JPH031451Y2 - - Google Patents
Info
- Publication number
- JPH031451Y2 JPH031451Y2 JP14298385U JP14298385U JPH031451Y2 JP H031451 Y2 JPH031451 Y2 JP H031451Y2 JP 14298385 U JP14298385 U JP 14298385U JP 14298385 U JP14298385 U JP 14298385U JP H031451 Y2 JPH031451 Y2 JP H031451Y2
- Authority
- JP
- Japan
- Prior art keywords
- dish
- shaped body
- membrane
- flange portion
- gas
- 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
- 239000003814 drug Substances 0.000 claims description 28
- 229940079593 drug Drugs 0.000 claims description 23
- 239000003795 chemical substances by application Substances 0.000 claims description 18
- 239000012528 membrane Substances 0.000 claims description 13
- 239000000463 material Substances 0.000 claims description 10
- 239000011888 foil Substances 0.000 claims description 9
- 239000012790 adhesive layer Substances 0.000 claims description 8
- 239000010410 layer Substances 0.000 claims description 5
- 238000002560 therapeutic procedure Methods 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 229920003023 plastic Polymers 0.000 claims description 4
- 239000004033 plastic Substances 0.000 claims description 4
- 239000002985 plastic film Substances 0.000 claims description 3
- 230000002093 peripheral effect Effects 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000005038 ethylene vinyl acetate Substances 0.000 description 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 230000009931 harmful effect Effects 0.000 description 3
- 238000012856 packing Methods 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 description 2
- 239000000006 Nitroglycerin Substances 0.000 description 2
- 239000002612 dispersion medium Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229960003711 glyceryl trinitrate Drugs 0.000 description 2
- 229940124597 therapeutic agent Drugs 0.000 description 2
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 description 1
- 229930000680 A04AD01 - Scopolamine Natural products 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- GJSURZIOUXUGAL-UHFFFAOYSA-N Clonidine Chemical compound ClC1=CC=CC(Cl)=C1NC1=NCCN1 GJSURZIOUXUGAL-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- STECJAGHUSJQJN-GAUPFVANSA-N Hyoscine Natural products C1([C@H](CO)C(=O)OC2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-GAUPFVANSA-N 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- STECJAGHUSJQJN-UHFFFAOYSA-N N-Methyl-scopolamin Natural products C1C(C2C3O2)N(C)C3CC1OC(=O)C(CO)C1=CC=CC=C1 STECJAGHUSJQJN-UHFFFAOYSA-N 0.000 description 1
- ZBBHBTPTTSWHBA-UHFFFAOYSA-N Nicardipine Chemical compound COC(=O)C1=C(C)NC(C)=C(C(=O)OCCN(C)CC=2C=CC=CC=2)C1C1=CC=CC([N+]([O-])=O)=C1 ZBBHBTPTTSWHBA-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229940035676 analgesics Drugs 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 229940124599 anti-inflammatory drug Drugs 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 229960002896 clonidine Drugs 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- BTVWZWFKMIUSGS-UHFFFAOYSA-N dimethylethyleneglycol Natural products CC(C)(O)CO BTVWZWFKMIUSGS-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 229960005309 estradiol Drugs 0.000 description 1
- 229930182833 estradiol Natural products 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- CGIGDMFJXJATDK-UHFFFAOYSA-N indomethacin Chemical compound CC1=C(CC(O)=O)C2=CC(OC)=CC=C2N1C(=O)C1=CC=C(Cl)C=C1 CGIGDMFJXJATDK-UHFFFAOYSA-N 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229960001783 nicardipine Drugs 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- STECJAGHUSJQJN-FWXGHANASA-N scopolamine Chemical compound C1([C@@H](CO)C(=O)O[C@H]2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-FWXGHANASA-N 0.000 description 1
- 229960002646 scopolamine Drugs 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Description
【考案の詳細な説明】
本考案は新規な皮膚透過療法剤容器、殊患部へ
の投与が容易であつて、その上、主剤である薬剤
が投与中揮散する恐れの少ない皮膚透過療法剤に
関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel container for a skin-permeating therapeutic agent, which is easy to administer to a particularly affected area, and is less likely to cause the main drug to volatilize during administration.
パツプ剤とは、本来多量の粉末薬品を含む粥状
又は泥状の塗布用薬剤を意味し、これを布帛に厚
く展延したものを患部に貼着することにより、消
炎や分泌物吸収の目的に使用されるもので、局方
品のカオリンパツプは従来から有名である。そし
てこの目的の使い捨て製品も発売されている。ま
た肩凝りなどの治療剤として、絆創膏に消炎、鎮
痛性薬剤を含有させた〇〇パスと称される製品が
広く出回つていることも周知のことである。 A poultice is a paste-like or slurry-like medicine that originally contains a large amount of powdered medicine, and is spread thickly on a cloth and applied to the affected area for the purpose of extinguishing inflammation and absorbing secretions. Kaolin buds, a pharmacopoeial product, have long been well-known. Disposable products for this purpose are also available. It is also well known that a product called 〇〇Pass, which is a bandage containing anti-inflammatory and analgesic drugs, is widely available as a treatment for stiff shoulders and the like.
しかるに近来に至り、皮膚透過性の薬剤を経皮
的に投与にしようとする皮膚透過療法(TTS)
の効果が認められるようになり、既にニトログリ
セリン、スコポラミン、エストラジオール、クロ
ニジン、インドメサジン、ニカルジピンなどを含
む皮膚透過療法剤が市販され又は臨床的に研究も
しくは動物実験の段階にある。 However, in recent years, transcutaneous therapy (TTS), which attempts to transdermally administer drugs that permeate the skin, has emerged.
The effectiveness of skin permeation therapy has been recognized, and skin permeation therapy agents including nitroglycerin, scopolamine, estradiol, clonidine, indomethazine, nicardipine, etc. are already on the market or are in the stage of clinical research or animal experiments.
ところで、今日実用化され又は研究の段階にあ
る皮膚透過療法剤(以下「TTS剤」と略称する)
は、一般に厚手アルミニウム箔製の浅い鍔付皿型
容器の内部に薬剤を収容すると共に、該容器の開
口面を直接EVA等の薬剤透過制御層を介して又
はさらにアルミ箔及び粘着剤層を介して弾性材製
の蓋材で被覆してなるものである。使用に際して
は、容器を除いた蓋材部分を、該部分の粘着剤層
を利用して薬剤部分が皮膚に当接するように適用
部位の皮膚面に貼着する。 By the way, there are skin permeation therapy agents (hereinafter abbreviated as "TTS agents") that are currently in practical use or are in the research stage.
Generally, the drug is stored inside a dish-shaped container with a shallow flange made of thick aluminum foil, and the opening surface of the container is directly passed through a drug permeation control layer such as EVA or further through an aluminum foil and adhesive layer. It is covered with a lid made of elastic material. In use, the lid part excluding the container is attached to the skin surface of the application site using the adhesive layer of the part so that the drug part comes into contact with the skin.
しかしながら、従来のこの種の製品は、保在時
には問題がないとしても、適用時には容器が取去
られているため、使用中に肝心の薬剤が気化して
しまつたり、又はビークルとして用いられている
溶媒が気化してしまつたりして用をなさなくなる
ことが少なくない。これらの欠点は、この種薬剤
が長時間(24時間以上)に亘る連続投与を主要な
目的とすだけに無視できない欠点である。さらに
ニトログリセリンのようなガスが有害な薬剤の場
合には、揮散したガスが周囲の過敏なヒトに頭
痛、脱力感などの有害作用を及ぼす場合もありう
る。 However, although conventional products of this type pose no problems when stored, the container is removed when applied, so the key drug may evaporate during use or may be used as a vehicle. It is not uncommon for the solvent in the solution to evaporate and become useless. These drawbacks cannot be ignored since the main purpose of this type of drug is continuous administration over a long period of time (24 hours or more). Furthermore, when the gas is a harmful drug such as nitroglycerin, the volatilized gas may have harmful effects such as headaches and weakness on sensitive people nearby.
(考案の目的)
本考案は、既在のTTS剤における主剤やビー
クルの揮散を有効に抑えることにより、予定され
た長時間に亘り有効に薬剤を奏効させると共に、
気化した薬剤又は溶媒のガスやによる有害作用を
なくした新規なTTS剤を提供するのを目的とす
る。(Purpose of the invention) The present invention effectively suppresses the volatilization of the base agent and vehicle in existing TTS agents, thereby making the agent effective over a planned long period of time, and
The purpose of the present invention is to provide a new TTS agent that eliminates the harmful effects of vaporized drugs or solvent gases.
(目的達成のための手段)
本考案に係るTTS剤は、以上の目的を達成す
るため、金属箔又は薄手硬質プラスチツクシート
等の気体不透過性の可塑性材料から形成された、
周辺部に鍔部分を有する浅い皿状体と、該皿状体
内に密着状態で収容された経皮作用性の薬剤と、
前記皿状体の開口面を覆う制御膜と、該制御膜の
周縁の鍔部分を覆い、かつその裏面が該鍔部分に
接着された環状のパツキンと、該パツキンの周縁
部に塗布された粘着材層を介して前記制御膜及び
パツキンの表面を覆う気体不透過性のカバー層と
からなる構成を採用する。(Means for achieving the object) In order to achieve the above object, the TTS agent according to the present invention is made of a gas-impermeable plastic material such as a metal foil or a thin hard plastic sheet.
a shallow dish-shaped body having a flange on the periphery; a transdermal drug housed in the dish-shaped body in close contact with each other;
A control film that covers the opening surface of the dish-shaped body, an annular gasket that covers a flange portion at the periphery of the control membrane and whose back surface is adhered to the flange portion, and an adhesive applied to the periphery of the gasket. A configuration is adopted that includes a gas-impermeable cover layer that covers the surface of the control membrane and the packing via a material layer.
以上の構成において、主体をなす鍔付皿状体は
金属箔又は薄手硬質プラスチツクシート等の気体
不透過性の可塑性材料から形成されるが、実用的
には厚手アルミニウム箔から作られるのが好まし
い。但しこの場合、内面には必要に応じ耐蝕性樹
脂による被覆が施される。 In the above configuration, the main body of the flanged plate is made of a gas-impermeable plastic material such as a metal foil or a thin hard plastic sheet, but practically it is preferably made of a thick aluminum foil. However, in this case, the inner surface is coated with a corrosion-resistant resin if necessary.
主剤は上の皿状体の内部へ塑性状態化又はゲル
状態化して収容される。種々の多糖類、乳糖、シ
リコーン樹脂、エタノール、アセトン、ジメチル
スルホキシド、エチレングリコール、ポリエチレ
ングリコールなどの化学物質が、基材のマトリツ
クス化や薬剤の可溶化のため使用される。なお、
本考案の目的上、薬剤は本容器の内面に密着して
いなければならない。 The base agent is stored inside the upper dish-shaped body in a plastic or gel state. Chemicals such as various polysaccharides, lactose, silicone resins, ethanol, acetone, dimethyl sulfoxide, ethylene glycol, and polyethylene glycol are used to matrix the substrate and solubilize the drug. In addition,
For purposes of this invention, the drug must be in intimate contact with the interior surface of the container.
制御膜は、薬剤が収容された容器の開口面を覆
うように鍔部の内側表面に貼着される。このもの
は種々の多孔性膜状材料又はエチレン・ビニルア
セテートコポリマー(EVA)又はエチレン・ビ
ニルアルコールコポリマーの如き非多孔質浸透性
材料から作られ、内部の薬剤の滲出速度を制御す
る。従つて、材料の種類や微孔の大きさ及び密度
などにより該滲出速度を自由に制御することがで
きる。このため、内部の薬剤は厳密に組成状態又
はゲル状態に在る必要はなく、粘稠な流動状態で
あつてもよい。 The control film is attached to the inner surface of the collar so as to cover the opening of the container containing the drug. It can be made from a variety of porous membrane materials or non-porous permeable materials such as ethylene vinyl acetate copolymer (EVA) or ethylene vinyl alcohol copolymer to control the rate of exudation of the drug therein. Therefore, the seepage rate can be freely controlled depending on the type of material, the size and density of the micropores, etc. Therefore, the drug inside does not need to be strictly in a composition state or a gel state, but may be in a viscous fluid state.
ウレタンフオーム又は軟質ゴム等のシーリング
材から作られた環状のパツキンは上記容器の鍔部
の外側に貼着される。このものは、後述のカバー
と鍔部との間に位置して貯蔵時及び使用時におけ
る薬剤や溶媒若しくは分散媒の揮散を防ぐと同時
に、皮膚に貼着した際の感触を柔らかくする。 An annular gasket made of a sealant such as urethane foam or soft rubber is attached to the outside of the flange of the container. This material is located between the cover and the flange, which will be described later, to prevent volatilization of the drug, solvent, or dispersion medium during storage and use, and at the same time provides a soft feel when applied to the skin.
気体不透過性のカバーは上記パツキン部を含む
制御膜の全面を覆い、使用時まで内容物の揮散や
乾燥を阻止する。本カバーはアルミ箔等の金属箔
を用いて作られるが、なるべくポリエチレンフイ
ルム又はシリコーン塗料等による離型加工を施さ
れているのが望ましい。 The gas-impermeable cover covers the entire surface of the control membrane, including the gasket, and prevents the contents from volatilizing and drying until use. This cover is made using metal foil such as aluminum foil, but it is preferable that the cover be subjected to a release process using polyethylene film or silicone paint.
(作用)
本案TTS剤の内部の薬剤や溶媒若しくは分散
媒は、使用時まで容器及びカバーに守られている
ので長く有効に保存される。さらに使用時におい
ても、薬剤等が気体不透過性の容器(カバー)に
より保護されているので、長時間に亘り薬効が持
続する。(Effect) The drug and solvent or dispersion medium inside the TTS agent of the present invention are protected by the container and cover until use, so they can be effectively stored for a long time. Furthermore, even during use, the drug and the like are protected by the gas-impermeable container (cover), so the drug's efficacy remains for a long time.
(実施例)
以下、実施例により考案具体化の二例を説明す
るが、例示は当然説明用のものであつて、考案思
想の内包・外延を示すものではない。(Examples) Hereinafter, two examples of embodiments of the invention will be explained using examples, but the examples are, of course, for illustrative purposes and do not indicate the connotation or extension of the idea of the invention.
実施例 1
第1図は、本考案に係るTTS剤の一例の中央
部縦断面図(但し材料の厚み誇張)、第2図は第
1図の剤の開封状態を示す断面図、第3図は同じ
くその斜視図、第4図はその使用状態を示す説明
図である。Example 1 Fig. 1 is a longitudinal cross-sectional view of the central part of an example of the TTS agent according to the present invention (however, the thickness of the material is exaggerated), Fig. 2 is a cross-sectional view showing the agent in Fig. 1 in an unsealed state, and Fig. 3 Similarly, FIG. 4 is a perspective view thereof, and FIG. 4 is an explanatory view showing its usage state.
剤の全体1は周辺部に、鍔3を備える厚手アル
ミ箔製の皿型容器2と、該容器内に充填された
TTS用薬剤4と、該容器の開口面を覆うEVA製
制御膜5と、該膜5の周縁部の鍔3面上に位置す
る環状のパツキン6と、該パツキン6と前記膜5
の両者を一体的に覆うアルミ箔製のカバー8とか
ら構成され、前記制御膜5及びパツキン6は接着
剤層7を介して鍔3の上面に、またカバー8は、
粘着剤層9を介してパツキン6の表面に夫々接着
されている。なお、カバー8の外面の一隅には、
開封用の把手10が付加されている。 The entire agent 1 is provided with a dish-shaped container 2 made of thick aluminum foil equipped with a flange 3 on the periphery, and a container filled in the container.
A TTS drug 4, an EVA control membrane 5 covering the opening surface of the container, an annular gasket 6 located on the flange 3 at the peripheral edge of the membrane 5, and the gasket 6 and the membrane 5.
The control film 5 and the packing 6 are attached to the upper surface of the collar 3 via an adhesive layer 7, and the cover 8 is
They are each adhered to the surface of the gasket 6 via an adhesive layer 9. In addition, in one corner of the outer surface of the cover 8,
A handle 10 for opening is added.
使用に際し把手10を引つ張ると、第2図及び
同第3図のようにカバー8だけが離れるので、粘
着剤層9を利用第4図の如くこれを適当な部位
(図では左胸部)に貼着する。この際、薬剤4は
容器2及びパツキン6により略々密閉状態に保た
れるので、長時間に亘り効力を持続する。 When the handle 10 is pulled during use, only the cover 8 will be separated as shown in Figures 2 and 3, so use the adhesive layer 9 and place it on a suitable area (left chest in the figure) as shown in Figure 4. Paste it on. At this time, the drug 4 is kept in a substantially airtight state by the container 2 and the gasket 6, so that its efficacy remains for a long time.
実施例 2
第5図は、考案の他の実施例を示す第1図と同
様の断面図である。Embodiment 2 FIG. 5 is a sectional view similar to FIG. 1 showing another embodiment of the invention.
本例においては、鍔3に段部3aが設けられて
いるので、薄い制御膜5と厚手のパツキン6の表
面(図では下面)を同一平面上に一致させること
ができる。本例では、さらに容器の底部に把手1
1が取付けられているので、使用後の取外しが容
易である。 In this example, since the collar 3 is provided with the stepped portion 3a, the surfaces (lower surfaces in the figure) of the thin control film 5 and the thick gasket 6 can be aligned on the same plane. In this example, there is also a handle on the bottom of the container.
1 is attached, so it can be easily removed after use.
(効果)
以上説明したように、本願考案によれば、長期
の保在に耐え、しかも長時間に亘り効力を持続す
る皮膚透過療法剤を提供できるので、医療上大き
な寄与を果しうる。(Effects) As explained above, according to the present invention, it is possible to provide a skin permeation therapeutic agent that can withstand long-term storage and maintains its efficacy over a long period of time, so it can make a significant medical contribution.
第1図は、本考案に係るTTS剤の一例の中央
部縦断面図(但し材料の厚み誇張)、第2図は第
1図の剤の開封状態を示す断面図、第3図は同じ
くその斜視図、第4図はその使用状態を示す説明
図、第5図は、考案の他の実施例を示す第1図と
同様の断面図である。図中の符号の意味は以下の
通り:1:本案薬剤全体、2:1の容器、3:2
の鍔部、11:2の把手部、4:1の薬剤、5:
1の制御膜、6:1のパツキン、7:ン1の接着
剤層、8:1のカバー、9:1の粘着剤層、1
0:8の把手部。
Figure 1 is a longitudinal cross-sectional view of the central part of an example of the TTS agent according to the present invention (however, the thickness of the material is exaggerated), Figure 2 is a cross-sectional view showing the agent in Figure 1 in an unsealed state, and Figure 3 is the same. FIG. 4 is a perspective view, FIG. 4 is an explanatory view showing the state of use thereof, and FIG. 5 is a sectional view similar to FIG. 1 showing another embodiment of the invention. The meanings of the symbols in the diagram are as follows: 1: whole drug, 2: 1 container, 3: 2
flange part, 11:2 handle part, 4:1 medicine, 5:
1 control film, 6:1 packing, 7:1 adhesive layer, 8:1 cover, 9:1 adhesive layer, 1
0:8 handle.
Claims (1)
気体不透過性の可塑性材料から形成された、周
辺部に鍔部分を有する浅い皿状体と、該皿状体
内に密着状態で収容された経皮作用性の薬剤
と、前記皿状体の開口面を覆う制御膜と、該制
御膜の周縁の鍔部分を覆い、かつ、その裏面が
該鍔部分に接着された環状のパツキンと、該パ
ツキンの周縁部に塗布された粘着材層を介して
前記制御膜及びパツキンの表面を覆う気体不透
過性のカバー層とからなることを特徴とする皮
膚透過療法剤。 (2) 制御膜の表面が気体不透過の膜で覆われ、該
膜はカバー層の除去と共に除去しうるように構
成されている登録請求の範囲第1項記載の剤。 (3) 皿状体が、その鍔部分に開封用の爪掛け部を
備える登録請求の範囲第1項記載の剤。[Scope of Claim for Utility Model Registration] (1) A shallow dish-shaped body made of a gas-impermeable plastic material such as a metal foil or a thin hard plastic sheet, and having a flange portion on the periphery, and an object inside the dish-shaped body. A transdermal drug housed in close contact with each other, a control membrane covering the opening surface of the dish-shaped body, and a flange portion at the periphery of the control membrane, the back surface of which is adhered to the flange portion. A skin permeation therapy agent comprising an annular patch and a gas-impermeable cover layer that covers the surface of the control membrane and the patch via an adhesive layer applied to the peripheral edge of the patch. (2) The agent according to claim 1, wherein the surface of the control membrane is covered with a gas-impermeable membrane, and the membrane is configured to be removable together with the removal of the cover layer. (3) The agent according to claim 1, wherein the dish-shaped body has a hook portion for opening the package on its flange portion.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14298385U JPH031451Y2 (en) | 1985-09-18 | 1985-09-18 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14298385U JPH031451Y2 (en) | 1985-09-18 | 1985-09-18 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6251142U JPS6251142U (en) | 1987-03-30 |
JPH031451Y2 true JPH031451Y2 (en) | 1991-01-17 |
Family
ID=31052237
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14298385U Expired JPH031451Y2 (en) | 1985-09-18 | 1985-09-18 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH031451Y2 (en) |
-
1985
- 1985-09-18 JP JP14298385U patent/JPH031451Y2/ja not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS6251142U (en) | 1987-03-30 |
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