JPH08126659A - Base material for medical care containing antifungal material and wound covering material - Google Patents
Base material for medical care containing antifungal material and wound covering materialInfo
- Publication number
- JPH08126659A JPH08126659A JP6269147A JP26914794A JPH08126659A JP H08126659 A JPH08126659 A JP H08126659A JP 6269147 A JP6269147 A JP 6269147A JP 26914794 A JP26914794 A JP 26914794A JP H08126659 A JPH08126659 A JP H08126659A
- Authority
- JP
- Japan
- Prior art keywords
- wound
- antibacterial
- antifungal
- medical
- base 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
Links
- 239000000463 material Substances 0.000 title claims abstract description 69
- 230000000843 anti-fungal effect Effects 0.000 title abstract 6
- 229940121375 antifungal agent Drugs 0.000 title abstract 4
- 239000000126 substance Substances 0.000 claims abstract description 26
- 239000000853 adhesive Substances 0.000 claims abstract description 25
- 230000001070 adhesive effect Effects 0.000 claims abstract description 25
- 239000012528 membrane Substances 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000000758 substrate Substances 0.000 claims abstract description 13
- 229910052588 hydroxylapatite Inorganic materials 0.000 claims abstract description 12
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 claims abstract description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000000741 silica gel Substances 0.000 claims abstract description 8
- 229910002027 silica gel Inorganic materials 0.000 claims abstract description 8
- 229910052751 metal Inorganic materials 0.000 claims abstract description 7
- 239000002184 metal Substances 0.000 claims abstract description 7
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 6
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 6
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052802 copper Inorganic materials 0.000 claims abstract description 6
- 239000010949 copper Substances 0.000 claims abstract description 6
- 229910052709 silver Inorganic materials 0.000 claims abstract description 6
- 239000004332 silver Substances 0.000 claims abstract description 6
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 6
- 239000011701 zinc Substances 0.000 claims abstract description 6
- 238000010030 laminating Methods 0.000 claims abstract 2
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 15
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims description 15
- 239000005871 repellent Substances 0.000 claims description 9
- 239000000835 fiber Substances 0.000 claims description 8
- 229920002635 polyurethane Polymers 0.000 claims description 7
- 239000004814 polyurethane Substances 0.000 claims description 7
- 229920000728 polyester Polymers 0.000 claims description 6
- 229920000742 Cotton Polymers 0.000 claims description 5
- 230000002940 repellent Effects 0.000 claims description 5
- 229920000297 Rayon Polymers 0.000 claims description 4
- 239000002964 rayon Substances 0.000 claims description 4
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 3
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims description 3
- 208000015181 infectious disease Diseases 0.000 abstract description 10
- 210000000416 exudates and transudate Anatomy 0.000 abstract description 8
- 229910021645 metal ion Inorganic materials 0.000 abstract description 8
- 241000894006 Bacteria Species 0.000 abstract description 6
- 239000012790 adhesive layer Substances 0.000 abstract description 4
- 230000000694 effects Effects 0.000 abstract description 3
- 238000004040 coloring Methods 0.000 abstract description 2
- 239000010410 layer Substances 0.000 abstract description 2
- 238000007654 immersion Methods 0.000 abstract 2
- 230000037305 epidermis formation Effects 0.000 abstract 1
- 230000001737 promoting effect Effects 0.000 abstract 1
- 206010052428 Wound Diseases 0.000 description 50
- 208000027418 Wounds and injury Diseases 0.000 description 50
- 230000000844 anti-bacterial effect Effects 0.000 description 45
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 33
- 229920001296 polysiloxane Polymers 0.000 description 15
- -1 polytetrafluoroethylene Polymers 0.000 description 10
- 229920000260 silastic Polymers 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000004743 Polypropylene Substances 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000004745 nonwoven fabric Substances 0.000 description 6
- 229920001155 polypropylene Polymers 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000004744 fabric Substances 0.000 description 5
- 239000010408 film Substances 0.000 description 5
- 239000000499 gel Substances 0.000 description 5
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 4
- 241000191967 Staphylococcus aureus Species 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 238000007598 dipping method Methods 0.000 description 4
- 230000035876 healing Effects 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 238000006266 etherification reaction Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 3
- 206010072170 Skin wound Diseases 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 229920001477 hydrophilic polymer Polymers 0.000 description 2
- 230000002757 inflammatory effect Effects 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- HFCUBKYHMMPGBY-UHFFFAOYSA-N 2-methoxyethyl prop-2-enoate Chemical compound COCCOC(=O)C=C HFCUBKYHMMPGBY-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 210000001339 epidermal cell Anatomy 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010559 graft polymerization reaction Methods 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 210000000265 leukocyte Anatomy 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 230000003020 moisturizing effect Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000000451 tissue damage Effects 0.000 description 1
- 231100000827 tissue damage Toxicity 0.000 description 1
- 239000003860 topical agent Substances 0.000 description 1
- 230000000472 traumatic effect Effects 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
- 230000029663 wound healing Effects 0.000 description 1
Landscapes
- Materials For Medical Uses (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は抗菌性を有する医療用基
材および創傷被覆材に関するものである。FIELD OF THE INVENTION The present invention relates to a medical base material having antibacterial properties and a wound dressing.
【0002】[0002]
【従来の技術】外傷性の皮膚創傷および採皮創等の創傷
および疾患に伴う創部に対する創傷保護材又は材料とし
ては、大別して創傷部を乾燥状態に保ち、外部からの感
染と体液の流出を防止し、痂皮形成によって治癒を行
う、いわゆるドライドレッシングと、適度の湿潤環境を
つくり、速やかに表皮細胞の遊走を行うウエットドレッ
シングが知られている。局方ガーゼがドライドレッシン
グ法に用いる材料の代表といえるが、滲出液の多い創な
どではガーゼと新生組織が固着したり、外部からの汚染
を防止しにくいといった問題がある。また、ウエットド
レッシングの一方法であるフィルムドレッシングでは水
蒸気透過性があるとはいえ、吸水性はないので滲出液が
多量な場合は、湿潤環境と閉塞状態から細菌の繁殖を招
く恐れがある。従って今のところ感染を防止または抑制
する機能を持った創傷被覆材などの医療用基材は少な
い。2. Description of the Related Art Wound-protecting materials or materials for wounds such as traumatic skin wounds and skin wounds and wounds associated with diseases are roughly classified to keep the wounds in a dry state to prevent infection from the outside and leakage of body fluids. So-called dry dressing, which prevents and heals by crusting, and wet dressing, which creates an appropriate moist environment and rapidly migrates epidermal cells, are known. Although gypsum gauze can be said to be a representative material used in the dry dressing method, there are problems that gauze and new tissue adhere to each other and it is difficult to prevent contamination from the outside in wounds with a large amount of exudate. Further, although film dressing, which is one of the wet dressing methods, has water vapor permeability, it does not absorb water, and therefore, when a large amount of exudate is present, there is a possibility that bacteria may propagate due to the wet environment and the closed state. Therefore, at present, there are few medical base materials such as wound dressings having a function of preventing or suppressing infection.
【0003】一方、現在使われている抗菌性の局所薬剤
は、耐性菌の発生、菌交代現象および白血球やCaの減
少症などを生じ、ゼオライトに抗菌性金属を含有させた
抗菌性材料は、樹脂に添加した後に変色するという欠点
がある。さらに、抗菌材料を含有した被覆材から抗菌剤
が脱落し、直接生体に接触するすることによって異物反
応が起きる問題点がある。On the other hand, the antibacterial topical agents currently used cause the development of resistant bacteria, the bacterial substitution phenomenon and the decrease of white blood cells and Ca, and the antibacterial material containing zeolite in an antibacterial metal is It has the drawback of discoloring after being added to the resin. Further, there is a problem that the antibacterial agent is dropped from the coating material containing the antibacterial material and directly contacts the living body to cause a foreign substance reaction.
【0004】[0004]
【発明が解決しようとする課題】本発明は、抗菌性を有
し、経時安定性に優れ変色する恐れがなく、生体に対し
て副作用が少なく、感染防止、疼痛緩和、表皮化を促進
する医療用基材および創傷被覆材を提供することを目的
としている。DISCLOSURE OF THE INVENTION The present invention is a medical treatment which has antibacterial properties, is excellent in stability over time, has no risk of discoloration, has few side effects on the living body, and promotes infection prevention, pain relief, and epidermal formation. An object is to provide a base material and a wound dressing.
【0005】[0005]
【課題を解決するための手段】上記目的は以下の本発明
により解決される。 (1) 銀、銅及び亜鉛よりなる群から選ばれた少なく
とも一種類の金属を担持したハイドロキシアパタイト及
び/又はシリカゲルを接着物質と共に支持体に被覆、浸
漬等により含有させたことを特徴とする医療用基材。 (2) 前記支持体が繊維構造体である上記(1)記載
の医療用基材。The above objects can be solved by the present invention described below. (1) Medical treatment characterized in that hydroxyapatite and / or silica gel supporting at least one metal selected from the group consisting of silver, copper and zinc are contained in a support together with an adhesive substance by coating, dipping or the like. Substrate. (2) The medical substrate according to (1) above, wherein the support is a fiber structure.
【0006】(3) 前記繊維構造体が織布、不織布及
び編布の少なくとも一つである上記(1)乃至(2)記
載の医療用基材。 (4) 前記接着物質が撥水性物質である上記(1)乃
至(3)記載の医療用基材。(3) The medical substrate according to the above (1) or (2), wherein the fibrous structure is at least one of woven fabric, non-woven fabric and knitted fabric. (4) The medical substrate according to the above (1) to (3), wherein the adhesive substance is a water-repellent substance.
【0007】(5) 前記撥水性物質がシリコーンであ
る上記(1)乃至(4)記載の医療用基材。 (6) 前記支持体の材質が、カルボキシメチルセルロ
ース、ポリエステル、ポリウレタン、コットン、又はレ
ーヨンである上記(1)乃至(5)記載の医療用基材。(5) The medical substrate according to the above (1) to (4), wherein the water repellent substance is silicone. (6) The medical base material according to the above (1) to (5), wherein the material of the support is carboxymethyl cellulose, polyester, polyurethane, cotton, or rayon.
【0008】(7) 上記(1)乃至(6)記載の医療
用基材に親水性多孔質膜が積層されてなる創傷被覆材。 (8) 抗菌性材料が支持体に対して0.1〜5.0mg/c
m2含有されている上記(7)記載の創傷被覆材。(7) A wound dressing material comprising a medical substrate as described in (1) to (6) above and a hydrophilic porous membrane laminated on the substrate. (8) Antibacterial material is 0.1-5.0 mg / c with respect to the support.
The wound dressing material according to (7) above, which contains m 2 .
【0009】(9) 銀、銅及び亜鉛よりなる群から選
ばれた少なくとも一種類の金属を担持したハイドロキシ
アパタイト及び/又はシリカゲルが接着物質に対して
0.5〜50重量%含有されている上記(7)乃至
(8)記載の創傷被覆材。 (10) 親水性多孔質膜がポリオレフィン、ハロゲン
化ポリオレフィン、又はこれらの混合物からなる上記
(7)乃至(9)記載の創傷被覆材。(9) Hydroxyapatite and / or silica gel carrying at least one metal selected from the group consisting of silver, copper and zinc is contained in an amount of 0.5 to 50% by weight based on the adhesive material. The wound dressing according to (7) to (8). (10) The wound dressing according to the above (7) to (9), wherein the hydrophilic porous membrane is made of polyolefin, halogenated polyolefin, or a mixture thereof.
【0010】本発明は抗菌性材料として、銀、銅及び亜
鉛よりなる群から選ばれた少なくとも一種類の金属を担
持したハイドロキシアパタイト及び/又はシリカゲルを
用いた抗菌性及び経時安定性(変色しない)に優れた医
療用基材及び創傷被覆材である。The present invention uses, as an antibacterial material, hydroxyapatite and / or silica gel carrying at least one metal selected from the group consisting of silver, copper and zinc, and has antibacterial properties and stability over time (no discoloration). An excellent medical base material and wound dressing.
【0011】本発明の抗菌性材料は、銀、銅、亜鉛など
の金属イオンを1000℃以上の高温焼結あるいはイオ
ン交換によりハイドロキシアパタイトまたはシリカゲル
に担持させたものを用いる。その際、ハイドロキシアパ
タイトまたはシリカゲルの粒径は0.1〜5μm、金属イ
オンの量はハイドロキシアパタイトに対して0.001
〜5重量%含まれていることが好ましい。具体的には、
アパサイダー(登録商標、サンギ株式会社製)が挙げら
れる。As the antibacterial material of the present invention, a material in which a metal ion such as silver, copper or zinc is carried on hydroxyapatite or silica gel by high temperature sintering at 1000 ° C. or more or ion exchange is used. At that time, the particle size of hydroxyapatite or silica gel is 0.1 to 5 μm, and the amount of metal ions is 0.001 relative to hydroxyapatite.
It is preferable that the content is up to 5% by weight. In particular,
Apacider (registered trademark, manufactured by Sangi Co., Ltd.) can be mentioned.
【0012】本発明の医療用基材及び創傷被覆材におい
て支持体は、特に限定しないが好ましくは、カルボキシ
メチルセルロース(以下、CMCとする)、ポリエステ
ル、ポリウレタン、コットン、又はレーヨンからなる繊
維構造体からなり、その構造は織布、不織布及び編布の
少なくとも一つの構造を有する。In the medical base material and wound dressing of the present invention, the support is not particularly limited, but is preferably a fibrous structure made of carboxymethyl cellulose (hereinafter referred to as CMC), polyester, polyurethane, cotton, or rayon. The structure has at least one structure of woven cloth, non-woven cloth and knitted cloth.
【0013】本発明の医療用基材及び創傷被覆材におい
て、抗菌性材料を支持体に被覆、浸漬等により含有させ
るために使用する接着物質は限定しないが撥水性物質で
あることが好ましく、具体的にはシリコーン、ポリウレ
タン、スチレン−ブタジエン−スチレンブロックコポリ
マー、及びポリテトラフルオロエチレンなどが挙げられ
る。その際、接着物質、好ましくは撥水性物質の量は繊
維構造体に対し5〜20重量%であるとよい。また上記
の接着物質は本発明の創傷被覆材においては支持体と親
水性多孔質膜を接着するためにも用いられる。In the medical base material and wound dressing material of the present invention, the adhesive substance used for containing the antibacterial material on the support by coating, dipping or the like is not limited, but is preferably a water repellent substance, Specific examples thereof include silicone, polyurethane, styrene-butadiene-styrene block copolymer, and polytetrafluoroethylene. At that time, the amount of the adhesive substance, preferably the water-repellent substance, may be 5 to 20% by weight based on the fibrous structure. Further, the above-mentioned adhesive substance is also used for adhering the support and the hydrophilic porous membrane in the wound dressing of the present invention.
【0014】本発明の創傷被覆材において親水性多孔質
膜は特に限定しないが、ポリエチレン、ポリプロピレン
のようなポリオレフィン、又はポリフッ化ビニリデン、
ポリ塩化ビニリデン、塩素化ポリエチレンのようなハロ
ゲン化ポリオレフィン、又はこれらの混合物で形成され
る多孔質膜の表面に親水性ポリマーを被覆したものを用
いる。その際、親水性のポリマーは特に限定はないが、
好ましい例としてはポリメトキシエチルアクリレート、
ポリジメチルアクリルアミド、メトキシアクリル酸エス
テル共重合体、ジメチルアクリルアミド共重合体があげ
られる。また、多孔質膜は孔径0.01〜1.0μm、水
蒸気透過率(JIS規格)は20〜10000g/m2・
24hrであることが好ましい。The hydrophilic porous membrane in the wound dressing of the present invention is not particularly limited, but may be polyethylene, polyolefin such as polypropylene, or polyvinylidene fluoride,
A porous membrane formed of polyvinylidene chloride, a halogenated polyolefin such as chlorinated polyethylene, or a mixture thereof is used, which is coated with a hydrophilic polymer. At that time, the hydrophilic polymer is not particularly limited,
Preferred examples include polymethoxyethyl acrylate,
Examples thereof include polydimethylacrylamide, methoxyacrylic acid ester copolymer, and dimethylacrylamide copolymer. The porous membrane has a pore size of 0.01 to 1.0 μm and a water vapor transmission rate (JIS standard) of 20 to 10000 g / m 2 ·.
It is preferably 24 hours.
【0015】さらに本発明の創傷被覆材において親水性
多孔質膜は弾性を付与するために、前記多孔質膜にアク
リル酸エステルなどの弾性を有する高分子を重合させて
弾性を付与することが好ましい。その際、弾性を有する
高分子としては、高分子反応あるいはグラフト重合など
で付与できるものであれば特に限定されないが、アクリ
ル酸n−ブチルが好ましい。また、弾性を付与した多孔
質膜は、孔径0.01〜1.0μm、水蒸気透過率200
〜10000g/m2・24hrであることが好ましい。Further, in the wound dressing of the present invention, in order to impart elasticity to the hydrophilic porous membrane, it is preferable to impart elasticity by polymerizing an elastic polymer such as acrylate ester to the porous membrane. . At that time, the polymer having elasticity is not particularly limited as long as it can be imparted by a polymer reaction or graft polymerization, but n-butyl acrylate is preferable. Further, the elastic porous film has a pore size of 0.01 to 1.0 μm and a water vapor transmission rate of 200.
It is preferably from 10000 g / m 2 · 24 hr.
【0016】また本発明の医療用基材及び創傷被覆材に
おいて、支持体を変えることにより様々な特性を持たせ
ることができる。例えば、支持体に非固着性のポリエス
テル等を用いると、創面に一次ドレッシングとして直接
使用することでガーゼが創に固着せず、速やかに滲出液
を透過させることができ、抗菌性材料により感染を防止
できる医療用基材及び創傷被覆材を得ることができる。
また、支持体にCMCを用いると創面からの滲出液を吸
水し、適度な湿潤環境を保つことができ、なおかつ抗菌
性材料により感染を防止し、疼痛を緩和させることので
きる医療用基材及び創傷被覆材を得ることができる。In the medical base material and wound dressing material of the present invention, various properties can be given by changing the support. For example, when non-adhesive polyester or the like is used for the support, gauze does not adhere to the wound by directly using it as a primary dressing on the wound surface, and exudate can be quickly permeated. A medical base material and a wound dressing which can be prevented can be obtained.
Further, when CMC is used as the support, a medical base material that absorbs the exudate from the wound surface and can maintain an appropriate moist environment, and that can prevent infection and relieve pain with an antibacterial material, A wound dressing can be obtained.
【0017】本発明の医療用基材は、上述した通り支持
体と抗菌性材料を含有した撥水性物質からなっている。
支持体に用いる基材を代えることにより、創傷部位を覆
い保護し、創面にガーゼが固着せず、滲出液を透過し、
治癒を促進させたり、滲出液を吸水し、適度な湿潤環境
を保ち、治癒を促進することができる。さらに、撥水生
物質に含有された抗菌性材料により感染が抑えられる。The medical substrate of the present invention comprises a support and a water-repellent substance containing an antibacterial material as described above.
By replacing the base material used for the support, the wound site is covered and protected, the gauze does not stick to the wound surface, and the exudate permeates,
Healing can be promoted and exudate can be absorbed by water to maintain an appropriate moist environment and accelerate healing. Further, infection is suppressed by the antibacterial material contained in the water repellent material.
【0018】本発明の医療用基材の製造方法としては特
に限定しないが、具体的には、溶媒、例えば、ヘキサ
ン、テトラヒドロフラン、メチルエチルケトン、ジエチ
ルエーテル、トルエンに、抗菌性材料、例えば、アパサ
イダー(登録商標、サンギ株式会社製)、バクテノン
(登録商標、ゲルテクノロジー社製)と、接着物質好ま
しくは撥水性物質である接着物質、例えば、シリコー
ン、ポリウレタン、スチレン−ブタジエン−スチレンブ
ロックコポリマー及びポリテトラオロエチレンを濃度5
〜20重量%程度溶解した接着物質溶液を作製し、ポリ
エステル、ポリウレタン、コットン、レーヨンまたはC
MCからなる支持体を、この溶液に浸漬またはスプレ
ー、ローラーなどを用いて塗布することにより接触させ
て所望の医療用基材を得ることができる。The method for producing the medical base material of the present invention is not particularly limited, but specifically, it is added to a solvent such as hexane, tetrahydrofuran, methyl ethyl ketone, diethyl ether or toluene, and an antibacterial material such as apacider (registered). Trademark, manufactured by Sangi Co., Ltd.), Bactenone (registered trademark, manufactured by Gel Technology Co., Ltd.), and an adhesive substance, preferably an adhesive substance which is a water repellent substance, such as silicone, polyurethane, styrene-butadiene-styrene block copolymer and polytetraoloethylene. The concentration 5
Approximately 20% by weight of dissolved adhesive substance solution is prepared, and polyester, polyurethane, cotton, rayon or C
A desired medical base material can be obtained by bringing a support made of MC into contact with the solution by applying it by dipping or spraying, using a roller or the like.
【0019】本発明の創傷被覆材は、上述した通り繊維
構造体好ましくはCMCからなる支持体と、接着剤層お
よび親水性多孔質膜が積層されてなり、前記支持体、接
着剤層及び親水性多孔質膜の少なくとも一つに抗菌性材
料が被覆及び/又は浸漬などにより含有され、抗菌性を
有する特徴とする創傷被覆材である。The wound dressing of the present invention comprises a support comprising a fibrous structure, preferably CMC, an adhesive layer and a hydrophilic porous membrane, which are laminated as described above, and the support, the adhesive layer and the hydrophilic layer are laminated. A wound dressing material having an antibacterial property, in which at least one of the porous membranes contains an antibacterial material by coating and / or dipping.
【0020】本発明の創傷被覆材は、CMCの繊維構造
体の創面からの滲出液を吸水し、適度な湿潤環境を保つ
作用と、親水性多孔質膜の高い水蒸気透過作用、水分透
過作用により創傷部位の治癒が行われる。また熱傷創な
どの感染の危険性のある創面では含有した抗菌性材料に
より菌による感染が防止される。また、抗菌性金属イオ
ンが、ハイドロキシアパタイトまたはシリカゲルに特異
的に強く吸着されているため、抗菌性金属イオンが溶出
することがなく経時的に着色を起こさない。The wound dressing of the present invention absorbs the exudate from the wound surface of the CMC fibrous structure and maintains an appropriate moist environment, and the hydrophilic porous membrane has high water vapor permeation and water permeation. Healing of the wound site is performed. In addition, on the wound surface having a risk of infection such as a burn wound, infection by bacteria is prevented by the contained antibacterial material. Further, since the antibacterial metal ions are strongly adsorbed specifically on the hydroxyapatite or silica gel, the antibacterial metal ions do not elute and coloring does not occur over time.
【0021】次に本発明の創傷被覆材の製造方法につい
て説明する。具体的には、CMCからなる織布、不織
布、編布などの高含水ゲル形成繊維構造体を作製する。
そして、得られた高含水ゲル形成繊維構造体を溶解しな
いように適当な溶媒、例えば、ヘキサン、テトラヒドロ
フラン、メチルエチルケトン、ジエチルエーテル、トル
エンに、接着物質好ましくは撥水性物質である接着物
質、例えば、シリコーン、ポリウレタン、スチレン−ブ
タジエン−スチレンブロックコポリマー、ポリテトラフ
ルオロエチレンを濃度を1〜10重量%程度溶解した接
着物質溶液を作製し、高含水ゲル形成繊維構造体をこの
溶液に浸漬、またはスプレー、ローラーなどを用いて塗
布することにより接触させ、高含水ゲル形成物質薄膜の
創傷部と接触しない部分となる面に接着物質を付着さ
せ、次にこの接着物質が付着された高含水ゲル形成繊維
構造体に、親水化処理したポリプロピレン製の多孔質膜
をラミネートすると所望の創傷被覆材を得ることができ
る。なお、抗菌性材料は予め接着物質または接着物質溶
液に含有させておく。Next, a method for manufacturing the wound dressing of the present invention will be described. Specifically, a highly hydrous gel-forming fiber structure such as a woven fabric, a non-woven fabric, or a knit fabric made of CMC is produced.
Then, in a suitable solvent, such as hexane, tetrahydrofuran, methyl ethyl ketone, diethyl ether, toluene, so as not to dissolve the resulting highly hydrous gel-forming fiber structure, an adhesive substance, preferably an adhesive substance that is a water-repellent substance, for example, silicone. , Polyurethane, styrene-butadiene-styrene block copolymer, polytetrafluoroethylene in a concentration of about 1 to 10% by weight to prepare a solution of an adhesive substance, and dip the high water content gel forming fiber structure in this solution, or spray, roller And the like, and the adhesive substance is adhered to the surface of the thin film of the highly hydrous gel-forming substance thin film, which is not in contact with the wound, and then the highly hydrous gel-forming fibrous structure to which the adhesive substance is adhered. When a hydrophilic porous polypropylene film is laminated on the It can be obtained of the wound dressing. The antibacterial material is previously contained in the adhesive substance or the adhesive substance solution.
【0022】[0022]
【実施例】以下、実施例を示して本発明をさらに具体的
に説明する。EXAMPLES The present invention will be described more specifically below with reference to examples.
【0023】(実施例1)抗菌性材料として、アパサイ
ダー(登録商標、サンギ株式会社製)またはバクテノン
(登録商標、ゲルテクノロジー社製)を用い、これらの
抗菌性材料を2.0mg/cm2濃度で予めヘキサン溶液中に
充分分散させ、5%のメディカルグレードサイラスティ
ック(登録商標)シリコーン(接着タイプA、ダウコー
ニング社製)と混合した。得られた抗菌性材料含有5%
シリコーンヘキサン溶液をポリエステルメッシュ(10
0本/インチ、マルチフィラメント)に被覆(ディプィ
ング)した。Example 1 Apacider (registered trademark, manufactured by Sangi Co., Ltd.) or Bactenone (registered trademark, manufactured by Gel Technology Co., Ltd.) was used as the antibacterial material, and these antibacterial materials were used at a concentration of 2.0 mg / cm 2. Was sufficiently dispersed in a hexane solution in advance and mixed with 5% of Medical Grade Silastic (registered trademark) silicone (adhesive type A, manufactured by Dow Corning). 5% containing the obtained antibacterial material
Add silicone hexane solution to polyester mesh (10
0 filaments / inch, multifilament) was coated (dipped).
【0024】(実施例2)抗菌性材料として、アパサイ
ダー(登録商標、サンギ株式会社製)またはバクテノン
(登録商標、ゲルテクノロジー社製)を用い、これらの
抗菌性材料を2.0mg/cm2濃度で予めヘキサン溶液中に
充分分散させ、5%のメディカルグレードサイラスティ
ック(登録商標)シリコーン(接着タイプA、ダウコー
ニング社製)と混合した。上記の抗菌性材料含有5%シ
リコーンヘキサン溶液を綿不織布(ベンリーゼ、旭化成
(株)製、目付18.5g/m2)に被覆(ディプィング)
した。(Example 2) As an antibacterial material, Apacider (registered trademark, manufactured by Sangi Co., Ltd.) or Bactenone (registered trademark, manufactured by Gel Technology Co., Ltd.) was used, and the concentration of these antibacterial materials was 2.0 mg / cm 2. Was sufficiently dispersed in a hexane solution in advance and mixed with 5% of Medical Grade Silastic (registered trademark) silicone (adhesive type A, manufactured by Dow Corning). A 5% silicone hexane solution containing the above antibacterial material was applied to a cotton nonwoven fabric (Benlize, Asahi Kasei
Co., Ltd., unit weight 18.5g / m 2 ) coating (diping)
did.
【0025】(実施例3)抗菌性材料として、アパサイ
ダー(登録商標、サンギ株式会社製)またはバクテノン
(登録商標、ゲルテクノロジー社製)を用い、これらの
抗菌性材料を0.25〜2.0mg/cm2濃度で予めヘキサン
溶液中に充分分散させ、5%のメディカルグレードサイ
ラスティック(登録商標)シリコーン(接着タイプA、
ダウコーニング社製)と混合した。上記の抗菌性材料含
有5%シリコーンヘキサン溶液をCMC不織布(東海染
工(株)製、目付18.5g/m2、エーテル化度0.40)
に被覆(ディプィング)した。Example 3 As an antibacterial material, Apacider (registered trademark, manufactured by Sangi Co., Ltd.) or Bactenone (registered trademark, manufactured by Gel Technology Co., Ltd.) was used, and 0.25 to 2.0 mg of these antibacterial materials were used. Pre-dispersed in hexane solution at a concentration of / cm 2 and 5% Medical Grade Silastic® silicone (adhesive type A,
Dow Corning). A 5% silicone hexane solution containing the above antibacterial material was used as a CMC non-woven fabric (manufactured by Tokai Senko Co., Ltd., basis weight 18.5 g / m 2 , etherification degree 0.40).
Was coated (dipped).
【0026】(試験例1)抗菌性試験 滅菌済みシャーレ上に固形培地(Muller Hinton Agar,M
HA,DIFCO製)を20ml/シャーレの割合でまき、平板と
し前培養されたStaphylococcus aureus(黄色ブドウ球
菌)、Pseudomonas aeruginosa(緑膿菌)を均一に塗抹
した。これに実施例1、2、3で得られた本発明に係わ
る医療用基材を8mmφの大きさに打ち抜きサンプルと
し、固定培地平板1枚あたり3カ所載せた。37℃で1
8時間倒置培養後、阻止円の有無、接触面の菌の発育を
観察した。結果を表1に示す。結果より、抗菌効果が確
認された。(Test Example 1) Antibacterial test A solid medium (Muller Hinton Agar, M) was placed on a sterilized petri dish.
HA, DIFCO) was sprinkled at a rate of 20 ml / dishes, and Staphylococcus aureus (Staphylococcus aureus) and Pseudomonas aeruginosa (Pseudomonas aeruginosa), which had been pre-cultured as a plate, were uniformly smeared. The medical base material according to the present invention obtained in Examples 1, 2 and 3 was punched out into a sample having a size of 8 mmφ and placed at three locations per fixed medium plate. 1 at 37 ° C
After inversion culture for 8 hours, the presence or absence of an inhibition circle and the growth of bacteria on the contact surface were observed. The results are shown in Table 1. From the results, the antibacterial effect was confirmed.
【0027】[0027]
【表1】 [Table 1]
【0028】(実施例4)抗菌性金属イオンを担持させ
たハイドロキシアパタイトとしてはアパサイダー(登録
商標、サンギ株式会社製)を用い、上記の材料を2.0m
g/cm2濃度で予めヘキサン溶液中に充分分散させ、5%
のメディカルグレードサイラスティック(登録商標)シ
リコーン(接着タイプA、ダウコーニング社製)と混合
した。上記の抗菌性金属イオンを担持させたハイドロキ
シアパタイト含有5%シリコーンヘキサン溶液を市販の
CMC製の不織布(東海染工(株)製、目付18.5g/m
2、エーテル化度0.40)にコーティングして厚さ約1
00μmの抗菌性CMC繊維構造体を得た。(Example 4) As the hydroxyapatite supporting the antibacterial metal ion, Apacider (registered trademark, manufactured by Sangi Co., Ltd.) was used, and the above material was added to 2.0 m.
Pre-dispersed in a hexane solution at a concentration of g / cm 2 to 5%
Medical Grade Silastic® Silicone (adhesive type A, Dow Corning). A 5% silicone hexane solution containing hydroxyapatite supporting the above-mentioned antibacterial metal ions was used as a commercially available CMC non-woven fabric (manufactured by Tokai Senko Co., Ltd., basis weight 18.5 g / m 2).
2 , the degree of etherification is 0.40) and the thickness is about 1
An antibacterial CMC fiber structure of 00 μm was obtained.
【0029】上記抗菌性CMC繊維構造体を展延したメ
ディカルグレードサイラスティック(登録商標)シリコ
ーン(MDX4−4210、ダウコーニング社製)上に
静置して60℃で加温後、ポリプロピレンと流動パラフ
ィンを溶融混練して膜状に成形した後、脱パラフィンし
て得たポリプロピレン多孔質膜をアルゴン雰囲気下でプ
ラズマ照射し、その後にメトキシエチルアクリレートモ
ノマーを導入することによりグラフト重合して作製した
親水化多孔質ポリプロピレン膜にゆっくり載せて接着さ
せ、再び60℃に加温することにより本発明の創傷被覆
材を作製した。The above-mentioned antibacterial CMC fiber structure was spread on a medical grade silastic (registered trademark) silicone (MDX4-4210, manufactured by Dow Corning) and heated at 60 ° C., and then polypropylene and liquid paraffin were added. Hydrophilization made by graft-polymerizing the polypropylene porous film obtained by melt-kneading and forming into a film shape, and then deparaffinizing and irradiating plasma under argon atmosphere, and then introducing methoxyethyl acrylate monomer. The wound dressing of the present invention was produced by slowly placing it on a porous polypropylene membrane to adhere it, and heating it again at 60 ° C.
【0030】(実施例5)市販のCMC製の不織布(東
海染工(株)■製、エーテル化度0.40)を5%のメデ
ィカルグレードサイラスティック(登録商標)シリコー
ン(接着タイプA、ダウコーニング社製)ヘキサン溶液
中に10秒間浸漬して厚さ約100μmの抗菌性CMC
繊維構造体を得た。Example 5 A commercially available non-woven fabric made of CMC (manufactured by Tokai Senko Co., Ltd., having an etherification degree of 0.40) was used as a 5% medical grade silastic (registered trademark) silicone (adhesive type A, Dow). (Corning Co., Ltd.) Antibacterial CMC with a thickness of about 100 μm immersed in a hexane solution for 10 seconds
A fibrous structure was obtained.
【0031】上記抗菌性CMC繊維構造体を、抗菌性金
属イオンを担持させたハイドロキシアパタイトとしてア
パサイダー(登録商標、サンギ株式会社製)を50重量
%含有させ展延したメディカルグレードサイラスティッ
ク(登録商標)シリコーン(MDX4−4210、ダウ
コーニング社製)上に静置して60℃で加温後、実施例
1に準拠して得られた親水化多孔質ポリプロピレン膜に
ゆっくり載せて接着させ、再び60℃に加温することに
より本発明の創傷被覆材を作製した。Medical grade silastic (registered trademark) obtained by spreading the above antibacterial CMC fiber structure containing 50% by weight of apacider (registered trademark, manufactured by Sangi Co., Ltd.) as hydroxyapatite supporting antibacterial metal ions. After standing still on silicone (MDX4-4210, Dow Corning) and heating at 60 ° C., it was slowly placed on and adhered to the hydrophilized porous polypropylene membrane obtained according to Example 1, and again 60 ° C. The wound dressing of the present invention was produced by heating the wound dressing.
【0032】(試験例2)抗菌性試験 滅菌済みシャーレ上に固形培地(Muller Hinton Agar,M
HA,DIFCO製)を20ml/シャーレの割合でまき、平板と
し前培養されたStaphylococcus aureus(黄色ブドウ球
菌)、Pseudomonas aeruginosa(緑膿菌)を均一に塗抹
した。Test Example 2 Antibacterial Test A solid medium (Muller Hinton Agar, M) was placed on a sterilized petri dish.
HA, DIFCO) was sprinkled at a rate of 20 ml / dishes, and Staphylococcus aureus (Staphylococcus aureus) and Pseudomonas aeruginosa (Pseudomonas aeruginosa), which had been pre-cultured as a plate, were uniformly smeared.
【0033】これに実施例4、5で得られた本発明に係
わる創傷被覆材を8mmφの大きさに打ち抜きサンプルと
し、固定培地平板1枚あたり3カ所載せた。37℃で1
8時間倒置培養後、阻止円の有無、接触面の菌の発育を
観察した。結果を表2に示す。結果より、抗菌効果が確
認された。The wound dressing material according to the present invention obtained in Examples 4 and 5 was punched out into a sample having a size of 8 mmφ and placed at three locations per fixed medium plate. 1 at 37 ° C
After inversion culture for 8 hours, the presence or absence of an inhibition circle and the growth of bacteria on the contact surface were observed. Table 2 shows the results. From the results, the antibacterial effect was confirmed.
【0034】[0034]
【表2】 [Table 2]
【0035】(試験例3)動物実験 実施例4、5で得られた本発明に係わる創傷被覆材を、
ラットの背部を剃毛し、デルマトームを用いて20×2
0mmの採皮創を作製後、そこに貼付した。炎症性、表皮
化率及び治癒状態を観察し、創傷被覆材としての実用性
を評価した。その結果、炎症性及び表皮化率について特
に悪影響は見られなかった。Test Example 3 Animal Experiment The wound dressing material according to the present invention obtained in Examples 4 and 5 was
The back of the rat is shaved and 20 × 2 using a dermatome
After preparing a 0 mm bark wound, it was attached thereto. The inflammatory property, the epidermalization rate and the healing state were observed, and the practicality as a wound dressing was evaluated. As a result, no particular adverse effects were found on the inflammatory property and the epidermalization rate.
【0036】(試験例4)経時着色変化 実施例4、5で得られた本発明に係わる創傷被覆材と、
本発明の抗菌性材料の代わりに、ゼオライトに抗菌性金
属を付与させた抗菌性材料であるバクテキラー(登録商
標、ニチメン(株)社製)を実施例4、5と同様の方法で
用いて作製した創傷被覆材(比較例1、2)を、1週間
室温に放置したところ、本発明に係わる創傷被覆材の外
観は変化はなかったが、各比較例の創傷被覆材は茶褐色
に変色した。(Test Example 4) Color Change with Time The wound dressing material according to the present invention obtained in Examples 4 and 5,
Instead of the antibacterial material of the present invention, Bactekiller (registered trademark, manufactured by Nichimen Co., Ltd.), which is an antibacterial material in which an antibacterial metal is added to zeolite, is produced in the same manner as in Examples 4 and 5. When the wound dressings (Comparative Examples 1 and 2) prepared above were left at room temperature for one week, the appearance of the wound dressings according to the present invention did not change, but the wound dressings of each Comparative Example turned brown.
【0037】[0037]
【発明の効果】本発明の医療用基材及び創傷被覆材は、
優れた抗菌性と経時安定性を有し、しかも皮膚欠損受傷
の際、疼痛を抑制し、創面の保湿性に優れ、潰瘍や熱傷
創等の感染を防止し、組織傷害の少ない創傷治癒を促進
できる。The medical base material and wound dressing of the present invention are
It has excellent antibacterial properties and stability over time. In addition, it suppresses pain when wounded with a skin defect, has excellent moisturizing properties on the wound surface, prevents infections such as ulcers and burn wounds, and promotes wound healing with less tissue damage. it can.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 小出 幹夫 神奈川県足柄上郡中井町井ノ口1500番地 テルモ株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Mikio Koide 1500 Inoguchi, Nakai-cho, Ashigarakami-gun, Kanagawa Terumo Corporation
Claims (5)
なくとも一種類の金属を担持したハイドロキシアパタイ
ト及び/又はシリカゲルを接着物質と共に支持体に含有
させたことを特徴とする医療用基材。1. A medical base material comprising a support containing at least one metal selected from the group consisting of silver, copper and zinc, and supporting hydroxyapatite and / or silica gel together with an adhesive substance. .
載の医療用基材。2. The medical substrate according to claim 1, wherein the support is a fiber structure.
乃至2記載の医療用基材。3. The adhesive material is a water repellent material.
The medical base material according to any one of claims 1 to 3.
ルロース、ポリエステル、ポリウレタン、コットン、又
はレーヨンである請求項1乃至3記載の医療用基材。4. The medical base material according to claim 1, wherein the material of the support is carboxymethyl cellulose, polyester, polyurethane, cotton, or rayon.
膜が積層されてなる創傷被覆材。5. A wound dressing obtained by laminating a hydrophilic porous membrane on the medical substrate according to claim 1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6269147A JPH08126659A (en) | 1994-11-01 | 1994-11-01 | Base material for medical care containing antifungal material and wound covering material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6269147A JPH08126659A (en) | 1994-11-01 | 1994-11-01 | Base material for medical care containing antifungal material and wound covering material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH08126659A true JPH08126659A (en) | 1996-05-21 |
Family
ID=17468340
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6269147A Pending JPH08126659A (en) | 1994-11-01 | 1994-11-01 | Base material for medical care containing antifungal material and wound covering material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH08126659A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998007929A1 (en) | 1996-08-16 | 1998-02-26 | Mitsubishi Materials Corporation | NOx REMOVING PAVEMENT STRUCTURE |
US6756060B1 (en) * | 1996-09-19 | 2004-06-29 | Usbiomaterials Corp. | Anti-inflammatory and antimicrobial uses for bioactive glass compositions |
JP2013099543A (en) * | 2012-12-27 | 2013-05-23 | Trustees Of Columbia Univ In The City Of New York | Zinc salt composition for coating medical product |
-
1994
- 1994-11-01 JP JP6269147A patent/JPH08126659A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1998007929A1 (en) | 1996-08-16 | 1998-02-26 | Mitsubishi Materials Corporation | NOx REMOVING PAVEMENT STRUCTURE |
US6756060B1 (en) * | 1996-09-19 | 2004-06-29 | Usbiomaterials Corp. | Anti-inflammatory and antimicrobial uses for bioactive glass compositions |
JP2013099543A (en) * | 2012-12-27 | 2013-05-23 | Trustees Of Columbia Univ In The City Of New York | Zinc salt composition for coating medical product |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU643058B2 (en) | Wound-covering materials | |
Gupta et al. | Textile-based smart wound dressings | |
JP2022523780A (en) | Antibacterial dressings, dressing components, and methods | |
US20060211972A1 (en) | Wound dressing | |
AU634164B2 (en) | Haemostatic wound dressing material | |
RU2437681C1 (en) | Wound covering with therapeutic action | |
Han | Interactive wound dressings | |
GB2399289A (en) | Hydrogel wound dressing | |
EP1601388B1 (en) | Hydrocolloid materials for use in wound healing | |
EP1493452A2 (en) | Antimicrobially active flexible hydrophilic polyurethane foam | |
CN116672488A (en) | Bismuth-containing burn dressing and preparation method thereof | |
JPH04303445A (en) | Wound covering material | |
JPH08126659A (en) | Base material for medical care containing antifungal material and wound covering material | |
JP2645098B2 (en) | Antibacterial agent-containing artificial skin and method for producing the same | |
KR20140097728A (en) | Wound dressing foam containing cuttlefish bone powder and method for preparing the same | |
JP2852954B2 (en) | Artificial skin and method for producing the same | |
JPH05337151A (en) | Wound cover material | |
JPH06245988A (en) | Material for coating wound | |
JPH04263855A (en) | Wound coating material | |
JP2896216B2 (en) | Wound dressing | |
JPH03242145A (en) | Wound covering material and production thereof | |
US20240157017A1 (en) | A medical dressing comprising a bacteriostatic composition | |
JPH03206032A (en) | Wound-covering material | |
JPH05337174A (en) | Cut covering material | |
JP2892790B2 (en) | Adhesive dressing |