JP3973420B2 - Method for producing wound dressing - Google Patents
Method for producing wound dressing Download PDFInfo
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- JP3973420B2 JP3973420B2 JP2001400101A JP2001400101A JP3973420B2 JP 3973420 B2 JP3973420 B2 JP 3973420B2 JP 2001400101 A JP2001400101 A JP 2001400101A JP 2001400101 A JP2001400101 A JP 2001400101A JP 3973420 B2 JP3973420 B2 JP 3973420B2
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Description
【0001】
【発明の属する技術分野】
この発明は、絆創膏やドレッシング剤等、身体の傷面を覆い保護する創傷被覆材の製造方法に関する。
【0002】
【従来の技術】
従来、例えば特開昭59−139267号公報に開示されているように、ゼラチンや寒天に消毒剤を混合してゼリー化し、皮膚表面の殺菌消毒洗浄を目的としたゼリー状消毒剤が提案されている。また、殺菌消毒溶液をブリスターパックし、使用時にこのパックを破壊して薬液をパッド部に染み込ませて使用する傷絆創膏等も提案されている。
【0003】
【発明が解決しようとする課題】
上記従来技術では、製造コストが高く、製品の長期安定性や使用時にパックを破壊する等の操作が難しい等の欠点があった。
【0004】
この発明は上記従来の問題点に鑑みてなされたもので、製造が容易であり、コストも安価で、使用しやすく、殺菌効果を長時間持続することができる創傷被覆材の製造方法を提供することを目的とする。
【0005】
【課題を解決するための手段】
この発明は、パッド部に殺菌剤を溶解した含水ゲル層を有する創傷被覆材である。上記含水ゲル層はゲル支持体に保持され、このゲル支持体は粘着剤支持材に保持されており、上記含水ゲル層、ゲル支持体、粘着剤支持材はいずれも透明な材料で形成されていても良い。
【0006】
上記含水ゲル層は、エチルアルコール又は水溶性殺菌剤等の薬剤を含む含水ゲルの層である。また、上記含水ゲル層は、加熱して溶解し、冷却により固化する高分子多糖類等の水溶性高分子材料から成る。上記高分子多糖類の水溶性高分子材料は、マンナン、寒天、ゼラチン、ジェランガム、アラビアゴム、またはトラガントゴム等であり、その他ポリビニルピロリドンでも良く、これらから選ばれた一または複数の材料から成る高分子材料である。
【0007】
また、上記含水ゲル層は、化学反応により固化する水溶性高分子材料から成る。上記水溶性高分子材料は、アルギン酸ナトリウム、またはポリビニルアルコールを含む合成高分子である。
【0008】
上記ゲル支持体は、不織布、織布、またはナイロン製の網体であるナイロンネットである。上記含水ゲル層は、樹脂フィルムで成形した浅い容器内に設けられている。
【0009】
また、粘着剤支持材は、不織布、織布、樹脂フィルム等であり、粘着剤を塗布可能なものであればよい。特に、織布や不織布で構成した場合、含水ゲル層からの水分蒸発を促進し、創傷面の冷却効果が高くなる。
【0010】
またこの発明は、含水ゲルを構成する高分子多糖類である水溶性高分子の水溶液を、ゲル支持体の片面に部分的に吸着させ、ゲル化した後、上記ゲル支持体を粘着剤支持材の粘着剤層に貼り付ける創傷被覆材の製造方法である。上記含水ゲル層は、シート状の上記ゲル支持体上に一体に形成し、打ち抜きにより所定の大きさに形成し、このゲル支持体を粘着剤支持材の粘着剤層に貼付するものである。
【0011】
【発明の実施の形態】
以下、この発明の実施の形態について図面に基づいて説明する。図1,図2はこの発明の第一実施形態を示すもので、この実施形態の創傷被覆材10は、長方形の薄いポリエステル等のフィルムやテープ、その他薄い織布や不織布等から成る粘着剤支持材12と、この粘着剤支持材12の一面に設けられた粘着剤層14、及びこの粘着剤層14が形成された側の面の中央部に設けられた含水ゲル層16を備えている。含水ゲル層16は、ゲル支持体18に保持されてパッド部15を形成し、粘着剤層14に貼り付けられている。
【0012】
粘着剤層14は、一面に形成されていても良いが、ウェーブ塗工等により粘着剤支持材12の面に部分的に形成されていることにより通気性を有し、含水ゲル層16の水分蒸発を妨げない。
【0013】
また、粘着剤支持材12、粘着剤層14、含水ゲル層16、及びゲル支持体18を全て透明な材料で形成することにより、本発明の創傷被覆材10を貼付した状態で、患部を外部から観察することができる。
【0014】
含水ゲル層16は、水と混合し加熱して溶解するとともに、冷却により固化する高分子多糖類の水溶性高分子材料から成るゲルの層である。この水溶性高分子材料としては、マンナン、寒天、ゼラチン、ジェランガム、ポリビニルピロリドン、アラビアゴム、またはトラガントゴムから選ばれた一または複数の材料から成る。ゲル形成材の配合量は、全体の0.1〜5%程度である。
【0015】
また、含水ゲル層16の材料は、化学反応によりゲル化する水溶性高分子材料であっても良い。この水溶性高分子材料は、アルギン酸ナトリウム、またはポリビニルアルコールを含む合成高分子である。
【0016】
ゲル支持体18は、不織布、織布の薄い布で、目付量が30〜100g/m2、好ましくは50〜70g/m2で、伸縮性のある不織布が最も好ましい。ゲル支持体18を形成する繊維は、ポリエステル、ポリプロピレン、アクリル等の合成繊維の他、レーヨン、パルプ、コットン等の繊維も使用し得る。またはナイロン製の網体であるナイロンネットを用いても良い。
【0017】
含水ゲル層16及び粘着剤層14は、剥離しやすいようにエンボス処理又はシリコン塗工したポリエステルフィルムの剥離フィルム20で覆われている。
【0018】
含水ゲル層16には、殺菌剤として、アクリノール、グルコン酸クロルヘキシジン、セチルピリジウム、エチルアルコール、イソプロパノール、塩化ベンザルコニウム、マレイン酸クロルフェニラミン等が配合されている。さらに、局所麻酔剤として、リドカイン、皮膚修復剤としてアラントイン等の薬剤を配合しても良い。
【0019】
さらに、含水ゲル層16には、保湿剤として、グリセリン、イソプロピルアルコール、エチレングリコール、ポリプロピレングリコール、ポリエチレングリコール、1,3−ブチレングリコール、その他のポリグリセリン等を用いることができる。保湿剤の配合量は、含水ゲル層16の重量に対して0.1〜10%程度、好ましくは0.5〜5%である。
【0020】
この実施形態の含水ゲル層16には、有機塩類、油分、界面活性剤、無機粉体、無機塩類、防腐剤、pH調整剤、顔料、香料、その他薬効成分などをその使用目的に応じて用いることができる。
【0021】
次に、この実施形態の創傷被覆材10の製造方法について説明する。まず、含水ゲル層16の形成は、所定の薄い型内に水溶性高分子の水溶液を加熱して流し込み、その水溶液がゲル化する前に、不織布等のゲル支持体18をこの水溶性高分子水溶液表面に被せ、ゲル支持体18中にその溶液を染みこませ、ゲル化させる。または、大型の不織布等の支持体形性材料の表面に水溶性高分子水溶液を流し、ゲル化させ、この後、所定形状に含水ゲル層16及びゲル支持体18とも切断しても良い。この場合、任意の大きさの含水ゲル層16を得ることができる。
【0022】
含水ゲル層16がゲル化した後、所定形状のゲル支持体18を粘着剤層14の中央部に貼り付ける。そして、剥離フィルム20を粘着剤層14及び含水ゲル層18表面に貼り付け、密封して包装する。
【0023】
この実施形態の創傷被覆材とその製造方法によれば、皮膚の創傷面に含水ゲル層16が接触するので、細胞の増殖を妨害することなく自然治癒を早めることができる。また、含水ゲル層16の表面は、滑らかで柔軟性があるため、凹凸の創傷面にも密着することができ、ゲル内の薬剤が均一に創傷部位に作用し、細菌の侵入も確実に阻止する。含水ゲル層16は、創傷部位に癒着することが無く、治癒が早く、創傷被覆材10の交換時にも疼痛がない。また、ゲル支持体18が通気性を有するので、含水ゲル層16からの水分の蒸発による気化熱により、患部を冷却することができる。さらに、粘着剤支持材12を織布や不織布で構成した場合、含水ゲル層からの水分蒸発を促進し、創傷面の冷却効果が高い。また、含水ゲル層16を備えたパッド部15を手で押圧することにより、容易に含水ゲル層16のゲルが破壊して、ゲルの溶液を分離するので、ゲル中の薬剤が創傷面に浸透しやすい。
【0024】
次にこの発明の第二実施形態について説明する。この実施形態の創傷被覆材24は、含水ゲル層16が薄いCPPのフィルム容器26内に収容され、粘着剤層14もこのフィルム容器26のフィルムの延長部28により被覆されているものである。
【0025】
この実施形態の創傷被覆材24の製造方法は、まず、フィルム容器26内に上記と同様の水溶性高分子水溶液を流し込み、ゲル化する前に不織布等のゲル支持体18をフィルム容器24の開口部に被せ、水溶性高分子溶液をゲル支持体18に染みこませる。この後冷却して、含水ゲル層16が形成され、このゲル支持体18及びフィルム容器26の延長部28に粘着剤支持材12の粘着剤層14を貼り付ける。この後、密封して包装する。
【0026】
この実施形態によっても上記と同様の効果を得ることができ、さらに、含水ゲル層16を包装後も型くずれ等しないように保護する。
【0027】
なお、この発明の創傷被覆材とその製造方法は上記各実施形態に限定されるものではなく、粘着剤支持材は、穴あき樹脂フィルムや薄い布や不織布等でも良い。また、含水ゲル層の形状は適宜設定可能なものである。含水ゲル層への殺菌剤やその他の薬剤の配合は、溶解させる以外に、乳化や分散させるものでも良い。
【0028】
【実施例】
以下、この発明の第一実施例の創傷被覆材について説明する。この実施例では、寒天1.5部を精製水97.3に混ぜて加熱溶解し、90℃で保温しながらグリセンリン1部、アクリノール0.2部を順次混合し溶解する。この溶液2.225gを50mm×45mm、深さ1mmの樹脂製容器に滴下して容器内に液を充填する。そして、溶液がゲル化する前に、53mm×48mmに裁断した目付100g/m2のポリプロピレン不織布を容器開口部に載せて、不織布に溶液を染みこませ、溶液を冷却固化させ、不織布と含水ゲル層を一体化する。ゲル化した後、含水ゲル層と一体化した不織布を樹脂製容器から分離し、不織布面を粘着テープに貼着して、粘着面及び含水ゲル層に、シリコン塗工したポリエステルフィルムを貼り付け、密封包装する。
【0029】
次に、この発明の第二実施例の創傷被覆材について説明する。この実施例では、寒天1.5部を精製水82.1部に混ぜて加熱溶解し、90℃で保温しながら、エチルアルコール15部に塩化ベンザルコニウム0.1部、塩酸リドカイン1部、塩酸ナファゾリン0.1部、及びマレイン酸クロルフェニラミン0.2部を溶解した溶液を分散し混合する。この溶液0.3gを、20mm×14mm、深さ1mmの凹部を有し凹部側の表面にシリコン塗工したCPP樹脂フィルム製の容器内に滴下し、容器に溶液を充填する。そして、溶液がゲル化する前に、溶液面に22mm×16mmに裁断した目付100g/m2のポリプロピレン不織布を容器開口部に載せて、不織布に溶液が染みこむようにし、溶液を冷却固化させ、不織布と含水ゲル層を一体化する。ゲル化した後、不織布が表面に露出したフィルム容器及びその延長部分に、粘着テープを貼り付けて密封包装する。
【0030】
【発明の効果】
この発明の創傷被覆材の製造方法によれば、簡単な装置で安価に創傷被覆材を製造することができる。そして、皮膚の創傷面に含水ゲル層が接触するので、ガーゼ等が創傷面に当たる絆創膏と比較して細胞の増殖を妨害することなく自然治癒を早めることができる。また、含水ゲル層の表面は、滑らかで柔軟性があるため、創傷面を痛めることなく凹凸の創傷面にも密着することができ、ゲル内の薬剤が均一に創傷部位に作用し、細菌の侵入も確実に阻止する。さらに、含水ゲル層は創傷部位に癒着することが無く、治癒が早く、創傷被覆材の交換時にも疼痛がない。さらに、含水ゲル層からの水分の蒸発による気化熱により、患部を冷却することができる。
【図面の簡単な説明】
【図1】 この発明の第一実施形態の創傷被覆材平面図である。
【図2】 この実施形態の創傷被覆材の断面図である。
【図3】 この発明の第二実施形態の創傷被覆材の断面図である。
【符号の説明】
10 創傷被覆材
12 粘着剤支持材
14 粘着剤層
15 パッド部
16 含水ゲル層
18 ゲル支持体
20 剥離フィルム[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a method for manufacturing a wound dressing material that covers and protects a wound surface of a body, such as a bandage and a dressing agent.
[0002]
[Prior art]
Conventionally, as disclosed in, for example, Japanese Patent Application Laid-Open No. 59-139267, a jelly-like disinfectant for the purpose of sterilization and cleaning of the skin surface has been proposed by mixing gelatin or agar with a disinfectant to jelly. Yes. In addition, a wound adhesive plaster or the like in which a sterilizing / disinfecting solution is blister packed, and the pack is destroyed during use and a chemical solution is soaked into a pad portion.
[0003]
[Problems to be solved by the invention]
The above prior art has drawbacks such as high manufacturing costs, long-term stability of the product, and difficult operations such as breaking the pack during use.
[0004]
The present invention has been made in view of the above-described conventional problems, and provides a method for manufacturing a wound dressing that is easy to manufacture, inexpensive, easy to use, and capable of maintaining a bactericidal effect for a long time. For the purpose.
[0005]
[Means for Solving the Problems]
The present invention is a wound dressing material having a hydrogel layer in which a disinfectant is dissolved in a pad portion. The hydrated gel layer is held on a gel support, the gel support is held on an adhesive support, and the hydrated gel layer, gel support, and adhesive support are all made of a transparent material. May be.
[0006]
The hydrated gel layer is a hydrated gel layer containing a drug such as ethyl alcohol or a water-soluble disinfectant. The hydrated gel layer is made of a water-soluble polymer material such as a polymer polysaccharide that dissolves by heating and solidifies by cooling. The water-soluble polymer material of the above-mentioned polymer polysaccharide is mannan, agar, gelatin, gellan gum, gum arabic, or tragacanth rubber, and may be polyvinyl pyrrolidone, or a polymer composed of one or more materials selected from these. Material.
[0007]
The hydrogel layer is made of a water-soluble polymer material that is solidified by a chemical reaction. The water-soluble polymer material is a synthetic polymer containing sodium alginate or polyvinyl alcohol.
[0008]
The gel support is a non-woven fabric, a woven fabric, or a nylon net that is a nylon net. The hydrated gel layer is provided in a shallow container formed of a resin film.
[0009]
Moreover, the adhesive support material is a nonwoven fabric, a woven fabric, a resin film, or the like, as long as it can apply the adhesive. In particular, when composed of a woven fabric or a non-woven fabric, moisture evaporation from the hydrated gel layer is promoted, and the cooling effect on the wound surface is enhanced.
[0010]
Further, the present invention also includes an aqueous solution of a water-soluble polymer, which is a polymeric polysaccharide constituting a hydrous gel, partially adsorbed on one side of a gel support and gelled, and then the gel support is used as an adhesive support. It is a manufacturing method of the wound dressing material affixed on this adhesive layer. The hydrated gel layer is formed integrally on the sheet-like gel support, formed into a predetermined size by punching, and the gel support is affixed to the pressure-sensitive adhesive layer of the pressure-sensitive adhesive support.
[0011]
DETAILED DESCRIPTION OF THE INVENTION
Hereinafter, embodiments of the present invention will be described with reference to the drawings. 1 and 2 show a first embodiment of the present invention. A
[0012]
The pressure-sensitive
[0013]
Further, by forming the pressure sensitive adhesive support material 12, the pressure sensitive
[0014]
The water-containing
[0015]
The material of the
[0016]
The gel support 18 is a non-woven fabric or a thin woven fabric, and has a basis weight of 30 to 100 g / m 2 , preferably 50 to 70 g / m 2 , and is most preferably a stretchable non-woven fabric. As the fibers forming the gel support 18, fibers such as rayon, pulp and cotton can be used in addition to synthetic fibers such as polyester, polypropylene and acrylic. Alternatively, a nylon net that is a nylon net may be used.
[0017]
The
[0018]
The water-containing
[0019]
Further, glycerin, isopropyl alcohol, ethylene glycol, polypropylene glycol, polyethylene glycol, 1,3-butylene glycol, other polyglycerin, and the like can be used for the
[0020]
In the water-containing
[0021]
Next, the manufacturing method of the wound dressing 10 of this embodiment is demonstrated. First, the water-containing
[0022]
After the
[0023]
According to the wound dressing of this embodiment and the manufacturing method thereof, the
[0024]
Next, a second embodiment of the present invention will be described. In the wound dressing 24 of this embodiment, the
[0025]
In the method of manufacturing the wound dressing 24 of this embodiment, first, a water-soluble polymer aqueous solution similar to the above is poured into the
[0026]
According to this embodiment, the same effect as described above can be obtained, and further, the
[0027]
In addition, the wound dressing material of this invention and its manufacturing method are not limited to said each embodiment, A perforated resin film, a thin cloth, a nonwoven fabric, etc. may be sufficient as an adhesive support material. Moreover, the shape of the hydrogel layer can be set as appropriate. The disinfectant and other chemicals may be mixed in the water-containing gel layer in addition to being dissolved or emulsified or dispersed.
[0028]
【Example】
Hereinafter, the wound dressing of the first embodiment of the present invention will be described. In this example, 1.5 parts of agar is mixed with 97.3 purified water and dissolved by heating, and 1 part of glycenline and 0.2 part of acrinol are sequentially mixed and dissolved while keeping at 90 ° C. 2.225 g of this solution is dropped into a resin container having a size of 50 mm × 45 mm and a depth of 1 mm, and the container is filled with the liquid. Then, before the solution gels, a polypropylene nonwoven fabric having a basis weight of 100 g / m 2 cut to 53 mm × 48 mm is placed on the opening of the container, the solution is soaked into the nonwoven fabric, the solution is cooled and solidified, and the nonwoven fabric and the hydrous gel Integrate the layers. After gelling, the nonwoven fabric integrated with the hydrogel layer is separated from the resin container, the non-woven fabric surface is attached to the adhesive tape, and a silicone-coated polyester film is applied to the adhesive surface and the hydrogel layer, Seal and package.
[0029]
Next, a wound dressing according to a second embodiment of the present invention will be described. In this example, 1.5 parts of agar was mixed with 82.1 parts of purified water and dissolved by heating. While keeping at 90 ° C., 15 parts of ethyl alcohol was mixed with 0.1 part of benzalkonium chloride, 1 part of lidocaine hydrochloride, A solution in which 0.1 part of naphazoline hydrochloride and 0.2 part of chlorpheniramine maleate are dissolved is dispersed and mixed. 0.3 g of this solution is dropped into a container made of a CPP resin film having a recess of 20 mm × 14 mm and a depth of 1 mm and silicon-coated on the surface of the recess, and the container is filled with the solution. Then, before the solution is gelled, a polypropylene nonwoven fabric having a basis weight of 100 g / m 2 cut to 22 mm × 16 mm on the solution surface is placed on the container opening so that the solution soaks into the nonwoven fabric, and the solution is cooled and solidified. The nonwoven fabric and the hydrogel layer are integrated. After the gelation, an adhesive tape is attached to the film container with the nonwoven fabric exposed on the surface and its extended portion, and hermetically packaged.
[0030]
【The invention's effect】
According to the method for manufacturing a wound dressing of the present invention, a wound dressing can be manufactured at low cost with a simple apparatus. And since a hydrous gel layer contacts the wound surface of skin, natural healing can be accelerated | stimulated without interfering with the proliferation of a cell compared with the adhesive bandage which gauze etc. contact | wins a wound surface. In addition, since the surface of the hydrogel layer is smooth and flexible, it can adhere to an uneven wound surface without damaging the wound surface. Certainly prevent intrusion. Furthermore, the hydrogel layer does not adhere to the wound site, cures quickly, and does not cause pain when the wound dressing is replaced. Further, the affected part can be cooled by heat of vaporization caused by evaporation of water from the hydrous gel layer.
[Brief description of the drawings]
FIG. 1 is a plan view of a wound dressing according to a first embodiment of the present invention.
FIG. 2 is a cross-sectional view of the wound dressing of this embodiment.
FIG. 3 is a cross-sectional view of a wound dressing according to a second embodiment of the present invention.
[Explanation of symbols]
DESCRIPTION OF
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001400101A JP3973420B2 (en) | 2001-12-28 | 2001-12-28 | Method for producing wound dressing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001400101A JP3973420B2 (en) | 2001-12-28 | 2001-12-28 | Method for producing wound dressing |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003190206A JP2003190206A (en) | 2003-07-08 |
| JP3973420B2 true JP3973420B2 (en) | 2007-09-12 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001400101A Expired - Lifetime JP3973420B2 (en) | 2001-12-28 | 2001-12-28 | Method for producing wound dressing |
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| Country | Link |
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| JP (1) | JP3973420B2 (en) |
Cited By (2)
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| US10543347B2 (en) | 2015-02-24 | 2020-01-28 | Medrx Co., Ltd. | Delivery system for percutaneous absorption drug preparation and method for manufacturing same |
| US10932955B2 (en) | 2015-11-12 | 2021-03-02 | Medrx Co., Ltd. | Percutaneous absorption agent delivery device and manufacturing method therefor |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101510925B1 (en) | 2008-12-16 | 2015-04-15 | 히사미쓰 세이야꾸 가부시키가이샤 | Pressure-sensitive adhesive tape package |
| MX2011006899A (en) * | 2008-12-25 | 2011-08-03 | Hisamitsu Pharmaceutical Co | Pressure-sensitive adhesive tape package. |
| USD692147S1 (en) | 2011-04-22 | 2013-10-22 | Hisamitsu Pharmaceutical Co., Ltd. | Medical patch |
| JP6130130B2 (en) * | 2012-12-04 | 2017-05-17 | シスメックス株式会社 | Body fluid collector |
| CN103040559B (en) * | 2012-12-21 | 2014-10-08 | 薛磊 | Convenient thoracic cavity sealing device |
| CN108633253A (en) * | 2017-01-19 | 2018-10-09 | 崔性铉 | The alleviation and treatment of the exudative skin disease of plasma proteins including atopic diseases pad |
| WO2019222520A1 (en) | 2018-05-16 | 2019-11-21 | The Board Of Trustees Of The Leland Stanford Junior University | Controlled hydrogel delivery of focal adhesion kinase inhibitor for decreased scar formation |
| CN113288587B (en) * | 2021-07-28 | 2021-09-21 | 南通跃香拉链有限公司 | Outdoor first aid is with stanching bandage |
-
2001
- 2001-12-28 JP JP2001400101A patent/JP3973420B2/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10543347B2 (en) | 2015-02-24 | 2020-01-28 | Medrx Co., Ltd. | Delivery system for percutaneous absorption drug preparation and method for manufacturing same |
| US10932955B2 (en) | 2015-11-12 | 2021-03-02 | Medrx Co., Ltd. | Percutaneous absorption agent delivery device and manufacturing method therefor |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2003190206A (en) | 2003-07-08 |
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