JP2001114671A - Cataplasm - Google Patents
CataplasmInfo
- Publication number
- JP2001114671A JP2001114671A JP32860499A JP32860499A JP2001114671A JP 2001114671 A JP2001114671 A JP 2001114671A JP 32860499 A JP32860499 A JP 32860499A JP 32860499 A JP32860499 A JP 32860499A JP 2001114671 A JP2001114671 A JP 2001114671A
- Authority
- JP
- Japan
- Prior art keywords
- cataplasm
- skin
- effect
- component
- patch
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
Links
Landscapes
- Medicinal Preparation (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、消炎鎮痛貼付剤に
関するものである。TECHNICAL FIELD The present invention relates to an anti-inflammatory analgesic patch.
【0002】[0002]
【従来の技術及び発明の解決しようとする課題】従来よ
り用いられている貼付剤は、一般的には成型パップ剤と
も呼ばれ、肩こり、筋肉疲労、打ち身等の疲労や打撲、
炎症それに伴う痛みなどに数多く用いられている。その
使用法も患部に貼り付けるだけと手軽なものとなってい
る。2. Description of the Related Art Patches conventionally used are generally referred to as molded cataplasms, and include stiff shoulders, muscular fatigue, bruises and other bruises.
It is widely used for pain associated with inflammation. Its usage is simple, just sticking it to the affected area.
【0003】しかし貼付剤は、その形態故に長時間皮膚
に接触している必要があること、また、本来外部から体
内への侵入を防ぐ役目を持つ皮膚を通して薬効成分を体
内に入れる必要があること等の理由により、効果が長時
間持続しない等の他、貼付剤の基剤や薬効成分等の皮膚
に対する刺激が常に問題となる。すなわち貼付部位での
かぶれや炎症が効果に対する副作用として存在するので
ある。[0003] However, the patch must be in contact with the skin for a long time because of its form, and it is necessary to put a medicinal ingredient into the body through the skin, which originally has a function of preventing invasion into the body from the outside. For these reasons, in addition to the effect not being maintained for a long time, irritation to the skin such as the base of the patch or the medicinal component always poses a problem. That is, rash and inflammation at the site of application are present as side effects on the effect.
【0004】このうち、基剤自体についてはかなり研究
が進み、低刺激性の基剤が使用されるようになってき
た。しかし、貼付剤としての形になると薬効成分や各種
の安定化剤、経皮吸収促進剤等の影響もあり、効果の裏
返しである刺激性の問題は解決されていない。特に、温
感タイプとされるトウガラシエキスあるいはノニル酸ワ
ニリルアミド等を含有するものは、皮膚の温感点を刺激
して血流を改善する効果があるが、それは同時に皮膚に
対する刺激による効果であり長時間の使用は皮膚の状態
を悪化させる可能性をもはらんでいる。発明者らは、貼
付剤の効果を落とすことなくしかも貼付剤全体として刺
激性の少ない安全なものという観点から鋭意研究を重ね
た結果、貼付部位の血流改善と皮膚表面の抗活性酸素効
果及び細胞賦活作用の組合せにより本発明を完成した。[0004] Of these, the base itself has been studied considerably, and a base having low irritation has come to be used. However, in the form of a patch, there are also effects of medicinal ingredients, various stabilizers, transdermal absorption enhancers, and the like, and the problem of irritation, which is the reverse of the effect, has not been solved. In particular, those containing hot pepper type pepper extract or nonylate vanillylamide have the effect of stimulating the hot spot of the skin and improving blood flow, but at the same time, it is the effect of irritation to the skin, which has a long effect. The use of time has the potential to worsen the condition of the skin. The inventors of the present invention have conducted intensive studies from the viewpoint of safe and less irritating as a whole patch without reducing the effect of the patch, and as a result, the blood flow improvement of the patch site and the anti-reactive oxygen effect on the skin surface and The present invention has been completed by a combination of cell activation effects.
【0005】[0005]
【課題を解決するための手段】本発明は、通常使用され
る鎮痛消炎成分と血流改善に良い影響を及ぼす遠赤外線
を発生する成分等、それに皮膚における抗酸化と細胞賦
活作用などに効果のある白金族元素のコロイドより成
る。消炎鎮痛成分には、第一世代と言われるメントー
ル、カンフル、サリチル酸等及びその誘導体とその組合
せのみならず第二世代と言われるインドメタシン等も用
いることが出来る。これらは消炎鎮痛の薬効をあらわ
す。DISCLOSURE OF THE INVENTION The present invention relates to a commonly used analgesic and anti-inflammatory component and a component that generates far-infrared rays that have a positive effect on blood flow improvement, and also has an effect on antioxidant and cell activating effects on the skin. Consists of a colloid of a platinum group element. As the anti-inflammatory analgesic component, not only menthol, camphor, salicylic acid and the like, which are said to be the first generation, and their derivatives and combinations thereof, but also indomethacin, which is said to be the second generation, can be used. These show the medicinal effects of anti-inflammatory analgesia.
【0006】遠赤外線を発生する成分としては、一例と
して麦飯石、電気石(トルマリン)、かんらん岩、蛇紋
岩、きん青石、絹雲母あるいはそれらを用いて作成され
たセラミックスが使用される。この微細粉末にしたもの
を通常0.1%乃至10%、好ましくは0.5%乃至5
%の濃度で使用する。これ以上量を増やしても効果は変
わらない。また、これ以上低いと効果が期待できない。
この遠赤外線発生成分は、その遠赤外線によりその部位
の血管を拡張して血流を改善し貼付剤の貼付部位を安定
に保つ。As a component for generating far-infrared rays, for example, barley stone, tourmaline, peridotite, serpentine, kyanite, sericite, or ceramics prepared using them are used. This fine powder is usually 0.1% to 10%, preferably 0.5% to 5%.
Use at a% concentration. Increasing the amount further does not change the effect. Further, if it is lower than this, the effect cannot be expected.
The far-infrared ray-generating component expands the blood vessel at the site by the far-infrared ray, improves blood flow, and stably maintains the patch application site.
【0007】白金族元素のコロイド化物として、特に好
ましくは白金及びパラジウムのコロイドを用いる。白金
及びパラジウムのコロイドは、粒子径が75μm以下と
なった白金及びパラジウムの比率が1:3乃至3:1、
特に約2:3であるようなのコロイドもしくはそれを含
有する溶液を用いることが望ましい。本発明において使
用される白金及びパラジウムのコロイドは、すでに公知
である方法、例えば、蒸発皿に蒸留水を入れ、これを冷
却しながらこの中に浸した2本の白金電極の間で30〜
100V程度の直流電流または105〜107程度の高
周波の高圧電流によってアークを飛ばすブレージッヒ法
等で製造されたものを使用できる。パラジウムコロイド
も同様にして白金電極をパラジウム電極に代えたブレー
ジッヒ法等により製造できる。これらのコロイドの製品
への配合量は、各々20乃至3000ppm、好ましく
は100乃至1000ppmである。これ以上量が少な
いと効果が出ない。またこれ以上多くてもコストのみ上
昇して効果が上がらない。As a colloidal product of a platinum group element, a colloid of platinum and palladium is particularly preferably used. The colloid of platinum and palladium has a particle diameter of 75 μm or less, and the ratio of platinum and palladium is 1: 3 to 3: 1,
In particular, it is desirable to use a colloid such as about 2: 3 or a solution containing it. The colloid of platinum and palladium used in the present invention can be prepared by a method known in the art, for example, by placing distilled water in an evaporating dish, and cooling the mixture between two platinum electrodes immersed therein.
It is possible to use one manufactured by a Bragg method or the like in which an arc is blown by a direct current of about 100 V or a high-frequency high current of about 10 5 to 10 7 . A palladium colloid can be similarly produced by a Bragg method or the like in which a platinum electrode is replaced with a palladium electrode. The content of these colloids in the product is 20 to 3000 ppm, preferably 100 to 1000 ppm. If the amount is less than this, the effect is not obtained. If the amount is more than this, only the cost increases and the effect is not improved.
【0008】このような白金及びパラジウムのコロイド
は、強い抗活性酸素効果と細胞賦活作用を持つので、貼
付剤に用いたとき、皮膚表面で基剤から発生する水分が
飽和して皮膚から薬物透過を促進するときに、同時に敏
感になった皮膚表面を保護し刺激から皮膚を守る。[0008] Since such colloids of platinum and palladium have a strong anti-reactive oxygen effect and a cell activating effect, when used as a patch, the moisture generated from the base material on the skin surface is saturated and the drug permeates from the skin. Promotes and simultaneously protects the sensitized skin surface and protects the skin from irritation.
【0009】貼付剤の基剤にはゼラチン、カルメロース
ナトリウム、メチルセルロース、ポリアクリル酸ナトリ
ウム等の通常使用されるものを用いることができる。こ
の基剤に適量の薬用成分、遠赤外線発生成分それに白金
及びパラジウムのコロイドを混ぜて練合して膏体とし、
成型パップ剤製造の定法により貼付剤を製造することが
できる。As the base of the patch, commonly used substances such as gelatin, carmellose sodium, methylcellulose and sodium polyacrylate can be used. An appropriate amount of medicinal component, far-infrared ray generating component and platinum and palladium colloid are mixed with this base and kneaded to form a plaster,
A patch can be produced by a standard method for producing a molded cataplasm.
【0010】[0010]
【実施の形態もしくは実施例】インドメタシン1%、3
00メッシュ以下に砕いた麦飯石3%と白金コロイド2
00ppm、パラジウムコロイド300ppmを経皮吸
収促進剤のd−リモネンとともに窒素気流下でポリアク
リル酸ナトリウムの基剤に練合し膏体として定法に従い
成型パップ剤を製造した。Embodiments or Examples Indomethacin 1%, 3
3% barley rice stone and platinum colloid 2 crushed to less than 00 mesh
00 ppm and 300 ppm of palladium colloid were kneaded with a base of sodium polyacrylate together with a transdermal absorption enhancer d-limonene under a nitrogen stream to prepare a plaster according to a standard method as a plaster.
【0011】[0011]
【発明の効果】本発明は、主成分の消炎鎮痛の薬効とと
もに、通常水分で飽和される貼付剤の接触部位の血流を
改善し薬効を持続させ、なおかつ細胞賦活作用と抗活性
酸素効果が貼付剤の刺激性を改善して貼付部位の皮膚を
守る、貼付剤の副作用を解決した画期的なものである。Industrial Applicability The present invention improves the blood flow at the contact site of a patch which is usually saturated with water, maintains the efficacy, and has a cell activating effect and an anti-reactive oxygen effect. It is an epoch-making solution that improves the irritancy of the patch and protects the skin at the patch site, eliminating the side effects of the patch.
Claims (4)
薬効成分を有する薬剤及び遠赤外線を発生する成分を併
用することを特徴とする消炎鎮痛貼付剤1. An anti-inflammatory analgesic patch characterized by using a colloidal substance of a platinum group element, a drug having a medicinal component for anti-inflammatory analgesia, and a component generating far-infrared rays.
化物に、白金、パラジウム、その他の白金族元素のうち
の1種類以上を用いることを特徴とする消炎鎮痛貼付剤2. An anti-inflammatory analgesic patch, wherein at least one of platinum, palladium and other platinum group elements is used as the colloidal product of the platinum group element according to claim 1.
トール、サリチル酸、カンフル、ボルネオール、グリチ
ルリチン酸及びそれぞれの誘導体、ハッカ油、ユーカリ
油、インドメタシンのうちの1種類以上であることを特
徴とする消炎鎮痛貼付剤3. The anti-inflammatory analgesic component used in claim 1 is one or more of menthol, salicylic acid, camphor, borneol, glycyrrhizic acid and derivatives thereof, peppermint oil, eucalyptus oil and indomethacin. Anti-inflammatory analgesic patch
成分が、麦飯石、電気石(トルマリン)、かんらん岩、
蛇紋岩、きん青石、絹雲母あるいはそれらを用いて作成
されたセラミックスのうちの1種類以上を0.1%乃至
10%の濃度で使用することを特徴とする消炎鎮痛貼付
剤4. The component that generates far-infrared rays used in claim 1 is malted stone, tourmaline, peridotite,
An anti-inflammatory analgesic patch characterized by using one or more of serpentine, kyanite, sericite or ceramics prepared using them at a concentration of 0.1% to 10%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32860499A JP2001114671A (en) | 1999-10-15 | 1999-10-15 | Cataplasm |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32860499A JP2001114671A (en) | 1999-10-15 | 1999-10-15 | Cataplasm |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2001114671A true JP2001114671A (en) | 2001-04-24 |
Family
ID=18212138
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP32860499A Pending JP2001114671A (en) | 1999-10-15 | 1999-10-15 | Cataplasm |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2001114671A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004073723A1 (en) * | 2003-02-20 | 2004-09-02 | She Tec Co., Ltd. | Medical drug containing fine particle of noble metal |
WO2004073722A1 (en) * | 2003-02-20 | 2004-09-02 | Shetech Co., Ltd. | Superoxide anion decomposing agent |
WO2007074749A1 (en) * | 2005-12-27 | 2007-07-05 | Apt Co., Ltd. | Prophylactic and/or therapeutic agent for chronic obstructive pulmonary disease |
JP2008156314A (en) * | 2006-12-26 | 2008-07-10 | Kose Corp | Atp production promotor |
JP2008266324A (en) * | 2007-03-29 | 2008-11-06 | Kose Corp | Liposome composition and external preparation for skin containing liposome composition |
JP2009167572A (en) * | 2008-01-18 | 2009-07-30 | Daiwabo Co Ltd | Antioxidant fabric, clothing, bedding and method for producing the same |
-
1999
- 1999-10-15 JP JP32860499A patent/JP2001114671A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004073723A1 (en) * | 2003-02-20 | 2004-09-02 | She Tec Co., Ltd. | Medical drug containing fine particle of noble metal |
WO2004073722A1 (en) * | 2003-02-20 | 2004-09-02 | Shetech Co., Ltd. | Superoxide anion decomposing agent |
US7838043B2 (en) | 2003-02-20 | 2010-11-23 | Apt Co., Ltd | Superoxide anion decomposing agent |
WO2007074749A1 (en) * | 2005-12-27 | 2007-07-05 | Apt Co., Ltd. | Prophylactic and/or therapeutic agent for chronic obstructive pulmonary disease |
JP2008156314A (en) * | 2006-12-26 | 2008-07-10 | Kose Corp | Atp production promotor |
JP2008266324A (en) * | 2007-03-29 | 2008-11-06 | Kose Corp | Liposome composition and external preparation for skin containing liposome composition |
JP2009167572A (en) * | 2008-01-18 | 2009-07-30 | Daiwabo Co Ltd | Antioxidant fabric, clothing, bedding and method for producing the same |
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