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JPH0436132B2 - - Google Patents
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JPH0436132B2 - - Google Patents

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Publication number
JPH0436132B2
JPH0436132B2 JP59119440A JP11944084A JPH0436132B2 JP H0436132 B2 JPH0436132 B2 JP H0436132B2 JP 59119440 A JP59119440 A JP 59119440A JP 11944084 A JP11944084 A JP 11944084A JP H0436132 B2 JPH0436132 B2 JP H0436132B2
Authority
JP
Japan
Prior art keywords
eva
patch
parts
vinyl acetate
added
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 - Lifetime
Application number
JP59119440A
Other languages
Japanese (ja)
Other versions
JPS615012A (en
Inventor
Minoru Kuroda
Kazunari Yoshe
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Daiichi Pharmaceutical Co Ltd
Saitama Daiichi Pharmaceutical Co Ltd
Original Assignee
Daiichi Pharmaceutical Co Ltd
Saitama Daiichi Pharmaceutical Co Ltd
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 Daiichi Pharmaceutical Co Ltd, Saitama Daiichi Pharmaceutical Co Ltd filed Critical Daiichi Pharmaceutical Co Ltd
Priority to JP11944084A priority Critical patent/JPS615012A/en
Publication of JPS615012A publication Critical patent/JPS615012A/en
Publication of JPH0436132B2 publication Critical patent/JPH0436132B2/ja
Granted legal-status Critical Current

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  • Medicinal Preparation (AREA)

Description

【発明の詳細な説明】 本発明は貼付剤、特にプラスター剤(硬膏剤)
の改良に関する。
[Detailed Description of the Invention] The present invention relates to a patch, especially a plaster (plaster).
Regarding the improvement of

プラスター剤は、比較的水分含量が低い天然ゴ
ム又は合成ゴム等の高分子を基剤として用いるも
のであるが、天然ゴム又はスチレン、イソブチレ
ン等のゴム質を用いたプラスター剤の製造法は文
献(例えば杉原正泰等編集「製剤工学ハンドブツ
ク」30版228ページ)等で明らかなとおり一次練
り、二次練り等の工程があり、フランネル、不織
布又はプラスチツクフイルム等(パツキング)上
へ展延する工程では溶媒を使用して展延するか、
あるいは加熱圧着して展延する等の方法が採用さ
れている。このようにプラスター剤の製造方法は
非常に複雑で、多大の時間及び労力を要するもの
である。
Plastering agents use polymers such as natural rubber or synthetic rubber, which have a relatively low water content, as a base material, but the manufacturing method of plastering agents using natural rubber or rubber materials such as styrene and isobutylene is described in the literature ( For example, as is clear from "Pharmaceutical Engineering Handbook" edited by Masayasu Sugihara et al., 30th edition, page 228), there are processes such as primary kneading and secondary kneading, and in the process of spreading onto flannel, nonwoven fabric, plastic film, etc. (packing), solvents are used. or spread it using
Alternatively, methods such as heat-pressing and spreading are employed. As described above, the method for producing plaster is very complicated and requires a great deal of time and effort.

そこで本発明者等は、上述の欠点等を有しない
優れたプラスター用基剤の探索について鋭意検討
した結果、エチレン酢酸ビニル共重合樹脂が目的
にかなうことを見いだし本発明を完成した。
Therefore, the present inventors conducted extensive research to find an excellent base material for plaster that does not have the above-mentioned drawbacks, etc., and as a result found that ethylene-vinyl acetate copolymer resin met the purpose and completed the present invention.

エチレン酢酸ビニル共重合体樹脂(以下EVA
と略す)を基剤とするプラスターを製するには、
初め90〜150℃程度に加温して基剤を溶かしたの
ち40〜130℃程度に温度を維持して、各種添加剤
を加えて混ぜ合わせれば良く、練る工程は不要で
あるばかりか、バツキングに展延する場合も基剤
が溶けているため、溶媒は不要であり、圧着する
必要がなく、単にバツキングの上に均一の厚みに
塗布するだけでよい。
Ethylene vinyl acetate copolymer resin (hereinafter referred to as EVA)
To make plaster based on
First, you can heat it to about 90 to 150℃ to melt the base, then maintain the temperature at about 40 to 130℃, add various additives, and mix. Not only is there no need for a kneading process, but it is also easy to mix. Since the base material is dissolved in the case of spreading, there is no need for a solvent, and there is no need for pressure bonding, and it is sufficient to simply apply it to a uniform thickness on the backing.

即ち、EVAを使用して貼付剤を製する場合繁
雑な操作は必要なく、従つて誤動作が加わる心配
がなく工程管理が容易であるばかりでなく、布地
に展延するとき流出する心配のない適度な粘弾性
を示し、かつ又皮膚への貼着性に優れたものであ
る。
In other words, when making a patch using EVA, there is no need for complicated operations, so there is no need to worry about malfunctions, and process control is easy. It exhibits good viscoelasticity and has excellent adhesion to the skin.

なお、EVAはエチレンと酢酸ビニルとの共重
合樹脂であり、従来包装、製本、木工類の接着
剤、或はパラフイン、ワツクス、アスフアルト等
の改質剤、粘着用テープ又はシートの粘着剤とし
て使用されうることは公知であるが、貼付剤用基
剤としての使用は本発明者等によりはじめて見い
出されたものである。
EVA is a copolymer resin of ethylene and vinyl acetate, and is conventionally used as an adhesive for packaging, bookbinding, and woodworking, as a modifier for paraffin, wax, asphalt, etc., and as an adhesive for adhesive tapes or sheets. Although it is known that it can be used as a patch base, the present inventors discovered for the first time its use as a base for a patch.

本発明の貼付剤用基剤としてEVAを使用する
場合、酢酸ビニル含量(けん化法)15〜50wt%
でメルトインデツクス(JIS:K−6760−1966)
が30〜500g/10分であるEVAが好ましい。酢酸
ビニル含量が高くなると皮膚への貼着性が良くな
り、融点も低く製造しやすくなる反面酢酸臭が強
くなり、皮膚にべとつきやすくなる。又、酢酸ビ
ニル含量が低くなるとEVAの結晶化度が増し、
ごわごわしたものとなり皮膚へ付きにくくなる。
従つて15〜50wt%程度のけん化度のEVAが好ま
しい。又、メルトインデツクスが大きくなると凝
集力が減少し流れやすくなり展延しにくくなると
同時にベトベトして使用感が悪くなる。又一方メ
ルトインデツクスが小さくなると凝集力が増大
し、皮膚への貼着性が悪くなる。従つて30〜500
(g/10分)程度のメルトインデツクスが好まし
い。
When using EVA as the base for the patch of the present invention, the vinyl acetate content (saponification method) is 15 to 50 wt%.
Melt index (JIS: K-6760-1966)
Preferably, EVA is 30 to 500 g/10 minutes. As the vinyl acetate content increases, adhesion to the skin improves, and the melting point decreases, making it easier to manufacture, but on the other hand, the acetic acid odor becomes stronger and the adhesive becomes more sticky to the skin. Also, as the vinyl acetate content decreases, the crystallinity of EVA increases,
It becomes stiff and difficult to adhere to the skin.
Therefore, EVA with a saponification degree of about 15 to 50 wt% is preferable. Furthermore, when the melt index increases, the cohesive force decreases, making it easy to flow and making it difficult to spread, and at the same time, it becomes sticky and has a poor feel when used. On the other hand, as the melt index decreases, the cohesive force increases and adhesion to the skin deteriorates. Therefore 30-500
(g/10 minutes) is preferable.

通常、貼付剤に特定の薬効成分を配合する場
合、その成分を溶解又は分散させる溶媒としてグ
リセリン、プロピレングリコール等のアルコール
類又は流動パラフイン、ワセリン、スクワラン等
の炭化水素類、オリーブ油、大豆油等の油脂類、
ラウリン酸、ミリスチン酸等の脂肪酸類等が考え
られるが、本発明に関しては炭化水素類が好まし
い。アルコール類、油脂類又は脂肪酸類は基剤
EVAとなじみが悪く、均一に溶解又は分散しに
くく、そのままでは用いられず可溶化、乳化等を
行わない限り、EVAと分離してしまい使用でき
ない。
Usually, when a specific medicinal ingredient is added to a patch, alcohols such as glycerin and propylene glycol, hydrocarbons such as liquid paraffin, petrolatum and squalane, olive oil and soybean oil are used as solvents to dissolve or disperse the ingredient. oils and fats,
Fatty acids such as lauric acid and myristic acid are possible, but hydrocarbons are preferred for the present invention. Alcohols, fats and oils, or fatty acids are the base
It is not compatible with EVA and is difficult to dissolve or disperse uniformly, so it cannot be used as it is and unless it is solubilized or emulsified, it will separate from EVA and cannot be used.

本発明の貼付剤において、添加成分等の影響に
より皮膚への貼着性が十分でないときには、ポリ
ブテン、ポリイソブチレン、テルペン樹脂又はオ
レフイン系樹脂の粘着剤をEVAに添加し、自由
に貼着性を調整することが出来る。
When the patch of the present invention does not have sufficient adhesion to the skin due to the influence of added ingredients, etc., an adhesive such as polybutene, polyisobutylene, terpene resin, or olefin resin can be added to EVA to freely improve the adhesion. It can be adjusted.

製造時の布地へのなじみ又は貼付剤を使用時の
皮膚へのなじみ(フイツト感又はゴワゴワした感
覚)は、EVAにジオクテルフタレート、塩素化
パラフイン、ノニルフエニルエーテル類等の可塑
剤を加えて自由に調整することができる。
To improve the conformability of the patch to fabric during manufacturing or to the skin when using the patch (feeling of a tight fit or stiffness), plasticizers such as diocterphthalate, chlorinated paraffin, and nonyl phenyl ethers are added to EVA. Can be adjusted freely.

以下に実施例を示すが、本発明は実施例に限定
されるものではない。実施例では消炎鎮痛剤とし
て用いられているdl−カンフル、−メントー
ル、サリチル酸メチル及びハツカ油を21:24:
24:31(重量比)で混ぜて主成分油として加えた
が、これらの消炎鎮痛剤に限定されずインドメタ
シン、ケトプロフエン、ジクロフエナツクナトリ
ウム又はステロイドホルモン類、ニトログリセリ
ン類、スコポラミン類等の薬物をも添加してもさ
しつかえないものである。又、パツキングとして
フランネル、不織布、塩化ビニルフイルム、ポリ
エチレンフイルム等のプラスチツクフイルム等を
用いることができ、塗布量も厚み0.01mm以上から
できるものである。
Examples are shown below, but the present invention is not limited to the examples. In the example, dl-camphor, -menthol, methyl salicylate, and peppermint oil, which are used as anti-inflammatory analgesics, were mixed at 21:24:
The oil was mixed at a ratio of 24:31 (weight ratio) and added as the main component, but drugs such as indomethacin, ketoprofen, diclofenac sodium, steroid hormones, nitroglycerin, and scopolamine were used, but were not limited to these anti-inflammatory analgesics. There is no problem even if it is added. Further, flannel, nonwoven fabric, plastic film such as vinyl chloride film, polyethylene film, etc. can be used as the packing, and the coating amount can be from 0.01 mm or more in thickness.

実施例 1 酢酸ビニル含量45wt%、メルトインデツクス
80(g/10分)のEVA(商品名エバフレツクス
45X)98.5部を130℃に加熱して溶融したのち攪
拌しつつ冷却し、90℃以下になつたことを確認し
て主成分油(前記)1.5部を加えかきまぜつつ、
綿布上に厚みが約1mmとなるように塗布して冷却
し、貼付剤を得た。
Example 1 Vinyl acetate content 45wt%, melt index
80 (g/10 min) EVA (product name: Evaflex)
Heat 98.5 parts of 45
It was applied onto cotton cloth to a thickness of about 1 mm and cooled to obtain a patch.

実施例 2 実施例1と同一EVA90部を130℃に加熱して溶
かしたのち、90〜100℃に冷却し、あらかじめ90
℃に加温した軽質流動パラフイン(日本薬局方適
合品)8.5部を加えよくかきまぜて均一に混合し
たのち、攪拌しつつ冷却し、90℃以下になつたこ
とを確認し、主成分油1.5部を加え、かきまぜつ
つ綿布上に厚みが約1mmとなるように塗布して冷
却し、貼付剤を得た。
Example 2 90 parts of the same EVA as in Example 1 was heated to 130°C and melted, then cooled to 90 to 100°C and preheated to 90°C.
Add 8.5 parts of light liquid paraffin (Japanese Pharmacopoeia compliant product) warmed to ℃ and stir well to mix uniformly. Cool while stirring. Confirm that the temperature is below 90℃, and add 1.5 parts of the main component oil. was added to the mixture, and the mixture was coated on a cotton cloth to a thickness of about 1 mm while stirring, and cooled to obtain a patch.

実施例 3 酢酸ビニル含量25wt%、メルトインデツクス
400(g/10分)のEVA(エバフレツクス310)60
部を130℃に加熱して溶かしたのち、ポリイソブ
チレン38.5部を加えてよくかき混ぜ、均等になる
まで混合する。攪拌しつつ冷却し、90℃以下にな
つたことを確認し、主成分油1.5部を加え、かき
混ぜつつ綿布上に厚みが約1mmとなるように塗布
して冷却し、貼付剤を得た。
Example 3 Vinyl acetate content 25wt%, melt index
400 (g/10 min) EVA (Evaflex 310) 60
After heating 1 part to 130℃ and melting it, add 38.5 parts of polyisobutylene and stir well until it is evenly mixed. The mixture was cooled while stirring, and after confirming that the temperature was below 90°C, 1.5 parts of the main component oil was added, and the mixture was coated on cotton cloth to a thickness of about 1 mm while stirring, and cooled to obtain a patch.

実施例 4 実施例3と同一EVA60部を130℃に加熱して溶
かしたのち、ポリイソブチレン37部及びポリオキ
シエチレンノニルフエニルエーテル1.5部を加え
てよくかき混ぜて均等になるまで混合する。攪拌
しつつ冷却し90℃以下になつたことを確認し、主
成分油1.5部を加え、かき混ぜつつ綿布上に厚み
が約1mmとなるように塗布して冷却し、貼付剤を
得た。
Example 4 After heating and melting 60 parts of the same EVA as in Example 3 to 130°C, 37 parts of polyisobutylene and 1.5 parts of polyoxyethylene nonyl phenyl ether were added and mixed well until uniform. After cooling with stirring and confirming that the temperature was below 90°C, 1.5 parts of the main component oil was added, and while stirring, the mixture was coated on cotton cloth to a thickness of about 1 mm and cooled to obtain a patch.

実施例 5 実施例1と同一EVA59部を130℃に加熱して溶
かしたのち、ポリブテン(平均分子量2350)10
部、軽質流動パラフイン(日本薬局方連合品)10
部、テルペン樹脂15部及びポリオキシエチレンノ
ニルフエニルエーテル4.5部を加えてかき混ぜて
均等にする。攪拌しつつ冷却し、90℃以下になつ
たことを確認し、主成分油1.5部を加え、かき混
ぜつつ綿布上に厚みが約1mmとなるように塗布し
て冷却し、貼付剤を得た。
Example 5 After heating and melting 59 parts of the same EVA as in Example 1 to 130°C, polybutene (average molecular weight 2350) 10
Part, light liquid paraffin (Japanese Pharmacopoeia Union product) 10
15 parts of terpene resin and 4.5 parts of polyoxyethylene nonyl phenyl ether and stir to equalize. The mixture was cooled while stirring, and after confirming that the temperature was below 90°C, 1.5 parts of the main component oil was added, and the mixture was coated on cotton cloth to a thickness of about 1 mm while stirring, and cooled to obtain a patch.

以上で得られた貼付剤はいずれも綿布へのなじ
みも良く、皮膚への貼着性及びべとつきともに優
れたものであつた。
All of the patches obtained above were compatible with cotton cloth and had excellent adhesion to the skin and stickiness.

Claims (1)

【特許請求の範囲】 1 酢酸ビニル含量が15〜50wt%で、メルトイ
ンデツクスが30〜500g/10分であるエチレン酢
酸ビニル共重合樹脂を用いることを特徴とする貼
付剤。 2 流動パラフイン又はスクワラン等の炭化水素
を1成分以上添加した特許請求の範囲第1項の貼
付剤。
[Scope of Claims] 1. A patch characterized by using an ethylene vinyl acetate copolymer resin having a vinyl acetate content of 15 to 50 wt% and a melt index of 30 to 500 g/10 minutes. 2. The adhesive patch according to claim 1, which contains one or more hydrocarbons such as liquid paraffin or squalane.
JP11944084A 1984-06-11 1984-06-11 Spreading plaster Granted JPS615012A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11944084A JPS615012A (en) 1984-06-11 1984-06-11 Spreading plaster

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11944084A JPS615012A (en) 1984-06-11 1984-06-11 Spreading plaster

Publications (2)

Publication Number Publication Date
JPS615012A JPS615012A (en) 1986-01-10
JPH0436132B2 true JPH0436132B2 (en) 1992-06-15

Family

ID=14761464

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11944084A Granted JPS615012A (en) 1984-06-11 1984-06-11 Spreading plaster

Country Status (1)

Country Link
JP (1) JPS615012A (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2612785A1 (en) * 1987-03-25 1988-09-30 Lhd Lab Hygiene Dietetique SELF-ADHESIVE DEVICE FOR DELIVERY OF A PERCUTANEOUS ACTIVE INGREDIENT
US4814168A (en) * 1988-03-04 1989-03-21 Noven Pharmaceuticals, Inc. Transdermal multipolymer drug delivery system
JP2788754B2 (en) * 1989-05-12 1998-08-20 日東電工株式会社 Sheet-shaped transdermal absorption device
DE4230588C1 (en) * 1992-09-12 1993-10-07 Lohmann Therapie Syst Lts Dexpanthenol-containing plaster for the transdermal application of steroid hormones and process for its production

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5414607A (en) * 1977-07-06 1979-02-03 Hitachi Ltd Transfer system for time sharing signal
JPS54117552A (en) * 1978-03-03 1979-09-12 Dai Ichi Seiyaku Co Ltd Preparation of hydrated compound of vinyl acetate resin and poultice composition containing it
JPS5777617A (en) * 1980-10-20 1982-05-15 Nichiban Co Ltd Plaster for cardiac disease
JPS5883961A (en) * 1981-11-13 1983-05-19 日東電工株式会社 Surgical member
JPS593965A (en) * 1982-06-29 1984-01-10 Fujitsu Ltd Semiconductor memory device

Also Published As

Publication number Publication date
JPS615012A (en) 1986-01-10

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