Carbon dioxide gas pack kit

JPWO2024262012A1Active Publication Date: 2024-12-26AMPLY CO LTD
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Patent Information

Application Number
JP2023559051
Authority / Receiving Office
JP · JP
Patent Type
Applications
Current Assignee / Owner
Filing Date
2023-06-23
Publication Date
2024-12-26
Estimated Expiration
2043-06-23

AI Technical Summary

Technical Problem

Carbon dioxide gas packs that turn into gels can block the movement of generated carbon dioxide gas, making it difficult for the gas to reach the skin, and they are prone to dripping until gelation occurs, with the gas also diffusing from non-skin surfaces.

Method used

A carbon dioxide pack kit comprising a viscous composition, a carbon dioxide adjuvant, and a sheet with an easily water-soluble calcium salt, where the sheet accelerates gelation at the contact surface with the skin, allowing efficient delivery of carbon dioxide gas.

Benefits of technology

The kit minimizes dripping and ensures efficient transdermal absorption of carbon dioxide gas by promoting gelation at the skin contact surface while maintaining fluidity elsewhere, enhancing skin absorption.

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Abstract

To provide a kit for a carbon dioxide gas pack which is less likely to drip and allows generated carbon dioxide gas to efficiently reach the skin. [Solution] A kit for a carbon dioxide gas pack comprising a viscous composition (A), a carbon dioxide supplement (B) and a sheet (C), wherein the viscous composition (A) comprises a carbonate, a thickener, water, a gelling agent that gels with calcium ions, and a poorly water-soluble calcium salt, the carbon dioxide supplement (B) comprises at least one of an acid and a substance that is hydrolyzed to produce an acid, and the sheet (C) has a readily water-soluble calcium salt attached thereto.
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Description

[Technical field]

[0001] The present invention relates to a kit for a carbon dioxide gas pack that generates carbon dioxide gas. [Background technology]

[0002] It is known that carbon dioxide gas, when absorbed transdermally (transmucosally), promotes blood circulation in the skin, subcutaneous tissue, and muscles, and activates metabolism. For this reason, in recent years, topical agents that generate carbon dioxide gas (hereinafter also referred to as "carbon dioxide gas packs") have been attracting attention in the fields of beauty and medicine. Such carbon dioxide gas packs are designed to generate carbon dioxide gas, and are used by applying them to the skin. When applied to the skin, the carbon dioxide gas pack generates carbon dioxide gas, which is released through the contact surface with the skin and absorbed transdermally.

[0003] Carbon dioxide gas packs are required to generate carbon dioxide gas continuously so that the gas can be absorbed through the skin, and the generated carbon dioxide gas must be able to move to the outer surface of the pack. For this reason, carbon dioxide gas packs generally use viscous materials (substances having viscosity) that exhibit fluidity. However, carbon dioxide gas packs made of viscous materials that exhibit fluidity have problems in that they may drip into the pack, and they also require the effort of wiping or washing after use.

[0004] Therefore, gelling carbon dioxide gas packs have been developed. For example, Patent Document 1 discloses a composition for preparing a carbon dioxide external preparation (hereinafter also referred to as the "carbon dioxide gas pack of Patent Document 1") that is composed of a substance that is hydrolyzed to generate an acid, a carbonate, a thickener, water, a gelling agent that gels with calcium ions, and a poorly water-soluble (water-insoluble) calcium salt. In the carbon dioxide gas pack of Patent Document 1, calcium ions generated from the poorly water-soluble calcium salt are allowed to act on the gelling agent to gel the carbon dioxide gas pack. [Prior art documents] [Patent documents]

[0005] [Patent Document 1] International Publication No. 2006 / 080398 Summary of the Invention [Problem to be solved by the invention]

[0006] If a carbon dioxide pack gels, the movement of the generated carbon dioxide gas is blocked by the gel, making it difficult for the carbon dioxide gas to reach the skin. For this reason, even if the carbon dioxide pack gels, it is required that it does not gel while the carbon dioxide gas is being absorbed through the skin.

[0007] In the carbon dioxide pack of Patent Document 1, a poorly water-soluble calcium salt is used as a source of calcium ions to be reacted with a gelling agent, thereby slowing down the gelling reaction rate. Poorly water-soluble calcium salts have lower solubility in water than readily water-soluble calcium salts, and generate calcium ions by reacting with acid, thereby slowing down the gelling reaction rate. In this way, the carbon dioxide pack of Patent Document 1 is able to achieve both gelation and delivery of carbon dioxide to the skin.

[0008] However, the carbon dioxide gas pack in Patent Document 1 exhibits fluidity (has viscosity) until it gels. Therefore, even with the carbon dioxide gas pack in Patent Document 1, there is still a problem that dripping occurs easily until it gels.

[0009] In addition, the carbon dioxide pack in Patent Document 1 is made to remain in a viscous, fluid state until it gels, allowing the generated carbon dioxide to move to the surface that comes into contact with the skin, but the carbon dioxide generated in the pack diffuses in all directions, so it is released not only from the surface that comes into contact with the skin, but also from the outer surface other than the surface that comes into contact with the skin. In other words, the carbon dioxide pack in Patent Document 1 has the problem that the generated carbon dioxide cannot efficiently reach the skin.

[0010] The present invention has been made to solve the above-mentioned problems, and aims to provide a carbon dioxide gas pack kit that is less likely to drip and can efficiently deliver the generated carbon dioxide gas to the skin. [Means for solving the problem]

[0011] The gist of the present invention is as follows. [1] A kit for a carbon dioxide gas pack comprising a viscous composition (A), a carbon dioxide supplement (B) and a sheet (C), wherein the viscous composition (A) comprises a carbonate, a thickener, water, a gelling agent that gels with calcium ions, and a poorly water-soluble calcium salt, the carbon dioxide supplement (B) comprises at least one of an acid and a substance that is hydrolyzed to produce an acid, and the sheet (C) has a readily water-soluble calcium salt attached thereto. [2] The carbon dioxide gas pack kit according to [1], wherein the sheet (C) is a fiber sheet made of fibers. [3] The sheet (C) has a coating amount of the water-soluble calcium salt of 1.0 to 100 g / m 2 The carbon dioxide gas pack kit according to [1] or [2]. [4] A kit for a carbon dioxide gas pack according to any one of [1] to [3], wherein the water-soluble calcium salt is a calcium salt having a solubility of 10.0 g / 100 ml or more in water at pH 7.0 at 20°C. [5] A sheet (C) for contacting with a mixture of a viscous composition (A) containing a carbonate, a thickener, water, a gelling agent that gels with calcium ions, and a poorly water-soluble calcium salt, and a carbon dioxide auxiliary (B) containing at least one of an acid and a substance that is hydrolyzed to produce an acid, the sheet (C) being characterized in that a readily water-soluble calcium salt is attached to the sheet (C). [6] The sheet (C) according to [5], which is a fiber sheet composed of fibers. [7] The amount of the water-soluble calcium salt attached is 1.0 to 100 g / m 2 The sheet (C) according to [5] or [6], [8] The sheet (C) according to any one of [5] to [7], wherein the water-soluble calcium salt is a calcium salt having a solubility of 10.0 g / 100 ml or more in water at 20°C and pH 7.0. Effect of the Invention

[0012] According to the present invention, it is possible to provide a kit for a carbon dioxide gas pack which is less likely to drip and which allows the generated carbon dioxide gas to efficiently reach the skin. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0013] Hereinafter, one embodiment of the present invention will be described.

[0014] This embodiment is a kit for a carbon dioxide gas pack including a viscous composition (A), a carbon dioxide adjuvant (B), and a sheet (C). First, of the viscous composition (A), the carbon dioxide adjuvant (B), and the sheet (C), the viscous composition (A) will be described.

[0015] The viscous composition (A) is a composition containing at least a carbonate, a thickener, water, a gelling agent that gels in the presence of calcium ions, and a poorly water-soluble calcium salt.

[0016] The carbonate contained in the viscous composition (A) is a source of carbon dioxide gas and generates carbon dioxide (carbon dioxide gas) by reacting with an acid. The carbonate may be any carbonate that generates carbon dioxide by reacting with an acid, and examples of the carbonate include ammonium carbonate, ammonium hydrogen carbonate, potassium carbonate, potassium hydrogen carbonate, potassium sesquicarbonate, sodium carbonate, sodium hydrogen carbonate, sodium sesquicarbonate, lithium carbonate, lithium hydrogen carbonate, lithium sesquicarbonate, cesium carbonate, cesium hydrogen carbonate, cesium sesquicarbonate, magnesium carbonate, magnesium hydrogen carbonate, calcium hydrogen carbonate, calcium carbonate, magnesium hydroxide carbonate, and barium carbonate, and one or more of these can be used. Of the carbonates mentioned above, it is preferable that the carbonate is a water-soluble carbonate such as sodium hydrogen carbonate or sodium carbonate.

[0017] The content of the carbonate is not particularly limited, but may be, for example, 0.1 to 10 mass% and preferably 0.1 to 5 mass% relative to 100 mass% of the viscous composition (A). When the viscous composition (A) contains two or more kinds of carbonates, the content of the carbonate refers to the total content of the carbonates contained.

[0018] The carbonates mentioned above also include poorly water-soluble calcium salts such as calcium carbonate. For such substances that are carbonates and poorly water-soluble calcium salts, the inclusion of the substances can be regarded as the inclusion of both the carbonates and poorly water-soluble calcium salts in the viscous composition (A). In addition to the substances that are carbonates and poorly water-soluble calcium salts, the viscous composition (A) may further contain a carbonate different from the substances, or may further contain a poorly water-soluble calcium salt different from the substances.

[0019] The thickener contained in the viscous composition (A) is not particularly limited, and one or more selected from natural polymers, semi-synthetic polymers, synthetic polymers, and inorganic substances can be used. The thickener may be acidic, neutral, or alkaline, but is preferably neutral or alkaline from the viewpoint of timely generation of carbon dioxide gas.

[0020] Examples of the neutral or alkaline thickener include the following.

[0021] Examples of natural polymers (neutral or alkaline thickeners) include plant-based polymers such as gum arabic, carrageenin, galactan, agar, quince seed, guar gum, tragacanth, mannan, locust bean gum, wheat starch, rice starch, tara gum, corn starch, and potato starch; microbial polymers such as curdlan, xanthan gum, succinoglucan, dextran, and pullulan; and protein-based polymers such as albumin, casein, collagen, gelatin, and fibroin. One or more of these may be used.

[0022] Examples of semi-synthetic polymers (neutral or alkaline thickeners) include cellulose-based polymers such as ethyl cellulose, carboxymethyl cellulose and its salts, carboxymethyl ethyl cellulose and its salts, carboxymethyl starch and its salts, croscarmellose and its salts, crystalline cellulose, cellulose acetate, cellulose acetate phthalate, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, hydroxypropyl methyl cellulose phthalate, methyl cellulose, and methyl hydroxypropyl cellulose; starch-based polymers such as pregelatinized starch, partially pregelatinized starch, carboxymethyl starch, dextrin, and methyl starch; alginic acid-based polymers such as sodium alginate, potassium alginate, ammonium alginate, and propylene glycol alginate; and other polysaccharide-based polymers such as sodium chondroitin sulfate and sodium hyaluronate. One or more of these may be used.

[0023] Examples of synthetic polymers (neutral or alkaline thickeners) include sodium polyacrylate, polyvinyl acetal diethylaminoacetate, polyvinyl alcohol, polyvinylpyrrolidone, methacrylic acid-ethyl acrylate copolymer, methacrylic acid-ethyl methacrylate copolymer, ethyl methacrylate-trimethylammonium ethyl methacrylate copolymer, and dimethylaminoethyl methacrylate-methyl methacrylate copolymer, and one or more of these can be used.

[0024] Examples of inorganic substances (neutral or alkaline thickeners) include hydrated silicon dioxide, colloidal alumina, bentonite, and laponite, and one or more of these can be used.

[0025] Examples of acidic thickeners include the following:

[0026] Examples of natural polymers (acidic thickeners) include alginic acid, pectin, and hyaluronic acid, examples of semi-synthetic polymers (acidic thickeners) include carboxyvinyl polymers, and examples of inorganic substances (acidic thickeners) include light anhydrous silicic acid, and these may be used alone or in combination of two or more.

[0027] The content of the thickener is not particularly limited, but may be, for example, 0.5 to 20% by mass, and preferably 1.0 to 10% by mass, relative to 100% by mass of the viscous composition (A). When the viscous composition (A) contains two or more types of thickeners, the content of the thickener mentioned above means the total content of the thickeners contained.

[0028] The above-mentioned thickeners include gelling agents such as sodium alginate that gel with calcium ions. For such substances that are thickeners and gelling agents that gel with calcium ions, the inclusion of the substance can be regarded as including both the thickener and the gelling agent that gels with calcium ions in the viscous composition (A). In addition to the substance that is a thickener and a gelling agent that gels with calcium ions, the viscous composition (A) may further include a thickener different from the substance, or may further include a gelling agent that gels with calcium ions different from the substance.

[0029] The water contained in the viscous composition (A) is not particularly limited, and natural water, tap water, distilled water, purified water, etc. can be used.

[0030] The content of water is not particularly limited, but can be, for example, 40 to 95% by mass relative to 100% by mass of the viscous composition (A).

[0031] The gelling agent contained in the viscous composition (A) that gels with calcium ions may be any substance that gels with the action of calcium ions, and is not particularly limited thereto. Examples include sodium alginate, carrageenan, tara gum, and locust bean gum, and one or more of these may be used. Of the gelling agents described above, the gelling agent that gels with calcium ions is preferably sodium alginate. In this specification, the term "gel" refers to a substance in which molecules are linked together by crosslinking or the like to form a three-dimensional network structure, the inside of which is filled with a solvent such as water.

[0032] The content of the gelling agent that gels with calcium ions is not particularly limited, but may be, for example, 0.5 to 10 mass% and preferably 1.0 to 5.0 mass% relative to 100 mass% of the viscous composition (A). When the viscous composition (A) contains two or more gelling agents, the content of the gelling agent refers to the total content of the gelling agents contained.

[0033] The poorly water-soluble calcium salt contained in the viscous composition (A) is a calcium salt having a solubility in water at pH 7.0 at 25° C. of less than 3.7 g / 100 ml. Examples of poorly water-soluble calcium salts contained in the viscous composition (A) include calcium carbonate, calcium sulfate, calcium alginate, calcium pyrophosphate, calcium monophosphate, calcium diphosphate, calcium silicate, calcium gluconate, and calcium benzoate, and one or more of these can be used. Among the poorly water-soluble calcium salts described above, the poorly water-soluble calcium salt is preferably calcium carbonate.

[0034] The content of the poorly water-soluble calcium salt is not particularly limited, but may be, for example, 0.1 to 5 mass% and preferably 0.3 to 3.0 mass% relative to 100 mass% of the viscous composition (A). When the viscous composition (A) contains two or more poorly water-soluble calcium salts, the content of the poorly water-soluble calcium salt refers to the total content of the poorly water-soluble calcium salts contained.

[0035] The viscous composition (A) may be composed of only the above-mentioned carbonate, thickener, water, gelling agent that gels with calcium ions, and poorly water-soluble calcium salt, but may also contain other components other than these components. Examples of such other components include components contained in known external preparations and cosmetics, and specifically include fragrances, colorants, surfactants, oils, moisturizing agents, alcohols, preservatives, antioxidants, pH adjusters, dispersants, sequestering agents, coloring inhibitors, ultraviolet absorbing and scattering agents, vitamins, amino acids, arbutin, kojic acid, nutrients, anti-inflammatory agents, vasodilators, hormones, astringents, antihistamines, bactericides, sebum suppressants, keratin peeling and dissolving agents, antiseborrheic agents, and antipruritic agents, and one or more of these may be contained.

[0036] The viscous composition (A) is a viscous material having a higher viscosity than water, and more specifically, a viscous material (sol substance) exhibiting fluidity. The viscosity of the viscous composition (A) is not particularly limited, but may be, for example, 20,000 to 1,100,000 mPa·s, and preferably 50,000 to 1,100,000 mPa·s. The viscosity means the viscosity measured using a Brookfield viscometer at 25°C, a rotation speed of 0.5 rpm, and a spindle number of LV4.

[0037] The pH of the viscous composition (A) is preferably weakly alkaline to weakly acidic (e.g., 4 to 9) from the viewpoint of application to the skin, and is preferably weakly alkaline to neutral (e.g., 7 to 9) from the viewpoint of timely generation of carbon dioxide gas.

[0038] The viscous composition (A) can be produced by appropriately mixing a carbonate, a thickener, water, a gelling agent that gels in the presence of calcium ions, and a poorly water-soluble calcium salt, and other components that may be included as necessary.

[0039] Next, the carbon dioxide supplement (B) contained in the carbon dioxide gas pack kit of this embodiment will be described.

[0040] The carbon dioxide auxiliary agent (B) is an agent for promoting a reaction in which carbon dioxide gas is generated in the viscous composition (A) when mixed with the viscous composition (A), and contains at least one of an acid and a substance that is hydrolyzed to produce an acid.

[0041] The acid that can be contained in the carbon dioxide adjuvant (B) may be any of organic acids and inorganic acids, and one or more of these may be used. The acid may be in the form of a salt.

[0042] Examples of organic acids include straight-chain fatty acids such as formic acid, acetic acid, propionic acid, butyric acid, and valeric acid; dicarboxylic acids such as oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, fumaric acid, maleic acid, phthalic acid, isophthalic acid, and terephthalic acid; acidic amino acids such as glutamic acid and aspartic acid; and oxyacids such as glycolic acid, malic acid, tartaric acid, citric acid, lactic acid, hydroxyacrylic acid, α-oxybutyric acid, glyceric acid, tartronic acid, salicylic acid, gallic acid, tropic acid, ascorbic acid, and gluconic acid. These may be used alone or in combination of two or more kinds.

[0043] Examples of inorganic acids include phosphoric acid, potassium dihydrogen phosphate, sodium dihydrogen phosphate, sodium sulfite, potassium sulfite, sodium pyrosulfite, potassium pyrosulfite, sodium acid hexametaphosphate, potassium acid hexametaphosphate, sodium acid pyrophosphate, potassium acid pyrophosphate, and sulfamic acid, and these can be used alone or in combination.

[0044] The substance that can be contained in the carbon dioxide adjuvant (B) and that generates an acid upon hydrolysis may be any substance that generates an acid upon contact with water, and is not particularly limited thereto. Examples include lactones and cyclic dimers of organic acids, and one or more of these can be used. The substance that generates an acid upon hydrolysis is preferably a crystalline lactone and / or cyclic dimer of an organic acid, and is preferably at least one selected from the group consisting of glucono-delta-lactone, pantolactone, D,L- or L-lactide (3,6-dimethyl-1,4-dioxane-2,5-dione), and D,L- or L-glycolide.

[0045] The content of the acid in the carbon dioxide adjuvant (B) and the content of the substance that generates an acid upon hydrolysis can be appropriately set in consideration of the amount of carbon dioxide gas generated and the time until gelation, but from the viewpoint of percutaneous absorption of more carbon dioxide gas, it is preferably 1 to 100 times (1 to 100 times by mass) the content of the carbonate contained in the viscous composition (A), more preferably 1 to 50 times (1 to 50 times by mass), and even more preferably 1 to 10 times (1 to 10 times by mass). On the other hand, from the viewpoint of ensuring sufficient time for percutaneous absorption of carbon dioxide gas, the content of the acid in the carbon dioxide adjuvant (B) is preferably 1 to 500 times (1 to 500 times by mass) the content of the poorly water-soluble calcium salt contained in the viscous composition (A), more preferably 5 to 400 times (5 to 400 times by mass), and even more preferably 8 to 20 times (8 to 20 times by mass). In addition, when the carbon dioxide adjuvant (B) contains both an acid and a substance that is hydrolyzed to produce an acid, the above-mentioned content refers to the total content of both of these substances. When the carbon dioxide adjuvant (B) contains only one of an acid and a substance that is hydrolyzed to produce an acid, the above-mentioned content refers to the content of either one of them.

[0046] The carbon dioxide adjuvant (B) may be composed only of the above-mentioned acid or a substance that generates an acid when hydrolyzed, but may also contain other components other than these components. Examples of other components include components contained in known external preparations and cosmetics, such as fragrances, colorants, surfactants, oils, moisturizing agents, alcohols, preservatives, antioxidants, pH adjusters, dispersants, sequestering agents, coloring inhibitors, ultraviolet absorbing / scattering agents, excipients, binders, stabilizers, disintegrants, lubricants, dispersion media, vitamins, amino acids, arbutin, kojic acid, nutrients, anti-inflammatory agents, vasodilators, hormones, astringents, antihistamines, bactericides, sebum suppressants, keratin peeling / dissolving agents, antiseborrheic agents, and antipruritic agents, and one or more of these may be contained.

[0047] The form of the carbon dioxide adjuvant (B) is not particularly limited and may be either liquid or solid, but is preferably in the form of a solid, and more preferably in the form of a particulate material such as granules, fine particles, or powder.

[0048] The carbon dioxide supplement (B) can be produced by appropriately mixing the above-mentioned acid or a substance that generates an acid when hydrolyzed with the above-mentioned other components that are contained as necessary. When the carbon dioxide supplement (B) is made into a granular form, it can be made into a granular form using a granulation method (compression molding method, extrusion granulation method, rolling granulation method, spray granulation method, stirring granulation method, etc.) that is usually used in the manufacture of pharmaceuticals. When the carbon dioxide supplement (B) is a granular material, its particle size is not particularly limited, but can be, for example, 1 to 1000 μm, and is preferably 5 to 600 μm. The particle size refers to the particle size determined by sieving using a sieve.

[0049] Next, the sheet (C) included in the carbon dioxide gas pack kit of this embodiment will be described.

[0050] The sheet (C) is a sheet that is placed over the mixture of carbon dioxide adjuvant (B) and viscous composition (A) (hereinafter also referred to as "mixture (A)(B)") applied to the skin so as to come into contact with the mixture, and has at least a water-soluble calcium salt attached thereto.

[0051] The water-soluble calcium salt attached to the sheet (C) is a calcium salt having a solubility of 3.7 g / 100 ml or more in water at pH 7.0 at 25° C. Examples of the water-soluble calcium salt include calcium chloride, calcium chlorate, calcium perchlorate, calcium permanganate, calcium formate, calcium glycerophosphate, calcium glutamate, calcium acetate, calcium salicylate, calcium hypochlorite, calcium bromide, calcium bromate, calcium nitrate, calcium lactate, calcium pantothenate, calcium propionate, and calcium phosphorylated oligosaccharides, and one or more of these may be used.

[0052] From the viewpoint of allowing the generated carbon dioxide gas to reach the skin more efficiently, the readily water-soluble calcium salt is, among the readily water-soluble calcium salts mentioned above, preferably a calcium salt having a solubility in water of pH 7.0 at 20°C of 10.0 g / 100 ml or more, more preferably a calcium salt having a solubility in water of pH 7.0 at 20°C of 30.0 g / 100 ml or more, even more preferably a calcium salt having a solubility in water of pH 7.0 at 20°C of 50.0 g / 100 ml or more, and particularly preferably calcium chloride.

[0053] The amount of the water-soluble calcium salt to be attached is not particularly limited, but from the viewpoint of allowing the generated carbon dioxide gas to reach the skin more efficiently, it is preferably 1.0 to 100 g / m 2 and preferably 1.5 to 80.0 g / m 2 More preferably, the thickness is 2.3 to 55.8 g / m 2 It is even more preferable that the adhesion amount of the readily water-soluble calcium salt (g / m 2) is the mass of water-soluble calcium salt per unit area of ​​the sheet, and the mass (g) of the water-soluble calcium salt attached to the sheet is multiplied by the area (m 2 ) The area of ​​the sheet means the projected area in the thickness direction of the sheet (the area of ​​the upper or lower surface of the sheet), and is an area that does not take into account minute gaps or pores formed between the raw materials (e.g., fibers) that make up the sheet. When holes (openings) are provided in the sheet, the area of ​​the holes (openings) is not taken into account in the area of ​​the sheet (is not included in the area of ​​the sheet).

[0054] As long as the sheet (C) has the above-mentioned water-soluble calcium salt attached thereto, other components other than the water-soluble calcium salt may be attached thereto. Examples of such other components include ascorbyl glucoside, 3-O-ethyl ascorbic acid, arbutin, sodium hyaluronate, hydrolyzed hyaluronic acid, sodium hydrolyzed hyaluronate, sodium acetylated hyaluronate, sodium carboxymethyl hyaluronate, hydrolyzed alkyl (C12-13) glyceryl hyaluronate, hydrolyzed collagen, niacinamide, and dipotassium glycyrrhizinate, and one or more of these can be used.

[0055] The sheet (C) may be made of any material to which a water-soluble calcium salt can be attached, and examples of the material include a film, a porous material, a foam, a nonwoven fabric, a woven fabric, and paper.

[0056] Examples of materials for the film, porous body, or foam include polyolefin resins (polyethylene, polypropylene, etc.), acrylic resins (polymethyl methacrylate, etc.), polyester resins (polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, etc.), polyvinyl alcohol, ethylene-vinyl alcohol copolymers, polyvinyl chloride, polyvinylidene chloride, polystyrene, polyurethane resins, polyacrylonitrile, fluorine-based resins, styrene-isoprene-styrene block copolymers, styrene-butadiene-styrene block copolymers, styrene-ethylene-propylene-styrene block copolymers, styrene-butadiene rubber, ethylene-vinyl acetate copolymers, polyamides, polysulfones, polyesters, styrenes, polyesters, or thermoplastic elastomers such as copolymer rubbers, and these may be used alone or in combination.

[0057] Examples of materials for the nonwoven fabric, woven fabric, and paper include polyester-based resins such as rayon, polyamide, polyethylene, and polyethylene terephthalate, polyolefin-based resins such as polypropylene, polyester ether, polyurethane-based resins, acrylic resins, polyvinyl alcohol, polystyrene-based resins, cotton, and hemp, and these can be used alone or in combination.

[0058] Among the above-mentioned materials, the sheet (C) is preferably a fiber sheet composed of fibers such as nonwoven fabric, woven fabric, and paper. When the sheet (C) is a fiber sheet, when the mixture (A) and (B) come into contact with the sheet (C), the water contained in the mixture (A) and (B) is likely to move into the fine gaps between the fibers constituting the sheet (C) due to capillary action. As a result, calcium ions are likely to be generated from the water-soluble calcium salt attached to the sheet (C), and the outer surface of the mixture (A) and (B) in contact with the sheet (C) can be gelled more quickly. The basis weight of the fiber sheet is not particularly limited, but is preferably 10 to 120 g / m 2 The following can be exemplified.

[0059] The shape of the sheet (C) is not particularly limited and can be appropriately set depending on the area to which the mixtures (A) and (B) are applied. The sheet (C) may have holes (openings) so as not to cover the eyes, nose, etc., or may have cuts so as to be deformed to fit the curved area.

[0060] The sheet (C) can be produced by adhering (fixing) a water-soluble calcium salt to a sheet substrate. The method for adhering the water-soluble calcium salt is not particularly limited, and a conventionally known method can be used. For example, a method of applying a solution in which a water-soluble calcium salt is dissolved or dispersed to a sheet substrate and drying the applied solution can be exemplified. The solution in which the water-soluble calcium salt is dissolved or dispersed is not particularly limited, and examples thereof include water and alcohol.

[0061] The carbon dioxide gas pack kit of this embodiment may be composed of only the above-mentioned viscous composition (A), carbon dioxide supplement (B), and sheet (C), but may also include other items. For example, the carbon dioxide gas pack kit of this embodiment may include a spatula for mixing the viscous composition (A) and the carbon dioxide supplement (B) in addition to the viscous composition (A), the carbon dioxide supplement (B), and the sheet (C).

[0062] Next, a method for using the carbon dioxide gas pack kit of this embodiment, which includes the viscous composition (A), the carbon dioxide supplement (B), and the sheet (C), will be described. The method for using the carbon dioxide gas pack kit of this embodiment includes at least three steps: a mixing step, a coating step, and a covering step.

[0063] The mixing step is a step of mixing the viscous composition (A) and the carbon dioxide adjuvant (B). By mixing the viscous composition (A) and the carbon dioxide adjuvant (B), an external preparation that generates carbon dioxide gas (carbon dioxide gas pack) is obtained. The viscous composition (A) and the carbon dioxide adjuvant (B) may be mixed in such a way that the acid contained in the carbon dioxide adjuvant (B) and the substance that generates an acid upon hydrolysis are not unevenly distributed (uniformly) in the viscous composition (A), and there is no particular limitation on the mixing method.

[0064] When the carbon dioxide adjuvant (B) contains an acid, when the viscous composition (A) and the carbon dioxide adjuvant (B) are mixed in the mixing step, the acid contained in the carbon dioxide adjuvant (B) reacts with the carbonate contained in the viscous composition (A) to generate carbon dioxide gas. The acid contained in the carbon dioxide adjuvant (B) also reacts with the poorly water-soluble calcium salt contained in the viscous composition (A) to generate calcium ions. The generated calcium ions react with the gelling agent contained in the viscous composition (A) to advance the gelling reaction.

[0065] In addition, when the carbon dioxide adjuvant (B) contains a substance that generates an acid upon hydrolysis, when the viscous composition (A) and the carbon dioxide adjuvant (B) are mixed in the mixing step, the substance in the carbon dioxide adjuvant (B) that generates an acid upon hydrolysis reacts with the water contained in the viscous composition (A) to generate an acid. The generated acid then reacts with the carbonate contained in the viscous composition (A) to generate carbon dioxide gas. The generated acid also reacts with the poorly water-soluble calcium salt contained in the viscous composition (A) to generate calcium ions. The generated calcium ions react with the gelling agent contained in the viscous composition (A) to proceed with the gelling reaction.

[0066] The application step is a step of applying a mixture of the viscous composition (A) and the carbon dioxide adjuvant (B) (i.e., mixture (A)(B)) to the skin. The method of applying the mixture (A)(B) is not particularly limited, but from the viewpoint of facilitating transdermal absorption of the generated carbon dioxide gas, it is preferable to apply the mixture (A)(B) so that the thickness of the mixture (A)(B) applied to the skin is 0.2 mm to 50.0 mm. Note that if the mixture (A)(B) gels, it becomes difficult for the carbon dioxide gas to be absorbed transdermally, so the application step is preferably performed immediately after the completion of the mixing step.

[0067] In the application process, when the mixture (A) and (B) are applied to the skin, some of the carbon dioxide gas generated in the mixture (A) and (B) is released from the contact surface with the skin, resulting in the carbon dioxide gas being absorbed transdermally.

[0068] The covering step is a step of covering the mixture (A) and (B) on the skin with the sheet (C) so that the sheet (C) comes into contact with the mixture (A) and (B) applied to the skin. When the sheet (C) covers the mixture (A) and (B) on the skin, it is sufficient that the area where the water-soluble calcium salt adheres comes into contact with the mixture (A) and (B), and it is not necessary for the entire surface of the sheet (C) to come into contact with the mixture (A) and (B).

[0069] In the covering step, the mixture (A)(B) applied to the skin is brought into contact with the sheet (C), and the water-soluble calcium salt attached to the sheet (C) is dissolved by the water contained in the mixture (A)(B), generating calcium ions. The calcium ions react with the gelling agent (a gelling agent that gels with calcium ions) contained in the mixture (A)(B), promoting the gelling reaction occurring in the mixture (A)(B). This promotion of the gelling reaction occurs at the contact surface (and its surrounding area) with the sheet (C) to which the water-soluble calcium salt is attached, so that the contact surface (and its surrounding area) of the mixture (A)(B) with the sheet (C) gels faster than the areas other than the contact surface (and its surrounding area) with the sheet (C) (hereinafter also referred to as "other areas"). Therefore, the mixture (A)(B) applied to the skin is less likely to drip.

[0070] In addition, since the gelation reaction is accelerated at the contact surface (and its surrounding area) of mixture (A) and (B) with sheet (C), even if the contact surface (and its surrounding area) with sheet (C) gels, the other areas can maintain their viscosity (fluidity). Therefore, the movement of carbon dioxide toward the contact surface with the skin is permitted, and carbon dioxide can be released from the contact surface with the skin. In addition, since the contact surface with sheet (C) has gelled, the movement of carbon dioxide toward the contact surface with sheet (C) is prevented, and the amount of carbon dioxide toward the contact surface with the skin increases, making it easier for more carbon dioxide to be released from the contact surface with the skin. As a result, the carbon dioxide generated in mixture (A) and (B) can reach the skin more efficiently.

[0071] From the viewpoint of more quickly preventing dripping of the mixture (A)(B) and more efficiently allowing the carbon dioxide gas generated in the mixture (A)(B) to reach the skin, the covering step is preferably performed immediately after the application step is completed. In addition, in the covering step, after the contact surface with the sheet (C) has gelled, the sheet (C) covered by the mixture (A)(B) may be peeled off from the mixture (A)(B).

[0072] The carbon dioxide gas pack kit of this embodiment can be used by a method including the mixing step, application step, and coating step described above. In addition to these steps, the kit may also include a leaving step of leaving the mixture (A)(B) from which carbon dioxide gas has been generated on the skin for a predetermined period of time in order to allow a greater amount of carbon dioxide gas to be absorbed percutaneously, and a removal step of removing the gelled mixture (A)(B) from the skin after the entire mixture (A)(B) has gelled.

[0073] The carbon dioxide gas pack kit of this embodiment described above can induce a first gelation in which the contact surface with the sheet (C) (and the surrounding area) of the mixture (A)(B) applied to the skin is gelled, followed by a second gelation in which other areas are gelled. Therefore, the carbon dioxide gas pack kit of this embodiment makes it difficult for the carbon dioxide gas pack (i.e., the mixture (A)(B)) to drip, and allows the carbon dioxide gas generated in the carbon dioxide gas pack (i.e., the mixture (A)(B)) to efficiently reach the skin. EXAMPLES

[0074] The present invention will be described in more detail below with reference to examples, but the present invention is not limited to these examples.

[0075] (Viscous composition (A)) The components shown in Table 1 below were prepared and mixed to obtain a viscous composition a. This was used as viscous composition (A). [Table 1]

[0076] (Carbon dioxide supplement (B)) Gluconodeltalactone (particle size of 10 to 500 μm) was prepared as the carbon dioxide adjuvant b. Nine times the amount of the carbon dioxide adjuvant b relative to the amount of calcium carbonate contained in the viscous composition (A) was used as the carbon dioxide adjuvant (B). [Table 2]

[0077] (Sheet (C)) A 20% by mass aqueous solution of calcium chloride was prepared and mixed with a nonwoven cotton sheet (basis weight 40 g / m 2 ) and dried to obtain nonwoven fabric sheets c1 to c10 (Table 3) with calcium chloride (solubility in water with a pH of 7.0 at 20°C: 74.5 g / 100 mL) attached thereto. These nonwoven fabric sheets were used as sheets (C). [Table 3]

[0078] [Examples and Comparative Examples] The viscous composition (A), the carbon dioxide adjuvant (B), and the sheet (C) were combined as shown in Table 4 below to obtain carbon dioxide gas pack kits of Examples 1 to 10 and Comparative Example 1. In Table 4 below, a indicates the viscous composition a, b indicates the carbon dioxide adjuvant b, and c1 to c10 indicate the nonwoven fabric sheets c1 to c10, respectively. [Table 4]

[0079] [Evaluation 1 (gelation confirmation test for the outer surface other than the surface that comes into contact with the skin)] For the carbon dioxide gas pack kits of each Example and Comparative Example, the carbon dioxide auxiliary (B) was added to the viscous composition (A), and the viscous composition (A) and the carbon dioxide auxiliary (B) were mixed. A measuring spoonful (about 5 g) was taken from the resulting mixture (A)(B) and applied to the skin. For Example 1, immediately after the mixture (A)(B) was applied to the skin, the sheet (C) was placed over the mixture (A)(B) so that the sheet (C) was in contact with the mixture (A)(B). On the other hand, for the Comparative Example, the mixture (A)(B) was left to stand after being applied to the skin.

[0080] In order to make the mixing time consistent between the examples and the comparative examples, the viscous composition (A) and the carbon dioxide adjuvant (B) were mixed for 30 seconds after the carbon dioxide adjuvant (B) was added to the viscous composition (A). In order to make the area of ​​the application consistent between the examples and the comparative examples, the mixtures (A) and (B) were applied to the same area of ​​the skin that had been marked in advance. The thickness of the mixtures (A) and (B) applied to the skin was about 5 mm.

[0081] For each example, after 3 minutes had elapsed since the mixture (A) and (B) were applied to the skin, the covering sheet (C) was peeled off from the mixture (A) and (B). After that, for each example and comparative example, the outer surface (side not in contact with the skin) of the mixture (A) and (B) was touched with a finger, and if the mixture (A) and (B) remained attached to the finger even after the finger was removed, it was judged as not gelling (evaluation: ×), and if the mixture (A) and (B) did not adhere to the finger, it was judged as gelling (evaluation: ◯). In addition, among the mixtures (A) and (B) that did not adhere to the finger, if the thickness of the gelled part was 0.5 mm or more, it was evaluated as ◎. The results are shown in Table 5.

[0082] [Evaluation 2 (gelling confirmation test on the surface that comes into contact with the skin)] In the same manner as in Evaluation 1, the mixture (A) and (B) were applied to the skin, and the sheet (C) was placed over the mixture (A) and (B) (covering with the sheet (C) was only in Example 1). In Example 1, 10 minutes had passed since the mixture (A) and (B) were applied to the skin, and the covering sheet (C) was peeled off from the mixture (A) and (B). Then, in both the Examples and Comparative Examples, the surface layer of the mixture (A) and (B) applied to the skin was removed with a spatula so that the thickness of the mixture (A) and (B) applied to the skin was 2 mm or less. The mixture (A) and (B) remaining on the skin were touched with a finger and then removed, and the mixture (A) and (B) that adhered to the finger and did not come off were judged to have not gelled (evaluation: ×), and the mixture (A) and (B) that did not adhere to the finger were judged to have gelled (evaluation: ◯). The results are shown in Table 2.

[0083] [Table 5]

[0084] As shown in Table 2, in Examples 1 to 10, the outer surfaces other than the surface in contact with the skin (the surface in contact with the sheet (C)) of the mixtures (A) and (B) were gelled 3 minutes after application to the skin, but the surface in contact with the skin had not gelled even after 10 minutes. On the other hand, in Comparative Example 1, the outer surfaces other than the surface in contact with the skin of the mixtures (A) and (B) were not gelled, nor was the surface in contact with the skin, 3 minutes after application to the skin. From these results, it was understood that the carbon dioxide gas pack kits of Examples 1 to 10 made the carbon dioxide gas packs (i.e., the mixtures (A) and (B)) less likely to drip, and allowed the carbon dioxide gas generated in the carbon dioxide gas packs (i.e., the mixtures (A) and (B)) to efficiently reach the skin.

[0085] In both Example 1 and Comparative Example 1, it was confirmed that the entire mixture (A) and (B) had gelled 30 minutes after application to the skin.

Claims

1. A kit for a carbon dioxide gas pack, comprising a viscous composition (A), a carbon dioxide supplement (B), and a sheet (C), The viscous composition (A) contains a carbonate, a thickener, water, a gelling agent that gels in the presence of calcium ions, and a poorly water-soluble calcium salt; The carbon dioxide auxiliary agent (B) comprises a substance that is hydrolyzed to produce an acid, A water-soluble calcium salt is adhered to the sheet (C), The poorly water-soluble calcium salt is a calcium salt having a solubility in water at 25° C. and pH 7.0 of less than 3.7 g / 100 ml, The water-soluble calcium salt is a calcium salt having a solubility of 3.7 g / 100 ml or more in water at 25° C. and pH 7.0, The gelling agent is at least one selected from the group consisting of sodium alginate, carrageenan, tara gum, and locust bean gum; the substance that generates an acid upon hydrolysis is one or more selected from the group consisting of glucono-delta-lactone, pantolactone, D,L- or L-lactide, and D,L- or L-glycolide; The carbon dioxide gas pack kit, wherein the sheet (C) is a fiber sheet made of fiber.

2. The sheet (C) has a coating amount of the water-soluble calcium salt of 1.0 to 100 g / m 2 2. The carbon dioxide gas pack kit according to claim 1,

3. 2. The kit for a carbon dioxide gas pack according to claim 1, wherein the readily water-soluble calcium salt is a calcium salt having a solubility in water at 20° C. and pH 7.0 of 10.0 g / 100 ml or more.

4. A sheet (C) for contacting a mixture of a viscous composition (A) containing a carbonate, a thickener, water, a gelling agent that gels with calcium ions, and a poorly water-soluble calcium salt, and a carbon dioxide auxiliary (B) containing a substance that is hydrolyzed to generate an acid, A water-soluble calcium salt is adhered to the sheet (C), The poorly water-soluble calcium salt is a calcium salt having a solubility in water at 25° C. and pH 7.0 of less than 3.7 g / 100 ml, The water-soluble calcium salt is a calcium salt having a solubility of 3.7 g / 100 ml or more in water at 25° C. and pH 7.0, The gelling agent is at least one selected from the group consisting of sodium alginate, carrageenan, tara gum, and locust bean gum; the substance that generates an acid upon hydrolysis is one or more selected from the group consisting of glucono-delta-lactone, pantolactone, D,L- or L-lactide, and D,L- or L-glycolide; The sheet (C) is a fiber sheet composed of fibers.

5. The amount of the readily water-soluble calcium salt attached is 1.0 to 100 g / m 2 The sheet (C) according to claim 4, which is

6. 5. The sheet (C) according to claim 4, wherein the readily water-soluble calcium salt is a calcium salt having a solubility in water at 20°C and pH 7.0 of 10.0 g / 100 ml or more.