WO2018230325A1 - Composition for use in oral cavity - Google Patents

Composition for use in oral cavity Download PDF

Info

Publication number
WO2018230325A1
WO2018230325A1 PCT/JP2018/020506 JP2018020506W WO2018230325A1 WO 2018230325 A1 WO2018230325 A1 WO 2018230325A1 JP 2018020506 W JP2018020506 W JP 2018020506W WO 2018230325 A1 WO2018230325 A1 WO 2018230325A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
zinc oxide
oil
hexagonal plate
oral cavity
Prior art date
Application number
PCT/JP2018/020506
Other languages
French (fr)
Japanese (ja)
Inventor
典浩 高下
卓 小倉
Original Assignee
ライオン株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by ライオン株式会社 filed Critical ライオン株式会社
Priority to KR1020197026233A priority Critical patent/KR20200015449A/en
Priority to CN201880007910.9A priority patent/CN110198699A/en
Publication of WO2018230325A1 publication Critical patent/WO2018230325A1/en

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/0241Containing particulates characterized by their shape and/or structure
    • A61K8/0254Platelets; Flakes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/27Zinc; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q11/00Preparations for care of the teeth, of the oral cavity or of dentures; Dentifrices, e.g. toothpastes; Mouth rinses

Definitions

  • the present invention relates to a composition for oral cavity that has an excellent whitening effect on teeth.
  • (1) has a problem in safety
  • (2) to (4) there is room for improvement in terms of simplicity because a fixing means may be used for whitening the teeth.
  • Development of a simple and effective whitening technique for teeth was desired.
  • This invention is made
  • (A) hexagonal plate-like zinc oxide has an excellent whitening effect on teeth, and when this is blended into an oral composition, It has been found that it has an excellent whitening effect that makes it whiter than the color. That is, according to the present invention, by blending (A) hexagonal plate-like zinc oxide into the oral composition, an excellent tooth whitening effect is provided, thereby allowing normal tooth brushing and washing without using fixing means. It has been found that even with the mouth alone, the whiteness of the teeth stands out, the brightness of the teeth increases, and the teeth can appear much whiter than the original color, and the present invention has been made.
  • Hexagonal plate-like zinc oxide is known as a component of skin cosmetics such as foundations as an ultraviolet light inhibitor, but in preparations applied to the oral cavity, amorphous particles are generally used as zinc oxide. It was done. Therefore, single crystal particles are not applied as zinc oxide, and the composition of hexagonal plate-like zinc oxide into the oral composition has not been known so far.
  • (A) hexagonal plate-like zinc oxide, particularly preferably hexagonal plate-like zinc oxide having a specific average particle diameter and average thickness, is an excellent tooth in an oral composition. The whitening effect of the present invention is achieved, and there is a special effect that cannot be obtained by using other white pigments.
  • the present invention not only the above-described whitening effect but also an astringent feeling derived from zinc oxide can be appropriately imparted by the component (A) to give a good feeling of use.
  • gear using the zinc oxide which is a white pigment is well-known (patent document 3), as above-mentioned, the zinc oxide used for a composition for oral cavity is usually an amorphous particle. Even with zinc oxide, the effect of the present invention cannot be obtained with irregularly shaped particles. As shown in a comparative example described later, the whitening effect is inferior when an amorphous zinc oxide powder is used instead of the component (A), and even when it is a hexagonal plate, mica titanium may be used.
  • the whitening effect is inferior, and the effect of the present invention is inferior in these.
  • the effect of making the teeth whiter is excellent and the astringent feeling is satisfied by the contribution of the film-forming ability of the component (A) and the retention in the oral mucosa. It is speculated that it can also be granted.
  • the present invention provides the following oral composition.
  • (A) A composition for oral cavity containing hexagonal plate-like zinc oxide.
  • [2] The oral composition according to [1], wherein the hexagonal plate-like zinc oxide has an average particle size of 0.1 to 10 ⁇ m.
  • [3] The oral composition according to [1] or [2], wherein the hexagonal plate-like zinc oxide has an average thickness of 0.01 to 1 ⁇ m.
  • [4] The composition for oral cavity according to any one of [1] to [3], wherein the average particle diameter / average thickness is 0.5 to 50 and represents the ratio between the average particle diameter and the average thickness of hexagonal plate-like zinc oxide .
  • composition for oral cavity according to [5] which is a dentifrice or mouthwash.
  • an oral composition having an excellent whitening effect on teeth can be provided.
  • the composition for oral cavity of the present invention can be effectively used for whitening teeth because it can easily and effectively whiten teeth and make the teeth whiter than the original color.
  • (A) hexagonal plate-like zinc oxide is blended in an oral composition as an active ingredient for whitening teeth.
  • Hexagonal plate-like zinc oxide has a whitening effect on teeth and gives a sense of convergence.
  • the hexagonal plate-like zinc oxide is not particularly limited as long as it is hexagonal and plate-like particles, and known single crystal hexagonal plate-like zinc oxide can be used.
  • the hexagonal plate-like zinc oxide can be used by being dispersed in water.
  • the average particle size of the hexagonal plate-like zinc oxide is preferably 0.1 ⁇ m or more, more preferably 0.5 ⁇ m or more, still more preferably 1 ⁇ m or more, particularly 1.5 ⁇ m or more, and preferably 10 ⁇ m or less, more preferably It is 8 ⁇ m or less, more preferably 5 ⁇ m or less. When it is 0.1 ⁇ m or more, the whitening effect is sufficiently exhibited. When the thickness is 10 ⁇ m or less, the convergence feeling is sufficiently exhibited.
  • the “particle size” of the hexagonal plate-like zinc oxide in the present invention is an average value of the lengths of the three diagonal lines of the hexagonal surface of the hexagonal plate-like particle.
  • the average particle size was calculated by image analysis, specifically, by randomly selecting 20 hexagonal plate-like zinc oxides, and measuring and averaging the lengths of the diagonal lines of each particle.
  • a scanning electron microscope (SEM) JSM7600F manufactured by JEOL Ltd. was used for the particle size measurement.
  • the particle size of each particle was measured by averaging the lengths of three hexagonal diagonal lines from the image from the Z-axis direction (the same applies hereinafter).
  • the average thickness of the hexagonal plate-like zinc oxide is preferably 0.01 ⁇ m or more, more preferably 0.1 ⁇ m or more, still more preferably 0.2 ⁇ m or more, and preferably 1 ⁇ m or less, more preferably 0.8 ⁇ m or less. More preferably, it is 0.7 ⁇ m or less.
  • the “thickness” of hexagonal plate-like zinc oxide in the present invention is a distance between two hexagonal surfaces of hexagonal plate-like particles.
  • said average thickness uses the scanning electron microscope (SEM) JSM7600F by JEOL Co., Ltd., 20 hexagonal plate-like zinc oxides were selected at random, and each particle
  • SEM scanning electron microscope
  • the hexagonal plate-like zinc oxide shows the ratio between the average particle diameter and the average thickness, and the average particle diameter / average thickness is preferably 0.5 or more, more preferably 1 or more, and further preferably 2 or more. Moreover, 50 or less is preferable, More preferably, it is 30 or less, and may be 5 or less. When the average particle size / average thickness is 0.5 or more, the whitening effect is sufficiently exhibited. When it is 50 or less, a feeling of convergence is sufficiently exhibited.
  • the oil absorption amount of hexagonal plate-like zinc oxide is preferably 45 g / 100 g or less, more preferably 36 g / 100 g or less.
  • the oil absorption was measured according to JIS K-5101-13-1.
  • hexagonal plate-like zinc oxide commercially available products can be used. Examples include hexagonal plate-like zinc oxide XZ series XZ-100F, XZ-300F, XZ-1000F, XZ-2000F, and XZ-3000F (all manufactured by Sakai Chemical Industry Co., Ltd.).
  • the compounding quantity of hexagonal plate-shaped zinc oxide is not restrict
  • the blending amount of the component (A) is preferably 0.1 to 30%, particularly preferably 0.1 to 20%, more preferably 0.1 to 5% of the whole composition, More preferably, it is 0.5 to 3%, and particularly preferably 1.0 to 2%.
  • the composition for oral cavity of this invention can be prepared also in sheet-like forms, such as a pack agent and a film agent, as mentioned later, in such a sheet-form preparation, (A) component is compared compositionally. Can be blended as much as possible.
  • the blending amount of the component (A) can be 0.1 to 95% of the whole composition from the viewpoint of the whitening effect and the feeling of use, but is preferably 0.1 to 20%, more preferably 0.1 to 5%.
  • (B) a surfactant it is preferable to further blend (B) a surfactant.
  • (B) a surfactant is added, the dispersibility of the component (A) is improved and the whitening effect is further increased.
  • surfactant examples include known anionic surfactants, nonionic surfactants, and amphoteric surfactants for oral use, and any of them may be used.
  • anionic surfactants include alkyl sulfates such as sodium lauryl sulfate, N-acyl sarcosine salts such as N-lauroyl sarcosine sodium, acyl amino acid salts such as N-acyl glutamate, and ⁇ -olefin sulfonic acids. Sodium etc. are mentioned.
  • Nonionic surfactants include sugar fatty acid esters such as sucrose fatty acid esters, sugar alcohol fatty acid esters, sorbitan fatty acid esters, glycerin fatty acid esters, polyglycerin fatty acid esters such as decaglyceryl monolaurate, and average added moles of ethylene oxide ( And polyoxyethylene fatty acid esters such as polyoxyethylene hydrogenated castor oil having an EO) of 10 to 60, fatty acid alkanolamides such as polyoxyethylene higher alcohol ethers and lauric acid diethanolamide.
  • sugar fatty acid esters such as sucrose fatty acid esters, sugar alcohol fatty acid esters, sorbitan fatty acid esters, glycerin fatty acid esters, polyglycerin fatty acid esters such as decaglyceryl monolaurate, and average added moles of ethylene oxide ( And polyoxyethylene fatty acid esters such as polyoxyethylene hydrogenated castor oil having an EO) of 10 to 60, fatty acid
  • amphoteric surfactants include betaine types such as alkylbetaines, alkyldimethylaminoacetic acid betaines, fatty acid amidopropyl betaines, fatty acid amidopropyldimethylaminoacetic acid betaines, betaine types such as alkylimidazolinium betaines, and N-fatty acid acyl-N.
  • examples include imidazoline type such as -carboxymethyl-N-hydroxyethylethylenediamine salt.
  • anionic surfactants are particularly preferable, anionic surfactants having a sulfonic acid group are more preferable, and alkyl sulfates and ⁇ -olefin sulfonates are more preferable.
  • the blending amount of the (B) surfactant is preferably from 0.1 to 10%, particularly preferably from 1 to 5%, based on the entire composition.
  • the composition for oral cavity of the present invention can be made into paste, gel, liquid such as liquid, solid, etc., and prepared as a toothpaste such as toothpaste, liquid dentifrice, liquid dentifrice, mouthwash, etc. obtain. Furthermore, it is also possible to prepare a form that can be applied to teeth without using a fixing means, specifically, a sheet-form oral preparation such as a pack or film. In particular, dentifrices or mouthwashes are preferred in terms of the manifestation and usability of this effect.
  • the pack agent is a preparation in which the plaster surface of a sheet is attached to a tooth, the support is peeled off, the plaster is transferred onto the tooth surface, and the plaster is used as a dentifrice or the like.
  • a film agent is a preparation in which the entire film is used as a dentifrice etc. by sticking the film to the tooth surface and brushing as it is.
  • a tooth having a length of 2.5 cm, a width of 2 cm, and a thickness of about 0.3 mm The size and shape can be adjusted.
  • components that are commonly blended for oral compositions can be blended as necessary, depending on the form and the like. It can be prepared by conventional methods. For example, abrasives, thickeners, binders, sweeteners, preservatives, colorants, fragrances, active ingredients other than the component (A), and the like can be blended.
  • various gelling agents can also be used in order to gelatinize and paste and to improve the applicability to a tooth and adhesiveness with a tooth.
  • abrasive examples include silica-based abrasives such as precipitated silica, aluminosilicate, zirconosilicate, calcium phosphate-based abrasives, calcium carbonate and the like (the amount is usually 2 to 50%, particularly 10 to 40%). ).
  • wetting agent examples include sugar alcohols such as sorbit and xylite, glycerin, propylene glycol, and polyhydric alcohols such as polyethylene glycol having an average molecular weight of 160 to 4000 (average molecular weight described in Quasi-drug Raw Material Standard 2006). (The amount is usually 5 to 50%).
  • binders include cellulose derivatives such as sodium carboxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, alginic acid or its derivatives such as sodium alginate, gums such as xanthan gum, organic binders such as carrageenan, polyvinyl alcohol, and sodium polyacrylate. And inorganic binders such as an agent, gelling silica, gelling aluminum silica, bee gum, and laponite (the blending amount is usually 0.1 to 10%).
  • sweetening agent examples include sodium saccharin
  • preservative examples include paraoxybenzoic acid esters such as methyl paraoxybenzoate, benzoic acid such as sodium benzoate, and salts thereof.
  • colorant examples include blue No. 1, yellow No. 4, titanium dioxide and the like.
  • Perfumes include peppermint oil, spearmint oil, anise oil, eucalyptus oil, winter green oil, cassia oil, clove oil, thyme oil, sage oil, lemon oil, orange oil, peppermint oil, cardamom oil, coriander oil, mandarin oil, Lime oil, lavender oil, rosemary oil, laurel oil, camomil oil, caraway oil, marjoram oil, bay oil, lemongrass oil, origanum oil, pine needle oil, neroli oil, rose oil, jasmine oil, grapefruit oil, sweetie Natural fragrances such as oil, bran oil, Iris concrete, absolute peppermint, absolute rose, orange flower, and processing of these natural fragrances (front reservoir cut, rear reservoir cut, fractional distillation, liquid-liquid extraction, essence, powder Perfumes, etc.) and menthol, Rubon, Anethole, Cineol, Methyl salicylate, Synamic aldehyde, Eugenol, 3-l-Ment
  • Active ingredients include fluorine-containing compounds such as sodium fluoride and sodium monofluorophosphate, cationic fungicides such as isopropylmethylphenol and cetylpyridinium chloride, enzymes such as anti-inflammatory agents and dextranase, and water-soluble phosphoric acid. Examples thereof include compounds, copper compounds, vitamins, plant extracts, calculus inhibitors, and plaque inhibitors.
  • the active ingredient can be blended in an effective amount as long as the effects of the present invention are not hindered.
  • the same material as the above-mentioned binder can be used as a gelling agent, but from the viewpoint of use feeling in the mouth, sodium carboxymethylcellulose, hydroxyethylcellulose, Cellulose derivatives such as hydroxypropyl cellulose, polyvinyl alcohol, and sodium alginate are preferred (the amount is preferably 1 to 5%).
  • the sheet-form oral preparation is not particularly limited as long as it can be applied to teeth, and there is no particular limitation on the shape, thickness, etc., usage form, and the like, even in a form that can be applied to one or more tooth surfaces.
  • it can also be used as a dentifrice by sticking on the tooth surface and brushing as it is after use.
  • the plaster composition is spread and integrated on the support so that the plaster composition is peelable.
  • a water-insoluble material is preferably used, and examples thereof include films, nonwoven fabrics, woven fabrics, and mesh fabrics of materials such as polypropylene, polyethylene, and polyurethane.
  • the film may be a single layer or a laminated film, or a laminated sheet of a film and unemployed cloth, woven cloth or net cloth.
  • the plaster composition may be protected by coating a release liner. These can use a commercial item.
  • Examples and Comparative Examples Prepare aqueous dispersions (simple systems) having the compositions shown in Tables 1 and 2 and dentifrices, mouth washes, packs or film preparations (formulation systems) having the compositions shown in Tables 3 to 7, respectively. Evaluation was performed by the method shown. The results are shown in the table.
  • the average particle diameter and average thickness of the samples used are shown in the table.
  • Zinc oxide powder, comparative product
  • Amorphous powder Japanese Pharmacopoeia zinc oxide, manufactured by Sakai Chemical Industry Co., Ltd., amorphous Average particle size 2 ⁇ m, average thickness 2 ⁇ m, oil absorption 59g / 100g Mica titanium (hexagonal plate, comparative product); TIMIRON MP-149, manufactured by Merck Ltd., single crystal, Average particle size 2 ⁇ m, average thickness 0.5 ⁇ m
  • the measuring method of said average particle diameter and average thickness is shown below. Measuring the average particle size; It was calculated by image analysis, and measured and analyzed in the same manner as described above using a scanning electron microscope (SEM) JSM7600F manufactured by JEOL. From the image from the Z-axis direction, the lengths of the three diagonal lines of the hexagon were measured to obtain the particle size, and the average particle size was calculated. Average thickness measurement method; Using a scanning electron microscope (SEM) JSM7600F manufactured by JEOL Ltd., measurement was performed in the same manner as described above, and an average value was obtained. The length of the plate-like upper and lower surfaces of the particles was measured to obtain the thickness, and the average thickness was calculated.
  • SEM scanning electron microscope
  • the measuring method of the average particle diameter of zinc oxide (hexagonal plate shape) and mica titanium (hexagonal plate shape) and average thickness is as described above, respectively, and the average particle size of zinc oxide (powdered shape) is The average thickness is measured by a laser diffraction scattering type particle size distribution measuring apparatus LA-920 manufactured by HORIBA, Ltd. Since the shape of zinc oxide (powder) is nearly spherical, the average particle size is defined as the average thickness for convenience. did. The oil absorption was measured according to JIS K-5101-13-1.
  • FIG. 1 shows a two-dimensional image of (A) zinc oxide (hexagonal plate) (taken using a scanning electron microscope (SEM) JSM7600F manufactured by JEOL Ltd.).
  • Evaluation method-1 Lightness measurement method of hydroxyapatite (HAP) plate and evaluation method of degree of whiteness (simple system) Zinc oxide was weighed and dispersed in 100 ml of water. A hydroxyapatite (HAP) plate having a diameter of 7 mm was put in this dispersion, and after 3 minutes, the HAP plate was taken out and lightly rinsed with 100 ml of water. This HAP plate was measured with a color difference meter (spectral color difference meter SE-2000, manufactured by Nippon Denshoku Industries Co., Ltd.) to obtain a value of ⁇ L which is an index of brightness. As a control, an untreated product (untreated HAP plate) was measured in the same manner.
  • the comparative example was similarly measured according to the above method.
  • a questionnaire was conducted on the degree of whiteness of the HAP plate for 10 subjects.
  • a score (1 to 4 points) was assigned based on the following criteria, and an average value was calculated from the obtained results. From the calculated average score, the degree of whiteness of the HAP plate was evaluated based on the following evaluation criteria.
  • An untreated HAP plate was used as a control.
  • Evaluation method-2 Lightness measurement method of hydroxyapatite (HAP) plate and evaluation method of degree of whiteness (formulation system) Dentifrices, packs (plasters), and film preparations were diluted three times with water to prepare a dispersion of about 100 ml, which was used as an evaluation solution. The mouthwash was directly used as an evaluation solution. A hydroxyapatite (HAP) plate having a diameter of 7 mm was put in this dispersion, and after 3 minutes, the HAP plate was taken out and lightly rinsed with 100 ml of water.
  • HAP hydroxyapatite
  • This HAP plate was measured with a color difference meter (spectral color difference meter SE-2000, manufactured by Nippon Denshoku Industries Co., Ltd.) to obtain a value of ⁇ L which is an index of brightness.
  • a color difference meter spectral color difference meter SE-2000, manufactured by Nippon Denshoku Industries Co., Ltd.
  • ⁇ L an index of brightness
  • an untreated product untreated HAP plate
  • the comparative example was similarly measured according to the above method. Further, the degree of whiteness of the HAP plate was evaluated in the same manner as in the evaluation method-1.
  • Evaluation method-3 Evaluation method of astringency (formulation system) A questionnaire was conducted on 10 subjects about the degree of convergence after using each preparation. A score (1 to 4 points) was assigned based on the following criteria, and an average value was calculated from the obtained results. Based on the average value of the calculated scores, the degree of convergence after brushing was evaluated based on the following evaluation criteria. In each dentifrice, tooth brushing was performed for each subject by taking about 1 g of the dentifrice composition on a toothbrush, brushing for 3 minutes, and rinsing the oral cavity with water. The other preparations were used in the usual manner.
  • the pack agent was prepared in the same shape by the same method as the adhesive sheet in the examples of JP-A-2016-117682, except that the plaster composition and the support having the above composition were used.
  • the plaster composition was applied to a support, and spread while being sandwiched between the support and a silicone coating surface of a release liner (BD binder of film binder 75E-001 manufactured by Fujimori Kogyo Co., Ltd.).
  • the obtained sheet was punched out for the upper jaw (width (parallel to the dentition) 62 mm, length 24 mm) and lower jaw (width 52 mm, height 24 mm), and cut and folded lines were also prepared. .
  • the pack agent was affixed to the tooth surface and the support was peeled off, it was used after brushing.
  • the film agent was prepared in a size of 2.5 cm in length, 2 cm in width, and 0.3 mm in thickness by a usual method. After the film agent was applied to the tooth surface, it was used after brushing.

Abstract

A composition for use in the oral cavity characterized by containing (A) hexagonal plate-like zinc oxide. The present invention makes it possible to provide a composition for use in the oral cavity having an excellent tooth whitening effect.

Description

口腔用組成物Oral composition
 本発明は、歯の美白(ホワイトニング)効果が優れる口腔用組成物に関する。 The present invention relates to a composition for oral cavity that has an excellent whitening effect on teeth.
 従来、歯を元の色よりも白く見せるための歯の化学的な美白技術として、下記のような提案がされている。
(1)漂白剤を用いた歯の美白。
(2)キレート剤、具体的にはポリリン酸塩などを用いた美白用組成物を、適用用具を用いて歯に保持、固定させることによる歯の美白(特許文献1;特開2000-281548号公報)。
(3)特定の溶剤及び共重合体を用いた非水系組成物を、適用用具を用いて歯に脱着可能に装着させることによる歯の美白(特許文献2;特開2006-8530号公報)。
(4)二酸化チタン、二酸化ケイ素、酸化亜鉛等の白色粉体を含有する組成物を、適用用具で歯に装着させたり、フィルム製剤に調製して歯に貼付することによって、白色粉末を固定し白く見せる方法(特許文献3;特許第483155号公報、特許文献4;特開2008-1649号公報)。
Conventionally, the following proposal has been made as a chemical whitening technique for teeth to make the teeth appear whiter than the original color.
(1) Whitening teeth using bleach.
(2) Whitening of teeth by holding and fixing a whitening composition using a chelating agent, specifically polyphosphate, etc. to the teeth using an application tool (Patent Document 1; JP 2000-281548 A) Publication).
(3) Whitening of a tooth by attaching a non-aqueous composition using a specific solvent and copolymer to the tooth so as to be detachable using an application tool (Patent Document 2; JP-A-2006-8530).
(4) Fix the white powder by applying a composition containing white powder such as titanium dioxide, silicon dioxide, zinc oxide, etc. to the teeth with an application tool, or preparing a film preparation and applying it to the teeth. A method of making it appear white (Patent Document 3; Japanese Patent No. 483155, Patent Document 4; Japanese Patent Application Laid-Open No. 2008-1649).
特開2000-281548号公報JP 2000-281548 A 特開2006-8530号公報JP 2006-8530 A 特許第483155号公報Japanese Patent No. 483155 特開2008-1649号公報JP 2008-1649 A
 しかしながら、(1)は安全面に問題があり、また、(2)~(4)では、歯の美白のために固定手段を用いることもあるため簡便性の面で改善の余地があり、より簡便かつ効果的な歯の美白技術の開発が望まれた。 However, (1) has a problem in safety, and in (2) to (4), there is room for improvement in terms of simplicity because a fixing means may be used for whitening the teeth. Development of a simple and effective whitening technique for teeth was desired.
 本発明は、上記事情に鑑みなされたもので、歯の美白効果が優れる口腔用組成物を提供することを目的とする。 This invention is made | formed in view of the said situation, and it aims at providing the composition for oral cavity which is excellent in the whitening effect of a tooth | gear.
 本発明者らは、上記目的を達成するため鋭意検討を行った結果、(A)六角板状酸化亜鉛が、歯の美白作用に優れ、これを口腔用組成物に配合すると、歯を元の色よりも白くする優れた美白効果を奏することを知見した。即ち、本発明によれば、口腔用組成物に(A)六角板状酸化亜鉛を配合することによって、優れた歯の美白効果を与え、これにより、固定手段を用いることなく通常の歯みがきや洗口だけでも、歯の白さが際立ち、歯の明るさも増し、歯を元の色よりも格段に白く見せることができることを見出し、本発明をなすに至った。 As a result of intensive studies to achieve the above object, the present inventors have found that (A) hexagonal plate-like zinc oxide has an excellent whitening effect on teeth, and when this is blended into an oral composition, It has been found that it has an excellent whitening effect that makes it whiter than the color. That is, according to the present invention, by blending (A) hexagonal plate-like zinc oxide into the oral composition, an excellent tooth whitening effect is provided, thereby allowing normal tooth brushing and washing without using fixing means. It has been found that even with the mouth alone, the whiteness of the teeth stands out, the brightness of the teeth increases, and the teeth can appear much whiter than the original color, and the present invention has been made.
 六角板状の酸化亜鉛は、紫外線防止剤としてファンデーション等の皮膚用化粧料の配合成分としては知られているものの、口腔内に適用する製剤では、一般的に酸化亜鉛として不定形の粒子が用いられていた。そのため、酸化亜鉛として、あえて単結晶の粒子を応用することはなく、口腔用組成物への六角板状酸化亜鉛の配合は今まで知られていなかった。これに対して、本発明では、(A)六角板状酸化亜鉛、特に好ましくは特定の平均粒径及び平均厚さの六角板状の酸化亜鉛が、口腔用組成物において、格段に優れた歯の美白効果を奏し、他の白色顔料の使用では得られない格別な作用効果を奏する。更に、本発明では、(A)成分によって上記の美白効果のみならず、酸化亜鉛由来の収斂感を適度に付与して良好な使用感を与えることもできる。
 なお、白色顔料である酸化亜鉛を使用した歯の美白技術は公知である(特許文献3)が、上述したように、口腔用組成物に使用される酸化亜鉛は通常、不定形の粒子であり、酸化亜鉛であっても不定形の粒子では、本発明の作用効果を得ることができない。後述の比較例にも示すように、(A)成分の代わりに、不定形の酸化亜鉛粉末を用いた場合は美白効果が劣り、また、六角板状であっても雲母チタンを用いた場合も美白効果が劣り、これらでは本発明の作用効果が劣る。
 本発明において、作用機序の詳細は明らかではないが、(A)成分の皮膜形成能や口腔粘膜等への滞留性が寄与することによって、歯を白く見せる効果が優れ、収斂感を満足に付与することもできると推測される。
Hexagonal plate-like zinc oxide is known as a component of skin cosmetics such as foundations as an ultraviolet light inhibitor, but in preparations applied to the oral cavity, amorphous particles are generally used as zinc oxide. It was done. Therefore, single crystal particles are not applied as zinc oxide, and the composition of hexagonal plate-like zinc oxide into the oral composition has not been known so far. On the other hand, in the present invention, (A) hexagonal plate-like zinc oxide, particularly preferably hexagonal plate-like zinc oxide having a specific average particle diameter and average thickness, is an excellent tooth in an oral composition. The whitening effect of the present invention is achieved, and there is a special effect that cannot be obtained by using other white pigments. Furthermore, in the present invention, not only the above-described whitening effect but also an astringent feeling derived from zinc oxide can be appropriately imparted by the component (A) to give a good feeling of use.
In addition, although the whitening technique of the tooth | gear using the zinc oxide which is a white pigment is well-known (patent document 3), as above-mentioned, the zinc oxide used for a composition for oral cavity is usually an amorphous particle. Even with zinc oxide, the effect of the present invention cannot be obtained with irregularly shaped particles. As shown in a comparative example described later, the whitening effect is inferior when an amorphous zinc oxide powder is used instead of the component (A), and even when it is a hexagonal plate, mica titanium may be used. The whitening effect is inferior, and the effect of the present invention is inferior in these.
In the present invention, although the details of the mechanism of action are not clear, the effect of making the teeth whiter is excellent and the astringent feeling is satisfied by the contribution of the film-forming ability of the component (A) and the retention in the oral mucosa. It is speculated that it can also be granted.
 従って、本発明は、下記の口腔用組成物を提供する。
〔1〕
 (A)六角板状酸化亜鉛を含有することを特徴とする口腔用組成物。
〔2〕
 六角板状酸化亜鉛の平均粒径が0.1~10μmである〔1〕に記載の口腔用組成物。
〔3〕
 六角板状酸化亜鉛の平均厚さが0.01~1μmである〔1〕又は〔2〕に記載の口腔用組成物。
〔4〕
 六角板状酸化亜鉛の平均粒径と平均厚さとの比率を示す、平均粒径/平均厚さが0.5~50である〔1〕~〔3〕のいずれかに記載の口腔用組成物。
〔5〕
 (A)成分を0.1~30質量%含有する非シート状の製剤である〔1〕~〔4〕のいずれかに記載の口腔用組成物。
〔6〕
 歯磨剤又は洗口剤である〔5〕に記載の口腔用組成物。
〔7〕
 (A)成分を0.1~95質量%含有するシート状の製剤である〔1〕~〔4〕のいずれかに記載の口腔用組成物。
〔8〕
 更に、(B)界面活性剤を0.1~10質量%含有する〔1〕~〔7〕のいずれかに記載の口腔用組成物。
〔9〕
 歯の美白用である〔1〕~〔8〕のいずれかに記載の口腔用組成物。
Accordingly, the present invention provides the following oral composition.
[1]
(A) A composition for oral cavity containing hexagonal plate-like zinc oxide.
[2]
The oral composition according to [1], wherein the hexagonal plate-like zinc oxide has an average particle size of 0.1 to 10 μm.
[3]
The oral composition according to [1] or [2], wherein the hexagonal plate-like zinc oxide has an average thickness of 0.01 to 1 μm.
[4]
The composition for oral cavity according to any one of [1] to [3], wherein the average particle diameter / average thickness is 0.5 to 50 and represents the ratio between the average particle diameter and the average thickness of hexagonal plate-like zinc oxide .
[5]
The composition for oral cavity according to any one of [1] to [4], which is a non-sheet-form preparation containing 0.1 to 30% by mass of component (A).
[6]
The composition for oral cavity according to [5], which is a dentifrice or mouthwash.
[7]
The oral composition according to any one of [1] to [4], which is a sheet-form preparation containing 0.1 to 95% by mass of component (A).
[8]
The oral composition according to any one of [1] to [7], further comprising (B) a surfactant in an amount of 0.1 to 10% by mass.
[9]
The oral composition according to any one of [1] to [8], which is used for whitening teeth.
 本発明によれば、歯の美白効果が優れる口腔用組成物を提供できる。本発明の口腔用組成物は、簡便かつ効果的に歯を美白し、歯を元の色よりも白くみせることもできることから、歯の美白用として有効に使用できる。 According to the present invention, an oral composition having an excellent whitening effect on teeth can be provided. The composition for oral cavity of the present invention can be effectively used for whitening teeth because it can easily and effectively whiten teeth and make the teeth whiter than the original color.
本発明の実施例で用いた(A)酸化亜鉛(六角板状)の形状を示す2次元の画像である。It is a two-dimensional image which shows the shape of (A) zinc oxide (hexagonal plate shape) used in the Example of this invention.
 本発明においては、(A)六角板状酸化亜鉛が、歯を美白するための有効成分として、口腔用組成物に配合される。 In the present invention, (A) hexagonal plate-like zinc oxide is blended in an oral composition as an active ingredient for whitening teeth.
 (A)六角板状酸化亜鉛は、歯の美白(ホワイトニング)作用を奏し、また、収斂感を与える。六角板状酸化亜鉛は、六角形で板状の粒子であればその種類などに制限はなく、公知の単結晶性の六角板状酸化亜鉛を使用し得る。なお、六角板状酸化亜鉛は、水に分散させて使用することができる。 (A) Hexagonal plate-like zinc oxide has a whitening effect on teeth and gives a sense of convergence. The hexagonal plate-like zinc oxide is not particularly limited as long as it is hexagonal and plate-like particles, and known single crystal hexagonal plate-like zinc oxide can be used. The hexagonal plate-like zinc oxide can be used by being dispersed in water.
 六角板状酸化亜鉛の平均粒径は、好ましくは0.1μm以上、より好ましくは0.5μm以上、更に好ましくは1μm以上、とりわけ1.5μm以上であり、また、10μm以下が好ましく、より好ましくは8μm以下、更に好ましくは5μm以下である。0.1μm以上であると、美白効果が十分に発揮される。10μm以下であると、収斂感が十分に発揮される。本発明における六角板状酸化亜鉛の「粒径」とは、六角板状粒子の六角形面の3本の対角線の長さの平均値である。
 上記平均粒径は、画像解析、具体的には六角板状酸化亜鉛20個をランダムに選択し、各粒子の対角線の長さをそれぞれ測定して平均することによって算出した。粒径測定には日本電子(株)製の走査電子顕微鏡(SEM)JSM7600Fを使用した。各粒子の粒径は、Z軸方向からの画像から六角形の3本の対角線の長さを測定し平均した(以下同様)。
The average particle size of the hexagonal plate-like zinc oxide is preferably 0.1 μm or more, more preferably 0.5 μm or more, still more preferably 1 μm or more, particularly 1.5 μm or more, and preferably 10 μm or less, more preferably It is 8 μm or less, more preferably 5 μm or less. When it is 0.1 μm or more, the whitening effect is sufficiently exhibited. When the thickness is 10 μm or less, the convergence feeling is sufficiently exhibited. The “particle size” of the hexagonal plate-like zinc oxide in the present invention is an average value of the lengths of the three diagonal lines of the hexagonal surface of the hexagonal plate-like particle.
The average particle size was calculated by image analysis, specifically, by randomly selecting 20 hexagonal plate-like zinc oxides, and measuring and averaging the lengths of the diagonal lines of each particle. For the particle size measurement, a scanning electron microscope (SEM) JSM7600F manufactured by JEOL Ltd. was used. The particle size of each particle was measured by averaging the lengths of three hexagonal diagonal lines from the image from the Z-axis direction (the same applies hereinafter).
 六角板状酸化亜鉛の平均厚さは、好ましくは0.01μm以上、より好ましくは0.1μm以上、更に好ましくは0.2μm以上であり、また、1μm以下が好ましく、より好ましくは0.8μm以下、更に好ましくは0.7μm以下である。平均厚さが0.01μm以上であると、美白効果が十分に発揮される。1μm以下であると、収斂感が十分に発揮される。本発明における六角板状酸化亜鉛の「厚さ」とは、六角板状粒子の六角形面2面間の距離である。
 なお、上記の平均厚さは、日本電子(株)製の走査電子顕微鏡(SEM)JSM7600Fを使用し、六角板状酸化亜鉛20個をランダムに選択し、Y軸方向からの画像から各粒子の厚さを測定して平均することによって算出した。各粒子の厚さは、板状の上面と下面との距離(長さ)を測定した(以下同様)。
The average thickness of the hexagonal plate-like zinc oxide is preferably 0.01 μm or more, more preferably 0.1 μm or more, still more preferably 0.2 μm or more, and preferably 1 μm or less, more preferably 0.8 μm or less. More preferably, it is 0.7 μm or less. When the average thickness is 0.01 μm or more, the whitening effect is sufficiently exhibited. When the thickness is 1 μm or less, a feeling of convergence is sufficiently exhibited. The “thickness” of hexagonal plate-like zinc oxide in the present invention is a distance between two hexagonal surfaces of hexagonal plate-like particles.
In addition, said average thickness uses the scanning electron microscope (SEM) JSM7600F by JEOL Co., Ltd., 20 hexagonal plate-like zinc oxides were selected at random, and each particle | grain was measured from the image from the Y-axis direction. The thickness was calculated by measuring and averaging. The thickness of each particle was measured by measuring the distance (length) between the plate-like upper surface and lower surface (the same applies hereinafter).
 六角板状酸化亜鉛は、上記の平均粒径と平均厚さとの比率を示す、平均粒径/平均厚さが、好ましくは0.5以上、より好ましくは1以上、更に好ましくは2以上であり、また、50以下が好ましく、より好ましくは30以下であり、5以下であってもよい。平均粒径/平均厚さが0.5以上であると、美白効果が十分に発揮される。50以下であると、収斂感が十分に発揮される。 The hexagonal plate-like zinc oxide shows the ratio between the average particle diameter and the average thickness, and the average particle diameter / average thickness is preferably 0.5 or more, more preferably 1 or more, and further preferably 2 or more. Moreover, 50 or less is preferable, More preferably, it is 30 or less, and may be 5 or less. When the average particle size / average thickness is 0.5 or more, the whitening effect is sufficiently exhibited. When it is 50 or less, a feeling of convergence is sufficiently exhibited.
 また、六角板状酸化亜鉛の吸油量は、好ましくは45g/100g以下、より好ましくは36g/100g以下である。吸油量は、JIS K-5101-13-1に準じ測定した。 Further, the oil absorption amount of hexagonal plate-like zinc oxide is preferably 45 g / 100 g or less, more preferably 36 g / 100 g or less. The oil absorption was measured according to JIS K-5101-13-1.
 このような六角板状酸化亜鉛としては、市販品を使用できる。例えば、六角板状酸化亜鉛XZシリーズのXZ-100F、XZ-300F、XZ-1000F、XZ-2000F、XZ-3000F(いずれも堺化学工業(株)製)等が挙げられる。 As such hexagonal plate-like zinc oxide, commercially available products can be used. Examples include hexagonal plate-like zinc oxide XZ series XZ-100F, XZ-300F, XZ-1000F, XZ-2000F, and XZ-3000F (all manufactured by Sakai Chemical Industry Co., Ltd.).
 (A)六角板状酸化亜鉛の配合量は、特に制限されないが、好ましくは組成物全体の0.1%(質量%、以下同様)以上、特に0.5%以上、とりわけ1%以上である。また、組成物全体の95%以下が好ましく、より好ましくは30%以下、特に20%以下、とりわけ10%以下である。0.1%以上であると、美白効果が十分に発揮され、また、収斂感が十分に発揮される。多く配合し過ぎないほうが、それ自身の金属味が強く発現するのを防止して使用感を良好に維持でき、この点で95%以下が良い。 (A) Although the compounding quantity of hexagonal plate-shaped zinc oxide is not restrict | limited in particular, Preferably it is 0.1% (mass%, the following is similar) or more of the whole composition, 0.5% or more especially, 1% or more especially. . Moreover, 95% or less of the whole composition is preferable, More preferably, it is 30% or less, Especially 20% or less, Especially 10% or less. When it is 0.1% or more, the whitening effect is sufficiently exhibited, and the convergence feeling is sufficiently exhibited. If not added too much, it is possible to prevent a strong metallic taste and maintain a good feeling of use. In this respect, 95% or less is good.
 更に、口腔用組成物として一般的な形態、例えば歯磨剤、洗口剤等の非シート状の形態に調製することができる。このような非シート状の製剤では、(A)成分の配合量は、組成物全体の0.1~30%、特に0.1~20%が好ましく、より好ましくは0.1~5%、更に好ましくは0.5~3%、とりわけ好ましくは1.0~2%である。
 また、本発明の口腔用組成物は、後述のようにパック剤、フィルム剤等のシート状の形態にも調製できるが、このようなシート状の製剤では、組成的に(A)成分を比較的多く配合可能である。この場合、(A)成分の配合量は、美白効果及び使用感の点から、組成物全体の0.1~95%とすることができるが、0.1~20%が好ましく、より好ましくは0.1~5%である。
Further, it can be prepared in a general form as a composition for oral cavity, for example, a non-sheet form such as a dentifrice and a mouthwash. In such a non-sheet-form preparation, the blending amount of the component (A) is preferably 0.1 to 30%, particularly preferably 0.1 to 20%, more preferably 0.1 to 5% of the whole composition, More preferably, it is 0.5 to 3%, and particularly preferably 1.0 to 2%.
Moreover, although the composition for oral cavity of this invention can be prepared also in sheet-like forms, such as a pack agent and a film agent, as mentioned later, in such a sheet-form preparation, (A) component is compared compositionally. Can be blended as much as possible. In this case, the blending amount of the component (A) can be 0.1 to 95% of the whole composition from the viewpoint of the whitening effect and the feeling of use, but is preferably 0.1 to 20%, more preferably 0.1 to 5%.
 本発明では、更に、(B)界面活性剤を配合することが好ましい。(B)界面活性剤を配合すると、(A)成分の分散性が向上し、美白効果がより高まる。 In the present invention, it is preferable to further blend (B) a surfactant. When (B) a surfactant is added, the dispersibility of the component (A) is improved and the whitening effect is further increased.
 界面活性剤としては、口腔用として公知のアニオン性界面活性剤、ノニオン性界面活性剤、両性界面活性剤等が挙げられ、何れでもよい。具体的にアニオン性界面活性剤としては、ラウリル硫酸ナトリウム等のアルキル硫酸塩、N-ラウロイルサルコシンナトリウム等のN-アシルサルコシン酸塩、N-アシルグルタミン酸塩等のアシルアミノ酸塩、α-オレフィンスルホン酸ナトリウムなどが挙げられる。
 ノニオン性界面活性剤としては、ショ糖脂肪酸エステル等の糖脂肪酸エステル、糖アルコール脂肪酸エステル、ソルビタン脂肪酸エステル、グリセリン脂肪酸エステル、モノラウリン酸デカグリセリル等のポリグリセリン脂肪酸エステル、エチレンオキサイドの平均付加モル数(E.O.)が10~60であるポリオキシエチレン硬化ヒマシ油等のポリオキシエチレン脂肪酸エステル、ポリオキシエチレン高級アルコールエーテル、ラウリン酸ジエタノールアミド等の脂肪酸アルカノールアミドなどが挙げられる。
 両性界面活性剤としては、アルキルベタイン、アルキルジメチルアミノ酢酸ベタイン,脂肪酸アミドプロピルベタイン,脂肪酸アミドプロピルジメチルアミノ酢酸ベタイン等の酢酸ベタイン型、アルキルイミダゾリニウムベタイン等のベタイン型、N-脂肪酸アシル-N-カルボキシメチル-N-ヒドロキシエチルエチレンジアミン塩等のイミダゾリン型が挙げられる。
 これらの中で、特にアニオン性界面活性剤が好ましく、スルホン酸基を有するアニオン性界面活性剤がより好ましく、アルキル硫酸塩、α-オレフィンスルホン酸塩がより好ましい。とりわけラウリル硫酸ナトリウム、テトラデセンスルホン酸ナトリウムが、(A)成分の分散性の点から好ましい。
 (B)界面活性剤の配合量は、組成物全体の0.1~10%が好ましく、特に好ましくは1~5%である。
Examples of the surfactant include known anionic surfactants, nonionic surfactants, and amphoteric surfactants for oral use, and any of them may be used. Specific examples of anionic surfactants include alkyl sulfates such as sodium lauryl sulfate, N-acyl sarcosine salts such as N-lauroyl sarcosine sodium, acyl amino acid salts such as N-acyl glutamate, and α-olefin sulfonic acids. Sodium etc. are mentioned.
Nonionic surfactants include sugar fatty acid esters such as sucrose fatty acid esters, sugar alcohol fatty acid esters, sorbitan fatty acid esters, glycerin fatty acid esters, polyglycerin fatty acid esters such as decaglyceryl monolaurate, and average added moles of ethylene oxide ( And polyoxyethylene fatty acid esters such as polyoxyethylene hydrogenated castor oil having an EO) of 10 to 60, fatty acid alkanolamides such as polyoxyethylene higher alcohol ethers and lauric acid diethanolamide.
Examples of amphoteric surfactants include betaine types such as alkylbetaines, alkyldimethylaminoacetic acid betaines, fatty acid amidopropyl betaines, fatty acid amidopropyldimethylaminoacetic acid betaines, betaine types such as alkylimidazolinium betaines, and N-fatty acid acyl-N. Examples include imidazoline type such as -carboxymethyl-N-hydroxyethylethylenediamine salt.
Among these, anionic surfactants are particularly preferable, anionic surfactants having a sulfonic acid group are more preferable, and alkyl sulfates and α-olefin sulfonates are more preferable. In particular, sodium lauryl sulfate and sodium tetradecenesulfonate are preferable from the viewpoint of dispersibility of the component (A).
The blending amount of the (B) surfactant is preferably from 0.1 to 10%, particularly preferably from 1 to 5%, based on the entire composition.
 本発明の口腔用組成物は、ペースト状、ゲル状、液体等の液状、固体等の形状にすることができ、練歯磨,液体歯磨,液状歯磨等の歯磨剤、洗口剤などとして調製し得る。更に、固定手段を使用しなくても歯に貼付し得る形態、具体的にはパック剤、フィルム剤等のシート状の口腔用製剤に調製することもできる。特に歯磨剤又は洗口剤が、本効果の発現性、使用性の点で好ましい。
 なお、ここで、パック剤とは、シートの膏体面を歯に貼り付けて支持体を剥がし、膏体を歯面上に移して、膏体を歯磨剤等として使用する製剤である。フィルム剤とは、フィルムを歯面に貼り付け、そのままブラッシングすることで、フィルム全体が歯磨剤等として使用される製剤であり、例えば縦2.5cm、横2cm、厚さ0.3mm程度の歯に適用可能な大きさ・形状に調製できる。
The composition for oral cavity of the present invention can be made into paste, gel, liquid such as liquid, solid, etc., and prepared as a toothpaste such as toothpaste, liquid dentifrice, liquid dentifrice, mouthwash, etc. obtain. Furthermore, it is also possible to prepare a form that can be applied to teeth without using a fixing means, specifically, a sheet-form oral preparation such as a pack or film. In particular, dentifrices or mouthwashes are preferred in terms of the manifestation and usability of this effect.
Here, the pack agent is a preparation in which the plaster surface of a sheet is attached to a tooth, the support is peeled off, the plaster is transferred onto the tooth surface, and the plaster is used as a dentifrice or the like. A film agent is a preparation in which the entire film is used as a dentifrice etc. by sticking the film to the tooth surface and brushing as it is. For example, a tooth having a length of 2.5 cm, a width of 2 cm, and a thickness of about 0.3 mm The size and shape can be adjusted.
 この場合、組成物の目的、剤型等に応じて、上述した成分以外にも口腔用組成物用として公知の通常配合される成分を必要に応じて配合することができ、形態等に応じた通常の方法で調製できる。例えば、研磨剤、粘稠剤、粘結剤、甘味剤、防腐剤、着色剤、香料、(A)成分以外の有効成分等を配合できる。また、シート剤では、ゲル化、ペースト化して歯への塗布性や歯との粘着性を高める目的で各種のゲル化剤を使用することもできる。 In this case, depending on the purpose of the composition, dosage form, and the like, in addition to the above-described components, components that are commonly blended for oral compositions can be blended as necessary, depending on the form and the like. It can be prepared by conventional methods. For example, abrasives, thickeners, binders, sweeteners, preservatives, colorants, fragrances, active ingredients other than the component (A), and the like can be blended. Moreover, in a sheet agent, various gelling agents can also be used in order to gelatinize and paste and to improve the applicability to a tooth and adhesiveness with a tooth.
 研磨剤としては、沈降性シリカ、アルミノシリケート、ジルコノシリケート等のシリカ系研磨剤、リン酸カルシウム系研磨剤、炭酸カルシウム等が挙げられる(配合量は、通常、2~50%、特に10~40%)。 Examples of the abrasive include silica-based abrasives such as precipitated silica, aluminosilicate, zirconosilicate, calcium phosphate-based abrasives, calcium carbonate and the like (the amount is usually 2 to 50%, particularly 10 to 40%). ).
 湿潤剤(粘稠剤)としては、ソルビット、キシリット等の糖アルコール、グリセリン、プロピレングリコール、平均分子量160~4000(医薬部外品原料規格2006記載の平均分子量)のポリエチレングリコール等の多価アルコールが挙げられる(配合量は、通常、5~50%)。 Examples of the wetting agent (thickening agent) include sugar alcohols such as sorbit and xylite, glycerin, propylene glycol, and polyhydric alcohols such as polyethylene glycol having an average molecular weight of 160 to 4000 (average molecular weight described in Quasi-drug Raw Material Standard 2006). (The amount is usually 5 to 50%).
 粘結剤としては、カルボキシメチルセルロースナトリウム、ヒドロキシエチルセルロース、ヒドロキシプロピルセルロース等のセルロース誘導体、アルギン酸ナトリウム等のアルギン酸又はその誘導体、キサンタンガム等のガム類、カラギーナン、ポリビニルアルコール、ポリアクリル酸ナトリウムなどの有機粘結剤、ゲル化性シリカ、ゲル化性アルミニウムシリカ、ビーガム、ラポナイト等の無機粘結剤が挙げられる(配合量は、通常、0.1~10%)。 Examples of binders include cellulose derivatives such as sodium carboxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, alginic acid or its derivatives such as sodium alginate, gums such as xanthan gum, organic binders such as carrageenan, polyvinyl alcohol, and sodium polyacrylate. And inorganic binders such as an agent, gelling silica, gelling aluminum silica, bee gum, and laponite (the blending amount is usually 0.1 to 10%).
 甘味剤としてはサッカリンナトリウム等、防腐剤としては、パラオキシ安息香酸メチル等のパラオキシ安息香酸エステル、安息香酸ナトリウム等の安息香酸又はその塩などが挙げられる。
 着色剤としては、青色1号、黄色4号、二酸化チタン等が挙げられる。
Examples of the sweetening agent include sodium saccharin, and examples of the preservative include paraoxybenzoic acid esters such as methyl paraoxybenzoate, benzoic acid such as sodium benzoate, and salts thereof.
Examples of the colorant include blue No. 1, yellow No. 4, titanium dioxide and the like.
 香料としては、ペパーミント油、スペアミント油、アニス油、ユーカリ油、ウィンターグリーン油、カシア油、クローブ油、タイム油、セージ油、レモン油、オレンジ油、ハッカ油、カルダモン油、コリアンダー油、マンダリン油、ライム油、ラベンダー油、ローズマリー油、ローレル油、カモミル油、キャラウェイ油、マジョラム油、ベイ油、レモングラス油、オリガナム油、パインニードル油、ネロリ油、ローズ油、ジャスミン油、グレープフルーツ油、スウィーティー油、柚油、イリスコンクリート、アブソリュートペパーミント、アブソリュートローズ、オレンジフラワー等の天然香料や、これら天然香料の加工処理(前溜部カット、後溜部カット、分溜、液液抽出、エッセンス化、粉末香料化等)した香料、及び、メントール、カルボン、アネトール、シネオール、サリチル酸メチル、シンナミックアルデヒド、オイゲノール、3-l-メントキシプロパン-1,2-ジオール、チモール、リナロール、リナリールアセテート、リモネン、メントン、メンチルアセテート、N-置換-パラメンタン-3-カルボキサミド、ピネン、オクチルアルデヒド、シトラール、プレゴン、カルビールアセテート、アニスアルデヒド、エチルアセテート、エチルブチレート、アリルシクロヘキサンプロピオネート、メチルアンスラニレート、エチルメチルフェニルグリシデート、バニリン、ウンデカラクトン、ヘキサナール、ブタノール、イソアミルアルコール、ヘキセノール、ジメチルサルファイド、シクロテン、フルフラール、トリメチルピラジン、エチルラクテート、エチルチオアセテート等の単品香料、更に、ストロベリーフレーバー、アップルフレーバー、バナナフレーバー、パイナップルフレーバー、グレープフレーバー、マンゴーフレーバー、バターフレーバー、ミルクフレーバー、フルーツミックスフレーバー、トロピカルフルーツフレーバー等の調合香料など、口腔用組成物に用いられる公知の香料素材を組み合わせて使用することができる。配合量は特に限定されないが、通常、上記の香料素材では0.000001~1%が好ましく、また、上記香料素材を使用した賦香用香料では0.1~2%が好ましい。 Perfumes include peppermint oil, spearmint oil, anise oil, eucalyptus oil, winter green oil, cassia oil, clove oil, thyme oil, sage oil, lemon oil, orange oil, peppermint oil, cardamom oil, coriander oil, mandarin oil, Lime oil, lavender oil, rosemary oil, laurel oil, camomil oil, caraway oil, marjoram oil, bay oil, lemongrass oil, origanum oil, pine needle oil, neroli oil, rose oil, jasmine oil, grapefruit oil, sweetie Natural fragrances such as oil, bran oil, Iris concrete, absolute peppermint, absolute rose, orange flower, and processing of these natural fragrances (front reservoir cut, rear reservoir cut, fractional distillation, liquid-liquid extraction, essence, powder Perfumes, etc.) and menthol, Rubon, Anethole, Cineol, Methyl salicylate, Synamic aldehyde, Eugenol, 3-l-Mentoxypropane-1,2-diol, Thymol, Linalool, Linarel acetate, Limonene, Menthone, Menthyl acetate, N-Substituted paramenthane 3-carboxamide, pinene, octylaldehyde, citral, pulegone, carbyl acetate, anisaldehyde, ethyl acetate, ethyl butyrate, allylcyclohexane propionate, methyl anthranilate, ethyl methyl phenyl glycidate, vanillin, undecalactone, Hexanal, butanol, isoamyl alcohol, hexenol, dimethyl sulfide, cycloten, furfural, trimethylpyrazine, ethyl lactate, ethyl Oral compositions such as single flavors such as oacetate, and other flavors such as strawberry flavor, apple flavor, banana flavor, pineapple flavor, grape flavor, mango flavor, butter flavor, milk flavor, fruit mix flavor, tropical fruit flavor, etc. It can be used in combination with known perfume materials used in the above. The blending amount is not particularly limited, but usually 0.000001 to 1% is preferable for the above fragrance materials, and 0.1 to 2% is preferable for the fragrance materials using the above fragrance materials.
 有効成分としては、フッ化ナトリウム,モノフルオロリン酸ナトリウム等のフッ素含有化合物、イソプロピルメチルフェノール,塩化セチルピリジニウム等のカチオン性殺菌剤、抗炎症剤、デキストラナーゼ等の酵素、水溶性のリン酸化合物や銅化合物、ビタミン類、植物抽出物、歯石防止剤、歯垢防止剤などが挙げられる。有効成分は、本発明の効果を妨げない範囲で有効量配合できる。 Active ingredients include fluorine-containing compounds such as sodium fluoride and sodium monofluorophosphate, cationic fungicides such as isopropylmethylphenol and cetylpyridinium chloride, enzymes such as anti-inflammatory agents and dextranase, and water-soluble phosphoric acid. Examples thereof include compounds, copper compounds, vitamins, plant extracts, calculus inhibitors, and plaque inhibitors. The active ingredient can be blended in an effective amount as long as the effects of the present invention are not hindered.
 シート状の口腔用製剤に調製する場合は、ゲル化剤として、上述した粘結剤と同様の物質を使用することができるが、口中での使用感の点から、カルボキシメチルセルロースナトリウム、ヒドロキシエチルセルロース、ヒドロキシプロピルセルロース等のセルロース誘導体、ポリビニルアルコール、アルギン酸ナトリウムが好ましい(配合量は、好ましくは1~5%)。 When preparing into a sheet-form oral preparation, the same material as the above-mentioned binder can be used as a gelling agent, but from the viewpoint of use feeling in the mouth, sodium carboxymethylcellulose, hydroxyethylcellulose, Cellulose derivatives such as hydroxypropyl cellulose, polyvinyl alcohol, and sodium alginate are preferred (the amount is preferably 1 to 5%).
 本発明において、シート状の口腔用製剤については、歯に適用できればその形、厚さ等の形状、使用形態などに特に制限はなく、1本又は2本以上の歯面に貼付可能な形態でもよく、また、歯面に貼付して使用後にそのままブラッシングすることで歯磨剤として使用することもできる。
 なお、パック剤は、支持体上に膏体組成物が剥離可能に展延されて一体化されていることが好ましい。支持体としては、水不溶性の材質のものを用いることが好ましく、ポリプロピレン、ポリエチレン、ポリウレタン等の材質のフィルムや不織布、織布、網布が挙げられる。前記フィルムは単層又は積層フィルム、あるいはフィルムと不職布、織布、網布との積層シートを使用できる。更に、剥離ライナーを被覆して膏体組成物を保護してもよい。これらは市販品を使用し得る。
In the present invention, the sheet-form oral preparation is not particularly limited as long as it can be applied to teeth, and there is no particular limitation on the shape, thickness, etc., usage form, and the like, even in a form that can be applied to one or more tooth surfaces. Well, it can also be used as a dentifrice by sticking on the tooth surface and brushing as it is after use.
In addition, it is preferable that the plaster composition is spread and integrated on the support so that the plaster composition is peelable. As the support, a water-insoluble material is preferably used, and examples thereof include films, nonwoven fabrics, woven fabrics, and mesh fabrics of materials such as polypropylene, polyethylene, and polyurethane. The film may be a single layer or a laminated film, or a laminated sheet of a film and unemployed cloth, woven cloth or net cloth. Further, the plaster composition may be protected by coating a release liner. These can use a commercial item.
 以下、実施例及び比較例を示し、本発明を具体的に説明するが、本発明は下記の実施例に制限されるものではない。なお、下記の例において%は特に断らない限りいずれも質量%を示す。 Hereinafter, although an Example and a comparative example are shown and this invention is demonstrated concretely, this invention is not restrict | limited to the following Example. In the following examples, “%” means “% by mass” unless otherwise specified.
 [実施例、比較例]
 表1、2に示す組成の水分散液(単純系)、表3~7に示す組成の歯磨剤、洗口剤、パック剤又はフィルム剤(製剤系)をそれぞれ常法によって調製し、下記に示す方法で評価した。結果を表に併記した。
[Examples and Comparative Examples]
Prepare aqueous dispersions (simple systems) having the compositions shown in Tables 1 and 2 and dentifrices, mouth washes, packs or film preparations (formulation systems) having the compositions shown in Tables 3 to 7, respectively. Evaluation was performed by the method shown. The results are shown in the table.
 使用原料の詳細を下記に示す。
(A)酸化亜鉛(六角板状);
 六角板状酸化亜鉛XZシリーズ(XZ-100F、300F、1000F、2000F、3000F)、堺化学工業(株)製、単結晶性
 XZ-100F:平均粒径0.1μm、平均厚さ0.03μm、吸油量42g/100g
 XZ-300F:平均粒径0.3μm、平均厚さ0.08μm、吸油量37g/100g
 XZ-1000F:平均粒径1μm、平均厚さ0.3μm、吸油量36g/100g
 XZ-2000F:平均粒径2μm、平均厚さ0.5μm、吸油量34g/100g
 XZ-3000F:平均粒径3μm、平均厚さ0.8μm、吸油量32g/100g
 これらの原料を適宜分級し、実験に使用した。使用したサンプルの平均粒径及び平均厚さはそれぞれ表に示した。
酸化亜鉛(粉末状、比較品);
 不定形の粉末、日本薬局方酸化亜鉛、堺化学工業(株)製、非晶性、
 平均粒径2μm、平均厚さ2μm、吸油量59g/100g
雲母チタン(六角板状、比較品);
 TIMIRON MP-149、メルク社製、単結晶性、
 平均粒径2μm、平均厚さ0.5μm
Details of the raw materials used are shown below.
(A) Zinc oxide (hexagonal plate shape);
Hexagonal zinc oxide XZ series (XZ-100F, 300F, 1000F, 2000F, 3000F), manufactured by Sakai Chemical Industry Co., Ltd., single crystal XZ-100F: average particle size 0.1 μm, average thickness 0.03 μm, Oil absorption 42g / 100g
XZ-300F: Average particle size 0.3 μm, average thickness 0.08 μm, oil absorption 37 g / 100 g
XZ-1000F: Average particle diameter 1 μm, average thickness 0.3 μm, oil absorption 36 g / 100 g
XZ-2000F: Average particle diameter 2 μm, average thickness 0.5 μm, oil absorption 34 g / 100 g
XZ-3000F: Average particle size 3 μm, average thickness 0.8 μm, oil absorption 32 g / 100 g
These raw materials were classified appropriately and used for experiments. The average particle diameter and average thickness of the samples used are shown in the table.
Zinc oxide (powder, comparative product);
Amorphous powder, Japanese Pharmacopoeia zinc oxide, manufactured by Sakai Chemical Industry Co., Ltd., amorphous
Average particle size 2μm, average thickness 2μm, oil absorption 59g / 100g
Mica titanium (hexagonal plate, comparative product);
TIMIRON MP-149, manufactured by Merck Ltd., single crystal,
Average particle size 2μm, average thickness 0.5μm
 上記の平均粒径、平均厚さの測定方法を下記に示す。
平均粒径の測定方法;
 画像解析で算出し、日本電子(株)製の走査電子顕微鏡(SEM)JSM7600Fを使用し、上記と同様に測定、解析して求めた。Z軸方向からの画像から六角形の3本の対角線の長さを測定して粒径とし、平均粒径を算出した。
平均厚さの測定方法;
 日本電子(株)製の走査電子顕微鏡(SEM)JSM7600Fを使用し、上記と同様に測定し、平均値を求めた。粒子の板状の上面と下面との長さを測定して厚さとし、平均厚さを算出した。
 なお、酸化亜鉛(六角板状)及び雲母チタン(六角板状)の平均粒径、平均厚さの測定法はそれぞれ上記の通りであり、また、酸化亜鉛(粉末状)の平均粒径は、(株)堀場製作所製のレーザ回折散乱式粒度分布測定装置LA-920によって測定し、平均厚さは、酸化亜鉛(粉末状)の形状が球状に近いため、便宜上、平均粒径を平均厚さとした。
 吸油量は、JIS K-5101-13-1に準じて測定した。
 また、(A)酸化亜鉛(六角板状)の2次元の画像(日本電子(株)製の走査電子顕微鏡(SEM)JSM7600Fを使用して撮影)を図1に示す。
The measuring method of said average particle diameter and average thickness is shown below.
Measuring the average particle size;
It was calculated by image analysis, and measured and analyzed in the same manner as described above using a scanning electron microscope (SEM) JSM7600F manufactured by JEOL. From the image from the Z-axis direction, the lengths of the three diagonal lines of the hexagon were measured to obtain the particle size, and the average particle size was calculated.
Average thickness measurement method;
Using a scanning electron microscope (SEM) JSM7600F manufactured by JEOL Ltd., measurement was performed in the same manner as described above, and an average value was obtained. The length of the plate-like upper and lower surfaces of the particles was measured to obtain the thickness, and the average thickness was calculated.
In addition, the measuring method of the average particle diameter of zinc oxide (hexagonal plate shape) and mica titanium (hexagonal plate shape) and average thickness is as described above, respectively, and the average particle size of zinc oxide (powdered shape) is The average thickness is measured by a laser diffraction scattering type particle size distribution measuring apparatus LA-920 manufactured by HORIBA, Ltd. Since the shape of zinc oxide (powder) is nearly spherical, the average particle size is defined as the average thickness for convenience. did.
The oil absorption was measured according to JIS K-5101-13-1.
FIG. 1 shows a two-dimensional image of (A) zinc oxide (hexagonal plate) (taken using a scanning electron microscope (SEM) JSM7600F manufactured by JEOL Ltd.).
評価方法-1:ハイドロキシアパタイト(HAP)板の明度測定方法及び白さの程度の評価方法(単純系)
 酸化亜鉛を量り取り、水100mlに分散させた。この分散液中に、直径7mmのハイドロキシアパタイト(HAP)板を入れ、3分間経過後、HAP板を取り出し、100mlの水で軽くすすいだ。このHAP板を色差計(分光色差計 SE-2000、日本電色工業(株)製)で測定し、明度の指標であるΔLの値を得た。対照として、未処理品(未処理のHAP板)を同様に測定した。比較例は、上記方法に準じて同様に測定した。
 また、10名の被験者に対し、HAP板の白さの程度についてアンケートを行った。下記の評点基準に基づき評点(1~4点)をつけ、得られた結果から平均値を算出した。算出した評点の平均値から、下記の評価基準に基づきHAP板の白さの程度を評価した。なお、未処理のHAP板を対照とした。
 〔評点基準〕
  4点:とても白くなった
  3点:白くなった
  2点:やや白くなった
  1点:白くならなかった
 〔評価基準〕
  ☆:平均値3.5点以上
  ◎:平均値3.0点以上3.5点未満
  ○:平均値2.5点以上3.0点未満
  △:平均値2.0点以上2.5点未満
  ×:平均値2.0点未満
Evaluation method-1: Lightness measurement method of hydroxyapatite (HAP) plate and evaluation method of degree of whiteness (simple system)
Zinc oxide was weighed and dispersed in 100 ml of water. A hydroxyapatite (HAP) plate having a diameter of 7 mm was put in this dispersion, and after 3 minutes, the HAP plate was taken out and lightly rinsed with 100 ml of water. This HAP plate was measured with a color difference meter (spectral color difference meter SE-2000, manufactured by Nippon Denshoku Industries Co., Ltd.) to obtain a value of ΔL which is an index of brightness. As a control, an untreated product (untreated HAP plate) was measured in the same manner. The comparative example was similarly measured according to the above method.
In addition, a questionnaire was conducted on the degree of whiteness of the HAP plate for 10 subjects. A score (1 to 4 points) was assigned based on the following criteria, and an average value was calculated from the obtained results. From the calculated average score, the degree of whiteness of the HAP plate was evaluated based on the following evaluation criteria. An untreated HAP plate was used as a control.
[Score standard]
4 points: very white 3 points: white 2 points: slightly white 1 point: not white [Evaluation Criteria]
☆: Average value 3.5 points or more ◎: Average value 3.0 points or more and less than 3.5 points ○: Average value 2.5 points or more and less than 3.0 points △: Average value 2.0 points or more and 2.5 points Less than ×: Average value less than 2.0 points
評価方法-2:ハイドロキシアパタイト(HAP)板の明度測定方法及び白さの程度の評価方法(製剤系)
 歯磨剤、パック剤(膏体)、フィルム剤は試料を水で3倍に希釈し、約100mlの分散液を作り、評価液とした。洗口剤は、そのまま評価液とした。この分散液中に、直径7mmのハイドロキシアパタイト(HAP)板を入れ、3分間経過後、HAP板を取り出し、100mlの水で軽くすすいだ。このHAP板を色差計(分光色差計 SE-2000、日本電色工業(株)製)で測定し、明度の指標であるΔLの値を得た。対照として、未処理品(未処理のHAP板)を同様に測定した。比較例は、上記方法に準じて同様に測定した。
 また、評価方法-1と同様にして、HAP板の白さの程度について評価した。
Evaluation method-2: Lightness measurement method of hydroxyapatite (HAP) plate and evaluation method of degree of whiteness (formulation system)
Dentifrices, packs (plasters), and film preparations were diluted three times with water to prepare a dispersion of about 100 ml, which was used as an evaluation solution. The mouthwash was directly used as an evaluation solution. A hydroxyapatite (HAP) plate having a diameter of 7 mm was put in this dispersion, and after 3 minutes, the HAP plate was taken out and lightly rinsed with 100 ml of water. This HAP plate was measured with a color difference meter (spectral color difference meter SE-2000, manufactured by Nippon Denshoku Industries Co., Ltd.) to obtain a value of ΔL which is an index of brightness. As a control, an untreated product (untreated HAP plate) was measured in the same manner. The comparative example was similarly measured according to the above method.
Further, the degree of whiteness of the HAP plate was evaluated in the same manner as in the evaluation method-1.
評価方法-3:収斂感の評価方法(製剤系)
 10名の被験者に対し、各製剤を使用後の収斂感の高さについてアンケートを行った。下記の評点基準に基づき評点(1~4点)をつけ、得られた結果から平均値を算出した。算出した評点の平均値から、下記の評価基準に基づきブラッシング後の収斂感の高さについて評価した。
 なお、歯磨剤において、歯みがきは、各被験者において、歯磨剤組成物約1gを歯ブラシにとり、3分間ブラッシング後、口腔内を水ですすぐことにより実施した。その他の製剤は、それぞれ常法で使用した。
 〔評点基準〕
  4点:収斂感を高く感じた
  3点:収斂感を感じた
  2点:やや収斂感を感じた
  1点:収斂感を感じなかった
 〔評価基準〕
  ☆:平均値3.5点以上
  ◎:平均値3.0点以上3.5点未満
  ○:平均値2.5点以上3.0点未満
  △:平均値2.0点以上2.5点未満
  ×:平均値2.0点未満
Evaluation method-3: Evaluation method of astringency (formulation system)
A questionnaire was conducted on 10 subjects about the degree of convergence after using each preparation. A score (1 to 4 points) was assigned based on the following criteria, and an average value was calculated from the obtained results. Based on the average value of the calculated scores, the degree of convergence after brushing was evaluated based on the following evaluation criteria.
In each dentifrice, tooth brushing was performed for each subject by taking about 1 g of the dentifrice composition on a toothbrush, brushing for 3 minutes, and rinsing the oral cavity with water. The other preparations were used in the usual manner.
[Score standard]
4 points: A feeling of convergence was high 3 points: A feeling of convergence was felt 2 points: A little feeling of convergence was felt 1 point: A feeling of convergence was not felt [Evaluation criteria]
☆: Average value 3.5 points or more ◎: Average value 3.0 points or more and less than 3.5 points ○: Average value 2.5 points or more and less than 3.0 points △: Average value 2.0 points or more and 2.5 points Less than ×: Average value less than 2.0 points
Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000001
Figure JPOXMLDOC01-appb-T000002
*;雲母チタンの平均粒径、厚さ及び両者の比率
Figure JPOXMLDOC01-appb-T000002
*: Average particle diameter of titanium mica, thickness, and ratio of both
Figure JPOXMLDOC01-appb-T000003
Figure JPOXMLDOC01-appb-T000003
Figure JPOXMLDOC01-appb-T000004
*;雲母チタンの平均粒径、厚さ及び両者の比率
Figure JPOXMLDOC01-appb-T000004
*: Average particle diameter of titanium mica, thickness, and ratio of both
Figure JPOXMLDOC01-appb-T000005
Figure JPOXMLDOC01-appb-T000005
Figure JPOXMLDOC01-appb-T000006
**;パック剤は、上記組成の膏体組成物、支持体を使用する以外は、特開2016-117682号公報の実施例の貼付シートと同様の方法で同様の形状に調製した。膏体組成物を支持体に塗布し、支持体と剥離ライナー(藤森工業(株)製のフィルム バイナ75E-001のBDニュウハク)のシリコーンコーティング面で挟み込みながら展延した。得られたシートを上顎用(横幅(歯列に平行方法)62mm、縦幅24mm)、下顎用(横幅52mm、縦幅24mm)の大きさで型抜きし、切れ込み及び折り返し線も作って調製した。パック剤を歯面に貼り付けて支持体を剥がした後、そのままブラッシングして使用した。
Figure JPOXMLDOC01-appb-T000006
**: The pack agent was prepared in the same shape by the same method as the adhesive sheet in the examples of JP-A-2016-117682, except that the plaster composition and the support having the above composition were used. The plaster composition was applied to a support, and spread while being sandwiched between the support and a silicone coating surface of a release liner (BD binder of film binder 75E-001 manufactured by Fujimori Kogyo Co., Ltd.). The obtained sheet was punched out for the upper jaw (width (parallel to the dentition) 62 mm, length 24 mm) and lower jaw (width 52 mm, height 24 mm), and cut and folded lines were also prepared. . After the pack agent was affixed to the tooth surface and the support was peeled off, it was used after brushing.
Figure JPOXMLDOC01-appb-T000007
***;フィルム剤は、通常の方法で縦2.5cm、横2cm、厚さ0.3mmの大きさに調製した。フィルム剤を歯面に貼り付けた後、そのままブラッシングして使用した。
Figure JPOXMLDOC01-appb-T000007
***; The film agent was prepared in a size of 2.5 cm in length, 2 cm in width, and 0.3 mm in thickness by a usual method. After the film agent was applied to the tooth surface, it was used after brushing.

Claims (9)

  1.  (A)六角板状酸化亜鉛を含有することを特徴とする口腔用組成物。 (A) A composition for oral cavity containing hexagonal plate-like zinc oxide.
  2.  六角板状酸化亜鉛の平均粒径が0.1~10μmである請求項1に記載の口腔用組成物。 The oral composition according to claim 1, wherein the hexagonal plate-like zinc oxide has an average particle size of 0.1 to 10 µm.
  3.  六角板状酸化亜鉛の平均厚さが0.01~1μmである請求項1又は2に記載の口腔用組成物。 The oral composition according to claim 1 or 2, wherein the hexagonal plate-like zinc oxide has an average thickness of 0.01 to 1 µm.
  4.  六角板状酸化亜鉛の平均粒径と平均厚さとの比率を示す、平均粒径/平均厚さが0.5~50である請求項1~3のいずれか1項に記載の口腔用組成物。 The composition for oral cavity according to any one of claims 1 to 3, wherein the average particle diameter / average thickness is 0.5 to 50 and represents a ratio between an average particle diameter and an average thickness of hexagonal plate-like zinc oxide. .
  5.  (A)成分を0.1~30質量%含有する非シート状の製剤である請求項1~4のいずれか1項に記載の口腔用組成物。 The oral composition according to any one of claims 1 to 4, which is a non-sheet preparation containing 0.1 to 30% by mass of component (A).
  6.  歯磨剤又は洗口剤である請求項5に記載の口腔用組成物。 The composition for oral cavity according to claim 5, which is a dentifrice or a mouthwash.
  7.  (A)成分を0.1~95質量%含有するシート状の製剤である請求項1~4のいずれか1項に記載の口腔用組成物。 The composition for oral cavity according to any one of claims 1 to 4, which is a sheet-form preparation containing 0.1 to 95% by mass of component (A).
  8.  更に、(B)界面活性剤を0.1~10質量%含有する請求項1~7のいずれか1項に記載の口腔用組成物。 The oral composition according to any one of claims 1 to 7, further comprising 0.1 to 10% by mass of (B) a surfactant.
  9.  歯の美白用である請求項1~8のいずれか1項に記載の口腔用組成物。 The composition for oral cavity according to any one of claims 1 to 8, which is used for whitening teeth.
PCT/JP2018/020506 2017-06-15 2018-05-29 Composition for use in oral cavity WO2018230325A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
KR1020197026233A KR20200015449A (en) 2017-06-15 2018-05-29 Oral Composition
CN201880007910.9A CN110198699A (en) 2017-06-15 2018-05-29 Composition for oral cavity

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2017117531A JP2019001747A (en) 2017-06-15 2017-06-15 Oral composition
JP2017-117531 2017-06-15

Publications (1)

Publication Number Publication Date
WO2018230325A1 true WO2018230325A1 (en) 2018-12-20

Family

ID=64659271

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2018/020506 WO2018230325A1 (en) 2017-06-15 2018-05-29 Composition for use in oral cavity

Country Status (4)

Country Link
JP (1) JP2019001747A (en)
KR (1) KR20200015449A (en)
CN (1) CN110198699A (en)
WO (1) WO2018230325A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022083996A1 (en) 2020-10-22 2022-04-28 Unilever Ip Holdings B.V. An oral care composition for whitening benefits

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5467596A (en) * 1977-11-09 1979-05-31 Matsushita Electric Ind Co Ltd Preparation of hexagonal plate zinc oxide crystal powder
JP2003183142A (en) * 2001-12-19 2003-07-03 Lion Corp Process and composition for whitening tooth
US20090017303A1 (en) * 2007-06-12 2009-01-15 Fas Alliances, Inc. Zinc oxide having enhanced photocatalytic activity
WO2015118777A1 (en) * 2014-02-07 2015-08-13 堺化学工業株式会社 Hexagonal plate-like zinc oxide particles, production method therefor, cosmetic, filler, resin composition, infrared reflective material, and coating composition

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS483155Y1 (en) 1970-10-08 1973-01-26
JP3997371B2 (en) 1999-01-28 2007-10-24 ライオン株式会社 Teeth whitening set
JP4548582B2 (en) 2004-06-22 2010-09-22 ライオン株式会社 Teeth whitening set
DE602006006790D1 (en) * 2006-03-22 2009-06-25 Procter & Gamble Zinc-containing oral compositions
JP4919009B2 (en) 2006-06-23 2012-04-18 ライオン株式会社 Tooth makeup set

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5467596A (en) * 1977-11-09 1979-05-31 Matsushita Electric Ind Co Ltd Preparation of hexagonal plate zinc oxide crystal powder
JP2003183142A (en) * 2001-12-19 2003-07-03 Lion Corp Process and composition for whitening tooth
US20090017303A1 (en) * 2007-06-12 2009-01-15 Fas Alliances, Inc. Zinc oxide having enhanced photocatalytic activity
WO2015118777A1 (en) * 2014-02-07 2015-08-13 堺化学工業株式会社 Hexagonal plate-like zinc oxide particles, production method therefor, cosmetic, filler, resin composition, infrared reflective material, and coating composition

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
IZUKA, YOSHINOBU ET AL.: "Effects of anionic surfactant on shape of zinc oxide particle", LECTURE ABSTRACTS OF THE 2015 RESEARCH PRESENTATION OF COLOR MATERIALS, 2015, pages 82 - 83 *
J AVIDI, M. ET AL.: "Zinc oxide nano-particles as sealer in endodontics and its sealing ability", CONTEMPORARY CLINICAL DENTISTRY, vol. 5, no. 1, January 2014 (2014-01-01), pages 20 - 24, Retrieved from the Internet <URL:doi:10.4103/0976-237X.128656> *
YOSHIDA, RYOHEI: "Multifunctional zinc oxide evolving make-up cosmetics", FRAGRANCE JOURNAL, vol. 43, December 2015 (2015-12-01), pages 31 - 35 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022083996A1 (en) 2020-10-22 2022-04-28 Unilever Ip Holdings B.V. An oral care composition for whitening benefits

Also Published As

Publication number Publication date
KR20200015449A (en) 2020-02-12
JP2019001747A (en) 2019-01-10
CN110198699A (en) 2019-09-03

Similar Documents

Publication Publication Date Title
JP5625647B2 (en) Dentifrice composition
JP2007145740A (en) Dentifrice composition
JP6367190B2 (en) Oral composition containing diamond particles
JP6092751B2 (en) Dentifrice composition
JP2003335646A (en) Dentifrice composition
JP2007161598A (en) Dentifrice composition
WO2018230325A1 (en) Composition for use in oral cavity
JP5168466B2 (en) Dentifrice composition
JPWO2017094582A1 (en) Oral composition
JP5948903B2 (en) Dentifrice composition and method for improving antiseptic power of dentifrice composition
JP2015117215A (en) Dentifrice composition
JP2010143842A (en) Dentifrice composition
KR20170058089A (en) Oral composition for tooth whitening
JP2011105682A (en) Toothpaste composition
JP2010111648A (en) Dentifrice composition
CN111902125A (en) Oral composition and bitterness improver for alpha-olefin sulfonate
JP6264292B2 (en) Dentifrice composition and tooth remineralization accelerator
JP2010037293A (en) Dentifrice composition
CN111031999B (en) Toothpaste composition
WO2016136719A1 (en) Toothpaste composition
JP5720416B2 (en) Gel oral composition and method for producing the same
WO2022075422A1 (en) Dentifrice composition
JP2006182658A (en) Toothpaste composition
JP2024000720A (en) Composition for oral cavity
JP2020193167A (en) Oral composition

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 18817663

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 20197026233

Country of ref document: KR

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 18817663

Country of ref document: EP

Kind code of ref document: A1