Oral composition

Abstract

To provide an oral cavity composition having an excellent balance between adhesion to a toothbrush and sharpness when squeezed out from a tube container. [Solution] The oral composition contains an abrasive and a binder, and when the tensile return forces in a 5 mm tensile test and a 10 mm tensile test are TF5 and TF10, respectively, the ratio of TF5 to TF10 (TF5 / TF10) is 1.1 or more and 10 or less, and the spinnability is 2 mm or more and less than 24 mm.

Description

[Technical field]

[0001] The present invention relates to an oral composition. [Background technology]

[0002] A technology for improving the ease of application of an oral composition to a toothbrush is described in Patent Document 1 (JP Patent Publication No. 2021-91654). The document describes a dentifrice composition containing one or more water-soluble polyvalent metal salts selected from water-soluble aluminum salts, water-soluble copper salts, and water-soluble zinc salts, xanthan gum, and a cationic polymer compound (Claim 1). According to the document, a dentifrice composition can be provided that has effects such as suppressing hypersensitivity, suppressing bad breath, and tightening gums due to the water-soluble polyvalent metal salt, and is easy to apply to a toothbrush because of its excellent moldability, and is also excellent in terms of dischargeability from a storage container even after storage because hardening over time is suppressed. This dentifrice composition can be formulated into a dentifrice composition that satisfactorily maintains the physical properties of the dentifrice composition, and that has a relatively small amount of abrasive or is free of abrasives, ensuring a gentle brushing experience with low irritation, and is particularly useful for suppressing hypersensitivity or bad breath and tightening gums (paragraph 0011). [Prior art documents] [Patent documents]

[0003] [Patent Document 1] Patent Publication No. 2021-91654 DISCLOSURE OF THEINVENTION [Problem to be solved by the invention]

[0004] The inventors' investigations have revealed that there is still room for improvement in the composition described in Patent Document 1 above in terms of improving adhesion to the toothbrush while also providing a desirable sharpness when squeezing the composition from the tube container.

[0005] The present invention provides an oral composition that has an excellent balance between adhesion to a toothbrush and ease of squeezing the composition out of a tube container. [Means for solving the problem]

[0006] According to the present invention, the following oral compositions are provided. [1] An oral composition comprising an abrasive and a binder, When the tensile return forces in a 5 mm tensile test and a 10 mm tensile test, which are measured by the following method 1, are designated as TF5 and TF10, respectively, the ratio of TF5 to TF10 (TF5 / TF10) is 1.1 or more and 10 or less, An oral composition having a stringiness of 2 mm or more and less than 24 mm as measured by the following method 2. (Method 1) Device name: Rheometer Jig used: Pressure / elasticity measuring pressure-sensitive shaft (Φ20mm) Measurement speed: 60mm / min Pull-up distance: 5mm or 10mm Filling container: 30mL plastic jar (diameter 43mm) Procedure: Fill the filling container with the oral composition until it is full, set it in the device, and then pull it up at the measurement speed. Measure the absolute value of the stress at each pull-up distance. Measure three times at each pull-up distance and use the average value as the TF5 or TF10. (Method 2) Device name: Rheometer Tool used: Pressure-sensitive shaft for measuring penetration (Φ15mm) Measurement speed: 1000mm / min Pulling distance: 50mm Filling container: 30mL plastic jar (diameter 43mm) Procedure: The oral composition is filled into the filling container until it is full, and after setting it in the device, it is pulled up at the measurement speed. The distance until the oral composition separates from the jig during pulling is measured. The average value of the pulling distance measured three times is regarded as the spinnability. [2] The oral composition described in [1], wherein the binder contains thickening silica. [3] The oral composition according to [1] or [2], wherein the binder comprises an organic binder. [4] The oral composition described in [3], wherein the organic binder is one or more selected from the group consisting of carboxymethylcellulose and its salts, xanthan gum, alginic acid and its salts, polyacrylic acid and its salts, carboxyvinyl polymers, hydroxyethyl cellulose, hydroxypropyl cellulose, pectin, tragacanth gum, gum arabic, guar gum, karaya gum, locust bean gum, gellan gum, tamarind gum, psyllium seed gum, polyvinyl alcohol, and carrageenan (excluding κ-carrageenan). [5] The oral composition described in any one of [1] to [4], wherein the abrasive contains abrasive silica. [6] An oral composition described in any one of [1] to [5], further comprising a humectant. [7] An oral composition described in any one of [1] to [6], which is a dentifrice composition. [8] An oral composition described in any one of [1] to [7], which is a toothpaste composition. [9] A dentifrice comprising the oral composition described in any one of [1] to [8] filled in a tube container.

[0007] Any combination of these configurations and conversion of the present invention between methods, devices, etc. are also valid aspects of the present invention. Effect of the Invention

[0008] According to the present invention, an oral composition can be obtained that has an excellent balance between adhesion to a toothbrush and sharpness when squeezed out of a tube container. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0009] Hereinafter, an embodiment of the present invention will be described. In this embodiment, the composition may contain each component alone or in combination of two or more kinds. In this specification, the symbol "to" indicating a numerical range means "greater than or equal to" or "less than or equal to," and both end numerical values ​​are included.

[0010] (Oral composition) In this embodiment, the oral composition contains an abrasive and a binder, and when the tensile return forces in a 5 mm tensile test and a 10 mm tensile test measured by the following method 1 are TF5 and TF10, respectively, the ratio of TF5 to TF10 (TF5 / TF10) is 1.1 to 10, and the stringiness measured by the following method 2 is 2 mm to less than 24 mm. (Method 1) Device name: Rheometer (e.g. CR-3000EX-S, manufactured by Sun Scientific Co., Ltd.) Jig used: Pressure / elasticity measuring pressure-sensitive shaft (Φ20mm) Measurement speed: 60mm / min Pull-up distance: 5mm or 10mm Filling container: 30mL plastic jar (diameter 43mm) Procedure: Fill the filling container with oral composition until it is full, set it in the device, and then pull it up at the measurement speed to measure the absolute value of the stress at each pull-up distance. The average value of three measurements at each pull-up distance is TF5 or TF10. In the procedure of Method 1, the numerical value of the stress during pulling is negative, so the recorded value is negative and the absolute value is positive.

[0011] (Method 2) Device name: Rheometer (e.g. CR-3000EX-S, manufactured by Sun Scientific Co., Ltd.) Tool used: Pressure-sensitive shaft for measuring penetration (Φ15mm) Measurement speed: 1000mm / min Pulling distance: 50mm Filling container: 30mL plastic jar (diameter 43mm) Procedure: Fill the filling container with the oral composition until it is full, set it in the device, and then pull it up at the measurement speed. Measure the distance until the oral composition separates from the jig while being pulled up. The average value of the three measurements up to the pulling distance is regarded as the stringiness.

[0012] Here, the measurement temperature in Measurement 1 and Measurement 2 is specifically room temperature (25° C.).

[0013] The present inventors have focused on the ingredients and physical properties as design guidelines for improving the balance between the adhesiveness of an oral composition to a toothbrush and the sharpness with which the oral composition can be squeezed out of a tube container when the oral composition is filled in the tube container. As a result, the inventors have newly discovered that by controlling the ingredients of the oral composition while controlling the tensile return force ratio (TF5 / TF10) and spinnability as indicators, it is possible to achieve a favorable balance between the good sharpness with which the oral composition filled in the tube container can be squeezed out of the tube container and excellent adhesiveness to a toothbrush. That is, in this embodiment, the oral composition contains a combination of an abrasive and a binder, and (TF5 / TF10) and spinnability are each within a specific range, so that the oral composition has an excellent balance between adhesion to a toothbrush and the sharpness when the oral composition filled in the tube container is squeezed out of the tube container. This also makes it possible to provide an oral composition that is excellent in ease of handling. For example, it is possible to reduce the oral composition falling off the toothbrush when the oral composition filled in the tube container is placed on the toothbrush, or adhesion to areas other than the desired area. It is also possible to suitably reduce dripping from the outlet when the oral composition filled in the tube container is squeezed out of the tube container. It is also possible to improve the handleability of the oral composition in the procedure from squeezing the dentifrice filled in the tube container onto the toothbrush to applying it to the oral cavity.

[0014] The ratio of the tensile return force TF5 in the 5 mm tensile test to the tensile return force TF10 in the 10 mm tensile test (TF5 / TF10) is 1.1 or more, preferably 1.15 or more, more preferably 1.2 or more, and even more preferably 1.25 or more, thereby improving the adhesion of the oral composition to the toothbrush. In addition, (TF5 / TF10) is not more than 10, preferably not more than 9, more preferably not more than 8, even more preferably not more than 7, and may be not more than 4. This makes it possible to obtain an oral composition whose discharge amount from a tube container can be easily controlled.

[0015] TF5 is preferably 1 gf or more, more preferably 5 gf or more, and further preferably 10 gf or more, thereby making it possible to obtain an oral composition that is less likely to spill from a tube or a toothbrush. Further, TF5 is preferably 100 gf or less, more preferably 75 gf or less, and further preferably 50 gf or less, whereby an oral composition that is easily separated from a tube container when squeezed can be obtained.

[0016] TF10 can be a value such that (TF5 / TF10) is in the above-mentioned range. TF10 may be, for example, 0.5 gf or more, and may be, for example, 50 gf or less.

[0017] The stringiness of the oral composition is 2 mm or more, more preferably 3 mm or more, and further preferably 5 mm or more, which can more stably improve the adhesion of the oral composition to a toothbrush. The spinnability of the oral composition is less than 24 mm, preferably 23 mm or less, more preferably 22 mm or less, and even more preferably 20 mm or less, thereby improving the sharpness of the oral composition.

[0018] Next, the components of the oral composition will be described. The oral composition includes an abrasive and a binder as described above.

[0019] (Abrasive) Examples of the abrasives include one or more selected from the group consisting of abrasive silica such as hydrous silicic acid (e.g., gel-processed silica, precipitated silica), anhydrous silicic acid, silica gel, and aluminosilicate; zeolites; calcium phosphate-based abrasives such as calcium hydrogen phosphate anhydrate, calcium hydrogen phosphate dihydrate, and calcium pyrophosphate; calcium carbonate-based abrasives such as calcium carbonate; and other inorganic abrasives such as aluminum hydroxide, alumina, magnesium carbonate, magnesium triphosphate, zirconium silicate, calcium triphosphate, hydroxyapatite, and calcium quaternary phosphate; and organic abrasives such as synthetic resin-based abrasives.

[0020] The abrasive preferably contains abrasive silica, more preferably contains hydrated silicic acid. It is also preferable that the abrasive contains anhydrous silicic acid. This makes it possible to more stably improve the balance between adhesion to the toothbrush and the sharpness when squeezed out of the tube container. The abrasive silica may be either crystalline silica or amorphous silica, or may be wet silica.

[0021] The average particle size of the abrasive silica is preferably 1 μm or more, more preferably 2 μm or more, even more preferably 3 μm or more, and even more preferably 5 μm or more, which can efficiently remove stains on the tooth surface. The average particle size of the abrasive silica is preferably 50 μm or less, more preferably 30 μm or less, and even more preferably 20 μm or less, thereby making it possible to obtain an oral composition that is smooth to the touch.

[0022] Here, the average particle size of the abrasive silica and the thickening silica described below is determined by measuring the particle size distribution of the particles on a volume basis using a commercially available laser diffraction / scattering type particle size distribution measuring device. 50 It can be said that:

[0023] It is also preferable that the abrasive is substantially free of calcium carbonate, which makes it possible to more stably improve the balance between adhesion to the toothbrush and sharpness when squeezed out of the tube container. Here, the oral composition not containing calcium carbonate specifically means that calcium carbonate is not intentionally blended into the oral composition, and more specifically means that the calcium carbonate content is 0.001 mass% or less based on the entire oral composition.

[0024] The content of the abrasive in the oral composition is preferably 5% by mass or more, more preferably more than 5% by mass, even more preferably more than 10% by mass, even more preferably more than 10% by mass, even more preferably more than 11% by mass, and even more preferably more than 13% by mass, based on the total amount of the oral composition. This allows for efficient removal of stains on the tooth surface. The content of the abrasive in the oral composition is preferably 30% by mass or less, more preferably less than 30% by mass, even more preferably 25% by mass or less, and even more preferably 20% by mass or less, based on the total amount of the oral composition. This makes it possible to obtain an oral composition that is excellent in smoothness when used.

[0025] (Binding agent) Examples of the binder include at least one selected from the group consisting of thickening silica such as hydrated silicic acid (e.g., gel-processed silica and precipitated silica) and anhydrous silicic acid (e.g., gel-processed silica, precipitated silica, and dry silica); other inorganic binders such as bentonite; and organic binders such as pullulan, gelatin, methyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, carboxymethyl cellulose and salts thereof, carrageenan, alginic acid and salts thereof, xanthan gum, polyacrylic acid and salts thereof, gum arabic, guar gum, locust bean gum, polyvinyl alcohol, and carboxyvinyl polymers. Specific examples of the above salts include alkali metal salts such as sodium salts and potassium salts.

[0026] The binder preferably contains an inorganic binder, and more preferably contains thickening silica, which can more stably improve the balance between adhesion to the toothbrush and sharpness when squeezed out from the tube container.

[0027] The thickening silica may be either crystalline silica or amorphous silica, and may be either dry silica or wet silica. The average particle size of the thickening silica is preferably 1 μm or more, more preferably 2 μm or more, even more preferably 5 μm or more, and even more preferably 10 μm or more, which allows the viscosity of the oral composition to be more efficiently maintained. The average particle size of the thickening silica is preferably 60 μm or less, more preferably 50 μm or less, and even more preferably 40 μm or less, thereby making it possible to obtain an oral composition that is smooth to the touch.

[0028] The oil absorption of the thickening silica, which is determined by the amount of boiled linseed oil absorbed according to the method described in JIS K 5101-13-2 (2004), is, for example, 0.1 mL / g or more, preferably 0.2 mL / g or more, and, for example, 5 mL / g or less, preferably 4 mL / g or less.

[0029] The content of the inorganic binder in the oral composition is preferably 2% by mass or more, more preferably 2.5% by mass or more, even more preferably 3% by mass or more, and even more preferably 4% by mass or more, based on the total oral composition. This makes it possible to obtain an oral composition that has excellent cushioning properties when brushing teeth. This also reduces irritation caused by the contact of the toothbrush with the teeth, gums, etc. The content of the inorganic binder in the oral composition is preferably 30% by mass or less, more preferably 25% by mass or less, even more preferably 20% by mass or less, and even more preferably 15% by mass or less, based on the total amount of the oral composition, thereby making it possible to obtain an oral composition having excellent surface smoothness.

[0030] The binder preferably contains an organic binder. When the binder contains thickening silica, it is preferable that the binder further contains an organic binder. This makes it possible to more stably improve the balance between adhesion to the toothbrush and sharpness when squeezed out of the tube container.

[0031] In view of the above, the organic binder preferably comprises one or more selected from the group consisting of carboxymethylcellulose and its salts (e.g., sodium carboxymethylcellulose), xanthan gum, alginic acid and its salts (e.g., sodium alginate), polyacrylic acid and its salts, carboxyvinyl polymers, hydroxyethylcellulose, hydroxypropylcellulose, pectin, tragacanth gum, gum arabic, guar gum, karaya gum, locust bean gum, gellan gum, tamarind gum, psyllium seed gum, polyvinyl alcohol, and carrageenan (preferably excluding κ-carrageenan, e.g., ι-carrageenan); More preferably, it contains one or more selected from the group consisting of carrageenan, sodium alginate, sodium carboxymethylcellulose and xanthan gum; More preferably, it contains two or more selected from the group consisting of carrageenan, sodium alginate, sodium carboxymethylcellulose, and xanthan gum; Even more preferably, it comprises sodium alginate or sodium carboxymethylcellulose and xanthan gum; Even more preferably, it contains sodium alginate and xanthan gum. Specific examples of the above salts include alkali metal salts such as sodium salts and potassium salts.

[0032] On the other hand, in terms of facilitating rinsing the oral cavity, it is also preferable that the oral composition does not contain xanthan gum. Specifically, the oral composition does not contain xanthan gum means that xanthan gum is not intentionally blended into the oral composition, and more specifically, the content of xanthan gum is 0.001% by mass or less based on the entire oral composition.

[0033] The content of the organic binder in the oral composition is preferably 0.2% by mass or more, more preferably 0.3% by mass or more, and even more preferably 1% by mass or more, based on the total amount of the oral composition, which allows the oral composition to have an appropriate viscosity. The content of the organic binder in the oral composition is preferably 15% by mass or less, more preferably 12% by mass or less, even more preferably 11% by mass or less, and even more preferably 10% by mass or less, based on the total oral composition, which allows the oral composition to be squeezed out of the tube container with better sharpness.

[0034] The mass ratio of the organic binder content to the inorganic binder content in the oral cavity composition (organic binder / inorganic binder) is preferably 0.05 or more, more preferably 0.1 or more, and even more preferably 0.2 or more, thereby making it possible to obtain an oral cavity composition that is smooth to the touch and has an excellent usability. Moreover, the mass ratio (organic binder / inorganic binder) is preferably 2.0 or less, more preferably 1.75 or less, even more preferably 1.5 or less, even more preferably 1.25 or less, and even more preferably 0.9 or less, thereby making it possible to obtain an oral composition that is excellent in sharpness when the oral composition is taken out of the tube container onto a toothbrush or the like.

[0035] The total content of the binder in the oral composition is preferably 2% by mass or more, more preferably 3% by mass or more, and even more preferably 5% by mass or more, based on the total oral composition, which can impart an appropriate viscosity to the oral composition. The total content of the binder in the oral composition is, for example, 45% by mass or less, preferably 15% by mass or less, more preferably 12% by mass or less, even more preferably 11% by mass or less, and even more preferably 10% by mass or less, based on the entire oral composition. This makes it possible to obtain an oral composition that is more compatible with saliva during tooth brushing. Also, excessive thickening of the oral composition can be suppressed.

[0036] The total content of silica in the oral composition is preferably 10% by mass or more, more preferably 15% by mass or more, and even more preferably 20% by mass or more, based on the total oral composition, which can appropriately suppress the fluidity of the oral composition. The total content of silica in the oral composition is, for example, 60% by mass or less, preferably 30% by mass or less, more preferably 27.5% by mass or less, and even more preferably 25% by mass or less, based on the total oral composition. This makes it possible to obtain an oral composition that is more compatible with saliva in the oral cavity, for example, when brushing teeth.

[0037] (Other ingredients) The oral composition may further contain ingredients other than those mentioned above, such as medicinal ingredients, thickeners, surfactants, humectants, flavoring agents, preservatives, fragrances, colorants, pH adjusters, solvents, solubilizers, bases, detergents, adsorbents, etc., which may be appropriately selected depending on the dosage form.

[0038] Examples of the medicinal ingredient include one or more selected from the group consisting of bactericides, anti-inflammatory agents, blood circulation promoters, tartar deposition inhibitors, stain removers, hypersensitivity inhibitors, vitamins, and plaque decomposing enzymes. There is no limitation on these medicinal ingredients as long as they can be used in medicines, etc.

[0039] Among the medicinal ingredients, examples of the bactericide include one or more selected from the group consisting of isopropylmethylphenol, cetylpyridinium chloride, benzalkonium chloride, benzethonium chloride, hinokitiol, chlorhexidine hydrochloride, alkyldiaminoethylglycine hydrochloride, sodium lauroyl sarcosine, and triclosan.

[0040] Examples of the anti-inflammatory agent include one or more selected from the group consisting of tranexamic acid, β-glycyrrhetinic acid, glycyrrhetinic acid, glycyrrhizinic acid, diammonium glycyrrhizinate, disodium glycyrrhizinate, trisodium glycyrrhizinate, dipotassium glycyrrhizinate, monoammonium glycyrrhizinate, stearyl glycyrrhetinate, ε-aminocaproic acid, sodium azulene sulfonate hydrate, allantoin, allantoin dihydroxyaluminum, epidihydrocholesterol, dihydrocholesterol, and lysozyme hydrochloride.

[0041] Examples of the blood circulation promoter include one or more selected from the group consisting of sodium chloride, tocopherol acetate, sodium bicarbonate, sodium hydrogen carbonate, and tocopherol nicotinate.

[0042] Examples of tartar deposit inhibitors include one or more selected from the group consisting of disodium hydrogen phosphate, disodium dihydrogen pyrophosphate, sodium pyrophosphate, anhydrous sodium pyrophosphate, tetrasodium pyrophosphate (anhydrous), disodium monohydrogen phosphate, sodium hydrogen phosphate hydrate, disodium hydrogen phosphate (crystalline), trisodium phosphate, and sodium polyphosphate.

[0043] Examples of stain removers include one or more selected from the group consisting of macrogol (Macrogol 200, Macrogol 300, Macrogol 400, Macrogol 600, Macrogol 1000, Macrogol 1500, Macrogol 1540, Macrogol 4000, Macrogol 6000, Macrogol 20000, etc.), sodium polyphosphate, and polyvinylpyrrolidone.

[0044] The dentin hypersensitivity suppressant may, for example, be at least one selected from the group consisting of potassium nitrate and water-soluble aluminum salts.

[0045] Examples of vitamin preparations include one or more selected from the group consisting of vitamin C and derivatives thereof, such as ascorbic acid, L-ascorbic acid, sodium ascorbate, sodium L-ascorbate, magnesium L-ascorbyl phosphate, pyridoxine hydrochloride, L-ascorbic acid 2-glucoside, ascorbyl tetra-2-hexyldecanoate, trisodium ascorbyl palmitate phosphate, 3-O-ethyl ascorbic acid, tocopherol, disodium isostearyl ascorbyl phosphate, and caprylyl 2-glyceryl ascorbate; and vitamin E and derivatives thereof, such as DL-α-tocopherol acetate, tocopherol acetate, dl-α-tocopherol nicotinate, and tocopherol nicotinate.

[0046] An example of a plaque decomposing enzyme is dextranase.

[0047] The thickening agent may be, for example, one commercially available as a pharmaceutical, food, or cosmetic raw material. The thickening agent may, for example, be one or more selected from the group consisting of polyhydric alcohols, more specifically sorbitol (sorbitol), glycerin, concentrated glycerin, diglycerin, ethylene glycol, propylene glycol, 1,3-butylene glycol, propanediol (1,3-propanediol), polyethylene glycol, polypropylene glycol, xylitol, maltitol, lactitol, trehalose, sodium hyaluronate, and hydrolyzed collagen.

[0048] Examples of the surfactant include anionic surfactants such as N-acylamino acid salts, α-olefin sulfonates, N-acylsulfonates, alkyl sulfates (e.g., sodium lauryl sulfate), and sulfates of glycerin fatty acid esters; Nonionic surfactants such as polyoxyethylene alkyl ethers, polyoxyethylene-polyoxypropylene block copolymers, polyoxyethylene hydrogenated castor oil, polyoxyethylene ethers of glycerin esters, sucrose fatty acid esters, alkylolamides, and glycerin fatty acid esters; and Examples of the surfactant include one or more selected from the group consisting of amphoteric surfactants such as alkyl betaine surfactants (e.g., coconut oil fatty acid amido alkyl betaine), amine oxide surfactants, and imidazolinium betaine surfactants (e.g., 2-alkyl-N-carboxymethyl-N-hydroxyethyl imidazolinium betaine). The surfactant may be a foaming agent.

[0049] The content of the surfactant in the oral composition is preferably 0.1% by mass or more, more preferably 0.5% by mass or more, and even more preferably 1% by mass or more, based on the total amount of the oral composition, thereby making it possible to obtain an oral composition that foams appropriately when brushing teeth. The content of the surfactant in the oral composition is preferably 5% by mass or less, more preferably 3% by mass or less, and even more preferably 2% by mass or less, based on the total amount of the oral composition. This makes it possible to obtain an oral composition with a cleaning power that does not remove too much oil from the oral cavity.

[0050] It is preferable that the oral composition further contains a humectant, which can provide the oral composition with better manufacturing stability. The humectant may be any one that is commercially available as a pharmaceutical, food, or cosmetic ingredient, such as a polyhydric alcohol, and more specifically, one or more selected from the group consisting of sorbitol, glycerin, concentrated glycerin, diglycerin, ethylene glycol, propylene glycol, 1,3-butylene glycol, propanediol (1,3-propanediol), polyethylene glycol, polypropylene glycol, sodium hyaluronate, and hydrolyzed collagen.

[0051] From the viewpoint of reducing irritation to the oral cavity, the humectant is preferably at least one selected from the group consisting of sorbitol, concentrated glycerin, and propylene glycol, and more preferably sorbitol or concentrated glycerin.

[0052] The content of the humectant in the oral composition is preferably 5% by mass or more, more preferably 10% by mass or more, and even more preferably 20% by mass or more, based on the total amount of the oral composition, thereby making it possible to obtain an oral composition having excellent moisturizing power in the oral cavity. The content of the humectant in the oral composition is preferably 50% by mass or less, more preferably 45% by mass or less, and even more preferably 40% by mass or less, based on the total oral composition. This makes it possible to obtain an oral composition that is easy to rinse with gargle.

[0053] Examples of flavoring agents include one or more selected from the group consisting of sodium L-glutamate, saccharin, saccharin sodium, sucrose, glucose, fructose, lactose, honey, aspartame, stevia, sucralose, inositol, D-sorbitol, D-mannitol, arabitol, raffinose, lactulose, lactitol, xylitol, erythritol, reduced palatinose, palatinose, Palatinit (registered trademark), acesulfame K, trehalose, maltose, maltosyl trehalose or maltitol, neohesperidin dihydrochalcone, perillartine, p-methoxycinnamic aldehyde, and thaumatin.

[0054] The flavoring agent is preferably at least one selected from the group consisting of xylitol, sodium saccharin, and saccharin, and more preferably at least one selected from the group consisting of xylitol and sodium saccharin, because it has a strong sweetness and can be used to adjust the taste even in small amounts.

[0055] Examples of preservatives include one or more selected from the group consisting of paraoxybenzoic acid esters such as sodium benzoate, methylparaben, ethylparaben, butylparaben, isopropylparaben, propylparaben, isobutylparaben, and benzylparaben; alcohols such as phenoxyethanol; sorbic acid, benzoic acid, dehydroacetic acid, propionic acid, and salts thereof; ethylenediaminetetraacetate, alkyldiaminoethylglycine hydrochloride, and ethylhexylglycerin. Specific examples of the above salts include alkali metal salts such as sodium salts and potassium salts; and alkaline earth metal salts such as calcium salts and magnesium salts.

[0056] The flavoring agent may, for example, be one or more selected from the group consisting of L-menthol, peppermint, spearmint, fruit flavorings, and peppermint oil.

[0057] Examples of colorants include one or more selected from the group consisting of natural colorants such as safflower red colorant, gardenia yellow colorant, gardenia blue colorant, perilla colorant, red koji colorant, red cabbage colorant, carrot colorant, hibiscus colorant, cacao colorant, spirulina blue colorant, and coumarind colorant; legal colorants such as Red No. 3, Red No. 104, Red No. 105, Red No. 106, Yellow No. 4, Yellow No. 5, Green No. 3, and Blue No. 1; riboflavin, and titanium dioxide.

[0058] Examples of pH adjusters include one or more selected from the group consisting of acids and alkalis and buffers, such as acetic acid, hydrochloric acid, sulfuric acid, nitric acid, citric acid, phosphoric acid, malic acid, gluconic acid, maleic acid, succinic acid, glutamic acid, pyrophosphoric acid, tartaric acid, acetic acid, sodium hydroxide, potassium hydroxide, sodium acetate, sodium carbonate, sodium citrate, sodium hydrogen citrate, phosphoric acid, sodium phosphate, sodium monohydrogen phosphate, sodium dihydrogen phosphate, and potassium dihydrogen phosphate.

[0059] Solvents include water; and lower alcohols such as ethanol, propanol, etc. The solvent may be a liquid base.

[0060] The content of water in the oral composition can be, for example, the remainder after removing the components other than water from the oral composition. The content of water in the oral composition can be, for example, 30 to 80% by mass, and preferably 32 to 70% by mass, based on the entire oral composition. It is also preferable that the oral composition does not contain ethanol, i.e., the ethanol content is 0% by mass, or the oral composition contains ethanol but the ethanol content is 5% by mass or less, which can suppress strong irritation in the oral cavity.

[0061] A solubilizer may be added to promote dissolution of the additives and medicinal ingredients in water. Examples of such solubilizers include polyhydric alcohols such as dipropylene glycol.

[0062] Other bases include, for example, sodium bicarbonate.

[0063] Detergents include, for example, sodium polyphosphate.

[0064] The adsorbent may, for example, be β-cyclodextrin.

[0065] Furthermore, in addition to the above-mentioned components, components generally suitable for use in oral compositions can also be appropriately blended within the scope of the present invention.

[0066] (Dosage form, etc.) Specific examples of oral compositions include dentifrices such as toothpaste. In addition, the oral composition is preferably a dentifrice composition, more preferably a toothpaste composition, which can further improve the ease of handling of the oral composition. From the same viewpoint, the oral composition is preferably in a paste or gel form.

[0067] The oral composition is preferably applied to the oral cavity by being placed on a toothbrush. Examples of toothbrushes that can be used with the oral cavity composition include known toothbrushes. Examples of materials for the bristle bundles of toothbrushes include resins, and more specifically, one or more types selected from the group consisting of saturated polyesters such as polyethylene terephthalate, polybutylene terephthalate, and polytrimethylene terephthalate, polyolefins such as polypropylene, polyamides such as nylon, and elastomer resins such as olefin elastomers and styrene elastomers. The toothbrush to be used with the oral composition may be a typical commercially available toothbrush.

[0068] (Manufacturing method) In this embodiment, the oral composition includes a step of blending, for example, an abrasive, a binder, and other ingredients as appropriate. Here, in order to obtain an oral composition having (TF5 / TF10) and spinnability each falling within a specific range, it is important to appropriately select, for example, the components and their blending ratios contained in the oral composition, as well as to appropriately select the manufacturing process for the oral composition. For example, it is important to appropriately select and combine the types and amounts of abrasives and binders contained in the oral composition to design the composition, and it is preferable to use a combination of abrasive silica and an inorganic binder, and more preferable to use a combination of abrasive silica and a thickening silica. It is also preferable to further add an organic binder to the oral composition. It is also preferable to further add a humectant to the oral composition. It is also preferable to carry out the manufacturing process of the oral composition under vacuum. For example, when the oral composition contains thickening silica, an organic binder, a humectant, and water, it is preferable to add thickening silica, an abrasive, and other components as appropriate during or after mixing the humectant, the organic binder, and the water, and stir and mix until uniform. It is also preferable to prepare a mixture of a part of the humectant and the organic binder in advance, add the mixture at the stage where the mixture is homogenized, and stir until further homogenized. It is more preferable to carry out these steps under vacuum.

[0069] (Toothpaste) In this embodiment, the dentifrice is the above-mentioned oral composition filled in a tube container, and preferably is a toothpaste composition filled in a tube container. In this embodiment, the oral composition has an excellent balance between adhesion to a toothbrush and ease of squeezing out of a tube container, and by filling this into a tube container to make a dentifrice, the dentifrice can be squeezed from the tube container onto a toothbrush with excellent ease of handling when applied to the oral cavity.

[0070] Oral compositions such as toothpaste compositions are preferably used by squeezing them out of a tube container. As the tube container, for example, a known container can be used. The material of the tube container may be one or more selected from the group consisting of resin materials such as polyethylene, polypropylene, polyethylene terephthalate, nylon, and metal materials such as aluminum. For example, the tube container may be a single-layer or multi-layer container made of these materials. The material of the innermost layer of the container is preferably one or more selected from the group consisting of polyethylene, polypropylene, and polyethylene terephthalate. For example, an aluminum laminated tube container may be used in which the material of the innermost layer of the container is polyethylene and further includes an aluminum layer.

[0071] The inner diameter of the discharge port of the tube container is preferably 1 mm or more, more preferably 2 mm or more, and further preferably 3 mm or more, which makes it possible to more stably reduce the excessive force required to discharge the oral composition. The inner diameter of the discharge port of the tube container is preferably 11 mm or less, more preferably 10 mm or less, and further preferably 9 mm or less, which can efficiently prevent dripping. The length of the tube container excluding the discharge port may be about 50 to 160 mm, and the outer circumferential length in the width direction of the tube container may be about 20 to 120 mm.

[0072] Although the embodiments of the present invention have been described above, these are merely examples of the present invention, and various configurations other than those described above can also be adopted. EXAMPLES

[0073] The present embodiment will be specifically described below with reference to examples and comparative examples, but the present embodiment is not limited to these examples.

[0074] (Examples 1 to 6, Comparative Examples 1 to 3) In this example, oral compositions, which are toothpaste compositions, were prepared and evaluated. The formulations, measurements, and evaluation results of each example are shown in Tables 1 and 2. The units of component amounts in Tables 1 and 2 are mass %, and the particle size of silica is the average particle size. Details of the components listed in Tables 1 and 2 are shown below. Sorbitol Kao: 70% sorbitol liquid, manufactured by Kao Corporation Concentrated glycerin for cosmetics: Concentrated glycerin, manufactured by Sakamoto Pharmaceutical Co., Ltd. Sodium alginate SHG: Sodium alginate, manufactured by Kohara Co., Ltd. NIKKOL SLS: Sodium lauryl sulfate, manufactured by Nikko Chemicals Caustic soda (48%): Sodium hydroxide solution, manufactured by Tatsumi Synthetic Chemical Co., Ltd.

[0075] (Preparation of oral composition) Sorbitol or glycerin and purified water were weighed into a beaker, and the organic binder was gradually added while stirring at 2500 rpm at 80°C using an emulsifying and dispersing device (Labo-lution, Primix) and a stirring section (Homodisper 2.5, Primix). After stirring and mixing for 3 minutes, abrasive silica, thickening silica (oil absorption 2.5 mL / g), sodium lauryl sulfate, and caustic soda were added in that order, stirring and mixing with a rubber spatula each time until the mixture was uniform.

[0076] (Tensile return force) TF5 and TF10 were measured at 25°C using Method 1 described above. Device name: Rheometer (CR-3000EX-S, Sun Scientific, detection limit: 0.1 gf) Jig used: Pressure / elasticity measuring pressure-sensitive shaft (Φ20mm) Measurement speed: 60mm / min Pull-up distance: 5mm or 10mm Filling container: 30mL plastic jar (diameter 43mm) The absolute stress value at each pulling distance was measured three times, and the average value was calculated and designated as TF5 and TF10. Although the measured values ​​were negative, the absolute values ​​(positive values) were used to compare the magnitude of the force. The ratio (TF5 / TF10) was obtained from TF5 and TF10.

[0077] (Threadability) This was carried out at 25°C according to Method 2 described above. Equipment name: Rheometer (CR-3000EX-S, manufactured by Sun Scientific Co., Ltd.) Tool used: Pressure-sensitive shaft for measuring penetration (Φ15mm) Measurement speed: 1000mm / min Pulling distance: 50mm Filling container: 30mL plastic jar (diameter 43mm) The distance the toothpaste composition separated from the jig during lifting was measured three times, and the average value was calculated.

[0078] (Evaluation method) (Adhesion to toothbrush) Each composition was filled into a 30 mL plastic pot (Φ43 mm). A toothbrush (manufactured by Lion Corporation) with a head size of 18 mm and bristles made of saturated polyester resin was impregnated with the composition until the head was flush with the surface of the toothbrush. The toothbrush was then lifted vertically at a speed of approximately 3 cm per second, at which point the mass (g) of the composition adhering to the toothbrush was measured and evaluated according to the following criteria: A: Adhesion amount 1.2g or more B: Adhesion amount 1.0g or more and less than 1.2g C: Adhesion amount less than 1.0g

[0079] (Sharpness) Each toothpaste composition was filled into a laminate tube (manufactured by Takemoto Container Co., Ltd.) made of low density polyethylene (LDPE) with a diameter of 19 mm and a size of 40Φ×130H. A one-touch cap (T-40Φ one-touch CAPII, manufactured by Takemoto Container Co., Ltd.) made of polypropylene with a diameter of 6 mm and a size of 39Φ×24H was attached as a cap, and the toothpaste composition was extruded from the tube for about 2.5 cm onto a paper towel, and the length of the composition that was pulled out as a string when the tube was pulled sideways at a speed of about 5 cm per second was measured and evaluated according to the following evaluation criteria. A: The length of the string is less than 20 mm B: The length of the stringy composition is 20 mm or more and less than 28 mm C: The length of the string is 28 mm or more.

[0080] [Table 1]

[0081] [Table 2]

Claims

1. An oral composition comprising an abrasive, a binder and a humectant, the abrasive comprises abrasive silica; The binder comprises at least one selected from the group consisting of xanthan gum, sodium alginate, and thickening silica; The humectant comprises at least one selected from the group consisting of sorbitol and glycerin; When the tensile return forces in a 5 mm tensile test and a 10 mm tensile test measured by the following method 1 are defined as TF5 and TF10, respectively, the ratio of TF5 to TF10 (TF5 / TF10) is 1.1 or more and 10 or less, An oral composition having a stringiness of 2 mm or more and less than 24 mm as measured by the following method 2. (Method 1) Device name: Rheometer Jig used: Pressure / elasticity measuring pressure-sensitive shaft (Φ20 mm) Measurement speed: 60mm / min Pull-up distance: 5mm or 10mm Filling container: 30mL plastic jar (diameter 43mm) Procedure: The oral composition is filled into the filling container until it is full, and then the container is set in the device. The container is pulled up at the measurement speed, and the absolute value of the stress at each pulling distance is measured. The average value of three measurements at each pulling distance is designated as TF5 or TF10. (Method 2) Device name: Rheometer Jig used: Pressure-sensitive shaft for measuring penetration (Φ15 mm) Measurement speed: 1000mm / min Pulling distance: 50 mm Filling container: 30mL plastic jar (diameter 43mm) Procedure: The oral composition is filled into the filling container until it is fully filled, and then the container is set in the device and then pulled up at the measurement speed. The distance until the oral composition separates from the jig during pulling is measured. The average value of the distance that is measured three times is regarded as the spinnability.

2. An oral composition as described in claim 1, wherein the content of the binder in the oral composition is 2% by mass or more and 45% by mass or less relative to the entire oral composition.

3. The oral composition of claim 1 or 2, wherein the binder comprises an organic binder.

4. An oral composition as described in claim 3, wherein the content of the organic binder in the oral composition is 0.2 mass% or more and 15 mass% or less with respect to the entire oral composition.

5. An oral composition as described in claim 1 or 2, wherein the content of the abrasive in the oral composition is 5% by mass or more and 30% by mass or less relative to the entire oral composition.

6. An oral composition as described in claim 1 or 2, wherein the content of the humectant in the oral composition is 5% by mass or more and 50% by mass or less relative to the entire oral composition.

7. 3. The oral composition according to claim 1 or 2, which is a dentifrice composition.

8. 3. The oral composition according to claim 1, which is a toothpaste composition.

9. An oral composition as described in claim 1 or 2, wherein the TF5 is 1 gf or more and 100 gf or less.

10. An oral composition as described in claim 1 or 2, wherein the TF10 is 0.5 gf or more and 50 gf or less.

11. A dentifrice comprising the oral composition according to claim 8 packed in a tube container.

Images