JPH05209318A - Calcium alginate fiber having excellent liquid absorbing property and covering material for medical use - Google Patents

Calcium alginate fiber having excellent liquid absorbing property and covering material for medical use

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Publication number
JPH05209318A
JPH05209318A JP4015018A JP1501892A JPH05209318A JP H05209318 A JPH05209318 A JP H05209318A JP 4015018 A JP4015018 A JP 4015018A JP 1501892 A JP1501892 A JP 1501892A JP H05209318 A JPH05209318 A JP H05209318A
Authority
JP
Japan
Prior art keywords
fiber
calcium alginate
physiological saline
calcium
covering material
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
JP4015018A
Other languages
Japanese (ja)
Inventor
Tatsuo Yamauchi
達夫 山内
Toshimasa Kuroda
俊正 黒田
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.)
Teijin Ltd
Original Assignee
Teijin 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 Teijin Ltd filed Critical Teijin Ltd
Priority to JP4015018A priority Critical patent/JPH05209318A/en
Publication of JPH05209318A publication Critical patent/JPH05209318A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain calcium alginate fiber having excellent liquid absorbing properties of electrolyte solutions such as bodily fluid, physiological saline solution, etc., and having good mechanical performances such as strength or brittleness. CONSTITUTION:The objective calcium alginate fiber has 20-50g/g absorptivity of physiological saline solution when immersed at 37 deg.C for 4hr and the objective medical covering material consisting of the fiber. Since the fiber and the material are excellent in the absorptivity of bodily fluid and adhesion to lesion, they prevent microbial infection and the proliferation, thus have healing promotion effect.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、体液等の電解質水溶液
の吸収性に優れたアルギン酸カルシウム繊維及びそれか
らなる医療用被覆材に関する。さらに詳しくは、体液の
吸収性に優れているため、創傷(機械的外力によるもの
だけでなく、熱傷、薬傷等も含む)や褥瘡の治療に適す
るアルギン酸カルシウム繊維及びそれからなる医療用被
覆材に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a calcium alginate fiber excellent in absorption of an aqueous electrolyte solution such as body fluid, and a medical covering material comprising the same. More specifically, the present invention relates to a calcium alginate fiber suitable for treating wounds (including not only those caused by mechanical external force but also burns, chemical injuries, etc.) and pressure ulcers because of its excellent absorption of body fluids, and a medical covering material comprising the same. ..

【0002】[0002]

【従来の技術】アルギン酸アルカリ金属塩の水溶液をカ
ルシウムイオンを含有する水溶液中に押し出してアルギ
ン酸カルシウム繊維を形成することは、例えば英国特許
第567641号、同第568771号、同57165
7号、特開昭61―174499号公報等が知られてい
る。このようにして得られたアルギン酸カルシウム繊維
は、一般的には、アルギン酸カルシウムの一部をナトリ
ウムの形態に転化された後、外科用縫合糸、ガーゼ、脱
脂綿などとして用いられてきた。
2. Description of the Related Art Extruding an aqueous solution of an alkali metal alginate into an aqueous solution containing calcium ions to form calcium alginate fibers is described in, for example, British Patent Nos. 567641, 568771 and 57165.
No. 7, JP-A-61-174499 and the like are known. The calcium alginate fiber thus obtained has been generally used as a surgical suture, gauze, absorbent cotton, etc. after converting a part of calcium alginate into a form of sodium.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、かかる
アルギン酸繊維は、脆い、弱い、及び水分に敏感である
という欠点があるばかりでなく、この繊維の表面はアル
ギン酸ナトリウム塩となっているため、創傷や褥瘡の被
覆材として用いた場合、傷部に繊維がべとつくといった
問題があった。一方、ナトリウム塩の形態に転換されて
いないアルギン酸カルシウム繊維は、脆くて弱いという
欠点があり、そのままでは実用に供し難いものである。
さらに、これらのアルギン酸繊維(例えばソルブサン、
カルトスタットの商品名で市販されている)は、体液の
吸収性が未だ不充分であった。
However, such alginate fibers have the drawbacks of being brittle, weak, and sensitive to moisture, and since the surface of the fibers is sodium alginate, it may cause damage to wounds and When used as a covering material for pressure ulcers, there was a problem that fibers were sticky to the wound. On the other hand, calcium alginate fibers that have not been converted to the sodium salt form have the drawback of being brittle and weak, and are difficult to put to practical use as they are.
In addition, these alginate fibers (eg sorbusan,
(Commercially available under the trade name of Kaltostat), the absorbability of body fluid was still insufficient.

【0004】本発明は、かかる従来技術を背景になされ
たもので、その目的は、水分に対する感受性が改善され
て取り扱いが容易でありながら、体液や生理食塩水等の
電解質溶液に対する高い吸液性を有し、且つ力学的特性
(強度、脆性)も良好で、創傷や褥瘡に好適に用いるこ
とのできるアルギン酸カルシウム繊維及びそれからなる
医療用被覆材を提供することにある。
The present invention has been made in view of the background of the prior art, and its object is to improve the sensitivity to water and to be easily handled, while having a high liquid absorbing property to an electrolyte solution such as body fluid or physiological saline. It is intended to provide a calcium alginate fiber which has excellent mechanical properties (strength and brittleness) and can be suitably used for wounds and pressure ulcers, and a medical covering material comprising the same.

【0005】[0005]

【課題を解決するための手段】本発明者らは、前記目的
を達成するために種々検討を重ねた結果、可溶性アルギ
ン酸塩を含む水溶液(ドープと称する)をカルシウム塩
を含有する紡糸浴中に紡糸するに際し、凝固浴中のカル
シウム塩濃度をドープ濃度に対応させて特定範囲にする
ことにより得られる繊維は、良好な電解質吸液性を有し
ながら改善された強度、脆性、及び水分感受性を有する
ことを見い出し本発明に到達した。
Means for Solving the Problems As a result of various studies to achieve the above object, the present inventors have found that an aqueous solution containing a soluble alginate (referred to as a dope) is added to a spinning bath containing a calcium salt. Upon spinning, the fiber obtained by adjusting the calcium salt concentration in the coagulation bath to a specific range corresponding to the dope concentration has improved strength, brittleness, and moisture sensitivity while having good electrolyte absorption. It has been found that the present invention has the present invention.

【0006】すなわち、本発明によれば、 1.下記式で表わされる生理食塩水吸収性Xが20〜5
0g/gであることを特徴とするアルギン酸カルシウム
繊維、 生理食塩水吸収性X=(A−B)/B (但し、Aは生理食塩水中に37℃下4時間浸漬した
後、350Gで10分間遠心脱水処理した後の繊維の重
量、Bは絶乾時の繊維の重量を表わす)及び 2.生理食塩水吸収性Xが25〜50g/gであるアル
ギン酸カルシウム繊維からなる医療用被覆材、が提供さ
れる。
That is, according to the present invention: The physiological saline absorbency X represented by the following formula is 20 to 5
Calcium alginate fiber characterized by being 0 g / g, physiological saline absorbability X = (AB) / B (where A is immersed in physiological saline at 37 ° C. for 4 hours and then at 350 G for 10 minutes) 1. The weight of the fiber after centrifugal dehydration treatment, B represents the weight of the fiber when absolutely dried) and 1. There is provided a medical covering material comprising calcium alginate fibers having a physiological saline absorbability X of 25 to 50 g / g.

【0007】本発明にかかるアルギン酸カルシウム繊維
は、水溶性のアルギン酸塩、例えばアルギン酸ナトリウ
ム塩、アルギン酸カリウム塩、アルギン酸ナトリウム塩
等の水溶液(紡糸ドープ)を、カルシウム塩を含有する
凝固液中に押し出すことによって得られるが、この際、
下記方法で測定した時の生理食塩水吸収性Xが20〜5
0g/gの範囲内にあることが肝要である。
The calcium alginate fiber according to the present invention is obtained by extruding an aqueous solution (spinning dope) of a water-soluble alginate, such as sodium alginate, potassium alginate and sodium alginate, into a coagulating solution containing calcium salt. It is obtained by
The physiological saline absorption X measured by the following method is 20 to 5
It is important to be within the range of 0 g / g.

【0008】アルギン酸カルシウム繊維Bg(絶乾重
量)を生理食塩水中に37℃下4時間浸漬し、次いで3
50Gの遠心力下10分間脱水した後、吸液したアルギ
ン酸カルシウム繊維の重量Agを測定する。この時、生
理食塩水吸収性Xは、下式 X=(A−B)/B:(g/g) で表わされる。
Calcium alginate fiber Bg (absolute dry weight) was immersed in physiological saline at 37 ° C. for 4 hours, and then 3
After dehydration under a centrifugal force of 50 G for 10 minutes, the weight Ag of the absorbed calcium alginate fiber is measured. At this time, the physiological saline absorbency X is represented by the following formula: X = (AB) / B: (g / g).

【0009】生理食塩水吸収性が20g/g未満の場合
には、アルギン酸繊維を外科及び医学用途例えば創傷被
覆材として使用する場合、体液吸収性が不充分となって
治癒促進効果は得られず、また繊維の強度及び脆性が不
充分となるため本発明の目的は達成できない。一方50
g/gを越える場合には、体液吸収時の形態保持性が低
下するため医療用被覆材として不適当になるだけでな
く、該繊維製造時の凝固浴のカルシウム塩濃度を低くす
る必要があるため、凝固性が低下して紡糸も困難にな
る。
When the physiological saline absorbency is less than 20 g / g, when the alginic acid fiber is used for surgical and medical applications such as a wound dressing, the body fluid absorbency becomes insufficient and a healing promoting effect cannot be obtained. Moreover, the strength and brittleness of the fibers are insufficient, so that the object of the present invention cannot be achieved. While 50
When it exceeds g / g, not only is it unsuitable as a medical covering material because the shape retention during absorption of body fluid is reduced, but it is also necessary to lower the calcium salt concentration in the coagulation bath during the production of the fiber. Therefore, the coagulability is lowered and spinning becomes difficult.

【0010】かかる本発明のアルギン酸カルシウム繊維
を製造する方法としては特に限定されないが、前記のア
ルギン酸塩水溶液(ドープ)を濾過して不溶物及びゴミ
等を除き脱泡した後、経0.05〜0.5mmの紡糸孔を
有する紡糸口金から、カルシウム塩溶液(例えば塩化カ
ルシウム水溶液)中に押し出す方法において、凝固浴の
カルシウムイオン濃度を、凝固浴温度、ドープ濃度、ド
ープ粘度等に応じて適宜変更することにより容易に得る
ことができる。すなわち、凝固浴中のカルシウムイオン
の濃度を、ドープ濃度及び紡糸条件に応じて調整するこ
とにより達成され、カルシウムイオン濃度が高くなりす
ぎると生理食塩水吸水性Xは小さくなりすぎ、逆にカル
シウムイオン濃度が低くなりすぎるとXは大きくなりす
ぎて本発明のアルギン酸繊維は得られなくなる。
The method for producing the calcium alginate fiber of the present invention is not particularly limited, but the above-mentioned alginate aqueous solution (dope) is filtered to remove insoluble matters and dusts, and then defoamed. In the method of extruding into a calcium salt solution (for example, calcium chloride aqueous solution) from a spinneret having 0.5 mm spinning holes, the calcium ion concentration of the coagulation bath is appropriately changed according to the coagulation bath temperature, dope concentration, dope viscosity, etc. Can be easily obtained. That is, it is achieved by adjusting the concentration of calcium ions in the coagulation bath according to the dope concentration and the spinning conditions. If the calcium ion concentration becomes too high, the physiological saline absorption X becomes too small, and conversely calcium ion When the concentration becomes too low, X becomes too large and the alginic acid fiber of the present invention cannot be obtained.

【0011】なお、用いるドープは紡糸可能な粘度範囲
にあればよく、これは可溶性アルギン酸塩の濃度、ドー
プ濃度、助剤の添加等により適宜調整すればよい。好ま
しい粘度は50〜2000ポイズの範囲であり、より好
ましくは100〜1500ポイズの範囲である。また凝
固浴としては、水溶性アルギン酸塩の陽イオンと交換し
てこれを不溶化しうるカルシウムイオンの水溶液(例え
ば塩化カルシウム)を含む水溶液が好ましいが、本発明
の目的を阻害しない範囲でカルシウムイオン以外の他の
金属イオンが含まれていてもよい。
The dope to be used may be in a viscosity range in which spinning is possible, and it may be appropriately adjusted by the concentration of soluble alginate, the concentration of dope, addition of an auxiliary agent and the like. The preferred viscosity is in the range of 50 to 2000 poise, more preferably 100 to 1500 poise. The coagulation bath is preferably an aqueous solution containing an aqueous solution of calcium ions (eg calcium chloride) that can be exchanged with the cations of the water-soluble alginate to insolubilize them, but other than calcium ions within the range not impairing the object of the present invention. Other metal ions may be included.

【0012】また、凝固したゲル状のアルギン酸繊維
は、水洗した後必要に応じて延伸することができる。こ
の水洗及び延伸を行なう際には、高温度下で行なうこと
が、洗浄効果が向上し、延伸倍率も大きくすることがで
きるので、強力向上の点で好ましい。
Further, the coagulated gel-like alginic acid fiber may be washed with water and stretched if necessary. When the washing and stretching are carried out at a high temperature, the washing effect can be improved and the stretching ratio can be increased, which is preferable from the viewpoint of improving the strength.

【0013】また洗浄、延伸された繊維は、乾燥工程に
供する前の段階で一旦脱水処理することが好ましく、脱
水工程を経ずに乾燥した場合には、単糸同士の膠着が発
生して後加工工程での取り扱い性が低下する場合があ
る。
The washed and drawn fibers are preferably dehydrated once before being subjected to the drying step. If the fibers are dried without undergoing the dehydration step, the single yarns will stick to each other after the drying. The handling property in the processing step may be deteriorated.

【0014】かくして得られる本発明のアルギン酸カル
シウム繊維は、例えば織編物、不織布、紙、シート、マ
ット等の面状体、トウ、綿等の繊維集合体、あるいは粉
体として利用できるが、適度な体液吸収性及び繊維物性
を有し、且つ創傷面に対して良好な密着性を有すること
から、布帛等の面状体になして医療用被覆材として用い
ることが望ましい。
The calcium alginate fiber of the present invention thus obtained can be used, for example, as a woven or knitted fabric, a non-woven fabric, a sheet such as a sheet, a mat or the like, a fiber aggregate such as tow or cotton, or a powder. Since it has body fluid absorbability and fiber physical properties, and has good adhesion to the wound surface, it is desirable to use it as a sheet material such as a cloth and use it as a medical covering material.

【0015】この際、体液吸収性を損わない範囲で、ま
た創傷や褥瘡の治療に支障を与えない範囲内で他の繊維
や剤を添加してもよい。
At this time, other fibers or agents may be added within a range that does not impair the absorbability of body fluids and within a range that does not hinder the treatment of wounds and pressure ulcers.

【0016】かかる剤としては、例えばコラーゲン、卵
殻膜、キチン、キトサンを例示することができ、これら
はドープ中に懸濁、分散させればよい。該剤の粒径は、
紡糸性の観点より紡糸孔径の0.5倍以下が望ましく、
またその配合割合は重量比で99.99:0.01〜5
0:50(アルギン酸塩:添加剤)の範囲が好ましく、
配合量が0.01重量%未満の場合には、創傷や褥瘡の
治癒促進効果は認められなくなる。一方50重量%を越
える場合には、紡糸性が低下すると同時に得られる繊維
の力学的特性が不充分となる。
Examples of such agents include collagen, eggshell membranes, chitin and chitosan, which may be suspended or dispersed in the dope. The particle size of the agent is
From the viewpoint of spinnability, 0.5 times or less of the spinning hole diameter is desirable,
The blending ratio is 99.99: 0.01-5 by weight.
The range of 0:50 (alginate: additive) is preferable,
If the content is less than 0.01% by weight, the effect of promoting the healing of wounds and pressure ulcers is not observed. On the other hand, when it exceeds 50% by weight, the spinnability is lowered and, at the same time, the mechanical properties of the obtained fiber are insufficient.

【0017】さらに本発明においては、患部及びその周
辺部の感染防止、感染部の化学療法、更には治癒の促進
を目的として、前記アルギン酸繊維中に薬剤を配合する
こともできる。添加する方法は任意で、水不溶性の薬剤
の場合には紡糸用ドープに添加する方法が好適である。
この場合、紡糸性の観点から薬剤の直径は紡糸孔径の
0.5倍以下の微粒子であることが好ましい。一方、水
溶性の薬剤の場合には製糸時や後加工時に凝固浴や水中
に溶出する場合もあるので、得られたアルギン酸カルシ
ウム繊維を、薬剤を含む溶液に含浸させた後乾燥する方
法が好ましい。いずれの添加方法によっても、薬剤は繊
維内部又は表面に添加されるので、褥瘡患部及びその周
辺部の感染防止、感染部の化学治療、更には治癒の促進
に対し、充分な効果を発揮することができる。
Further, in the present invention, a drug may be incorporated in the alginic acid fiber for the purpose of preventing infection of the affected area and its peripheral area, chemotherapeutic treatment of the infected area, and promoting healing. The method of addition is arbitrary, and in the case of a water-insoluble drug, the method of addition to the spinning dope is suitable.
In this case, from the viewpoint of spinnability, it is preferable that the diameter of the drug is fine particles having a diameter of 0.5 times the spinning hole diameter or less. On the other hand, in the case of a water-soluble drug, it may be eluted into the coagulation bath or water during spinning or post-processing, so the method of impregnating the obtained calcium alginate fiber with a solution containing the drug and then drying is preferred. .. Regardless of the method of addition, the drug is added to the inside or surface of the fiber, so it should exert a sufficient effect on the prevention of infection of the pressure ulcer affected area and its surrounding area, the chemical treatment of the infected area, and the promotion of healing. You can

【0018】好適に用いられる薬剤としては、例えば、
(1)患部及びその周辺部の感染防止、感染部の治療を
目的に用いられる薬剤として、ポビンドンヨード、グル
コン酸クロルヘキシジン、マーキュロクロム、ヨウ素、
ヨードチンキ、チメロサール、ブロメゾール等の殺菌消
毒剤、スルファジアジン、スルファジアジン銀のような
外用サルファ剤、硫酸フラジオマイシン、硫酸ゲンタマ
イシン、エリスロマイシン、テトラサイクリン等の抗生
物質があげられ、これらは単独で使用してもよいし、ま
た二種以上組み合わせて用いてもよい。また、(2)患
部治癒の促進を目的に用いられる薬剤として、ヒアルロ
ン酸塩、コンドロイチン硫酸塩、ゼラチン、表在性炎症
疾患治療剤(例えば、1,4―ジメチル―7―イソプロ
ピルアズレン)、繊維素溶解酵素剤(例えば、フィブリ
ノリジン、デオキシリボヌクレアーゼ)、組織吸収賦活
剤(例えば、幼牛血液抽出物)、抗潰瘍剤(例えば、ベ
ンダザック、グアイアズレン)、潰瘍治療剤(例えば、
Alクロロヒドロキシアラントイネート)、表皮形成促
進剤(例えば、上皮細胞増殖因子)、肉芽形成促進剤
(例えば、プロスタグランジンE1 )、更には、フィブ
ロネクチン、線維芽細胞増殖因子、アミノ酸(特に、メ
チオニン、ヒスチジン、アルギニン、シスチン)、各種
ビタミン類、アンドロゲン、ヒスタミン、成長ホルモン
などがあげられ、これらも単独で使用してもよいし、ま
た二種以上組み合わせて用いてもよい。
Examples of the drug preferably used include, for example,
(1) Pobindon iodine, chlorhexidine gluconate, mercury chrome, iodine, as a drug used for the purpose of preventing infection of the affected area and its peripheral area and treating the infected area,
Iodotinki, thimerosal, bactericidal disinfectants such as bromezole, sulfadiazine, external sulfa agents such as silver sulfadiazine, fradiomycin sulfate, gentamicin sulfate, erythromycin, and antibiotics such as tetracycline, and these may be used alone, Moreover, you may use it in combination of 2 or more type. (2) Hyaluronate, chondroitin sulfate, gelatin, superficial inflammatory disease therapeutic agent (eg, 1,4-dimethyl-7-isopropylazulene), fiber Dissolving enzyme agents (eg, fibrinolidine, deoxyribonuclease), tissue absorption enhancers (eg, calf blood extract), anti-ulcer agents (eg, bendazac, guaiazulene), ulcer treatment agents (eg,
Al chlorohydroxy allantoinate), an epidermal formation promoter (for example, epidermal growth factor), a granulation formation promoter (for example, prostaglandin E 1 ), further, fibronectin, a fibroblast growth factor, an amino acid (particularly, Methionine, histidine, arginine, cystine), various vitamins, androgen, histamine, growth hormone and the like can be mentioned, and these may be used alone or in combination of two or more kinds.

【0019】[0019]

【実施例】以下実施例により本発明をさらに詳細に説明
するが、本発明はこれらにより何等制限されるものでは
ない。
The present invention will be described in more detail with reference to the following examples, but the present invention is not limited thereto.

【0020】[0020]

【実施例1】アルギン酸ナトリウム(ナカライデスク
(株)製、1000cps)の3重量%水溶液を調製
し、加圧濾過機を用い、濾紙(No63F、東洋濾紙
(株)製)を通過させて濾過した。この水溶液を、湿式
紡糸機を用いて吐出速度1.4ml/min で表1記載の各
種濃度の塩化カルシウム水溶液中に紡出した。この際、
0.2mmの口径を有する30ホールの口金を用いた。得
られたゲル状の繊維を延伸(延伸倍率1.36倍)し、
十分に洗浄した後、乾燥し、巻取速度4.9m/minで
巻取った。得られた繊維の生理食塩水の吸収性を前記の
方法に従い測定した。また常法に従って引張強度を測定
した。結果は表1に示す。
Example 1 A 3% by weight aqueous solution of sodium alginate (Nakarai Desk Co., Ltd., 1000 cps) was prepared and filtered through a filter paper (No 63F, Toyo Roshi Kaisha, Ltd.) using a pressure filter. .. This aqueous solution was spun into a calcium chloride aqueous solution having various concentrations shown in Table 1 at a discharge rate of 1.4 ml / min using a wet spinning machine. On this occasion,
A 30-hole die having a diameter of 0.2 mm was used. The obtained gel-like fiber is stretched (stretching ratio 1.36 times),
After thoroughly washing, it was dried and wound at a winding speed of 4.9 m / min. The absorbency of physiological saline in the obtained fiber was measured according to the method described above. Further, the tensile strength was measured according to a conventional method. The results are shown in Table 1.

【0021】また、得られた繊維(No.1〜6)を平
織となし、創傷部にあててその治癒効果を調べたとこ
ろ、いずれも良好な結果が得られた。
Further, when the obtained fibers (No. 1 to 6) were formed into a plain weave and applied to a wound part and the healing effect was examined, good results were obtained in all cases.

【0022】[0022]

【実施例2】アルギン酸ナトリウム水溶液の濃度及び塩
化カルシウム水溶液の濃度を表2記載の如く変更する以
外は実施例1と同様に行なった。結果は表2に示す。
Example 2 Example 1 was repeated except that the concentrations of the sodium alginate aqueous solution and the calcium chloride aqueous solution were changed as shown in Table 2. The results are shown in Table 2.

【0023】[0023]

【実施例3】アルギン酸ナトリウム(ナカライデスク
(株)製、1000cps)に対し、ヒアルロン酸ナト
リウム(ナカライデスク(株)製、微生物由来)をアル
ギン酸ナトリウム/ヒアルロン酸ナトリウム重量比が9
6/4になるように混合した。この混合物の3重量%水
溶液を調製し、加圧濾過機を用い、濾紙(No63F、
東洋濾紙(株)製)を通過させて濾過した。この水溶液
を、湿式紡糸機を用いて吐出速度1.4ml/min で0.
05mol /リットルの塩化カルシウム水溶液に紡出し
た。この際、0.2mmの口径を有する30ホールの口金
を用いた。得られたゲル状の繊維を延伸(延伸倍率1.
36倍)し、十分に洗浄した後、乾燥し、巻取速度4.
9m/min で巻取った。得られた繊維は5mmに切断し、
通常の抄紙濃度になるように水を加えて分散させ、TA
PPI標準シートマシンを用いて坪量100g/m2
なるよう抄造した。紡糸及び抄紙時、ヒアルロン酸の凝
固浴等への溶出は見られなかった。
[Example 3] Sodium alginate (manufactured by Nakarai Desk Co., Ltd., 1000 cps) was added to sodium alginate (manufactured by Nakarai Desk Co., Ltd., microorganism-derived) at a sodium alginate / sodium hyaluronate weight ratio of 9
Mix to 6/4. A 3 wt% aqueous solution of this mixture was prepared, and a filter paper (No63F,
It was passed through Toyo Roshi Kaisha, Ltd. and filtered. This aqueous solution was mixed with a wet spinning machine at a discharge rate of 1.4 ml / min.
It was spun into an aqueous solution of calcium chloride of 05 mol / liter. At this time, a 30-hole die having a diameter of 0.2 mm was used. The gel fiber thus obtained was stretched (stretching ratio 1.
36 times), thoroughly washed and then dried, and winding speed 4.
It was wound up at 9 m / min. The obtained fiber is cut into 5 mm,
Add water to obtain a normal papermaking concentration and disperse it
Paper was made using a PPI standard sheet machine so that the basis weight was 100 g / m 2 . No elution of hyaluronic acid to the coagulation bath was observed during spinning and papermaking.

【0024】得られた繊維の生理食塩水吸水性は30g
/gであった。
The water absorption of the obtained fiber is 30 g.
/ G.

【0025】[0025]

【実施例4】ドープ濃度を4%とし、得られた延伸糸を
エタノールで脱水する以外には実施例3と同様にして製
糸した。得られた繊維は押し込み捲縮機にかけた後、3
cm長に切断し、これをカードに通してウェブとし、次い
でニードルパンチして目付200g/m2 の不織布を得
た。
Example 4 A yarn was produced in the same manner as in Example 3 except that the dope concentration was 4% and the obtained drawn yarn was dehydrated with ethanol. The obtained fiber was put into a crimping machine and then 3
It was cut into cm length, passed through a card to make a web, and then needle punched to obtain a nonwoven fabric having a basis weight of 200 g / m 2 .

【0026】[0026]

【実施例5】アルギン酸ナトリウム(ナカライデスク
(株)製、1000cps)に対し、卵殻膜の微粉末
(平均粒径10μm)をアルギン酸ナトリウム/卵殻膜
重量比が15/1になるように混合した。この混合物の
3.2重量%水溶液を調製し、加圧濾過機を用い、ナス
ロンフィルター(日本精線(株)製、ファインボアN
F、NF―14、80μm)を通過させて濾過した。こ
の水溶液を、湿式紡糸機を用いて吐出速度2.1ml/mi
n で0.05mol /リットルの塩化カルシウム水溶液中
に紡出した。この際、0.2mmの口径を有する30ホー
ルの口金を用いた。得られたゲル状の繊維を延伸(延伸
倍率1.29倍)し、十分に洗浄した後、エタノールを
付与し脱水させ、乾燥し、巻取速度4.9m/min で巻
取った。得られた繊維は5mmに切断し、通常の抄紙濃度
になるように水を加えて分散させ、TAPPI標準シー
トマシンを用いて坪量100g/m2 となるように抄造
した。
Example 5 Sodium alginate (manufactured by Nakarai Desk Co., Ltd., 1000 cps) was mixed with a fine powder of egg shell membrane (average particle size 10 μm) so that the weight ratio of sodium alginate / egg shell membrane was 15/1. A 3.2 wt% aqueous solution of this mixture was prepared, and a Naslon filter (manufactured by Nippon Seisen Co., Ltd., Finebore N) was used using a pressure filter.
F, NF-14, 80 μm) and filtered. Discharge rate of this aqueous solution was 2.1 ml / mi using a wet spinning machine.
It was spun into an aqueous solution of calcium chloride of 0.05 mol / l. At this time, a 30-hole die having a diameter of 0.2 mm was used. The obtained gel-like fiber was stretched (stretching ratio 1.29 times), thoroughly washed, then ethanol was added thereto to dehydrate it, and it was dried and wound up at a winding speed of 4.9 m / min. The obtained fiber was cut into 5 mm, water was added and dispersed to obtain a usual papermaking concentration, and papermaking was performed using a TAPPI standard sheet machine so that the basis weight was 100 g / m 2 .

【0027】[0027]

【実施例6】実施例3及び5で得られたアルギン酸繊維
紙について、前記の方法に従い、生理食塩水の吸収性を
測定した。また、牛血清の吸収性についても生理食塩水
の場合と同様の方法で測定した。なお比較例として、市
販のアルギン酸創傷被覆材(ARGIDERM: Viaderm Pharma
cuticals社製)についても同様の評価を行なった。結果
を表3に示す。
Example 6 With respect to the alginic acid fiber papers obtained in Examples 3 and 5, the absorbency of physiological saline was measured according to the method described above. Also, the absorbability of bovine serum was measured by the same method as in the case of physiological saline. As a comparative example, a commercially available alginate wound dressing (ARGIDERM: Viaderm Pharma
The same evaluation was performed for “Cuticals”. The results are shown in Table 3.

【0028】[0028]

【実施例7】実施例1において、凝固浴カルシウム濃度
を0.05mol /リットルにして得た繊維を5mm長にカ
ットし、次いで抄紙して得た目付100g/m2 の紙及
び実施例3,5で得られた紙に、ヨードチンキを1m2
当り500mlの割合で含浸させた後、乾燥した。これら
の紙を10日間絶食させた体重3kgの家兎の脱毛した第
3転子上の皮膚に家兎の自重を加圧して発生させた家兎
の褥瘡部に貼付したところ、正常な肉芽形成、傷周辺部
からの治癒等、順調な治癒過程が観察され、褥面での細
菌感染巣も見られなかった。また褥面への密着性、褥面
からの剥離性、体液の吸収性も充分満足しうるものであ
った。なかでも、実施例3及び5で得られた試料を用い
た場合、治癒が早かった。
Example 7 In Example 1, fibers obtained by adjusting the concentration of calcium in the coagulating bath to 0.05 mol / liter were cut into a length of 5 mm, and then paper-made to obtain 100 g / m 2 of basis weight and Example 3, 1m 2 of tincture of iodine on the paper obtained in 5
After impregnation at a rate of 500 ml per unit, it was dried. When these papers were fasted for 10 days and attached to the pressure ulcer part of the rabbit generated by pressurizing the dead weight of the rabbit on the depilated third trochanter of a rabbit weighing 3 kg, normal granulation was observed. A smooth healing process such as healing from the wound periphery was observed, and no bacterial infection was found on the face of the foot. Further, the adhesion to the face of the foot, the releasability from the face of the foot, and the absorbability of body fluid were also sufficiently satisfactory. Among them, when the samples obtained in Examples 3 and 5 were used, healing was fast.

【0029】[0029]

【表1】 [Table 1]

【0030】[0030]

【表2】 [Table 2]

【0031】[0031]

【表3】 [Table 3]

【0032】[0032]

【発明の効果】本発明のアルギン酸カルシウム繊維は、
体液の吸収性、傷への密着性に優れているので、創傷・
褥瘡の被覆材として使用した場合、患部の細菌感染・繁
殖を阻止することができ、治癒促進効果を有する。さら
に本発明の繊維は、従来のものに比べて、強度、脆性、
水分に対する感受性が改善され、その取り扱い性が向上
しているので、創傷や褥瘡に対して使用した場合、良好
な治療が可能になるといった長所をも有する。
The calcium alginate fiber of the present invention is
Since it excels in absorbing body fluids and adhering to wounds,
When used as a covering material for pressure ulcer, it can prevent bacterial infection and reproduction of the affected part and has a healing promoting effect. Furthermore, the fiber of the present invention has strength, brittleness, and
Since the sensitivity to water is improved and the handleability thereof is improved, it has an advantage that good treatment is possible when used for a wound or pressure ulcer.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 下記式で表わされる生理食塩水吸収性X
が20〜50g/gであることを特徴とするアルギン酸
カルシウム繊維。 生理食塩水吸収性X=(A−B)/B (但し、Aは生理食塩水中に37℃下4時間浸漬した
後、350Gで10分間遠心脱水処理した後の繊維の重
量、Bは絶乾時の繊維の重量を表わす。)
1. A physiological saline absorption X represented by the following formula:
Is 20 to 50 g / g, calcium alginate fiber. Saline absorbability X = (A−B) / B (where A is the weight of the fiber after being immersed in physiological saline at 37 ° C. for 4 hours and then subjected to centrifugal dehydration at 350 G for 10 minutes, and B is absolutely dried) Indicates the weight of the fiber at the time.)
【請求項2】 コラーゲン、卵殻膜、キチン、キトサン
の群より選ばれる少なくとも一種以上を、繊維の重量に
対して0.01〜50重量%含有する請求項1記載のア
ルギン酸カルシウム繊維。
2. The calcium alginate fiber according to claim 1, which contains 0.01 to 50% by weight based on the weight of the fiber of at least one selected from the group consisting of collagen, eggshell membranes, chitin and chitosan.
【請求項3】 生理食塩水吸収性Xが25〜50g/g
であるアルギン酸カルシウム繊維からなる医療用被覆
材。
3. A physiological saline absorbency X is 25 to 50 g / g.
A medical dressing made of calcium alginate fiber.
JP4015018A 1992-01-30 1992-01-30 Calcium alginate fiber having excellent liquid absorbing property and covering material for medical use Pending JPH05209318A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4015018A JPH05209318A (en) 1992-01-30 1992-01-30 Calcium alginate fiber having excellent liquid absorbing property and covering material for medical use

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4015018A JPH05209318A (en) 1992-01-30 1992-01-30 Calcium alginate fiber having excellent liquid absorbing property and covering material for medical use

Publications (1)

Publication Number Publication Date
JPH05209318A true JPH05209318A (en) 1993-08-20

Family

ID=11877126

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4015018A Pending JPH05209318A (en) 1992-01-30 1992-01-30 Calcium alginate fiber having excellent liquid absorbing property and covering material for medical use

Country Status (1)

Country Link
JP (1) JPH05209318A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10502287A (en) * 1994-07-11 1998-03-03 イー アール スクイブ アンド サンズ インコーポレーテッド Alginate fabrics, their production and use
JP2002512857A (en) * 1998-04-29 2002-05-08 テヴネ,ファブリス Reinforcing implants for tissue sutures
JP2004527453A (en) * 2000-06-30 2004-09-09 アピメド メディカル ハニー リミテッド Improvements on the use of honey in coatings
EP2020455A2 (en) * 2007-07-30 2009-02-04 Idemitsu Technofine Co. Ltd Fiber, fiber assembly, and fiber producing method
JP2009089859A (en) * 2007-10-05 2009-04-30 Idemitsu Technofine Co Ltd Wound covering material
CN105401337A (en) * 2015-10-22 2016-03-16 江苏伟创力新材料有限公司 Alginate fiber spunlace non-woven fabric and manufacturing method thereof
CN105624832A (en) * 2014-11-07 2016-06-01 中国科学院大连化学物理研究所 Method for preparing calcium alginate microfibers having bat structure based on micro-fluidic technology
JP2018513287A (en) * 2015-04-16 2018-05-24 青島大学 Method for producing alginate fiber having salt resistance and detergent resistance
WO2019100711A1 (en) * 2017-11-21 2019-05-31 青岛明月海藻集团有限公司 Calcium alginate non-woven fabric and preparation method therefor

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH10502287A (en) * 1994-07-11 1998-03-03 イー アール スクイブ アンド サンズ インコーポレーテッド Alginate fabrics, their production and use
JP2002512857A (en) * 1998-04-29 2002-05-08 テヴネ,ファブリス Reinforcing implants for tissue sutures
JP2004527453A (en) * 2000-06-30 2004-09-09 アピメド メディカル ハニー リミテッド Improvements on the use of honey in coatings
EP2020455A2 (en) * 2007-07-30 2009-02-04 Idemitsu Technofine Co. Ltd Fiber, fiber assembly, and fiber producing method
JP2009089859A (en) * 2007-10-05 2009-04-30 Idemitsu Technofine Co Ltd Wound covering material
CN105624832A (en) * 2014-11-07 2016-06-01 中国科学院大连化学物理研究所 Method for preparing calcium alginate microfibers having bat structure based on micro-fluidic technology
CN105624832B (en) * 2014-11-07 2017-09-22 中国科学院大连化学物理研究所 The method that the calcium alginate microfibre of tool bat structure is prepared based on microflow control technique
JP2018513287A (en) * 2015-04-16 2018-05-24 青島大学 Method for producing alginate fiber having salt resistance and detergent resistance
CN105401337A (en) * 2015-10-22 2016-03-16 江苏伟创力新材料有限公司 Alginate fiber spunlace non-woven fabric and manufacturing method thereof
WO2019100711A1 (en) * 2017-11-21 2019-05-31 青岛明月海藻集团有限公司 Calcium alginate non-woven fabric and preparation method therefor

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