JPS6051108A - Rubber pressure-sensitive adhesive plaster - Google Patents

Rubber pressure-sensitive adhesive plaster

Info

Publication number
JPS6051108A
JPS6051108A JP58160056A JP16005683A JPS6051108A JP S6051108 A JPS6051108 A JP S6051108A JP 58160056 A JP58160056 A JP 58160056A JP 16005683 A JP16005683 A JP 16005683A JP S6051108 A JPS6051108 A JP S6051108A
Authority
JP
Japan
Prior art keywords
rubber
oil
plaster
sensitive adhesive
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.)
Pending
Application number
JP58160056A
Other languages
Japanese (ja)
Inventor
Mareyoshi Sawaguchi
希能 澤口
Yusuke Ito
祐輔 伊藤
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 JP58160056A priority Critical patent/JPS6051108A/en
Publication of JPS6051108A publication Critical patent/JPS6051108A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:Rubber pressure-sensitive adhesive plaster obtained by blending plaster consisting of rubber pressure-sensitive adhesive with a purified oil contained in a plant belonging to the genus Citrus, existing stably without causing decomposition of drug after long period preservation. CONSTITUTION:Rubber pressure-sensitive adhesive plaster obtained by blending plaster consisting of a rubber pressure-sensitive adhesive substance (e.g., natural rubber, styrene-butadiene rubber, or polybutene rubber) with a purified oil (e.g., lemon oil, orange oil, pummelo oil, lime oil) contained in a plant belonging to the genus Citrus. When a phenolic hydroxyl group-containing compound, an amine compound, etc. is used as a drug, it has tendency to lower remedying effect by decomposition or volatilization, etc., but the use of the plaster can keep the drug stably. The plaster may be further blended with a tackifier, an adjustor for bond strength and retention power, a filler, an emulsifying agent, etc.

Description

【発明の詳細な説明】 (技術分野) 本発明はゴム系粘着性物質よりなる膏体の改良に関する
DETAILED DESCRIPTION OF THE INVENTION (Technical Field) The present invention relates to improvements in plasters made of rubber-based adhesive substances.

(従来技術) 従来、外皮に投与する薬物は殺菌剤、消毒剤、皮屑゛刺
激剤などの外皮、その下部組織に局所的に作用させるこ
とを目的とするものであった。しかし、近年全身作用を
有する薬物を外皮より投与する試゛めがなされており、
種々の薬物の外皮投与が提案ないし試みられている。
(Prior Art) Conventionally, drugs administered to the integument include bactericidal agents, disinfectants, dermal irritants, and the like, intended to locally act on the integument and its underlying tissues. However, in recent years, attempts have been made to administer drugs with systemic effects through the skin.
Transdermal administration of various drugs has been proposed or attempted.

薬物の外皮投与は、たとえば粘着性物質よりなる膏体に
薬物を配合した粘着性貼付製剤の形態にて行われている
が、ゴム系粘着性物質よりなる何体に薬物を配合した製
剤を長期保存した場合、薬物の分解、揮散などにより当
該製剤による治療効果が著しく低下する傾向がある。と
りわLJフェノール性氷水酸基含有化合物アミン系化合
物などは、2〜3年の貯蔵によって使用に耐えなくなる
ものも少なくない。特に、消炎鎮痛剤としてのサリチル
酸メチル、サリチル酸モノグリコール、などのサリチル
酸誘導体、カブサイシン、ノニル酸バニリルアミド、ト
ウガラシエキスなどの皮膚刺激剤、ジフェンヒドラミン
などのエタノールアミン系抗ヒスタミン剤、d4−α−
トコフェロールなどのビタミンEなどの経口による含量
低下が著しい。
Therapeutic administration of drugs is carried out, for example, in the form of adhesive patch preparations in which the drug is blended into a plaster made of an adhesive substance, but long-term administration of drugs in which the drug is blended into a paste made of a rubber-based adhesive substance is carried out over a long period of time. When stored, the therapeutic effect of the preparation tends to decrease significantly due to decomposition, volatilization, etc. of the drug. Among LJ phenolic hydroxyl group-containing compounds, amine compounds, etc., many become unusable after being stored for 2 to 3 years. In particular, salicylic acid derivatives such as methyl salicylate and monoglycol salicylate as anti-inflammatory analgesics, skin irritants such as kabsaicin, nonylic acid vanillylamide, and hot pepper extract, ethanolamine type antihistamines such as diphenhydramine, and d4-α-
The content of vitamin E such as tocopherol is significantly reduced by oral administration.

従って、薬物を配合しても当該薬物の分解が進行しない
ゴム系粘着性物質よりなる膏体ないし、粘着性貼付製剤
の開発が望まれている。
Therefore, it is desired to develop a plaster or an adhesive patch made of a rubber-based adhesive material that does not allow the decomposition of the drug to progress even when the drug is mixed therein.

(発明の開示) かかる実情下に、本発明者らは種々研究を重ねてきたと
ころ、ゴム系粘着性物質よりなる膏体にミカン属植物の
精油を配合しておけば、当該膏体に薬物を配合しても薬
物が分解することなく安定に存在することを見いだした
(Disclosure of the Invention) Under these circumstances, the present inventors have conducted various studies and found that if the essential oil of a citrus plant is blended into a plaster made of a rubber-based adhesive substance, drugs can be added to the plaster. It was discovered that the drug existed stably without decomposition even when mixed with the drug.

本発明はかかる新知見に基づいて完成されたものであり
、ゴム系粘着性物質よりなる膏体に、ミカン属植物の精
油を配合してなることを特徴とするゴム系粘着性膏体、
当該膏体に更に薬物を配合してなるゴム系粘着性膏体、
即ち粘着性貼付製剤に関する。
The present invention has been completed based on this new knowledge, and includes a rubber-based adhesive paste comprising a rubber-based adhesive substance mixed with essential oil of a plant of the genus Citrus;
A rubber-based adhesive paste formed by further blending a drug into the paste,
That is, it relates to adhesive patch preparations.

本発明膏体によれば、薬物の安定化が図られることはも
ちろんのこと、たとえばパップ剤に特有の臭がミカン属
植物の精油によって緩和される。
According to the plaster of the present invention, not only the drug is stabilized, but also the odor characteristic of poultices, for example, is alleviated by the essential oil of the Citrus genus plant.

ゴム系粘着性物質としては、ゴJ・、系粘着性貼イτ1
製剤用として従来から使用されごいるジエン系高分子化
合物、具体的には天然ゴム、合成ゴム、これらの混合物
などがあげられる。合成ゴムとしては、スチレン−イソ
プレン−スチレンブロック共重合体ゴム、スチレン−ブ
タジェンゴム、ポリブテンゴム、ブチルゴム、シリコー
ンゴムなどがあげられる。
As a rubber-based adhesive substance, rubber-based adhesive paste τ1 is used.
Diene-based polymer compounds conventionally used for pharmaceutical preparations include natural rubber, synthetic rubber, and mixtures thereof. Examples of the synthetic rubber include styrene-isoprene-styrene block copolymer rubber, styrene-butadiene rubber, polybutene rubber, butyl rubber, and silicone rubber.

ゴム系粘着性物質よりなる膏体中には、さらに第三成分
としてテルペン系樹脂、石油系樹脂などの粘着性付与剤
、流動パラフィン、動植物油(たとえば、オ′リーブ油
、大豆油、牛脂、トン脂)、ポリブテン、低級イソプレ
ン、ワックスなどの接着力・保持力調整剤、酸化チタン
、酸化亜鉛、メタケイ酸アルミニウム、硫酸カルシウム
、リン酸カルシウムなどの充填剤、水および乳化剤(た
とえば、ソルビタンモノオレエート、ラウリルスルホン
酸ナトリウム)、乳化助剤(たとえば、ステアリン酸マ
グネシウム、ステアリン酸アルミニウム)などを配合し
てもよい。
The paste made of rubber-based adhesive substances further contains tackifiers such as terpene-based resins and petroleum-based resins, liquid paraffin, animal and vegetable oils (for example, olive oil, soybean oil, beef tallow, etc.) as third components. Adhesion/retention force regulators such as tonne (tonne resin), polybutene, lower isoprene, wax, fillers such as titanium oxide, zinc oxide, aluminum metasilicate, calcium sulfate, calcium phosphate, water and emulsifiers (for example, sorbitan monooleate, (sodium lauryl sulfonate), emulsification aids (eg, magnesium stearate, aluminum stearate), etc. may also be blended.

本発明にて使用されるミカン属植物としては、たとえば
レモン、シトロン、ライム、ダイダイ、ベルカモソト、
グレープフルーツ、ザポン、オレンジ、ランシュウミカ
ン、ポンカン、キンカン、ユズ、カボス、ハツサク、ネ
ーブルオレンジ、イコカン、サマーオレンジなどが列挙
される。
Examples of plants of the genus Citrus used in the present invention include lemon, citron, lime, daidai, berkamosoto,
Grapefruit, zapon, orange, orchid mandarin orange, ponkan, kumquat, yuzu, kabosu, hatsusaku, navel orange, kokan, summer orange, etc. are listed.

ミカン属の精油としては、たとえばレモン油、オレンジ
油、ザポン油、ライム油などがあげられる。
Examples of essential oils of the citrus genus include lemon oil, orange oil, zapon oil, and lime oil.

これらは、合成品、ミカン属植物由来のもののいずれで
もよいが、複数種の精油を用いることが好ましい。従っ
て、天然由来のものは、採取した複数種精油を、特定精
油を分離することなく、そのまま用いることが好ましく
、また合成のものは任意の2種以上を混合して用いるこ
とが好ましい。勿論、ある任意のミカン属植物に含まれ
るすべての種類の精油を使用する必要はなく、その中の
任意の複数種の精油を用いてもよい。
These may be synthetic products or those derived from plants of the genus Citrus, but it is preferable to use multiple types of essential oils. Therefore, it is preferable to use naturally derived essential oils as they are without separating the specific essential oils, and it is preferable to use a mixture of two or more types of synthetic essential oils. Of course, it is not necessary to use all kinds of essential oils contained in a given Citrus genus plant, and any plural kinds of essential oils among them may be used.

天然のミカン属植物から採取したものとしては、水蒸気
蒸溜によるもの、圧搾点よるもの、溶媒抽出によるもの
などのいずれもが好適に使用される。
As for those collected from natural Citrus genus plants, those obtained by steam distillation, those obtained by pressing point, those obtained by solvent extraction, etc. are preferably used.

ミカン属植物の精油の配合量はゴム系粘着性物質に対し
て、0.01〜5重量%程度、好ましくは0.1〜2重
量%程度、さらに好ましくは0.2〜1重量%程度であ
る。
The blending amount of the essential oil of the Citrus genus plant is about 0.01 to 5% by weight, preferably about 0.1 to 2% by weight, and more preferably about 0.2 to 1% by weight based on the rubber adhesive substance. be.

本発明の膏体に配合される薬物は粘着性貼付製剤化して
投与されうる薬物であれば特に制限はなく、たとえば経
皮吸収性薬物(ただし、経皮吸収助剤などの助けによっ
て経皮吸収されるものであってもよく、また局所性薬物
、全身性薬物のいずれでもよい)、皮膚疾患治療用薬物
、皮膚刺激性薬物、不定愁訴治療用薬物などがあげられ
る。特に、フェノール性水酸基含有化合物、アミン系化
合物などは、従来のゴム系粘着性物質よc9なる丹体中
における含量低下が著しいので、本発明膏体はかかる薬
物を製剤化する場合に特にその意義がある。フェノール
性水酸基含有化合物としては、たとえばサリチル酸誘導
体(サリチル酸モノグルリコール、サリチル酸メチルな
ど)、ビタミンEおよびその誘導体、カブサイシンなど
があげられ、またアミン系化合物としてはジフェンヒド
ラミンなどのエタノールアミン系抗ヒスタミン薬物、ク
ロルファラミンなどのエチレンジアミン系抗ヒスタミン
薬物、リドカインなどがあげられる。その他の薬効成分
としては、たとえばβ−メントール、d7!−カンファ
ー、チモール、d−ボルネオールなどの感冷性刺激性薬
物、インドメタシン、ジクロフェナックナトリウムなど
の非ステロイド系抗炎症性薬物、デキサメタシン、ベタ
メタシンなどのステロイド系抗炎症剤、クロルヘキジジ
ンジグリコネート、アクリノールなどの殺菌剤、トウガ
ラシエキス、ノニル酸バニリルアミド、カブサイシン、
ショウキョウエキス、カンタリスチンキ、カンタリジン
などの温感性皮膚刺激性薬物、シコン、トウキなどの生
薬類等があげられれる。
There are no particular restrictions on the drug that can be incorporated into the paste of the present invention, as long as it can be administered in the form of an adhesive patch. Examples include drugs for treating skin diseases, drugs for skin irritation, and drugs for treating indefinite complaints. In particular, the content of phenolic hydroxyl group-containing compounds, amine compounds, etc. in the c9 complex is significantly lower than that of conventional rubber-based adhesive substances, so the paste of the present invention has particular significance when formulating such drugs. There is. Examples of phenolic hydroxyl group-containing compounds include salicylic acid derivatives (monoglylic salicylate, methyl salicylate, etc.), vitamin E and its derivatives, kabsaicin, and amine compounds include ethanolamine antihistamines such as diphenhydramine; Examples include ethylenediamine antihistamine drugs such as chlorphalamine, and lidocaine. Other medicinal ingredients include β-menthol, d7! - Cold-sensitive irritants such as camphor, thymol, d-borneol, nonsteroidal anti-inflammatory drugs such as indomethacin, diclofenac sodium, steroidal anti-inflammatory drugs such as dexamethacin, betamethacin, chlorhexidine diglyconate, acrinol Fungicides such as chili pepper extract, nonylic acid vanillylamide, kabsaicin,
Examples include heat-sensitive skin irritating drugs such as ginger extract, cantharis tincture, and cantharidin, and crude drugs such as sycamore and turmeric.

なお、本発明粘着性貼付製剤を調整するあたってはゴム
系着性物質にまず薬物を添加した後にミカン属植物の精
油を添加してもよいことは言うまでもない。
It goes without saying that in preparing the adhesive patch preparation of the present invention, the drug may be added to the rubber-based adhesive substance first, and then the essential oil of the Citrus genus plant may be added.

また、本発明粘着性貼付製剤は、通常、布、プラスチッ
クフィルムなどの支持体に展延して用いられる。
Further, the adhesive patch preparation of the present invention is usually used by being spread on a support such as cloth or plastic film.

以下に実施例および実験例を示して本発明をより具体的
に説明するが、本発明はこれらに限定されるものではな
い。
EXAMPLES The present invention will be described in more detail below with reference to Examples and Experimental Examples, but the present invention is not limited thereto.

以下の記載において「部」とあるは「重量部」を意味す
る。
In the following description, "parts" means "parts by weight."

実施例1 スチレン−ブタジェン−スチレンゴム43部と天然ロジ
ン25部を15(lに保持されたニーグーで20分間練
り、これにレモン油圧搾精油1部を加えて混合し、70
分間混練する。次ぎにボリブデン5部、流動パラフィン
7部、酸化チタン粉末6部、タルク5部を添加し、1部
分間混練した後、90℃まで冷却してからサリチル酸モ
ノグリコール5部、ノニル酸バニリルアミドo、 02
 fa、ジフンヒドラミン0.8部を加え混合し、織布
上に0.21の厚みで塗布し貼付剤を得る。
Example 1 43 parts of styrene-butadiene-styrene rubber and 25 parts of natural rosin were kneaded for 20 minutes in a Niguu maintained at 15 liters, and 1 part of lemon hydraulically squeezed essential oil was added thereto and mixed.
Knead for a minute. Next, 5 parts of bolybdenum, 7 parts of liquid paraffin, 6 parts of titanium oxide powder, and 5 parts of talc were added, and after kneading for 1 part, the mixture was cooled to 90°C, and then 5 parts of monoglycol salicylate, vanillylamide nonylate, 0.02
fa and 0.8 parts of diphunhydramine are added and mixed, and the mixture is coated on a woven fabric to a thickness of 0.21 to obtain a patch.

実施例2 実施例1において、レモン油圧搾精油の代わりにベルモ
ソト油(水蒸気蒸溜品)1部を配合し、それ以外は実施
例1と同様にして貼付剤を得る。
Example 2 A patch is obtained in the same manner as in Example 1, except that 1 part of vermoso oil (steam distilled product) is blended in place of the lemon oil pressure-pressed essential oil.

比較例1 実施例1において、レモン油圧搾精油を加えないこと以
外は実施例1と同様の操作にて貼付剤を得る。
Comparative Example 1 A patch is obtained in the same manner as in Example 1, except that the lemon oil pressure extraction essential oil is not added.

実験例1 実施例1〜2および比較例1で得たサンプルを、アルミ
ニウムポリエチレンラミネートフィルムに密封して、4
0°Cにて3ケ月間保存した後、各薬物の定量を行い、
その含量低下率をもとめ、その結果を第1表に示した。
Experimental Example 1 The samples obtained in Examples 1 to 2 and Comparative Example 1 were sealed in an aluminum polyethylene laminate film, and
After storing at 0°C for 3 months, each drug was quantified.
The content reduction rate was determined and the results are shown in Table 1.

第1表中における分解率は理論値を100%ととして計
算したものである。
The decomposition rates in Table 1 are calculated based on the theoretical value of 100%.

下表から明らかなように、本発明膏体中に配合された薬
物は極めて安定に存在する。
As is clear from the table below, the drug compounded in the paste of the present invention exists extremely stably.

第1表 特許出願人 日東電気工業株式会社 0Table 1 Patent applicant: Nitto Electric Industry Co., Ltd. 0

Claims (4)

【特許請求の範囲】[Claims] (1) ゴム系粘着性物質よりなる膏体に、ミカン属植
物に含まれる精油を配合してなることを特徴とするゴム
系粘着性膏体。
(1) A rubber-based adhesive paste comprising a paste made of a rubber-based adhesive substance mixed with an essential oil contained in a plant of the genus Citrus.
(2) ミカン属植物がレモン、シトロン、ライム、ダ
イダイ、ベル力モット、グレープフルーツ、ザポン、オ
レンジ、ランシュウミカン、ポンカン、キンカン、ユズ
、カボス、ハツサク、ネーブルオレンジ、イヨカン、サ
マーオレンジである特許請求の範囲第(1)項記載のゴ
ム系粘着性膏体。
(2) A patent claim in which the Citrus genus plants are lemons, citrons, limes, daidai daisies, vermilots, grapefruits, zapons, oranges, mandarin oranges, ponkans, kumquats, yuzu, kabosu, honeysuckle, navel oranges, iyocans, and summer oranges. A rubber-based adhesive paste according to item (1).
(3) さらに薬物を配合してなる特許請求の範囲第(
1)項または第(2)項記載のゴム系粘着性膏体。
(3) Claim No.
The rubber adhesive paste described in item 1) or item (2).
(4)薬物がフェノール性水酸基又は/及びアミノ基を
有するものである特許請求の範囲第(3)項記載のゴム
系粘着性膏体。
(4) The rubber adhesive paste according to claim (3), wherein the drug has a phenolic hydroxyl group and/or an amino group.
JP58160056A 1983-08-31 1983-08-31 Rubber pressure-sensitive adhesive plaster Pending JPS6051108A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58160056A JPS6051108A (en) 1983-08-31 1983-08-31 Rubber pressure-sensitive adhesive plaster

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58160056A JPS6051108A (en) 1983-08-31 1983-08-31 Rubber pressure-sensitive adhesive plaster

Publications (1)

Publication Number Publication Date
JPS6051108A true JPS6051108A (en) 1985-03-22

Family

ID=15706948

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58160056A Pending JPS6051108A (en) 1983-08-31 1983-08-31 Rubber pressure-sensitive adhesive plaster

Country Status (1)

Country Link
JP (1) JPS6051108A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2814072A1 (en) * 2000-09-20 2002-03-22 Ceetal Sa Lab Composition for sanitizing cows' teats, comprises a film-forming polymer and a liquid citrus extract in an aqueous medium
CN114869864A (en) * 2022-05-10 2022-08-09 黄山市信德成胶业有限公司 Thermoplastic styrene-butadiene rubber system plaster matrix adhesive

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2814072A1 (en) * 2000-09-20 2002-03-22 Ceetal Sa Lab Composition for sanitizing cows' teats, comprises a film-forming polymer and a liquid citrus extract in an aqueous medium
WO2002030437A1 (en) * 2000-09-20 2002-04-18 Laboratoires Ceetal S.A. Citrus composition for hygiene, care or protection of teats
CN114869864A (en) * 2022-05-10 2022-08-09 黄山市信德成胶业有限公司 Thermoplastic styrene-butadiene rubber system plaster matrix adhesive

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