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JP2005075755A - Antiphlogistic-sedative plaster and method for producing the same - Google Patents

Antiphlogistic-sedative plaster and method for producing the same Download PDF

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JP2005075755A
JP2005075755A JP2003306105A JP2003306105A JP2005075755A JP 2005075755 A JP2005075755 A JP 2005075755A JP 2003306105 A JP2003306105 A JP 2003306105A JP 2003306105 A JP2003306105 A JP 2003306105A JP 2005075755 A JP2005075755 A JP 2005075755A
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base
inflammatory analgesic
plaster
analgesic patch
skin
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Fumiko Ishiguro
文子 石黒
Takashi Maki
剛史 牧
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DAIKYO YAKUHIN KOGYO KK
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DAIKYO YAKUHIN KOGYO KK
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Abstract

<P>PROBLEM TO BE SOLVED: To obtain an antiphlogistic-sedative plaster having enhanced effectiveness and safety, by making a conventional antiphlogistic-sedative plaster to contain "SHIUNKO" of Chinese medicine. <P>SOLUTION: This antiphlogistic-sedative plaster is characterized by containing the SHIUNKO of Chinese medicine in a substrate containing a skin irritant. The SHIUNKO is preferably compounded in an amount of 5 to 50 wt. %. At least one selected from indomethacin, ketoprofen, flurbiprofen, felbinac, capsicum extract, nonylic acid vanillylamide, menthol, camphor, methyl salicylate, and glycol salicylate is contained in the substrate as the skin irritant. <P>COPYRIGHT: (C)2005,JPO&NCIPI

Description

本発明は消炎鎮痛貼付剤及びその製造法に関するものである。   The present invention relates to an anti-inflammatory analgesic patch and a method for producing the same.

紫雲膏は華岡青洲が考案した軟膏と言われ、湿疹、乾癬、角皮症、ひび、あかぎれ、かぶれ、やけど、痔、には特に良く効き、他に、水虫、うおのめ、たこ、にきび、いぼ、あせも、円形脱毛症、外傷、凍傷、潰瘍、脱肛等いろんな皮膚疾患に効き、手元にあると重宝する薬である。   Shiunko is said to be an ointment devised by Hanaoka Aoshima, and works particularly well for eczema, psoriasis, keratoderma, cracks, scabs, rashes, burns, and wrinkles. In addition, athlete's foot, corn, octopus, acne, warts It is a medicine that is useful when it is at hand, and is effective for various skin diseases such as alopecia areata, trauma, frostbite, ulcer, and anal prolapse.

通常、紫雲膏の材料としては、例えば次の組成及び量を用いる。
ごま油・・・・1000g
ミツロウ・・・・300g
豚油・・・・・・・30g
当帰・・・・・・・80g
紫根・・・・・・120g
Usually, the following composition and amount are used as the material for the purple cloud.
Sesame oil ... 1000g
Beeswax ... 300g
Pork oil ... 30g
Togo ... 80g
Murasakine ... 120g

作り方は、先ずゴマ油を煮てミツロウ及び豚油を溶かす。次に、当帰を加え、140℃に保つ。これに紫根を加え15分くらい、140℃を保ちながら沸騰させる。沸騰させたものを布で濾し、撹拌しながらゆっくり混ぜて固める。尚、ミツロウは夏多く、冬少なくする。   To make it, first boil sesame oil and dissolve beeswax and pork oil. Next, add a return and keep at 140 ° C. Add purple root to this and boil for 15 minutes while maintaining 140 ° C. Filter the boiled material with a cloth and mix slowly with stirring to harden. Beeswax is often in summer and less in winter.

この紫雲膏を利用した貼付剤としては、通気性を有する柔軟な樹脂からなる樹脂シート基材層に、紫雲膏、塩化リゾチーム、糖質の少なくとも1つを含有する膏体層を担持させた蓐瘡等の治療用貼付剤が既に提案されている(例えば、特許文献1参照)。しかしながら、この公知の貼付剤は、蓐瘡治療等用の貼付剤であり、蓐瘡治療のための紫雲膏が膏体層に配合されているにすぎないものである。   As a patch using this purple cloud plaster, a paste sheet layer containing at least one of purple cloud paste, lysozyme chloride, and sugar is supported on a resin sheet base layer made of a flexible resin having air permeability. A patch for treatment of acne or the like has already been proposed (see, for example, Patent Document 1). However, this known patch is a patch for treating pressure ulcers and the like, and is simply a purple cloud for treating pressure ulcers blended in the plaster layer.

一方、貼付剤については、消炎鎮痛成分を配合し、腰痛・肩こり・筋肉痛等の炎症をおさめる消炎鎮痛貼付剤が広く市販されている。これらは温感貼付剤と冷感貼付剤とに大別され、温感貼付剤は慢性腰痛症や急性腰痛症の発症数日後以降に使用され、冷感貼付剤は炎症による局所の発熱を抑えると共に炎症部位の拡大を防ぐ目的で使用される。   On the other hand, anti-inflammatory analgesic patches containing anti-inflammatory analgesic ingredients to suppress inflammation such as low back pain, stiff shoulders, and muscle pain are widely marketed. These are broadly classified into warm patches and cold patches, and warm patches are used several days after the onset of chronic low back pain or acute low back pain, and cold patches suppress local fever caused by inflammation. At the same time, it is used for the purpose of preventing the spread of inflammatory sites.

この2種類の貼付剤を成分から説明すると、温感貼付剤には、皮膚に温感を与えるトウガラシエキスやノニル酸ワニリルアミド等が含有され、トウガラシエキスは、その辛味成分であるカプサイシンが局所の血管を拡張させ、患部の血流増加により、損傷した組織の修復を早めたり、腰部筋の血流障害による腰痛を改善する。またノニル酸ワニリルアミドはカプサイシンの誘導体であり、同様の機序で血行を改善する。   These two types of patches will be explained from the components. The warm patch contains a pepper extract, nonyl acid vanillylamide, and the like that gives the skin a warm feeling. Capsicin, which is a pungent component of capsicin, is a local blood vessel. By expanding the blood flow in the affected area, the damaged tissue can be repaired more quickly, or low back pain due to lumbar muscle blood flow disturbance can be improved. Nonylic acid vanillylamide is a derivative of capsaicin and improves blood circulation by the same mechanism.

冷感貼付剤には、メントールやカンフル等の清涼成分が含有され、炎症による局所の発熱を抑えると共に、炎症部位の拡大を防ぐ。また、メントール等が知覚神経の末梢に作用し軽度の知覚麻痺を起こすため、鎮痛作用も期待でき、炎症性疼痛疾患の急性期に多く使用される。   The cooling patch contains refreshing components such as menthol and camphor, which suppresses local fever caused by inflammation and prevents the inflammation from spreading. In addition, since menthol and the like act on the periphery of sensory nerves to cause mild sensory paralysis, an analgesic action can be expected, and it is often used in the acute phase of inflammatory pain diseases.

登録実用新案第3036689号Registered Utility Model No. 3036689

以上のように消炎鎮痛貼付剤については、インドメタシン、ケトプロフェン、フルルビプロフェン、フェルビナク等の他、トウガラシエキス、ノニル酸ワニリルアミド、メントール、カンフル等の皮膚刺激成分が添加されており、皮膚刺激に対して敏感な人にとっては消炎鎮痛貼付剤を貼ることにより、今度は皮膚自体がかぶれを生じる場合があった。特に、温感貼付剤は皮膚刺激が強く、発赤・発疹などのかぶれの副作用が出現しやく、入浴時に貼付していた部位が強く痛む場合があった。   As described above, the anti-inflammatory analgesic patch contains skin irritation ingredients such as capsicum extract, nonyl acid vanillylamide, menthol and camphor in addition to indomethacin, ketoprofen, flurbiprofen, felbinac, etc. For those who are sensitive, the skin itself may be irritated by applying an anti-inflammatory analgesic patch. In particular, warm patches have strong skin irritation, rash side effects such as redness and rash are likely to appear, and the site applied at the time of bathing sometimes hurts strongly.

本発明は、従来の消炎鎮痛貼付剤に漢方処方の「紫雲膏」を含有させることにより、有効性と安全性を高めることができる。具体的には、酸化防止又は酸化遅延効果および貼着によるかぶれの低減、薬剤刺激の緩和、貼着基剤に対する適度な貼着力の付与、適度な貼着力に対する角質損傷の軽減、紫雲膏成分であるトウキ、シコンによる皮膚への積極的な保護作用を目的とする。   According to the present invention, the effectiveness and safety can be enhanced by including the traditional anti-inflammatory analgesic patch containing “Shiunko” as a Chinese medicine. Specifically, anti-oxidation or oxidation delay effect and reduction of rash caused by sticking, mitigation of drug irritation, imparting proper sticking power to sticking base, reducing keratinous damage to moderate sticking force, The purpose is to protect the skin positively by certain Toki and Shikon.

請求項1に記載された発明に係る消炎鎮痛貼付剤は、皮膚刺激成分を含む基剤中に漢方処方の紫雲膏を含有することを特徴とするものである。   The anti-inflammatory analgesic patch according to the invention described in claim 1 is characterized in that the base containing a skin irritant component contains a Chinese medicine prescription Shiunko.

請求項2に記載された発明に係る消炎鎮痛貼付剤は、請求項1に記載の基剤がプラスター剤であることを特徴とするものである。   The anti-inflammatory analgesic patch according to the invention described in claim 2 is characterized in that the base of claim 1 is a plaster.

請求項3に記載された発明に係る消炎鎮痛貼付剤は、請求項1又は2に記載の基剤中に紫雲膏が重量比5%以上50%未満配合されていることを特徴とするものである。   The anti-inflammatory analgesic patch according to the invention described in claim 3 is characterized in that shiunko is blended in the base of claim 1 or 2 in a weight ratio of 5% or more and less than 50%. is there.

請求項4に記載された発明に係る消炎鎮痛貼付剤は、請求項1〜3の何れか1項に記載の皮膚刺激成分として、インドメタシン、ケトプロフェン、フルルビプロフェン、フェルビナク、トウガラシエキス、ノニル酸ワニリルアミド、メントール、カンフル、サリチル酸メチル、サリチル酸グリコールから選ばれた1つ以上の成分が基剤中に含まれていることを特徴とするものである。   The anti-inflammatory analgesic patch according to the invention described in claim 4 is a skin irritation component according to any one of claims 1 to 3, wherein indomethacin, ketoprofen, flurbiprofen, felbinac, red pepper extract, nonylic acid One or more components selected from vanillyl amide, menthol, camphor, methyl salicylate and glycol salicylate are contained in the base.

請求項5に記載された発明に係る消炎鎮痛貼付剤は、請求項4に記載の皮膚刺激成分として、ノニル酸ワニリルアミドが基剤中に0.001〜0.5重量%含まれていることを特徴とするものである。   The anti-inflammatory analgesic patch according to the invention described in claim 5 is characterized in that 0.001 to 0.5% by weight of nonyl acid vanillylamide is contained in the base as a skin irritation component according to claim 4. It is.

請求項6に記載された発明に係る消炎鎮痛貼付剤の製造法は、請求項1〜5の何れかに記載の消炎鎮痛貼付剤の製造法において、
加熱混練された基剤を2〜4日間冷暗所で放置した後、該基剤からなる基剤層を支持体上に形成した後、2〜4日間冷暗所で放置することを特徴とするものである。
The method for producing an anti-inflammatory analgesic patch according to the invention described in claim 6 is the method for producing an anti-inflammatory analgesic patch according to any one of claims 1 to 5,
The heat-kneaded base is left to stand in a cool and dark place for 2 to 4 days, and then a base layer composed of the base is formed on a support and then left to stand in a cool and dark place for 2 to 4 days. .

本発明は以上説明した通り、従来の消炎鎮痛貼着剤に漢方処方の「紫雲膏」を含有させることにより、有効性と安全性を高めることができる。具体的には、具体的には、酸化防止又は酸化遅延効果および貼着によるかぶれの低減、薬剤刺激の緩和、貼着基剤に対する適度な貼着力の付与、適度な貼着力に対する角質損傷の軽減、紫雲膏成分であるトウキ、シコンによる皮膚への積極的な保護作用を得ることができるという効果がある。   As described above, according to the present invention, the effectiveness and safety can be improved by including the traditional anti-inflammatory analgesic adhesive in the form of Chinese medicine “Shiunko”. Specifically, anti-oxidation or oxidation delay effect and reduction of rash caused by sticking, alleviation of drug irritation, imparting proper sticking force to sticking base, reducing keratin damage to moderate sticking force In addition, there is an effect that an active protective action can be obtained on the skin by Toki and Sikon, which are components of purple cloud.

本発明による消炎鎮痛貼付剤は、皮膚刺激成分を含む基剤中に漢方処方の紫雲膏を含有してなるものであるため、消炎鎮痛剤としての有効性と安全性を高めることができ、酸化防止又は酸化遅延効果及び貼付によるかぶれを低減することができるものである。   Since the anti-inflammatory analgesic patch according to the present invention comprises Kampo-formed purple cloud plaster in a base containing a skin irritant component, the effectiveness and safety as an anti-inflammatory analgesic can be improved, and oxidation It can prevent or reduce the oxidation delay effect and rash caused by sticking.

本発明の貼付剤における基剤としては、パップ剤或いはプラスター剤の何れでも含有する意味であるが、水分含量が多いパップ剤の場合には油性成分の多い紫雲膏が基剤中に安定に分散保持され難く、従って製剤上及び製品安定性の面でプラスター剤が好適である。   As a base in the patch of the present invention, it means to contain either a poultice or a plaster, but in the case of a poultice having a high water content, purple cloud with a lot of oily components is stably dispersed in the base. Plasters are preferred because they are difficult to retain and are therefore in terms of formulation and product stability.

本発明の貼付剤において基剤中に添加される紫雲膏の配合割合については、基剤中重量比で5以上50%未満とすることが好ましい。5重量%より少なければ、紫雲膏の皮膚疾患への効能が発揮できず、50重量%以上配合すれば、好適な消炎鎮痛成分の配合に支承を生じ、また、皮膚への貼付力も低減することになる。   In the patch of the present invention, it is preferable that the blending ratio of shimo-gypsum added to the base is 5 or more and less than 50% by weight in the base. If it is less than 5% by weight, the effect of Shimo-gaku on skin diseases cannot be demonstrated, and if it is added in an amount of 50% by weight or more, support for the combination of suitable anti-inflammatory and analgesic ingredients is produced, and the adhesive strength to the skin is also reduced. become.

本発明の貼付剤における皮膚刺激成分としては、インドメタシン、ケトプロフェン、フルルビプロフェン、フェルビナク、トウガラシエキス、ノニル酸ワニリルアミド、メントール、カンフル、サリチル酸メチル、サリチル酸グリコールから選ばれた1つ以上の成分が基剤中に含まれているものが挙げられる。これら皮膚刺激成分が含有されていても同時に含有する紫雲膏がかぶれを低減する相乗的な効果を発揮する。より具体的には、皮膚刺激成分としてのノニル酸ワニリルアミドが基剤中に0.001〜0.5重量%含有させても、紫雲膏がかぶれを低減することができる。   The skin irritation component in the patch of the present invention is based on one or more components selected from indomethacin, ketoprofen, flurbiprofen, felbinac, capsicum extract, nonyl acid vanillylamide, menthol, camphor, methyl salicylate, and salicylate glycol. What is contained in the agent is mentioned. Even if these skin-irritating ingredients are contained, the purple cloud contained simultaneously exhibits a synergistic effect of reducing rash. More specifically, even if nonylic acid vanillylamide as a skin irritant component is contained in the base in an amount of 0.001 to 0.5% by weight, violet cloud can reduce rash.

本発明の消炎鎮痛貼付剤は、紫雲膏成分中にミツロウが配合されているためであるか基剤が、加熱ニーダ等で加熱混練された基剤は、アメ状に軟らかくなり、粘着力も甚大となった。そこで、本発明の消炎鎮痛貼付剤の製造法では、加熱混練された基剤を2〜4日間冷暗所で放置した後、該基剤からなる基剤層を支持体上に形成した後、2〜4日間冷暗所で放置する工程を備える。これにより、消炎鎮痛貼付剤は適度な堅さと、適度な粘着性が得られる。   The anti-inflammatory analgesic patch of the present invention is because the beeswax is blended in the purple cloud paste component, or the base is heat-kneaded with a heating kneader or the like, and the base becomes soft and has a large adhesive strength. became. Therefore, in the method for producing an anti-inflammatory analgesic patch of the present invention, after the heated and kneaded base is left in a cool and dark place for 2 to 4 days, a base layer composed of the base is formed on the support, A step of leaving it in a cool and dark place for 4 days is provided. As a result, the anti-inflammatory analgesic patch has an appropriate hardness and an appropriate adhesiveness.

実施例A.消炎鎮痛貼付剤の製造1
実施例として紫雲膏を、5重量%(実施例1)、20重量%(実施例2)、33重量%(実施例3)、50重量%(実施例4)配合したもの、比較例1として紫雲膏を配合しないものを作成した。具体的には、次の表1に示す組成を加熱混合して硬膏基剤を作成し、圧延(カレンダ)ロールによる圧延塗布し、剥離紙を重ねて裁断することにより、消炎鎮痛貼付剤を製造した。
Example A.1. Manufacture of anti-inflammatory analgesic patches 1
As a comparative example 1, as a working example, Shimogyo was blended with 5 wt% (Example 1), 20 wt% (Example 2), 33 wt% (Example 3), and 50 wt% (Example 4). The thing which does not mix | blend Shimo-gypsum was created. Specifically, an anti-inflammatory analgesic patch is produced by heating and mixing the composition shown in the following Table 1 to prepare a plaster base, rolling and applying with a roll (calendar) roll, and cutting the release paper on top of each other. did.

また、比較例1として、トウキ軟エキス、シコン軟エキスを添加して他の基剤成分をほぼ同じとした比較例を作成した。皮膚刺激成分としては、L−メントール、ノニル酸ワニリルアミド、サリチル酸メチルが添加されている。   In addition, as Comparative Example 1, a comparative example was prepared in which toki soft extract and shikon soft extract were added and other base components were substantially the same. As a skin irritating component, L-menthol, nonyl acid vanillylamide, and methyl salicylate are added.

より具体的な製造工程は、次の通りである。先ず、ニーダーで硬膏基剤を作成した。具体的には、80℃〜100℃のニーダーに生ゴム、ポリイソブチレン、酸化チタン、炭酸カルシウム、テルペン樹脂からなるゴム基剤を投入して混練した後、ポリブテン、エステルガム、アクリル酸メチル・アクリル酸−2−エチルヘキシル共重合樹脂エマルジョン、天然ゴムラテックスからなる粘着付与剤を投入して混練した。   A more specific manufacturing process is as follows. First, a plaster base was prepared with a kneader. Specifically, a rubber base made of raw rubber, polyisobutylene, titanium oxide, calcium carbonate, and terpene resin is put into a kneader at 80 ° C. to 100 ° C. and kneaded, and then polybutene, ester gum, methyl acrylate / acrylic acid A tackifier comprising 2-ethylhexyl copolymer resin emulsion and natural rubber latex was added and kneaded.

得られた硬膏基剤にL−メントール、サリチル酸メチル、ノニル酸ワニリルアミド、及び、紫雲膏(又は、トウキ軟エキス、シコン軟エキス)の有効成分を投入して混練し、硬膏基剤を完成させた。その後、圧延(カレンダ)ロールによる圧延塗布により支持体上に均一に塗布し、剥離紙を重ねて、所望の形状に裁断することにより、消炎鎮痛貼付剤を得た。尚、これに薬効成分を期待する薬剤は乳化基剤中に混合して添加する。また、硬膏基剤は耐熱性の剥離紙上に圧延塗布した後、支持体を重ねて、所望の形状に裁断してもよい。   Active ingredients of L-menthol, methyl salicylate, nonylic acid vanillylamide, and Shimogaku (or Toki soft extract, Shikon soft extract) were added to the obtained plaster base and kneaded to complete the plaster base. . Then, the anti-inflammatory analgesic patch was obtained by apply | coating uniformly on a support body by rolling application | coating by a rolling (calendar) roll, piled up a release paper, and cut | judging to a desired shape. In addition, the drug which expects a medicinal ingredient is mixed and added to the emulsifying base. Alternatively, the plaster base may be roll-coated on a heat-resistant release paper, and then the support may be overlaid and cut into a desired shape.

しかしながら、得られた消炎鎮痛剤は、紫雲膏成分中にミツロウが配合されているためであるか詳細は不明ではあるが、基剤がアメ状で軟らかく、粘着力も甚大であり、そのままでは製品として使用は不向きであった。そこで、工程を工夫した。   However, although the details of the anti-inflammatory analgesic agent obtained are due to the inclusion of beeswax in the purple cloud paste component, the base is candy-like and soft, and the adhesive strength is enormous. Use was unsuitable. Therefore, the process was devised.

図1は本発明の消炎鎮痛貼付剤の製造工程を示した工程図である。図に示す通り、ニーダで混練した硬膏基剤を一旦冷暗所で2日から4日間放置した。その後、硬膏基剤を圧延(カレンダ)ロールによる圧延塗布し、剥離紙を重ねて裁断した消炎鎮痛貼付剤を冷暗所で再度2日から4日間放置した。尚、圧延塗布工程としては、圧延ロールを通常の95℃から85℃に下げて行った。その結果、得られた消炎鎮痛貼付剤は適度な堅さと、適度な粘着性が得られたため、これを製品とした。   FIG. 1 is a process diagram showing the production process of the anti-inflammatory analgesic patch of the present invention. As shown in the figure, the plaster base kneaded with a kneader was once left in a cool and dark place for 2 to 4 days. Thereafter, the anti-inflammatory analgesic patch applied by rolling the plaster base with a rolling (calendar) roll and cut by overlapping release paper was left again in a cool and dark place for 2 to 4 days. In addition, as a rolling application | coating process, the rolling roll was lowered | hung from normal 95 degreeC to 85 degreeC. As a result, since the obtained anti-inflammatory analgesic patch had an appropriate hardness and an appropriate adhesiveness, it was used as a product.

Figure 2005075755
Figure 2005075755

実施例B.消炎鎮痛貼付剤の特徴
表1に示した消炎鎮痛貼付剤を用いて、被験者10名に対し腕に3時間貼付して、以下の項目について観察した。観察項目については、1.皮膚への接着性、2.効き目感、3.剥離時の痛み、4.剥がした後の皮膚の状態であり、各々について、該当する項目について点数を与え各々を計算した。結果を次の表2〜表5に示す。
Example B. Characteristics of anti-inflammatory analgesic patch Using the anti-inflammatory analgesic patch shown in Table 1, it was applied to the arm for 10 hours for 10 subjects, and the following items were observed. Regarding observation items: 1. Adhesion to the skin 2. Effective feeling; 3. Pain when peeling; It was the state of the skin after peeling, and for each, a score was given for the corresponding item and each was calculated. The results are shown in the following Tables 2 to 5.

Figure 2005075755
Figure 2005075755

表2に示した通り、油脂が配合されている紫雲膏であっても、5%〜33%の配合では、貼着性に大幅な差はなかったが、50%の配合では著しく接着力が低下した。また、ゴム基剤に対する粘着付与剤の配合率は同じにしたが、紫雲膏が50%未満であれば、接着性には支承はなく、油脂を含有する紫雲膏の配合により、皮膚に対する好適な粘着性を獲得していることが判った。   As shown in Table 2, even in the case of purple gypsum blended with fats and oils, there was no significant difference in sticking property with 5% to 33% blending. Declined. Moreover, although the compounding ratio of the tackifier to the rubber base was the same, there is no support for the adhesiveness if the amount of purple cloud is less than 50%. It turns out that it has acquired adhesiveness.

Figure 2005075755
Figure 2005075755

効き目感とは、簡単に説明するならば、接着した際に皮膚刺激成分が皮膚を刺激して得られる感覚であり、表3に示す通り、効き目感に関連する薬剤自体に差がないため、比較例及び実施例1,2,3について殆ど差がないことが確認された。   The effect feeling is, if briefly explained, a sensation obtained by stimulating the skin when the skin irritation component is adhered, and as shown in Table 3, there is no difference in the drug itself related to the effect feeling. It was confirmed that there was almost no difference between the comparative example and Examples 1, 2, and 3.

Figure 2005075755
Figure 2005075755

Figure 2005075755
Figure 2005075755

表4に示す通り、比較例の剥離時の痛みは接着力だけに起因するのではなく、後述の皮膚の状態から判断して、かぶれもその原因の1つではないかと思われた。実施例については、油脂成分を含有している紫雲膏が配合されているため、接着性がその分阻害される傾向にあるため、剥離時の痛みもなく、逆に程良い接着性となったのではないかと思われた。   As shown in Table 4, the pain at the time of exfoliation in the comparative example was not caused solely by the adhesive strength, but it was thought that rash was one of the causes as judged from the skin condition described later. As for the examples, since the purple cloud containing the fat and oil component is blended, the adhesiveness tends to be inhibited accordingly, so there was no pain at the time of peeling, and the adhesiveness was moderately reversed. I thought it was.

また、表5に示す通り、皮膚刺激成分は同等であるのに対して、紫雲膏を配合したものでは、角質が剥がれるほどの損傷はなかった。   In addition, as shown in Table 5, the skin irritation component was the same, whereas the blend containing shiunko was not damaged to the extent that the keratin was peeled off.

実施例C.消炎鎮痛貼付剤の製造2
実施例Aでは、皮膚刺激成分としては、d1一カンフル、L−メントール、ノニル酸ワニリルアミド、サリチル酸メチルが添加されているものを製造したが、その他の消炎鎮痛貼付剤として、インドメタシンとL−メント−ルとが添加された別の消炎鎮痛貼付剤を製造した。具体的には、次の表6に示す組成で消炎鎮痛貼付剤を製造した。
Example C. Manufacture of anti-inflammatory analgesic patches 2
In Example A, as a skin irritant component, d1 monoflux, L-menthol, nonylic acid vanillylamide, and methyl salicylate were added, but other anti-inflammatory analgesic patches include indomethacin and L-mento Another anti-inflammatory analgesic patch to which was added was prepared. Specifically, anti-inflammatory analgesic patches were prepared with the compositions shown in Table 6 below.

また、比較例2として、トウキ軟エキス、シコン軟エキスを添加して他の基剤成分をほぼ同じとした比較例を作成し、実施例2と同様に消炎鎮痛貼付剤の特徴を検証したが、実施例Bと同様に比較例2では角質が剥がれるほどの損傷が発生したのに対して、実施例5のものは角質が剥がれるほどの損傷はなかった。   In addition, as Comparative Example 2, a comparative example was prepared by adding toki soft extract and sycon soft extract to make the other base components substantially the same, and the characteristics of the anti-inflammatory analgesic patch were verified in the same manner as in Example 2. As in Example B, in Comparative Example 2, damage to the extent that the keratin was peeled occurred, whereas in Example 5, there was no damage to the extent that the keratin was peeled off.

Figure 2005075755
Figure 2005075755

本発明の消炎鎮痛貼付剤の製造工程を示した工程図である。It is process drawing which showed the manufacturing process of the anti-inflammatory analgesic patch of this invention.

Claims (6)

皮膚刺激成分を含む基剤中に漢方処方の紫雲膏を含有することを特徴とする消炎鎮痛貼付剤。   An anti-inflammatory analgesic patch characterized by containing Kampo-prescription shiungaku in a base containing a skin irritation component. 基剤がプラスター剤であることを特徴とする請求項1に記載の消炎鎮痛貼付剤。   The anti-inflammatory analgesic patch according to claim 1, wherein the base is a plaster. 基剤中に紫雲膏が重量比5%以上50%未満配合されていることを特徴とする請求項1又は2に記載の消炎鎮痛貼付剤。   3. The anti-inflammatory analgesic patch according to claim 1 or 2, wherein the base is formulated with 5% or more and less than 50% by weight. 皮膚刺激成分として、インドメタシン、ケトプロフェン、フルルビプロフェン、フェルビナク、トウガラシエキス、ノニル酸ワニリルアミド、メントール、カンフル、サリチル酸メチル、サリチル酸グリコールから選ばれた1つ以上の成分が基剤中に含まれていることを特徴とする請求項1〜3の何れか1項に記載の消炎鎮痛貼付剤。   As a skin irritation component, the base contains one or more components selected from indomethacin, ketoprofen, flurbiprofen, felbinac, pepper extract, nonyl acid vanillylamide, menthol, camphor, methyl salicylate, and salicylate glycol. The anti-inflammatory analgesic patch according to any one of claims 1 to 3. 皮膚刺激成分として、ノニル酸ワニリルアミドが基剤中に0.001〜0.5重量%含まれていることを特徴とする請求項4に記載の消炎鎮痛貼付剤。   The anti-inflammatory analgesic patch according to claim 4, wherein 0.001 to 0.5% by weight of nonyl acid vanillylamide is contained in the base as a skin irritation component. 請求項1〜5の何れかに記載の消炎鎮痛貼付剤の製造法において、
加熱混練された基剤を2〜4日間冷暗所で放置した後、該基剤からなる基剤層を支持体上に形成した後、2〜4日間冷暗所で放置することを特徴とする消炎鎮痛貼付剤の製造法。
In the method for producing an anti-inflammatory analgesic patch according to any one of claims 1 to 5,
An anti-inflammatory analgesic patch characterized in that after the heat-kneaded base is left in a cool dark place for 2 to 4 days, a base layer comprising the base is formed on a support and then left in a cool dark place for 2 to 4 days. Manufacturing method.
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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007018210A1 (en) * 2005-08-10 2007-02-15 Hisamitsu Pharmaceutical Co., Inc. Adhesive patch less irritative to skin
CN102579602A (en) * 2012-03-06 2012-07-18 徐金红 Medicinal composition for treating eczema
CN104721397A (en) * 2015-03-03 2015-06-24 广西大学 Traditional Chinese medicine composition
CN104940631A (en) * 2015-07-06 2015-09-30 福建省古方医药投资管理有限公司 Ointment and preparation method thereof
WO2015174876A1 (en) * 2014-04-28 2015-11-19 Global Treat Srl. Ointment for the treatment of hemorrhoidal disease
CN108186948A (en) * 2018-03-08 2018-06-22 山西忻州兴华皮肤病专科医院 A kind of Chinese medicine preparation for treating qi depression to blood stasis psoriasis pustulosa

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JPH0336689Y2 (en) * 1982-11-08 1991-08-02
JPH07509453A (en) * 1992-07-23 1995-10-19 シュヴァルツ ファルマ アクチエンゲゼルシャフト Active substance plasters for low-melting and/or volatile active substances
JP2003113077A (en) * 2001-09-28 2003-04-18 Lion Corp Patch

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JPH0336689Y2 (en) * 1982-11-08 1991-08-02
JPH01151523A (en) * 1988-11-10 1989-06-14 Yamanouchi Pharmaceut Co Ltd 'shiun-ko' poultice and preparation thereof
JPH07509453A (en) * 1992-07-23 1995-10-19 シュヴァルツ ファルマ アクチエンゲゼルシャフト Active substance plasters for low-melting and/or volatile active substances
JP2003113077A (en) * 2001-09-28 2003-04-18 Lion Corp Patch

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007018210A1 (en) * 2005-08-10 2007-02-15 Hisamitsu Pharmaceutical Co., Inc. Adhesive patch less irritative to skin
JP2007045738A (en) * 2005-08-10 2007-02-22 Hisamitsu Pharmaceut Co Inc Patches with reduced skin irritation
CN102579602A (en) * 2012-03-06 2012-07-18 徐金红 Medicinal composition for treating eczema
WO2015174876A1 (en) * 2014-04-28 2015-11-19 Global Treat Srl. Ointment for the treatment of hemorrhoidal disease
US20170143768A1 (en) * 2014-04-28 2017-05-25 Global Treat Srl Ointment for the treatment of hemorrhoidal disease
CN104721397A (en) * 2015-03-03 2015-06-24 广西大学 Traditional Chinese medicine composition
CN104940631A (en) * 2015-07-06 2015-09-30 福建省古方医药投资管理有限公司 Ointment and preparation method thereof
CN108186948A (en) * 2018-03-08 2018-06-22 山西忻州兴华皮肤病专科医院 A kind of Chinese medicine preparation for treating qi depression to blood stasis psoriasis pustulosa

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