JPS609221Y2 - patch - Google Patents

patch

Info

Publication number
JPS609221Y2
JPS609221Y2 JP6540780U JP6540780U JPS609221Y2 JP S609221 Y2 JPS609221 Y2 JP S609221Y2 JP 6540780 U JP6540780 U JP 6540780U JP 6540780 U JP6540780 U JP 6540780U JP S609221 Y2 JPS609221 Y2 JP S609221Y2
Authority
JP
Japan
Prior art keywords
drug
layer
adhesive layer
adhesive
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.)
Expired
Application number
JP6540780U
Other languages
Japanese (ja)
Other versions
JPS56165044U (en
Inventor
哲夫 堀内
三郎 大塚
祐輔 伊藤
Original Assignee
日東電工株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by 日東電工株式会社 filed Critical 日東電工株式会社
Priority to JP6540780U priority Critical patent/JPS609221Y2/en
Publication of JPS56165044U publication Critical patent/JPS56165044U/ja
Application granted granted Critical
Publication of JPS609221Y2 publication Critical patent/JPS609221Y2/en
Expired legal-status Critical Current

Links

Landscapes

  • Medicinal Preparation (AREA)

Description

【考案の詳細な説明】 この考案は基材に形成された粘着剤層に薬剤を保持させ
てなる貼付剤に関するものである。
[Detailed Description of the Invention] This invention relates to a patch in which a drug is retained in an adhesive layer formed on a base material.

一般に、この種貼付剤では、薬剤と粘着性ポリマーなど
とを一緒に混ぜ合せて薬剤含有の粘着剤層を構成しであ
るから、薬剤が粘着剤層の表面から効率よく放散されに
くい傾向にある。
Generally, in this type of patch, the drug and an adhesive polymer are mixed together to form the drug-containing adhesive layer, so the drug tends to be difficult to diffuse efficiently from the surface of the adhesive layer. .

このため、上記薬剤の放出を促進させる放出補助物質、
いわゆるアジュバントを粘着剤層に含ませることが試み
られているが、これによっても期待する程の効果を上げ
られない場合がある。
For this reason, a release auxiliary substance that promotes the release of the above drug,
Attempts have been made to include so-called adjuvants in the adhesive layer, but even this may not be as effective as expected.

この考案は上記事情に鑑みてなされたものであり、薬剤
と粘着性ポリマーなどとを一緒に混ぜ合わせる手段に委
ねることをやめ、基材に形成した粘着剤組成物だけから
なる層に、薬剤を含む組成物を埋入しかつ粘着剤層表面
に露出させた薬剤主体の貯薬層を形成することにより、
粘着剤層表面から薬剤を効果的に放出させうるようにし
た貼付剤を提供することを目的とする。
This idea was made in view of the above circumstances, and instead of relying on a method of mixing drugs and adhesive polymers together, it is possible to apply drugs to a layer consisting only of an adhesive composition formed on a base material. By forming a drug-based storage layer in which the composition containing the drug is embedded and exposed on the surface of the adhesive layer,
An object of the present invention is to provide a patch that can effectively release a drug from the surface of an adhesive layer.

以下、この考案の一実施例を図面にしたがって説明する
An embodiment of this invention will be described below with reference to the drawings.

第1図において、1は基材で、繊維シートもしくは合成
樹脂フィルムあるいはこれらの混成物などで構成されて
いる。
In FIG. 1, reference numeral 1 denotes a base material, which is made of a fiber sheet, a synthetic resin film, or a hybrid thereof.

ここで繊維シートとしては不織布、布、紙などがあり、
また合成樹脂フィルムとしては、ポリエチレン、ポリ塩
化ビニル、ポリウレタンフィルム、ポリアクリルフィル
ム、エチレン酢酸ビニル共重合体フィルムなどがある。
Here, fiber sheets include nonwoven fabric, cloth, paper, etc.
Examples of synthetic resin films include polyethylene, polyvinyl chloride, polyurethane films, polyacrylic films, and ethylene-vinyl acetate copolymer films.

2は上記基材1の主面に形成された粘着剤組成物からな
る粘着剤層、3は上記粘着剤層2内に散在的に埋入され
た薬剤主体の貯薬層で、各貯薬層3は上記粘着剤層2の
表面に露出する状態に埋設されている。
2 is an adhesive layer made of an adhesive composition formed on the main surface of the base material 1; 3 is a drug-based drug storage layer scattered in the adhesive layer 2; The layer 3 is embedded in the pressure-sensitive adhesive layer 2 so as to be exposed on the surface thereof.

なお薬剤としては身体面に対して移着ないし吸着させる
ことができるものであれば広く適用でき、たとえばペニ
シリンのような抗生物質、リドカインのような麻酔剤、
サリチルアミド、サリチル酸ナトリウムのような鎮痛消
炎剤などがあげられる。
As a drug, it can be widely applied as long as it can be transferred or adsorbed to the body surface, such as antibiotics such as penicillin, anesthetics such as lidocaine,
These include pain-relieving anti-inflammatory drugs such as salicylamide and sodium salicylate.

上記構成からなる貼付剤は、たとえば各種粘着性ポリマ
ーに必要に応じて粘着付与剤その他の公知の添加剤を配
合してなる粘着剤組成物を加熱溶融して、基材1の主面
に塗布し、この塗布された粘着剤組成物が冷えきらない
うちに、多数個の注射針を持った注入器具によって、薬
剤を含む組成物、たとえばポリマーその他の常温で固形
の物質に薬剤と必要に応じて放出補助物質、いわゆるア
ジュバントを配合してなるものを、上記同様に加熱溶融
した状態で、上記粘着剤組成物中に散在的に注入腰その
後組成物を自然冷却して固化させるなどの方法によって
製造することができる。
The patch having the above structure is produced by heating and melting an adhesive composition made by blending various adhesive polymers with tackifiers and other known additives as necessary, and applying the adhesive composition to the main surface of the base material 1. Then, before the applied adhesive composition has cooled down completely, a drug-containing composition, such as a polymer or other substance that is solid at room temperature, is injected with the drug using an injection device with multiple injection needles. A release auxiliary substance, a so-called adjuvant, is mixed into the adhesive composition in the same manner as above, heated and melted, and then injected sporadically into the pressure-sensitive adhesive composition.Then, the composition is then naturally cooled and solidified. can be manufactured.

なお薬剤を含む組成物に用いられる常温で固形の物質と
してはポリビニルアルコールなどの各種ポリマーやその
他ワックス、グリースなどがあるが、これらの固形物質
は薬剤を放散させやすいつまり薬剤を溶解させやすいの
であって、しかも粘着剤層2のポリマー成分と相溶しに
くいものが選択使用される。
Substances that are solid at room temperature and used in drug-containing compositions include various polymers such as polyvinyl alcohol, waxes, and greases, but these solid substances tend to dissipate drugs, that is, they tend to dissolve drugs. Moreover, those which are hardly compatible with the polymer component of the adhesive layer 2 are selected and used.

このように上記構成においては粘着剤層2に薬剤を直接
混入させるのではなく、上記粘着剤層2中に部分的に薬
剤主体の貯薬層3を設けるようにしているから、薬剤の
含有密度の高い部分が粘着剤層2に局部的に存在するこ
とになるとともに、各貯薬層3が粘着剤層2の表面に露
出して薬剤放出時のバイパス路として作用することから
、従来に比し、薬物の放出性は著しく向上する。
In this way, in the above structure, the drug is not directly mixed into the adhesive layer 2, but the drug storage layer 3 mainly composed of the drug is provided partially in the adhesive layer 2, so that the drug content density can be reduced. Since a high portion of the drug exists locally in the adhesive layer 2, and each drug storage layer 3 is exposed on the surface of the adhesive layer 2 and acts as a bypass path during drug release, it is compared to the conventional method. However, drug release properties are significantly improved.

一方上記構成において薬剤主体の貯薬層3により、薬剤
が短期間のうちに、放出されてしまうおそれがあれば、
上記貯薬層3の表面側に、薬剤の放散を抑制する放散抑
制剤層を上記貯層部3の構成要素の1つとして存在させ
ればよい。
On the other hand, in the above configuration, if there is a risk that the drug will be released in a short period of time due to the drug storage layer 3 mainly consisting of the drug,
A diffusion suppressing agent layer that suppresses diffusion of the drug may be provided on the surface side of the drug storage layer 3 as one of the constituent elements of the storage layer 3.

この放散抑制剤層は薬剤を含む組成物に使用するポリマ
ーないしその他の固形物質に比し、薬剤を溶解させにく
いものであればよい。
This diffusion-inhibiting agent layer may be made of a material that is less likely to dissolve the drug than the polymer or other solid substance used in the drug-containing composition.

ところで、上記薬剤を主体とする貯薬層3、つまり薬剤
を含む組成物に使用するポリマーないしその他の固形物
質としては、前記のとおり上記粘着剤層2におけるポリ
マーに相溶しにくいものが選択されるが、それでも上記
貯薬層3における薬剤あるいはアジュバントが上記粘着
剤層2との境界からこの粘着剤層2側へ移行するおそれ
は少なからず存在する。
By the way, as the polymer or other solid substance used in the drug storage layer 3 mainly containing the drug, that is, the composition containing the drug, a polymer or other solid substance that is hardly compatible with the polymer in the adhesive layer 2 is selected as described above. However, there is still a considerable possibility that the drug or adjuvant in the drug storage layer 3 may migrate from the boundary with the adhesive layer 2 to the adhesive layer 2 side.

かかる移行により貯薬層3を設けた意義が失なわれるだ
けでなく、粘着剤層が可塑化されて強度的にも低下する
おそれがある。
Due to such migration, not only the purpose of providing the drug storage layer 3 is lost, but also the adhesive layer may be plasticized and its strength may be reduced.

これを防止するために粘着剤層2を紫外線その他により
架橋処理するか、あるいは第2図に示すように、上記境
界にたとえばトランスイソプレンの如き薬剤やアジュバ
ントを透過させにくい物質で隔壁4を形成することによ
り、上記移行の問題を解消し得るとともに、ポリマー同
志の相溶性も防止できる。
In order to prevent this, the adhesive layer 2 is cross-linked using ultraviolet rays or the like, or, as shown in FIG. 2, a barrier wall 4 is formed at the boundary with a substance that is difficult for drugs or adjuvants to pass through, such as trans-isoprene. By doing so, the above-mentioned migration problem can be solved, and compatibility between polymers can also be prevented.

隔壁4を設ける場合は、第3図のように内筒Maに薬剤
を含む組成物3′を、外筒Mbに隔壁4形戒用の物質4
′を容するようにした2重筒注射針Mを用いることによ
り容易に形成できるものである。
When the partition wall 4 is provided, as shown in FIG.
This can be easily formed by using a double-barreled injection needle M that accommodates the .

勿論、この場合でも、必要に応じて前述した放出抑制剤
層を貯薬層3の表面側に形成することができる。
Of course, even in this case, the above-mentioned release inhibitor layer can be formed on the surface side of the drug storage layer 3 if necessary.

以上のように、この考案は基材に形成した粘着剤層の中
に、上記粘着剤層表面に露出させた薬剤主体の貯薬層を
形成することにより、薬物の放散性が向上し、しかもそ
の薬効を長期間にわたって維持し得る貼付剤を提供する
ことができる。
As described above, this invention improves drug dispersion by forming a drug-based storage layer exposed on the surface of the adhesive layer in the adhesive layer formed on the base material. A patch that can maintain its medicinal efficacy over a long period of time can be provided.

【図面の簡単な説明】[Brief explanation of drawings]

第1図はこの考案に係る貼付剤の一例を示す一部拡大断
面図、第2図は同貼付剤の変形例を示す一部拡大断面図
、第3図は2重筒注射針の説明図である。 1・・・・・・基剤、2・・・・・・粘着剤層、3・・
・・・・貯薬層。
Fig. 1 is a partially enlarged sectional view showing an example of the patch according to this invention, Fig. 2 is a partially enlarged sectional view showing a modification of the patch, and Fig. 3 is an explanatory diagram of a double barrel injection needle. It is. 1...Base, 2...Adhesive layer, 3...
...Drug storage layer.

Claims (1)

【実用新案登録請求の範囲】[Scope of utility model registration request] 基材の主面に粘着剤組成物だけを層状に形成し、この粘
着剤層中に薬剤を含む組成物を散在的に埋入して薬剤主
体の貯薬層を形成するとともに、各貯薬層を上記粘着剤
層の表面に露出させた貼付剤。
Only the adhesive composition is formed in a layer on the main surface of the base material, and a composition containing a drug is scattered in this adhesive layer to form a drug-based drug storage layer. A patch in which a layer is exposed on the surface of the adhesive layer.
JP6540780U 1980-05-12 1980-05-12 patch Expired JPS609221Y2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6540780U JPS609221Y2 (en) 1980-05-12 1980-05-12 patch

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6540780U JPS609221Y2 (en) 1980-05-12 1980-05-12 patch

Publications (2)

Publication Number Publication Date
JPS56165044U JPS56165044U (en) 1981-12-07
JPS609221Y2 true JPS609221Y2 (en) 1985-04-02

Family

ID=29659558

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6540780U Expired JPS609221Y2 (en) 1980-05-12 1980-05-12 patch

Country Status (1)

Country Link
JP (1) JPS609221Y2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3634016A1 (en) * 1986-04-17 1987-10-29 Lohmann Gmbh & Co Kg AREA-BASED THERAPEUTIC SYSTEM, METHOD FOR THE PRODUCTION THEREOF AND ITS USE

Also Published As

Publication number Publication date
JPS56165044U (en) 1981-12-07

Similar Documents

Publication Publication Date Title
US4031894A (en) Bandage for transdermally administering scopolamine to prevent nausea
US4262003A (en) Method and therapeutic system for administering scopolamine transdermally
US5310559A (en) Device for controlled release and delivery to mammalian tissue of pharmacologically active agents incorporating a rate controlling member which comprises an alkylene-alkyl acrylate copolymer
AU2006216955B2 (en) Transdermal systems having control delivery system
EP0400078B1 (en) Printed transdermal drug delivery device
RU2396951C2 (en) Adhesive pharmaceutical bisopropol-containing composition
US8440222B2 (en) Reservoir system with closed membrane
AU2796192A (en) Device for administering drug transdermally with a controlled temporal change in skin flux
WO2002045700A2 (en) Absorbing agents and cover layer which is impermeable to active substances and which contains channel-formers or removable protective layer of a transdermal therapeutic system
IE61305B1 (en) Transdermal therapeutic system, its use and process for the production thereof
JPH041127A (en) Plaster for medical treatment
JP2010521525A (en) Transdermal system, production method, and stabilization of amorphous drug
CN101842065A (en) Transdermal delivery system comprising a coated release liner
TWI621448B (en) Rivastigmine transdermal compositions and methods of using the same
JP4824963B2 (en) Patch and patch preparation
US7029693B2 (en) Percutaneously absorptive preparation
JPS609221Y2 (en) patch
JPH06199659A (en) Apparatus for percutaneous treatment
JP6148861B2 (en) Patch
US20030203697A1 (en) Patch and production method thereof
JPH0459296B2 (en)
JPS6342602B2 (en)
JP2869167B2 (en) Sustained-release patch preparation
JP4167750B2 (en) Transdermal absorption base and percutaneous absorption preparation containing the base
JP3098095B2 (en) Patch using a moisture-permeable support