JPH0490764A - Covering material for wound - Google Patents

Covering material for wound

Info

Publication number
JPH0490764A
JPH0490764A JP20499690A JP20499690A JPH0490764A JP H0490764 A JPH0490764 A JP H0490764A JP 20499690 A JP20499690 A JP 20499690A JP 20499690 A JP20499690 A JP 20499690A JP H0490764 A JPH0490764 A JP H0490764A
Authority
JP
Japan
Prior art keywords
wound
porous
membrane
hydrophilic polymer
polyolefin membrane
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.)
Granted
Application number
JP20499690A
Other languages
Japanese (ja)
Other versions
JP2896210B2 (en
Inventor
Mikio Koide
小出 幹夫
Masato Onishi
誠人 大西
Yukio Kiyota
清田 由紀夫
Takeo Katakura
片倉 健男
Akira Takahashi
晃 高橋
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.)
Terumo Corp
Original Assignee
Terumo Corp
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 Terumo Corp filed Critical Terumo Corp
Priority to JP20499690A priority Critical patent/JP2896210B2/en
Priority to AU81524/91A priority patent/AU640507B2/en
Priority to DE1991608136 priority patent/DE69108136T2/en
Priority to EP19910402183 priority patent/EP0470007B1/en
Publication of JPH0490764A publication Critical patent/JPH0490764A/en
Application granted granted Critical
Publication of JP2896210B2 publication Critical patent/JP2896210B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To promote a regeneration of skins by bonding a hydrophilic polymer chemically onto one surface of a porous polyolefin film to make a surface contacting a skin missing part lubricate by hydration. CONSTITUTION:A wound cover material is a porous polyolefin film or a porous polyolefin halide film bonded to a hydrophilic polymer chemically. In the cover material thus obtained, a pore diameter is preferably in a range of 0.01-1.0mum and a steam permeability in a range of 200-5000mg/m<2> per 24 hours. An antibacterial metal is evaporated and held on a surface where the hydrophilic polymer is bonded, thereby enabling the prevention of infection to wounds.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、創傷被覆材に関するものである。詳しく述べ
ると、本発明は創傷、熱傷等による皮膚欠損受傷の際、
該皮膚欠損部位に適用され、該皮膚欠損部位と接する面
を水和潤滑状態にして、表皮再生を促進する創傷被覆材
に関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to wound dressings. Specifically, the present invention provides treatment for skin defects caused by wounds, burns, etc.
The present invention relates to a wound dressing that is applied to the skin defect site and promotes epidermal regeneration by bringing the surface in contact with the skin defect site into a hydrated and lubricated state.

〔従来の技術〕[Conventional technology]

外傷性の皮膚創傷および採皮創等の創傷および疾患に伴
う創部に対する創傷治療方法としては、大別して創傷部
を乾燥状態に保ち、癲皮を形成させて治癒を行う、いわ
ゆるdry dressingと、適度の湿潤環境をつ
くり、速やかな表皮細胞の遊走を行うwet dres
singとが知られており、後者は創傷の治癒も速やか
であり、創傷部表面の乾燥壊死が少なく、創面の保護効
果も有することなどが知られている。
Wound treatment methods for wounds such as traumatic skin wounds and skin harvest wounds, as well as wounds associated with diseases, can be broadly divided into dry dressing, which keeps the wound dry and forms epidermis, and heals. Wet dress creates a moist environment for rapid migration of epidermal cells.
The latter is known to have rapid wound healing, less dry necrosis on the surface of the wound, and a protective effect on the wound surface.

しかし、yet dressjngの一方法であるサー
ジカルドレープを用いる方法では、浸出液の貯留が多く
創面に再吸収されるおそれがあり、また感染の危険も大
きく、接着剤が直接創面と接するため、創傷治癒に有害
と思われる問題点があることが指摘されている。また、
創面から剥がれやすいこともあり、創面と接する部分に
小さな突起を付けたものもあるが、逆に除去困難という
欠点を有するなどの問題点があった。
However, with the method of using a surgical drape, which is one method of yet dressing, a large amount of exudate accumulates and there is a risk of reabsorption into the wound surface, and there is also a high risk of infection, and the adhesive comes into direct contact with the wound surface, making it difficult for wound healing to occur. It has been pointed out that there are problems that seem to be harmful. Also,
Because they tend to peel off from the wound surface, some have small protrusions attached to the part that comes in contact with the wound surface, but they have the disadvantage of being difficult to remove.

これらの問題点を解決するため近年では被覆材の創傷部
と接触する部位にコラーゲン、キチン、フィブリン等の
生体高分子を用いるもの、あるいはゴム系の素材中に保
湿成分を分散させ密着・非癒着・高含水状態の確保など
を図ったもの、さらには本発明者らが以前提案した創傷
部に接触する部位の少なくとも一部が撓水性物質により
被覆された生体適合性のヒドロゲル形成性の支持層(例
えば、カルボキシメチルセルロース、アルギン酸塩系、
ヒアルロン酸塩系、ポリ(メタ)アクリル酸塩系)と、
該支持層の創傷部に接触する部位とは反対側に形成され
た水分透過調節層とからなる創傷被覆材(特開昭82−
183780号公報)等があり、一定の成果をおさめて
いる。
In order to solve these problems, in recent years, dressings that use biopolymers such as collagen, chitin, and fibrin in the part of the dressing that comes into contact with the wound, or that have moisturizing ingredients dispersed in rubber-based materials, have been developed to provide better adhesion and non-adhesion.・Those designed to maintain a high water content state, and furthermore, a biocompatible hydrogel-forming support layer in which at least a portion of the part that contacts the wound area is coated with a water-repellent substance, as previously proposed by the present inventors. (For example, carboxymethylcellulose, alginate-based,
hyaluronate-based, poly(meth)acrylate-based),
A wound dressing comprising a moisture permeation regulating layer formed on the side of the supporting layer opposite to the part that contacts the wound (Japanese Patent Application Laid-open No. 1982-
183780), and has achieved a certain degree of success.

一方、dry dressingとして多孔質高分子膜
があるが、この場合dress+ngが創面に固着して
しまい剥す際に出血を伴う為、最近では創面と接触する
部位には非粘着性多孔フィルム(Melol in@)
Sfflith & Nephew Lia+jted
)を使用したドレッシングが市販されている。
On the other hand, porous polymer membranes are available as dry dressings, but in this case dress+ng sticks to the wound surface and causes bleeding when removed, so recently non-adhesive porous films (Melol in@ )
Sfflith & Nephew Lia+jted
) is commercially available.

また創傷面や傷口の縫合部では感染が起こりやすい為、
抗菌剤を含有したクリーム基剤を使用して感染防止を行
っている。しかし、抗菌剤をガーゼに練り込んだ場合、
滲出液とともにガーゼ包帯に約57%が染み込み、創面
に約21%しか到達しない。またクリーム基剤では毎日
のように創傷面に塗り込むなど操作上面倒である。
In addition, infection is likely to occur on the wound surface and the sutured part of the wound.
A cream base containing antibacterial agents is used to prevent infection. However, when antibacterial agents are kneaded into gauze,
About 57% of the exudate soaks into the gauze bandage, and only about 21% reaches the wound surface. In addition, cream-based products are cumbersome to use, as they have to be applied to the wound surface every day.

〔発明が解決しようとする課題〕[Problem to be solved by the invention]

上記従来の被覆材もある程度の効果は有しているが、創
傷部と接触する部分の生体適合性を有する基剤層の形成
に用いられている材料が、分解、脱落しやすく、創傷被
覆材としての使用時における物性に問題があり、さらに
、その分解、離脱物が異物として認識されることがあり
、創傷部の治癒を遅延させる危険性があった。また、支
持層の創傷部に接触する部位とは反対側に形成される水
分透過調節層は、適度な水分透過能と細菌侵入阻止能を
有していることが必要とされるが、この両者の性質を満
足させる材料は、かなり限定されるものであった。
Although the conventional dressings mentioned above are effective to some extent, the material used to form the biocompatible base layer in the part that comes into contact with the wound easily decomposes and falls off. There are problems with the physical properties when used as a wound, and furthermore, the decomposition and detachment may be recognized as foreign matter, posing the risk of delaying the healing of the wound. In addition, the moisture permeation regulating layer formed on the side of the support layer opposite to the part that contacts the wound area is required to have appropriate moisture permeability and bacterial invasion prevention ability; Materials that satisfy these properties are quite limited.

そこで、本発明は創面への良好な密着性を有し、創傷部
と接触しても容易に分解、離脱することがなく、創傷部
の治癒、特に表皮再生が促進され、創傷部の早期の治癒
を行うことができ、また多孔質ポリオレフィン膜が水蒸
気透過性を兼ね備えた創傷被覆材を提供することを目的
とする。
Therefore, the present invention has good adhesion to the wound surface, does not easily decompose or detach even if it comes into contact with the wound, promotes healing of the wound, especially epidermal regeneration, and promotes early recovery of the wound. The object of the present invention is to provide a wound dressing that is capable of healing and whose porous polyolefin membrane is water vapor permeable.

また広範囲熱傷や■度熱傷では感染が起こりやすい為、
抗菌剤を含有したクリーム基剤を使用して感染防止を行
っている。しかし、このうち滲出液とともにガーゼ包帯
に約57%が染み込み、創傷面には約21%しか到達し
ない。また、クリーム基剤では毎日のように創傷面に塗
り込むなど操作上面倒である。この膜に抗菌性のある金
属を蒸着させれば、外部からの感染防止のみならず、創
面が細菌により汚染されている場合にも適応することが
できる。
In addition, extensive burns and second-degree burns are susceptible to infection, so
A cream base containing antibacterial agents is used to prevent infection. However, about 57% of the exudate soaks into the gauze bandage, and only about 21% reaches the wound surface. In addition, cream-based products are cumbersome to use, as they have to be applied to the wound surface every day. By depositing an antibacterial metal on this membrane, it can not only prevent infection from the outside, but also be used when the wound surface is contaminated with bacteria.

〔課題を解決するための手段〕[Means to solve the problem]

上記目的は下記の構成を有する創傷被覆材によって達成
される。
The above object is achieved by a wound dressing having the following structure.

(1)多孔質ポリオレフィン膜あるいは多孔質ハロゲン
化ポリオレフィン膜の一方の表面に親水性ポリマーを化
学的に結合させてなることを特徴とする創傷被覆材。
(1) A wound dressing material characterized by having a hydrophilic polymer chemically bonded to one surface of a porous polyolefin membrane or a porous halogenated polyolefin membrane.

(2)多孔質ポリオレフィン膜の平均孔径が0.01〜
1.0−である1項に記載の創傷被覆材。
(2) The average pore diameter of the porous polyolefin membrane is 0.01~
The wound dressing according to item 1, which is 1.0-.

(3)多孔質ポリオレフィン膜の水蒸気透過率が200
〜5000mg/ rn” ・24hrである1または
2項に記載の創傷被覆材。
(3) Water vapor permeability of porous polyolefin membrane is 200
The wound dressing according to item 1 or 2, which has a dosage of ~5000 mg/rn"/24 hr.

(4)多孔質ポリオレフィン膜あるいは多孔質ハロゲン
化ポリオレフィン膜の親水性ポリマーを結合させた面に
抗菌性を有する金属を蒸着させてなる1乃至3項のいず
れかの項に記載の創傷被覆材。
(4) The wound dressing material according to any one of items 1 to 3, comprising a porous polyolefin membrane or a porous halogenated polyolefin membrane, on which a hydrophilic polymer-bonded surface is coated with a metal having antibacterial properties.

本発明の創傷被覆材は、上記のように多孔質ポリオレフ
ィン股あるいは多孔質ハロゲン化ポリオレフィン膜に親
水性ポリマーを化学的に結合させたものからなり、皮膚
欠損部位に接する面を水和潤滑状態にして1、表皮再生
を促進することができる。
The wound dressing of the present invention is made of a porous polyolefin crotch or a porous halogenated polyolefin membrane with a hydrophilic polymer chemically bonded to it, as described above, and keeps the surface in contact with the skin defect site in a hydrated and lubricated state. 1. It can promote epidermal regeneration.

本発明に用いられる膜は多孔質ポリオレフィン膜あるい
は多孔質ハロゲン化ポリオレフィン膜であり、汎用で低
価格な面を考慮すると、ポリエチレン、ポリプロピレン
、ポリフッ化ビニリデン、ポリ塩化ビニリデン、塩素化
ポリエチレンなどが好ましい。多孔質ポリオレフィン膜
あるいは多孔質ハロゲン化ポリオレフィン膜に結合させ
る親水性ポリマーとしてはメトキシエチルアクリレート
あるいはN−ジメチルアクリルアミドがあげられ、これ
らを上記ポリオレフィン膜にグラフト重合させることに
より化学的に結合させるポリメトキシエチルアクリレー
トは生体適合性に優れており、生体組織と接触しても異
物反応が少ないという利点ををする。得られた被覆材は
、孔径0,01〜1.0μm、水蒸気透過率200〜5
000mg/ m” ・24hrの範囲内にあるものが
よい。
The membrane used in the present invention is a porous polyolefin membrane or a porous halogenated polyolefin membrane, and polyethylene, polypropylene, polyvinylidene fluoride, polyvinylidene chloride, chlorinated polyethylene, etc. are preferable in view of general use and low cost. Hydrophilic polymers to be bonded to the porous polyolefin membrane or porous halogenated polyolefin membrane include methoxyethyl acrylate or N-dimethylacrylamide, and polymethoxyethyl acrylate and N-dimethylacrylamide are chemically bonded to the polyolefin membrane by graft polymerization. Acrylate has excellent biocompatibility and has the advantage of less foreign body reaction when it comes into contact with living tissue. The obtained coating material has a pore size of 0.01 to 1.0 μm and a water vapor permeability of 200 to 5.
000mg/m”・24hr is preferable.

本発明において抗閑剤として使用される金属は銀、銅又
は亜鉛等であるか、抗菌性の点から銀が好ましい。また
膜表面に存在させる金属は2種類以上であっても良いし
、金属単体、酸化物または塩の状態であってもよい。そ
して多孔質膜に存在させる金属の量については、特に限
定されないが、コスト而、溶出金属による2次汚染等か
ら、膜表面に存在させる金属は膜表面のX線光電子スペ
クトルによる金属原子/炭素原子の存在比が0.02〜
5.0の範囲内にあるものが良い。金属原子/炭素原子
が5.0を越えると、膜表面での金属存在比が過剰とな
り、抗菌性を有するものの、孔径が付着した金属により
、縮小化して膜本来の水蒸気透過性が失われてしまう。
The metal used as the antifungal agent in the present invention is silver, copper, zinc, etc., and silver is preferred from the viewpoint of antibacterial properties. Further, two or more types of metals may be present on the film surface, or they may be in the form of a single metal, an oxide, or a salt. The amount of metal present in the porous membrane is not particularly limited, but due to cost and secondary contamination due to eluted metals, the amount of metal present on the membrane surface is determined by the X-ray photoelectron spectrum of the membrane surface. The abundance ratio is 0.02~
A value within the range of 5.0 is good. When the metal atom/carbon atom ratio exceeds 5.0, the metal abundance ratio on the membrane surface becomes excessive, and although it has antibacterial properties, the pore size is reduced by the attached metal and the membrane loses its original water vapor permeability. Put it away.

又、過剰に金属が付着してこの金属が薄膜化してしまう
と、孔が閉塞されたり、金属層が衝撃等で剥離するばか
りか、非経済的である。逆に金属原子/炭素原子比が0
.02以下であると、安定した抗菌性が失われる虞があ
る。
Furthermore, if an excessive amount of metal adheres and the metal becomes thin, the pores may become clogged, the metal layer may peel off due to impact, etc., and this is uneconomical. Conversely, the metal atom/carbon atomic ratio is 0
.. If it is less than 02, stable antibacterial properties may be lost.

〔作  用〕[For production]

本発明の創傷被覆材は例えば次のようにして製造される
。まず、ポリプロピレン粉末に所定量の流動パラフィン
及び結晶核形成剤を加えて溶融混練しベレット化する。
The wound dressing of the present invention is manufactured, for example, as follows. First, a predetermined amount of liquid paraffin and a crystal nucleating agent are added to polypropylene powder and melt-kneaded to form pellets.

このベレットを150〜200℃で溶融し、Tダイ付押
出機により押出し、冷却固定化液中に導き冷却固定化し
てフィルムにし、該フィルム中の流動パラフィンの抽出
を行い、135°C程度の空気中で約2分間熱処理を行
い、ポリプロピレン膜の多孔質膜を得る。該膜にメトキ
シエチルアクリレートをプラズマ開始表面グラフト重合
し、親水化処理したポリプロピレン膜の多孔質膜を得る
。この膜の湿潤下での表面の潤滑性を表1に示した。
This pellet is melted at 150 to 200°C, extruded using an extruder equipped with a T-die, introduced into a cooling fixation liquid, cooled and fixed, and made into a film, and the liquid paraffin in the film is extracted. A heat treatment is performed for about 2 minutes in a polypropylene film to obtain a porous polypropylene film. Plasma-initiated surface graft polymerization of methoxyethyl acrylate is performed on the membrane to obtain a porous polypropylene membrane subjected to hydrophilic treatment. Table 1 shows the surface lubricity of this film under wet conditions.

表 1 創傷被覆材の表面潤滑性 材料表面の湿潤下での表面潤滑性の度合を、平均摩擦係
数(摩擦抵抗)と摩擦係数の変動(いわゆるさらさら感
)より求めることができる。
Table 1 Surface Lubricity of Wound Dressing Material The degree of surface lubricity of the surface of a material under wet conditions can be determined from the average coefficient of friction (frictional resistance) and the variation in the coefficient of friction (so-called dry feeling).

未処理のポリプロピレン膜では平均摩擦係数と摩擦係数
の変動が高い値を示すのに対して、メトキシエチルアク
リレートで親水化処理を施すと、低い値を示し、湿潤下
で非常にざらつき感か低く、ぬるぬるとした水和状態と
なる。
While the untreated polypropylene film shows high values of average friction coefficient and friction coefficient variation, the hydrophilic treatment with methoxyethyl acrylate shows low values, with very low roughness under wet conditions. It becomes a slimy hydrated state.

次にこの多孔質膜を真空蒸着用のペルジャー内に収容し
、ペルジャー内を減圧し、所定時間銀を真空蒸着する。
Next, this porous membrane is placed in a Pel jar for vacuum deposition, the pressure inside the Pel jar is reduced, and silver is vacuum deposited for a predetermined period of time.

尚、膜表面に金属を存在させる方法は、他にスパッタリ
ング法、イオンビーム法等があり、特に限定されない。
Note that the method for making metal present on the film surface is not particularly limited, and there are other methods such as sputtering method and ion beam method.

上記で得られた金属が膜に蒸着した多孔質膜上に、アク
リル系の接着剤を精密被覆用具(アプリケーター)を用
いて塗布させることにより、本発明の創傷被覆材が作成
される。
The wound dressing of the present invention is prepared by applying an acrylic adhesive using a precision coating tool (applicator) onto the porous membrane on which the metal obtained above is vapor-deposited.

本発明の創傷被覆材は、膜表面に金属を存在させたので
、この金属による抗菌作用によって、細菌の増殖が抑制
される。
Since the wound dressing of the present invention has metal present on the membrane surface, the antibacterial action of this metal suppresses the growth of bacteria.

〔実 施 例〕〔Example〕

以下、実施例を示して本発明をさらに具体的に説明する
Hereinafter, the present invention will be explained in more detail with reference to Examples.

実施例 1 メルトフローインデックスが30及び0.3のポリプロ
ピレン混合物(混合重量比1(10: 40) 100
重量部当り、400重量部の流動パラフィン(平均分子
量324)及び0.3重量部の結晶核形成剤としての1
.3,2.4−ビス(p−エチルベンジリデン)ソルビ
トールを二軸型押出機により溶融混練し、ペレット化し
た。このベレットを上記二輪型押出機を用いて150〜
200℃で溶融し、スリット0.6wのTダイより空気
中に押出しフィルム状にし、このフィルム状物をTダイ
直下に置かれたがイドローラーによって冷却固定化液中
に導き冷却固定化した後巻取る。この巻取ったフィルム
状物を一定寸法に切断し、縦横両方向に固定し、1.1
.2−トリクロロ−L2,2−トリフルオロエタン中に
lO分間計4同浸漬して、フィルム状物中の流動パラフ
ィンの抽出を行う。次いで135℃の空気中で2分間熱
処理を行って、孔径0,6趨、膜厚140μのポリプロ
ピレン製多孔質膜を得た。
Example 1 Polypropylene mixture with melt flow index of 30 and 0.3 (mixing weight ratio 1 (10:40) 100
Per part by weight, 400 parts by weight of liquid paraffin (average molecular weight 324) and 0.3 parts by weight of 1 as a crystal nucleating agent.
.. 3,2.4-bis(p-ethylbenzylidene) sorbitol was melt-kneaded using a twin-screw extruder and pelletized. This pellet was processed using the above two-wheeled extruder to
It was melted at 200°C and extruded into a film through a T-die with a slit of 0.6W into the air, and this film-like material was placed directly under the T-die and was guided into a cooling fixing liquid by an idle roller and cooled and fixed. Wind it up. Cut this rolled-up film-like material into a certain size, fix it both vertically and horizontally, and 1.1
.. The liquid paraffin in the film-like material is extracted by immersing it in 2-trichloro-L2,2-trifluoroethane for a total of 4 1O minutes. Next, heat treatment was performed in air at 135° C. for 2 minutes to obtain a polypropylene porous membrane having a pore size of 0.6 and a thickness of 140 μm.

この膜にN、N−ジメチルアクリルアミドをプラズマ開
始表面グラフト重合し親水化したポリプロピレン膜を得
た。
This membrane was subjected to plasma-initiated surface graft polymerization of N,N-dimethylacrylamide to obtain a hydrophilic polypropylene membrane.

実施例 2 ポリフッ化ビニリデン粉末(三菱油化■製Kynar 
K2O2) 18重量部をアセトン73.8重量部及び
ジメチルホルムアミド8.2uffi部に溶解してなる
溶液を、ポリエチレンテレフタレートフィルム上にキャ
ストした後、1.1.2−トリフルオロエタン浴中に5
分間浸漬し、乾燥して平均孔径0.45ums膜厚13
5節のポリフッ化ビニリデン多孔質膜を得た。
Example 2 Polyvinylidene fluoride powder (Kynar manufactured by Mitsubishi Yuka)
A solution of 18 parts by weight of K2O2) dissolved in 73.8 parts by weight of acetone and 8.2 parts of dimethylformamide was cast onto a polyethylene terephthalate film, and then 1.1.
Soak for minutes, dry, average pore size 0.45 um, film thickness 13
A five-node polyvinylidene fluoride porous membrane was obtained.

この膜にN、N−ジメチルアクリルアミドをプラズマ開
始表面グラフト重合し親水化したポリフッ化ビニリデン
膜を得た。
This membrane was subjected to plasma-initiated surface graft polymerization of N,N-dimethylacrylamide to obtain a hydrophilic polyvinylidene fluoride membrane.

実施例 3 実施例1で得られた多孔質膜に銀をスパッタリング蒸着
する。このスパッタリング蒸着は、まず多孔質膜を真空
蒸着用のペルジャーに設置し、10’Torrにまず減
圧した後、シャーターを開いて多孔質膜に所定時間銀を
スパッタリング蒸着した。
Example 3 Silver is deposited on the porous membrane obtained in Example 1 by sputtering. In this sputtering deposition, the porous film was first placed in a Pel jar for vacuum deposition, the pressure was first reduced to 10' Torr, the shutter was opened, and silver was deposited on the porous film by sputtering for a predetermined period of time.

試験例 1 [抗菌性の評価コ Hut lcr −Hilton Agar(Difc
o社製)をオートクレーブにかけた後50℃に保ち、2
0m1ずつシャーレに分注し、1時間室温に放置し固め
た。菌は平板で培養した後、トリス緩衝液中に各種の菌
を懸濁して菌液とし、培地上に綿棒で3回ずつ全体に塗
布した。実施例3の方法で調製した試料を直径8關に切
りぬき、菌を塗布した培地上に置き、37℃で18時間
培養した。結果を表1に示した。
Test Example 1 [Antibacterial evaluation method Hut lcr - Hilton Agar (Difc
(manufactured by company o) was autoclaved and kept at 50℃,
0ml each was dispensed into petri dishes and left to solidify at room temperature for 1 hour. After culturing the bacteria on a flat plate, each type of bacteria was suspended in Tris buffer to obtain a bacterial solution, which was applied to the entire surface of the medium three times using a cotton swab. The sample prepared by the method of Example 3 was cut into 8 diameter pieces, placed on a culture medium coated with bacteria, and cultured at 37°C for 18 hours. The results are shown in Table 1.

試験例 2 実施例3の方法で調製した本発明の創傷被覆材と、多孔
質ポリプロピレン膜に銀を蒸着させた親水性ポリマーを
介しない創傷被覆材について、試験例1と同様の方法で
抗菌性の評価を行なった。
Test Example 2 Antibacterial properties were tested in the same manner as in Test Example 1 for the wound dressing of the present invention prepared by the method of Example 3 and the wound dressing without a hydrophilic polymer in which silver was vapor-deposited on a porous polypropylene membrane. We conducted an evaluation.

結果を表2に示す。The results are shown in Table 2.

〔発明の効果〕〔Effect of the invention〕

本発明の創傷被覆材は熱傷、採皮創および皮膚剥削傷、
外傷性皮膚欠損側等の疾患ないし、創傷による患部に適
用された際に、適当な水蒸気透過性と創面との接触面を
水和潤滑状態にして、創面に密着し表皮再生を促進する
ことができ、特に抗菌性を付与した金属を保持させるこ
とによって、傷口への感染を防止することができる。
The wound dressing of the present invention can be applied to burns, skin harvest wounds and dermabrasion wounds,
When applied to areas affected by diseases such as traumatic skin defects or wounds, it provides appropriate water vapor permeability and hydrates and lubricates the contact surface with the wound surface, allowing it to adhere closely to the wound surface and promote epidermal regeneration. In particular, by retaining metals that have antibacterial properties, infection of wounds can be prevented.

親水性ポリマーと抗菌性金属を被覆材表面で共存させた
場合は、親水性ポリマーを共存させないときと比較して
殺菌能力が向上する。これは、被覆材表面に導入された
親水性ポリマーが、水分により膨潤して構造がルーズに
なることにより、金属イオンの脱離、拡散が促進される
ため、抗菌性が向上するものと推定される。
When a hydrophilic polymer and an antibacterial metal coexist on the surface of a coating material, the bactericidal ability is improved compared to when a hydrophilic polymer is not coexisting. This is thought to be because the hydrophilic polymer introduced onto the surface of the coating material swells with moisture and becomes loose in structure, promoting the desorption and diffusion of metal ions, thereby improving antibacterial properties. Ru.

Claims (4)

【特許請求の範囲】[Claims] (1)多孔質ポリオレフィン膜あるいは多孔質ハロゲン
化ポリオレフィン膜の一方の表面に親水性ポリマーを化
学的に結合させてなることを特徴とする創傷被覆材。
(1) A wound dressing material characterized by having a hydrophilic polymer chemically bonded to one surface of a porous polyolefin membrane or a porous halogenated polyolefin membrane.
(2)多孔質ポリオレフィン膜の平均孔径が0.01〜
1.0μmである請求項1に記載の創傷被覆材。
(2) The average pore diameter of the porous polyolefin membrane is 0.01~
The wound dressing according to claim 1, which has a diameter of 1.0 μm.
(3)多孔質ポリオレフィン膜の水蒸気透過率が200
〜5000mg/m^2・24hrである請求項1また
は2に記載の創傷被覆材。
(3) Water vapor permeability of porous polyolefin membrane is 200
The wound dressing according to claim 1 or 2, which has a content of ~5000 mg/m^2.24 hr.
(4)多孔質ポリオレフィン膜あるいは多孔質ハロゲン
化ポリオレフィン膜の親水性ポリマーを結合させた面に
抗菌性を有する金属を蒸着させてなる請求項1乃至3の
いずれかの項に記載の創傷被覆材。
(4) The wound dressing material according to any one of claims 1 to 3, wherein a metal having antibacterial properties is vapor-deposited on the surface to which a hydrophilic polymer is bonded to a porous polyolefin membrane or a porous halogenated polyolefin membrane. .
JP20499690A 1990-08-03 1990-08-03 Wound dressing Expired - Lifetime JP2896210B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP20499690A JP2896210B2 (en) 1990-08-03 1990-08-03 Wound dressing
AU81524/91A AU640507B2 (en) 1990-08-03 1991-07-31 Wound-covering materials
DE1991608136 DE69108136T2 (en) 1990-08-03 1991-08-02 Wound covering material.
EP19910402183 EP0470007B1 (en) 1990-08-03 1991-08-02 Wound-covering materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20499690A JP2896210B2 (en) 1990-08-03 1990-08-03 Wound dressing

Publications (2)

Publication Number Publication Date
JPH0490764A true JPH0490764A (en) 1992-03-24
JP2896210B2 JP2896210B2 (en) 1999-05-31

Family

ID=16499736

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20499690A Expired - Lifetime JP2896210B2 (en) 1990-08-03 1990-08-03 Wound dressing

Country Status (2)

Country Link
JP (1) JP2896210B2 (en)
AU (1) AU640507B2 (en)

Also Published As

Publication number Publication date
JP2896210B2 (en) 1999-05-31
AU640507B2 (en) 1993-08-26
AU8152491A (en) 1992-02-06

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