JPH0236517Y2 - - Google Patents
Info
- Publication number
- JPH0236517Y2 JPH0236517Y2 JP20083686U JP20083686U JPH0236517Y2 JP H0236517 Y2 JPH0236517 Y2 JP H0236517Y2 JP 20083686 U JP20083686 U JP 20083686U JP 20083686 U JP20083686 U JP 20083686U JP H0236517 Y2 JPH0236517 Y2 JP H0236517Y2
- Authority
- JP
- Japan
- Prior art keywords
- bioabsorbable
- wound
- fibers
- tear strength
- cellulose
- 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
Links
- 229920003043 Cellulose fiber Polymers 0.000 claims description 12
- 239000000835 fiber Substances 0.000 claims description 9
- 239000004744 fabric Substances 0.000 claims description 8
- 229920001059 synthetic polymer Polymers 0.000 claims description 8
- 238000009941 weaving Methods 0.000 claims description 7
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- 238000000034 method Methods 0.000 claims description 2
- 238000010030 laminating Methods 0.000 claims 1
- 239000002985 plastic film Substances 0.000 claims 1
- 229920006255 plastic film Polymers 0.000 claims 1
- 206010052428 Wound Diseases 0.000 description 12
- 208000027418 Wounds and injury Diseases 0.000 description 12
- 239000002390 adhesive tape Substances 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- 208000025865 Ulcer Diseases 0.000 description 4
- 238000009940 knitting Methods 0.000 description 4
- 231100000397 ulcer Toxicity 0.000 description 4
- 229920000954 Polyglycolide Polymers 0.000 description 3
- 229920002678 cellulose Polymers 0.000 description 3
- 239000001913 cellulose Substances 0.000 description 3
- 210000002919 epithelial cell Anatomy 0.000 description 3
- 210000000416 exudates and transudate Anatomy 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000004633 polyglycolic acid Substances 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- 208000035874 Excoriation Diseases 0.000 description 2
- 208000004210 Pressure Ulcer Diseases 0.000 description 2
- 206010040943 Skin Ulcer Diseases 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 210000001124 body fluid Anatomy 0.000 description 2
- 239000010839 body fluid Substances 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 208000035475 disorder Diseases 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000035876 healing Effects 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 230000008338 local blood flow Effects 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 231100000019 skin ulcer Toxicity 0.000 description 2
- 230000000451 tissue damage Effects 0.000 description 2
- 231100000827 tissue damage Toxicity 0.000 description 2
- 230000008733 trauma Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 230000029663 wound healing Effects 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- 206010016322 Feeling abnormal Diseases 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 229920000747 poly(lactic acid) Polymers 0.000 description 1
- 229920002463 poly(p-dioxanone) polymer Polymers 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 239000000622 polydioxanone Substances 0.000 description 1
- 229920005594 polymer fiber Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229940126585 therapeutic drug Drugs 0.000 description 1
Description
【考案の詳細な説明】
(産業上の利用分野)
本考案は、ヤケド、擦過傷等外傷に起因する潰
傷、局部の血行障害による潰瘍褥瘡など皮膚潰瘍
に対して組織損傷を防止し、創部保護と優れた治
癒効果を発揮する被覆材に関する。[Detailed description of the invention] (Field of industrial application) This invention prevents tissue damage and protects skin ulcers such as ulcers caused by trauma such as burns and abrasions, and ulcers and pressure ulcers caused by local blood circulation disorders. and dressing materials that exhibit excellent healing effects.
(従来技術)
従来より上記創傷の治療に対しては、治療薬を
塗布したり、或は、消毒ガーゼを当てて包帯を巻
き付けたり、カツト絆、傷絆などと称する片面粘
着テープ付ガーゼを貼着して保護している。(Prior Art) Conventionally, the above-mentioned wounds have been treated by applying therapeutic drugs, applying disinfectant gauze and wrapping bandages, or pasting gauze with one-sided adhesive tape called Katsuto Kizuna, Kizuki Kizuna, etc. Wear it to protect it.
(考案が解決しようとする問題点)
しかしながら、かかる従来のものは取り外し、
又は手当の際に創傷表面を保護している滲出液水
泡を破つてしまい創傷基層に上皮細胞の形成がで
きにくく患者にも苦痛を与える。そのまま放置し
ても体内に吸収されることがなく創傷部の細菌感
染や排泄物による汚染が起り易いため取り代えを
要する。創傷面の摩擦及び取り外しの際には疼痛
がさけられない。治癒しかけた創傷面を傷めやす
く患部が乾きにくい等の問題点がある。(Problem that the invention attempts to solve) However, such conventional ones can be removed,
Alternatively, during treatment, the exudate blisters that protect the wound surface may burst, making it difficult for epithelial cells to form in the wound base layer, causing pain to the patient. Even if left as is, it will not be absorbed into the body and the wound will likely become infected with bacteria or contaminated with excrement, so it must be replaced. Pain is inevitable during friction and removal of the wound surface. There are problems such as easily damaging the surface of a wound that is about to heal and making it difficult for the affected area to dry.
(問題を解決するための手段)
本考案は前記の欠点をカバーしたもので、その
構成において、生体吸収性の合成高分子繊維とセ
ルロース系繊維を交編織して成りこれの引裂強さ
を10〜300gに調整して成ることに特徴を有する
生体吸収性創傷被覆材に関する。(但し、引裂強
さはJIS L−1096法の測定による)
即ち、本考案は生体吸収性の高分子材料と吸水
性のセルロース系繊維の組み合せより成り、前記
した従来の欠点を解消したものである。(Means for Solving the Problems) The present invention covers the above-mentioned drawbacks, and its structure is made by interweaving bioabsorbable synthetic polymer fibers and cellulose fibers, which has a tear strength of 10%. The present invention relates to a bioabsorbable wound dressing characterized in that the weight is adjusted to 300g. (However, the tear strength is measured by JIS L-1096 method.) In other words, the present invention is made of a combination of a bioabsorbable polymer material and a water-absorbing cellulose fiber, and eliminates the above-mentioned conventional drawbacks. be.
本考案を構成する生体吸収性の合成高分子とし
てはポリグリコール酸が吸収性、強力調整の面で
最適であるが、場合によつてはポリラクチド、ポ
リジオキサノン、ポリカプロラクトン等の適用も
可能である。また、引裂強さを10〜300gと特定
したのは10g未満では製造過程における保形性に
問題がありメツシユ状の編、織物として取り扱え
ないためであり、また、300gを越えると柔軟性
が付与されないため肌触りが悪く、また、適度に
脆化されていないため取外しの際に苦痛を与え、
また体内への吸収にも必要以上に時間がかかるの
で好ましくない。かかる強度の調整は、ポリグリ
コール酸を例にとると、編、織成後そのまま大気
中に長期的に放置してもよいが、短時間での処理
は熱処理が効果的で、例えば、熱水中での処理は
好適には90℃で約3時間、高圧蒸気による処理は
例えば、120℃で約30分処理するのが好ましく創
部添布後2〜3日で紛々になる程度に処理される
のが望ましい。 As the bioabsorbable synthetic polymer constituting the present invention, polyglycolic acid is most suitable in terms of absorbability and strength adjustment, but polylactide, polydioxanone, polycaprolactone, etc. may also be used in some cases. In addition, the tear strength was specified as 10 to 300 g because if it is less than 10 g, there will be problems with shape retention during the manufacturing process and it cannot be handled as a mesh-like knit or woven fabric, and if it exceeds 300 g, flexibility will be imparted. It feels bad to the touch because it is not embrittled, and it is painful to remove because it is not properly embrittled.
Also, it takes longer than necessary for absorption into the body, which is undesirable. To adjust the strength of polyglycolic acid, for example, it is possible to leave it in the air for a long time after knitting and weaving, but heat treatment is effective for short-term treatment, such as hot water treatment. It is preferable that the treatment be carried out at 90°C for about 3 hours, and the treatment with high-pressure steam should be carried out at 120°C for about 30 minutes. It is desirable to
また、これと交編織されるセルロース系繊維と
しては精練され、吸水性を高めた30〜100番手の
綿糸が好適である。これを2〜10本おきに用い
る。 Further, as the cellulose fiber to be mixed and woven with this, 30 to 100 count cotton yarn, which has been refined and has increased water absorption, is suitable. Use this every 2 to 10 times.
更に、交編織にかかる編、織組織は通常よく知
られているところの平、綾、朱子等の織組織、
平、フライス、両面、トリコツト等の編組織を任
意に選択して用いることができ、また、生体吸収
性高分子繊維糸とセルロース系繊維糸との交編、
交織率はその目的により任意に選択して用いるも
のであるが、セルロース系繊維糸を2〜10本おき
に用いるのが好適である。 Furthermore, the knitting and weaving structures involved in interwoven weaving are usually well-known weaving structures such as flat, twill, and satin.
Knitting structures such as flat, milled, double-sided, and tricot can be arbitrarily selected and used, and cross-knitting of bioabsorbable polymer fiber yarn and cellulose fiber yarn,
The weaving rate can be selected arbitrarily depending on the purpose, but it is preferable to use every 2 to 10 cellulose fiber yarns.
(作用)
本考案は、生体吸収性合成高分子繊維と吸水吸
湿性のセルロース系繊維との交編織物から成り立
つているため、下記の作用、効果を有する。(Function) Since the present invention is composed of an interwoven fabric of bioabsorbable synthetic polymer fibers and water-absorbing cellulose fibers, it has the following functions and effects.
即ち、生体吸収合成高分子繊条層は、皮膚によ
く密着し体液滲出液はセルロース系編、織成物に
吸収排出するので上皮細胞の遊送を助け、傷の治
療が促進される。また、生体吸収性繊条は柔軟性
のある加工を施してあるため創傷部によく密着す
ると共に一定の短い期間内に分解、強力低下を起
す。更に、生体吸収性材料のため、治癒までその
まま放置しても傷口を損傷したり、苦痛を与える
ことがない。 That is, the bioabsorbable synthetic polymer filament layer adheres well to the skin, and body fluid exudates are absorbed and excreted into the cellulose-based fabric, thereby aiding the migration of epithelial cells and promoting wound healing. Furthermore, since the bioabsorbable fibers have been processed to be flexible, they adhere well to the wound area and decompose and lose strength within a certain short period of time. Furthermore, since it is a bioabsorbable material, it will not damage the wound or cause pain even if it is left as is until it heals.
(実施例) 以下、その構成について例示する。(Example) The configuration will be illustrated below.
第1図は本考案の構成を例示したもので、片面
粘着テープ1の粘着テープ面に生体吸収性の合成
高分子繊条とセルロース系繊維を交織して成る織
物地2を貼着して成る。尚、かかる片面粘着テー
プ1は第2図の断面図に示すように、合成樹脂フ
イルム3の上に粘着剤4を塗布して成るものであ
る。 Figure 1 shows an example of the configuration of the present invention, in which a woven fabric 2 made by interweaving bioabsorbable synthetic polymer fibers and cellulose fibers is adhered to the adhesive tape surface of a single-sided adhesive tape 1. . The single-sided adhesive tape 1 is made by coating a synthetic resin film 3 with an adhesive 4, as shown in the sectional view of FIG.
かかる構成において、織物地2は第3図のよう
に固有粘度1.2のポリグリコール酸を溶融紡糸し
て18フイラメントでフイラメント当り2.5デニー
ルの糸を得これを45℃にて4倍延伸して配向性を
高めた吸収性繊維糸5と精練処理された60番手の
綿糸6を綿糸がタテ糸、ヨコ糸共4本おきに位置
するように平織で構成したものであり、これを更
にオートクレーブ中で121℃にて30分間処理し柔
軟且つ、手でちぎれる程度の強力即ち、引裂き強
さを150gに調整したものである。 In this structure, the fabric 2 is made by melt-spinning polyglycolic acid with an intrinsic viscosity of 1.2 to obtain yarn with 18 filaments and 2.5 denier per filament, as shown in FIG. It is made of absorbent fiber yarn 5 with increased viscosity and 60 count cotton yarn 6 that has been scoured in a plain weave so that the cotton yarns are positioned every fourth in both the warp and weft, and this is further woven in an autoclave for 121 It was processed at ℃ for 30 minutes to make it flexible and strong enough to be torn by hand, that is, the tear strength was adjusted to 150 g.
(考案の効果)
本考案は以上の構成であるため、皮膚によく密
着し体液滲出液はセルロース系繊維で吸収排出さ
れるため上皮細胞の遊送を助け、傷の治療が促進
され、また、これが柔軟性のある加工を施してあ
るため創傷部を刺激することなくよく密着する。
更に、生体吸収性材料のため、治癒までそのまま
放置しても傷口を損傷したり、苦痛を与えること
がなくヤケド、擦過傷等外傷に起因する潰傷、局
部の血行障害による潰瘍褥瘡など皮膚潰瘍に対し
て組織損傷を防止し、創部保護と優れた治癒効果
を発揮する。(Effects of the invention) Since the present invention has the above structure, it adheres well to the skin and body fluid exudates are absorbed and discharged by the cellulose fibers, which helps the migration of epithelial cells and promotes wound healing. It has been treated to be flexible, so it adheres well to the wound without irritating it.
Furthermore, since it is a bioabsorbable material, it will not damage the wound or cause pain even if left until it heals, and will not cause skin ulcers such as burns, ulcers caused by trauma such as abrasions, ulcers and bedsores due to local blood circulation disorders. It prevents tissue damage, protects the wound, and exhibits excellent healing effects.
また、第4図に示すように前記の如く構成した
交織物の肌に接しない面側に更にセルロース繊維
糸単独にて編成した生地7を重ね合せて二重の構
成とすると吸収性を高めると共にクツシヨン性を
付与することができる利点がある。かかる構成は
前記した生体吸収性合成高分子と吸水吸湿性のセ
ルロース系繊維との交編織比において極端に吸水
吸湿性のセルロース系繊維の比率が低いか、また
は生体吸収性合成高分子のみから成り立つている
ときに好適である。 Further, as shown in FIG. 4, if a fabric 7 knitted solely from cellulose fiber yarn is further superimposed on the side of the mixed fabric constructed as described above that does not come in contact with the skin to form a double structure, absorbency will be increased and It has the advantage of imparting cushioning properties. Such a structure has an extremely low ratio of water-absorbing and hygroscopic cellulose-based fibers in the weaving ratio of the above-mentioned bio-absorbable synthetic polymer and water-absorbing and hygroscopic cellulose-based fibers, or consists only of bio-absorbable synthetic polymers. It is suitable when you are
第1図は本考案の構成を例示した正面図、第2
図は第1図A−A線断面図、第3図は本考案の織
物地を例示した正面図、第4図は他の構成例を示
した斜視図。
1……片面粘着テープ、2……織物地、5……
生体吸収性繊維糸、6……綿糸、7……セルロー
ス系繊維単独編地。
Figure 1 is a front view illustrating the configuration of the present invention;
The figures are a sectional view taken along the line A-A in FIG. 1, FIG. 3 is a front view illustrating the fabric of the present invention, and FIG. 4 is a perspective view illustrating another example of the structure. 1... Single-sided adhesive tape, 2... Woven fabric, 5...
Bioabsorbable fiber yarn, 6... Cotton yarn, 7... Cellulose fiber single knitted fabric.
Claims (1)
繊維を交編織して成りこれの引裂強さを10〜
300gに調整して成ることを特徴とする生体吸
収性創傷被覆材。 (但し、引裂強さはJIS L−1096法の測定に
よる) 2 セルロース系繊維より成る編織物と重ね合せ
た構成より成ることを特徴とする実用新案登録
請求の範囲第1項記載の生体吸収性創傷被覆
材。 3 粘着材がコーテイングされたプラスチツクフ
イルムシート上に貼着されて成ることを特徴と
する実用新案登録請求の範囲第1項記載の生体
吸収性創傷被覆材。[Claims for Utility Model Registration] 1. Made by mixing and weaving bioabsorbable synthetic polymer fibers and cellulose fibers, the tear strength of which is 10~10.
A bioabsorbable wound dressing characterized by being adjusted to 300g. (However, the tear strength is measured according to JIS L-1096 method.) 2. Bioabsorbability according to claim 1 of the utility model registration claim, characterized in that it is constructed by laminating a knitted fabric made of cellulose fibers. Wound dressings. 3. The bioabsorbable wound dressing according to claim 1, which is made of a plastic film sheet coated with an adhesive.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20083686U JPH0236517Y2 (en) | 1986-12-26 | 1986-12-26 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP20083686U JPH0236517Y2 (en) | 1986-12-26 | 1986-12-26 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63103642U JPS63103642U (en) | 1988-07-05 |
JPH0236517Y2 true JPH0236517Y2 (en) | 1990-10-04 |
Family
ID=31163727
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP20083686U Expired JPH0236517Y2 (en) | 1986-12-26 | 1986-12-26 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0236517Y2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2619972B2 (en) * | 1990-06-29 | 1997-06-11 | 株式会社ニッショー | Medical prosthetic materials |
-
1986
- 1986-12-26 JP JP20083686U patent/JPH0236517Y2/ja not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS63103642U (en) | 1988-07-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2293752B1 (en) | Wound dressing | |
US4984570A (en) | Knitted hydrophobic web wound dressing | |
Rajendran et al. | Developments in medical textiles | |
US3903882A (en) | Composite dressing | |
EP1904011B1 (en) | Wound dressing material | |
AU2012314476B2 (en) | Improved wound dressing | |
US3896802A (en) | Flexible flocked dressing | |
US20130096524A1 (en) | Wound treatment article, containing a portion of modified natural fibers or synthetic fibers | |
US20100042034A1 (en) | Wound care product, comprising textile ribbons with fibres having gel-forming properties, and fibres not having gel-forming properties | |
GB2568101A (en) | Antimicrobial dressing | |
JP2009542353A (en) | Growth-stimulated wound dressing with improved contact surface | |
IL46797A (en) | Synthetic surgical dressing | |
AU2012348349B2 (en) | Non-adherent wound dressings and related methods therefor | |
EP2760487B1 (en) | Wound dressings and related methods therefor | |
EP3288512B1 (en) | Wound dressing | |
EP1435247B1 (en) | Wound dressings comprising an alginate fabric and a superabsorbent | |
JPH0236517Y2 (en) | ||
EP0849388A1 (en) | Fabrication process for non-woven fabric and products thereof | |
RU2240140C2 (en) | Medicinal multilayer bandage and articles based on such bandage | |
JPH0425131Y2 (en) | ||
EP1005844B1 (en) | Bandage cloth having an extended therapeutic action | |
RU2126692C1 (en) | Dressing for treating wounds | |
RU29463U1 (en) | Textile-based multilayer medical napkin | |
JP2000176000A (en) | Bandage for wound | |
ES2575784T3 (en) | Improved wound dressing |