JPH0566149B2 - - Google Patents
Info
- Publication number
- JPH0566149B2 JPH0566149B2 JP60027269A JP2726985A JPH0566149B2 JP H0566149 B2 JPH0566149 B2 JP H0566149B2 JP 60027269 A JP60027269 A JP 60027269A JP 2726985 A JP2726985 A JP 2726985A JP H0566149 B2 JPH0566149 B2 JP H0566149B2
- Authority
- JP
- Japan
- Prior art keywords
- gauze
- medical
- weight
- affected area
- salt
- 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.)
- Expired - Lifetime
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- Materials For Medical Uses (AREA)
Description
〔産業上の利用分野〕
本発明は新規な医療用被覆材、更に詳しくはヒ
アルロン酸またはその塩類または更にトリプトフ
アン、ヒスチジン、尿酸またはその塩類を医療用
ガーゼまたは医療用不織布に表面処理することを
特徴とする新規な医療用被覆材に関する。
〔従来の技術〕
従来の医療用ガーゼ、医療用不織布等はほう
帯、処置用マスク等に用いられる直接傷口、炎症
部または皮膚に接触することが多く、防炎性や吸
水性を向上する目的で従来のガーゼの改良も考慮
され、各種不織布が検討され、材質としてもポリ
塩化ビニル、ポリスチレン、ポリプロピレン、ポ
リエステル、ポリアミド、ポリウレタン等の合成
高分子などが使用されてきた。しかしこのような
材質の繊維および不織布は生体適合性の劣るばか
りか保温性も全く示さないことから、最近では吸
水性の大きいレーヨン等が使用されるようになつ
たが、吸水および吸液後その滲み出し、ベトツキ
がみられ衛生上にも問題が残る。また患部などに
直接被覆する被覆材や外科用覆布などは、患部か
らの滲み出す液体が固まつて、はがれ性を著しく
低下し、完治直前の傷を再び悪化させることがあ
る。また患部の乾燥は皮膚の張力により傷みを増
すことになり、必ずしも満足できるものではなか
つた。
更に救急絆創膏のパツドガーゼ、アクリノール
付きパツドガーゼやアクリノール湿潤ガーゼ、眼
帯用ガーゼ、眼帯用アクリノール付きガーゼのよ
うな殺菌、傷の保護を目的とする各種ガーゼにお
いても、炎症部位の乾燥を防止することは困難で
あり、通気性を維持してなおかつ乾燥を防止する
ことは困難であつた。
〔発明が解決しようとする問題点〕
本発明は従来使用されていたガーゼおよび絆創
膏のパツドガーゼ、外科用覆布など患部に直接被
覆する場合、炎症部あるいは傷口にそれ等が密着
し、剥離不能となる場合があり、完全治瘉を遅ら
せあるいは再び傷を付けてしまうようなことが多
かつた。そこでこれ等を解決すべくアルミシート
を貼り合わせた各種被覆材などが考えられ、被覆
材と炎症部の剥離性を改良すべき努力が払われて
いる。しかし、アルミシートの場合患部への酸素
補給、水分保持さらにはアルミシートによる断熱
効果のため、炎症部の放熱を妨げ必ずしも治瘉効
果に良いとは思われない。またいずれの方法にお
いても、患部の通気性を保ちつつ乾燥をおさえる
ことは困難であり、従つて乾燥とともに患部に痛
み、かゆみが感じられ、必ずしも満足な方法では
なかつた。
そこで本発明者等はこれ等問題を解決すべく鋭
意検討を重ねた結果、医療用ガーゼ、外科用覆布
など患部と直接接触する材質、例えばガーゼ、脱
脂綿、アクリノール湿潤ガーゼ、不織布などを保
湿成分水溶液に浸漬または保湿成分水溶液を噴霧
することにより、被覆材の剥離性、患部の治瘉効
果を改良しようとするものである。
〔問題を解決するための手段〕
本発明被覆材は患部の乾燥を防止し、かつ通気
性を良くし、炎症または傷の治瘉を促進しようと
するもので、ガーゼ、脱脂綿、不織布、人工皮膚
に皮膚構成成分であるヒアルロン酸またはそのナ
トリウム塩、カリウム塩、アンモニウム塩、アミ
ノ酸塩、カルシウム塩、アミン塩処理するもの
で、ガーゼ、脱脂綿、不織布への付着率は0.01〜
2重量%好ましくは0.01〜1重量%であり浸漬ま
たは噴霧処理が望ましい。0.01重量%以下では効
果がなく、2重量%以上は効果と経済性から必要
ない。
トリプトフアン、ヒスチジン、尿酸またはその
塩類の併用添加はヒアルロン酸の酸化的低分子化
を防止し、ヒアルロン酸の保湿性を維持し、治瘉
を促進するものである。
本発明でいうトリプトフアン、ヒスチジン、尿
酸またはその塩類とは、トリプトフアンまたはそ
の塩類としてはDL−トリプトフアン、L−トリ
プトフアン及びこれらの塩酸塩、酢酸塩、硫酸塩
をさし、ヒスチジンまたはその塩類とはL−ヒス
チジン及びこれの塩酸塩、酢酸塩、硫酸塩をさ
し、尿酸またはその塩類とは、尿酸、尿酸ナトリ
ウム、尿酸カリウム、尿酸カルシウム、尿酸水素
ナトリウム、尿酸水素カリウム、尿酸水素カルシ
ウム、尿酸水素アンモニウム、尿酸アミノ酸塩、
尿酸アミン塩などをいい、ガーゼ、不織布などへ
の付着率は0.005〜1.5重量%、好ましくは0.01〜
1重量%である。0.005重量%以下では目的とす
る効果が得られず1.5重量%以上は溶解性と効果
の点で必要ない。
本発明の医療用被覆材が適用できるのは、医療
包帯、医療用ガーゼ、眼帯などであり、医療用衛
生用品としては脱脂綿、ナプキン、タンポン、清
浄綿、絆創膏、紙おむつ、人工皮膚、縫合糸など
である。これらに使用される材料としては木綿お
よびレーヨン、ポリ塩化ビニル、ポリアクリルエ
ステル、ポリエステル、ナイロン、ポリエチレ
ン、ポリプロピレン、ポリオレフイン、セルロー
スエステルなどの合成高分子系不織布、キチン繊
維およびキチン不織布、羊腸糸、キチン縫合糸、
豚皮、牛皮などが適用出来る。
本発明でガーゼ、不織布などにヒアルロン酸ま
たはその塩類、トリプトフアン、ヒスチジン、尿
酸またはその塩類を付着させる方法は、これらを
水またはアルコールなどの溶剤に溶解し、浸漬ま
たは噴霧して付着させ、そのまま使用するか、
水、溶剤などを除去乾燥して使用する。
〔実施例〕
以下実施例によつて本発明を説明する。
実施例 1
ヒアルロン酸ナトリウム(純度95%以上)0.3
gを精成水100mlによく溶解し、医療用ガーゼ
(日局)(木綿)、レーヨン不織布、ナイロン不織
布、ポリプロピレン不織布、豚皮を5cm×5cmに
切断後5分浸漬し、以下条件で保湿度を調べた。
なお表中数字は原布に対する保水率で表わした。
[Industrial Application Field] The present invention is a novel medical covering material, more specifically, it is characterized by surface-treating medical gauze or medical nonwoven fabric with hyaluronic acid or its salts, or tryptophan, histidine, uric acid, or its salts. This invention relates to a new medical dressing material. [Prior art] Conventional medical gauze, medical non-woven fabrics, etc. are used for bandages, treatment masks, etc., and often come into direct contact with wounds, inflamed areas, or skin, and are intended to improve flame resistance and water absorption. Consideration has also been given to improving conventional gauze, and various nonwoven fabrics have been investigated, and synthetic polymers such as polyvinyl chloride, polystyrene, polypropylene, polyester, polyamide, and polyurethane have been used as materials. However, fibers and nonwoven fabrics made of such materials not only have poor biocompatibility but also have no heat retention properties.Recently, highly water-absorbing materials such as rayon have been used, but after absorbing water and absorbing the liquid, It oozes and becomes sticky, which also poses a hygiene problem. Furthermore, in the case of dressings, surgical coverings, etc. that are applied directly to the affected area, the liquid exuding from the affected area will solidify, significantly reducing the removability of the wound, and may worsen the wound that is about to heal completely. Furthermore, dryness of the affected area increases the damage due to the tension of the skin, which is not always satisfactory. Furthermore, it is difficult to prevent dryness of inflamed areas even with various types of gauze intended for sterilization and wound protection, such as emergency bandage patch gauze, patch gauze with acrinol, acrinol wet gauze, eye patch gauze, and eye patch gauze with acrinol. Therefore, it was difficult to maintain breathability and prevent drying. [Problems to be Solved by the Invention] The present invention solves the problem that when conventionally used gauze, adhesive bandages, surgical coverings, etc. are applied directly to the affected area, they stick tightly to the inflamed area or wound and cannot be removed. In some cases, complete healing may be delayed or the wound may be reinjured. In order to solve these problems, various types of covering materials made by laminating aluminum sheets have been considered, and efforts are being made to improve the releasability of the covering material and the inflamed area. However, in the case of aluminum sheets, the aluminum sheet supplies oxygen to the affected area, retains moisture, and has an insulating effect due to the aluminum sheet, which prevents heat radiation from the inflamed area and is not necessarily considered to be effective in curing the disease. In addition, in either method, it is difficult to prevent dryness while maintaining the air permeability of the affected area, and the dryness causes pain and itchiness in the affected area, so these methods are not necessarily satisfactory. Therefore, as a result of intensive studies to solve these problems, the inventors of the present invention have added moisturizing ingredients to materials that come into direct contact with the affected area, such as medical gauze and surgical coverings, such as gauze, absorbent cotton, acrinol wet gauze, and non-woven fabrics. By immersing it in an aqueous solution or spraying it with an aqueous moisturizing component solution, it is intended to improve the removability of the dressing and the healing effect of the affected area. [Means for solving the problem] The dressing of the present invention is intended to prevent dryness of the affected area, improve breathability, and promote healing of inflammation or wounds. It is treated with hyaluronic acid, a skin component, or its sodium salt, potassium salt, ammonium salt, amino acid salt, calcium salt, or amine salt, and the adhesion rate to gauze, absorbent cotton, and nonwoven fabric is 0.01 ~
The amount is 2% by weight, preferably 0.01 to 1% by weight, and immersion or spraying treatment is desirable. If it is less than 0.01% by weight, it is ineffective, and if it is more than 2% by weight, it is not necessary from the viewpoint of effectiveness and economy. The combined addition of tryptophan, histidine, uric acid, or their salts prevents the oxidative degradation of hyaluronic acid into low molecular weight molecules, maintains the moisturizing properties of hyaluronic acid, and promotes curing. In the present invention, tryptophan, histidine, uric acid, or salts thereof refer to DL-tryptophan, L-tryptophan, and their hydrochlorides, acetates, and sulfates; - Refers to histidine and its hydrochloride, acetate, and sulfate; uric acid or its salts refer to uric acid, sodium urate, potassium urate, calcium urate, sodium hydrogen urate, potassium hydrogen urate, calcium hydrogen urate, and ammonium hydrogen urate. , uric acid amino acid salt,
Refers to uric acid amine salts, etc., and the adhesion rate to gauze, nonwoven fabrics, etc. is 0.005 to 1.5% by weight, preferably 0.01 to 1.5% by weight.
It is 1% by weight. If it is less than 0.005% by weight, the desired effect cannot be obtained, and if it is more than 1.5% by weight, it is not necessary in terms of solubility and effectiveness. The medical dressing of the present invention can be applied to medical bandages, medical gauze, eye patches, etc. Medical hygiene products include absorbent cotton, napkins, tampons, clean cotton, bandages, disposable diapers, artificial skin, sutures, etc. It is. Materials used for these include synthetic polymer nonwoven fabrics such as cotton and rayon, polyvinyl chloride, polyacrylic ester, polyester, nylon, polyethylene, polypropylene, polyolefin, and cellulose ester, chitin fibers and chitin nonwoven fabrics, sheep intestinal thread, and chitin. suture,
Pork skin, cow skin, etc. can be used. The method of attaching hyaluronic acid or its salts, tryptophan, histidine, uric acid or its salts to gauze, nonwoven fabric, etc. in the present invention is to dissolve them in a solvent such as water or alcohol, apply them by dipping or spraying, and use them as they are. Or,
Remove water, solvent, etc. and dry before use. [Example] The present invention will be explained below with reference to Examples. Example 1 Sodium hyaluronate (purity 95% or more) 0.3
Dissolve g in 100 ml of purified water, cut medical gauze (Japanese) (cotton), rayon non-woven fabric, nylon non-woven fabric, polypropylene non-woven fabric, pigskin into 5 cm x 5 cm and soak for 5 minutes to determine the moisture content under the following conditions. I looked into it.
Note that the numbers in the table are expressed as water retention rates relative to the original fabric.
【表】【table】
【表】
実施例 2
左右両足甲の火傷患者に火傷後7日経過時より
2日間、すなわち薄い皮の生成が認められた時、
左右甲患部にはコロジオン処理ガーゼを当て、左
右甲患部には、木綿ガーゼのヒアルロン酸ナトリ
ウム処理後さらにコロジオン処理したガーゼを当
て、2日間治療した。なお12時間間経過時点で新
しいものと取りかえた。
なお患部の火傷度は何れも同程度であつたが右
足は面積約30cm2左足は約1/3の大きさであつた。[Table] Example 2 A patient with burns on both the left and right insteps was treated for 2 days from 7 days after the burn, that is, when the formation of thin skin was observed.
Collodion-treated gauze was applied to the affected areas of the left and right insteps, and cotton gauze treated with sodium hyaluronate and then collodion-treated gauze was applied to the affected areas of the left and right insteps for treatment for 2 days. It was replaced with a new one after 12 hours had passed. The severity of burns on the affected areas was the same in both cases, but the area on the right leg was about 30 cm2, and the area on the left leg was about 1/3 of the same size.
【表】
右足患部は30時間後中断し、通常方法による治
療を行なつた。その結果、右足については面積が
大きかつたこともあり薄皮の裂け目は一回の試験
では何とも言えないが、かゆみが出たことは乾燥
しすぎに基づくものでさらに続行すれば悪化し
た。
左足患部はかゆももなく順調な治瘉効果があつ
た。
実施例 3
眼瞼4針縫合患者にリバノール含浸ガーゼおよ
びリバノール含浸ガーゼにさらにヒアルロン酸ナ
トリウム0.1%、尿酸ナトリウム0.03%の混合水
溶液を粉霧し眼帯下患部に覆布した。なお本発明
者らは患部の治瘉に影響のないよう6時間毎に交
互に使用した。その結果リバノール含浸ガーゼ使
用の場合、3時間経過頃より縫合部につれる感じ
がありやや痛みを感じた。
一方、本発明品は全く異状がなく繰り返し3回
行つても何ら異状は無かつた。[Table] Treatment for the affected area of the right leg was discontinued after 30 hours, and treatment was performed using the usual method. As a result, since the area of the right foot was large, it was difficult to say anything about the tearing of the thin skin from a single test, but the itching that appeared was due to excessive dryness and would worsen if continued. There was no itching in the affected area of the left leg, and the healing effect was good. Example 3 A mixed aqueous solution of 0.1% sodium hyaluronate and 0.03% sodium urate was sprayed onto ribanol-impregnated gauze and ribanol-impregnated gauze for a patient who had undergone four-stitch eyelid suturing, and the affected area was covered with ophthalmia. The present inventors used the drugs alternately every 6 hours so as not to affect the healing of the affected area. As a result, in the case of using Rivanol-impregnated gauze, after about 3 hours, there was a feeling of tightening towards the sutured area and a slight pain was felt. On the other hand, the product of the present invention had no abnormalities at all, and no abnormalities were observed even after repeated testing three times.
Claims (1)
ン酸またはその塩を0.01〜2.0重量%になるよう
に表面処理することを特徴とする新規な医療用被
覆材。 2 医療用ガーゼまたは医療用不織布にヒアルロ
ン酸またはその塩を0.01〜2.0重量%およびトリ
プトフアン、ヒスチジン、尿酸またはその塩類か
ら選ばれる1種または2種以上0.005〜1.5重量%
になるように表面処理することを特徴とする新規
な医療用被覆材。[Scope of Claims] 1. A novel medical covering material, characterized in that medical gauze or medical nonwoven fabric is surface-treated with hyaluronic acid or its salt in an amount of 0.01 to 2.0% by weight. 2 Medical gauze or medical nonwoven fabric containing 0.01 to 2.0% by weight of hyaluronic acid or its salt and 0.005 to 1.5% by weight of one or more types selected from tryptophan, histidine, uric acid, or its salts.
A novel medical dressing material characterized by surface treatment to make it look like this.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60027269A JPS61187866A (en) | 1985-02-14 | 1985-02-14 | Novel medical cover material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60027269A JPS61187866A (en) | 1985-02-14 | 1985-02-14 | Novel medical cover material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61187866A JPS61187866A (en) | 1986-08-21 |
| JPH0566149B2 true JPH0566149B2 (en) | 1993-09-21 |
Family
ID=12216355
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60027269A Granted JPS61187866A (en) | 1985-02-14 | 1985-02-14 | Novel medical cover material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61187866A (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5990096A (en) * | 1990-09-18 | 1999-11-23 | Hyal Pharmaceutical Corporation | Formulations containing hyaluronic acid |
| US5767106A (en) * | 1992-02-21 | 1998-06-16 | Hyal Pharmaceutical Corporation | Treatment of disease and conditions associated with macrophage infiltration |
| FR2840801B1 (en) * | 2002-06-18 | 2005-06-03 | Cie De Rech En Composants Impl | COMPOSITE PROTHETIC IMPLANT |
| US20070270523A1 (en) * | 2004-11-05 | 2007-11-22 | Kaneka Corporation | Method of Modifying Blood Contact Material and Blood Contact Material Inhibited from Activating Granulocyte |
| WO2008024893A2 (en) * | 2006-08-23 | 2008-02-28 | Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services | Derivatives of uric and thiouric acid for oxidative stress-related diseases |
| TWI482634B (en) | 2013-10-24 | 2015-05-01 | Ind Tech Res Inst | Biomedical composition |
| JP6856221B2 (en) * | 2017-10-11 | 2021-04-07 | 国立大学法人鳥取大学 | Wound healing promotion sheet and its manufacturing method |
-
1985
- 1985-02-14 JP JP60027269A patent/JPS61187866A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS61187866A (en) | 1986-08-21 |
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