JPH02280772A - Percutaneous medicine-gradually exerting-coated material - Google Patents
Percutaneous medicine-gradually exerting-coated materialInfo
- Publication number
- JPH02280772A JPH02280772A JP1105178A JP10517889A JPH02280772A JP H02280772 A JPH02280772 A JP H02280772A JP 1105178 A JP1105178 A JP 1105178A JP 10517889 A JP10517889 A JP 10517889A JP H02280772 A JPH02280772 A JP H02280772A
- Authority
- JP
- Japan
- Prior art keywords
- medicine
- transdermal
- percutaneous
- drug
- transdermal drug
- 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.)
- Granted
Links
- 239000000463 material Substances 0.000 title claims abstract description 19
- 239000003814 drug Substances 0.000 claims abstract description 59
- 239000011230 binding agent Substances 0.000 claims abstract description 16
- 239000004744 fabric Substances 0.000 claims abstract description 14
- 239000011248 coating agent Substances 0.000 claims abstract description 13
- 238000000576 coating method Methods 0.000 claims abstract description 13
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- -1 lactone compound Chemical class 0.000 claims abstract description 7
- 229920000642 polymer Polymers 0.000 claims abstract description 6
- 229940079593 drug Drugs 0.000 claims description 52
- 238000013268 sustained release Methods 0.000 claims description 13
- 239000012730 sustained-release form Substances 0.000 claims description 13
- 238000013269 sustained drug release Methods 0.000 claims description 9
- 239000000843 powder Substances 0.000 claims description 6
- 230000002459 sustained effect Effects 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 5
- 230000001070 adhesive effect Effects 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 2
- 239000008187 granular material Substances 0.000 claims 2
- 239000000853 adhesive Substances 0.000 claims 1
- 238000004898 kneading Methods 0.000 claims 1
- 230000035900 sweating Effects 0.000 abstract description 5
- 239000004745 nonwoven fabric Substances 0.000 abstract description 2
- 239000002245 particle Substances 0.000 abstract description 2
- 229920001225 polyester resin Polymers 0.000 abstract description 2
- 239000004645 polyester resin Substances 0.000 abstract description 2
- 239000002759 woven fabric Substances 0.000 abstract description 2
- 239000011344 liquid material Substances 0.000 abstract 1
- 230000007704 transition Effects 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 description 5
- 239000010419 fine particle Substances 0.000 description 4
- 230000029058 respiratory gaseous exchange Effects 0.000 description 4
- 150000003431 steroids Chemical class 0.000 description 3
- IMCGHZIGRANKHV-AJNGGQMLSA-N tert-butyl (3s,5s)-2-oxo-5-[(2s,4s)-5-oxo-4-propan-2-yloxolan-2-yl]-3-propan-2-ylpyrrolidine-1-carboxylate Chemical compound O1C(=O)[C@H](C(C)C)C[C@H]1[C@H]1N(C(=O)OC(C)(C)C)C(=O)[C@H](C(C)C)C1 IMCGHZIGRANKHV-AJNGGQMLSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000003110 anti-inflammatory effect Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229920006237 degradable polymer Polymers 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000001647 drug administration Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- GUGOEEXESWIERI-UHFFFAOYSA-N Terfenadine Chemical compound C1=CC(C(C)(C)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 GUGOEEXESWIERI-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 230000001760 anti-analgesic effect Effects 0.000 description 1
- 230000003474 anti-emetic effect Effects 0.000 description 1
- 230000001387 anti-histamine Effects 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 230000001754 anti-pyretic effect Effects 0.000 description 1
- 229940125683 antiemetic agent Drugs 0.000 description 1
- 239000002111 antiemetic agent Substances 0.000 description 1
- 239000000739 antihistaminic agent Substances 0.000 description 1
- 239000002246 antineoplastic agent Substances 0.000 description 1
- 239000003908 antipruritic agent Substances 0.000 description 1
- 239000002221 antipyretic Substances 0.000 description 1
- 150000003976 azacycloalkanes Chemical class 0.000 description 1
- 239000002327 cardiovascular agent Substances 0.000 description 1
- 229940125692 cardiovascular agent Drugs 0.000 description 1
- 239000003218 coronary vasodilator agent Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229940125697 hormonal agent Drugs 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 201000003152 motion sickness Diseases 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 229940024473 salicylic acid emollient and protective preparations Drugs 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 230000003637 steroidlike Effects 0.000 description 1
- 230000005068 transpiration Effects 0.000 description 1
Landscapes
- Media Introduction/Drainage Providing Device (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Medicinal Preparation (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は経皮薬物投与技術に係る経皮薬物徐放被服材に
関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a transdermal drug sustained release dressing material related to transdermal drug administration technology.
[従来の技術]
濃度を調整しながら薬物を徐々に放出する材料である薬
物徐放剤としては、従来より湿布薬等としてのものが一
部に応用されている。[Prior Art] As a sustained drug release agent, which is a material that gradually releases a drug while adjusting the concentration, it has been used in some cases as a poultice and the like.
[発明が解決しようとする課題]
しかし、これらの湿布薬は一般に基布に塗着したペース
ト状の蒸散性添加材と混練した薬剤を皮肩面に接着保持
させて使用するものであり、徐放速度が比較的短く、ま
た制御することが難しいといった問題を有していた。ま
たこれらの湿布薬では皮膚面に密着してしまうため、皮
膚呼吸や発汗を妨げる等の問題から長期間の連続使用及
び広範囲の同時使用ができないものであった。[Problems to be Solved by the Invention] However, these poultices are generally used by adhering and holding a paste-like transpiration additive applied to a base fabric and a drug mixed with the shoulder surface of the skin. The problem was that the release rate was relatively short and it was difficult to control. Furthermore, since these poultices adhere closely to the skin surface, they cannot be used continuously for a long period of time or used simultaneously over a wide range of problems, such as preventing the skin from breathing and sweating.
本発明は上記問題に鑑みてなされたものであり、「着る
」感覚で投薬することができると共に、皮膚呼吸や発汗
を妨げることがなく長期に亘って投薬制御することが可
能な経皮薬物徐放被服材を提供することを目的とするも
のである。The present invention was made in view of the above problems, and provides a transdermal drug that can be administered with the feeling of "wearing it" and can be controlled over a long period of time without interfering with skin respiration or sweating. The purpose is to provide radiation clothing materials.
[課題を解決するための手段]
本発明に係る経皮薬物徐放被服材は、経皮薬物を基布に
塗着したバインダー内に徐放作用をもたせるように存在
させたもので、移行により粉粒体又は液体の経皮薬物を
バインダーから経時的に滲出せしめることを要旨とする
。また、該経皮薬物徐放被服材は、経皮薬物の微粉を経
時的に分解又は昇華する性質を有する高分子化合物液S
(以下「コーティング被膜」と称する)によってコーテ
ィングすることが好ましく、該コーティングした経皮薬
物の微粉を適宜バインダーを介して可撓性シート状基布
の表面に塗着し、経皮薬物徐放層を形成することを要旨
とするものである。[Means for Solving the Problems] The transdermal drug sustained release dressing material according to the present invention is a material in which a transdermal drug is present in a binder coated on a base fabric so as to have a sustained release effect. The gist of this method is to cause a powder or liquid transdermal drug to ooze out from a binder over time. In addition, the transdermal drug sustained release dressing material is made of a polymer compound liquid S that has the property of decomposing or sublimating the fine powder of the transdermal drug over time.
(hereinafter referred to as a "coating film"), the coated transdermal drug fine powder is applied to the surface of a flexible sheet-like base fabric via an appropriate binder, and a transdermal drug sustained release layer is formed. Its purpose is to form a
また上記バインダーが粘着性を有する場合は、経皮薬物
徐放層の表面に多孔性シートを被着した構造にすること
もできる。Further, when the binder has adhesive properties, a porous sheet may be attached to the surface of the transdermal drug sustained release layer.
上記経皮薬物の代わりに、経皮薬物と経皮吸収促進薬物
の混成物からなる微粒子を、経時的に分解又は昇華する
性質を有する高分子化合物被膜によってコーティングし
た構造が好ましい。Instead of the above-mentioned transdermal drug, a structure in which fine particles consisting of a mixture of a transdermal drug and a transdermal absorption-promoting drug are coated with a polymeric compound film having a property of decomposing or sublimating over time is preferable.
上記経皮薬物徐放被服材は、下着やサポータ又は夜具の
構造に縫製して使用することを要旨とするものである。The gist of the above-mentioned transdermal sustained drug release clothing material is to be used by sewing it into the structure of underwear, supporters, or nightwear.
[作用]
経皮薬物徐放被服材によって例えばサポータを構成した
場合、経皮薬物徐放被服材に形成した経皮薬物徐放層を
形成しているバインダー内の経皮薬物が移行によって滲
出し、皮膚を通して投薬される。この時コーティング被
膜を設けた経皮薬物では該コーティング被膜の解消によ
って放出されるようになる。該高分子化合物被膜のコー
ティングは1例えばオキシ酸とラクトン化合物からなる
化合物の種類を変えることにより解消時間が変えられる
ため、長時間に亘って経皮薬物の放出速度を制御するこ
とができる。[Function] For example, when a supporter is made of a transdermal sustained drug release dressing, the transdermal drug in the binder forming the sustained transdermal drug release layer formed on the sustained transdermal drug release dressing material oozes out due to migration. , administered through the skin. At this time, transdermal drugs provided with a coating are released when the coating is dissolved. Since the resolution time of the polymer compound coating can be changed by changing the type of compound, for example, an oxyacid and a lactone compound, the release rate of the transdermal drug can be controlled over a long period of time.
また使用に際して該サポータが「着る」感覚で使用する
ことができ、皮膚面に接触してはいるものの、皮膚に貼
着するなど、その面を密封することがないため皮膚呼吸
や発汗を妨げることがなく、長期間の連続使用及び広範
囲の同時使用を可能にし、経皮薬物の投与を行うことが
できる。In addition, the supporter can be used as if it were being "worn", and although it is in contact with the skin surface, it does not adhere to the skin or seal that surface, so it does not prevent the skin from breathing or sweating. This allows for long-term continuous use, wide range of simultaneous use, and transdermal drug administration.
[実施例]
以下、本発明に係る経皮薬物徐放被服材の図面に従って
説明する。[Example] Hereinafter, a transdermal sustained drug release dressing according to the present invention will be described with reference to the drawings.
第1図は第一の実施例を示す顕微鏡的拡大断面の説明図
であり、符号1は片面に経皮薬物徐放層2を形成した、
織成布1編成布或は不織布等からなる可撓性の基布であ
る。上記経皮薬物徐放層2は、後述する経皮薬物3及び
経皮吸収促進薬物4の微粒子を、それぞれオキシ酸とラ
クトン化合物からなる経時分解性高分子化合物によりコ
ーティング被膜5を構成すると共に、これらをポリエス
テル樹脂等の溶解したバインダー6中に混練したもので
あり、適宜層厚に塗着してある。FIG. 1 is an explanatory diagram of a microscopically enlarged cross-section showing the first embodiment, in which reference numeral 1 indicates a transdermal sustained drug release layer 2 formed on one side.
It is a flexible base fabric made of a woven fabric, a non-woven fabric, or the like. The above-mentioned transdermal drug sustained release layer 2 has fine particles of a transdermal drug 3 and a transdermal absorption-promoting drug 4, which will be described later, coated with a time-degradable polymer compound consisting of an oxyacid and a lactone compound, respectively, and forms a coating film 5. These are kneaded into a dissolved binder 6 such as polyester resin, and coated to an appropriate layer thickness.
また第2図は粘着性を有するバインダーを使用した他の
実施例を示すものであり、前記第一の実施例におけるバ
インダー6は粘着性を有している。Further, FIG. 2 shows another embodiment using a binder having adhesive properties, and the binder 6 in the first embodiment has adhesive properties.
この場合、経皮薬物徐放層2の表面に可撓性を有するフ
ィルム或は織成布、編成布或は不織布等からなる多孔性
シート7を貼着した構造になる。In this case, the transdermal drug sustained release layer 2 has a structure in which a porous sheet 7 made of a flexible film, woven cloth, knitted cloth, nonwoven cloth, etc. is adhered to the surface of the transdermal drug sustained release layer 2.
尚、他の実施態様として前記各実施例におけるコーティ
ング被膜5の構造を廃止することもできることはいうま
でもなく、バインダー6を選ぶことによって経皮薬物3
を微粒子のほか液体の状態で使用することもできる。It goes without saying that in other embodiments, the structure of the coating film 5 in each of the above embodiments can be abolished, and by selecting the binder 6, the transdermal drug 3
can be used in the form of liquid as well as fine particles.
経 のコーティング 理
経皮薬物は粒径10μm以下に粉砕した後、該微粒子を
オキシ酸とラクトン化合物からなる経時分解性高分子化
合物によってコーティング被膜を形成する。このときオ
キシ酸とラクトン化合物の種類を変え、それぞれ分解解
消時間を異にするようにその化合物の組合せを変える。After pulverizing the dermatological drug to a particle size of 10 μm or less, the fine particles are coated with a time-degradable polymer compound consisting of an oxyacid and a lactone compound. At this time, the types of oxyacid and lactone compound are changed, and the combination of the compounds is changed so that the decomposition resolution time is different for each.
経皮吸収促進薬物のコーティング処理についても同様で
ある。The same applies to the coating treatment of drugs that promote transdermal absorption.
冠血管拡張剤
(3)ホルモン剤
(4)解熱・鎮痛・消炎・鎮痒剤
ステロイド製剤、非ステロイド製剤、抗ヒスタミン製剤
(5)制吐薬
(8)ホルモン薬
舒m隻
経皮薬物として使用可能な薬剤の例
A1局所適応薬剤
(1)消炎鎮痛剤
サリチル酸製剤、ステロイド製剤、非ステロイド製剤
(2)抗腫瘍剤
B、全身適応薬剤
(1)乗物酔防止剤
(2)循環器用剤
経溝11又促m曳
(1)アザシクロアルカン2オン
1アルキル−2ピロリドン−5カルボン酸の脂肪族炭化
水素エステル
ピロリドン誘導体
(2)その他
Darmsiac、 5epas
兼jUL佳9JU1匹
(1)サポータ、細帯、マスク等の医療補助用品。Coronary vasodilators (3) Hormonal agents (4) Antipyretic, analgesic, antiinflammatory, and antipruritic agents Steroid preparations, non-steroid preparations, antihistamine preparations (5) Antiemetics (8) Hormonal drugs Can be used as transdermal drugs Examples of drugs A1 Locally applicable drugs (1) Anti-inflammatory and analgesic salicylic acid preparations, steroid preparations, non-steroidal preparations (2) Antitumor agent B, systemically applicable drugs (1) Anti-motion sickness agents (2) Cardiovascular agents (1) Aliphatic hydrocarbon ester pyrrolidone derivative of azacycloalkane 2-one 1-alkyl-2-pyrrolidone-5-carboxylic acid (2) Other Darmsiac, 5epas, 1 UL, 9JU (1) Supporter, stripe, mask, etc. medical aid supplies.
(2)アンダーシャツ、パンツ、ブリーフ、靴下等の衣
類。(2) Clothing such as undershirts, pants, briefs, socks, etc.
(3)シーツ、布団カバー、枕カバー等の寝具。(3) Bedding such as sheets, duvet covers, pillowcases, etc.
[発明の効果コ
以上述べたように本発明に係る経皮薬物徐放被服材によ
れば、基布に積層した経皮薬物徐放層から経皮薬物がコ
ーティング被膜の解消によって予め31I!した時間を
経て徐放され、経皮薬物の放出速度を自由に制御するこ
とができるため、安全性の高い投薬を行うことができる
。また使用に際して着る感覚で使用することができ、皮
膚面が密封されないため皮膚呼吸や発汗を妨げることが
なく、長期間の連続使用及び広範囲の同時使用を可能に
することができると同時に経皮薬物投与の利点を兼備す
る長所を有するものであり1本発明実施後の医薬業界に
及ぼす影響は極めて大きい。[Effects of the Invention] As described above, according to the sustained transdermal drug release clothing material of the present invention, the transdermal drug is released from the sustained transdermal drug release layer laminated on the base fabric to 31I! Since the release rate of the transdermal drug can be freely controlled, it is possible to administer the drug with high safety. In addition, it can be used as if it were worn, and since the skin surface is not sealed, it does not impede skin breathing or sweating, making it possible to use it continuously for a long period of time and to use it simultaneously over a wide range of areas. It has the advantage of having advantages in administration, and the influence it will have on the pharmaceutical industry after implementation of the present invention will be extremely large.
薬物徐放被服材の実施例を示す顕微鏡的拡大断面の説明
図である。FIG. 2 is an explanatory diagram of an enlarged microscopic cross section showing an example of a sustained drug release dressing material.
1・・・基布、2・・・経皮薬物徐放層、3・・・経皮
薬物。1... Base fabric, 2... Transdermal drug sustained release layer, 3... Transdermal drug.
4・・・経皮吸収促進薬物、5・・・コーティング被膜
、6・・・バインダー、7・・・多孔性シート。4... Transdermal absorption promoting drug, 5... Coating film, 6... Binder, 7... Porous sheet.
Claims (6)
して可撓性シート状基布の表面に塗着し、経皮薬物徐放
層を形成してなる経皮薬物徐放被服材。(1) A transdermal drug sustained release dressing material formed by applying transdermal drug powder or liquid to the surface of a flexible sheet-like base fabric via an appropriate binder to form a transdermal drug sustained release layer. .
分解又は昇華する性質を有する高分子化合物被膜によっ
てコーティングしてある請求項1記載の経皮薬物徐放被
服材。(2) The transdermal drug sustained release dressing material according to claim 1, wherein the transdermal drug is composed of powder or granules, and the powder or granules are coated with a polymeric compound film having a property of decomposing or sublimating over time.
層の表面に多孔性シートを被着してなる請求項1又は2
記載の経皮薬物徐放被服材。(3) Claim 1 or 2, wherein the binder is adhesive and a porous sheet is attached to the surface of the transdermal sustained drug release layer.
The transdermal sustained drug release dressing material described above.
合物被膜が、オキシ酸とラクトン化合物からなる種類を
異にする化合物の組合せである請求項1乃至3記載の経
皮薬物徐放被服材。(4) The transdermal sustained drug release dressing material according to any one of claims 1 to 3, wherein the polymeric compound coating having the property of decomposing or sublimating over time is a combination of different types of compounds consisting of an oxyacid and a lactone compound. .
の混成物をバインダーと混練してなる請求項1乃至4記
載の経皮薬物徐放被服材。(5) The sustained transdermal drug release dressing material according to any one of claims 1 to 4, which is made by kneading a mixture of a transdermal drug and a transdermal absorption-promoting drug with a binder instead of the transdermal drug.
含浸、乾燥させたことを特徴とする請求項1記載の経皮
薬物徐放被服材。(6) The sustained transdermal drug release dressing material according to claim 1, wherein the transdermal drug is a liquid, and the transdermal drug is directly impregnated into a base fabric and dried.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1105178A JPH02280772A (en) | 1989-04-24 | 1989-04-24 | Percutaneous medicine-gradually exerting-coated material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1105178A JPH02280772A (en) | 1989-04-24 | 1989-04-24 | Percutaneous medicine-gradually exerting-coated material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02280772A true JPH02280772A (en) | 1990-11-16 |
JPH0428391B2 JPH0428391B2 (en) | 1992-05-14 |
Family
ID=14400425
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1105178A Granted JPH02280772A (en) | 1989-04-24 | 1989-04-24 | Percutaneous medicine-gradually exerting-coated material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02280772A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPWO2004089347A1 (en) * | 2003-04-10 | 2006-07-06 | テイカ製薬株式会社 | Tulobuterol-containing percutaneous absorption preparation and patch using the same |
-
1989
- 1989-04-24 JP JP1105178A patent/JPH02280772A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPWO2004089347A1 (en) * | 2003-04-10 | 2006-07-06 | テイカ製薬株式会社 | Tulobuterol-containing percutaneous absorption preparation and patch using the same |
Also Published As
Publication number | Publication date |
---|---|
JPH0428391B2 (en) | 1992-05-14 |
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