JPH0442020B2 - - Google Patents
Info
- Publication number
- JPH0442020B2 JPH0442020B2 JP59188436A JP18843684A JPH0442020B2 JP H0442020 B2 JPH0442020 B2 JP H0442020B2 JP 59188436 A JP59188436 A JP 59188436A JP 18843684 A JP18843684 A JP 18843684A JP H0442020 B2 JPH0442020 B2 JP H0442020B2
- Authority
- JP
- Japan
- Prior art keywords
- chitin
- skin
- porous
- burns
- water
- 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
Links
- 229920002101 Chitin Polymers 0.000 claims description 29
- 239000000463 material Substances 0.000 claims description 21
- 238000011282 treatment Methods 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 3
- 238000000465 moulding Methods 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 2
- 206010052428 Wound Diseases 0.000 description 25
- 208000027418 Wounds and injury Diseases 0.000 description 25
- 210000003491 skin Anatomy 0.000 description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 210000000416 exudates and transudate Anatomy 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 8
- -1 polypropylene Polymers 0.000 description 7
- 230000001681 protective effect Effects 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000001179 sorption measurement Methods 0.000 description 5
- 230000003179 granulation Effects 0.000 description 4
- 238000005469 granulation Methods 0.000 description 4
- 238000003306 harvesting Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229920003169 water-soluble polymer Polymers 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 229920001817 Agar Polymers 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 3
- 239000008272 agar Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 238000004108 freeze drying Methods 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 206010053615 Thermal burn Diseases 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000001112 coagulating effect Effects 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 210000000981 epithelium Anatomy 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 230000035876 healing Effects 0.000 description 2
- 229930014626 natural product Natural products 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 230000037380 skin damage Effects 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- 241000238424 Crustacea Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 102000009123 Fibrin Human genes 0.000 description 1
- 108010073385 Fibrin Proteins 0.000 description 1
- BWGVNKXGVNDBDI-UHFFFAOYSA-N Fibrin monomer Chemical compound CNC(=O)CNC(=O)CN BWGVNKXGVNDBDI-UHFFFAOYSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- OVRNDRQMDRJTHS-FMDGEEDCSA-N N-acetyl-beta-D-glucosamine Chemical group CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O OVRNDRQMDRJTHS-FMDGEEDCSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 210000000170 cell membrane Anatomy 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 229920001436 collagen Polymers 0.000 description 1
- 230000001054 cortical effect Effects 0.000 description 1
- 238000002316 cosmetic surgery Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002500 effect on skin Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 210000002615 epidermis Anatomy 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229950003499 fibrin Drugs 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 230000008571 general function Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- CZMAXQOXGAWNDO-UHFFFAOYSA-N propane-1,1,2-triol Chemical compound CC(O)C(O)O CZMAXQOXGAWNDO-UHFFFAOYSA-N 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 230000000472 traumatic effect Effects 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Materials For Medical Uses (AREA)
Description
【発明の詳細な説明】
本発明は、創傷被覆保護材に関するものであ
り、さらに詳しくは熱傷、採皮創、剥削創、外傷
性削皮創などの皮膚欠損傷に対し好ましく用いら
れる保護材に関し、多孔性キチン成形体からなる
皮膚欠損傷に対する保護材に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a wound covering and protection material, and more particularly to a protection material preferably used for skin damage such as burns, dermabrasion wounds, abrasion wounds, and traumatic dermabrasion wounds. This invention relates to a protective material for skin damage made of a porous chitin molded body.
従来から、熱傷、採皮創等の皮膚欠損傷に対し
ての好ましい治療は、形成外科及び皮膚科領域に
おいて大きな課題であり、その創傷被覆保護材と
して多くの材料が検討されてきた。例えば、合成
物からなるものとしてナイロン、ポリエステル、
ポリプロピレン、レーヨン等の特殊織物(直径数
百ミクロンの単繊維がループ状又は毛羽状に表面
に突出している。)これら織物とシリコーンシー
トとの積層体、ホルマル化ビニルアルコールスポ
ンジ、エチレン酸化物とポリオキシプロピレング
リコールとのブロツク共重合体のゲル化物あるい
は抗生物質含有軟膏をしみこませた“ソフラチユ
ール”ガーゼ(日本ルセル)等があり、また生物
材料を素材としてものとしてフイブリン膜、プラ
ズマ膜、さらにはコラーゲン繊維を不織布とした
もの(商品名:メイパツク 明治製菓販売)、豚
の背部の真皮層を減菌凍結乾燥したポーシンスキ
ン等がある。 BACKGROUND OF THE INVENTION Conventionally, preferable treatments for skin defects such as burns and skin extraction wounds have been a major issue in the fields of plastic surgery and dermatology, and many materials have been investigated as wound covering and protective materials. For example, nylon, polyester,
Special fabrics such as polypropylene and rayon (single fibers with a diameter of several hundred microns protrude from the surface in the form of loops or fluff.) Laminated products of these fabrics and silicone sheets, formalized vinyl alcohol sponge, ethylene oxide and polyester There are gelatinized block copolymers with oxypropylene glycol and "Sofuratyur" gauze (Nippon Lucelle) impregnated with antibiotic-containing ointment, and products made from biological materials such as fibrin membranes, plasma membranes, and even collagen. There are non-woven fibers (product name: Meipatsuku, sold by Meiji Seika) and Poshinskin, which is made by sterilizing and freeze-drying the dermal layer of the pig's back.
しかしながら、これらの材料は皮層欠損傷のた
めの保護材として必ずしも満足のできる材料では
なかつた。すなわち、一般に創傷被覆保護材とし
ての機能は新生皮膚が形成されるまでの創面から
の生体成分の喪失防止、感染防止、肉芽、上皮形
成生成の補助であり、そのためには強度、患部へ
の密着性、吸水性及び浸出液の吸着性、透湿性、
組織適合性、非抗原性、新生皮膚促進性等の性質
を有することが必要である。しかし、従来の合成
物質からなるものでは、これらの性質のうち吸水
性や浸出液の吸着性、透湿性等が劣り、天然物か
らなるものでは強度、浸出液の吸着性等が劣り、
特に深い傷の場合には治療後、数日間でどろどろ
にとけてしまう等の欠点があつた。したがつて、
これらの従来の合成物や天然物で傷の保護を行つ
た場合には、結果として肉芽、上皮形成等が十分
に行われていなかつた。例えば、熱傷に関してい
えば、その損傷の程度に応じて度熱傷、浅在
度熱傷、深在度熱傷、度熱傷にわけられるが
従来のものは浅在度熱傷、すなわち軽度な熱傷
の治療に限られ、また植皮後の採皮創の治療にも
中間分層植皮によるもの程度にかぎられるという
欠点があつた。 However, these materials were not necessarily satisfactory as protective materials for cortical defects. In other words, the general function of a wound covering material is to prevent the loss of biological components from the wound surface until new skin is formed, prevent infection, and assist in the formation of granulation and epithelium. properties, water absorption and exudate adsorption, moisture permeability,
It is necessary to have properties such as histocompatibility, non-antigenicity, and ability to promote new skin. However, conventional synthetic materials have poor water absorption, exudate adsorption, moisture permeability, etc., while natural products have poor strength, exudate adsorption, etc.
Particularly in the case of deep wounds, it had the disadvantage that it would become mushy within a few days after treatment. Therefore,
When wounds were protected with these conventional synthetic or natural products, granulation, epithelial formation, etc. did not occur sufficiently as a result. For example, when it comes to burns, they are classified into degree burns, superficial degree burns, deep degree burns, and degree burns, depending on the degree of damage. Conventional burns are limited to the treatment of superficial degree burns, that is, mild burns. Furthermore, the treatment of skin harvest wounds after skin grafting also had the drawback of being limited to intermediate-thickness skin grafting.
本発明者らは、患部への密着性、浸出液の吸着
性が良好で、浸出液が患部へ貯留せず、治癒に到
るまで溶解又は損傷を起こさず、好ましい肉芽、
上皮の形成が行われる創傷被覆保護材を開発する
べく鋭意研究した結果、キチンからなる多孔性成
形体が創傷被覆保護材として優れていることを見
出し、本発明に到達したものである。 The present inventors have found favorable granulation, which has good adhesion to the affected area and adsorption of exudate, does not accumulate exudate in the affected area, and does not dissolve or damage until healing occurs.
As a result of intensive research aimed at developing a wound covering material in which epithelium is formed, it was discovered that a porous molded article made of chitin is excellent as a wound covering material, and the present invention was thus achieved.
すなわち、本発明は湿式成形法により製造され
た多孔性キチン成形体からなる創傷被覆保護材で
ある。 That is, the present invention is a wound covering protection material made of a porous chitin molded article produced by a wet molding method.
本発明において、キチンとは、甲殻類、昆虫類
の外骨格等を塩酸処理並びにカ性ソーダ処理して
蛋白質及びカルシウワ分を分離精製することによ
つて得られるポリ(N−アセチル−D−グルコサ
ミン)あるいはそれらの誘導体をいう。キチンの
誘導体としては、アセチルグルコサミン基の一部
が脱アセチル化したもの、エーテル化物、エステ
ル化物、カルボキシメチル化物、ヒドロキシエチ
ル化物、o−エチル化物等があげられ、好ましい
具体例としてはポリ〔N−アセチル−6−O−
(2′−ヒドロキシエチル)−D−グルコサミン〕,
ポリ〔N−アセチル−6−O−(エチル)−D−グ
ルコサミン〕等があげられる。 In the present invention, chitin refers to poly(N-acetyl-D-glucosamine) obtained by treating the exoskeleton of crustaceans and insects with hydrochloric acid and caustic soda to separate and purify protein and calcium. ) or their derivatives. Examples of chitin derivatives include those in which acetylglucosamine groups are partially deacetylated, etherified products, esterified products, carboxymethylated products, hydroxyethylated products, o-ethylated products, etc. Preferred specific examples include poly[N -acetyl-6-O-
(2'-hydroxyethyl)-D-glucosamine],
Examples include poly[N-acetyl-6-O-(ethyl)-D-glucosamine].
これらキチンから得る多孔性キチン成形体とは
乾燥状態で測定された気孔率(B/A×100%;B:
単位重量の多孔性成形体に含まれる細孔の容積、
A:単位重量の多孔性成形体の全容積)が90%以
上である成形体、例えばシート状、棒状、繊維状
等の湿式成形可能な成形体を意味する。 The porous chitin molded body obtained from these chitins has a porosity measured in a dry state (B/A x 100%; B: volume of pores contained in a porous molded body per unit weight,
A: Means a molded product whose total volume per unit weight of the porous molded product is 90% or more, such as a wet-formable molded product such as a sheet, rod, or fiber shape.
かかる多孔性キチン成形体は、例えば以下のご
とき方法によつて製造することができる。 Such porous chitin molded bodies can be produced, for example, by the following method.
精製されたキチンを、公知のキチンの溶剤、例
えばジメチルアセトアミドと塩化リチウムの混合
物、N−メチルピロリドンと塩化リチウムの混合
物、トリクロル酢酸とハロゲン化炭化水素の混合
物に0.5〜15重量%程度の濃度で溶解してドープ
を得る。このドープに、常温で固体である水溶性
高分子、例えばポリビニルアルコール、ポリエチ
レングライコール、ポリプロピレングライコー
ル、寒天、水溶性デンプン、蛋白質等、好ましく
はポリビニルアルコール又は寒天をドープ中に均
一に分散させる。その際、キチンドープ対水溶性
高分子の比率は1/5〜5/1(重量比)の範囲
から選ぶのが好ましい。水溶性高分子の混合され
たキチンドープは、形枠等に流し込んだり、スリ
ツト状ダイから押し出す等の方法で好ましい形状
を保たせながら、凝固液にて凝固を行う。凝固液
としては例えば水又はメチルアルコール、エチル
アルコール、プロピルアルコール、ブチルアルコ
ール等のアルコール類、又はアセトン等のケトン
類が好ましく用いられる。溶剤が十分に除去さ
れ、凝固が終了した後、凝固物は水又は水溶液で
処理を行う。一般には水溶性高分子は低温で、こ
の凝固物中から除去し難いので、60℃〜125℃の
高温での処理が好ましく、時間は30分以上が好ま
しい。処理後の十分に洗浄された成形体は含水率
の高いスポンジ状を呈しており、この状態から乾
燥体を得るには、一般的な常温乾燥を行つてもよ
いが、凍結乾燥法が好ましく使用される。すなわ
ち、水を含んだままで成形体を約−40℃の温度で
凍結した後、10℃の温度で凍結乾燥を行うのが好
ましい。 The purified chitin is added to a known chitin solvent such as a mixture of dimethylacetamide and lithium chloride, a mixture of N-methylpyrrolidone and lithium chloride, a mixture of trichloroacetic acid and a halogenated hydrocarbon at a concentration of about 0.5 to 15% by weight. Dissolve to obtain dope. A water-soluble polymer that is solid at room temperature, such as polyvinyl alcohol, polyethylene glycol, polypropylene glycol, agar, water-soluble starch, protein, etc., preferably polyvinyl alcohol or agar, is uniformly dispersed in this dope. At that time, the ratio of chitin dope to water-soluble polymer is preferably selected from the range of 1/5 to 5/1 (weight ratio). The chitin dope mixed with a water-soluble polymer is solidified in a coagulating liquid while maintaining a desired shape by pouring into a form or extruding from a slit die. As the coagulating liquid, for example, water, alcohols such as methyl alcohol, ethyl alcohol, propyl alcohol, and butyl alcohol, or ketones such as acetone are preferably used. After the solvent has been sufficiently removed and coagulation has been completed, the coagulated product is treated with water or an aqueous solution. In general, water-soluble polymers are difficult to remove from the coagulated material at low temperatures, so treatment at a high temperature of 60° C. to 125° C. is preferred, and the treatment time is preferably 30 minutes or more. The molded product that has been thoroughly washed after processing has a sponge-like shape with a high moisture content. To obtain a dried product from this state, ordinary room temperature drying may be performed, but freeze-drying is preferably used. be done. That is, it is preferable to freeze the molded product at a temperature of about -40°C while containing water, and then freeze-dry it at a temperature of 10°C.
本発明における多孔性キチン成形体としては、
上記のごとくにして得られた多孔性キチン成形体
をアルカリ溶液中で処理したものが好ましく用い
られる。アルカリ処理を行うための好ましい条件
は、例えばカ性ソーダの5〜60W/V%水溶液を
用い、温度10〜120℃で1分間以上処理するもの
である。本発明において、とくに好ましく用いら
れる多孔性キチン成形体は、処理後、中和された
ものが25℃、2V/V%酢酸水溶液に浸漬された
ときに溶解しないものである。 The porous chitin molded article in the present invention includes:
A porous chitin molded article obtained as described above treated in an alkaline solution is preferably used. Preferred conditions for carrying out the alkali treatment are, for example, using a 5 to 60 W/V% aqueous solution of caustic soda at a temperature of 10 to 120° C. for one minute or more. In the present invention, the porous chitin molded article particularly preferably used is one that does not dissolve when it is neutralized after treatment and immersed in a 2V/V% acetic acid aqueous solution at 25°C.
本発明における多孔性キチン成形体は、滅菌の
うえ、創傷被覆保護材として使用されるが、とく
に好ましいのは1g/mm2以上の湿潤強度を有する
ものである。このように高い湿潤強度をもつもの
が創傷被覆保護材として好ましく、特に熱傷、植
皮後の採皮創等の治療に対してめざましい効果を
発揮する。すなわち、皮膚欠損傷の創傷被覆保護
材として使用した場合、浸出液の吸着が良好であ
り、患部への浸出液の貯留が少なくなり、長期使
用後も体液による溶解が起こらず、患部が適度な
湿潤状態に保たれるために、良好な新生皮膚の再
生が行われるという画期的な効果を有するもので
ある。 The porous chitin molded article according to the present invention is used as a wound covering material after sterilization, and it is particularly preferable to have a wet strength of 1 g/mm 2 or more. Materials with such high wet strength are preferable as wound covering and protective materials, and are particularly effective in treating burns, skin-grafted wounds after skin grafting, and the like. In other words, when used as a wound dressing for skin defects, it has good adsorption of exudate, reduces accumulation of exudate in the affected area, prevents dissolution by body fluids even after long-term use, and leaves the affected area moderately moist. This has the revolutionary effect of ensuring good regeneration of new skin.
本発明の創傷被覆保護材は、浅在熱傷度、中
間分層植皮の採皮創等はもちろんのこと、従来の
創傷被覆保護材では治療ができなかつた深在熱傷
度、厚い分層植皮の採皮創の保護材として極め
て効果的に使用できる。 The wound dressing of the present invention can be used not only for superficial burns and intermediate-thickness skin graft wounds, but also for deep burns and thick split-thickness skin grafts that cannot be treated with conventional wound dressings. It can be used extremely effectively as a protective material for skin harvest wounds.
以下、実施例をあげ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
キチン粉末(共和油脂製)を100メツシユに粉
砕し、1N−HClにて4℃で1時間処理し、さら
に3%NaOH液中で3時間、90〜100℃で加熱
し、水洗をくりかえし乾燥した。得られたキチン
を室温で、塩化リチウム8重量%を含んだジメチ
ルアセトアミド溶媒に濃度が2重量%になるよう
に溶解して透明な液を得たのち、1480メツシユス
テンレスネツトにて加圧濾過し、さらに撹拌を行
いながら減圧下で脱泡を行つてキチンドープを得
た。Example 1 Chitin powder (manufactured by Kyowa Yushi Co., Ltd.) was ground into 100 meshes, treated with 1N-HCl at 4°C for 1 hour, heated in 3% NaOH solution for 3 hours at 90-100°C, and washed with water. Dry repeatedly. The obtained chitin was dissolved at room temperature in a dimethylacetamide solvent containing 8% by weight of lithium chloride to a concentration of 2% by weight to obtain a clear liquid, which was then filtered under pressure using a 1480 mesh stainless steel net. Then, defoaming was performed under reduced pressure while stirring to obtain a chitin dope.
このキチンドープ100gにポバールUF−170GS
(ユニチカケミカル株式会社製;重合度170、ケン
化度95%以上)50gを添加し、撹拌翼を有したビ
ーカー中で1時間撹拌して均一な分散液を作成し
た。この分散液をガラス板上へ1mmの厚さで流延
し、その後約25℃の水に浸漬して十分に凝固及び
洗浄を行つてシートを得た。次いで、このシート
を水に浸漬した後、沸とう状態で5時間処理して
シート状キチン成形体を得た。この成形体を−40
℃で凍結した後、10℃で凍結乾燥を行つて、多孔
質キチン成形体を得た。この成形体の気孔率は
99.2%であり、湿潤強度は4.5g/mm2であつた。 100g of this chitin dope and Poval UF-170GS
(manufactured by Unitika Chemical Co., Ltd.; degree of polymerization 170, degree of saponification 95% or more) was added and stirred for 1 hour in a beaker equipped with a stirring blade to prepare a uniform dispersion. This dispersion was cast onto a glass plate to a thickness of 1 mm, and then immersed in water at about 25°C to sufficiently coagulate and wash to obtain a sheet. Next, this sheet was immersed in water and then treated in a boiling state for 5 hours to obtain a sheet-like chitin molded article. This molded body is −40
After freezing at 10°C, freeze-drying was performed at 10°C to obtain a porous chitin molded body. The porosity of this molded body is
99.2%, and the wet strength was 4.5 g/mm 2 .
このシート(たて120mm、よこ120mm、厚み0.8
mm)を滅菌して、創傷被覆保護材として使用し
た。 This sheet (length 120mm, width 120mm, thickness 0.8
mm) was sterilized and used as a wound dressing.
すなわち、背部皮膚に広範囲の熱傷を得て、深
在の熱傷度と判定された30才の男性の患部に対
して、この多孔質シートを創面に2枚貼付し、木
綿製ガーゼにて上部を保護した。 Specifically, two of these porous sheets were applied to the affected area of a 30-year-old man who had extensive burns on his back skin and were determined to be deep burns, and the upper part was covered with cotton gauze. Protected.
6日後、シートは損傷をうけることなく初期の
状態を保ち、かつ体内からの浸出液を吸着し、湿
潤状態となり、その一部はシート上に重ねた木綿
のガーゼに達していた。さらに、患部面は浸出液
の貯留が少なく、適切な湿潤状態を保つていた。
治療を続けて12日後シートは乾燥状態となり、容
易に患部から剥離することができ、患部には正常
な新生表皮が形成されて、治療が十分に行われた
ということを示していた。 After 6 days, the sheet remained undamaged and remained in its original state, adsorbed exudates from the body, and became moist, some of which had reached the cotton gauze layered on the sheet. Furthermore, there was little accumulation of exudate on the affected area and it maintained an appropriate moist state.
After 12 days of continued treatment, the sheet became dry and could be easily peeled off from the affected area, and normal new epidermis was formed on the affected area, indicating that the treatment had been sufficiently performed.
実施例 2
実施例1で得たキチン粉末を塩化リチウム8重
量%を含んだジメチルアセトアミド溶液に1重量
%溶解して、濾過、脱泡を行い、透明なキチンド
ープを得た。このドープ100gに寒天粉末100gを
添加して混合液を作成した。この液をたて15cm、
よこ15cm、深さ1mmの型枠に流し込み、メタノー
ルで凝固して、含まれている溶剤を除去してシー
トを得た。このシートを水に浸漬して121℃のオ
ートクレーブ中で1時間処理を行つた後、さらに
40%カ性ソーダ液で121℃、1時間のオートクレ
ーブ処理を行つた後、中和及び水洗を十分に行
い、さらに水を含んだままで−40℃で凍結したの
ち、10℃で凍結乾燥を行つたところ、湿潤強度
6.5g/mm2、気孔率99.2%の厚み0.8mmの多孔性キ
チンシートが得られた。Example 2 The chitin powder obtained in Example 1 was dissolved at 1% by weight in a dimethylacetamide solution containing 8% by weight of lithium chloride, and filtered and defoamed to obtain a transparent chitin dope. A mixed solution was prepared by adding 100 g of agar powder to 100 g of this dope. Pour this liquid 15cm tall,
The mixture was poured into a mold with a width of 15 cm and a depth of 1 mm, solidified with methanol, and the solvent contained therein was removed to obtain a sheet. After immersing this sheet in water and treating it in an autoclave at 121℃ for 1 hour,
After autoclaving with 40% caustic soda solution at 121℃ for 1 hour, thoroughly neutralize and wash with water, freeze at -40℃ while still containing water, and freeze-dry at 10℃. Finally, wet strength
A porous chitin sheet with a weight of 6.5 g/mm 2 and a porosity of 99.2% and a thickness of 0.8 mm was obtained.
この多孔性キチンシートを滅菌の上、厚い分層
植皮後の採皮創の保護材として使用した。すなわ
ち、患者は37才の女性で背部皮膚の採皮創にたて
12mmの2枚が貼付され、その上部を木綿製ガーゼ
で保護した。6日後、この保護材面には多くの浸
出液が認められ、患部には浸出液が少なく、肉芽
の生成が認められた。14日後には新生皮膚が形成
され、患部の治癒が良好であることを示してい
た。 This porous chitin sheet was sterilized and used as a protective material for a skin harvest wound after thick split-thickness skin grafting. Specifically, the patient was a 37-year-old woman who had a skin harvest wound on her back.
Two 12mm pieces were attached, and the upper part was protected with cotton gauze. After 6 days, a lot of exudate was observed on the surface of the protective material, and less exudate was observed in the affected area, and granulation was observed. After 14 days, new skin was formed, indicating that the affected area was healing well.
Claims (1)
形体からなる創傷被覆保護材。 2 多孔性キチン成形体が、湿潤強度が1g/mm2
以上のものである特許請求の範囲第1項記載の創
傷被覆保護材。 3 多孔性キチン成形体が、湿式成形後にアルカ
リ処理されたものである特許請求の範囲第1項記
載の創傷被覆保護材。[Scope of Claims] 1. A wound covering protection material comprising a porous chitin molded article produced by a wet molding method. 2 The porous chitin molded body has a wet strength of 1 g/mm 2
The wound covering protection material according to claim 1, which is as described above. 3. The wound covering protection material according to claim 1, wherein the porous chitin molded body is subjected to alkali treatment after wet molding.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59188436A JPS6164256A (en) | 1984-09-07 | 1984-09-07 | Wound covering protective material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59188436A JPS6164256A (en) | 1984-09-07 | 1984-09-07 | Wound covering protective material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6164256A JPS6164256A (en) | 1986-04-02 |
JPH0442020B2 true JPH0442020B2 (en) | 1992-07-10 |
Family
ID=16223641
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59188436A Granted JPS6164256A (en) | 1984-09-07 | 1984-09-07 | Wound covering protective material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6164256A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0622559B2 (en) * | 1985-09-02 | 1994-03-30 | ユニチカ株式会社 | Porous chitin molding for hemostasis |
JPS62238209A (en) * | 1986-04-08 | 1987-10-19 | Nippon Bio Kemikaruzu Kk | Production of spongy material for cosmetic |
JP2580136B2 (en) * | 1986-11-11 | 1997-02-12 | ユニチカ株式会社 | Wound covering protective material |
JPS63209661A (en) * | 1987-02-25 | 1988-08-31 | ユニチカ株式会社 | Wound protective material |
JPH074244B2 (en) * | 1991-06-25 | 1995-01-25 | 日本水産株式会社 | Microorganism-immobilized carrier and method for producing the same |
PL226837B1 (en) * | 2012-08-24 | 2017-09-29 | Celther Polska Spółka Z Ograniczoną Odpowiedzialnością | Active polymer layer formed of chitin derivatives, especially for dressing and its use |
-
1984
- 1984-09-07 JP JP59188436A patent/JPS6164256A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6164256A (en) | 1986-04-02 |
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