Patent Application
20150297477
This invention relates to an oral care composition comprising a fluoride ion source and a buffer. This invention also relates to a method of providing fluoride to the oral cavity of a mammal. The invention further relates to a method of treating or preventing a disease or condition of the oral cavity of a mammal. The invention further relates to the use of a buffer for controlling the pH of an oral care composition comprising fluoride.
It is commonly accepted that fluoride anti caries efficacy is related to the prior formation of a CaF2 depot (ideally in form of a layer) on the enamel surface (Rølla G., ACTA ODONTOL SCAND 46 (1988)). For efficient formation of CaF2, conditions need to be slightly acidic since under neutral pH conditions, calcium phosphates form more readily than CaF2 even with the little phosphate that is available in saliva. Due to the relatively high buffer capacity of saliva (a consequence of the high level of carbonate ions), intra oral pH conditions are rarely kept at the advantageous slightly acidic level for the entire duration of product application.
Fluoride can be provided by oral care products. The majority of oral care products are formulated at neutral pH. Therefore, they do not effectively form CaF2 layers and there is poor fluoride uptake onto the enamel surface of the teeth. A few oral care products are formulated at a slightly acidic pH, but do not maintain the intra oral pH at the desired level during application of the oral care product.
EP0691124 discloses attempts to increase fluoride uptake by adding polymers to an oral care composition. A copolymer of N-vinylpyrrolidone and acrylic acid is used to improve the bioadhesion of bactericidal compounds and/or to provide an enhanced fluoride uptake.
It would be desirable to improve the fluoride uptake from fluoride-containing oral care products. It has now surprisingly been found that fluoride uptake from oral care products can be increased by providing an oral care composition comprising a buffer that can counteract the buffering effect of saliva and hold the pH of the oral care composition at the slightly acidic level necessary to ensure formation of CaF2 layers. The buffer is able to buffer the oral care composition at the desired pH and also yield a stable product.
According to a first aspect of the present invention there is provided an oral care composition comprising an orally acceptable vehicle, a fluoride ion source and a buffer having a pKa of less than 7.0 wherein the pH of the oral composition is greater than 3.5 and less than 5.0, and wherein the oral composition has an acid number greater than or equal to 4.5.
Optionally, the buffer is selected from α-hydroxy acids, dicarboxylic acids, phosphoric acid, amino acids, diphosphoric acid, salts of α-hydroxy acids, salts of dicarboxylic acids, salts of phosphoric acid, salts of amino acids, salts of diphosphoric acid and combinations thereof. Optionally, the buffer may be selected from succinic acid, tartaric acid, malic acid, fumaric acid, glutamic acid, lactic acid, suberic acid, adipic acid, sebacic acid, glutaric acid, azelaic acid, salts of succinic acid, salts of tartaric acid, salts of malic acid, salts of fumaric acid, salts of glutamic acid, salts of lactic acid, salts of suberic acid, salts of adipic acid, salts of sebacic acid, salts of glutaric acid, salts of azelaic acid and combinations thereof. Preferably the buffer is selected from fumaric acid, salts of fumaric acid, malic acid, salts of malic acid, succinic acid, salts of succinic acid and combinations thereof. The buffer may be a mixture of any one or any combination of these acid and salts. Optionally the buffer comprises an aqueous solution of an acid and a salt.
Optionally the buffer comprises an aqueous solution of an acid and a salt of the acid, and the ratio of acid:salt is from 2:1 to 1:2. Optionally, the buffer comprises an aqueous solution of an acid and a salt of the acid, and the ratio of acid:salt is from 1.5:1 to 1:1.5. In one embodiment the ratio of acid:salt is 1:1.
Optionally, the buffer is present at a level from 0.05 to 5.00 weight % or 0.1 to 3.00 weight % based on the total weight of the composition. Further optionally, the buffer is present at a level from 0.50 to 2.00% weight % based on the total weight of the composition. In one embodiment, the buffer is present at a level of 0.7 to 1.8 weight %. In another embodiment, the buffer is present at a level of 1.4 to 1.6 weight %.
Optionally, the fluoride ion is selected from sodium fluoride, potassium fluoride, stannous fluoride, amine fluoride and combinations thereof. Optionally the fluoride ion is present at a level from 100 ppm to 10000 ppm. Further optionally, the fluoride ion is present a level from 150 ppm to 2000 ppm, 150 ppm to 1800 ppm or 150 to 1500 ppm. Further optionally, the fluoride ion is present at a level of 250 ppm to 2000 ppm, 250 ppm to 1800 ppm or 250 ppm to 1500 ppm.
Optionally the pH of the oral composition is greater than or equal to 3.5. Further optionally, the pH of the oral composition is from 4.2 to 4.8, from 4.3 to 4.7, from 4.4 to 4.7 or from 4.4 to 4.6. Optionally the pH of the composition is 4.5.
Optionally, the buffer has a pKa from 2.5 to 6.0. Further optionally the buffer has a pKa from 3.5 to 5.6, from 4.0 to 5.6 or from 4.2 to 5.6.
Optionally the oral composition has an acid number greater than or equal to 4.5. Optionally the acid number is greater than or equal to 6.0, 6.45, 7.0, 8.0, 9.0 or 10.0. Optionally the acid number is less than 25 or further optionally less than 18.
Optionally the oral composition is a dentifrice, toothpaste, mouthrinse, mouthwash, strip or a solid or liquid gel. Preferably the oral composition is a dentifrice or mouthrinse.
Optionally the buffer is selected from an aqueous solution of succinic acid and the sodium or potassium salt of succinic acid, an aqueous solution of tartaric acid and the sodium or potassium salt of tartaric acid, an aqueous solution of malic acid and the sodium or potassium salt of malic acid, an aqueous solution of fumaric acid and the sodium or potassium salt of fumaric acid, an aqueous solution of glutamic acid and the sodium or potassium salt of glutamic acid, an aqueous solution of lactic acid and the sodium or potassium salt of lactic acid, an aqueous solution of suberic acid and the sodium or potassium salt of suberic acid, an aqueous solution of adipic acid and the sodium or potassium salt of adipic acid, an aqueous solution of sebacic acid and the sodium or potassium salt of sebacic acid, an aqueous solution of glutaric acid and the sodium or potassium salt of glutaric acid and an aqueous solution of azelaic acid and the sodium or potassium salt of azelaic acid and combinations thereof; the buffer is present at a level from 0.05 to 5.00 weight % based on the total weight of the composition; the pH of the composition is from 4.2 to 4.8 and the oral care composition has an acid number greater than or equal to 6.0.
According to a further aspect of the invention there is provided a method of providing fluoride ions to the oral cavity of a mammal comprising contacting a composition according to the invention with the oral cavity.
According to a further aspect of the invention there is provided a method of treating or preventing a disease or condition of the oral cavity of a mammal comprising applying a composition according to the invention to the oral cavity.
According to a further aspect of the invention there is provided a method of decreasing dental cavity formation in mammalian teeth comprising applying a composition according to the invention to the oral cavity of a mammal.
According to a further aspect of the invention there is provided a method of re-mineralizing teeth in a mammal comprising applying a composition according to the invention to the oral cavity of a mammal.
According to a further aspect of the invention there is provided a composition according to the invention for use in a method of providing fluoride ions to the oral cavity of a mammal.
According to a further aspect of the invention there is provided a composition according to the invention for use in a method of treating or preventing a disease or condition of the oral cavity of a mammal.
According to a further aspect of the invention there is provided a composition according to the invention for use in a method of decreasing dental cavity formation in mammalian teeth.
According to a further aspect of the invention there is provided a composition according to the invention for use in a method of re-mineralizing mammalian teeth.
According to a further aspect of the invention there is provided use of a buffer having a pKa of less than 7.0 for controlling the pH of an oral care composition comprising a fluoride ion source, the buffer controlling the pH of the composition such that the pH is greater than 3.5 and less than 5.0 and buffering the composition such that the oral care composition has an acid number greater than or equal to 4.5.
According to a further aspect of the invention there is also provided an oral care composition comprising an orally acceptable vehicle, a fluoride ion source and a buffer having a pKa of less than 7.0 wherein the pH of the oral composition is greater than 3.5 and less than 5.0, and wherein the oral composition has an acid number greater than or equal to 4.5 wherein the buffer controls the pH of the composition to be greater than 3.5 and less than 5.0, and buffers the composition such that the oral care composition has an acid number greater than or equal to 4.5.
The compositions may contain additional therapeutic and non-therapeutic components.
This invention is predicated on the finding by the present inventors that in oral care compositions comprising fluoride, fluoride uptake from the oral care composition can be increased by including a buffer in the oral care composition to maintain the intra oral pH at a slightly acidic level during application of the oral care composition.
The features and benefits of the invention are illustrated by reference to the preferred embodiments. Accordingly, the invention expressly should not be limited to such preferred embodiments illustrating some possible non-limiting combination of features that may exist alone or in other combinations of features. It should be understood that the detailed description and specific examples, while indicating embodiments of the invention, are intended for purposes of illustration only and are not intended to limit the scope of the invention.
As referred to herein, all compositional percentages are by weight of the total composition, unless otherwise specified.
The dentifrice composition according to the invention comprises an orally acceptable vehicle. As used herein, an “orally acceptable vehicle” refers to a material or combination of materials that are safe for use in the compositions of the invention, commensurate with a reasonable benefit/risk ratio.
The composition may contain any conventional excipients or carriers, although these will vary depending on the dosage form or means of dosage selected. Excipients or carriers can include, for example, humectants, glycerin, sorbitol, xylitol, and/or propylene glycol, water or other solvents.
Surfactants may be included, if desired. Examples of suitable surfactants include water-soluble salts of higher fatty acid monoglyceride monosulfates, such as the sodium salt of monosulfated monoglyceride of hydrogenated coconut oil fatty acids; higher alkyl sulfates such as sodium lauryl sulfate; alkyl aryl sulfonates such as sodium dodecyl benzene sulfonate; higher alkyl sulfoacetates, such as sodium lauryl sulfoacetate; higher fatty acid esters of 1,2-dihydroxypropane sulfonate; and the substantially saturated higher aliphatic acyl amides of lower aliphatic amino carboxylic compounds, such as those having 12-16 carbons in the fatty acid, alkyl or acyl radicals; and the like. Examples of the last mentioned amides include N-lauryl sarcosine, and the sodium, potassium and ethanolarmine salts of N-lauryl, N-myristoyl, or N-palmitoyl sarcosine. Others include, for example, nonanionic polyoxyethylene surfactants, such as Polyoxamer 407, Steareth 30, Polysorbate 20, and castor oil; and amphoteric surfactants, such as cocamidopropyl betaine (tegobaine), and cocamidopropyl betaine lauryl glucoside; condensation products of ethylene oxide with various hydrogen containing compounds that are reactive therewith and have long hydrocarbon chains (e.g., aliphatic chains of from 12 to 20 carbon atoms), which condensation products (ethoxamers) contain hydrophilic polyoxyethylene moieties, such as condensation products of poly (ethylene oxide) with fatty acids, fatty alcohols, fatty amides and other fatty moieties, and with propylene oxide and polypropylene oxides.
In an embodiment, the oral composition includes a surfactant system that is sodium lauryl sulfate (SLS). Optionally, the orally acceptable vehicle comprises sorbitol which is present in an amount of from 10 to 25 wt % based on the weight of the composition, further optionally from 12 to 18 wt % based on the weight of the composition.
Any orally acceptable particulated fluoride ion can be used, including potassium, sodium and ammonium fluorides and monofluorophosphates, stannous fluoride, indium fluoride, amine fluorides such as olaflur (N′-octadecyltrimethylendiamine-N,N,N′-tris(2-ethanol)-dihydrofluoride), and mixtures thereof. One or more fluoride ions are optionally present in an amount providing a clinically efficacious amount of soluble fluoride ion to the oral composition. Optionally the fluoride ion is present at a level from 100 ppm to 10000 ppm based on the total weight of the composition. Further optionally, the fluoride ion is present a level from 150 ppm to 2000 ppm, 150 ppm to 1800 ppm or 150 to 1500 ppm. Further optionally, the fluoride ion is present at a level of 250 ppm to 2000 ppm, 250 ppm to 1800 ppm or 250 ppm to 1500 ppm.
Optionally, the toothpaste composition further comprises sodium monofluorophosphate in an amount of from 0.75 to 1.5 wt % based on the weight of the composition.
A buffer in an aqueous solution of a weak acid and its conjugate base or a weak base and its conjugate acid. Buffer solutions maintain the pH of a solution by means of the equilibrium between the acid and its conjugate base (or the base and its conjugate acid).
The pKa value of an acid is a measure of the strength of an acid in solution. The Ka or acid dissociation constant (also known as the acidity constant or acid-ionization constant) is the equilibrium constant for the dissociation of an acid (HA) into its conjugate base (A−) and a proton (H+). The pKa is the logarithmic measure and is equal to −log10 Ka. Polyprotic acids that can lose more than proton can have successive pKa dissociation values for dissociation of successive protons. The pKa of an acid can be determined by titration. The pKa is determined at 25° C. unless otherwise stated. Apart from the required acid-base properties the buffer needs to be sufficiently soluble in the oral care formula backbone. Acids that are rather poorly soluble as a free acid but readily soluble in the form of an alkali salt form a reservoir of acid that is not in solution and is thus behaving neutral on taste. It is, however, available for buffering. While buffering takes place during the intra oral application of the product the acid solubilizes at the same rate as the protons are consumed by saliva. Since the concentration of free solubilized acid remains small during that process the influence on taste is minimal. Fumaric acid is an acid that works according to the mechanism described.
The acid number is a measure quantifying the buffering capacity of a product. The acid number or acid value expresses in milligrams the quantity of potassium hydroxide needed to neutralise the free acids present in 1 g of the product. The determination can be carried out e.g. by an adaptation of the method according to the protocol described in the European Pharmacopoeia 7.0 section 2.5.1. dissolving samples in water instead of ethanol/petroleum ether; and monitoring the end point with a pH electrode instead of with phenolphthalein indicator.
Sample preparation: Weigh sample in a 150 ml beaker. The amount of sample depends on the expected acid value. As a guideline use approximately 5.0 g for toothpaste or gels or approximately 10 mL to 20 mL for mouth rinses. Add 50 mL of water pH 9 prepared previously and stir the sample until it's completely dissolved or until the resulting suspension is homogeneous. Titrate slowly and under stirring the sample solution using a 0.1N potassium hydroxide solution. End point of the titration is reached, when the pH of the solution is exactly 9.00 and it remains stable for at least 15 seconds (the drift should be less than 0.1 pH units/minute, or less than 0.025 pH units during 15 seconds). Calculation of the acid value is done as described above. This parameter yields the amount of protons neutralized but does not provide information on the pH at which buffering occurs. A product can have a high acid number but would do little to keep the pH constant at a particular pH of interest. Therefore the buffer substance must additionally have a pKa close to the desired pH that is to be kept constant. Ideally, the pKa of the buffer is within the range of the desired pH±1. The acid number of the oral composition is at least greater than or equal to 4.5. Optionally, the acid number is greater than or equal to 6.0. Optionally the acid number is greater than or equal to 6.45, 7.0, 8.0, 9.0 or 10.0. Optionally the acid number is less than 25 or further optionally less than 18.
pH
In order to increase the fluoride uptake from the composition, the compositions of the present invention are buffered to maintain the pH at a slightly acidic level. By “slightly acidic” it is meant that the oral composition has a pH of less than 7.0 but greater than 3.5. An example of a pH that is considered slightly acidic is a pH of from 3.5 to 6.0 or from 4.0 to 6.0, or from 3.5 to 5.0 or from 4.0 to 5.0. A pH of 4.5 is considered to be slightly acidic in the context of this invention. Measurement of the pH can be carried by a procedure based on the method described in the European Pharmacopoeia 7.0, section 2.2.36. The fluoride concentration is measured at a constant ionic strength by using a fluoride selective electrode, Constant ionic strength in the measuring solution is ensured by the use of a TISAB (total ionic strength adjustment buffer). Fluoride is always measured as ionic fluoride (F−). Analysis is performed by measuring the difference in electrical potential of fluoride selective (ISE) and reference electrode immersed in the measuring solution.
Sample preparation for toothpaste: Weigh a sample of approximately 200 mg to the nearest 0.1 milligram on the bottom of a 50 mL plastic beaker and add exactly 20.0 mL deionized water. Let stir for 5 minutes or until the sample is completely dissolved and the resulting suspension is homogeneous. Proceed to measurement of the pH as described above.
Sample preparation for mouthrinse: Weigh a sample of approximately 1000 mg to the nearest milligram in a 50 mL plastic beaker and add 19.0 mL deionized water. Stir until the sample solution is homogenous. Proceed to measurement of the pH as described above.
Optionally the pH of the oral composition is greater than 4.0. Further optionally, the pH of the oral composition is from 4.2 to 4.8. Further optionally, the pH of the oral composition is 4.5.
The compositions of the invention may optionally comprise an additional orally acceptable thickening agent, selected from one or more of, without limitation, silica, polyvinyl pyrrolidone, which may be linear or cross-linked, carbomers, also known as carboxyvinyl polymers, carrageenans, also known as Irish moss and more particularly -carrageenan (iota-carrageenan), high molecular weight polyethylene glycols (such as CARBOWAX®, available from The Dow Chemical Company), cellulosic polymers such as hydroxyethylcellulose, carboxymethylcellulose (CMC) and salts thereof, e.g., CMC sodium, natural gums such as karaya, xanthan gum, gum arabic and tragacanth, and colloidal magnesium aluminum silicate and mixtures of the same.
The cellulose polymer may be selected from one or more of hydroxypropylmethyl cellulose (HPMC), hydroxyethylpropyl cellulose (HEPC), hydroxybutylmethyl cellulose (HBMC), and carboxymethyl cellulose (CMC).
Optionally, such additional thickening agents are present in a total amount of 0.1 wt % to 50 wt %, for example 0.1 wt % to 35 wt % or 1 wt % to 15 wt %, based on the weight of the composition.
The compositions of the invention may also include a polymeric adherent material that attaches to the surface of a mammalian tooth and/or to the heterogeneous biofilm which also may be present on a tooth's surface. Attachment may occur by any means, such as ionic interaction, van der Waals forces, hydrophobic-hydrophilic interactions, etc. The adherent material may be, for example, any homopolymers or copolymers (hereinafter referred to collectively as a “polymers”) that adhere to the surface of a tooth. For example, the composition may additionally include poly (ethylene oxide) polymers (such as POLYOX from Dow Chemical), linear PVP and cross-linked PVP, PEG/PPG copolymers (such as BASF Pluracare L1220), ethylene oxide (EO)-propylene oxide (PO) block copolymers (such as polymers sold under the trade mark Pluronic available from BASF Corporation), ester gum, shellac, pressure sensitive silicone adhesives (such as BioPSA from Dow-Corning), methacrylates, or mixtures thereof. In an embodiment, a copolymer comprises (PVM/MA). In an embodiment, a copolymer comprises poly (methylvinylether/maleic anhydride). In another embodiment, a copolymer comprises poly (methylvinylether/maleic acid). In another embodiment, a copolymer comprises poly (methylvinylether/maleic acid) half esters. In another embodiment, a copolymer comprises poly (methylvinylether/maleic acid) mixed salts.
In some embodiments, the composition further comprises polymer thickeners selected from (i) polyethylene glycol, (ii) polyethylene glycol-polypropylene glycol block co-polymers having a molecular weight of at least 5000, and (iii) combinations thereof. In some embodiments, the composition comprises an ethylene oxide, propylene oxide block co-polymer of formula (ethylene oxide)x-(propylene oxide)y wherein x is an integer of 80-150, e.g. 100-130, e.g. 118, and y is an integer 30-80, e.g. 60-70, e.g. 66, having an average molecular weight of greater than 5000, e.g., 8000-13000 Da, e.g. 9800;
In some embodiments, the composition comprises an ethylene oxide, propylene oxide block co-polymer of average molecular weight greater than 5000 Da, being substantially free of an ethylene oxide, propylene oxide block co-polymer of average molecular weight less than 5000 Da. Optionally, the ethylene oxide, propylene oxide block co-polymer is present in an amount of from 5 wt % to 10 wt % based on the weight of the composition. Block copolymers of ethylene oxide/propylene oxide are useful, but higher molecular weight, e.g., >5000 Da are preferred, e.g. including PLURACARE® L1220 (available from BASF, Wyandotte, Mich., United States of America). In some embodiments, the composition further comprises polyethylene glycol of average molecular weight 400 to 800 Da, e.g., 600 Da. Low or medium molecular weight polyethylene glycol, e.g., PEG 400, PEG 600, PEG 800, PEG 1000 and mixtures thereof are useful in the compositions of some embodiments of the invention. Further optionally, the polyethylene glycol may be present in an amount of from 5 wt % to 15 wt % based on the weight of the composition.
Polymers of any molecular weight may be used, including, for example molecular weights of 50,000 to 500,000, 500,000 to 2,500,000 or 2,500,000 to Ser. No. 10/000,000 (calculated by either number average or weight average). Commercially-available polymers may be used in the present invention. It is understood that over time, the exact size, weight and/or composition of a commercially-available polymer may change. Based on the disclosure set forth herein, the skilled artisan will understand how to determine whether such polymers are useful in the invention.
Some embodiments may further comprise an abrasive. Optionally, the oral care compositions may comprise from 5 to 15 wt % abrasive based on the weight of the composition. Where abrasives are present, the average particle size is generally 0.1 to 30 microns, for example 1 to 20 or 5 to 15 microns.
The abrasive may comprise a calcium abrasive, such as a calcium phosphate salt, (e.g., calcium pyrophosphate, dicalcium orthophosphate dihydrate, tricalcium phosphate, calcium pyrophosphate), calcium sulfate and/or calcium polymetaphosphate. The oral composition may comprise abrasive particulates selected from sodium bicarbonate, silica, iron oxide, aluminium oxide, perlite, plastic particles, e.g., polyethylene, and combinations thereof. Any type of silica may be used, such as hydrated silica, precipitated silica or silica gel. Optionally, the composition may comprise, as a thickener and also as an abrasive, silica particles in an amount of from 1 to 3 wt % based on the weight of the composition. In a typical embodiment, the calcium abrasive comprises calcium pyrophosphate. In another embodiment, the calcium abrasive comprises calcium carbonate. Optionally, the composition is a toothpaste comprising a calcium pyrophosphate abrasive. Further optionally, the calcium pyrophosphate is present in an amount of from 10 wt % to 20 wt % based on the weight of the composition.
The compositions may comprise silica that has a particle size and an amount and distribution in the composition so that the silica has a dual function, and functions not only as a dentin tubule-occluding particulate but also as an abrasive particulate. Such a dual function particulate may be provided by a commercially available silica such as INEOS AC43, available in commerce from Ineos Silicas, Warrington, United Kingdom. In an embodiment, such silica has a median particle size less than 8 μm, for example from 3 μm to 5 m.
The compositions of the present invention may further comprise an abrasive useful for example as a polishing agent. Any orally acceptable abrasive can be used, but type, fineness, (particle size) and amount of abrasive should be selected so that tooth enamel is not excessively abraded in normal use of the composition. Suitable abrasives include silica, for example in the form of precipitated silica or as admixed with alumina, insoluble phosphates, and mixtures thereof. Among insoluble phosphates useful as abrasives are orthophosphates, polymetaphosphates and pyrophosphates. Illustrative examples are dicalcium orthophosphate dihydrate, calcium pyrophosphate, calcium pyrophosphate, tricalcium phosphate, calcium polymetaphosphate and insoluble sodium polymetaphosphate.
In an embodiment, the abrasive particles may be initially present in the toothpaste composition having the desired particle size, or may be initially present in the composition at a larger size, so long as the structure of the particles is such that it fractures or breaks into the desired particle size upon application of mechanical force by, e.g., a toothbrush, when brushing.
Flavorants, sweeteners, colorants, foam modulators, mouth-feel agents and others additively may be included if desired, in the composition. These may be included in any combination of one or more additional ingredients.
The compositions of the present invention may comprise a surface active agent (surfactant). Suitable surfactants include without limitation water-soluble salts of C8-20alkyl sulfates, sulfonated monoglycerides of C8-20 fatty acids, sarcosinates, taurates, sodium lauryl sulfate, sodium cocoyl monoglyceride sulfonate, sodium lauryl sarcosinate, sodium lauryl isoethionate, sodium laureth carboxylate and sodium dodecyl benzenesulfonate, and cocoamidopropyl betaine. In some embodiments, the composition may additionally comprise a surfactant, e.g., sodium lauryl sulfate (SLS).
The oral care composition may include any other therapeutic, cosmetic, and/or aesthetic materials as may be desired. Examples include desensitizing agents (e.g. a nitrate salt, an arginine ester, a bicarbonate salt, potassium nitrate, an arginine-bicarbonate-phytate complex, potassium citrate, and arginine, among others), a chemical whitening agent (such as a peroxide releasing compound), an opaque whitening agent (such as hydroxyapatite) and an anticalculus agent.
The composition according to the invention may also comprise one or more further agents typically selected from an anti-plaque agent, an anti-caries agent, a whitening agent, desensitizing agent, antimicrobial agent, antibacterial agent, cleaning agent, a flavouring agent, a sweetening agent, adhesion agents, viscosity modifiers, diluents, surfactants, foam modulators, emulsifiers, abrasives, pH modifying agents, humectants, mouth feel agents, colorants, preservatives, tartar control (anticalculus) agent, saliva stimulating agent, nutrient and combinations thereof.
The humectants may be selected from for example glycerin, propylene glycol or a combination thereof. In some embodiments, the oral care composition comprises from 20 to 60 wt % humectant based on the weight of the composition. In some embodiments, the composition comprises propylene glycol in an amount of from 10 wt % to 20 wt % based on the weight of the composition. In some embodiments, the composition comprises glycerin in an amount of from 25 wt % to 40 wt % based on the weight of the composition.
Suitable anticalculus agents include without limitation phosphates and polyphosphates (for example pyrophosphates), polyaminopropanesulfonic acid (AMPS), hexametaphosphate salts, zinc citrate trihydrate, polypeptides, polyolefin sulfonates, polyolefin phosphates, diphosphonates. Typically, the anticalculus agent is present at 0.1 wt % to 30 wt % based on the weight of the composition. The oral composition may include a mixture of different anticalculus agents. In some embodiments, the composition additionally comprises a tartar control agent, e.g., selected from tetrasodium pyrophosphate (TSPP) and sodium tripolyphosphate (STPP). In one embodiment, tetrasodium pyrophosphate (TSPP) and sodium tripolyphosphate (STPP) are used. The anticalculus agent comprises TSPP at 1-2 wt % and STPP at 7 wt % to 10 wt %, each based on the weight of the composition.
The compositions may include a stannous ion or a stannous ion source. Suitable stannous ion sources include without limitation stannous fluoride, other stannous halides such as stannous chloride dihydrate, stannous pyrophosphate, organic stannous carboxylate salts such as stannous formate, acetate, gluconate, lactate, tartrate, oxalate, malonate and citrate, stannous ethylene glyoxide and the like. One or more stannous ion sources are optionally and illustratively present in a total amount of 0.01% to 10 wt %, for example 0.1 wt % to 7 wt % or 1 wt % to 5 wt %, each based on the weight of the composition.
In some embodiments, the compositions of the invention optionally comprise an antimicrobial (e.g., antibacterial) agent, e.g., triclosan. A further illustrative list of useful antibacterial agents is provided in such as those listed in U.S. Pat. No. 5,776,435 to Gaffar et al., the contents of which are incorporated herein by reference. One or more antimicrobial agents are optionally present in an antimicrobial effective total amount, typically 0.05 wt % to 10 wt %, for example 0.1 wt % to 3 wt %, each based on the weight of the composition.
In some embodiments, the compositions of the invention optionally comprise an antioxidant. Any orally acceptable antioxidant can be used, including butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), vitamin A, carotenoids, vitamin E, flavonoids, polyphenols, ascorbic acid, herbal antioxidants, chlorophyll, melatonin, and mixtures thereof.
The compositions of the invention may optionally comprise a sialagogue or saliva-stimulating agent, an antiplaque agent, an anti-inflammatory agent, and/or a desensitizing agent.
It is preferred that the when the oral care composition is a dentifrice, the vehicle ingredients in particular provide a dentifrice with a viscosity of 10,000 CPS to 700,000 CPS, preferably 30,000 CPS to 300,000 CPS.
Colorants may be used in a single phase toothpaste or a two-phase toothpaste for forming a striped toothpaste. Such colorants may be selected from pigments, dyes, lakes and agents imparting a particular luster or reflectivity such as pearling agents. In various embodiments, 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 FD&C dyes and pigments, talc, mica, magnesium carbonate, magnesium silicate, silica, titanium dioxide, zinc oxide, red, yellow, brown and black iron oxides, ferric ammonium ferrocyanide, manganese violet, ultramarine, titanated mica, bismuth oxychioride, and mixtures thereof. One or more colorants are optionally present in a total amount of 0.001% to 20%, for example 0.01% to 10% or 0.1% to 5%.
Optionally, the toothpaste composition further comprises titanium dioxide in an amount of from 0.05 to 0.15 wt % based on the weight of the composition. Such titanium dioxide addition has been found to whiten the slightly yellowish appearance of the toothpaste caused by the addition of the guar gum binder.
While ingredients are sometimes identified herein by category, e.g., humectant, antioxidant, thickener, etc., this identification is for convenience and clarity, but is not intended to be limiting. All of the ingredients in the compositions may have functions in addition to their primary function, and may contribute to the overall properties of the composition, including its stability, efficacy, consistency, mouthfeel, taste, odor and so forth.
It is understood that while general attributes of each of the above categories of materials may differ, there may be some common attributes and any given material may serve multiple purposes within two or more of such categories of materials. Preferably, the carrier is selected for compatibility with other ingredients of the composition.
The toothpaste composition of the invention may be prepared by any means known in the art.
Toothpaste formulation based on a silica base were prepared by using various concentrations of 1:1 buffer solutions prepared from the acids and their sodium/potassium salts. The acid/salt mixtures have been employed at levels from 0.5% to 2.00% total buffer concentration in the final formulation. The yielding toothpaste met all the stability criteria after accelerated aging from 6 months at 40° C.
The pastes have been submitted to Enamel Fluoride Uptake (EFU) testing according to FDA Method #40. This method determines the fluoride uptake into caries like subsurface lesions affected by an in vitro treatment of tooth specimen with slurries of toothpastes. The buffered recipes were referenced against toothpastes of identical formula but without the buffering substance. Formulations tested are in Table 1. Results are summarized in Table 2.
For all paste with additional buffer the fluoride uptake was significantly higher than for the respective controls. Also a dose effect for the amount of buffer used was observed.
Additionally, selected pastes were tested for the rermineralization potential. To do so, specimen derived from human teeth were initially demineralized (baseline) and then alternately exposed to an acid challenge (demineralization pH 5.00, 4 h daily) and a slurry of the toothpaste (remineralization, 4 treatments per day) for 20 days. Between acid exposure and treatments the specimens were stored in saliva. The degree of mineralization of the specimen was investigated by micro hardness measurements (VMH) and compared to the baseline. The higher the gain in hardness the more efficient the remineralization potential of the used product is. Again the pastes were referenced against paste of identical formula but without the buffering substance. Results are summarized in Table 3.
In all cases the hardness improvement was significantly higher than for the respective control toothpaste. The results are in accordance with the EFU data. The buffered toothpastes also show an increased remineralization potential compared to state of the art toothpastes.
It can be seen that pastes with increased buffer capacity lead to an improved fluoride uptake in caries-like lesions. Thus pastes according to the invention will have an increased anti-cavity effect compared to state of the art pastes.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2012/074286 | 12/3/2012 | WO | 00 |
