WO2009133637A1 - 外用シート剤および外用シート剤セット - Google Patents
外用シート剤および外用シート剤セット Download PDFInfo
- Publication number
- WO2009133637A1 WO2009133637A1 PCT/JP2008/068108 JP2008068108W WO2009133637A1 WO 2009133637 A1 WO2009133637 A1 WO 2009133637A1 JP 2008068108 W JP2008068108 W JP 2008068108W WO 2009133637 A1 WO2009133637 A1 WO 2009133637A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- hydrogen storage
- sheet
- porous material
- adhesive
- external
- Prior art date
Links
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/70—Web, sheet or filament bases ; Films; Fibres of the matrix type containing drug
- A61K9/7023—Transdermal patches and similar drug-containing composite devices, e.g. cataplasms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
Definitions
- the present invention relates to an external sheet agent and an external sheet agent set, and more particularly, to an external sheet agent and an external sheet agent set that generate hydrogen efficiently and continuously at a lower cost.
- Patent Document 1 discloses that a negative adhesive is generated in the adhesive layer of an outer skin adhesive type patch in which a hydrophilic adhesive layer containing moisture is laminated on one side of a film-like or sheet-like support.
- An external patch containing a body is disclosed.
- Patent Document 2 discloses a negative ion generator containing a negative ion generator and a hygroscopic body as essential components.
- the hydrogen occluded in the hydrogen occlusion porous material is quickly taken into the cells that make up the human body when taken directly into the body as edible hydrogen, and produces ATP via the citric acid circuit in the mitochondria.
- hydrogen is released and active oxygen such as hydroxy radicals and superoxide radicals are eliminated as water. It is known that this causes a physiological response to activate the cells.
- coral calcium powder is kneaded by adding water to a mass ratio of 55% and a flour mass ratio of 45%. After forming into a plate shape and drying, the dried molded body is oxidized and fired at 700 ° C. for 4 hours, and then reduced and fired at 650 ° C.
- Patent Document 4 discloses an antioxidant composition obtained by mixing brown rice powder and calcined calcium calcium powder adsorbed with hydrogen. JP 2003-171265 A JP 2003-169852 A JP 2005-245265 A JP 2007-217351 A
- Patent Document 1 can reduce the influence due to the change in the amount of moisture in the air, since the negative ion generator is contained in the adhesive layer containing moisture, it has already been stored. Negative ions are generated, and sufficient negative ions cannot be generated during use, and it has been desired to generate negative ions and the like efficiently and continuously.
- Patent Document 2 can reduce the influence due to the change in the amount of moisture in the air, it requires a hygroscopic body, which is costly and labor intensive, and negative ions and the like can be produced at a lower cost. There has been a demand for a sheet for external use that is generated efficiently and continuously.
- Patent Documents 3 and 4 are mainly related to food, there is room for improvement with regard to providing hydrogen to the skin efficiently and continuously as an external preparation.
- an object of the present invention is to solve the above-mentioned problems of the prior art, and to provide an external sheet agent and an external sheet agent set that generate hydrogen efficiently and continuously at a lower cost.
- the present inventors have found that the object can be achieved by not allowing the sheet having the pressure-sensitive adhesive and the hydrogen storage porous material to coexist during storage, The present invention has been completed.
- the external sheet of the present invention is characterized in that a hydrogen storage porous material is disposed on a sheet having an adhesive on one side.
- the hydrogen storage porous material is composed of hydrogen storage calcined coral calcium, hydrogen storage zeolite, hydrogen storage charcoal, hydrogen storage activated carbon, hydrogen storage barley stone, hydrogen storage tourmaline and hydrogen storage rare earth ore. It is preferable that it is 1 or more types selected from the group which consists of.
- the external sheet of the present invention is preferably formed by adding an organic acid to the hydrogen storage porous material, and the organic acid is citric acid, tartaric acid, lactic acid, glycolic acid, malic acid, dilute hydrochloric acid, acetic acid, One or more selected from the group consisting of oxalic acid and D-glucuronic acid are preferred.
- the hydrogen storage porous material is a tablet provided with a recess for receiving the organic acid.
- the hydrogen storage porous material is in the form of a paste, powder or granules.
- the external sheet of the present invention preferably has an aluminum layer on a sheet having an adhesive on one side, and a hydrogen storage porous material is disposed on the aluminum layer. It is preferable to have an aluminum layer on the lower side of a sheet having an adhesive on one side.
- the external sheet set of the present invention is characterized by comprising a sheet having an adhesive on one side, a hydrogen storage porous material, and an organic acid.
- the hydrogen storage porous material is preferably a tablet provided with a recess for receiving the organic acid.
- Another external sheet set of the present invention is characterized by comprising a sheet having an adhesive on one side and a hydrogen storage porous material in the form of a paste, powder or granules.
- the external sheet of the present invention is obtained by disposing a hydrogen storage porous material on a sheet having an adhesive on one side.
- the arrangement method is not limited as long as it is disposed on the sheet having the adhesive immediately before the hydrogen-occlusion porous material is attached to the skin, and a tablet or the like is applied by applying a paste or the like. Also good. Since the hydrogen storage porous material is placed before being attached to the skin, a large amount of hydrogen is immediately generated after placement at a lower cost, and hydrogen is generated until the organic acid is placed. Therefore, hydrogen can be generated for a long time. Therefore, by applying the external sheet of the present invention to pain, inflammation sites, etc., hydrogen can permeate into cells oxidized by active oxygen over time, and inflammation can be suppressed by its reducing power. It can be expected to have an anti-inflammatory and analgesic action that is not immediately available.
- the sheet for external use of the present invention can be used not only for humans but also for animals such as dogs, cats, horses and cows.
- animals such as dogs, cats, horses and cows.
- hydrogen can penetrate into cells oxidized by active oxygen over time, and inflammation can be suppressed by its reducing power, Expected to have an immediate anti-inflammatory / analgesic action that has never been seen before.
- it can be suitably used for the treatment of legs such as racehorses.
- the hydrogen storage porous material used in the present invention is not limited as long as it is porous and can store hydrogen, and the desired effect can be obtained.
- hydrogen storage calcined coral calcium, hydrogen storage zeolite, hydrogen storage It is preferably at least one selected from the group consisting of charcoal, hydrogen storage activated carbon, hydrogen storage barleystone, hydrogen storage tourmaline and hydrogen storage rare earth ore, more preferably hydrogen storage calcined coral calcium or hydrogen storage zeolite. .
- the porous material is oxidized and fired in an oxidation firing furnace at 700 ° C. for 4 hours. After the temperature is returned to normal temperature, it is manufactured by two-stage firing such as oxidation firing and reduction firing, such as reduction firing at 650 ° C. for 4 hours in an atmosphere of N 2 gas: H 2 gas (90 vol.%: 10 vol.%). can do.
- coral calcium used as a porous material is calcium contained in sandy fossil corals deposited on the sea floor, and fossil corals are rich in minerals such as magnesium and potassium in addition to calcium. Moreover, it is a natural material that is highly water-soluble and easily ionized, and therefore has high absorption efficiency into the human body. Such coral calcium is not particularly limited as long as the desired effect of the present invention can be obtained.
- zeolite used as a porous material is an aluminosilicate with fine pores in the crystal, and natural or synthetic products produced from crystal cavities formed in volcanic rocks and lava in hot spring areas are used. be able to. Zeolite has a bonded structure formed by silicon and aluminum mediating oxygen, and can store hydrogen in the pores by molecular adsorption.
- charcoal, activated carbon, barley stone, tourmaline and rare earth ore used as porous materials can use charcoal, activated carbon, barley stone, tourmaline and rare earth ore available on the market and occlude hydrogen.
- a hydrogen storage porous material can be obtained.
- the dosage form of the hydrogen storage porous material is not particularly limited, and may take the form of a liquid, sol or gel fluid (for example, paste), powder, granule, tablet and the like.
- other components may be added to the hydrogen occlusion porous material so long as the effects of the present invention are not impaired.
- the addition includes means such as dropping.
- the organic acid dissolves the hydrogen-absorbing porous material immediately before being applied to the skin, so that a large amount of hydrogen is generated immediately and very little hydrogen is generated until the organic acid is added. Hydrogen can be generated for a long time.
- the organic acid is not limited as long as it reacts with the hydrogen-absorbing porous material to generate hydrogen, but preferably citric acid, tartaric acid, lactic acid, glycolic acid, malic acid, dilute hydrochloric acid (for example, hydrochloric acid) Somonade), acetic acid (eg, cereal vinegar), oxalic acid and D-glucuronic acid, and more preferably citric acid that is readily available.
- the organic acid needs to be a solution, preferably a 10 to 30% by mass citric acid aqueous solution, and more preferably a 20% by mass citric acid aqueous solution. Further, the aqueous solution may contain other components as long as the effects of the present invention are not impaired.
- the mixing ratio of the hydrogen storage porous material and the organic acid is preferably 5: 1 to 5: 3, more preferably 5: 1 to 5: 2. It is preferable that the mixing ratio of the hydrogen storage porous material and the organic acid is 5: 1 to 5: 3 because a more appropriate amount of hydrogen can be generated over a long period of time.
- FIG. 1 is a perspective view showing an embodiment of a sheet according to the present invention.
- seat agent of this invention is the tablet 1 in which the hydrogen storage porous substance provided the recessed part 2 which receives the said organic acid.
- the organic acid is received by the concave portion 2 of the tablet 1, so that the organic acid can dissolve the hydrogen-absorbing porous material immediately before being attached to the skin, and a large amount of hydrogen can be generated immediately and immediately.
- hydrogen generation is extremely small, so that hydrogen can be generated for a long time.
- the number and position of the recesses 2 in the tablet 1 are not limited, but preferably one recess 2 for receiving the organic acid is provided on one side of the tablet.
- FIG. 2 is a perspective view showing an embodiment of the hydrogen storage porous material tablet according to the present invention
- FIG. 3 is a cross-sectional view showing an embodiment of the hydrogen storage porous material tablet according to the present invention
- FIG. 4 is a perspective view showing another embodiment of the hydrogen storage porous material tablet according to the present invention
- FIG. 5 is a cross section showing another embodiment of the hydrogen storage porous material tablet according to the present invention.
- Examples of the shape of the tablet 1 are tableting types that are usually used in pharmaceuticals and health foods, and examples thereof include a disc shape, a lens shape, a button shape, and a trapezoid shape, and preferably a lens shape. (FIGS. 2 and 3) or button shape (FIGS. 4 and 5).
- the size of the tablet 1 is not particularly limited, but the diameter 1a is preferably 4 to 30 mm, and more preferably 8 to 15 mm. Further, the thickness 1b of the tablet 1 is appropriately selected according to the diameter 1a of the tablet 1, and is preferably 2 to 10 mm, and more preferably 3 to 5 mm. Furthermore, the mass of the tablet 1 is preferably 100 to 1000 mg, and more preferably 200 to 500 mg.
- the size 2a, 2b of the recess 2 in the tablet 1 is not limited as long as it can receive and store the added organic acid, but the ratio of the tablet 1 to the diameter 1a and the thickness 1b is preferably 20 -80%, more preferably 40-60%.
- a calcium processed food (trade name: hydrogen every day, manufactured by Sante Corporation) can be used with a recess 2 provided.
- FIG. 6 is a perspective view showing another embodiment of the seat according to the present invention.
- the external sheet of the present invention is obtained by applying a hydrogen-occlusion porous material 4 in the form of a paste, powder or granules onto a sheet 3 having an adhesive.
- a hydrogen-occlusion porous material 4 in the form of a paste, powder or granules onto a sheet 3 having an adhesive.
- the hydrogen-occlusion porous material 4 is not limited as long as it is a paste, powder or granule containing the hydrogen-occlusion porous material, and contains other components as long as the effects of the present invention are not impaired. Also good.
- this hydrogen storage porous material 4 for example, Sante Care (fucoidan paste, manufactured by Sante Global Co., Ltd.) can be used.
- the hydrogen storage porous material 4 includes 0.5 g to 5.0 g of hydrogen storage coral calcium (hydrogen bulk powder), 0.05 to 1.0 g of Igis seaweed powder, and citric acid powder. It is preferable to contain 0.1 to 2.0 g.
- kaolin (mud) and citric acid it is preferable to use kaolin (mud) and citric acid to add a base material having a pH of 4 to 5, for example, 1 to 10 g of kaolin (mud) and 0.1 to 10 g of citric acid. Mix well for the small dish, and the pH of the substrate can be 4-5.
- the method of application and the like is not particularly limited, and it can be applied by being dispersed in a substance that does not react with the hydrogen occlusion porous material 4 in the form of paste, powder or granules. Similarly to the above, it is preferable to add an organic acid to the hydrogen storage porous material 4.
- FIG. 7 is a perspective view showing an embodiment of a sheet having an aluminum layer in the present invention.
- the external sheet of the present invention preferably has an aluminum layer 8 on a sheet 3 having an adhesive on one side, and a hydrogen storage porous material 4 is disposed on the aluminum layer 8. Since the aluminum layer 8 is on the surface having the adhesive, it is essential that the size of the aluminum layer 8 is smaller than the sheet 3 having the adhesive in consideration of the adhesiveness of the external sheet to the skin.
- FIG. 8 is a perspective view showing another embodiment of a sheet having an aluminum layer in the present invention.
- the external sheet of the present invention preferably has an aluminum layer 9 on the lower side of the sheet 3 having an adhesive on one side.
- the production method of the aluminum layers 8 and 9 in the present invention is not particularly limited as long as the aluminum layer can be produced.
- the aluminum layers 8 and 9 are produced by aluminum vapor deposition, or a commercially available aluminum foil is bonded. Can be produced.
- the sheet that can be used in the present invention is not particularly limited as long as the desired effect of the present invention can be obtained.
- the sheet is flexible and does not impair the feeling of use as a sheet for external use.
- a sheet formed of natural fibers and / or artificial fibers or a sheet formed of a polymer material can be appropriately selected and used.
- these materials may be used alone, or may be used as a sheet-like laminate in which at least two kinds selected from these materials are laminated.
- Examples of the sheet made of natural fibers and / or artificial fibers include paper, cloth, towels, blankets, knitted fabrics, quilts, non-woven fabrics, and woven fabrics.
- Examples of the natural fiber include cotton, kapok, flax, ramie, cannabis, jute, shiro, manila hemp, sisal hemp, coyer fiber, etc.
- Examples include animal fibers such as camel hair, alpaca hair, mohair, and eyelashes.
- the artificial fibers include, for example, recycled fibers such as artificial silk, sufu, viscose, and bemberg, or polyamide fibers, polyester fibers, polyacrylic fibers, polyvinyl alcohol fibers, polyalkylene paraoxybenzoate fibers, Examples thereof include synthetic fibers such as polyurethane fibers, polyvinylidene chloride fibers, polyvinyl chloride fibers, polyacrylonitrile fibers, polyethylene fibers, polypropylene fibers, and polyclar, or semi-synthetic fibers such as acetate artificial fibers.
- recycled fibers such as artificial silk, sufu, viscose, and bemberg
- polyamide fibers polyester fibers
- polyacrylic fibers such as polyvinyl alcohol fibers, polyalkylene paraoxybenzoate fibers
- synthetic fibers such as polyurethane fibers, polyvinylidene chloride fibers, polyvinyl chloride fibers, polyacrylonitrile fibers, polyethylene fibers, polypropy
- the sheet made of the polymer material examples include polyethylene, polypropylene, polyamide, polyester, polyurethane, ethylene-vinyl acetate copolymer, polyvinyl chloride, polybutadiene, cellophane, polychloroprene, polyamino acid, and nitrile rubber. It is possible to use a sheet in which a synthetic resin such as butyl rubber or silicone rubber or a synthetic rubber or the like is thinly formed, and if necessary, a foam (breathable) or non-breathable (non-breathable) foamed foam. Can also be used. In this case, in the case of non-breathable (non-breathable) sheets or foams, breathability (moisture permeability) is imparted by perforating or stretching in a range that does not allow the generated hydrogen to diffuse to the outside. You can also
- the size and shape of the sheet are not limited as long as the desired effect of the present invention can be obtained, and can be appropriately determined according to the site to be used.
- 6.5 cm ⁇ 4.2 cm, 9 A rectangular shape of 0.0 cm ⁇ 6.0 cm, 13.0 cm ⁇ 7.2 cm, 18 cm ⁇ 24 cm, or a circular shape having a diameter of 22 mm can be used.
- the thickness of such a sheet is preferably 15 to 250 ⁇ m, and more preferably 30 to 100 ⁇ m.
- the pressure-sensitive adhesive that can be used in the present invention is not particularly limited as long as the desired effect of the present invention can be obtained without reacting with the above-described hydrogen storage porous material and the above-mentioned organic acid. It can be worn.
- Such an adhesive only needs to be provided on one side of the sheet, and may be provided on a part or the entire surface of the sheet, and is generally formed as an adhesive layer. Further, such an adhesive preferably has an adhesive strength that does not peel naturally during use, and preferably does not easily lose adhesiveness even when it comes into contact with moisture due to sweating, etc. Is a known lipophilic pressure-sensitive adhesive.
- the pressure-sensitive adhesive examples include a vinyl acetate pressure-sensitive adhesive, an acrylic pressure-sensitive adhesive, a polyvinyl alcohol-based pressure-sensitive adhesive, a polyvinyl acetal-based pressure-sensitive adhesive, a vinyl chloride-based pressure-sensitive adhesive, a polyamide-based pressure-sensitive adhesive, and a polyethylene-based pressure-sensitive adhesive.
- a thermoplastic adhesive such as an adhesive or a cellulose adhesive, or a rubber adhesive such as a nitrile rubber adhesive, a butyl rubber adhesive, or a chloroprene adhesive is preferably used. Is not particularly limited, but is preferably about 10 to 70 ⁇ m.
- a tackifier an inorganic filler, an anti-aging agent, an antioxidant, an ultraviolet absorber, and a pigment are generally added to the pressure-sensitive adhesive within a range that does not impair the effects of the present invention. Etc. can be added.
- the external sheet set of the present invention is characterized by comprising a sheet having an adhesive on one side, the hydrogen storage porous material and the organic acid, and the hydrogen storage porous material contains an organic acid. It is preferable that it is a tablet provided with the recessed part to receive.
- Another external sheet set according to the present invention is characterized by comprising a sheet having an adhesive on one side and a hydrogen storage porous material in the form of a paste, powder or granules. By setting it as such an external sheet agent set, the external sheet agent of this invention can be obtained more easily.
- FIGS. 9 and 10 are diagrams showing how to use the external sheet.
- the method for using the external sheet is to arrange the hydrogen storage porous material 1 on the sheet 3 having an adhesive on one side (FIG. 9A), and to store the hydrogen storage porous material 1.
- the external sheet 6 is adhered to the skin (FIG. 9C).
- another method for using an external sheet is to apply a hydrogen storage porous material 4 in the form of a paste, powder or granules on a sheet 3 having an adhesive on one side. Later (FIG. 10A), the external sheet 7 is adhered to the skin (FIG. 10B).
- the effect of the present invention by the hydrogen storage porous material and the organic acid can be realized, and it is oxidized by active oxygen by being attached to pain, an inflammatory site, etc.
- Hydrogen can permeate into the cells over time, and inflammation can be suppressed by its reducing power, and an unprecedented immediate anti-inflammatory and analgesic action can be expected.
- Example 1 (Production of hydrogen storage porous material) Calcium processed food (trade name: hydrogen every day, manufactured by Sante Corporation) is used as a tablet, and a concave portion with a diameter of 4.5 mm and a depth of 3 mm is formed in the center of the tablet, and hydrogen storage porous Material tablet A was prepared.
- Calcium processed food (trade name: hydrogen every day, manufactured by Sante Corporation) is used as a tablet, and a concave portion with a diameter of 4.5 mm and a depth of 3 mm is formed in the center of the tablet, and hydrogen storage porous Material tablet A was prepared.
- Example 1 by using an external sheet A that efficiently and continuously generates hydrogen, symptoms such as rheumatoid arthralgia, low back pain, hay fever, general fatigue, and cold are alleviated. We were able to.
- Example 2 Preparation of external sheet B
- Sante Care (fucoidan paste, manufactured by Sante Global Co., Ltd.) was applied to the adhesive surface of a commercially available adhesive bandage tape having a diameter of 22 mm to prepare an external sheet agent B.
- Example 3 (Preparation of external sheet C) Hydrogen-absorbing coral calcium (hydrogen bulk powder) 700 mg, Igis seaweed powder 200 mg, and citric acid powder 100 mg were mixed, and this mixture was made into one bag. Six such sachets, 5 g of kaolin (mud) and 2 g of citric acid were placed in a small dish and mixed well to obtain a substrate (pH 4-5). The obtained base material was applied to the adhesive surface of a commercially available L-size adhesive bandage tape (18 cm ⁇ 24 cm) to produce an external sheet C.
- a commercially available L-size adhesive bandage tape (18 cm ⁇ 24 cm
- Example 4 (Preparation of sheet D for external use) Hydrogen-absorbing coral calcium (hydrogen bulk powder) 700 mg, Igis seaweed powder 200 mg, and citric acid powder 100 mg were mixed, and this mixture was made into one bag. Six such sachets, 5 g of kaolin (mud) and 2 g of citric acid were placed in a small dish and mixed well to obtain a substrate (pH 4-5). An aluminum sheet was adhered to the adhesive surface of a commercially available L-size adhesive bandage tape (18 cm ⁇ 24 cm), and the base material obtained was applied to the adhesive surface of the adhesive bandage tape (18 cm ⁇ 24 cm) to prepare an external sheet D. .
Landscapes
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
1a 錠剤の直径
1b 錠剤の厚さ
2 錠剤の凹部
2a 凹部の直径
2b 凹部の深さ
3 粘着剤を含有するシート
4 ペースト状、粉末状または顆粒状である水素吸蔵多孔質物質
5 有機酸
6,7 外用シート剤
8、9 アルミ層
実施例1
(水素吸蔵多孔質物質の作製)
錠剤としてカルシウム加工食品(商品名:毎日水素、(株)サンテ・コーポレーション社製)を使用し、該錠剤の中央に、直径4.5mm、深さ3mmの凹部を形成して、水素吸蔵多孔質物質錠剤Aを作製した。
クエン酸1gを5mLの精製水に溶解して、有機酸水溶液Aを調整し、5mLスポイト瓶に保存した。
直径22mmの市販の創膏テープの粘着面に水素吸蔵多孔質物質錠剤Aを粘着し、有機酸水溶液Aをスポイトで1滴(0.4mL)滴下して、外用シート剤Aを作製した。
(リュウマチ関節痛試験)
リュウマチ関節痛を有するボランティア9名(関節19箇所)に対し、有機酸水溶液Aを1滴スポイトで滴下後の外用シート剤Aを、リュウマチ関節痛の部位に、粘着した。痛みを、0~10点の段階で、10点が最も痛い状態を表す数値で評価した。外用シート剤Aの粘着前は10点であったが、外用シート剤Aの粘着後は、ボランティア9名全員について、0~1点に顕著に改善された。また、いずれも鎮痛効果は5分以内に改善され、即効性を示した。
腰痛症を有するボランティア5名に対し、有機酸水溶液Aを1滴スポイトで滴下後の外用シート剤Aを、腰部に、粘着した。痛みを、0~10点の段階で、10点が最も痛い状態を表す数値で評価した。外用シート剤Aの粘着前は10点であったが、外用シート剤Aの粘着後は、ボランティア5名全員について、0~1点に顕著に改善された。
花粉症を有するボランティア12名に対し、有機酸水溶液Aを1滴スポイトで滴下後の外用シート剤Aを、星状神経節(ツボ)の両側に、粘着した。外用シート剤Aを粘着することにより、ボランティア12名全員について、鼻閉、鼻汁が改善された。
感冒を発症しているボランティア3名に対し、有機酸水溶液Aを1滴スポイトで滴下後の外用シート剤Aを、肺経のツボに、粘着した。外用シート剤Aを粘着することにより、ボランティア3名全員について、顕著に改善された。
全身疲労感を感じているボランティア1名に対し、有機酸水溶液Aを1滴スポイトで滴下後の外用シート剤Aを、副腎と胸腺の部位に、粘着した。外用シート剤Aを粘着することにより、ボランティア1名全員について、顕著に改善された。
波動測定器(ゼロサーチ)を作製し、該波動測定器で、外用シート剤Aの皮膚への粘着による影響を観察した。その結果、アドレナリンおよびノルアドレナリンの共鳴反応の消失が確認された。また、エンドルフィンおよびセロトニンの共鳴の増加が確認された。さらに、ATP(アデノシントリホスフェイト)の共鳴の顕著な増加が確認された。
(外用シート剤Bの作製)
直径22mmの市販の絆創膏テープの粘着面に、サンテケア(フコイダンペースト、(株)サンテグローバル社製)を塗布して、外用シート剤Bを作製した。
(外用シート剤Cの作製)
水素吸蔵サンゴカルシウム(水素原末)700mg、イギス海藻粉末200mg、クエン酸粉末100mgを混合し、この混合物を1袋とした。かかる混合物6包、カオリン(泥)5gおよびクエン酸2gを小皿にとり、十分に混合し、基材(pH4~5)とした。得られた基材を市販のLサイズ絆創膏テープ(18cm×24cm)の粘着面に塗布して、外用シート剤Cを作製した。
右前脚挫傷のサラブレッドで、トレーニングへの移動を嫌がるほど痛みを感じていたサラブレッドを使用した。かかるサラブレッドの右脛に外用シート剤Cを貼付した。外用シート剤Cの貼付後1日目で、サラブレッドがコースでの追い切り800~1000mを軽快に走ることができ、痛みが軽快し鎮痛効果があることを示した。なお、従来の治療であるアイシングでは脚の血行不全はよくならず、外用シート剤Cにより従来にはない治療効果が得られた。
右前脚骨折のサラブレッドで、骨折の激しい痛みのため、すぐにギブスで固定しているサラブレッドを使用した。ギブスを外して、かかるサラブレッドの骨折部位に直接外用シート剤Cを貼付し、ギブスで再固定した。外用シート剤Cの貼付後数時間で、骨折の痛みが軽快し鎮痛効果があることを示した。1日1回の外用シート剤Cの貼付を3日間繰り返すことで、完全に痛みを除くことができた。
(外用シート剤Dの作製)
水素吸蔵サンゴカルシウム(水素原末)700mg、イギス海藻粉末200mg、クエン酸粉末100mgを混合し、この混合物を1袋とした。かかる混合物6包、カオリン(泥)5gおよびクエン酸2gを小皿にとり、十分に混合し、基材(pH4~5)とした。市販のLサイズ絆創膏テープ(18cm×24cm)の粘着面にアルミ箔を接着し、かかる絆創膏テープ(18cm×24cm)の粘着面に得られた基材を塗布して、外用シート剤Dを作製した。
Claims (21)
- 片面側に粘着剤を有するシート上に、水素吸蔵多孔質物質を配設してなることを特徴とする外用シート剤。
- 前記水素吸蔵多孔質物質が、水素吸蔵焼成サンゴカルシウム、水素吸蔵ゼオライト、水素吸蔵木炭、水素吸蔵活性炭、水素吸蔵麦飯石、水素吸蔵トルマリンおよび水素吸蔵レアアース鉱石からなる群より選ばれた1種以上である請求項1記載の外用シート剤。
- 前記水素吸蔵多孔質物質に有機酸を添加してなる請求項2記載の外用シート剤。
- 前記有機酸が、クエン酸、酒石酸、乳酸、グリコール酸、リンゴ酸、希塩酸、酢酸、シュウ酸およびD-グルクロン酸からなる群より選ばれた1種以上である請求項3記載の外用シート剤。
- 前記水素吸蔵多孔質物質が、前記有機酸を受け止める凹部を設けた錠剤である請求項3記載の外用シート剤。
- 前記水素吸蔵多孔質物質が、前記有機酸を受け止める凹部を設けた錠剤である請求項4記載の外用シート剤。
- 前記水素吸蔵多孔質物質がペースト状、粉末状または顆粒状である請求項1記載の外用シート剤。
- 前記水素吸蔵多孔質物質がペースト状、粉末状または顆粒状である請求項2記載の外用シート剤。
- 前記水素吸蔵多孔質物質がペースト状、粉末状または顆粒状である請求項3記載の外用シート剤。
- 前記水素吸蔵多孔質物質がペースト状、粉末状または顆粒状である請求項4記載の外用シート剤。
- 前記片面側に粘着剤を有するシート上にアルミ層を有し、該アルミ層上に水素吸蔵多孔質物質を配設してなる請求項1記載の外用シート剤。
- 前記片面側に粘着剤を有するシート上にアルミ層を有し、該アルミ層上に水素吸蔵多孔質物質を配設してなる請求項2記載の外用シート剤。
- 前記片面側に粘着剤を有するシート上にアルミ層を有し、該アルミ層上に水素吸蔵多孔質物質を配設してなる請求項5記載の外用シート剤。
- 前記片面側に粘着剤を有するシート上にアルミ層を有し、該アルミ層上に水素吸蔵多孔質物質を配設してなる請求項7記載の外用シート剤。
- 前記片面側に粘着剤を有するシートの下側に、アルミ層を有する請求項1記載の外用シート剤。
- 前記片面側に粘着剤を有するシートの下側に、アルミ層を有する請求項2記載の外用シート剤。
- 前記片面側に粘着剤を有するシートの下側に、アルミ層を有する請求項5記載の外用シート剤。
- 前記片面側に粘着剤を有するシートの下側に、アルミ層を有する請求項7記載の外用シート剤。
- 片面側に粘着剤を有するシート、水素吸蔵多孔質物質および有機酸からなることを特徴とする外用シート剤セット。
- 前記水素吸蔵多孔質物質が、前記有機酸を受け止める凹部を設けた錠剤である請求項19記載の外用シート剤セット。
- 片面側に粘着剤を有するシートと、ペースト状、粉末状または顆粒状の水素吸蔵多孔質物質からなることを特徴とする外用シート剤セット。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2009525844A JP5301442B2 (ja) | 2008-04-28 | 2008-10-03 | 外用シート剤および外用シート剤セット |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008116666 | 2008-04-28 | ||
JP2008-116666 | 2008-04-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2009133637A1 true WO2009133637A1 (ja) | 2009-11-05 |
Family
ID=41254865
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2008/068108 WO2009133637A1 (ja) | 2008-04-28 | 2008-10-03 | 外用シート剤および外用シート剤セット |
Country Status (3)
Country | Link |
---|---|
JP (1) | JP5301442B2 (ja) |
KR (1) | KR20110004850A (ja) |
WO (1) | WO2009133637A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013189379A (ja) * | 2012-03-12 | 2013-09-26 | Kracie Home Products Ltd | 水素発生材 |
CN109925319A (zh) * | 2019-04-09 | 2019-06-25 | 苏州雨泉富氢生物科技有限公司 | 一种氢气膜及其制备方法 |
Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63180054U (ja) * | 1987-05-12 | 1988-11-21 | ||
JPH0421521U (ja) * | 1990-06-14 | 1992-02-24 | ||
WO1999024043A1 (fr) * | 1997-11-07 | 1999-05-20 | Medion Research Laboratories Inc. | Compositions visqueuses contenant du dioxyde de carbone |
JP2000239092A (ja) * | 1999-02-22 | 2000-09-05 | Nippon Kayaku Co Ltd | ガス発生剤成形体 |
JP2000319187A (ja) * | 1999-05-06 | 2000-11-21 | Medion Research Laboratories Inc | 二酸化炭素経皮・経粘膜吸収用組成物 |
WO2002080941A1 (fr) * | 2001-04-06 | 2002-10-17 | Masaya Tanaka | Compositions destinees a preparer des agents exterieurs du dioxyde de carbone |
JP2003144520A (ja) * | 2001-11-14 | 2003-05-20 | Takeo Suda | 花粉症ツボ刺激貼付剤 |
WO2004004745A1 (ja) * | 2002-07-05 | 2004-01-15 | Neochemir Inc. | 二酸化炭素外用剤及び二酸化炭素外用剤調製用材料 |
JP2005245265A (ja) * | 2004-03-03 | 2005-09-15 | Sozoteki Seibutsu Kogaku Kenkyusho:Kk | 食べるマイナス水素イオンの製造方法 |
JP2006036743A (ja) * | 2004-07-22 | 2006-02-09 | Santamonica:Kk | 外用貼付剤 |
JP3129640U (ja) * | 2006-12-11 | 2007-03-01 | 第一商事株式会社 | 複合多層剤 |
JP2007217351A (ja) * | 2006-02-17 | 2007-08-30 | Amimoto Giken Kk | 抗酸化組成物及びこれを含む食品・医薬品・化粧品 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3472514B2 (ja) * | 1999-10-22 | 2003-12-02 | 株式会社コーヨーサムシング | マイナスイオン発生の繊維製品とその製造法 |
JP2003169852A (ja) * | 2001-12-05 | 2003-06-17 | Ooshin Seiyaku Kk | マイナスイオン発生剤、これを用いたマイナスイオン発生シート及びマイナスイオン発生貼付剤 |
JP2003171265A (ja) * | 2001-12-05 | 2003-06-17 | Ooshin Seiyaku Kk | 外用貼付剤 |
JP3906425B2 (ja) * | 2002-10-25 | 2007-04-18 | 明子 菅原 | 溶解タンク、溶解液製造方法、繊維製品、羽毛製品、壁紙、溶解液成分の付着方法、洗濯用柔軟剤、不織紙 |
-
2008
- 2008-10-03 WO PCT/JP2008/068108 patent/WO2009133637A1/ja active Application Filing
- 2008-10-03 JP JP2009525844A patent/JP5301442B2/ja active Active
- 2008-10-03 KR KR1020107022482A patent/KR20110004850A/ko not_active Application Discontinuation
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63180054U (ja) * | 1987-05-12 | 1988-11-21 | ||
JPH0421521U (ja) * | 1990-06-14 | 1992-02-24 | ||
WO1999024043A1 (fr) * | 1997-11-07 | 1999-05-20 | Medion Research Laboratories Inc. | Compositions visqueuses contenant du dioxyde de carbone |
JP2000239092A (ja) * | 1999-02-22 | 2000-09-05 | Nippon Kayaku Co Ltd | ガス発生剤成形体 |
JP2000319187A (ja) * | 1999-05-06 | 2000-11-21 | Medion Research Laboratories Inc | 二酸化炭素経皮・経粘膜吸収用組成物 |
WO2002080941A1 (fr) * | 2001-04-06 | 2002-10-17 | Masaya Tanaka | Compositions destinees a preparer des agents exterieurs du dioxyde de carbone |
JP2003144520A (ja) * | 2001-11-14 | 2003-05-20 | Takeo Suda | 花粉症ツボ刺激貼付剤 |
WO2004004745A1 (ja) * | 2002-07-05 | 2004-01-15 | Neochemir Inc. | 二酸化炭素外用剤及び二酸化炭素外用剤調製用材料 |
JP2005245265A (ja) * | 2004-03-03 | 2005-09-15 | Sozoteki Seibutsu Kogaku Kenkyusho:Kk | 食べるマイナス水素イオンの製造方法 |
JP2006036743A (ja) * | 2004-07-22 | 2006-02-09 | Santamonica:Kk | 外用貼付剤 |
JP2007217351A (ja) * | 2006-02-17 | 2007-08-30 | Amimoto Giken Kk | 抗酸化組成物及びこれを含む食品・医薬品・化粧品 |
JP3129640U (ja) * | 2006-12-11 | 2007-03-01 | 第一商事株式会社 | 複合多層剤 |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013189379A (ja) * | 2012-03-12 | 2013-09-26 | Kracie Home Products Ltd | 水素発生材 |
CN109925319A (zh) * | 2019-04-09 | 2019-06-25 | 苏州雨泉富氢生物科技有限公司 | 一种氢气膜及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
KR20110004850A (ko) | 2011-01-14 |
JP5301442B2 (ja) | 2013-09-25 |
JPWO2009133637A1 (ja) | 2011-08-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6487039B2 (ja) | スキンケア組成物の送達のためのデバイス | |
JP4527724B2 (ja) | 発熱体及び型成形発熱体用包材 | |
JP4490971B2 (ja) | 発熱体 | |
WO2006006653A1 (ja) | マイクロヒーター及びその製造方法 | |
JPWO2006006662A1 (ja) | 発熱体 | |
JPWO2006006652A1 (ja) | 発熱体 | |
WO2006006654A1 (ja) | ヒートクロス及びその製造方法 | |
WO2004061045A1 (ja) | 発熱組成物及び発熱体 | |
EP3348242B1 (en) | Heating compress | |
WO2006006648A1 (ja) | 発熱組成物、発熱体及び発熱体の製造方法 | |
DK2533773T3 (en) | TOPICAL DERMAL delivery device for delivering nitric oxide | |
WO2006006657A1 (ja) | 関節周囲部用温熱包装体 | |
CN102335069A (zh) | 一种药贴 | |
WO2004098537A3 (en) | Activation agents on the surface of encapsulation vesicles | |
WO2006006645A1 (ja) | 発熱混合物の製造方法、発熱混合物、発熱組成物及び発熱体 | |
JP5301442B2 (ja) | 外用シート剤および外用シート剤セット | |
JP2007136053A (ja) | 膏薬温熱用具 | |
JP2001238906A (ja) | 発熱体組成物、発熱体及びその製造方法 | |
TWI623332B (zh) | Tong nose improvement appliance | |
WO2006006649A1 (ja) | 湿潤性発熱組成物圧縮体、発熱体及び湿潤性発熱組成物圧縮体の製造方法 | |
WO2006006660A1 (ja) | 発熱ラップ | |
CN202122720U (zh) | 一种药贴 | |
JP2007275084A (ja) | 温灸器 | |
JP2010132618A (ja) | 外用剤、外用シート剤および外用シート剤セット | |
JP2003169852A (ja) | マイナスイオン発生剤、これを用いたマイナスイオン発生シート及びマイナスイオン発生貼付剤 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 2009525844 Country of ref document: JP |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 08874115 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 20107022482 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: 08874115 Country of ref document: EP Kind code of ref document: A1 |