JPH0197468A - Wound covering material - Google Patents

Wound covering material

Info

Publication number
JPH0197468A
JPH0197468A JP62254490A JP25449087A JPH0197468A JP H0197468 A JPH0197468 A JP H0197468A JP 62254490 A JP62254490 A JP 62254490A JP 25449087 A JP25449087 A JP 25449087A JP H0197468 A JPH0197468 A JP H0197468A
Authority
JP
Japan
Prior art keywords
base material
alumina
wound
ceramic powder
infrared rays
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
JP62254490A
Other languages
Japanese (ja)
Inventor
Nobuyuki Inoue
信之 井上
Tadashi Murakami
正 村上
Shuji Kadowaki
門脇 周治
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.)
Japan Vilene Co Ltd
Original Assignee
Japan Vilene 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 Japan Vilene Co Ltd filed Critical Japan Vilene Co Ltd
Priority to JP62254490A priority Critical patent/JPH0197468A/en
Publication of JPH0197468A publication Critical patent/JPH0197468A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To safely and continuously perform the treatment of a wound by far infrared rays for a necessary period, by bonding an alumina-silica ceramic powder containing a heavy metal emitting far infrared rays having a specific wavelength to a base material using a resin binder and specifying the pH of the whole. CONSTITUTION:An alumina-silica ceramic layer 2 is formed to the surface of a base material 1. In use, alumina-silica ceramic layer 2 is provided so as to become the surface side of a wound. The alumina-silica ceramic powder contains substantially no heavy metal and one generating far infrared rays having a peak wavelength of 4-12mum when heated to the bodily temp. of a human being or a temp. range of about room temp. is used. A wound covering material prepared by bonding this ceramic powder to the base material 1 by a resin binder is adjusted to 6-8 in its pH as a whole. As the wound covering material, polydimethylsiloxane as the binder and a material using a high pressure steam sterilizable nylon or cotton fibers as the base material 1 are desirably combined.

Description

【発明の詳細な説明】 [産業上の利用分野コ 本発明は創傷被覆材に関する。さらに詳しくは、本発明
は放出された遠赤外線によって創傷面の保護および治癒
の促進をはかりう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. More specifically, the present invention relates to a wound dressing that can protect a wound surface and promote healing by emitted far infrared rays.

[従来の技術] ピークの波長が4〜12−程度の遠赤外線が食品の鮮度
保持や人体の代謝促進に効果があることは一般に知られ
ている(「遠赤外線の時代」、今野和義著、昭和61年
、■人間と歴史社発行、131〜250頁参照)。また
、近年遠赤外線による健康促進効果を期待するべく布、
紙、不織布、プラスチックフィルムなどの基布に接着剤
などで人体の体温程度の熱量で遠赤外線を放射する遠赤
外線照射粉末を固定した人体用遠赤外線照射布(実開昭
55−27533号公報、同55−27549号公報お
よび同55−17L145号公報参照)や遠赤外線サウ
ナのように機器を用いて病気の治療や健康増進をはかっ
た例も報告されている(「新遠赤外線療法」、山崎敏子
著、昭和59年、■人間と歴史社発行、107〜172
頁参照)。
[Prior Art] It is generally known that far infrared rays with a peak wavelength of about 4 to 12 - are effective in keeping food fresh and promoting metabolism in the human body ("The Age of Far Infrared Rays", written by Kazuyoshi Konno, 1986, ■Published by Human and History Publishing, see pages 131-250). In addition, in recent years, in hopes of promoting health through far infrared rays, cloth,
Far-infrared irradiation cloth for the human body (Utility Model Application Publication No. 55-27533, (Refer to Publications No. 55-27549 and No. 55-17L145) and far-infrared saunas have been reported to treat diseases and improve health using equipment (``New Far-Infrared Therapy'', Yamazaki Written by Toshiko, 1982, published by Human and History Company, 107-172
(see page).

[発明が解決しようとする問題点コ 前記人体用遠赤外線照射布は受傷や欠損していない非受
傷皮膚に適用するばあいには、被覆材を滅菌する必要が
なく、生体適合性についても問題なく使用しつるが、直
接または薬剤処置後にガーゼを置いた創面上より被覆し
ようとするばあいには、安全性、滅菌性および生体適合
性に問題がある。
[Problems to be solved by the invention] When the far-infrared irradiated cloth for the human body is applied to uninjured skin that is not injured or damaged, there is no need to sterilize the dressing material, and there are also problems regarding biocompatibility. However, there are problems with safety, sterility, and biocompatibility when trying to cover the wound directly or with gauze placed after drug treatment.

また前記機器による治療は症状に応じて遠赤外線の波長
、放射量や放射率などを変更することができるといった
長所があるが、その設備のある所でないと治療すること
ができないという制約があった。
In addition, treatment using the above-mentioned equipment has the advantage of being able to change the far-infrared wavelength, radiation amount, emissivity, etc. depending on the symptom, but it has the limitation that treatment cannot be performed unless the equipment is available. .

そこで本発明者らは前記従来技術の問題点に鑑みて大が
かりな機器を用いることなく、創傷に対して遠赤外線に
よる治療を安全かつ必要期間にわたり継続的に行ないう
る手段を見出すべく鋭意研究を重ねた結果、かかる問題
点を解決しつることは勿論のこと、科学的に創傷を冶癒
しうる創傷被覆材をはじめて見出し、本発明を完成する
に至った。
Therefore, in view of the problems of the prior art described above, the present inventors have conducted extensive research in order to find a means to safely and continuously treat wounds with far infrared rays for a necessary period of time without using large-scale equipment. As a result, they have found for the first time a wound dressing material that not only solves these problems but also can scientifically heal wounds, and have completed the present invention.

[問題点を解決するための手段] 本発明はヒトの体温ないし室温程度の温度領域でピーク
の波長が4〜12加である遠赤外線を放射する重金属を
含まないアルミナ−シリカ系セラミック粉末を、樹脂バ
インダーを用いて基材に付着せしめ、全体のI)Hが6
〜8となるように調整された創傷被覆材に関する。
[Means for Solving the Problems] The present invention uses alumina-silica ceramic powder that does not contain heavy metals and emits far infrared rays with a peak wavelength of 4 to 12 mm in the temperature range of human body temperature or room temperature. It is attached to the base material using a resin binder, and the overall I)H is 6.
-8.

[作用および実施例コ 本発明に用いられるアルミナ−シリカ系セラミック粉末
は純度の高いkQ 20 sおよび5i02を主成分と
し、JV 203および5i02を75重量%以上、好
ましくは95重量%以上含むものである。
[Operations and Examples] The alumina-silica ceramic powder used in the present invention has high purity kQ 20 s and 5i02 as main components, and contains JV 203 and 5i02 in an amount of 75% by weight or more, preferably 95% by weight or more.

該アルミナ−シリカ系セラミック粉末に含まれるAg2
Osと5i02との組成比(重量比)は30/−3= 70〜70/ 30、なかんづ<40/80〜80/ 
40であるのが好ましい。なお、該アルミナ−シリカ系
セラミック粉末中にたとえばZrs T1% Co5C
rなどの重金属が含まれているばあい、創傷面に悪影響
を及ぼすことがあるので、かかる重金属は実質的に含ま
れないことが望ましく、たとえば、創傷被覆材を試料と
して4 V/V%酢酸溶液で60℃、30分間溶出した
ときの試料表面積1 ciあたりの重金属の検出は硫化
ナトリウム比色法によるとき検出限界1μg / ml
で検出されないことが望ましい。
Ag2 contained in the alumina-silica ceramic powder
The composition ratio (weight ratio) of Os and 5i02 is 30/-3 = 70-70/30, Nakazu<40/80-80/
Preferably, it is 40. In addition, for example, Zrs T1% Co5C is contained in the alumina-silica ceramic powder.
If heavy metals such as r are contained, they may have an adverse effect on the wound surface, so it is desirable that such heavy metals be substantially free of the wound dressing material. The detection limit of heavy metals per 1 ci of sample surface area when eluted with a solution at 60°C for 30 minutes is 1 μg/ml using the sodium sulfide colorimetric method.
It is desirable that it not be detected.

前記アルミナ−シリカ系セラミック粉末はたとえばヒト
の体温ないし室温程度の温度領域に加熱したときにピー
クの波長が4〜12卯の遠赤外線を発生するものである
The alumina-silica ceramic powder emits far-infrared rays having a peak wavelength of 4 to 12 μm when heated to a temperature range of, for example, human body temperature or room temperature.

前記アルミナ−シリカ系セラミック粉末の粒子径は通常
1〜50加となるように粉砕して調整されるが、本発明
においてはとくに限定されるものではない。
The particle size of the alumina-silica ceramic powder is usually adjusted by grinding to a particle size of 1 to 50, but is not particularly limited in the present invention.

本発明に用いられる樹脂バインダーとしては、耐熱性お
よび生体適合性に優れたものが選ばれる。かかる樹脂バ
インダーとしては、とくにポリジメチルシロキサンが好
ましい。
As the resin binder used in the present invention, one with excellent heat resistance and biocompatibility is selected. As such a resin binder, polydimethylsiloxane is particularly preferred.

ただし、えられた創傷被覆材を滅菌バッグで包装し、エ
チレンオキサイドガス滅菌やγ線滅菌などを行なって製
品化するばあいには樹脂バインダーとしてポリウレタン
やポリアクリレートなどを用いてもよい。
However, when the obtained wound dressing is packaged in a sterilized bag and subjected to ethylene oxide gas sterilization, gamma ray sterilization, etc. to produce a product, polyurethane, polyacrylate, or the like may be used as the resin binder.

前記アルミナ−シリカ系セラミック粉末の使用量は、樹
脂バインダー100部(重量部、以下同様)に対して1
0〜70部、なかんづ<30〜50部であるのが好まし
い。該使用量は10部未満であるばあい、遠赤外線の放
射量か小さくなってその放射による効果が小さくなりす
ぎ、また70部をこえるばあい、基材に付着せしめるの
が困難となる。かかるセラミック粉末の使用量は前記範
囲内で遠赤外線の放射量に応じて適宜調整される。
The amount of the alumina-silica ceramic powder used is 1 part by weight (parts by weight, same hereinafter) of the resin binder.
Preferably, the amount is 0 to 70 parts, and <30 to 50 parts. If the amount used is less than 10 parts, the amount of far-infrared rays emitted will be too small and the effect of the radiation will be too small, and if it exceeds 70 parts, it will be difficult to adhere to the substrate. The amount of the ceramic powder to be used is appropriately adjusted within the above range depending on the amount of far-infrared radiation.

本発明に用いられる基祠としては、高圧蒸気滅菌を施す
ことができ、しかも毒性の小さいたとえばポリエステル
、ナイロン、綿などの原料からなる織布、不織布あるい
はフィルムなどがあげられる。かかる基材は手術用など
のように無菌性が重要視され、滅菌される必要があるも
のについて有効である。
Examples of the base used in the present invention include woven fabrics, nonwoven fabrics, and films made of raw materials such as polyester, nylon, and cotton, which can be subjected to high-pressure steam sterilization and have low toxicity. Such a base material is effective for applications where sterility is important and must be sterilized, such as for surgical applications.

前記セラミック粉末を樹脂バインダーにより基材に付着
した創傷被覆材は、そのpT(が全体として6〜8であ
ることが望ましい。これは、創傷被覆材のplが5以下
または9以上のばあい、該セラミック粉末を用いてつく
られたシートを用いて創傷面を直接被覆したときには強
い刺激痛をもたらすと同時に化学熱傷が引きおこされ、
創傷を悪化させることがあるからである。このpH調整
は、セラミック粉末を水に分散したばあいのpHがセラ
ミックの原料組成や焼成方法などによって変動しやすい
ので樹脂バインダー側で調整するか、あるいはセラミッ
ク粉末を樹脂バインダーで基材に付着した後、局数性ま
たは弱塩基性溶液で処理することにより調整するのが好
ましい。後者のばあい、たとえば創傷被覆材がアルカリ
性を呈するものであれば、酢酸、ギ酸などの弱酸性溶液
に浸漬後、水洗、乾燥を行なえばよく、酸性であればア
ンモニア水などの弱塩基性溶液に浸漬後、水洗、乾燥す
ればよい。
The wound dressing in which the ceramic powder is attached to the base material with a resin binder preferably has a pT of 6 to 8 as a whole. This means that if the pl of the wound dressing is 5 or less or 9 or more, When a sheet made of the ceramic powder is used to directly cover a wound surface, it causes strong irritating pain and at the same time causes chemical burns.
This is because it may worsen the wound. This pH adjustment can be done either on the resin binder side, or after the ceramic powder is attached to the base material with a resin binder, as the pH when ceramic powder is dispersed in water tends to fluctuate depending on the ceramic raw material composition and firing method. Preferably, the adjustment is carried out by treatment with a polyhydric or weakly basic solution. In the latter case, for example, if the wound dressing is alkaline, it can be soaked in a weakly acidic solution such as acetic acid or formic acid, then washed with water and dried; if it is acidic, it can be soaked in a weakly basic solution such as ammonia water. After soaking, wash with water and dry.

なお創傷被覆材には使用前に滅菌が施されている必要が
ある。かかる滅菌法としては、エチレンオキサイドガス
滅菌、γ線照射滅菌、高圧蒸気滅菌などがあるが、とく
に病院で日常広く行なわれている高圧蒸気滅菌法がもっ
とも信頼性が高い。この方法で使用することができる該
創傷被覆材としてはバインダーにポリジメチルシロキサ
ンを、基材にポリエステル、ナイロン、綿などの高圧蒸
気滅菌可能な繊維を用いた材料を組合せたものが望まし
い。
The wound dressing must be sterilized before use. Such sterilization methods include ethylene oxide gas sterilization, γ-ray irradiation sterilization, and high-pressure steam sterilization, but high-pressure steam sterilization, which is widely used in hospitals on a daily basis, is the most reliable. The wound dressing material that can be used in this method is preferably a material in which the binder is polydimethylsiloxane and the base material is a fiber that can be sterilized by high-pressure steam, such as polyester, nylon, or cotton.

前記アルミナ−シリカ系セラミック粉末を樹脂バインダ
ーを用いて基材に付着せしめる方法についてはとくに限
定はなく、かかる方法としては、たとえばセラミック粉
末を樹脂バインダーと混合し、これをコーティング、プ
リント、含浸法などの公知の方法によって付着せしめる
方法があげられる。基材に付着されるアルミナ−シリカ
系セラミック粉末の量は放射される遠赤外線量に応じて
調整される。
There are no particular limitations on the method of attaching the alumina-silica ceramic powder to the base material using a resin binder, and such methods include, for example, mixing ceramic powder with a resin binder and coating, printing, impregnating, etc. An example of this is a method of attaching it by a known method. The amount of alumina-silica ceramic powder attached to the base material is adjusted depending on the amount of far infrared rays emitted.

かくしてえられる被覆材の一実施態様の断面を第1図に
示す。第1図において、基材(1)の表面上にアルミナ
−シリカ系セラミック層(2)が形成されている。使用
に際しては前記アルミナ−シリカ系セラミック層(2)
が創傷面側となるように設けて使用される。なお本発明
の被覆材はそのまま使用してもよく、またさらに粘着シ
ート基材の中央部に該被覆材を傷当てパッドとして付着
させ、粘着面を離型シートで覆って絆創膏として使用し
てもよい。
A cross-section of one embodiment of the dressing thus obtained is shown in FIG. In FIG. 1, an alumina-silica ceramic layer (2) is formed on the surface of a base material (1). When used, the alumina-silica ceramic layer (2)
It is used with the side facing the wound side. The dressing of the present invention may be used as it is, or it may be used as a bandage by attaching the dressing to the center of an adhesive sheet base material as a wound dressing pad and covering the adhesive surface with a release sheet. good.

つぎに本発明の創傷被覆材を実施例に基づいてさらに詳
細に説明するが、本発明はかかる実施例のみに限定され
るものではない。
Next, the wound dressing of the present invention will be explained in more detail based on Examples, but the present invention is not limited to these Examples.

実施例1〜4 ポリエステル繊維(繊度:3デニール、繊維長:64m
m)を用い、水流絡合法によってノーバインダー不織布
(目付:80g/rr?)をつくり、これを基材とした
。粒子径が2〜4 lJmの範囲にある遠赤外線セラミ
ック粉末の組成を第1表に示すように調整し、該セラミ
ック粉末とバインダーの懸濁液中に基材を含浸した後乾
燥して第1表に示すセラミック粉末およびバインダーの
付着量を有する創傷被覆材をえた。
Examples 1 to 4 Polyester fiber (fineness: 3 denier, fiber length: 64 m
A binder-free nonwoven fabric (fabric weight: 80 g/rr?) was made by the hydroentanglement method using the material M), and this was used as a base material. The composition of a far-infrared ceramic powder having a particle size in the range of 2 to 4 lJm was adjusted as shown in Table 1, and a base material was impregnated into a suspension of the ceramic powder and a binder, and then dried. Wound dressings were obtained having the amounts of ceramic powder and binder deposited as shown in the table.

[以下余白] かくしてえられ被覆材を所定の寸法に裁断し、これを用
いて高圧蒸気滅菌後、臨床試験を試みた。対象疾患は裸
皮面でハーフサイドテストで評価した。その結果を以下
に示す。
[Margins below] The thus obtained dressing material was cut to a predetermined size, and after sterilization using high-pressure steam, a clinical trial was conducted. Target diseases were evaluated using a half-side test on the naked skin surface. The results are shown below.

症例1 36オの女性の大腿部の皮膚を、通常皮膚移植の際に用
いられているデルマトームを用いて長さ約10(711
%幅約5cm5厚さ18/1000インチ(約0.46
mm)だけ採取したあとの裸皮部を軟膏で処理し、その
上半分を実施例1でえられた創傷被覆材で処理し、つい
で裸皮部全体にその上からガーゼドレッシングを施した
Case 1 The skin of the thigh of a 36-year-old woman was cut into a length of about 10 mm (711 cm) using a dermatome, which is normally used for skin grafting.
% Width approx. 5 cm 5 Thickness 18/1000 inch (approx. 0.46
The bare skin part after harvesting only 2 mm) was treated with ointment, the upper half was treated with the wound dressing obtained in Example 1, and then a gauze dressing was applied over the entire bare skin part.

3ケ月経過したのち、ガーゼドレッシングをはずしたと
ころ、創傷被覆材で被覆されていなかった裸皮部には、
部分的に赤黒い斑痕を有し、全体としてケロイドに近い
赤っぽい紫色を呈する周囲の皮膚よりも盛り上がった弾
力性のない厚みのある皮膚が形成されていた。一方、創
傷被覆材で被覆されていた裸皮部には、正常の新生した
皮膚と同色の肥厚化していない皮膚が形成されていた。
After 3 months, when the gauze dressing was removed, the bare skin that had not been covered with the wound dressing showed
The skin had thick, inelastic skin that was raised higher than the surrounding skin, which had reddish-black spots in some areas, and an overall reddish-purple color similar to that of a keloid. On the other hand, unthickened skin of the same color as normal new skin was formed on the bare skin that had been covered with the wound dressing.

症例2 43才の女性の大腿部の皮膚を症例1と同様にして採皮
し、採皮したあとの裸皮部を2種類の抗菌性の軟膏で処
置した後、上半分を実施例3でえられた被覆材で被覆し
、ついで裸皮部全体にその上からガーゼドレッシングを
施した。4ケ月間経過したのち、ガーゼドレッシングを
はずしたところ、創傷被覆材で被覆されていなかった裸
皮部には、部分的に赤黒い斑痕を残し、全体としてケロ
イドに近い褐色を呈する周囲の皮膚よりも盛り上がった
弾力性のない厚みのある皮膚が形成されていた。
Case 2 The thigh skin of a 43-year-old woman was harvested in the same manner as in Case 1. After the skin was harvested, the naked skin was treated with two types of antibacterial ointment, and the upper half was treated with Example 3. The skin was covered with the resulting dressing material, and then a gauze dressing was applied over the entire bare skin area. After 4 months had passed, when the gauze dressing was removed, the bare skin that had not been covered by the wound dressing had reddish-dark spots in some areas, and the overall appearance was darker than the surrounding skin, which had a brownish color similar to that of a keloid. Thick, raised skin with no elasticity had formed.

一方、創傷被覆材で被覆されていた裸皮部には正常の新
生した皮膚と同色の肥厚化していない皮膚が形成されて
いた。
On the other hand, unthickened skin of the same color as normal new skin was formed in the bare skin area that had been covered with the wound dressing.

上記の結果より、本発明の創傷被覆材は創傷の治癒の促
進をはかりうることかわかる。
The above results demonstrate that the wound dressing of the present invention can promote wound healing.

[発明の効果コ 本発明の創傷被覆材は体温によって放射される遠赤外線
によって創傷面の保護および治癒をはかりうるものであ
り、傷当てパッドをはじめ、絆創膏などとして好適に使
用しうるちのである。
[Effects of the Invention] The wound dressing material of the present invention can protect and heal the wound surface by far infrared rays emitted by body temperature, and can be suitably used as a dressing pad, bandage, etc. .

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の被覆材の一実施例を示す断面図である
。 (図面の主要符号) (1):基 材
FIG. 1 is a sectional view showing one embodiment of the covering material of the present invention. (Main symbols in the drawing) (1): Base material

Claims (1)

【特許請求の範囲】 1 ヒトの体温ないし室温程度の温度領域でピークの波
長が4〜12μmである遠赤外線を放射する重金属を含
まないアルミナ−シリカ系セラミック粉末を、樹脂バイ
ンダーを用いて基材に付着せしめてなり、全体のpHが
6〜8となるように調整された創傷被覆材。2 樹脂バ
インダーがポリジメチルシロキサンであり、基材が高圧
蒸気滅菌可能な繊維またはフィルムである特許請求の範
囲第1項記載の創傷被覆材。 3 高圧蒸気滅菌可能な繊維がポリエステル、ナイロン
または綿からなるものである特許請求の範囲第2項記載
の創傷被覆材。 4 高圧蒸気滅菌可能なフィルムがポリエステルまたは
ナイロンからなるものである特許請求の範囲第2項記載
の創傷被覆材。
[Claims] 1. An alumina-silica ceramic powder containing no heavy metals that emits far infrared rays with a peak wavelength of 4 to 12 μm in the temperature range of human body temperature or room temperature is used as a base material using a resin binder. A wound dressing that is made by adhering to the skin and has an overall pH of 6 to 8. 2. The wound dressing according to claim 1, wherein the resin binder is polydimethylsiloxane, and the base material is a fiber or film that can be autoclaved. 3. The wound dressing according to claim 2, wherein the autoclave sterilizable fiber is made of polyester, nylon, or cotton. 4. The wound dressing according to claim 2, wherein the autoclave sterilizable film is made of polyester or nylon.
JP62254490A 1987-10-08 1987-10-08 Wound covering material Pending JPH0197468A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62254490A JPH0197468A (en) 1987-10-08 1987-10-08 Wound covering material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62254490A JPH0197468A (en) 1987-10-08 1987-10-08 Wound covering material

Publications (1)

Publication Number Publication Date
JPH0197468A true JPH0197468A (en) 1989-04-14

Family

ID=17265774

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62254490A Pending JPH0197468A (en) 1987-10-08 1987-10-08 Wound covering material

Country Status (1)

Country Link
JP (1) JPH0197468A (en)

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