyl peroxide is relatively insoluble in water, so it can be desirable to form a suspension of the benzoyl peroxide in aqueous media in the impregnant composition and for the purpose of stabilization and entrainment therein. Further, the surfactant system is selected to provide for release of the benzoyl peroxide from the porous article upon contact with the skin and retention of a residue or portion of the benzoyl peroxide after the composition has been rinsed or otherwise substantially removed from the skin.
  • The surfactant system (one or more surfactants) is present in the impregnant composition in an amount of about 0.1 wt % to about 75 wt % of the total composition. Preferably, the surfactant system is present from about 4 wt % to about 40 wt % of the total composition. More preferably, the surfactant system is present from about 10 wt % to about 30 wt % of the total composition.
  • The surfactant system may have surfactants known in the art, such as anionic, nonionic, amphoteric, cationic, and zwitterionic surfactants. Preferred systems have one or more anionic surfactants for the cleansing and lathering effects.
  • The surfactant system preferably has one or more anionic surfactants present in an amount of about 0.1 wt % to about 75 wt % and more preferably about 4 wt % to about 40 wt % based on the total weight of surfactants in the surfactant system.
  • Examples of useful anionic surfactants include carboxylates, amino acid derivatives, alkyl sulphates, alkyl ether sulfates, sulphonates, isethionates, taurates, sulfosuccinates, alkyl sulfoacetates, phosphates, alkyl phosphates, lauramine oxide, and any combination thereof. Preferred anionic surfactants include salts of fatty acid esters having from 12 to 20 carbon atoms, such as sodium methyl cocoyl taurate; salts of fatty acid isethionates having from 12 to 20 carbon atoms, such as sodium cocoyl isethionate; salts of fatty acid sulfoacetates having from 12 to 20 carbons, such as sodium lauryl sulfoacetate; and disalts of fatty acid sulfosuccinates having from 12 to 20 carbons, such as disodium laureth sulfosuccinate.
  • In preferred compositions, salts of fatty acid esters having from 12 to 20 carbon atoms and salts of fatty acid isethionates having from 12 to 20 carbons are together present at a total of about 8 to about 30 wt %, such as about 8 to about 20 wt % active material (e.g., sodium cocoyl isethionate), typically about 9 to about 15 wt % active material (e.g., about 10 to about 12% active material), but alternatively about 12 to about 27 wt % based on the total weight of the composition. In one aspect, the salt is sodium methyl cocoyl taurate. In this and other aspects, a relatively lower concentration can be suitable (e.g., about 1 to about 15 wt %, such as about 2 to about 8 wt % active material).
  • In more preferred compositions, salts of fatty acid sulfoacetates having from 12 to 20 carbons and disalts of fatty acid sulfosuccinates having from 12 to 20 carbons are together present at a total of about 1 to about 10 wt %, more preferably at a total of about 2 to about 8 wt %, and most preferably at a total of about 3 to about 6 wt % based on the total weight of the composition.
  • Examples of useful nonionic surfactants include alkanolamides, amine oxides, esterified carboxylic acids, ethoxylated alcohols, poloxamers, and any combination thereof.
  • Examples of useful amphoteric/zwitterionic surfactants include betaine surfactants, such as cocamidopropyl betaine and lauramidopropyl betaine.
  • Examples of useful cationic surfactants include alkylamines, alkylimidazolines, and quaternary ammonium compounds. Examples of cationic surfactants include, benzethonium chloride, cetrimide, cetylpyridinium chloride, stearalkonium chloride and dicetyldimonium chloride.
  • The impregnant composition can be aqueous or nonaqueous or aqueous/nonaqueous, i.e., an emulsion. In an aqueous composition, water can be present as a carrier or solvent for suspending, dispersing, and/or dissolving composition ingredients. In an aqueous composition, the water is present in the composition at up to 90 wt %, preferably about 10 wt % to about 90 wt %, and more preferably from about 20 wt % to about 80 wt %, and most preferably from about 40 wt % to about 80 wt % based on the total weight of the composition. Useful nonaqueous and/or hydrophilic solvents include monohydric alcohols, polyhydric alcohols, and C12-15 alkyl benzoates and can be present in the composition in the percentages indicated above for water.
  • Selection of viscosity is important to the storage stability of the liquid impregnant composition and the rheology or flow properties of the composition during impregnation of the porous article. Viscosity may also vary depending on the form of the composition employed, e.g., gel, dispersion, emulsion, or suspension. The gel form is preferred. Viscosity of the composition is preferably from about 500 cP to about 3,000,000 cP, more preferably about 30,000 cP to about 150,000 cP, and most preferably about 35,000 cP to about 65,000 cP.
  • The viscosity of the composition can be regulated with the presence of one or more gelling agents and/or a thickening agents as optional ingredient(s). The gelling agent(s) and/or thickening agents are present in the composition at up to 30 wt %, preferably from about 0.1 wt % to about 10 wt % based on the total weight of the composition.
  • Examples of useful gelling agents include various cellulose agents, including cellulose ethers such as carboxymethylcellulose sodium, carboxymethylcellulose calcium, hydroxypropyl cellulose, hydroxyethylmethyl cellulose, ethylcellulose, hydroxyethylcellulose, methylcellulose, hydroxypropylcellulose, and hydroxypropylmethylcellulose. A preferred cellulose ether is hydroxypropylmethylcellulose. Other useful cellulose agents include cellulose gum, xanthan gum, gum arabic, gum tragacanth, locust bean gum, guar gum, derivatives thereof, and any combination thereof. The gelling agent(s) (and other possible components of the composition) preferably do not stain or otherwise impair hair, skin, and/or clothing.
  • When one or more cellulose ethers are present, it is preferably present from about 0.1 wt % to about 3 wt % and more preferably from about 0.45 wt % to about 1 wt % in the composition.
  • Other useful gelling agents useful include polyacrylic polymers, carboxy vinyl polymers such as carboxypolymethylene, derivatives thereof, and any combination thereof. A preferred polyacrylic polymer is the carbomers, such as the Carbopol polymers available from Noveon Inc. A preferred polyacrylic polymer is an acrylates/C10-30 alkyl acrylate crosspolymer.
  • Preferred polyacrylic polymers are carbomers. Examples of suitable carbomers are Carbopol 1342, Carbopol 940, Carbopol 941, Carbopol 980, Carbopol 981, Carbopol 1382, Carbopol 971P, Carbopol 974P, Carbopol 71G, Carbopol 910, Carbopol 934, Carbopol 934P, Carbopol 5984, Carbopol ETD, Carbopol Ultrez 10, Carbopol Ultrez 21, Pemulen TR-1, Pemulen TR-2, and any combination of the foregoing. Carbopol 1342 is a preferred carbomer.
  • When one or more polyacrylic polymers are present, it is preferably present from about 0.1 wt % to about 3 wt % and more preferably from about 0.45 wt % to about 1 wt % in the composition.
  • Examples of useful thickening agents include fatty alcohols of 10 to 24 carbon atoms, such as cetyl alcohol, cetearyl alcohol, cetostearyl alcohol, stearyl alcohol, lauryl alcohol, myristyl alcohol, arachidyl alcohol, behenyl alcohol, oleyl alcohol, and erucyl alcohol; fatty acids of 10 to 24 carbon atoms, such as stearic acid, myristic acid, lauric acid, arachidic acid, behenic acid, oleic acid, and erucic acid; fatty esters of 10 to 24 carbon atoms, such as sodium stearate, glyceryl monostearate and glyceryl monooleate; magnesium aluminum silicate; xanthan gum; PEG-150 pentaerythrityl tetrastearate; derivatives thereof; and any combination thereof. Preferred thickening agents are fatty alcohols, fatty acids, and fatty esters. More preferred thickening agents are fatty alcohols. A most preferred thickening agent is cetyl alcohol.
  • When one or more fatty alcohols, fatty acids, or fatty esters of 10 to 24 carbon atoms are present in the composition, it is preferably present from about 0.5 wt % to about 10 wt % and more preferably from about 0.5 wt % to about 3 wt %.
  • The thickening agent may also take the form of one or more organic waxes, such as emulsifying wax (nonionic emulsifying wax), anionic emulsifying wax, cetyl ester wax, microcrystalline wax, white wax, yellow wax, paraffin, synthetic waxes such as high molecular weight organic esters, and any combination of the foregoing.
  • The thickening agent may also take the form of one or more of the following: chitosan, carrageenan, colloidal silicon dioxide, hydroxypropyl starch, kaolin, polycarbophil, propylene glycol alginate, sodium alginate, alginic acid, tragacanth, acacia, trehalose, and any combination of the foregoing.
  • Preferred compositions further have a moisturizer. In some instances, benzoyl peroxide can dry out areas of the body to which compositions having it are applied. In these instances, it is desirable to include a moisturizer in the composition to help the body retain moisture to offset the drying effect of the benzoyl peroxide. Examples of useful moisturizers include glycerin, pentylene glycol, butylene glycol, polyethylene glycol, sodium pyrrolidone carboxylate, alpha-hydroxy acids, beta-hydroxy acids, polyhydric alcohols, ethoxylated and propoxylated polyols, polyols, polysaccharides, panthenol, pantethine, hexylene glycol, propylene glycol, polypropylene glycol, octyldodecanol, dipropylene glycol, sorbitol, sodium hyaluronate, sodium pyrrolidone carboxylic acid (sodium PCA), derivatives thereof, and any combination thereof. Preferred moisturizers are glycerin, sodium hyaluronate, and sodium PCA.
  • The composition may optionally further have a humectant. Examples of useful humectants include sorbitol, glycerin, sorbitol syrup, E965 maltitol, maltitol, maltitol syrup, E1200 polydextrose, E1518 glyceryl triacetate, triacetin, glyceryl triacetate, 1,2,3-propanetriyl triacetate, 1,2,3-propanetriol triacetate, triacetylglycerol, E1520 propylene glycol, 1,2-propanediol, 1,2-dihydroxypropane, methylethylene glycol, propane-1,2-diol, E420 sorbitol, propylene glycol, polyethylene glycol (PEG) esters, PEG-20 stearate, PEG-40 stearate, PEG-150 stearate, PEG-150 distearate, PEG-100 stearate, laureth-12, ceteareth-20, laureth-23, glycereth-7, glycereth-12, glycereth-26, PEG-4, PEG-6, PEG-8, PEG-12, PEG-32, PEG-75, PEG-150, derivatives thereof, and any combination thereof.
  • The composition optionally further has a pH modifier. Examples of useful pH modifiers include inorganic hydroxides, inorganic oxides, inorganic salts of weak acids, inorganic acids, organic acids, inorganic oxides, derivatives thereof, and any combination thereof. Examples of useful inorganic hydroxides include ammonium hydroxide, alkali metal hydroxide, alkaline earth metal hydroxides. Sodium hydroxide is a preferred pH modifier.
  • Examples of useful inorganic oxides include magnesium oxide, calcium oxide, derivatives thereof, and any combination thereof.
  • Examples of useful inorganic salts of weak acids useful herein include ammonium phosphate (dibasic), alkali metal salts of weak acids such as sodium acetate, sodium borate, sodium metaborate, sodium carbonate, sodium bicarbonate, sodium phosphate (tribasic), sodium phosphate (dibasic), potassium carbonate, potassium bicarbonate, potassium citrate, potassium acetate, potassium phosphate (dibasic), potassium phosphate (tribasic), alkaline earth metal salts of weak acids such as magnesium phosphate and calcium phosphate, derivatives thereof, and any combination thereof.
  • Examples of useful inorganic acids include hydrochloric acid, hydrofluoric acid, hydrobromic acid, nitric acid, nitrous acid, hydrocyanic acid, perchloric acid, chlorous acid, sulfurous acid, hypochlorous acid, phosphoric acid, acetic acid, sulfuric acid, derivatives thereof, and any combination thereof.
  • Examples of useful organic acids include lactic acid, citric acid, glutamic acid, methanoic acid, ethanoic acid, maleic acid and salts, glycolic acid and salts, benzoic acid, phenol, monochloroethanoic acid, dichloroethanoic acid, trichloroethanoic acid, butanoic acid, salicylic acid, glycolic acid, salts thereof, and any suitable combination thereof.
  • The composition optionally further has a chelating agent. Examples of useful chelating agents include citric acid, isopropyl (mono) citrate, stearyl citrate, lecithin citrate, gluconic acid, tartaric acid, oxalic acid, phosphoric acid, sodium tetrapyrophosphate, potassium monophosphate, sodium hexametaphosphate, calcium hexametaphosphate, sorbitol, glycine (aminoacetic acid), methyl glucamine, triethanolamine (trolamine), EDTA, DEG (dihydroxyethylglycine), DPTA (diethylene triamine pentaacetic acid), NTA (Nitrilotriacetic Acid), HEDTA (N-(hydroxyethyl)-ethylenetriaminetriacetic acid), aminocarboxylates, dimercaperol (BAL), larixinic acid (Maltol), unidentate ligands (fluoride and cyanide ions), diphenylthiocarbazone, O-phenanthroline, barium diphenylamine sulfonate, sodium glucoheptonate, 8-hydroxyquinoline, olefin complexes (such as dicyclopentadienyl iron), porphyrins, phosphonates, pharmaceutically acceptable salts thereof, derivatives thereof, and any combination thereof.
  • The composition may further have one or more zinc compounds useful as an astringent. The one or more zinc compounds is selected from the group consisting of water soluble, poorly water soluble and water insoluble zinc salts, compounds and complexes, such as zinc acetate, zinc bacitracin, zinc bromide, zinc caprylate, zinc chloride, zinc citrate, zinc fluoride, zinc formate, zinc glycolate, zinc glycinate, zinc iodate, zinc lactate, zinc nitrate, zinc nitrite, zinc oleate, zinc oxalate, zinc oxide, zinc permanganate, zinc peroxide, zinc phenolsulfonate, zinc phosphate, zinc propionate, zinc pyrophosphate, zinc ricinoleate, zinc salicylate, zinc selenate, zinc silicate, zinc selenide, zinc sulfate, zinc stearate, zinc sulfide, zinc tannate, zinc tartrate, zinc valerate, zinc peptides, and zinc protein complexes. Preferred compounds are zinc lactate and zinc acetate. The one or more zinc compounds is present in an amount about 0.001% to about 30% and more preferably between about 0.1% to about 10%.
  • In addition to the ingredients enumerated above, the composition optionally may have other ingredients and excipients known in the art as useful in dermatological compositions.
  • The method of the present invention employs a porous article impregnated with the anti-acne composition to deliver the composition to the skin of a user. The porous article of the delivery system allows for easy application of the composition.
  • The porous article is preferably made of a material in which the composition is capable of being absorbed and/or adsorbed yet still allowing transmission to the skin to provide suitable contact/bioavailability after application. The porous article can be made from a drapeable or flexible plastic foam, a sponge, a woven or nonwoven natural or synthetic fiber fabric or cloth, including that of gauze, felt, cotton, paper, or any other material capable of absorbing and/or adsorbing the composition. Preferably, the porous article is made of synthetic or natural material and woven or non-woven material. Most preferably, the porous article is made of a non-woven synthetic material(s) in the form of a cloth article. The porous article is flexible and can be easily manipulated by hand.
  • The porous article can be composed of a single layer or be formed of two or more layers. Different layers can be made of the same or different materials. The porous articles are of discrete size and can be of various forms or shapes, for example, rectangular, circular, or oval. The porous articles can also take the form of a pattern, such as a glove or mitten.
  • The impregnated porous articles are supplied to the user in the form of a package or container. A plurality of porous articles may be supplied together in a single package or container, or porous articles may be supplied individually packaged. In one embodiment, the porous articles are supplied as individually packaged and hermetically sealed so as to better and more efficiently maintain the moisture content of the articles. The porous articles are also packaged so as to not allow leakage of liquid composition from the container or package. The package or container may be constructed of any material that provides a sufficient barrier to air and/or moisture permeation, such as foil, a plastic-lined foil, or a suitable plastic composition. A plurality of individually packaged impregnated porous articles may be in turn packaged in a larger package or container, such as a box.
  • If desired, the container may take the form of a plastic, metal, or glass jar suitable for receiving and retaining a plurality of the porous articles. The plastic, metal, or glass jar is made of a suitable plastic, metal, or glass material that does not react with the impregnant composition.
  • The porous articles are preferably supplied in a moistened state so at to facilitate immediate use by the end user. The article is contacted with an area of the skin affected by acne by touching, dabbing, rubbing, wiping, or similar mechanical motion or action. The contact may be carried out by hand or with by hand in conjunction with a mechanical implement, such as a trowel, brush, or other pad holder that permits a pad surface to contact skin. Contact may be maintained for any period of time but is preferably maintained for a period of time sufficient to effect a desirable degree of cleansing action and deposition of benzoyl peroxide from the article to the skin. Although not deemed to be limiting, the typical user will contact, e.g., rub the article on the surface of the skin for about five seconds or more and more typically about 10 seconds to 30 seconds. When the impregnant composition has a lathering surfactant(s), the user will typically contact the affected area with the article so as to produce a lather simultaneous with the cleansing effect. At the conclusion of contact with the skin, the impregnant composition imparted to the skin, together with any dirt, oils, or lather, are removed by any practical means, such as rinsing off with water or contact with a wet or dry washcloth, towel, or other cloth. Alternately, the impregnant composition may be removed by wiping thoroughly with the composition itself. In that case, the residual benzoyl peroxide may be similar to the originally applied amount. Residual amounts of benzoyl peroxide, an ingredient only sparingly soluble in water, remain on the skin to provide a residual anti-acne effect when the applied amount is removed by rinsing. The amount of residual benzoyl peroxide can be up to about 50 wt % of the applied amount, typically up to 20 wt % and more typically from about 0.1 wt % to about 10 wt % of the benzoyl peroxide originally present in the impregnant composition in the porous article. In other words, the proportion of residual benzoyl peroxide can be considerably less compared to the amount of benzoyl peroxide originally present in the impregnant composition in the porous article but still measurable (and therapeutically and/or prophylactically effective) on the skin.
  • The method of the present invention can be used to treat existing acne or to facilitate the prevention of acne. Any area of the skin can be treated, although the face and the back are the areas more commonly susceptible to the occurrence of acne.
  • In an alternate embodiment, the porous articles may be supplied substantially dry, i.e., the water in the impregnant composition (containing the benzoyl peroxide) has been partially or wholly reduced. In this instance, the end user must moisten the porous article with water or other liquid solvent prior to contacting the skin with the article.
  • The impregnant compositions are stable, i.e., the compositions substantially maintain phase stability and homogeneous dispersion of benzoyl peroxide therewithin at ambient temperature conditions.
  • The foaming cloth provides efficacious lathering and cleaning of the face. The lather is desirably easily washed of and imparts a cosmetically elegant feel to the skin. After washing, a residual amount of benzoyl peroxide remains on the skin to reduce or diminish the incidence of acne.
  • The following are examples of the present invention and are not to be construed as limiting.
  • EXAMPLES
  • Formulations for impregnant compositions were made. A goal was to provide products with good foaming characteristics and/or good skin application properties and good safety profile. The active formulations are amenable to coating on a non-woven material to make impregnated cloth articles.
  • Formulations containing benzoyl peroxide as an active ingredient at a concentration of 3%, 6%, and 9% (w/w) were made. Since benzoyl peroxide is practically insoluble in water, the formulations were designed as aqueous gels, wherein the benzoyl peroxide was homogeneously suspended. However, solvents for some or all of the benzoyl peroxide also or alternatively can be used in similar formulations.
  • Examples 1 to 3
  • Three formulations were made. The gelling agent used in the formulations was Carbopol 1342. Each of three foaming agents including sodium methyl cocoyl taurate, sodium cocoyl isethionate, and lauramidopropyl betaine were selected since they provided good foaming characteristics. The pH of the formulations was targeted at 5.0-5.5 since it was found to be the most stable and appropriate pH range for benzoyl peroxide topical formulations. The formulation compositions are provided in Table 1.
  • TABLE 1
    (Formulation Compositions of Examples 1 to 3)
    % (w/w)
    Ingredient 3% Cleanser 6% Cleanser 9% Cleanser
    Carbomer 1342, NF 0.90 0.70 0.70
    Purified Water, USP 9.918 21.539 32.301
    Docusate Sodium, USP 0.028 0.062 0.092
    Simethicone Emulsion, 0.007 0.015 0.023
    USP
    Benzoyl Peroxide, USP 4.270 9.264 13.894
    (75%)*
    Sodium Methyl Cocoyl 7.00 7.00 7.00
    Taurate
    Sodium Cocoyl Isethionate 11.25 11.25 11.25
    Lauramidopropyl Betaine 6.00 6.00 6.00
    Glycolic Acid, 70% 0.72 0.72 0.72
    Zinc Lactate 0.20 0.20 0.20
    Sodium Hydroxide, USP qs. pH 5.0 qs. pH 5.0 qs. pH 5.0
    (25%)
    Purified Water, USP qs. 100% qs. 100% qs. 100%
    pH 5.01 5.00 5.00
    Viscosity (T-C @ 5 RPM) 33,000 cP 16,300 cP 27,000 cP
    *BPO was added with 15% overage in 6% and 9% formulations and was added with 6% overage in the 3% formulation. Depending on the circumstances, other overages or no overage may be used.
  • Example 4
  • The gelling agent was changed from Carbopol 1342 to Carbopol 940. In addition, 2 thickening agents, methyl gluceth 20 and PEG-150 pentaerythrityl tetrastearate, were added.
  • TABLE 2
    (Formulation Composition of Example 4) (6% Benzoyl Peroxide)
    Ingredient % (w/w)
    A Purified Water, USP 32.81
    Methyl Gluceth 20 2.00
    B Purified Water, USP 5.00
    Glycolic Acid, 70% 0.72
    Zinc Lactate 0.20
    C Carbomer 940, NF 0.70
    D Purified Water, USP 20.00
    Docusate Sodium, USP 0.05
    Simethicone Emulsion, USP 0.01
    E Benzoyl Peroxide, USP (75%) 9.26%
    F Sodium Methyl Cocoyl Taurate 7.00
    PEG-150 Pentaerythrityl 0.10
    Tetrastearate
    Sodium Cocoyl Isethionate 11.25
    G Lauramidopropyl Betaine 6.00
    H Sodium Hydroxide, USP (25%) qs. pH 5.0-5.5
    I Purified Water, USP qs. 100%
  • Examples 5 to 8
  • Additional formulations were made to enhance physical stability using different combinations of thickening agents. The formulations are set forth in Table 3.
  • TABLE 3
    (Formulations for Examples 5 to 8)
    Formulation Thickening Agents Results
    Example 5 PEG-150 Pentaerythrityl Phase separation
    Tetrastearate and occurred even though
    Lauramidopropyl Betaine there were also some
    (increased process changes by
    concentrations) adding zinc lactate and
    glycolic acid towards
    the end.
    Example 6 PEG-150 Pentaerythrityl Phase separation
    Tetrastearate and occurred.
    xanthan gum
    Example 7 Xanthan gum Phase separation
    occurred.
    Example 8 Hydroxypropyl Formulation was fluffy
    methylcellulose,
    Magnesium Aluminum
    Silicate, cetyl
    alcohol, and Carbopol
    Example 9 Hydroxypropyl Formulation was fluffy
    methylcellulose,
    Veegum, PEG-150
    Pentaerythrityl
    Tetrastearate, and
    Carbopol
  • Examples 10 to 14
  • Methyl gluceth 20 in Example 4 was replaced with cetyl alcohol and hydroxypropyl methylcellulose and magnesium aluminum silicate were removed. Additional moisturizers were added. These included 0.1% allantoin, 0.01% sodium hyaluronate, and 0.1% sodium PCA. Lauramidopropyl betaine was replaced with cocamidopropyl betaine.
  • TABLE 4
    (Formulations for Examples 10 to 14)
    % (w/w)
    3% BPO 3% BPO 6% BPO 9% BPO
    Cleanser Cleanser Cleanser Cleanser
    Ingredient Example 10 Example 11 Example 12 Example 13
    A Purified Water, USP 42.86 42.76 38.40 33.83
    Carbomer 1342, NF 0.70 0.80 0.70 0.70
    Hydroxypropyl 0.30 0.30 0.30 0.30
    Methylcellulose
    Allantoin 0.10 0.10 0.10 0.10
    Sodium Hyaluronate 0.01 0.01 0.01 0.01
    B Sodium Methyl 7.00 7.00 7.00 7.00
    Cocoyl Taurate
    Sodium Cocoyl 11.25 11.25 11.25 11.25
    Isethionate
    Cetyl Alcohol, NF 1.00 1.00 1.00 1.00
    C Purified Water, USP 20.00 20.00 20.00 20.00
    Docusate Sodium, 0.05 0.05 0.05 0.05
    USP
    Simethicone 0.01 0.01 0.01 0.01
    Emulsion, USP
    D Benzoyl Peroxide, 4.70 4.70 9.16 13.73
    USP (75%)*
    E Cocamidopropyl 6.00 6.00 6.00 6.00
    Betaine
    F Sodium PCA 0.10 0.10 0.10 0.10
    G Purified Water, USP 5.00 5.00 5.00 5.00
    Glycolic Acid, 70% 0.72 0.72 0.72 0.72
    Zinc Lactate 0.20 0.20 0.20 0.20
    H Sodium Hydroxide, qs. qs. qs. qs.
    USP (25%) pH 5.0-5.5 pH 5.0-5.5 pH 5.0-5.5 pH 5.0-5.5
    I Purified Water, USP qs. 100% qs. 100% qs. 100% qs. 100%
    pH 5.27 5.23 5.23
    Viscosity (T-C @ 5 RPM) 25,000 cP 70,000 cP 60-70,000 cP 66-79,000 cP
    *These 3% cleansers contained 18% overage. 6% and 9% cleansers contained 15% overage. Other related formulations may contain other overages or no overages depending on circumstances.
  • The formulation of Example 11 was made with a higher concentration of carbomer (0.8%). The viscosity of this formulation was 70,000 cP.
  • The formulations were prepared according to the following:
    • 1. In main vessel, mix and heat Phase A to 65-70° C.
    • 2. Continue mixing Phase A until all gums are completely hydrated.
    • 3. At 65-70° C., add Phase B into Phase A and mix until uniform.
    • 4. Begin cooling main batch to 50° C.
    • 5. In a separate vessel, mix and heat Phase C to 65-70° C. Continue mixing until all docusate sodium is dissolved.
    • 6. Cool Phase C to 50° C. and add Phase D.
    • 7. Homogenize combined Phase C with fine screen for 5 minutes.
    • 8. Pass combined Phase C-D through microfluidizer@25,000 psi (one pass) directly into main batch under homogenization.
    • 9. Continue homogenization for 10 minutes and switch to propeller mixing with sweep agitation.
    • 10. Add Phase E to main batch and mix until uniform.
    • 11. Add Phase F to main batch and mix until uniform.
    • 12. Premix and warm (30° C.) Phase G until clear. Add to batch and mix until uniform.
    • 13. Adjust pH of batch to 5.0-5.5 with Phase H.
    • 14. qs batch to 100% with purified water (Phase I).
    Examples 14 to 17
  • The formulations were further modified to adjust viscosity according to the following:
      • 1. Removed cocamidopropyl betaine and added 2 levels of glycerin (0.5% and 2%)
      • 2. Removed cocamidopropyl betaine and added 2 levels of glycerin (0.5% and 2%), plus added sodium lauryl sulfoacetate and disodium laureth sulfosuccinate
      • 3. Removed cocamidopropyl betaine and added 2 levels of glycerin (0.5% and 2%), plus added sodium lauryl sulfoacetate and disodium laureth sulfosuccinate and lauramine oxide
      • 4. Removed sodium lauryl sulfoacetate and disodium laureth sulfosuccinate betaine, added 2 levels of glycerin (0.5% and 2%), added lauramine oxide.
  • Formulations are set forth below in Table 8.
  • TABLE 8
    (Formulations for Examples 14 to 17)
    Glycerin
    Example # Stepan Mild LSB % (w/w) Viscosity (cP)
    Example 14 Without sodium 0.5 65,000
    lauryl sulfoacetate
    and disodium laureth
    sulfosuccinate
    Example 15 Without sodium 2.0 39,000
    lauryl sulfoacetate
    and disodium laureth
    sulfosuccinate
    Example 16 With sodium lauryl 0.5 72,000
    sulfoacetate and
    disodium laureth
    sulfosuccinate
    Example 17 With sodium lauryl 2.0 49,400
    sulfoacetate and
    disodium laureth
    sulfosuccinate
  • Formulations having sodium lauryl sulfoacetate and disodium laureth sulfosuccinate had a higher viscosity than formulations without them. Formulations having a higher concentration of glycerin had a lower viscosity than the formulations containing a lower concentration of glycerin.
  • Examples 18 to 21
  • The 3% and 6% formulations having adjusted HPMC and Carbopol levels were made. The formulations had two different levels of glycerin (0.5% and 0.1%). The formulations are set forth in Table 9.
  • TABLE 9
    (Formulation Compositions of Examples 18 to 21)
    3% BPO 3% BPO 6% BPO 6% BPO
    Cleanser Cleanser Cleanser Cleanser
    Phase Ingredient Example 18 Example 19 Example 20 Example 21
    A Purified Water, USP 42.56 42.86 38.06 38.11
    Sodium Hyaluronate 0.01 0.01 0.01 0.01
    B Carbomer 1342, NF 0.80 0.90 0.70 0.90
    C Hydroxypropyl 0.50 0.45 0.30 0.45
    Methylcellulose (HPMC)
    D Allantoin 0.10 0.10 0.10 0.10
    Glycerin, USP 0.50 0.10 0.50 0.10
    E Sodium Methyl Cocoyl 7.00 7.00 7.00 7.00
    Taurate
    Sodium Cocoyl Isethionate 11.25 11.25 11.25 11.25
    Cetyl Alcohol, NF 1.00 1.50 1.00 1.00
    F sodium lauryl 4.00 4.00 4.00 4.00
    sulfoacetate and disodium
    laureth sulfosuccinate
    G Purified Water, USP 20.00 20.00 20.00 20.00
    Docusate Sodium, USP 0.05 0.05 0.05 0.05
    Simethicone Emulsion, USP 0.01 0.01 0.01 0.01
    H Benzoyl Peroxide, USP 4.72 4.72 9.44 9.44
    (75%)*
    I Sodium PCA 0.10 0.10 0.10 0.10
    J Purified Water, USP 5.00 5.00 5.00 5.00
    Glycolic Acid, 70% 0.72 0.72 0.72 0.72
    Zinc Lactate 0.20 0.20 0.20 0.20
    K Sodium Hydroxide, USP q.s. q.s. q.s. q.s.
    (25%) pH 5.0-5.5 pH 5.0-5.5 pH 5.0-5.5 pH 5.0-5.5
    L Purified Water, USP qs. 100% qs. 100% qs. 100% qs. 100%
    Total 100.00 100.00 100.00 100.00
    *All formulations contained 18% overage of benzoyl peroxide.
  • The formulations were prepared according to the following:
    • 1. In main vessel, mix and heat Phase A to 70° C.
    • 2. Continue mixing Phase A until all sodium hyaluronate is completely hydrated.
    • 3. At 70° C., add Phase B into Phase A and mix until all carbomer is hydrated.
    • 4. Add Phase C and mix until all hydroxypropyl methylcellulose is dispersed and hydrated.
    • 5. Maintain 70° C. and add Phase D. Mix until dissolved and uniform.
    • 6. Maintain 70° C. and add Phase E. Mix until completely melted and uniform.
    • 7. Homogenize batch gently being careful not to aerate batch.
    • 8. Add Phase F to batch and mix until uniform.
    • 9. In an appropriately sized vessel, mix and heat Phase G to 55° C. Continue mixing until all Docusate Sodium is dissolved.
    • 10. Cool Phase C to 50° C. and add Phase H.
    • 11. Homogenize combined Phase GH with fine screen for 5 minutes.
    • 12. Cool main batch to 55-60° C. and add Phase GH and mix until uniform using propeller and sweep mixing.
    • 13. **If batch size will allow, homogenize entire batch at this point to make batch uniform.
      • Air must not be incorporated into the batch.
    • 14. Add Phase I and mix until uniform.
    • 15. Premix and warm (30° C.) Phase J until clear. Add to batch and mix until uniform.
    • 16. Adjust pH of batch to 5.0-5.5 with Phase K.
    • 17. qs batch to 100% with purified water (Phase L).
    • 18. Mix and cool batch to 20-25° C.
  • In addition to the modification of the formulations, the methods of making were slightly modified for the formulations of Example 18 and Example 20. Phase GH was added after the batch was cooled to 35-40° C. The temperature was kept in this range with to enhance the chemical stability of benzoyl peroxide in the formulations. At this temperature the batch was thick, so the temperature was changed to 55-60° C. for the formulations of Example 19 and Example 21.
  • Example 22
  • A 9% formulation was made. The formulation is set forth in Table 10.
  • TABLE 10
    (Formulation Composition of Example 22)
    % (w/w)
    9%
    Ingredient Cleanser
    Sodium Hyaluronate 0.01
    Carbomer 1342, NF 0.90
    Hydroxypropyl 0.45
    Methylcellulose
    Glycerin, USP 0.10
    Sodium Methyl Cocoyl 7.00
    Taurate
    Sodium Cocoyl Isethionate 11.25
    Cetyl Alcohol, NF 1.00
    sodium lauryl sulfoacetate 4.00
    and disodium laureth
    sulfosuccinate
    Docusate Sodium 0.05
    Simethicone Emulsion, USP 0.01
    Benzoyl Peroxide, USP 14.16
    (75%)*
    Sodium PCA 0.10
    Glycolic Acid, 70% 0.72
    Zinc Lactate 0.20
    Sodium Hydroxide, USP q.s.
    (25%) pH 5.0-5.5
    Purified Water, USP q.s. 100%
    Total 100.00
    *The formulation has an 18% overage of benzoyl peroxide.
  • Example 23
  • Impregnated porous articles can be prepared using the formulations of the foregoing examples. For instance, impregnated cloth articles can be prepared by exposing a non-woven fabric or cloth to an amount that is suitable to contact the acne-affected area of the skin.
  • Consumer Use Study (Example 24) and Comparative Examples A and B
  • A cloth article useful in the method of the present invention and two commercial anti-acne compositions (A and B) were compared in a consumer/user study for efficacy and desirable product features.
  • A consumer research guidance test was conducted to evaluate the attributes of a facial cleansing cloth (BPO Foaming Cloth) useful in the method of the present invention. The study was conducted at two separate testing facilities. The following Table 11 is a summary of the number of subjects in each age group and gender that completed the study.
  • TABLE 11
    Combined
    Facilities Location # 1 Location # 2
    (n = 193) (n = 118) (n = 75)
    Age 17 to 22 years old 141 86 55
    Groups 23 to 30 years old 52 32 20
    Male Subjects 69 52 17
    Gender Female Subjects 124 66 58
  • There was no attrition from this study at either test location. Subjects 001 through 042 participated in a pilot study at Location #1.
  • All subjects were assigned to wash their face with the BPO Foaming Cloth with or without rinsing. Subjects were also assigned to use one of the following commercial facial cleansers (comparative compositions not of the present invention) as determined by a randomization design:
      • BPO Cleanser (Benzoyl Peroxide 6%)
      • BPO Wash (Benzoyl Peroxide 4%)
  • The order of test material usage was also determined by the randomization design. All subjects were blinded to all three test materials.
  • Test Material Descriptions
    (A) Test material 0357-06CC/0125-07C
    identification number (TMIN):
    (B) Test material BPO Foaming Cloth (Benzoyl
    identification: Peroxide 6%)
    (C) Physical description: White, opaque, medication-coated
    cloth applicator
    (D) Test material 0358-06CC/0162-07C
    identification number (TMIN):
    (E) Test material BPO Cleanser (Benzoyl Peroxide
    identification: 6%)
    (F) Physical description: White, opaque cream
    (G) Test material 0359-06CC/0163-07C
    identification number (TMIN):
    (H) Test material BPO Wash (Benzoyl Peroxide 4%)
    identification:
    (I) Physical description: White, opaque cream
  • The BPO Cleanser (benzoyl peroxide 6%) used as a comparison composition in the consumer research guidance test had the following ingredients: benzoyl peroxide, glycerin USP, petrolatum USP, C12-15 alkyl benzoate, sodium cocoyl isethionate, special petrolatum fraction, sodium C14-16 olefin sulfonate, zinc lactate, carbomer, potassium metaphosphate NF, titanium dioxide USP, trolamine NF, glycolic acid, lavender extract, and menthol USP.
  • The BPO Wash (benzoyl peroxide 4%) used as a comparison composition in the consumer research guidance test had the following ingredients: benzoyl peroxide, alpha olefin sulfonate, cetosteryl alcohol NF, glycerin USP, glyceryl monostearate SE, methylparaben NF, phosphoric acid NF, propylene glycol USP, sodium PCA, and white soft paraffin USP.
  • The formulation for the impregnant composition in the BPO Foaming Cloth (Benzoyl Peroxide 6%) used in the consumer research guidance test is set forth below in Table 12.
  • TABLE 12
    (Formulation for BPO Foaming Cloth)
    Phase CTFA Name Percent
    A DEIONIZED WATER 37.21
    SODIUM HYALURONATE 0.01
    B ACRYLATES/C10-30 ALKYL 0.90
    ACRYLATE CROSSPOLYMER
    C HYDROXYPROPYL 0.45
    METHYLCELLULOSE
    D ALLANTOIN 0.10
    GLYCERIN 0.1
    E SODIUM METHYL COCOYL 7.00
    TAURATE
    SODIUM COCOYL ISOTHIANOATE 11.25
    CETYL ALCOHOL 1.0
    F SODIUM LAURYL SULFOACETATE 4.00
    AND DISODIUM LAURETH
    SULFOSUCCINATE
    G DEIONIZED WATER 20.00
    DOCUSATE SODIUM 0.05
    SIMETHICONE 0.01
    H BENZOYL PEROXIDE 9.44
    I SODIUM PCA 0.10
    J DEIONIZED WATER 5.00
    GLYCOLIC ACID 0.72
    ZINC LACTATE 0.20
    K SODIUM HYDROXIDE 25% 1.56
    100.00
  • Subjects were provided with the following usage instructions for each cleanser:
  • BPO Foaming Cloth:
      • Wet the provided facial cleanser cloth with a light stream of tap water.
      • Lather and gently wash face with cloth. Do not scrub.
      • Rinse thoroughly and pat dry.
    BPO Cleanser or BPO Wash
      • Lightly wet face and hands with water.
      • Dispense an approximately dime-sized amount onto one hand.
      • Lather in the hands and apply to the face as you would your normal cleanser.
      • Rinse face thoroughly and pat dry.
  • Subjects rested quietly in the clinic for at least five minutes prior to washing with the first assigned cleanser (BPO Foaming cloth). At least five minutes after washing with the first cleanser, subjects used the second assigned cleanser (BPO Cleanser or BPO Wash) as instructed.
  • The first and second washes for subject 054 were separated by two (2) minutes instead of five (5) minutes. This deviation is not expected to have an impact on the outcome of the study.
  • After completion of washing with the BPO Foaming Cloth, subjects completed a Product Attribute Questionnaire regarding product use. After completion of the final wash, subjects completed a Comparative Questionnaire comparing the BPO Foaming Cloth to the other cleanser (BPO Cleanser or BPO Wash) they were assigned to use.
  • Questionnaires were tabulated and a top 2 box analysis was performed. Questionnaire analyses were conducted separately for each testing facility, age group, and gender combination. All differences were considered significant at the p≦0.05 level. The tables below present the results of the questionnaire tabulations for both testing facilities combined.
  • In the Product Attribute Questionnaire, subjects rated their agreement with statements regarding the test material using the following scale:
      • 1=Strongly Agree
      • 2
      • 3=Somewhat Agree
      • 4
      • 5=Strongly Disagree
  • Table 13 presents the results of the top 2 box (positive responses: score of 1 or 2)/bottom 2 box (negative responses: score of 4 or 5) analysis of the questionnaires regarding product attributes. The number of subjects with the specific response is listed, followed by the percentage of the total subject population in parentheses. An asterisk (*) indicates that the proportion of subjects responding positively for a given statement is statistically greater than the proportion of subjects responding negatively.
  • TABLE 13
    (Results of Top 2 Box Analysis for the Product Attribute
    Questionnaire: BPO Foaming Cloth)
    All Subjects Male Subjects Female Subjects
    Bottom 2 Bottom 2 Bottom 2
    Top 2 box Box Top 2 box Box Top 2 box Box
    1. Convenient All (17-30 yrs) *164 14 (7.2%)  *55  9 (13.0%) *109 5 (4.0%)
    to use (84.9%) (79.7%) (87.9%)
    17-22 yrs *122 11 (7.8%)  *50  8 (12.9%) *72 3 (3.7%)
    old (86.5%) (80.6%) (91.1%)
    23-30 yrs *42 3 (5.7%) 5  1 (14.2%) *37 2 (4.4%)
    old (80.7%) (71.4%) (82.2%)
    2. Easy to All (17-30 yrs) *166 16 (8.2%)  *53  8 (11.5%) *113 8 (6.4%)
    use (86.0%) (76.8%) (91.1%)
    17-22 yrs *123 9 (6.3%) *49 6 (9.6%) *74 3 (3.7%)
    old (87.2%) (79.0%) (93.6%)
    23-30 yrs *43  7 (13.4%) 4  2 (28.5%) *39  5 (11.1%)
    old (82.6%) (57.1%) (86.6%)
    3. Portable All (17-30 yrs) *178 7 (3.6%) *58 5 (7.2%) *120 2 (1.6%)
    (92.2%) (84.0%) (96.7%)
    17-22 yrs *128 5 (3.5%) *52 4 (6.4%) *76 1 (1.2%)
    old (90.7%) (83.8%) (96.2%)
    23-30 yrs *50 2 (3.8%) 6  1 (14.2%) *44 1 (2.2%)
    old (96.1%) (85.7%) (97.7%)
    4. Easy to All (17-30 yrs) *155 13 (6.7%)  *52  7 (10.1%) *103 6 (4.8%)
    use in the (80.3%) (75.3%) (83.0%)
    shower 17-22 yrs *115 8 (5.6%) *47 5 (8.0%) *68 3 (3.7%)
    old (81.5%) (75.8%) (86.0%)
    23-30 yrs *40 5 (9.6%) 5  2 (28.5%) *35 3 (6.6%)
    old (76.9%) (71.4%) (77.7%)
    5. Easy to All (17-30 yrs) *168 11 (5.6%)  *53  7 (10.1%) *115 4 (3.2%)
    use at the (87.0%) (76.8%) (92.7%)
    sink 17-22 yrs *123 8 (5.6%) *48 6 (9.6%) *75 2 (2.5%)
    old (87.2%) (77.4%) (94.9%)
    23-30 yrs *45 3 (5.7%) 5  1 (14.2%) *40 2 (4.4%)
    old (86.5%) (71.4%) (88.8%)
    6. Amount of All (17-30 yrs) *157 10 (5.1%)  *46  8 (11.5%) *111 2 (1.6%)
    lather/foam (81.3%) (66.6%) (89.5%)
    was appealing 17-22 yrs *114 8 (5.6%) *41  7 (11.2%) *73 1 (1.2%)
    old (80.8%) (66.1%) (92.4%)
    23-30 yrs *43 2 (3.8%) 5  1 (14.2%) *38 1 (2.2%)
    old (82.6%) (71.4%) (84.4%)
    7. Provided All (17-30 yrs) *163 11 (5.6%)  *51  7 (10.1%) *112 4 (3.2%)
    adequate (84.4%) (73.9%) (90.3%)
    amount of 17-22 yrs *118 8 (5.6%) *47 6 (9.6%) *71 2 (2.5%)
    lather/foam old (83.6%) (75.8%) (89.8%)
    23-30 yrs *45 3 (5.7%) 4  1 (14.2%) *41 2 (4.4%)
    old (86.5%) (57.1%) (91.1%)
    8. Provided All (17-30 yrs) *179 6 (3.1%) *58 4 (5.7%) *121 2 (1.6%)
    enough lather (92.7%) (84.0%) (97.5%)
    to cover face 17-22 yrs *129 5 (3.5%) *52 4 (6.4%) *77 1 (1.2%)
    old (91.4%) (83.8%) (97.4%)
    23-30 yrs *50 1 (1.9%) *6 0 (0.0%) *44 1 (2.2%)
    old (96.1%) (85.7%) (97.7%)
    9. Provided All (17-30 yrs) *123 18 (9.3%)  *37 10 (14.4%) *86 8 (6.4%)
    enough lather (63.7%) (53.6%) (69.3%)
    to cover 17-22 yrs *87 15 (10.6%) *33 10 (16.1%) *54 5 (6.3%)
    chest old (61.7%) (53.2%) (68.3%)
    23-30 yrs *36 3 (5.7%) 4 0 (0.0%) *32 3 (6.6%)
    old (69.2%) (57.1%) (71.1%)
    10. Provided All (17-30 yrs) *90 37 (19.1%) 26 16 (23.1%) *64 21 (16.9%)
    enough lather (46.6%) (37.6%) (51.6%)
    to cover back 17-22 yrs *60 26 (18.4%) 23 14 (22.5%) *37 12 (15.1%)
    old (42.5%) (37.0%) (46.8%)
    23-30 yrs *30 11 (21.1%) 3  2 (28.5%) *27  9 (20.0%)
    old (57.6%) (42.8%) (60.0%)
    11. Provided All (17-30 yrs) 50 69 (35.7%) 16 26 (37.6%) 34 43 (34.6%)
    adequate (25.9%) (23.1%) (27.4%)
    amount of 17-22 yrs *33 56 (39.7%) 14 24 (38.7%) 19 32 (40.5%)
    lather to old (23.4%) (22.5%) (24.0%)
    cover face, 23-30 yrs 17 13 (25.0%) 2  2 (28.5%) 15 11 (24.4%)
    chest, & back old (32.6%) (28.5%) (33.3%)
    12. Easily All (17-30 yrs) *165 10 (5.1%)  *55  7 (10.1%) *110 3 (2.4%)
    washed off (85.4%) (79.7%) (88.7%)
    17-22 yrs *122 8 (5.6%) *50 6 (9.6%) *72 2 (2.5%)
    old (86.5%) (80.6%) (91.1%)
    23-30 yrs *43 2 (3.8%) 5  1 (14.2%) *38 1 (2.2%)
    old (82.6%) (71.4%) (84.4%)
    13. Left skin All (17-30 yrs) *159 13 (6.7%)  *55 6 (8.6%) *104 7 (5.6%)
    feeling (82.3%) (79.7%) (83.8%)
    smooth 17-22 yrs *117 10 (7.0%)  *49 6 (9.6%) *68 4 (5.0%)
    old (82.9%) (79.0%) (86.0%)
    23-30 yrs *42 3 (5.7%) *6 0 (0.0%) *36 3 (6.6%)
    old (80.7%) (85.7%) (80.0%)
    14. Cosmetically All (17-30 yrs) *129 17 (8.8%)  *38 6 (8.6%) *91 11 (8.8%) 
    elegant (66.8%) (55.0%) (73.3%)
    17-22 yrs *92 13 (9.2%)  *34 5 (8.0%) *58  8 (10.1%)
    old (65.2%) (54.8%) (73.4%)
    23-30 yrs *37 4 (7.6%) 4  1 (14.2%) *33 3 (6.6%)
    old (71.1%) (57.1%) (73.3%)
    15. Left my All (17-30 yrs) *175 9 (4.6%) *60 6 (8.6%) *115 3 (2.4%)
    face feeling (90.6%) (86.9%) (92.7%)
    clean 17-22 yrs *129 7 (4.9%) *55 5 (8.0%) *74 2 (2.5%)
    old (91.4%) (88.7%) (93.6%)
    23-30 yrs *46 2 (3.8%) 5  1 (14.2%) *41 1 (2.2%)
    old (88.4%) (71.4%) (91.1%)
    16. Cleansed All (17-30 yrs) *168 6 (3.1%) *58 4 (5.7%) *110 2 (1.6%)
    my face very (87.0%) (84.0%) (88.7%)
    well 17-22 yrs *123 5 (3.5%) *53 4 (6.4%) *70 1 (1.2%)
    old (87.2%) (85.4%) (88.6%)
    23-30 yrs *45 1 (1.9%) 5 0 (0.0%) *40 1 (2.2%)
    old (86.5%) (71.4%) (88.8%)
    In the At Sink or
    At the Sink Shower in Shower
    17. When would All All (17-30 yrs) 64 (33.1%) 29 (15.0%) 100 (51.8%) 
    you use the Subjects 17-22 yrs 44 (31.2%) 22 (15.6%) 75 (53.1%)
    Cleansing Cloth old
    23-30 yrs 20 (38.4%)  7 (13.4%) 25 (48.0%)
    old
    Male All (17-30 yrs) 25 (36.2%) 14 (20.2%) 30 (43.4%)
    Subjects 17-22 yrs 22 (35.4%) 13 (20.9%) 27 (43.5%)
    old
    23-30 yrs  3 (42.8%)  1 (14.2%) 3 (42.8%)
    old
    Female All (17-30 yrs) 39 (31.4%) 15 (12.0%) 70 (56.4%)
    Subjects 17-22 yrs 22 (27.8%)  9 (11.3%) 48 (60.7%)
    old
    23-30 yrs 17 (37.7%)  6 (13.3%) 22 (48.8%)
    old
  • After completion of the final wash, subjects completed a comparative questionnaire regarding the BPO Foaming Cloth and the other cleanser (BPO Cleanser or BPO Wash) which they were assigned to use. Subjects selected which product they preferred for each attribute.
  • Table 14 presents the results of the top 2 box/bottom 2 box analysis of the questionnaires regarding product preference. The number of subjects with the specific response is listed, followed by the percentage of the total subject population in parentheses. An asterisk (*) indicates that the proportion of subjects who selected BPO Foaming Cloth for a given statement is statistically greater than the proportion of subjects who selected the other assigned cleanser (BPO Cleanser or BPO Wash).
  • TABLE 14
    (Results of Top 2 Box Analysis for
    the Comparison Questionnaires)
    BPO Foaming Cloths BPO Foaming Cloths
    vs. BPO Cleanser vs. BPO Wash (Benzoyl
    (Benzoyl Peroxide 6%) Peroxide 4%)
    CLOTH PADS CLEANSER CLOTH PADS CREAMY WASH
    1. More All All (17-30 yrs) *78 19 *77 19
    convenient to Subjects (80.4%) (19.5%) (80.2%) (19.7%)
    use 17-22 yrs *58 13 *57 13
    old (81.6%) (18.3%) (81.4%) (18.5%)
    23-30 yrs *20 6 *20 6
    old (76.9%) (23.0%) (76.9%) (23.0%)
    Male All (17-30 yrs) *27 9 *24 9
    Subjects (75.0%) (25.0%) (72.7%) (27.2%)
    17-22 yrs *25 8 *22 7
    old (75.7%) (24.2%) (75.8%) (24.1%)
    23-30 yrs 2 1 2 2
    old (66.6%) (33.3%) (50.0%) (50.0%)
    Female All (17-30 yrs) *51 10 *53 10
    Subjects (83.6%) (16.3%) (84.1%) (15.8%)
    17-22 yrs *33 5 *35 6
    old (86.8%) (13.1%) (85.3%) (14.6%)
    23-30 yrs *18 5 *18 4
    old (78.2%) (21.7%) (81.8%) (18.1%)
    2. Easier to All All (17-30 yrs) *71 26 *69 27
    use Subjects (73.1%) (26.8%) (71.8%) (28.1%)
    17-22 yrs *52 19 *52 18
    old (73.2%) (26.7%) (74.2%) (25.7%)
    23-30 yrs *19 7 17 9
    old (73.0%) (26.9%) (65.3%) (34.6%)
    Male All (17-30 yrs) 24 12 22 11
    Subjects (66.6%) (33.3%) (66.6%) (33.3%)
    17-22 yrs 22 11 20 9
    old (66.6%) (33.3%) (68.9%) (31.0%)
    23-30 yrs 2 1 2 2
    old (66.6%) (33.3%) (50.0%) (50.0%)
    Female All (17-30 yrs) *47 14 *47 16
    Subjects (77.0%) (22.9%) (74.6%) (25.3%)
    17-22 yrs *30 8 *32 9
    old (78.9%) (21.0%) (78.0%) (21.9%)
    23-30 yrs *17 6 15 7
    old (73.9%) (26.0%) (68.1%) (31.8%)
    . More All All (17-30 yrs) *95 2 *91 5
    portable Subjects (97.9%) (2.0%) (94.7%) (5.2%)
    17-22 yrs *69 2 *67 3
    old (97.1%) (2.8%) (95.7%) (4.2%)
    23-30 yrs *26 0 *24 2
    old (100.0%) (0.0%) (92.3%) (7.6%)
    Male All (17-30 yrs) *36 0 *30 3
    Subjects (100.0%) (0.0%) (90.9%) (9.0%)
    17-22 yrs *33 0 *28 1
    old (100.0%) (0.0%) (96.5%) (3.4%)
    23-30 yrs 3 0 2 2
    old (100.0%) (0.0%) (50.0%) (50.0%)
    Female All (17-30 yrs) *59 2 *61 2
    Subjects (96.7%) (3.2%) (96.8%) (3.1%)
    17-22 yrs *36 2 *39 2
    old (94.7%) (5.2%) (95.1%) (4.8%)
    23-30 yrs *23 0 *22 0
    old (100.0%) (0.0%) (100.0%) (0.0%)
    4. Lather/foam All All (17-30 yrs) *81 16 *77 19
    was more Subjects (83.5%) (16.4%) (80.2%) (19.7%)
    appealing 17-22 yrs *59 12 *56 14
    old (83.0%) (16.9%) (80.0%) (20.0%)
    23-30 yrs *22 4 *21 5
    old (84.6%) (15.3%) (80.7%) (19.2%)
    Male All (17-30 yrs) *30 6 *25 8
    Subjects (83.3%) (16.6%) (75.7%) (24.2%)
    17-22 yrs *28 5 *23 6
    old (84.8%) (15.1%) (79.3%) (20.6%)
    23-30 yrs 2 1 2 2
    old (66.6%) (33.3%) (50.0%) (50.0%)
    Female All (17-30 yrs) *51 10 *52 11
    Subjects (83.6%) (16.3%) (82.5%) (17.4%)
    17-22 yrs *31 7 *33 8
    old (81.5%) (18.4%) (80.4%) (19.5%)
    23-30 yrs *20 3 *19 3
    old (86.9%) (13.0%) (86.3%) (13.6%)
    5. Provides a All All (17-30 yrs) *85 12 *72 24
    more adequate Subjects (87.6%) (12.3%) (75.0%) (25.0%)
    amount of 17-22 yrs *62 9 *53 17
    lather foam old (87.3%) (12.6%) (75.7%) (24.2%)
    23-30 yrs *23 3 *19 7
    old (88.4%) (11.5%) (73.0%) (26.9%)
    Male All (17-30 yrs) *30 6 19 14
    Subjects (83.3%) (16.6%) (57.5%) (42.4%)
    17-22 yrs *28 5 18 11
    old (84.8%) (15.1%) (62.0%) (37.9%)
    23-30 yrs 2 1 1 3
    old (66.6%) (33.3%) (25.0%) (75.0%)
    Female All (17-30 yrs) *55 6 *53 10
    Subjects (90.1%) (9.8%) (84.1%) (15.8%)
    17-22 yrs *34 4 *35 6
    old (89.4%) (10.5%) (85.3%) (14.6%)
    23-30 yrs *21 2 *18 4
    old (91.3%) (8.6%) (81.8%) (18.1%)
    6. Produced All All (17-30 yrs) *84 13 *71 25
    more lather to Subjects (86.5%) (13.4%) (73.9%) (26.0%)
    cover face 17-22 yrs *62 9 *50 20
    old (87.3%) (12.6%) (71.4%) (28.5%)
    23-30 yrs *22 4 *21 5
    old (84.6%) (15.3%) (80.7%) (19.2%)
    Male All (17-30 yrs) *31 5 20 13
    Subjects (86.1%) (13.8%) (60.6%) (39.3%)
    17-22 yrs *28 5 17 12
    old (84.8%) (15.1%) (58.6%) (41.3%)
    23-30 yrs 3 0 3 1
    old (100.0%) (0.0%) (75.0%) (25.0%)
    Female All (17-30 yrs) *53 8 *51 12
    Subjects (86.8%) (13.1%) (80.9%) (19.0%)
    17-22 yrs *34 4 *33 8
    old (89.4%) (10.5%) (80.4%) (19.5%)
    23-30 yrs *19 4 *18 4
    old (82.6%) (17.3%) (81.8%) (18.1%)
    . Produced All All (17-30 yrs) *79 18 *61 35
    more lather to Subjects (81.4%) (18.5%) (63.5%) (36.4%)
    cover chest 17-22 yrs *57 14 41 29
    old (80.2%) (19.7%) (58.5%) (41.4%)
    23-30 yrs *22 4 *20 6
    old (84.6%) (15.3%) (76.9%) (23.0%)
    Male All (17-30 yrs) *28 8 16 17
    Subjects (77.7%) (22.2%) (48.4%) (51.5%)
    17-22 yrs *25 8 14 15
    old (75.7%) (24.2%) (48.2%) (51.7%)
    23-30 yrs 3 0 2 2
    old (100.0%) (0.0%) (50.0%) (50.0%)
    Female All (17-30 yrs) *51 10 *45 18
    Subjects (83.6%) (16.3%) (71.4%) (28.5%)
    17-22 yrs *32 6 27 14
    old (84.2%) (15.7%) (65.8%) (34.1%)
    23-30 yrs *19 4 *18 4
    old (82.6%) (17.3%) (81.8%) (18.1%)
    8. Produced All All (17-30 yrs) *79 18 *60 36
    more lather to Subjects (81.4%) (18.5%) (62.5%) (37.5%)
    cover back 17-22 yrs *58 13 40 30
    old (81.6%) (18.3%) (57.1%) (42.8%)
    23-30 yrs *21 5 *20 6
    old (80.7%) (19.2%) (76.9%) (23.0%)
    Male All (17-30 yrs) *29 7 16 17
    Subjects (80.5%) (19.4%) (48.4%) (51.5%)
    17-22 yrs *26 7 14 15
    old (78.7%) (21.2%) (48.2%) (51.7%)
    23-30 yrs 3 0 2 2
    old (100.0%) (0.0%) (50.0%) (50.0%)
    Female All (17-30 yrs) *50 11 *44 19
    Subjects (81.9%) (18.0%) (69.8%) (30.1%)
    17-22 yrs *32 6 26 15
    old (84.2%) (15.7%) (63.4%) (36.5%)
    23-30 yrs *18 5 *18 4
    old (78.2%) (21.7%) (81.8%) (18.1%)
    9. Produced All All (17-30 yrs) *78 19 57 39
    more lather to Subjects (80.4%) (19.5%) (59.3%) (40.6%)
    cover face, 17-22 yrs *56 15 38 32
    chest, back old (78.8%) (21.1%) (54.2%) (45.7%)
    and trunk 23-30 yrs *22 4 *19 7
    old (84.6%) (15.3%) (73.0%) (26.9%)
    Male All (17-30 yrs) *27 9 17 16
    Subjects (75.0%) (25.0%) (51.5%) (48.4%)
    17-22 yrs *24 9 15 14
    old (72.7%) (27.2%) (51.7%) (48.2%)
    23-30 yrs 3 0 2 2
    old (100.0%) (0.0%) (50.0%) (50.0%)
    Female All (17-30 yrs) *51 10 *40 23
    Subjects (83.6%) (16.3%) (63.4%) (36.5%)
    17-22 yrs *32 6 23 18
    old (84.2%) (15.7%) (56.0%) (43.9%)
    23-30 yrs *19 4 *17 5
    old (82.6%) (17.3%) (77.2%) (22.7%)
    10. More All All (17-30 yrs) *73 24 *74 22
    Cosmetically Subjects (75.2%) (24.7%) (77.0%) (22.9%)
    Elegant 17-22 yrs *54 17 *55 15
    old (76.0%) (23.9%) (78.5%) (21.4%)
    23-30 yrs *19 7 *19 7
    old (73.0%) (26.9%) (73.0%) (26.9%)
    Male All (17-30 yrs) *25 11 *27 6
    Subjects (69.4%) (30.5%) (81.8%) (18.1%)
    17-22 yrs *23 10 *25 4
    old (69.6%) (30.3%) (86.2%) (13.7%)
    23-30 yrs 2 1 2 2
    old (66.6%) (33.3%) (50.0%) (50.0%)
    Female All (17-30 yrs) *48 13 *47 16
    Subjects (78.6%) (21.3%) (74.6%) (25.3%)
    17-22 yrs *31 7 *30 11
    old (81.5%) (18.4%) (73.1%) (26.8%)
    23-30 yrs *17 6 *17 5
    old (73.9%) (26.0%) (77.2%) (22.7%)
    11. Which All All (17-30 yrs) *75 22 *75 21
    product do you Subjects (77.3%) (22.6%) (78.1%) (21.8%)
    prefer 17-22 yrs *56 15 *56 14
    old (78.8%) (21.1%) (80.0%) (20.0%)
    23-30 yrs *19 7 *19 7
    old (73.0%) (26.9%) (73.0%) (26.9%)
    Male All (17-30 yrs) *28 8 22 11
    Subjects (77.7%) (22.2%) (66.6%) (33.3%)
    17-22 yrs *26 7 20 9
    old (78.7%) (21.2%) (68.9%) (31.0%)
    23-30 yrs 2 1 2 2
    old (66.6%) (33.3%) (50.0%) (50.0%)
    Female All (17-30 yrs) *47 14 *53 10
    Subjects (77.0%) (22.9%) (84.1%) (15.8%)
    17-22 yrs *30 8 *36 5
    old (78.9%) (21.0%) (87.8%) (12.1%)
    23-30 yrs *17 6 *17 5
    old (73.9%) (26.0%) (77.2%) (22.7%)
  • The following Table 15 summarizes the results of the top 2 box/bottom 2 box analysis for the Product Attribute Questionnaire. An asterisk (*) indicates that a statistically significant proportion of subjects responded positively (Strongly Agree/Agree—score of 1 or 2) than negatively (Disagree/Strongly Disagree—score of 4 or 5).
  • TABLE 15
    (Summary of Results for the Product Attribute Questionnaire -
    The Monadic Ratings of the BPO Foaming Cloth)
    All Subjects Male Subjects Female Subjects
    All 17-22 yrs 23-30 yrs All 17-22 yrs 23-30 yrs All 17-22 yrs 23-30 yrs
    (17-30 yrs) old old (17-30 yrs) old old (17-30 yrs) old old
    1. Convenient to use * * * * * * * *
    2. Easy to use * * * * * * * *
    3. Portable * * * * * * * *
    4. Easy to use in the shower * * * * * * * *
    5. Easy to use at the sink * * * * * * * *
    6. Amount of lather was appealing * * * * * * * *
    7. Provided adequate amount * * * * * * * *
    of foam
    8. Provided enough lather to * * * * * * * * *
    cover face
    9. Provided enough lather to * * * * * * * *
    cover chest
    10. Provided enough lather to * * * * * *
    cover back
    11. Provided lather to cover *
    face/chest/back
    12. Easily washed off * * * * * * * *
    13. Left skin feeling smooth * * * * * * * *
    14. Cosmetically elegant * * * * * * * *
    15. Left my face feeling clean * * * * * * * *
    16. Cleansed my face very well * * * * * * * *
  • The following Tables 16 and 17 summarize the results of the top 2 box/bottom 2 box analysis for the Comparative Questionnaire. An asterisk (*) indicates that a statistically significant proportion of subjects selected BPO Foaming Cloth for a given statement than the other assigned cleanser (BPO Cleanser or BPO Wash).
  • TABLE 16
    (Summary of Results for the Comparative Questionnaire for
    the BPO Foaming Cloth vs. the BPO Cleanser)
    BPO Foaming Cloth vs.
    BPO Cleanser (Benzoyl Peroxide 6%)
    All Subjects Male Subjects Female Subjects
    All 17-22 yrs 23-30 yrs All 17-22 yrs 23-30 yrs All 17-22 yrs 23-30 yrs
    (17-30 yrs) old old (17-30 yrs) old old (17-30 yrs) old old
    1. More convenient to use * * * * * * * *
    2. Easier to use * * * * * *
    3. More portable * * * * * * * *
    4. Lather/foam was more appealing * * * * * * * *
    5. Provides more adequate * * * * * * * *
    amount of lather
    6. Produced more lather to cover * * * * * * * *
    face
    7. Produced more lather to * * * * * * * *
    cover chest
    8. Produced more lather to * * * * * * * *
    cover back
    9. Produced more lather to * * * * * * * *
    cover face/chest/back/trunk
    10. More Cosmetically Elegant * * * * * * * *
    11. Which product do you prefer * * * * * * * *
  • TABLE 17
    (Summary of Results for the Comparative Questionnaire for the
    BPO Foaming Cloth vs. the BPO Wash)
    BPO Foaming Cloth vs.
    BPO Wash (Benzoyl Peroxide 4%)
    All Subjects Male Subjects Female Subjects
    All 17-22 yrs 23-30 yrs All 17-22 yrs 23-30 yrs All 17-22 yrs 23-30 yrs
    (17-30 yrs) old old (17-30 yrs) old old (17-30 yrs) old old
    1. More convenient to use * * * * * * * *
    2. Easier to use * * * *
    3. More portable * * * * * * * *
    4. Lather/foam was more appealing * * * * * * * *
    5. Provides more adequate * * * * * *
    amount of lather
    6. Produced more lather to * * * * * *
    cover face
    7. Produced more lather to * * * *
    cover chest
    8. Produced more lather to * * * *
    cover back
    9. Produced more lather to * * *
    cover face/chest/back/trunk
    10. More Cosmetically Elegant * * * * * * * *
    11. Which product do you prefer * * * * * *
  • Overall, the results from the Product Attribute Questionnaire (only used for BPO Foaming Cloth) were very positive with statistically significant top wins for all questions. Moreover, the results from the Comparative Questionnaires showed significant wins for the BPO Foaming Cloth compared to BPO Cleanser and BPO Wash for questions 1-4 (related to convenience of use and aesthetic properties), and questions 5-9 (related to product coverage). Questions 10 and 11 showed significant wins for BPO Foaming Cloth Pads (Question 10: “More Cosmetically Elegant” and Question 11: “Product Preference”).
  • The BPO Foaming Cloth may provide a higher degree of lathering compared to the BPO Cleanser and the BPO Wash. Further, the BPO Foaming Cloth may impart a higher degree of cosmetically elegant feel to the skin compared to the BPO Cleanser and the BPO Wash. Further, the BPO Foaming Cloth may leave a higher degree of a residual benzoyl peroxide on the skin compared to the BPO Cleanser and the BPO Wash after wash-off.
  • Foaming Tendency
  • The foaming tendency of the BPO Foaming Cloth was also tested and compared to that of the BPO Cleanser and the BPO Wash.
  • The test method employed was ASTM D-3519-88. The test method was used to measure foaming tendency in aqueous media under high shear conditions (blender test). The testing was performed with deionized (DI) water and hard water (100 ppm) in triplicate. The test samples were prepared by cutting two pads of BPO Foaming Cloths into small pieces and adding them to 190 mL of water. The test samples for BPO Cleanser and BPO Wash were prepared by adding 10 mL of the test product into 190 mL of water. The test samples were equilibrated for 1 hour in a 25±1° C. water bath. The foam volume was determined after blending for 30 seconds using a blender with a glass jar agitating between 8000 and 9000 rpm. The residual foam height was also determined after allowing the blender to stand undisturbed for 5 minutes.
  • Data Summary
  • The testing results of maximum foam height and residual foam height after 5 min are summarized in Table 18. When DI water was used as the test medium, the maximum foam height generated by BPO Foaming Cloths was 7.4±0.3 cm. The residual foam height after 5 minutes remained high at 5.6±0.3 cm for BPO Foaming Cloths. Comparing to other cleansing products, the maximum foam height generated by BPO Cloths was 4 and 3 times of that by BPO Cleanser and BPO Wash, respectively. The residual foam height after 5 minutes for BPO Foaming Cloths was 19 and 4 times of that for BPO Cleanser and BPO Wash, respectively.
  • Similar results were obtained when hard water was used as the test medium. The maximum foam height generated by BPO Foaming Cloths was 6.1±0.3 cm. The residual foam height after 5 minutes remained high at 4.5±0.3 cm for BPO Foaming Cloths. Comparing to other cleansing products, the maximum foam height generated by BPO Foaming Cloths was 3 and 2 times of that by BPO Cleanser and BPO Wash, respectively. The residual foam height after 5 minutes for BPO Foaming Cloths was 6 and 3 times of that for BPO Cleanser and BPO Wash, respectively. The results are set forth below in Table 18.
  • TABLE 18
    (Blender Foam Volume Test Results)
    BPO Foaming BPO Cleanser
    Testing Cloths 6% BPO Wash 4%
    Medium Test Parameters Average STDEV Average STDEV Average STDEV
    DI Water Fm (maximum foam height) 7.4 0.3 1.8 0.1 2.8 0.1
    (cm)
    Fr (residual foam after 5.6 0.3 0.3 0.2 1.4 0.3
    5 min) (cm)
    Hard Water Fm (maximum foam height) 6.1 0.3 1.9 0.2 3.1 0.3
    (100 ppm) (cm)
    Fr (residual foam after 4.5 0.3 0.7 0.2 1.6 0.1
    5 min) (cm)
    STDEV—standard deviation
  • It should be understood that the foregoing description is only illustrative of the present invention. Various alternatives and modifications can be devised by those skilled in the art without departing from the invention. Accordingly, the present invention is intended to embrace all such alternatives, modifications and variances which fall within the scope of the appended claims.

Claims (45)

1. An anti-acne composition, comprising:
(a) water;
(b) benzoyl peroxide;
(c) a thickening agent comprising carbomer 1342 or Pemulen TR-1, hydroxypropyl methylcellulose, and cetyl alcohol;
(d) a cleansing agent component comprising sodium methyl cocoyl taurate and sodium cocoyl isethionate in an amount sufficient to render the composition foamable and to maintain a substantially homogeneous dispersion of the benzoyl peroxide in the composition;
(e) glycolic acid; and
(f) and zinc lactate.
2. An anti-acne composition, comprising:
(a) water;
(b) benzoyl peroxide;
(c) a salt of a fatty acid ester having from 12 to 20 carbon atoms; and
(d) a salt of a fatty acid isethionate having from 12 to 20 carbon atoms,
wherein the salt of a fatty acid ester and the salt of a fatty acid isethionate are present in an amount sufficient to render the composition foamable and to maintain a substantially homogeneous dispersion of the benzoyl peroxide in the composition.
3. The composition of claim 2, wherein the salt of a fatty acid ester is sodium methyl cocoyl taurate.
4. The composition of claim 2, wherein the salt of a fatty acid isethionate is sodium cocoyl isethionate.
5. The composition of claim 2, wherein the salt of a fatty acid ester and the salt of a fatty acid isethionate are present at a total of about 8 to about 30 wt % based on the total weight of the composition.
6. The composition of claim 2, further comprising a salt of a fatty acid sulfoacetate having from 12 to 20 carbons and a disalt of a fatty acid sulfosuccinate having from 12 to 20 carbons.
7. The composition of claim 6, wherein the salt of a fatty acid sulfoacetate is sodium lauryl sulfoacetate and the disalt of a fatty acid sulfosuccinate is disodium laureth sulfosuccinate.
8. The composition of claim 6, wherein the salt of a fatty acid sulfoacetate and the disalt of a fatty acid sulfosuccinate are present at a total of about 1 to about 10 wt % based on the total weight of the composition.
9. An anti-acne composition, comprising:
(a) water;
(b) benzoyl peroxide;
(c) a cellulose ether; and
(d) a polyacrylic polymer,
wherein the cellulose ether and the polyacrylic polymer are present in an amount sufficient to impart stability to the composition.
10. The composition of claim 9, further comprising an additional ingredient selected from the group consisting of a fatty alcohol of 10 to 24 carbon atoms, a fatty acid of 10 to 24 carbon atoms, a fatty ester of 10 to 24 carbon atoms, an organic wax, chitosan, carrageenan, colloidal silicon dioxide, hydroxypropyl starch, kaolin, polycarbophil, propylene glycol alginate, sodium alginate, alginic acid, tragacanth, acacia, and trehalose, and any combination of the foregoing, wherein the cellulose ether, the polyacrylic polymer, and the additional ingredient are present in an amount sufficient to impart stability to the composition.
11. The composition of claim 9, wherein the cellulose ether is present from about 0.1 wt % to about 3 wt % and the polyacrylic polymer is present from about 0.1 wt % to about 3 wt %.
12. The composition of claim 11, wherein the cellulose ether is present from about 0.1 wt % to about 3 wt %, the polyacrylic polymer is present from about 0.1 wt % to about 3 wt %, and the additional ingredient is present from about 0.5 wt % to about 10 wt %.
13. The composition of claim 12, wherein the additional ingredient is a fatty alcohol, wherein the fatty alcohol is selected from the group consisting of lauryl alcohol, cetyl alcohol, cetearyl alcohol, myristyl alcohol, stearyl alcohol, arachidyl alcohol, behenyl alcohol, oleyl alcohol, erucyl alcohol, and any combination of the foregoing.
14. The composition of claim 10, wherein the additional ingredient is the fatty alcohol of 10 to 24 carbon atoms, and wherein the fatty alcohol of 10 to 24 carbon atoms is cetyl alcohol.
15. The composition of claim 10, wherein the additional ingredient is an organic wax, wherein the organic wax is selected from the group consisting of an emulsifying wax (nonionic emulsifying wax), an anionic emulsifying wax, a cetyl ester wax, a microcrystalline wax, a white wax, a yellow wax, paraffin, and any combination of the foregoing.
16. The composition of claim 9, wherein the cellulose ether is selected from the group consisting of carboxymethylcellulose sodium, carboxymethylcellulose calcium, hydroxypropyl cellulose, hydroxyethylmethyl cellulose, ethylcellulose, hydroxyethylcellulose, methylcellulose, hydroxypropylcellulose, and hydroxypropylmethylcellulose.
17. The composition of claim 16, wherein the cellulose ether is hydroxypropylmethylcellulose.
18. The composition of claim 9, wherein the polyacrylic polymer is a carbomer.
19. The composition of claim 18, wherein the carbomer is selected from the group consisting of Carbopol 1342, Carbopol 940, Carbopol 941, Carbopol 980, Carbopol 981, Carbopol 1382, Carbopol 971P, Carbopol 974P, Carbopol 71G, Carbopol 910, Carbopol 934, Carbopol 934P, Carbopol 5984, Carbopol ETD, Carbopol Ultrez 10, Carbopol Ultrez 21, Pemulen TR-1, Pemulen TR-2, and any combination of the foregoing.
20. A method for treating acne on the skin, comprising:
(a) providing a flexible porous article impregnated with a cleansing composition having a carrier, benzoyl peroxide, and one or more cleansing agents selected from sodium methyl cocoyl taurate, sodium cocoyl isethionate, and mixtures thereof;
(b) contacting an area of the skin affected by acne with the porous article such that the skin is contacted by the composition; and
(c) removing the composition from the skin wherein residual benzoyl peroxide remains on the skin in an anti-acne effective amount.
21. A method for treating acne on the skin, comprising:
(d) providing a flexible porous article impregnated with a cleansing composition having a carrier, benzoyl peroxide, and one or more cleansing agents;
(e) contacting an area of the skin affected by acne with the porous article such that the skin is contacted by the composition; and
(f) removing the composition from the skin wherein residual benzoyl peroxide remains on the skin in an anti-acne effective amount.
22. The method of claim 21, wherein the contacting of the skin with the porous article is carried out by rubbing the skin with the porous article.
23. The method of claim 21, wherein the contacting of the skin with the porous article results in lathering of the composition on the skin.
24. The method of claim 21, wherein the composition is removed from the skin by rinsing.
25. The method of claim 24, wherein the rinsing is with water.
26. The method of claim 21, wherein the composition is removed from the skin by wiping.
27. The method of claim 21, wherein the wiping is with a wet towel or cloth.
28. The method of claim 21, wherein the wiping is with a dry towel or cloth or with the flexible porous article.
29. The method of claim 21, wherein the absorbent porous article is a non-woven fabric or cloth article.
30. The method of claim 21, wherein one or more cleansing agents is one or more surfactants.
31. The method of claim 21, wherein the one or more surfactants is present from about 4 wt % to about 40 wt % of the total composition.
32. The method of claim 21, wherein the one or more surfactants is one or more anionic surfactants.
33. The method of claim 32, wherein the one or more anionic surfactants is selected from the group consisting of sodium lauryl sulfoacetate, disodium laureth sulfosuccinate, lauramine oxide, cocamidopropyl betaine, lauramidopropyl betaine, lauryl sulfoacetate, sodium methyl cocoyl taurate, sodium cocoyl isethionate, and any combination thereof.
34. The method of claim 33, wherein the one or more surfactants is selected from the group consisting of sodium lauryl sulfoacetate, disodium laureth sulfosuccinate, lauramine oxide, lauryl sulfoacetate, sodium methyl cocoyl taurate, sodium cocoyl isethionate, and any combination thereof.
35. The method of claim 21, wherein the benzoyl peroxide is present in the composition in an amount of about 1 wt % to about 15 wt % based on the total weight of the composition.
36. The method of claim 21, wherein the benzoyl peroxide is present in the composition in an amount of about 3 wt % to about 9 wt % based on the total weight of the composition.
37. The method of claim 21, wherein the composition further has one or more moisturizers.
38. The method of claim 21, wherein the composition further has one or more zinc compounds.
39. The method of claim 21, wherein the composition is aqueous.
40. The method of claim 21, wherein the composition is nonaqueous.
41. The method of claim 21, wherein the composition is an emulsion.
42. The method of claim 21, wherein the composition is a suspension.
43. The method of claim 21, wherein the composition is a dispersion.
44. The method of claim 21, wherein the area of the skin affected by acne is the face.
45. The method of claim 21, wherein the porous article is a cloth article.
US12/716,130 2009-03-05 2010-03-02 Methods and compositions for treating acne Abandoned US20100226948A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US12/716,130 US20100226948A1 (en) 2009-03-05 2010-03-02 Methods and compositions for treating acne
US13/335,151 US8263097B2 (en) 2009-03-05 2011-12-22 Methods and compositions for treating acne

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US15781709P 2009-03-05 2009-03-05
US30680810P 2010-02-22 2010-02-22
US12/716,130 US20100226948A1 (en) 2009-03-05 2010-03-02 Methods and compositions for treating acne

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US13/335,151 Continuation US8263097B2 (en) 2009-03-05 2011-12-22 Methods and compositions for treating acne

Publications (1)

Publication Number Publication Date
US20100226948A1 true US20100226948A1 (en) 2010-09-09

Family

ID=42678462

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/716,130 Abandoned US20100226948A1 (en) 2009-03-05 2010-03-02 Methods and compositions for treating acne
US13/335,151 Expired - Fee Related US8263097B2 (en) 2009-03-05 2011-12-22 Methods and compositions for treating acne

Family Applications After (1)

Application Number Title Priority Date Filing Date
US13/335,151 Expired - Fee Related US8263097B2 (en) 2009-03-05 2011-12-22 Methods and compositions for treating acne

Country Status (2)

Country Link
US (2) US20100226948A1 (en)
WO (1) WO2010101934A1 (en)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2012170866A1 (en) * 2011-06-10 2012-12-13 Norac Pharma Benzoyl peroxide microparticle process
WO2014076136A1 (en) * 2012-11-13 2014-05-22 Galderma S.A. Bpo wash emulsion composition
US20150148425A1 (en) * 2013-11-25 2015-05-28 The Dial Corporation Antimicrobial composition exhibiting increased efficacy
CN105764475A (en) * 2013-11-22 2016-07-13 欧莱雅 Clay based product in sheet form for cosmetic applications
US20170296453A1 (en) * 2014-10-02 2017-10-19 Pierre Fabre Dermo-Cosmetique Cosmetic and/or pharmaceutical composition in the form of a dispersion, method for preparing same and use thereof for skin treatment
RU2638799C2 (en) * 2012-07-09 2017-12-15 Пьер Фабр Дермо-Косметик Zinc coceth sulphate application in capacity of antibacterial agent for propionibacterium acnes
US20190151394A1 (en) * 2017-11-17 2019-05-23 Ying Tung Chen Prebiotic Acne Treatment
JP2019514891A (en) * 2016-04-25 2019-06-06 ロレアル Hypoallergenic cleaning composition with makeup removal properties
RU2706695C2 (en) * 2012-11-13 2019-11-20 Галдерма С.А Gel detergent composition containing benzoyl peroxide (bpo)
US20200179409A1 (en) * 2015-08-05 2020-06-11 Cmpd Licensing, Llc Topical compositions and methods of formulating the same
US10688117B2 (en) 2011-05-27 2020-06-23 Galderma S.A. Topical wash composition for use in acne patients
WO2021041312A1 (en) * 2019-08-26 2021-03-04 L'oreal Silicone-free, low-friction cleanser with high-foaming properties
US20210386638A1 (en) * 2017-06-06 2021-12-16 Dual-Shave LLC Shave-cleanser composition
WO2023112664A1 (en) * 2021-12-14 2023-06-22 ロート製薬株式会社 Pharmaceutical composition for external application which contains benzoyl peroxide
US11684567B2 (en) 2015-08-05 2023-06-27 Cmpd Licensing, Llc Compositions and methods for treating an infection
US11793783B2 (en) 2015-08-05 2023-10-24 Cmpd Licensing, Llc Compositions and methods for treating an infection

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100226948A1 (en) * 2009-03-05 2010-09-09 Medicis Pharmaceutical Corporation Methods and compositions for treating acne
GB0912481D0 (en) 2009-07-17 2009-08-26 Reckitt Benckiser Healthcare I Skincare compositions
GB2512343A (en) * 2013-03-27 2014-10-01 Reckitt Benckiser Brands Ltd Skincare compositions
CN114149876A (en) * 2016-06-09 2022-03-08 阿科玛股份有限公司 Organic peroxide dispersions

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5086075A (en) * 1985-01-24 1992-02-04 Board Of Regents, The University Of Texas System Therapeutic compositions containing benzoyl peroxide
US5648389A (en) * 1995-10-27 1997-07-15 Medicis Pharmaceutical, Inc. Compositions for the treatment of dermatological disorders and methods for their use
US6294186B1 (en) * 1997-06-04 2001-09-25 Peter William Beerse Antimicrobial compositions comprising a benzoic acid analog and a metal salt
US6338855B1 (en) * 1996-10-25 2002-01-15 The Procter & Gamble Company Cleansing articles for skin and/or hair which also deposit skin care actives
US6352724B1 (en) * 1995-03-13 2002-03-05 Lesli A. Taylor Method for treating acne and/or rosacea
US20040191300A1 (en) * 2001-06-21 2004-09-30 Beiersdorf Ag Cosmetic or dermatological impregnated cloths
US20050025817A1 (en) * 2003-07-03 2005-02-03 Bhatia Kuljit S. Delivery system for topical medications
US20060051384A1 (en) * 2004-09-07 2006-03-09 3M Innovative Properties Company Antiseptic compositions and methods of use
US20060172904A1 (en) * 2005-01-31 2006-08-03 L'oreal Makeup-removing composition
US20070269537A1 (en) * 2003-02-10 2007-11-22 Bioderm Research Skin Condition Improvement Including Acne, Rosacea, and Topical Wounds by Artemisia Annua Extract via Iron Siderophore Trojan Horse Delivery System
US20090017147A1 (en) * 2005-01-14 2009-01-15 Sederma Cosmetic or Dermopharmaceutical Composition Comprising an Euglena Extract
US8263097B2 (en) * 2009-03-05 2012-09-11 Medicis Pharmaceutical Corporation Methods and compositions for treating acne

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2163947B (en) 1984-09-06 1988-06-29 Noel Douglas Lempriere Non-woven personal washing cloth
US4758467A (en) 1987-02-26 1988-07-19 Lempriere Noel D Disposable personal washing cloth
FR2628319B1 (en) 1988-03-09 1990-12-07 Oreal PHARMACEUTICAL AND COSMETIC COMPOSITIONS BASED ON BENZOYL PEROXIDE AND QUATERNARY AMMONIUM SALTS
GB9409945D0 (en) 1994-05-17 1994-07-06 Bioglan Lab Ltd A medicated wipe
US5879693A (en) 1997-01-30 1999-03-09 Circle Laboratories, Inc. Individually packaged disposable single acne pad
US5951991A (en) 1997-05-22 1999-09-14 The Procter & Gamble Company Cleansing products with improved moisturization
EP1011629B1 (en) 1997-09-05 2012-03-21 The Procter & Gamble Company Cleansing and conditioning products for skin or hair with improved deposition of conditioning ingredients
JP2001516712A (en) 1997-09-12 2001-10-02 ザ、プロクター、エンド、ギャンブル、カンパニー Cleansing and conditioning products for skin or hair
US6524594B1 (en) * 1999-06-23 2003-02-25 Johnson & Johnson Consumer Companies, Inc. Foaming oil gel compositions
US7074747B1 (en) 1999-07-01 2006-07-11 Johnson & Johnson Consumer Companies, Inc. Cleansing compositions
US7115535B1 (en) 1999-08-02 2006-10-03 The Procter & Gamble Company Personal care articles comprising batting
EP1373348A1 (en) 2001-03-09 2004-01-02 Regenesis, Llc Cosmetic sponges
FR2826270B1 (en) 2001-06-22 2005-01-28 Oreal WIPES AND USES IN THE COSMETIC FIELD
US20030194425A1 (en) 2002-04-11 2003-10-16 L'oreal Moist cleansing, skin care or cosmetic article
DE10301841A1 (en) 2003-01-20 2004-07-29 Beiersdorf Ag Cosmetic composition for impregnating cleansing wipes comprises cocoamidopropyl betaine, sodium laureth sulfate, sodium lauroyl glutamate, sodium lauroyl sarcosinate and polyethylene glycol 9 cocoglyceride
DE10301839A1 (en) 2003-01-20 2004-07-29 Beiersdorf Ag Surface-structured dry-look wipes useful for skin cleansing are impregnated with a cleansing composition comprising defined amounts of sarcosinate and alkyl glucoside
US7776355B2 (en) 2003-07-03 2010-08-17 Medics Pharmaceutical Corporation Delivery system for topical medications
DE602005007862D1 (en) 2004-02-19 2008-08-14 Reckitt & Colman Overseas SKIN CARE INCLUDING SALICYLIC ACID
US20060177505A1 (en) 2005-01-31 2006-08-10 L'oreal Cleaning composition in solid form
US20070099812A1 (en) 2005-10-27 2007-05-03 Luizzi Joseph M Exothermic cleansing article
US20070099813A1 (en) 2005-10-27 2007-05-03 Luizzi Joseph M Effervescent cleansing article
US20080026039A1 (en) 2006-07-26 2008-01-31 Stiefel Laboratories, Inc. Benzoyl peroxide pads and formulations therefor
US20090018200A1 (en) 2007-07-12 2009-01-15 L'oreal Composition containing a phenanthrenol
EP2273974A2 (en) 2008-05-09 2011-01-19 Tolmar, Inc. Proguanil to treat skin/mucosal diseases
US8308702B2 (en) 2010-04-21 2012-11-13 Johnson & Johnson Consumer Companies, Inc. Foaming porous pad for use with a motorized device

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5086075A (en) * 1985-01-24 1992-02-04 Board Of Regents, The University Of Texas System Therapeutic compositions containing benzoyl peroxide
US6352724B1 (en) * 1995-03-13 2002-03-05 Lesli A. Taylor Method for treating acne and/or rosacea
US5648389A (en) * 1995-10-27 1997-07-15 Medicis Pharmaceutical, Inc. Compositions for the treatment of dermatological disorders and methods for their use
US6338855B1 (en) * 1996-10-25 2002-01-15 The Procter & Gamble Company Cleansing articles for skin and/or hair which also deposit skin care actives
US6294186B1 (en) * 1997-06-04 2001-09-25 Peter William Beerse Antimicrobial compositions comprising a benzoic acid analog and a metal salt
US20040191300A1 (en) * 2001-06-21 2004-09-30 Beiersdorf Ag Cosmetic or dermatological impregnated cloths
US20070269537A1 (en) * 2003-02-10 2007-11-22 Bioderm Research Skin Condition Improvement Including Acne, Rosacea, and Topical Wounds by Artemisia Annua Extract via Iron Siderophore Trojan Horse Delivery System
US20050025817A1 (en) * 2003-07-03 2005-02-03 Bhatia Kuljit S. Delivery system for topical medications
US20060051384A1 (en) * 2004-09-07 2006-03-09 3M Innovative Properties Company Antiseptic compositions and methods of use
US20090017147A1 (en) * 2005-01-14 2009-01-15 Sederma Cosmetic or Dermopharmaceutical Composition Comprising an Euglena Extract
US20060172904A1 (en) * 2005-01-31 2006-08-03 L'oreal Makeup-removing composition
US8263097B2 (en) * 2009-03-05 2012-09-11 Medicis Pharmaceutical Corporation Methods and compositions for treating acne

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10688117B2 (en) 2011-05-27 2020-06-23 Galderma S.A. Topical wash composition for use in acne patients
WO2012170866A1 (en) * 2011-06-10 2012-12-13 Norac Pharma Benzoyl peroxide microparticle process
RU2638799C2 (en) * 2012-07-09 2017-12-15 Пьер Фабр Дермо-Косметик Zinc coceth sulphate application in capacity of antibacterial agent for propionibacterium acnes
RU2647479C2 (en) * 2012-11-13 2018-03-15 Галдерма С.А. Composition for face washing as emulsion containing benzoyl peroxide
AU2013346891B2 (en) * 2012-11-13 2018-02-08 Galderma Holding SA BPO wash emulsion composition
US11446272B2 (en) 2012-11-13 2022-09-20 Galderma Holding SA BPO wash emulsion composition
RU2706695C2 (en) * 2012-11-13 2019-11-20 Галдерма С.А Gel detergent composition containing benzoyl peroxide (bpo)
US10610594B2 (en) 2012-11-13 2020-04-07 Galderma S.A. BPO wash gel composition
WO2014076136A1 (en) * 2012-11-13 2014-05-22 Galderma S.A. Bpo wash emulsion composition
US20160287493A1 (en) * 2013-11-22 2016-10-06 L'oreal Clay based product in sheet form for cosmetic applications
CN105764475A (en) * 2013-11-22 2016-07-13 欧莱雅 Clay based product in sheet form for cosmetic applications
US20150148425A1 (en) * 2013-11-25 2015-05-28 The Dial Corporation Antimicrobial composition exhibiting increased efficacy
US20170296453A1 (en) * 2014-10-02 2017-10-19 Pierre Fabre Dermo-Cosmetique Cosmetic and/or pharmaceutical composition in the form of a dispersion, method for preparing same and use thereof for skin treatment
US11793783B2 (en) 2015-08-05 2023-10-24 Cmpd Licensing, Llc Compositions and methods for treating an infection
US11684567B2 (en) 2015-08-05 2023-06-27 Cmpd Licensing, Llc Compositions and methods for treating an infection
US20200179409A1 (en) * 2015-08-05 2020-06-11 Cmpd Licensing, Llc Topical compositions and methods of formulating the same
EP3452175A4 (en) * 2016-04-25 2020-02-26 L'oreal Gentle cleansing compositions with makeup removal properties
JP2021155422A (en) * 2016-04-25 2021-10-07 ロレアル Gentle cleansing compositions with makeup removal properties
JP7169194B2 (en) 2016-04-25 2022-11-10 ロレアル Mild cleansing composition with makeup-removing properties
JP2019514891A (en) * 2016-04-25 2019-06-06 ロレアル Hypoallergenic cleaning composition with makeup removal properties
US20210386638A1 (en) * 2017-06-06 2021-12-16 Dual-Shave LLC Shave-cleanser composition
US11878069B2 (en) * 2017-06-06 2024-01-23 Dual-Shave LLC Shave-cleanser composition
US20190151394A1 (en) * 2017-11-17 2019-05-23 Ying Tung Chen Prebiotic Acne Treatment
CN114340592A (en) * 2019-08-26 2022-04-12 欧莱雅 Silicone-free low-friction cleaners with high foam properties
WO2021041312A1 (en) * 2019-08-26 2021-03-04 L'oreal Silicone-free, low-friction cleanser with high-foaming properties
WO2023112664A1 (en) * 2021-12-14 2023-06-22 ロート製薬株式会社 Pharmaceutical composition for external application which contains benzoyl peroxide

Also Published As

Publication number Publication date
US20120082710A1 (en) 2012-04-05
US8263097B2 (en) 2012-09-11
WO2010101934A1 (en) 2010-09-10

Similar Documents

Publication Publication Date Title
US8263097B2 (en) Methods and compositions for treating acne
US9730870B2 (en) Sodium hypochlorite-based body wash compositions
US20050095261A1 (en) Antimicrobial topical compositions for treatment of rosacea
US5346886A (en) Topical α-1-antitrypsin, non-aqueous lipid miscible, benzalkonium chloride compositions for treating skin
JP2002541182A (en) Antimicrobial wipes provide improved immediate bacterial reduction
AU2020201781B2 (en) Composition, system and method for treating skin
JP2014519503A (en) Cleaning composition
JP2003183153A (en) Skin detergent containing anti-aging active agent
US20110236503A1 (en) Topical Skincare Composition
JP2007505093A (en) Skin care compositions and methods
JP6448377B2 (en) Cleansing lotion
JPH03123732A (en) Massage material
JP6448376B2 (en) Lotion
KR20170066652A (en) Cleansing lotion, sheet cosmetic product, and cosmetic method
WO2008057411A1 (en) Kits containing benzoyl peroxide pads and another acne-treating composition, and formulations and methods of use therefor
JP2000507248A (en) Acne treatment
JP2000191514A (en) Sebum remover composition
US20230033248A1 (en) Compositions and methods for enhanced decontamination
US20140023728A1 (en) Iodine Liquid Soap, Dispenser and Method
US20080026039A1 (en) Benzoyl peroxide pads and formulations therefor
US20230413812A1 (en) Sanitizing compositions containing ionic liquid
JP7355493B2 (en) Skin cleansing composition
CA3231023A1 (en) Ointments for treating dry skin
KR20240054383A (en) Ointment to treat dry skin
RU2351310C2 (en) Compositions for skin care and methods

Legal Events

Date Code Title Description
AS Assignment

Owner name: MEDICIS PHARMACEUTICAL CORPORATION, ARIZONA

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:JITPRAPHAI, WARANUSH;GANS, EUGENE;REEL/FRAME:024360/0200

Effective date: 20100401

AS Assignment

Owner name: GOLDMAN SACHS LENDING PARTNERS LLC, NEW YORK

Free format text: SECURITY AGREEMENT;ASSIGNOR:MEDICIS PHARMACEUTICAL CORPORATION;REEL/FRAME:030281/0433

Effective date: 20130423

STCB Information on status: application discontinuation

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

AS Assignment

Owner name: BARCLAYS BANK PLC, AS SUCCESSOR AGENT, NEW YORK

Free format text: NOTICE OF SUCCESSION OF AGENCY;ASSIGNOR:GOLDMAN SACHS LENDING PARTNERS, LLC;REEL/FRAME:034749/0689

Effective date: 20150108