WO2009045949A2 - Foamable fluoride oral care composition - Google Patents
Foamable fluoride oral care composition Download PDFInfo
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- WO2009045949A2 WO2009045949A2 PCT/US2008/078091 US2008078091W WO2009045949A2 WO 2009045949 A2 WO2009045949 A2 WO 2009045949A2 US 2008078091 W US2008078091 W US 2008078091W WO 2009045949 A2 WO2009045949 A2 WO 2009045949A2
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- composition
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- fluoride
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- surface active
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q11/00—Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/046—Aerosols; Foams
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/20—Halogens; Compounds thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/20—Halogens; Compounds thereof
- A61K8/21—Fluorides; Derivatives thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/36—Carboxylic acids; Salts or anhydrides thereof
- A61K8/365—Hydroxycarboxylic acids; Ketocarboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/90—Block copolymers
Definitions
- One present practice to reduce dental caries in children is the periodic application, e.g., 1 to 2 times per year, of a foamable fluoride composition having a relatively high concentration of a fluoride releasing salt, e.g., 1-3% by weight sodium fluoride, that is packaged in an aerosol container in combination with an aerosol propellant.
- the composition is dispensed from the container into the trough of a dental tray as a dense, stable, non-flowable foam which is superimposed about and into engagement with the teeth to be treated, to affect fluoride uptake by the dental enamel.
- conventional dental foams may be effective and are in present commercial use, in practice, the thick, dense foam that is produced may cause the patient to experience discomfort during treatment. Additionally, upon completion of treatment, the residual dense foam may be difficult and/or time consuming to remove from the patient's mouth. For at least these reasons, conventional foams may discourage professional usage and patient compliance with the fluoride treatment.
- the invention includes a low density foamable oral care composition
- a low density foamable oral care composition comprising an aqueous solution of: a fluoride ion releasable salt; a surface active agent selected from the group consisting of nonionic surfactants, zwitterionic surfactants, betaine surfactants, and mixtures thereof; and an acidifying agent in an amount sufficient to adjust the pH of the composition to about 3 to about 5, wherein the composition is substantially free of precipitates when maintained at a temperature of 4.4°C (40°F) for 12 hours.
- an oral care composition is any composition that is suitable for administration or application to the oral cavity of a human or animal subject for enhancing health, hygiene or appearance of the subject, preferably providing such benefits as the prevention or treatment of a physiologic condition or disorder, the provision of sensory, decorative or cosmetic benefits, and combinations thereof.
- an oral care composition is not intentionally swallowed, but is rather retained in the oral cavity for a time sufficient to effect the intended utility.
- compositions to be used in this invention are, accordingly, pharmaceutically- or cosmetically- acceptable.
- a “pharmaceutically acceptable” or “cosmetically acceptable” component, or a component used in a “safe and effective amount” is one that is suitable for use with humans and/or animals to provide the desired therapeutic, prophylactic, sensory, decorative, or cosmetic benefit without undue adverse effects (such as toxicity, irritation, and allergic response) commensurate with a reasonable benefit/risk ratio.
- the present invention provides a low density, foamable, dental fluoride foam.
- the composition is packaged in a foam generating container.
- the composition comprises an aqueous solution of a water soluble fluoride ion releasable salt; a surfactant selected from the group consisting of nonionic surfactants, zwitterionic surfactants, betaine surfactants, and mixtures thereof; and an orally compatible acidifying agent in an amount sufficient to adjust the pH of the composition to about 3 to about 5.
- the composition is a clear solution substantially free of precipitates when held at a temperature of 4.4°C (40°F) for 12 hours.
- substantially free of precipitates means that the composition does not contain any precipitates that can be seen with the human eye, that is, without the aid of an artificial device.
- the composition has an upper solubility temperature greater than about 29.4 0 C (85°F), preferably greater than about 31.TC (100 0 F), and a lower solubility temperature less than about 4.4°C (40 0 F), thus providing a stable and substantially clear solution.
- the composition When dispensed from the container into the trough of a dental tray, the composition forms a low density, rapidly collapsible foam which substantially liquefies in about 1 minute, or less, after being dispensed from a foam generating container and placed in contact with a patient's teeth, from which it can be readily rinsed and removed from the patient's mouth.
- colladible foam as it is used in the present application means a foam that collapses, i.e., becomes substantially liquid in a period of no more than about 2 minutes after its formation in the dental tray trough and placement on the patient's teeth. After this short period of time, the aerosol foam is substantially collapsed to a liquid and the patient's teeth is simply rinsed free of the residual foam.
- the orally acceptable dentifrice carrier used to prepare the foamable oral composition comprises a water-phase.
- Water employed in the preparation of commercially suitable dental foams, toothpastes, gels, and mouthwashes should preferably be deionized and free of organic impurities.
- Water generally comprises of about 85% to 98%, preferably of about 90% to 95%, of the foamable dental fluoride compositions herein, hi one embodiment, deionized water is provided at a level of about 91%. The water is free water which is added, plus that which is introduced with other materials and ingredients.
- the water soluble fluoride ion releasable salt of the present invention is a fluoride ion source useful, for example, as an anticaries agent.
- the sources of fluoride ions, or fluoride-providing agents may be slightly soluble in water or may be fully water-soluble. They are characterized by their ability to release fluoride ions in water, by their freedom from undesired reaction with other compounds of the oral preparation, and by their anticaries activity. Any orally acceptable fluoride ion source can be used.
- Non-limiting examples include soluble alkali metal or alkaline earth metal salts such as sodium fluoride, potassium fluoride, and calcium fluoride; ammonium fluoride; a copper fluoride such as cuprous fluoride; zinc fluoride; barium fluoride; sodium fluorosilicate; ammonium fluorosilicate; sodium fluorozirconate; sodium monofluorophosphate; aluminum mono- and di-fluorophosphate; and fluorinated sodium calcium pyrophosphate.
- Alkali metal and tin fluorides such as sodium and stannous fluorides, indium fluoride, sodium monofluorophosphate (MFP), and mixtures thereof are preferred.
- amine fluorides are used, including olaflur (N 1 - octadecyltrimethylendiami ⁇ e-N,N,N'- tris(2-ethanol)-dihydrofluoride).
- the amount of fluoride-providing agent is dependent to some extent upon the type of compound, its solubility, and the type of oral preparation, but it must be a non-toxic amount.
- water-soluble fluoride ion releasable salts are used and provided in a safe and effective amount.
- One or more fluoride ion sources are typically present in an amount that provides about 5,000 p.p.m to about 50,000 p.p.m. of fluoride ion, alternatively about 10,000 p.p.m.
- Surface active agents include components that may function as a surfactant, emulsifier, and/or foam modulator. Surface active agents generally increase prophylactic action by thoroughly dispersing the fluoride ions throughout the oral cavity. Suitable emulsifying agents include those that are reasonably stable and foam throughout a wide pH range. In addition, preferred surface active agents form stable compositions at low temperatures such as 4.4°C (40 0 F). This renders the instant compositions more cosmetically acceptable and increases the available of actives that remain in solution.
- the organic surface-active material is preferably selected from nonionic and zwitterionic surfactants. Mixtures of surfactants can also be used.
- oral compositions contain one or more surfactants in the range of about 0.1% to about 3%, and preferably of about 0.6% to about 1.5%, wherein all percentages are by weight based on the total weight of the oral composition.
- Suitable nonionic surfactants include ethylene oxide/propylene oxide block copolymers (e.g., Poloxamers or Pluronic® surfactants); polyethylene oxide condensates of alkyl phenols; products derived from the condensation of ethylene oxide with the reaction product of propylene oxide and ethylene diamine; ethylene oxide condensates of aliphatic alcohols; long chain tertiary amine oxides; long chain tertiary phosphine oxides; long chain dialkyl sulfoxides; and condensates of sorbitan esters of fatty acids with ethylene oxide (polysorbates).
- Poloxamers or Pluronic® surfactants e.g., Pluronic® surfactants
- polyethylene oxide condensates of alkyl phenols products derived from the condensation of ethylene oxide with the reaction product of propylene oxide and ethylene diamine
- ethylene oxide condensates of aliphatic alcohols long chain tertiary amine oxides
- Non-limiting examples of sorbitan ester ethoxylates include sorbitan fatty acid esters with of about 20 to about 60 moles of ethylene oxide (e.g., the Tween® surfactants, a trademark of ICI Americas, Inc., Wilmington, Delaware, U.S.A.
- Particularly preferred polysorbates are Polysorbate 20 (polyoxyethylene 20 sorbitan monolaurate, Tween® 20) and Polysorbate 80 (polyoxyethylene 20 sorbitan mono-oleate, Tween® 80).
- Suitable poloxamer surfactants include poly(oxyethylene)- poly(oxypropylene) block copolymers having an average molecular weight of about 3,000 to about 15,000. Intermediate average molecular weights may be of about 6,000 to about 15,000 with a preferred average molecular weight of about 10,000 to about 15,000.
- Such copolymers are known commercially by the non-proprietary name of poloxamers, the name being used in conjunction with a numeric suffix to designate the individual identification of each copolymer. Poloxamers have varying contents of ethylene oxide and propylene oxide, resulting in a wide range of chemical structures and molecular weights.
- One preferred poloxamer is Poloxamer 407, available, for example, under the tradename Pluronic F127 by BASF of Mount Olive, New Jersey, U.S.A.
- Zwitterionic surface active agents can be broadly described as those containing both a negative and a positive charged group. In various embodiments, they are derivatives of aliphatic quaternary ammonium, phosphonium, and sulfomum compounds, in which the aliphatic radicals can be straight chain or branched of about 8 carbons or more, and preferably 8 to about 18 or 20 carbons.
- the positively charged group is typically a quaternary ammonium group, while the negatively charged group is generally an anionic water-solubilizing group such as carboxy, sulfonate, sulfate, phosphate or phosphonate.
- a suitable of a suitable zwitterionic surfactant is 4-(N,N-di(2-hydroxyethyl)-N-octadecylammonio)-butane- 1 -carboxylate.
- betaine surfactants such as those disclosed in United States Patent No. 5,180,577, the disclosure of which is incorporated herein by reference.
- Preferred betaines include those derived structurally from N,N- dimethylglycine. They contain a quaternary nitrogen and a carboxylate group separated by a single methylene group.
- Typical alkyldimethyl betaines include decyl betaine, cocobetaine, myristyl betaine, palmityl betaine, lauryl betaine, cetyl betaine, stearyl betaine, and the like.
- amidobetaines include cocoamidoethyl betaine, cocoamidopropyl betaine, lauramidopropyl betaine, and the like. To illustrate, amidopropyl betaines are represented by the formula:
- RCO represents a fatty acid residue and R contains of about 6 to 24 carbon atoms or greater, preferably of about 8 to 20 carbon atoms, more preferably about 12 to 18 carbon atoms.
- Cocamidopropyl betaine is a preferred commercial embodiment where RCO is derived from coconut oil. In one embodiment, cocoamidopropyl betaine is present at a level of about 1%.
- the surfactants provide suitable foaming characteristics and have a Hydrophile-Lipophile Balance (HLB) value of at least 12.
- HLB Hydrophile-Lipophile Balance
- HLB Hydrophile-Lipophile Balance
- the present invention provides a stable oral composition that is clear in appearance and substantially free from precipitates.
- the compositions are stable over a range of temperature about 4.4 0 C (4O 0 F) to at least about 29.4°C (85°F), and more preferably to at least 100 0 F. Further, the compositions preferably remain stable in solution at low temperatures such as 4O 0 F for extended periods, such as 12 hours or more.
- compositions further contain propellant gases such as those disclosed below, and maintain low temperature stability.
- precipitation points can also be measured on other surfactant solutions, including those formulated according to the present invention with a fluoride ion source and other additives.
- the cloud point is referred to as the solubility limit of the particular solution; it is the temperature above (for an upper limit) or below (for a lower limit) which an aqueous solution of a water-soluble surfactant becomes turbid.
- the compositions exhibit an upper solubility temperature, or upper cloud point, greater than about 9.4 0 C (85°F), preferably greater than 37.7 0 C (100 0 F), and a lower solubility temperature, or lower cloud point, less than about 4.4 0 C (40 0 F), preferably less than about 1.6 0 C (35 0 F).
- pH modifying agents among those useful herein include acidifying agents to lower pH, basifying agents to raise pH, and buffering agents to control pH within a desired range.
- one or more compounds selected from acidifying, basifying and buffering agents can be included to provide a pH of about 2 to about 6, or in various embodiments of about 3 to about 5, of about 3 to about 4, and of about 3.5 to about 4.
- Any orally acceptable pH modifying agent can be used, including without limitation carboxylic, phosphoric and sulfonic acids, acid salts (e.g., monosodium citrate, disodium citrate, monosodium malate, etc.), alkali metal hydroxides such as sodium hydroxide, carbonates such as sodium carbonate, bicarbonates, sesquicarbonates, borates, silicates, phosphates (e.g., monosodium phosphate, trisodium phosphate, pyrophosphate salts, etc.), imidazole and mixtures thereof.
- acid salts e.g., monosodium citrate, disodium citrate, monosodium malate, etc.
- alkali metal hydroxides such as sodium hydroxide
- carbonates such as sodium carbonate, bicarbonates, sesquicarbonates, borates, silicates
- phosphates e.g., monosodium phosphate, trisodium phosphate, pyrophosphate
- Acidifying agents useful in the practice of the present invention include inorganic acids such as phosphoric acid, hydrochloric acid and hydrofluoric acid and organic acids such as malic acid, hydroxysuccinic acid, citric acid and tartaric acid and mixtures thereof.
- the acidifying agent is present in the foamable composition in an amount ranging of about 0.5 to about 3.5% by weight to adjust the pH to between about 3 to about 5.
- One or more pH modifying agents are optionally present in a total amount effective to maintain the composition in an orally acceptable pH range.
- the malic acid is present at a level of about 3% by weight.
- a buffering salt such as sodium hydrogen phosphate, is included in the compositions to inhibit tooth demineralization exposed to the acidified foam.
- the sodium hydrogen phosphate is provided such that the composition contains about 0.1M phosphate ions.
- the sodium hydrogen phosphate is present at a level of about 1.4% (e.g., about 1.38%).
- the rapidly collapsible fluoride dental foams contain a sweetening agent.
- Sweeteners among those useful herein include orally acceptable natural or artificial, nutritive or non-nutritive sweeteners.
- Such sweeteners include dextrose, polydextrose, sucrose, maltose, dextrin, dried invert sugar, mannose, xylose, ribose, fructose, levulose, galactose, corn syrup (including high fructose corn syrup and corn syrup solids), partially hydrolyzed starch, hydrogenated starch hydrolysate, sorbitol, mannitol, xylitol, mallitol, isomalt, aspartame, neotame, saccharin and salts thereof, sucralose, dipeptide-based intense sweeteners, cyclamates, dihydrochalcones and mixtures thereof.
- sodium saccharinate may be mentioned by way of one presently preferred example.
- One or more sweeteners are optionally present in a total amount depending strongly on the particular sweetener(s) selected, but typically at levels of about 0.005% to about 5%, optionally about 0.1 to about 1%, preferably 0.25 and about 0.35% relative to the total weight to of the composition.
- the foams may also contain preservatives such as sodium benzoate, methyl parahydroxybenzoate, propyl parahydroxybenzoate and the like in quantities of between 0.01 and 0.5% by weight relative to the total weight of the composition, hi one embodiment, the sodium benzoate is present at a level of about 0.1%.
- a flavoring substance in proportions of preferably between about 0.5 and about 5% relative to the total weight of the foam expelled from the aerosol device is generally present in the composition.
- Flavorants among those useful herein include any material or mixture of materials operable to enhance the taste of the composition. Any orally acceptable natural or synthetic flavorant can be used, such as flavoring oils, flavoring aldehydes, esters, alcohols, similar materials, and combinations thereof.
- Flavorants include vanillin, sage, marjoram, parsley oil, spearmint oil, cinnamon oil, oil of wintergreen (methylsalicylate), peppermint oil, clove oil, bay oil, anise oil, eucalyptus oil, citrus oils, fruit oils and essences including those derived from lemon, orange, lime, grapefruit, apricot, banana, grape, apple, mandarin, strawberry, cherry, pineapple, etc., bean- and nut-derived flavors such as coffee, cocoa, cola, peanut, almond, etc., adsorbed and encapsulated flavorants, and mixtures thereof. Also encompassed within flavorants herein are ingredients that provide fragrance and/or other sensory effect in the mouth, including cooling or warming effects.
- Such ingredients include menthol, menthyl acetate, menthyl lactate, camphor, eucalyptus oil, eucalyptol, anethole, eugenol, cassia, oxanone, ⁇ -irisone, propenyl guaiethol, thymol, linalool, benzaldehyde, cin ⁇ amaldehyde, N-ethyl- p-menthan-3-carboxamine, N,2,3-trimethyl-2-isopropylbutanamide, 3-1- menthoxypropane-l,2-diol, cinnamaldehyde glycerol acetal (CGA), methone glycerol acetal (MGA) and mixtures thereof.
- One or more flavorants are optionally present in a total amount of about 0.01% to about 5%, optionally in various embodiments about 0.05 to about 2%, and more preferably about
- the propellants used in the pressurized aerosol container in which the foamable composition of the present invention may be packaged are selected from among compressed air, nitrous oxide, and carbon dioxide and, more typically, a volatile hydrocarbon or mixture of volatile hydrocarbons (typically with 3 to 6 carbon atoms) having a vapor pressure of about 15 to about 80 psig, preferably about 30 to about 70 psig, at about 20°C.
- volatile hydrocarbons is also intended to include the halohydrocarbons.
- a particularly preferred propellant is the product sold by Diversified CPC International, Charmahon, Illinois, U.S.A. under the name Aeron A-46 ("A-46").
- A-46 is a mixture of isobutane and propane with a vapor pressure of 46 psig at about 20° C.
- the propellant comprises about 75 to about 85 wt % propane and about 15 to about 25 wt % iso-butane.
- the dental foam composition comprises about 5 to about 20 wt % of the compressed liquid propellant, more preferably about 7 to about 10 wt % of the propellant.
- the present invention may optionally use two propellants, referred to in the art as a dual-propellant system.
- the two main functions for the volatile propellant components are: (1) to propel the dentifrice from the dispensing container, and (2) to cause the dispensed composition to foam.
- the same propellant composition is used for both purposes, in other embodiments different propellants are used.
- the function of the latter propellant may alternatively be referred to as a blowing agent, or foaming agent. Blowing agents are added to the formulation to cause the formulation to foam and do not supply the major mechanical energy used to propel the dentifrice from its container.
- Foam modulators optionally useful herein include materials operable to increase amount, thickness or stability of foam generated by the composition (e.g., dentifrice compositions) upon agitation.
- Any orally acceptable foam modulator can be used, including polyethylene glycols (PEGs), also known as polyoxyethylenes.
- PEGs polyethylene glycols
- High molecular weight PEGs are suitable, including those having an average molecular weight of about 200,000 to about 7,000,000, for example about 500,000 to about 5,000,000 or about 1,000,000 to about 2,500,000.
- One or more PEGs are optionally present in a total amount of about 0.1% to about 10%, more preferably of about 0.2% to about 5%, and even more preferably of about 0.25% to about 2%.
- Viscosity modifiers among those optionally useful herein include mineral oil, petrolatum, clays and organomodified clays, silica and mixtures thereof. In various embodiments, such viscosity modifiers are operable to inhibit settling or separation of ingredients or to promote redispersibility upon agitation of a liquid composition. One or more viscosity modifiers are optionally present in a total amount between about 0.01% to about 10%, more preferably between about 0.1% to about 5% by weight of the composition.
- Colorants among those optionally useful herein include pigments, dyes, lakes and agents imparting a particular luster or reflectivity such as pearling agents.
- colorants are operable to provide a white or light-colored coating on a dental surface, to act as an indicator of locations on a dental surface that have been effectively contacted by the composition, and/or to modify appearance, in particular color and/or opacity, of the composition to enhance attractiveness to the consumer.
- Any orally acceptable colorant can be used, including talc, mica, magnesium carbonate, calcium carbonate, magnesium silicate, magnesium aluminum silicate, silica, titanium dioxide, zinc oxide, red, yellow, brown and black iron oxides, ferric ammonium ferrocyanide, manganese violet, ultramarine, titaniated mica, bismuth oxychloride, FD&C dyes, and mixtures thereof.
- One or more colorants are optionally present in a total amount of about 0.001% to about 20%, for example of about 0.01% to about 10% or of about 0.1% to about 5%.
- the foamable fluoride compositions of the present invention are prepared by blending the fluoride salt and acidifying agent with the surfactant, sweetening agent, flavor and preservative in an aqueous solution.
- the resulting aqueous solution containing about 85 to about 98% by weight water, and preferably about 90 to about 95% by weight water, is added in a predetermined amount to a foam generating container.
- an appropriate aerosol valve is securely fitted to the mouth of the container.
- the container is then charged through the aerosol valve with an aerosol propellant of about 4% to 1.0%, preferably 7% of the relative fill weight of the aerosol container.
- a dispensing actuator and spout assembly is then fitted onto the valve.
- Suitable pressure differential dispensers for use with a dual-propellant system include those comprising a collapsible product-containing bag being disposed within a rigid container which contains a propellant fluid, commonly referred to as a bag- in-can assembly.
- a propellant fluid commonly referred to as a bag- in-can assembly.
- operation of a manually actuated dispensing valve permits the release of the composition, the propellant fluid being separated from the product by the fluid impermeable bag.
- the fluid impermeable bag systems commonly include bags made of chemically inert polymers and those described in U.S. Patent No. 6,622,943, to Poisson, et al., issued September 23, 2003 and U.S. Patent No. 6,789,702, to O'Conner et al., issued September 14, 2004.
- the foam generating container is shaken well and rotated to align the dispensing spout with the trough of a dental tray.
- the actuator is pressed to dispense an amount of fluoride foam that substantially fills the volume defined by the trough.
- the tray is then placed in a patient's mouth so as to superimpose the trough and its fluoride foam content about and into engagement with the teeth to be treated.
- the fluoride foam is maintained in engagement with the teeth for about 1 to 4 minutes to effect the fluoride treatment of the teeth.
- the foam that is formed in the trough is "fluffy", with a relatively light body, as distinguished from the common dense foam, and collapses readily so as to allow for quick and easy removal of the residual treatment foam by simple aspiration or water rinsing of the mouth.
- the foam upon dispensing, may exist in foam form for about 2 minutes, about 100 seconds, about 90 second before collapsing or liquefies.
- a foamable fluoride treatment composition having the ingredients listed in Table 1 is prepared by dissolving the ingredients in water, in the order listed, at room temperature.
- a foamable fluoride treatment composition having the ingredients listed in Table 2 is prepared by dissolving the ingredients in water, in the order listed, at room temperature by the method described previously in Example 1.
- the surfactant comprises Pluronic F- 127, and no cocamidopropyl betaine is added to the composition.
- This composition is similarly placed in a 4.4°C (40°F) refrigerator for at least 12 hours, and the resulting composition is clear, not cloudy, and does not have any visible precipitated particles.
- a foamable fluoride treatment composition having the ingredients listed in Table 3 is prepared by dissolving the ingredients in water, in the order listed, at room temperature by the method described previously in Example 1.
- the surfactant comprises sodium lauryl sulfate, and no Pluronic F- 127 or cocamidopropyl betaine is added to the composition.
- This composition is similarly placed in a 4.4°C (40°F) refrigerator for at least 12 hours, and the resulting composition is cloudy, and does not have visible precipitated particles.
Abstract
Description
Claims
Priority Applications (13)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08834922A EP2194959B1 (en) | 2007-10-01 | 2008-09-29 | Foamable oral care composition |
MX2010003135A MX2010003135A (en) | 2007-10-01 | 2008-09-29 | Foamable fluoride oral care composition. |
BRPI0817913A BRPI0817913B1 (en) | 2007-10-01 | 2008-09-29 | low density foamy oral care composition and low density foamy dental fluoride composition packed in a foam generator container. |
JP2010528050A JP5705542B2 (en) | 2007-10-01 | 2008-09-29 | Effervescent fluoride oral care composition |
AT08834922T ATE547093T1 (en) | 2007-10-01 | 2008-09-29 | FOAMABLE ORAL CARE COMPOSITION |
CN200880110003.3A CN101815499B (en) | 2007-10-01 | 2008-09-29 | Foamable fluoride oral care composition |
PL08834922T PL2194959T3 (en) | 2007-10-01 | 2008-09-29 | Foamable oral care composition |
CA2700540A CA2700540C (en) | 2007-10-01 | 2008-09-29 | Foamable fluoride oral care composition |
DK08834922.0T DK2194959T3 (en) | 2007-10-01 | 2008-09-29 | Foam-proof oral care preparation |
ES08834922T ES2383038T3 (en) | 2007-10-01 | 2008-09-29 | Foamable composition for oral care |
AU2008308948A AU2008308948B2 (en) | 2007-10-01 | 2008-09-29 | Foamable fluoride oral care composition |
ZA2010/02224A ZA201002224B (en) | 2007-10-01 | 2010-03-29 | Foamable fluoride oral care composition |
HK10110016.7A HK1143533A1 (en) | 2007-10-01 | 2010-10-25 | Foamable oral care composition |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/865,457 US8802060B2 (en) | 2007-10-01 | 2007-10-01 | Foamable fluoride oral care composition |
US11/865,457 | 2007-10-01 |
Publications (2)
Publication Number | Publication Date |
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WO2009045949A2 true WO2009045949A2 (en) | 2009-04-09 |
WO2009045949A3 WO2009045949A3 (en) | 2009-06-18 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/US2008/078091 WO2009045949A2 (en) | 2007-10-01 | 2008-09-29 | Foamable fluoride oral care composition |
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US (1) | US8802060B2 (en) |
EP (1) | EP2194959B1 (en) |
JP (1) | JP5705542B2 (en) |
CN (1) | CN101815499B (en) |
AR (1) | AR068598A1 (en) |
AT (1) | ATE547093T1 (en) |
AU (1) | AU2008308948B2 (en) |
BR (1) | BRPI0817913B1 (en) |
CA (1) | CA2700540C (en) |
CO (1) | CO6270242A2 (en) |
DK (1) | DK2194959T3 (en) |
ES (1) | ES2383038T3 (en) |
HK (1) | HK1143533A1 (en) |
MX (1) | MX2010003135A (en) |
MY (1) | MY153728A (en) |
PL (1) | PL2194959T3 (en) |
RU (1) | RU2442562C2 (en) |
TW (1) | TWI411445B (en) |
WO (1) | WO2009045949A2 (en) |
ZA (1) | ZA201002224B (en) |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH704048A2 (en) | 2010-11-03 | 2012-05-15 | Roland Dr Zettel | Dentifrice. |
KR101687405B1 (en) * | 2010-11-22 | 2016-12-19 | (주)아모레퍼시픽 | Oral composition for preventing gingival disease containing natural forming agents |
CN104023796B (en) * | 2011-12-20 | 2018-02-09 | 高露洁-棕榄公司 | Oral care composition |
US20130344009A1 (en) * | 2012-06-22 | 2013-12-26 | Children Oral Care, Llc | Foaming oral care formulation and system and method of forming and using same |
RU2523560C1 (en) * | 2013-02-15 | 2014-07-20 | Закрытое акционерное общество "Брынцалов-А" | Disinfectant antiseptic agent in gel form for care of hand skin |
FR3012333B1 (en) * | 2013-10-24 | 2015-11-13 | Ouali Razira | LIQUID TOOTHPASTE COMPRISING A HYDROLISA OF CHICOREOUS LEAVES, IN PARTICULAR IN THE STADIUM OF ENDIVE |
CN104721063B (en) * | 2013-12-19 | 2018-05-08 | 高露洁-棕榄公司 | Dentrifice composition comprising zinc oxide and zinc citrate |
NO339503B1 (en) | 2014-06-18 | 2016-12-19 | Meda Otc Ab | Composition for the prevention or treatment of dental erosion |
GB201811061D0 (en) | 2018-07-05 | 2018-08-22 | GlaxoSmithKline Consumer Healthcare UK IP Ltd | Novel composition |
KR20210138671A (en) * | 2019-04-29 | 2021-11-19 | 히데토시 니시오 | how to whiten teeth |
CN110946319A (en) * | 2019-11-20 | 2020-04-03 | 许达勇 | Nicotine propellant and preparation method thereof |
CN110859765A (en) * | 2019-12-17 | 2020-03-06 | 北京天一恒康医疗器械有限公司 | Fluorinated foam for preventing dental caries |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4568540A (en) * | 1984-04-18 | 1986-02-04 | Johnson & Johnson | Oral hygiene compositions |
US5071637A (en) * | 1989-10-06 | 1991-12-10 | Pellico Michael A | Foamable fluoride compositions and method |
US5073363A (en) * | 1989-10-06 | 1991-12-17 | Pellico Michael A | Foamable fluoride gels and method |
WO2001076533A1 (en) * | 2000-04-05 | 2001-10-18 | Colgate-Palmolive Company | Foamable dental fluoride composition |
Family Cites Families (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2747092C2 (en) | 1977-10-20 | 1984-01-05 | Württembergische Parfümerie - Fabrik GmbH, 7332 Eislingen | Dentifrices containing dyes |
US4383987A (en) * | 1981-06-26 | 1983-05-17 | Colgate/Palmolive Company | Foaming dentifrice containing nonionic surface active agent |
US4528182A (en) * | 1983-07-13 | 1985-07-09 | Colgate-Palmolive Company | Stable antiplaque dentifrice with improved foaming |
US4770634A (en) | 1986-06-11 | 1988-09-13 | Pellico Michael A | Method for treating teeth with foamable fluoride compositions |
US4828849A (en) | 1988-01-14 | 1989-05-09 | Warner-Lambert Company | Surfactant inhibition of dental plaque |
US5180577A (en) | 1990-10-09 | 1993-01-19 | Colgate-Palmolive | Stabilized bis biguanide/anionic active ingredient compositions |
CN1054504C (en) | 1993-03-15 | 2000-07-19 | 科尔加特·帕尔莫利弗公司 | Antibacterial antiplaque oral composition |
US5624906A (en) * | 1994-12-08 | 1997-04-29 | Lever Brothers Company, Division Of Conopco, Inc. | Oral hygiene compositions comprising heteroatom containing alkyl aldonamide compounds |
US5599526A (en) | 1995-06-01 | 1997-02-04 | Viscio; David B. | Visually clear gel dentifrice |
US5824289A (en) | 1996-03-05 | 1998-10-20 | Sultan Dental Products | Dental fluoride foam |
JPH1087456A (en) | 1996-09-11 | 1998-04-07 | Sunstar Inc | Non-aerosol type foamy composition for oral cavity |
JPH10139643A (en) | 1996-09-14 | 1998-05-26 | Sunstar Inc | Oral cavity composition |
JPH10114637A (en) | 1996-10-12 | 1998-05-06 | Sunstar Inc | Non-aerosol type foam oral cavity composition |
JPH10114636A (en) | 1996-10-12 | 1998-05-06 | Sunstar Inc | Non-aerosol type foam oral cavity composition |
JP3618205B2 (en) | 1997-10-09 | 2005-02-09 | サンスター株式会社 | Foam-type fluorine coating agent |
US6142338A (en) | 1998-12-16 | 2000-11-07 | Pellicano; Joseph J. | Foamer and process for dispensing non-aerosol fluoride foam |
JP2000281156A (en) | 1999-03-31 | 2000-10-10 | Koike Kagaku Kk | Aerosol container |
US6415800B2 (en) | 2000-01-14 | 2002-07-09 | The Gillette Company | Method of shaving and a dispensing apparatus therefor |
EP1284911B1 (en) | 2000-05-19 | 2006-11-15 | The Gillette Company | System for dispensing multi-component products |
US7186416B2 (en) * | 2003-05-28 | 2007-03-06 | Stiefel Laboratories, Inc. | Foamable pharmaceutical compositions and methods for treating a disorder |
US20040247534A1 (en) * | 2003-06-06 | 2004-12-09 | Sultan Dental Products, Ltd | Foamable fluoride gel compositions and methods of treatment using the same |
AU2005304373B2 (en) | 2004-11-09 | 2011-05-26 | Discus Dental, Llc. | Dental whitening systems comprising transition metal salt activator |
JP4996845B2 (en) | 2005-11-14 | 2012-08-08 | サンスター株式会社 | Foam-type fluorine coating agent |
-
2007
- 2007-10-01 US US11/865,457 patent/US8802060B2/en active Active
-
2008
- 2008-09-29 CN CN200880110003.3A patent/CN101815499B/en not_active Expired - Fee Related
- 2008-09-29 EP EP08834922A patent/EP2194959B1/en not_active Not-in-force
- 2008-09-29 JP JP2010528050A patent/JP5705542B2/en not_active Expired - Fee Related
- 2008-09-29 BR BRPI0817913A patent/BRPI0817913B1/en not_active IP Right Cessation
- 2008-09-29 WO PCT/US2008/078091 patent/WO2009045949A2/en active Application Filing
- 2008-09-29 AT AT08834922T patent/ATE547093T1/en active
- 2008-09-29 MY MYPI2010001218A patent/MY153728A/en unknown
- 2008-09-29 DK DK08834922.0T patent/DK2194959T3/en active
- 2008-09-29 PL PL08834922T patent/PL2194959T3/en unknown
- 2008-09-29 MX MX2010003135A patent/MX2010003135A/en active IP Right Grant
- 2008-09-29 CA CA2700540A patent/CA2700540C/en not_active Expired - Fee Related
- 2008-09-29 ES ES08834922T patent/ES2383038T3/en active Active
- 2008-09-29 AU AU2008308948A patent/AU2008308948B2/en not_active Ceased
- 2008-09-29 RU RU2010117170/15A patent/RU2442562C2/en not_active IP Right Cessation
- 2008-09-30 AR ARP080104276A patent/AR068598A1/en unknown
- 2008-09-30 TW TW097137437A patent/TWI411445B/en not_active IP Right Cessation
-
2010
- 2010-03-29 ZA ZA2010/02224A patent/ZA201002224B/en unknown
- 2010-04-12 CO CO10041954A patent/CO6270242A2/en not_active Application Discontinuation
- 2010-10-25 HK HK10110016.7A patent/HK1143533A1/en not_active IP Right Cessation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4568540A (en) * | 1984-04-18 | 1986-02-04 | Johnson & Johnson | Oral hygiene compositions |
US5071637A (en) * | 1989-10-06 | 1991-12-10 | Pellico Michael A | Foamable fluoride compositions and method |
US5073363A (en) * | 1989-10-06 | 1991-12-17 | Pellico Michael A | Foamable fluoride gels and method |
WO2001076533A1 (en) * | 2000-04-05 | 2001-10-18 | Colgate-Palmolive Company | Foamable dental fluoride composition |
Also Published As
Publication number | Publication date |
---|---|
PL2194959T3 (en) | 2012-08-31 |
MX2010003135A (en) | 2010-04-07 |
WO2009045949A3 (en) | 2009-06-18 |
RU2010117170A (en) | 2011-11-10 |
AR068598A1 (en) | 2009-11-18 |
EP2194959A2 (en) | 2010-06-16 |
BRPI0817913B1 (en) | 2016-10-11 |
ES2383038T3 (en) | 2012-06-15 |
JP5705542B2 (en) | 2015-04-22 |
CA2700540C (en) | 2013-08-27 |
BRPI0817913A2 (en) | 2014-10-07 |
ATE547093T1 (en) | 2012-03-15 |
CO6270242A2 (en) | 2011-04-20 |
CA2700540A1 (en) | 2009-04-09 |
CN101815499B (en) | 2015-09-02 |
TWI411445B (en) | 2013-10-11 |
JP2010540645A (en) | 2010-12-24 |
US20090087391A1 (en) | 2009-04-02 |
RU2442562C2 (en) | 2012-02-20 |
TW200920409A (en) | 2009-05-16 |
EP2194959B1 (en) | 2012-02-29 |
HK1143533A1 (en) | 2011-01-07 |
ZA201002224B (en) | 2013-03-27 |
AU2008308948A1 (en) | 2009-04-09 |
AU2008308948B2 (en) | 2012-07-05 |
US8802060B2 (en) | 2014-08-12 |
DK2194959T3 (en) | 2012-06-25 |
MY153728A (en) | 2015-03-13 |
CN101815499A (en) | 2010-08-25 |
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