JP3228562U - Nano thin film medicated compress - Google Patents

Nano thin film medicated compress Download PDF

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JP3228562U
JP3228562U JP2020003102U JP2020003102U JP3228562U JP 3228562 U JP3228562 U JP 3228562U JP 2020003102 U JP2020003102 U JP 2020003102U JP 2020003102 U JP2020003102 U JP 2020003102U JP 3228562 U JP3228562 U JP 3228562U
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縱曜光
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Abstract

【課題】柔軟に皮膚に付着し、かぶれを生じないナノ薄膜薬用湿布を提供する。【解決手段】漢方医薬成分原料をナノレベルに磨砕して高分子ゲル層化剤と混合して形成したゲル層35と、柔軟性と伸縮性を有するポリウレタン製等の弾性層及び弾性層とゲル層の間に塗層し、紫外線を照射して硬化した接着層37とからなり、ゲル層による貼付剤と弾性層からなる伸縮面32を有し、伸縮面には平均孔径200〜300ナノメートルの孔331が均一に分布して形成される。貼付面31となるゲル層を剥離フィルム10で覆い、伸縮面となる弾性層の外側を保護フィルム20で覆う。【選択図】図2PROBLEM TO BE SOLVED: To provide a nano-thin film medicated compress that flexibly adheres to skin and does not cause a rash. SOLUTION: A gel layer 35 formed by grinding a Chinese herbal medicine ingredient raw material to a nano level and mixing it with a polymer gel layering agent, and an elastic layer and an elastic layer made of polyurethane or the like having flexibility and elasticity. It is composed of an adhesive layer 37 that is coated between gel layers and cured by irradiating with ultraviolet rays, has an elastic surface 32 composed of an adhesive by the gel layer and an elastic layer, and the elastic surface has an average pore diameter of 200 to 300 nanometers. The metric holes 331 are formed evenly distributed. The gel layer to be the sticking surface 31 is covered with the release film 10, and the outside of the elastic layer to be the elastic surface is covered with the protective film 20. [Selection diagram] Fig. 2

Description

本考案は湿布に関し、特に薬用成分を含むゲル層を利用したナノ薄膜薬用湿布に関する。 The present invention relates to a poultice, and particularly to a nano-thin film medicated poultice using a gel layer containing a medicinal component.

従来の薬用湿布は粘着層を一枚の層にコーテイングし、一枚の剥離フィルムによって粘着層を覆って構成される。上述の粘着層は粘着剤と精油といった二つの成分を含み、該精油は漢方の薬草から抽出される。そのため、薬用湿布は人体外の肌に貼付できると共に漢方医薬の薬草効果を奏する。 Conventional medicated compresses are constructed by coating an adhesive layer into a single layer and covering the adhesive layer with a single release film. The above-mentioned adhesive layer contains two components, an adhesive and an essential oil, and the essential oil is extracted from Chinese herbs. Therefore, the medicinal compress can be applied to the skin outside the human body and has the herbal effect of Chinese herbs.

従来の薬用湿布は以下の欠点がある。
まず、精油は揮発性のために気散して薬用湿布の使用期限を縮めさせ、効果が劣化する。
次に、分厚い層は肌の表面に貼りにくく、捲れたり、剥がれたりする。特に、関節の部分に貼付した湿布はより外れやすく、剥がれやすい。
さらに、粘着層は皮膚と接触することで、肌が薬草のエキスを吸収することを助ける。反対に、精油は皮膚のかぶれを引き起こす可能性があり、ひどい場合は肌を傷つける。
従って、上述のような従来の薬用湿布の欠点のある構造を改善することは本考案の課題である。
Conventional medicated compresses have the following drawbacks.
First, the essential oil is volatile and dissipates, shortening the expiration date of the medicated compress and deteriorating its effect.
Next, the thick layer is difficult to stick to the surface of the skin and can be rolled up or peeled off. In particular, the compress attached to the joint part is easier to come off and peel off.
In addition, the adhesive layer comes into contact with the skin, helping it absorb the herbal extracts. Essential oils, on the other hand, can cause skin irritation and, in severe cases, can hurt the skin.
Therefore, it is an object of the present invention to improve the defective structure of the conventional medicated compress as described above.

特開2011−161166号公報Japanese Unexamined Patent Publication No. 2011-161166 実用新案登録第3174656号公報Utility Model Registration No. 3174656

本考案が解決しようとする課題は、従来の薬用湿布の構造における欠点について解決したナノ薄膜薬用湿布を提供する。 The problem to be solved by the present invention is to provide a nano-thin film medicated compress that solves the shortcomings in the structure of the conventional medicated compress.

本考案のナノ薄膜薬用湿布の主な目的は、ゲル層を採用して、生薬の効果を引き出し、皮膚のかぶれを防ぐ。
ゲル層の作成は、Moghania philippinensis35〜40%、当帰4〜7%、山奈4〜7%、乳香4〜7%、没薬(もつやく)4〜7%、白▲し▼(びゃくし)4〜7%、川▲きゅう▼(せんきゅう)4〜7%、秦▲ぎょう▼(じんぎょう)4〜7%、桂枝4〜7%、延胡索(えんごさく)4〜7%、冬緑油(とうりょくゆ)4〜7%と薄荷脳4〜7%を直径65〜100nmの微粉末に磨砕して混合・調剤した微粉末薬用成分90〜94%を低アレルギー性で粘着性を有する高分子化合物6〜10と混合して化学架橋又は物理的架橋によりゲル層を形成する。
The main purpose of the nano-thin film medicated compress of the present invention is to adopt a gel layer to bring out the effects of crude drugs and prevent skin irritation.
The gel layer was created by Moghania philippinensis 35-40%, Toki 4-7%, Yamana 4-7%, Frankincense 4-7%, Myrrh 4-7%, White ▲ ▼ (Byakushi) 4 ~ 7%, River ▲ Kyu ▼ (Senkyu) 4-7%, Hata ▲ Gyo ▼ (Jingyo) 4-7%, Keishi 4-7%, Myrrh (Engosaku) 4-7%, 9-7% of winter green oil and 4-7% of myrrh brain are ground into fine powder with a diameter of 65-100 nm and mixed / prepared. 90-94% of fine powder medicinal ingredients are hypoallergenic. A gel layer is formed by chemical cross-linking or physical cross-linking by mixing with polymer compounds 6 to 10 having adhesiveness.

ゲル層を有する湿布は、紫外線硬化型接着剤を柔軟性と伸縮性を有するポリウレタン(PU)製等の薄いシート状若しくは薄膜状の弾性層とゲル層の間に塗層し、紫外線を照射することで硬化して接着層が形成されることで、弾性層とゲル層が貼り合わされ、ゲル層の外側面は湿布の貼付面とし、弾性層の外側面は湿布の伸縮面とし、伸縮面には平均孔径が200〜300ナノメートルの孔を均一に分布して形成して通気性を持たせ、貼付面と伸縮面がある湿布が製造される。
湿布の貼付面を覆う剥離フィルムは、湿布の貼付面として使用するゲル層の外側を覆わせる。
湿布の伸縮面に付着する保護フィルムは、伸縮面として使用される弾性層の外側に付着させる。
A wet cloth having a gel layer is irradiated with ultraviolet rays by applying an ultraviolet curable adhesive between a thin sheet-like or thin thin elastic layer made of polyurethane (PU) or the like having flexibility and elasticity and the gel layer. By curing and forming an adhesive layer, the elastic layer and the gel layer are bonded together, and the outer surface of the gel layer is used as the adhesive surface of the wet cloth, and the outer surface of the elastic layer is used as the elastic surface of the wet cloth. Is formed by uniformly distributing pores having an average pore diameter of 200 to 300 nanometers to provide air permeability, and a wet cloth having a sticking surface and an elastic surface is produced.
The release film covering the poultice sticking surface covers the outside of the gel layer used as the poultice sticking surface.
The protective film that adheres to the stretchable surface of the compress adheres to the outside of the elastic layer used as the stretchable surface.

上述のような方法によって、本考案のナノ薄膜薬用湿布を製造する。主な目的は、薬用成分のナノの構造体を長時間に保存することで、湿布の使用期限を延長させ、かぶれる発生率を低下させ、従来技術における欠点を有効に解決する。 The nano-thin film medicated compress of the present invention is produced by the method as described above. The main purpose is to extend the expiration date of the compress, reduce the incidence of irritation, and effectively solve the drawbacks of the prior art by storing the nanostructure of the medicinal ingredient for a long time.

このため、本考案のナノ薄膜薬用湿布は、湿布の構造として貼付面と伸縮面とを含む。ゲル層は直径65〜100nmの微粉末を含み、該ゲル層の外側は湿布の貼付面として使用される。また、弾性層はゲル層の内側に接着され、該弾性層は湿布の外側の伸縮面として使用される。
該弾性層とゲル層の間には接着層があり、該接着層は紫外線硬化型接着剤層である。
該貼付面にゲル層の周囲を一周して囲む粘着物層があり、該粘着物層は弾性層に付着して形成され、湿布を患部に粘着させる。
Therefore, the nano-thin film medicated poultice of the present invention includes a sticking surface and an elastic surface as the structure of the poultice. The gel layer contains a fine powder having a diameter of 65 to 100 nm, and the outside of the gel layer is used as a sticking surface of a compress. Further, the elastic layer is adhered to the inside of the gel layer, and the elastic layer is used as an elastic surface on the outside of the compress.
There is an adhesive layer between the elastic layer and the gel layer, and the adhesive layer is an ultraviolet curable adhesive layer.
The sticking surface has an adhesive layer that surrounds the gel layer around the gel layer, and the adhesive layer is formed by adhering to the elastic layer to adhere the compress to the affected area.

また、本考案のナノ薄膜薬用湿布は少なくとも一枚の剥離フィルムと一枚の保護フィルムとを含む。該剥離フィルムは湿布の貼付面を覆い、該保護フィルムは湿布の伸縮面に付着する。さらに、切り離し線が剥離フィルムを大きい面積部と小さい面積部とに分割する。 Further, the nano-thin film medicated compress of the present invention includes at least one release film and one protective film. The release film covers the sticking surface of the compress, and the protective film adheres to the stretchable surface of the compress. Further, the separation line divides the release film into a large area portion and a small area portion.

本考案のナノ薄膜薬用湿布は、前記方法に従って製作したナノ薄膜薬用湿布に限らず、ゲル層を利用してナノサイズ級の微粉末からなる薬用成分の構造体を長期にわたって保存でき、生薬の効果と湿布の使用期限を延長させ、皮膚のかぶれを防げ、またはかぶれる発生率を低下させ、従来技術における欠点を有効に解決する。
また、該弾性層は通気性があり、防水性も優れ、多方向に伸びて広げられるため、本考案のナノ薄膜薬用湿布はしっかり人体の皮膚に付着でき、外れたり、はがれたりするなどの問題を心配しなくてもよい。
The nano-thin film medicated poultice of the present invention is not limited to the nano-thin film medicated poultice produced according to the above method, and the structure of the medicinal component composed of nano-sized fine powder can be stored for a long period of time by using the gel layer. It prolongs the expiration date of the compress, prevents skin irritation, or reduces the incidence of irritation, and effectively solves the drawbacks of the prior art.
In addition, since the elastic layer is breathable, has excellent waterproofness, and can be stretched and spread in multiple directions, the nano-thin film medicated compress of the present invention can firmly adhere to the skin of the human body, causing problems such as detachment and peeling. You don't have to worry about it.

図1は、本考案に係るナノ薄膜薬用湿布を示す立体図である。FIG. 1 is a three-dimensional view showing a nano-thin film medicated compress according to the present invention. 図2は、本考案に係るナノ薄膜薬用湿布を示す分解図である。FIG. 2 is an exploded view showing a nano-thin film medicated compress according to the present invention. 図3は、本考案の湿布本体の立体断面図である。FIG. 3 is a three-dimensional cross-sectional view of the compress body of the present invention. 図4は、本考案のナノ薄膜薬用湿布を製造する工程図である。FIG. 4 is a process diagram for manufacturing the nano-thin film medicated compress of the present invention.

以下に図面を参照して本考案の具体的内容を詳細に説明する。 The specific contents of the present invention will be described in detail below with reference to the drawings.

先ず、図1のように、湿布30の片面は剥離フィルム10があり、もう片面は短い保護フィルム20と長い保護フィルム25がある。長い保護フィルム25は短い保護フィルム20の一部分を重ねて覆う。
図中で、一本の切り離し線12によって剥離フィルム10を大きい面積部14と小さい面積部16を分ける。
First, as shown in FIG. 1, one side of the compress 30 has a release film 10, and the other side has a short protective film 20 and a long protective film 25. The long protective film 25 covers a part of the short protective film 20 in an overlapping manner.
In the figure, the release film 10 is divided into a large area portion 14 and a small area portion 16 by a single separation line 12.

図2は、該剥離フィルム10を切り離し線12に沿って切り離し、大きい面積部14と小さい面積部16をそれぞれ切り離し辺が形成される。該切り離し辺はぎざぎざであるため、その個所から大きい面積部14と小さい面積部16を捲ると、それぞれ湿布30の貼付面31から剥がれて剥離される。
また、前記長い保護フィルム25は波状の捲り辺27があり、短い保護フィルム20を覆う個所から該捲り辺27を捲ると、長い保護フィルム25を連続して湿布30の伸縮面32の一部分から剥がれて剥離される。また、該短い保護フィルム20も波状の捲り辺22があり、該捲り辺22は同様に捲られ、短い保護フィルム22は連続して残りの伸縮面32から剥離される。
剥離フィルム10と保護フィルム25とを剥離した湿布30は多辺形薄膜体である。
図3に示すように、該貼付面31は粘着物層34がゲル層35の外周領域を囲んで一周して形成され、該伸縮面32は湿布の外側の弾性層33からなる。
In FIG. 2, the release film 10 is separated along the separation line 12, and the large area portion 14 and the small area portion 16 are separated from each other to form a side. Since the cut-off side is jagged, when the large area portion 14 and the small area portion 16 are rolled up from the portion, they are peeled off from the sticking surface 31 of the compress 30 respectively.
Further, the long protective film 25 has a wavy winding side 27, and when the winding side 27 is rolled from a portion covering the short protective film 20, the long protective film 25 is continuously peeled off from a part of the elastic surface 32 of the compress 30. Is peeled off. Further, the short protective film 20 also has a wavy winding side 22, the winding side 22 is similarly wound, and the short protective film 22 is continuously peeled from the remaining elastic surface 32.
The compress 30 from which the release film 10 and the protective film 25 are peeled off is a polyhedron thin film body.
As shown in FIG. 3, the sticking surface 31 is formed by the adhesive layer 34 surrounding the outer peripheral region of the gel layer 35, and the elastic surface 32 is composed of the elastic layer 33 on the outside of the compress.

本実施例では、該粘着物層34が弾性層33に付着し、ゲル層35の周囲を囲んで形成される。いくつかの他の実施例では、粘着物層がなく、該貼付面31はゲル層35が湿布の外側表面となるが、これらも本考案の変更・応用の許容範囲内にある。
該弾性層33とゲル層35の間には接着層37があり、該接着層37は紫外線硬化型接着剤層であり、例えば、UV接着剤である。
In this embodiment, the adhesive layer 34 adheres to the elastic layer 33 and is formed so as to surround the gel layer 35. In some other embodiments, there is no sticky layer and the sticking surface 31 has a gel layer 35 as the outer surface of the compress, which is also within the permissible range of modifications and applications of the present invention.
There is an adhesive layer 37 between the elastic layer 33 and the gel layer 35, and the adhesive layer 37 is an ultraviolet curable adhesive layer, for example, a UV adhesive.

該ゲル層35には直径65〜100ナノメートル(nm)の微粉末36を含む。該顆粒36はMoghania philippinensis35〜40%、当帰4〜7%、山奈4〜7%、乳香4〜7%、没薬(もつやく)4〜7%、白▲し▼(びゃくし)4〜7%、川▲きゅう▼(せんきゅう)4〜7%、秦▲ぎょう▼(じんぎょう)4〜7%、桂枝3〜5%、延胡索(えんごさく)4〜7%、冬緑油(とうりょくゆ)4〜7%と薄荷脳4〜7%などの生薬を磨砕した微粉末から形成される。 The gel layer 35 contains a fine powder 36 having a diameter of 65 to 100 nanometers (nm). The granules 36 are Moghania philippinensis 35-40%, Toki 4-7%, Yamana 4-7%, Frankincense 4-7%, Myrrh 4-7%, White ▲ ▼ (Byakushi) 4-7. %, River ▲ Kyu ▼ (Senkyu) 4-7%, Hata ▲ Gyo ▼ (Jingyo) 4-7%, Katsura 3-5%, Corydalis yangosaku 4-7%, Winter green It is formed from fine powder obtained by grinding crude drugs such as 4-7% oil and 4-7% myrrh brain.

使用時、該湿布30の貼付面31を人体に向け、該ゲル層35を皮膚の表面に貼り付けるため、微粉末36が皮膚の外側に集中する。該伸縮面32は湿布30の外側にあり、人体関節の伸縮と回転、または皮膚の収縮に適応する。 At the time of use, the sticking surface 31 of the compress 30 is directed toward the human body, and the gel layer 35 is stuck on the surface of the skin, so that the fine powder 36 is concentrated on the outside of the skin. The stretchable surface 32 is on the outside of the compress 30 and adapts to the stretch and rotation of human joints or the contraction of the skin.

図4は工程図であり、ナノ薄膜薬用湿布の生産プロセスを簡単に紹介する。
ゲル層の作成40は、Moghania philippinensis35〜40%、当帰4〜7%、山奈4〜7%、乳香4〜7%、没薬(もつやく)4〜7%、白▲し▼(びゃくし)4〜7%、川▲きゅう▼(せんきゅう)4〜7%、秦▲ぎょう▼(じんぎょう)4〜7%、桂枝4〜7%、延胡索(えんごさく)4〜7%、冬緑油(とうりょくゆ)4〜7%と薄荷脳4〜7%を直径65〜100nmの微粉末に磨砕して混合・調剤した微粉末薬用成分90〜94%を低アレルギー性で粘着性を有する高分子化合物6〜10と混合して化学架橋又は物理的架橋によりゲル層を形成する。
FIG. 4 is a process diagram and briefly introduces the production process of the nano-thin film medicated compress.
Creation of gel layer 40 is Moghania philippinensis 35-40%, Toki 4-7%, Yamana 4-7%, Frankincense 4-7%, Myrrh 4-7%, White ▲ ▼ (Byakushi) 4-7%, River ▲ Kyu ▼ (Senkyu) 4-7%, Hata ▲ Gyo ▼ (Jingyo) 4-7%, Keishi 4-7%, Myrrh (Engosaku) 4-7% , Winter green oil (Toryokuyu) 4-7% and myrrh brain 4-7% are ground into fine powder with a diameter of 65-100 nm and mixed / prepared. 90-94% of fine powder medicinal ingredients are hypoallergenic. A gel layer is formed by chemical cross-linking or physical cross-linking by mixing with polymer compounds 6 to 10 having sex and adhesiveness.

図4の工程41で形成されるゲル層を有する湿布は、紫外線硬化型接着剤をポリウレタン(PU)製の弾性層とゲル層の間に塗層し、紫外線を照射することで硬化して接着層が形成されることで、弾性層33とゲル層35が貼り合わされ、ゲル層35の外側面は湿布の貼付面31とし、弾性層33の外側面は湿布の伸縮面32とし、伸縮面32には平均的に孔径が200〜300ナノメートルの孔331が均一に分布して形成されることにより通気性を付与し、ゲル層と弾性層とからなる貼付剤と伸縮面がある湿布が製造される。
工程42で形成される湿布の貼付面を覆う剥離フィルムは、剥離フィルムを貼付面として使用するゲル層の外側を覆わせる。
さらに、工程43で形成される湿布の伸縮面に付着する保護フィルムは、保護フィルムを伸縮面として使用される弾性層の外側に付着させる。
The wet cloth having a gel layer formed in step 41 of FIG. 4 is coated with an ultraviolet curable adhesive between an elastic layer made of polyurethane (PU) and a gel layer, and is cured and adhered by irradiating with ultraviolet rays. By forming the layer, the elastic layer 33 and the gel layer 35 are bonded to each other, and the outer surface of the gel layer 35 is the adhesive surface 31 of the wet cloth, and the outer surface of the elastic layer 33 is the elastic surface 32 of the wet cloth. The pores 331 having a pore diameter of 200 to 300 nanometers are uniformly distributed and formed to provide air permeability, and a patch consisting of a gel layer and an elastic layer and a wet cloth having an elastic surface are manufactured. Will be done.
The release film that covers the sticking surface of the compress formed in step 42 covers the outside of the gel layer that uses the release film as the sticking surface.
Further, the protective film attached to the elastic surface of the compress formed in step 43 attaches the protective film to the outside of the elastic layer used as the elastic surface.

このように、上述方法に従って製作したナノ薄膜薬用湿布は、ゲル層を利用してナノサイズ級微粉末(の顆粒)の構造体を長期にわたって保存でき、生薬の効果と湿布の使用期限を延長させ、皮膚のかぶれを防げ、またはかぶれる発生率を低下させ、従来技術における欠点を有効に解決する。また、該弾性層は通気性があり、防水性も優れ、多方向に伸びて広げられるため、本考案のナノ薄膜薬用湿布はしっかり人体の皮膚に付着でき、外れたり、はがれたりするなどの問題を心配しなくてもいい。 As described above, the nano-thin film medicated wet cloth produced according to the above method can store the structure of nano-sized fine powder (granule) for a long period of time by utilizing the gel layer, and prolongs the effect of the crude drug and the expiration date of the wet cloth. , Prevents skin irritation, or reduces the incidence of irritation, effectively resolving shortcomings in the prior art. In addition, since the elastic layer is breathable, has excellent waterproofness, and can be stretched and spread in multiple directions, the nano-thin film medicated compress of the present invention can firmly adhere to the skin of the human body, causing problems such as detachment and peeling. You don't have to worry about it.

10 剥離フィルム
12 切り離し線
14 大きい面積部
16 小さい面積部
20 短い保護フィルム
22、27 捲り辺
25 長い保護フィルム
30 湿布
31 貼付面
32 伸縮面
33 弾性層
331 孔
34 粘着物層
35 ゲル層
36 顆粒
37 接着層
40 ゲル層の作成
41 ゲル層を有する湿布
42 湿布の貼付面を覆う剥離フィルム
43 湿布の伸縮面に付着する保護フィルム


10 Release film 12 Separation line 14 Large area 16 Small area 20 Short protective film 22, 27 Rolled side 25 Long protective film 30 Poultice 31 Sticking surface 32 Elastic surface 33 Elastic layer 331 Hole 34 Adhesive layer 35 Gel layer 36 Granules 37 Adhesive layer 40 Creation of gel layer 41 Poultice with gel layer 42 Release film covering the sticking surface of the compress 43 Protective film adhering to the elastic surface of the compress


Claims (7)

ゲル層と、弾性層とを含むナノ薄膜薬用湿布であって、
上記湿布には貼付面と伸縮面とを含み、
上記ゲル層は、直径65〜100nmの微粉末からなる薬用成分を含み、該ゲル層の外側は湿布の貼付面として使用され、
また、上記弾性層はゲル層の内側に接着されて、湿布の外側の伸縮面として使用され、該伸縮面には平均孔径200〜300ナノメートルの孔が均一に分布して形成されることを特徴とするナノ薄膜薬用湿布。
A nano-thin film medicated compress containing a gel layer and an elastic layer.
The compress includes a sticking surface and an elastic surface,
The gel layer contains a medicinal component composed of a fine powder having a diameter of 65 to 100 nm, and the outside of the gel layer is used as a sticking surface of a compress.
Further, the elastic layer is adhered to the inside of the gel layer and used as an elastic surface on the outside of the compress, and holes having an average pore diameter of 200 to 300 nanometers are uniformly distributed and formed on the elastic surface. A featured nano-thin film medicated compress.
上記弾性層とゲル層の間には接着層があることを特徴とする請求項1のナノ薄膜薬用湿布。 The nano-thin film medicated compress according to claim 1, wherein an adhesive layer is provided between the elastic layer and the gel layer. 上記接着層は、紫外線硬化型接着剤層であることを特徴とする請求項2のナノ薄膜薬用湿布。 The nano-thin film medicated compress according to claim 2, wherein the adhesive layer is an ultraviolet curable adhesive layer. 上記貼付面には、ゲル層の周囲を一周して囲んで弾性層に付着する粘着物層があることを特徴とする請求項2のナノ薄膜薬用湿布。 The nano-thin film medicated compress according to claim 2, wherein the sticking surface has an adhesive layer that surrounds the gel layer and adheres to the elastic layer. 一枚の剥離フィルムにより湿布の前記貼付面を覆うことを特徴とする請求項1のナノ薄膜薬用湿布。 The nano-thin film medicated compress according to claim 1, wherein the sticking surface of the compress is covered with a single release film. 上記剥離フィルムは切り離し線によって大きい面積部と小さい面積部に分けられることを特徴とする請求項5のナノ薄膜薬用湿布。 The nano-thin film medicated compress according to claim 5, wherein the release film is divided into a large area portion and a small area portion by a separation line. 少なくとも一枚の保護フィルムにより湿布の伸縮面を覆うことを特徴とする請求項1のナノ薄膜薬用湿布。

The nano-thin film medicated wet cloth according to claim 1, wherein the elastic surface of the wet cloth is covered with at least one protective film.

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