JPS6055045B2 - patch - Google Patents

patch

Info

Publication number
JPS6055045B2
JPS6055045B2 JP13350382A JP13350382A JPS6055045B2 JP S6055045 B2 JPS6055045 B2 JP S6055045B2 JP 13350382 A JP13350382 A JP 13350382A JP 13350382 A JP13350382 A JP 13350382A JP S6055045 B2 JPS6055045 B2 JP S6055045B2
Authority
JP
Japan
Prior art keywords
aluminum
parts
drug
patch
water
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
JP13350382A
Other languages
Japanese (ja)
Other versions
JPS5925318A (en
Inventor
希能 澤口
哲夫 堀内
廣昭 佐々木
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.)
Nitto Denko Corp
Original Assignee
Nitto Electric Industrial 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 Nitto Electric Industrial Co Ltd filed Critical Nitto Electric Industrial Co Ltd
Priority to JP13350382A priority Critical patent/JPS6055045B2/en
Publication of JPS5925318A publication Critical patent/JPS5925318A/en
Publication of JPS6055045B2 publication Critical patent/JPS6055045B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は含有されている薬物を長期間安定的に維持する
含水系骨休を構成成分とする貼付剤に関するものである
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a patch comprising a water-containing anti-inflammatory agent that stably maintains the drug contained therein over a long period of time.

一般に、サリチル酸メチル、サリチル酸モノグリコール
、ノニル酸バニリルアミド、酢酸トコフェロール、カプ
サイシン、インドメタシンの如き消炎鎮痛剤を含水系骨
体中に含有させてなる、所謂パツプ剤においては、エス
テル結合や酸アミド結合などの加水分解により、数ケ月
で薬物が分解され、薬効成分が半減されることが多いも
のである。
In general, so-called poultices containing anti-inflammatory analgesics such as methyl salicylate, monoglycol salicylate, vanillylamide nonylate, tocopherol acetate, capsaicin, and indomethacin in a water-containing bone body contain ester bonds, acid amide bonds, etc. Due to hydrolysis, drugs are often broken down over a period of several months, and their medicinal properties are often halved.

かかる加水分解による薬物の減少を防止するために、含
水系骨体中の水のPHを調整したり、骨休の主成分を改
良したりして、薬物の安定化を計つているが、未だ満足
するものが開発されるに至つていないのが実情である。
In order to prevent drug loss due to hydrolysis, efforts have been made to stabilize the drug by adjusting the pH of water in the water-containing bone body and improving the main components of bone loss. The reality is that nothing satisfactory has yet been developed.

本発明者達はかかる従来技術の状況に鑑み鋭意検討の結
果、薬物の安定化剤として高級脂肪酸アルミニュウム塩
を用いることによつて、薬効成分を長期間維持すること
を知見し、本発明に至つたものである。即ち本発明は、
薬物含有含水系骨休を用いてなる貼付剤において、薬物
の安定化剤として高級脂肪酸アルミニュウム塩を用いて
なることを特徴とするものである。
As a result of intensive studies in view of the state of the prior art, the present inventors found that by using higher fatty acid aluminum salt as a drug stabilizer, the medicinal ingredients can be maintained for a long period of time, and the present invention has been achieved. It is ivy. That is, the present invention
A patch using a drug-containing water-containing patch is characterized in that a higher fatty acid aluminum salt is used as a drug stabilizer.

本発明の実施に当つて用いられる含水系骨休としては、
グリセリン、ガンチッ、ゼラチンの如き粘性成分とケイ
ソウ±、タルクの如き固形成分と水とからなる、従来知
られる泥状骨体、又は合成樹脂をベース成分とし、乳化
剤又は乳化助剤を用いて、W/ 0又は0/W型エマル
ジョンとなしゲル化させてなる含水ゲル状骨体などが用
いられ、含水量は冷感及び粘着性などの点から3踵量%
以下とされる。
The water-containing bone rest used in carrying out the present invention includes:
Using a conventionally known muddy skeleton or synthetic resin as a base component consisting of a viscous component such as glycerin, ganchi, gelatin, a solid component such as diatomaceous material and talc, and water, and using an emulsifier or an emulsifying aid, W. /0 or 0/W type emulsion and water-containing gel-like bone formed by gelling are used, and the water content is 3% by heel weight from the viewpoint of cooling sensation and stickiness.
The following shall apply.

また高級脂肪酸アルミニュウム塩としては、脂肪酸のc
級が8〜3噌で、1〜3個の脂肪酸を有するアルミニュ
ウム塩が好ましいものであり、例えばモノステアリン酸
アルミニュウム、ジステアリン酸アルミニュウム、トリ
ステアリン酸アルミニュウム、モノパルミチン酸アルミ
ニュウム、ジパルミチン酸アルミニュウム、トリノニル
酸アルjミニニウムなどが挙げられる。
In addition, as higher fatty acid aluminum salts, fatty acid c
Preferred are aluminum salts having a grade of 8-3 and having 1-3 fatty acids, such as aluminum monostearate, aluminum distearate, aluminum tristearate, aluminum monopalmitate, aluminum dipalmitate, trinonyl. Examples include acid aluminum and the like.

これらの高級脂肪酸アルミニュウム塩は、骨体中に0.
01〜3重量%の範囲で添加するのが好ましいものであ
る。
These higher fatty acid aluminum salts have a concentration of 0.0% in the bone body.
It is preferable to add it in an amount of 0.01 to 3% by weight.

本発明の実施に当つて用いられる薬物として;は、サリ
チル酸メチル、サリチル酸モノグリコール、ノニル酸バ
ニリルアミド、酢酸トコフェロール、カプサイシン、イ
ンドメタシン、の如き消炎鎮痛剤以外に、エステル結合
又は酸アミド結合などにより加水分解される薬物も挙げ
ることができる。
In addition to anti-inflammatory drugs such as methyl salicylate, monoglycol salicylate, nonylic acid vanillylamide, tocopherol acetate, capsaicin, and indomethacin, the drugs used in the practice of the present invention include hydrolyzed by ester bond or acid amide bond. Also mentioned are the drugs that are used.

薬物は膏体中に2喧量%以下の範囲で配合するのが好ま
しいものである。本発明の薬物含有含水膏体中に高級脂
肪酸アルミニュウム塩を配合してある貼付剤が経日での
薬物安定性に優れる事実は、以下の実施例により実証さ
れる。
It is preferable that the drug is incorporated into the plaster in an amount of 2% or less. The fact that the patch of the present invention in which a higher fatty acid aluminum salt is blended into the drug-containing water-containing plaster has excellent drug stability over time is demonstrated by the following examples.

実施例1 イソプレンゴム5部(重量部以下同じ)とスチレンーイ
ソプレンースチレンプロツク共重合体ゴム35部とを、
15(代)に保持されたロールで2紛間素練りしたのち
、これにジステアリン酸アルミニュウム0.7部とトリ
ノニル酸アルミニュウム1.7部とを添加して均一に混
合する。
Example 1 5 parts of isoprene rubber (same parts below) and 35 parts of styrene-isoprene-styrene block copolymer rubber,
After masticating the two powders using a roll held at 15, 0.7 parts of aluminum distearate and 1.7 parts of aluminum trinonylate were added thereto and mixed uniformly.

次に石油系合成テルペン樹脂13部と天然ロジン7部と
を添加混合し、系を95℃まで冷却後、ポリブテン5部
、流動パラフィン14.18部、サリチル酸メチル3部
、サリチル酸モノグリコール3部、酢酸トコフエノール
0.5部、ノニル酸バニリルアミド0.02部及びソル
ビタンモノオレート2部を添加して系を均一に混合し、
これに精製水1嘔を加えて混合後、織布上に0.8Wr
!nの厚みで塗布してゲル化させ、貼付剤を得る。実施
例2 実施例1において、トリノニル酸アルミニュウムを配合
せず、ジステアリン酸アルミニュウムのみを2部を添加
した以外は、実施例1と同様の操作で貼付剤を得る。
Next, 13 parts of petroleum-based synthetic terpene resin and 7 parts of natural rosin were added and mixed, and after cooling the system to 95°C, 5 parts of polybutene, 14.18 parts of liquid paraffin, 3 parts of methyl salicylate, 3 parts of monoglycol salicylate, Add 0.5 parts of tocophenol acetate, 0.02 parts of vanillylamide nonylate, and 2 parts of sorbitan monooleate, mix the system uniformly,
Add 1 oz of purified water to this and mix it, then apply 0.8 Wr on the woven fabric.
! The adhesive is applied to a thickness of n and gelled to obtain a patch. Example 2 A patch was obtained in the same manner as in Example 1, except that aluminum trinonylate was not blended and only 2 parts of aluminum distearate was added.

第1表に実施例1〜2の試験結果を示す。Table 1 shows the test results of Examples 1 and 2.

第1表中における分解量は、上記各貼付剤をアルミニュ
ウム箔を積層してなる不透湿性基材にて密封包装し、4
CfCで3ケ月保存後理論値を100%として計算した
ものである。また比較例は実施例1において、トリノニ
ル酸アルミニュウム及びジステアリン酸アルミニュウム
を配合していないものである。上記実施例からも明らか
な如く、含水系膏体において、高級脂肪酸アルミニュウ
ム塩を安定化剤として用いると、経日ての薬物の加水分
解による分解が少ない事実が顕著である。
The amount of decomposition in Table 1 is calculated by packaging each of the above patches in a moisture-impermeable base material made of laminated aluminum foil,
Calculations were made with the theoretical value after storage for 3 months in CfC set as 100%. Further, a comparative example is the same as in Example 1, except that aluminum trinonylate and aluminum distearate are not blended. As is clear from the above examples, when a higher fatty acid aluminum salt is used as a stabilizer in a water-containing paste, it is remarkable that the drug is less likely to be degraded by hydrolysis over time.

Claims (1)

【特許請求の範囲】[Claims] 1 薬物含有含水系膏体を用いてなる貼付剤において、
薬物の安定化剤として高級脂肪酸アルミニュウム塩を用
いてなることを特徴とする貼付剤。
1. In a patch using a drug-containing water-containing plaster,
A patch characterized by using higher fatty acid aluminum salt as a drug stabilizer.
JP13350382A 1982-07-29 1982-07-29 patch Expired JPS6055045B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13350382A JPS6055045B2 (en) 1982-07-29 1982-07-29 patch

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13350382A JPS6055045B2 (en) 1982-07-29 1982-07-29 patch

Publications (2)

Publication Number Publication Date
JPS5925318A JPS5925318A (en) 1984-02-09
JPS6055045B2 true JPS6055045B2 (en) 1985-12-03

Family

ID=15106287

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13350382A Expired JPS6055045B2 (en) 1982-07-29 1982-07-29 patch

Country Status (1)

Country Link
JP (1) JPS6055045B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0430757Y2 (en) * 1987-03-28 1992-07-24

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0699291B2 (en) * 1985-06-14 1994-12-07 ライオン株式会社 Oral composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0430757Y2 (en) * 1987-03-28 1992-07-24

Also Published As

Publication number Publication date
JPS5925318A (en) 1984-02-09

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