JPS5827247B2 - Treatment adhesive tape or sheet - Google Patents
Treatment adhesive tape or sheetInfo
- Publication number
- JPS5827247B2 JPS5827247B2 JP55040860A JP4086080A JPS5827247B2 JP S5827247 B2 JPS5827247 B2 JP S5827247B2 JP 55040860 A JP55040860 A JP 55040860A JP 4086080 A JP4086080 A JP 4086080A JP S5827247 B2 JPS5827247 B2 JP S5827247B2
- Authority
- JP
- Japan
- Prior art keywords
- sensitive adhesive
- adhesive layer
- pressure
- drug
- adhesive tape
- 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.)
- Expired
Links
Landscapes
- Medicinal Preparation (AREA)
Description
【発明の詳細な説明】
本発明は各種皮膚疾患の治療、その他消炎、鎮痛等に適
した治療用接着テープもしくはシートに関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a therapeutic adhesive tape or sheet suitable for treating various skin diseases, as well as for anti-inflammatory and analgesic purposes.
薬物を経皮吸収させるのに角層の含水量を高くすると、
毛包−脂腺系だけでなく角層を直接通る吸収路も直接利
用できるので、効果的な皮膚吸収を行わしめることがで
きる。Increasing the water content of the stratum corneum for transdermal absorption of drugs
Since not only the hair follicle-sebaceous gland system but also the absorption path that passes directly through the stratum corneum can be used directly, effective skin absorption can be achieved.
このため、皮膚疾患の治療として、最近、皮膚に軟膏等
の外用薬を塗り不透過性のフィルムでこの上を覆い効果
的な薬剤の吸収を図る密封包帯療法(ODT療法)が普
及している。For this reason, occlusive bandage therapy (ODT therapy), which involves applying external medicine such as ointment to the skin and covering it with an impermeable film to ensure effective drug absorption, has recently become popular as a treatment for skin diseases. .
しかし、この密封包帯療法は、患部への取付けが面倒で
あるばかりでなく、嵩張ること、剥れ易いこと、患部の
面積が太きかったり患部の形状が複雑であったりすると
きは患部へ密着しにくい等の欠点があった。However, this occlusive bandage therapy is not only troublesome to attach to the affected area, but also bulky, easy to peel off, and is difficult to apply when the affected area is large or has a complicated shape. It had drawbacks such as being difficult to use.
この欠点を改善するため、例えば特公昭5231405
号公報に見られるように、薬剤を含む感圧性接着剤層が
不透過性のフィルムの片面に設けられた接着テープが提
案されている。In order to improve this drawback, for example,
As seen in the publication, an adhesive tape has been proposed in which a pressure-sensitive adhesive layer containing a drug is provided on one side of an impermeable film.
このような従来の接着テープは、感圧性接着剤層の表面
に適当な溶媒と共に薬剤を塗布することによって、又は
、薬剤を感圧性接着剤溶液に混合して塗布することによ
って製造されていた。Such conventional adhesive tapes have been manufactured by applying a drug together with a suitable solvent to the surface of a pressure-sensitive adhesive layer, or by mixing the drug into a pressure-sensitive adhesive solution and applying it.
そのため、前者の方法によると、薬剤は感圧性接着剤層
の表面に単に塗布されているので、患部へ急速に吸収さ
れてしまう欠点があり、又、後者の方法によると、薬剤
は感圧性接着剤層の内部に分散しているので、患部へ吸
収されるのに非常に長時間を要する欠点があり、いずれ
にしても患部へ望ましい速度で徐徐に吸収せしめること
は困難であった。Therefore, according to the former method, the drug is simply applied to the surface of the pressure-sensitive adhesive layer, which has the disadvantage that it is rapidly absorbed into the affected area, and according to the latter method, the drug is simply applied to the surface of the pressure-sensitive adhesive layer. Since it is dispersed inside the drug layer, it has the disadvantage that it takes a very long time for it to be absorbed into the affected area, and in any case, it has been difficult to gradually absorb it into the affected area at a desired rate.
本発明は、上記従来の欠点に鑑み、簡便に使用でき、し
かも薬剤を患部に望ましい速度で徐々に吸収せしめるこ
との可能な治療用接着テープもしくはシートを提供する
ことを目的とする。SUMMARY OF THE INVENTION In view of the above-mentioned drawbacks of the conventional art, it is an object of the present invention to provide a therapeutic adhesive tape or sheet that is easy to use and is capable of gradually absorbing a drug into an affected area at a desired rate.
本発明の要旨は、基材フィルムの片面に多孔性の感圧性
接着剤層が設けられ、該接着剤層の孔内に薬剤が入り込
んで吸着されてなることを特徴とする、治療用接着テー
プもしくはシートに存する。The gist of the present invention is a therapeutic adhesive tape, characterized in that a porous pressure-sensitive adhesive layer is provided on one side of a base film, and a drug is absorbed into the pores of the adhesive layer. Or it exists on the sheet.
本発明に用いられる基材フィルムとしては、ポリエチレ
ンフィルム、エチレン−酢酸ビニル共重合体フィルム、
軟質ポリ塩化ビニルフィルム、セロハンフィルム等もし
くはこれらをコロナ処理等で表面処理した可撓性を有す
るフィルムが好適に使用される。The base film used in the present invention includes polyethylene film, ethylene-vinyl acetate copolymer film,
A flexible polyvinyl chloride film, a cellophane film, etc., or a flexible film obtained by surface-treating these with corona treatment or the like is preferably used.
基材フィルムの厚みとしては50〜100ミクロンの範
囲が好ましい。The thickness of the base film is preferably in the range of 50 to 100 microns.
本発明に用いられる感圧性接着剤としては、ゴム系の感
圧性接着剤、即ち天然ゴム、イソプレンゴム、スチレン
−ブタジェンゴム等に粘着付与樹脂、軟化剤等を加えた
もの、アクリル系の感圧性接着剤、即ちアクリル酸アル
キルエステル、メタクリル酸アルキルエステル等を主成
分とする共重合体等、その他シリコン系感圧性接着剤、
ウレタン系感圧性接着剤等が好適に使用される。Pressure-sensitive adhesives used in the present invention include rubber-based pressure-sensitive adhesives, such as natural rubber, isoprene rubber, styrene-butadiene rubber, etc., to which tackifying resins, softeners, etc. are added, and acrylic-based pressure-sensitive adhesives. copolymers containing acrylic acid alkyl esters, methacrylic acid alkyl esters, etc. as main components; other silicone-based pressure-sensitive adhesives;
Urethane pressure sensitive adhesives and the like are preferably used.
アクリル系の感圧性接着剤を用いる場合は特にそのアル
キル基の炭素数が4〜12のものが好ましい。When using an acrylic pressure-sensitive adhesive, it is particularly preferable that the alkyl group has 4 to 12 carbon atoms.
本発明に用いられる薬剤としては、デキサメサゾン、フ
レドニゾロン、ヒドロコルチゾン、酢酸ヒドロコルチゾ
ン、ベタメタシン等の副腎皮質ホルモン、その他消炎剤
や抗ヒスタミン剤、殺菌剤等が目的に応じて適宜使用さ
れる。As the drug used in the present invention, adrenocortical hormones such as dexamethasone, frednisolone, hydrocortisone, hydrocortisone acetate, betamethacin, other anti-inflammatory agents, antihistamines, bactericidal agents, etc. are used as appropriate depending on the purpose.
本発明においては上記基材フィルムの片面に多孔性の感
圧性接着剤層を設けるのである。In the present invention, a porous pressure-sensitive adhesive layer is provided on one side of the base film.
多孔性の感圧性接着剤層の典型的な形式方法としては以
下の通りである。Typical formats for porous pressure sensitive adhesive layers are as follows.
基材フィルム上に感圧性接着剤溶液を塗布し、半乾燥状
態で、貧溶剤中へ浸漬し、その後、加熱、乾燥せしめて
多孔性の感圧性接着剤層を形成する。A pressure-sensitive adhesive solution is applied onto the base film, immersed in a poor solvent in a semi-dry state, and then heated and dried to form a porous pressure-sensitive adhesive layer.
この場合の貧溶剤とは、メタノール、エタノール、水等
であり、これらの混合物を用いても良いし、又、若干の
良溶剤を加え溶解性を調節しても良い。The poor solvent in this case is methanol, ethanol, water, etc. A mixture of these may be used, or a small amount of a good solvent may be added to adjust the solubility.
感圧性接着剤層の多孔性は、感圧性接着剤溶液を塗布し
たのち、貧溶剤中へ浸漬するまでの時間、即ち、このと
きの感圧性接着剤層に残存する良溶剤の量、及び貧溶剤
の種類によって制御することができる。The porosity of the pressure-sensitive adhesive layer is determined by the time from application of the pressure-sensitive adhesive solution to immersion into a poor solvent, that is, the amount of good solvent remaining in the pressure-sensitive adhesive layer at this time, and the amount of good solvent remaining in the pressure-sensitive adhesive layer at this time. It can be controlled by the type of solvent.
感圧性接着剤は適当に架橋せしめるのが、使用した場合
に患部へ接着剤が残ることがなくなるので、好ましく、
架橋は、ジインシアネート、金属塩、ジェポキシ、電子
線照射等によって行なうことができる。It is preferable to properly crosslink the pressure-sensitive adhesive, since this will prevent the adhesive from remaining on the affected area when used.
Crosslinking can be carried out using diincyanate, metal salts, jepoxy, electron beam irradiation, and the like.
多孔性の感圧性接着剤層を形成する方法は、上記方法の
他、発泡剤を用いる方法、感圧性接着剤の溶液中に水を
分散せしめて塗布、乾燥せしめる方法、感圧性接着剤に
水で溶解する物質を混入して、塗布の後、本で抽出する
方法等が適宜採用できる。In addition to the above methods, methods for forming a porous pressure-sensitive adhesive layer include a method using a foaming agent, a method in which water is dispersed in a solution of a pressure-sensitive adhesive, and then applied and dried. A method of mixing a substance that dissolves in water, applying it, and then extracting it using a book can be adopted as appropriate.
本発明においては上記多孔性の感圧性接着剤層に薬剤を
吸着せしめるのである。In the present invention, a drug is adsorbed onto the porous pressure-sensitive adhesive layer.
薬剤の吸着は、通常行なわれる方法、即ち、適当な溶剤
に薬剤を溶解せしめ、その中に多孔性の感圧性接着剤層
が設けられた接着テープもしくはシートを浸漬する方法
とか、溶剤に溶解せしめた薬剤溶液を多孔性の感圧性接
着剤層に塗布或は噴霧する方法等が適宜採用される。Adsorption of the drug can be carried out in the usual manner, that is, by dissolving the drug in a suitable solvent and dipping an adhesive tape or sheet provided with a porous pressure-sensitive adhesive layer therein, or by dissolving the drug in the solvent. A method of coating or spraying a drug solution on a porous pressure-sensitive adhesive layer is appropriately employed.
そうすると多孔性の感圧性接着剤層の該多孔の中に薬剤
が入り込んで吸着される。Then, the drug enters into the pores of the porous pressure-sensitive adhesive layer and is adsorbed.
多孔性の感圧性接着剤層に吸着される薬剤の量としては
、薬剤の種類により異なるが、該接着剤層1crttあ
たり約1〜100μmが好ましい。The amount of drug adsorbed on the porous pressure-sensitive adhesive layer varies depending on the type of drug, but is preferably about 1 to 100 μm per crtt of the adhesive layer.
而して本発明の治療用接着テープもしくはシートを患部
に貼れば、多孔性の感圧性接着剤層に吸着されている薬
剤が徐々に、例えば5〜20時間かかつて放出され、効
果的に経皮吸収される。When the therapeutic adhesive tape or sheet of the present invention is applied to the affected area, the drug adsorbed to the porous pressure-sensitive adhesive layer is gradually released over a period of, for example, 5 to 20 hours, and is effectively treated over time. Absorbed through the skin.
薬剤の放出速度は、上記多孔性の感圧性接着剤層の孔径
や数を調節することにより、用途、薬剤の種類等に合わ
せて望ましいものに制御することができる。The drug release rate can be controlled to a desired value depending on the application, the type of drug, etc. by adjusting the pore diameter and number of the porous pressure-sensitive adhesive layer.
上述のとおり、本発明の治療用接着テープもしくはシー
トは、基材フィルムの片面に多孔性の感圧性接着剤層が
設けられ、該接着剤層の孔内に薬剤が入り込んで吸着さ
れてなるから、簡便に使用でき、しかも薬剤を患部に望
ましい速度で吸収せしめることができる。As mentioned above, the therapeutic adhesive tape or sheet of the present invention has a porous pressure-sensitive adhesive layer provided on one side of the base film, and the drug enters and is adsorbed into the pores of the adhesive layer. It is easy to use and allows the drug to be absorbed into the affected area at a desired rate.
以下に本発明の実施例を示す。Examples of the present invention are shown below.
実施例 1
2エチルへキシルアクリレート28 重量部無水マレ
イン酸 1 重量部スチレン
1 重量部ベンゾイルパーオキサ
イド 0.1重量部酢酸エチル
70 重量部上記組成物を反応容器に投入し、
窒素気流中にて80℃で20時間重合を行ない、感圧性
接着剤溶液を作成した。Example 1 2 Ethylhexyl acrylate 28 parts by weight Maleic anhydride 1 part by weight Styrene
1 part by weight benzoyl peroxide 0.1 part by weight ethyl acetate
Pour 70 parts by weight of the above composition into a reaction vessel,
Polymerization was carried out at 80° C. for 20 hours in a nitrogen stream to prepare a pressure-sensitive adhesive solution.
次に、厚み70μのエチレン−酢酸ビニル共重合体フィ
ルム(酢酸ビニル含有量10重量%)をコロナ放電処理
して基材フィルムを得た。Next, an ethylene-vinyl acetate copolymer film (vinyl acetate content: 10% by weight) having a thickness of 70 μm was subjected to corona discharge treatment to obtain a base film.
上記感圧性接着剤溶液に酢酸亜鉛をo、i重量部添加し
たのち、基材フィルムの片面に約100μの厚みに塗布
し、40℃で30分間乾燥したのち、重量比50:50
のメタノールと水の混合液に浸漬し、その後70℃で2
時間乾燥して、多孔性の感圧性接着剤層(厚み約50μ
)が設けられた接着テープを得た。After adding o and i parts by weight of zinc acetate to the above pressure-sensitive adhesive solution, it was applied to one side of the base film to a thickness of about 100μ, and after drying at 40°C for 30 minutes, the weight ratio was 50:50.
immersed in a mixture of methanol and water, then heated at 70℃ for 2 hours.
After drying for a while, a porous pressure-sensitive adhesive layer (approximately 50μ thick) is formed.
) was obtained.
この接着テープの多孔性の感圧性接着剤層の表面に、プ
レドニゾロンを含むエタノール溶液を噴霧し、1c4あ
たり40μダのプレドニゾロンを含有する治療用接着テ
ープを得た。An ethanol solution containing prednisolone was sprayed onto the surface of the porous pressure-sensitive adhesive layer of this adhesive tape to obtain a therapeutic adhesive tape containing 40 μda of prednisolone per 1 c4.
この治療用接着テープを患部に貼り、3時間後、6時間
後に剥して治療用接着テープに残存しているプレドニゾ
ロン量の分析をした。This therapeutic adhesive tape was applied to the affected area, and after 3 and 6 hours, it was removed and the amount of prednisolone remaining on the therapeutic adhesive tape was analyzed.
その結果、3時間後には18μグ、6時間後には5μ2
のプレドニゾロンが残存しており、多孔性の感圧性接着
剤層に吸着されているプレドニゾロンが徐々に放出され
患部に吸収されていることが確認された。As a result, 18μg after 3 hours and 5μ2 after 6 hours.
of prednisolone remained, and it was confirmed that the prednisolone adsorbed to the porous pressure-sensitive adhesive layer was gradually released and absorbed into the affected area.
尚、治療用接着テープ中のプレドゾロンの分析は、テー
プをメタノールで抽出し、抽出液を液体クロマトグラフ
ィーを用いて分離したのち、紫外吸収スペクトロメータ
ーを用いて定量した。For analysis of predzolone in the therapeutic adhesive tape, the tape was extracted with methanol, the extract was separated using liquid chromatography, and then quantified using an ultraviolet absorption spectrometer.
実施例 2
実施例1と同じ感圧性接着剤溶液を同様の方法で基材フ
ィルムの片面に塗布し、40℃で10分間乾燥したのち
、重量比70:30のメタノールと水の混合液に浸漬し
、その後70℃で2時間乾燥して、多孔性の感圧性接着
剤層(厚み約50μ)が設けられた接着テープを得た。Example 2 The same pressure-sensitive adhesive solution as in Example 1 was applied to one side of the base film in the same manner, dried at 40°C for 10 minutes, and then immersed in a mixture of methanol and water at a weight ratio of 70:30. Then, it was dried at 70° C. for 2 hours to obtain an adhesive tape provided with a porous pressure-sensitive adhesive layer (thickness: about 50 μm).
この接着テープの多孔性の感圧性接着剤層に、プレドニ
ゾロンを含むエタノール溶液を塗布し、1crAあたり
42μグのプレドニゾロンを含有する治療用接着テープ
を得た。An ethanol solution containing prednisolone was applied to the porous pressure-sensitive adhesive layer of this adhesive tape to obtain a therapeutic adhesive tape containing 42 μg of prednisolone per crA.
この治療用接着テープを患部に貼り、6時間後、12時
間後、24時間後に剥して、接着テープ中に残存してい
るプレドニゾロン量を分析した。This therapeutic adhesive tape was applied to the affected area and removed after 6, 12, and 24 hours, and the amount of prednisolone remaining in the adhesive tape was analyzed.
その結果、6時間後に30μm、12時間後に18μグ
、24時間後に3μグのプレドニゾロンが残存しており
、多孔性の感圧性接着剤層に吸着されているプレドニゾ
ロンが徐々に、実施例1と比較して比較的ゆっくりした
速度で放出されていることが確認された。As a result, 30 μg of prednisolone remained after 6 hours, 18 μg after 12 hours, and 3 μg after 24 hours, and the prednisolone adsorbed on the porous pressure-sensitive adhesive layer gradually decreased compared to Example 1. It was confirmed that it was released at a relatively slow rate.
Claims (1)
けられ、該接着剤層の孔内に薬剤が入り込んで吸着され
てなることを特徴とする治療用接着テープもしくはシー
ト。 2 接着剤層の孔内に吸着される薬剤の量が、接着剤層
1crAあたり1〜100μmである、特許請求の範囲
第1項記載の治療用接着テープもしくはシート。[Claims] 1. A therapeutic adhesive tape, characterized in that a porous pressure-sensitive adhesive layer is provided on one side of a base film, and a drug enters and is adsorbed into the pores of the adhesive layer. Or a sheet. 2. The therapeutic adhesive tape or sheet according to claim 1, wherein the amount of the drug adsorbed into the pores of the adhesive layer is 1 to 100 μm per crA of the adhesive layer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55040860A JPS5827247B2 (en) | 1980-03-28 | 1980-03-28 | Treatment adhesive tape or sheet |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP55040860A JPS5827247B2 (en) | 1980-03-28 | 1980-03-28 | Treatment adhesive tape or sheet |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56138113A JPS56138113A (en) | 1981-10-28 |
| JPS5827247B2 true JPS5827247B2 (en) | 1983-06-08 |
Family
ID=12592290
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP55040860A Expired JPS5827247B2 (en) | 1980-03-28 | 1980-03-28 | Treatment adhesive tape or sheet |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5827247B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5823367B2 (en) * | 1980-08-29 | 1983-05-14 | 日東電工株式会社 | Adhesive tape formulation |
| US5633009A (en) * | 1990-11-28 | 1997-05-27 | Sano Corporation | Transdermal administration of azapirones |
| CN103381130A (en) * | 2012-05-03 | 2013-11-06 | 3M创新有限公司 | Antibacterial transfusion glue sticker |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5919926B2 (en) * | 1980-01-16 | 1984-05-09 | 日東電工株式会社 | drug administration member |
-
1980
- 1980-03-28 JP JP55040860A patent/JPS5827247B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56138113A (en) | 1981-10-28 |
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