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TWI577395B - Nano - silver colloidal wound dressing film and its preparation method - Google Patents

Nano - silver colloidal wound dressing film and its preparation method Download PDF

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Publication number
TWI577395B
TWI577395B TW105118493A TW105118493A TWI577395B TW I577395 B TWI577395 B TW I577395B TW 105118493 A TW105118493 A TW 105118493A TW 105118493 A TW105118493 A TW 105118493A TW I577395 B TWI577395 B TW I577395B
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film
nano silver
surfactant
wound dressing
ethanol solution
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TW105118493A
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TW201742637A (en
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Cheng-Wei Chen
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Chen ming-hong
Cheng-Wei Chen
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Priority to TW105118493A priority Critical patent/TWI577395B/en
Priority to CN201610737147.8A priority patent/CN107496970A/en
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Publication of TWI577395B publication Critical patent/TWI577395B/en
Publication of TW201742637A publication Critical patent/TW201742637A/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/24Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds; Derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42Use of materials characterised by their function or physical properties
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42Use of materials characterised by their function or physical properties
    • A61L15/46Deodorants or malodour counteractants, e.g. to inhibit the formation of ammonia or bacteria
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/10Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing inorganic materials
    • A61L2300/102Metals or metal compounds, e.g. salts such as bicarbonates, carbonates, oxides, zeolites, silicates
    • A61L2300/104Silver, e.g. silver sulfadiazine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/40Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
    • A61L2300/404Biocides, antimicrobial agents, antiseptic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/60Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a special physical form
    • A61L2300/602Type of release, e.g. controlled, sustained, slow

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Epidemiology (AREA)
  • Hematology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Materials For Medical Uses (AREA)
  • Medicinal Preparation (AREA)

Description

含奈米銀膠體傷口敷料薄膜及其製備方法 Nano silver colloid wound dressing film and preparation method thereof

本發明提供一種含奈米銀膠體傷口敷料薄膜,特別是有關於一種具有高度拉張力與吸水力,並且對於抗菌銀離子具有緩釋作用的含奈米銀膠體傷口敷料薄膜及其製備方法。 The invention provides a nano silver colloid wound dressing film, in particular to a nano silver colloid wound dressing film which has high tensile tension and water absorption and has a sustained release effect on antibacterial silver ions and a preparation method thereof.

皮膚為人體最大器官,具有阻隔外界有害物質入侵第一道防線,避免水份、離子流失及調節體溫之功能。而意外災難(如火災、交通事故),經常造成大範圍皮膚器官受損壞,引起感染、水離子喪失或溫度衡定調節異常而危害生命。 The skin is the largest organ of the human body, and it has the function of blocking the invasion of harmful substances from the outside to prevent the loss of moisture, ions and regulating body temperature. Accidental disasters (such as fires and traffic accidents) often cause damage to a wide range of skin organs, causing infection, loss of water ions, or abnormal temperature regulation and life-threatening.

通常二級、三級以上的中、重度燒燙傷入院傷患,醫護人員經常會於傷口清創處理後,以經消化道或非經消化道給予抗生素藥物作用於全身,或局部給藥直接在傷口上塗佈抗菌劑並覆蓋上一層滅菌紗布,施加以彈性繃帶固定。 Usually secondary or tertiary grades of moderate to severe burns are admitted to hospital. Medical staff often apply antibiotics to the whole body via the digestive or non-digestive tract after debridement, or local administration. The wound is coated with an antibacterial agent and covered with a layer of sterile gauze, applied with an elastic bandage.

而初期傷口因大量液體(如血液、壞死組織、免疫細胞等組成)會因滲出而浸潤污染覆蓋的紗布,故需經常性的更換。惟因網狀纖維狀的紗布覆蓋時,紗布容易進入傷口與組織交纏,因此,在更換紗布時,容易因拉扯動作,隨之撕去患者新生的皮膚組織細胞,造成傷患極大的不適 與疼痛,更有可能造成病患的傷口二次傷害與感染。 In the initial wound, a large amount of liquid (such as blood, necrotic tissue, immune cells, etc.) will infiltrate the contaminated gauze due to exudation, so it needs to be replaced frequently. However, when the gauze is covered by the reticular fibrous gauze, the gauze easily enters the wound and the tissue is intertwined. Therefore, when the gauze is changed, it is easy to pull off the patient's newborn skin tissue cells, causing great discomfort. With pain, it is more likely to cause secondary damage and infection to the wound of the patient.

故而在中,為能夠因應傷口敷料技術發展之需求,伴隨著終端傷口復原的需求,爭取醫護端的信任與潛力市場,尚需發展製造傷口敷料相關技術,可以達到環保目的,更可節省製造成本,且能有效形成保護傷口抗菌敷料。 Therefore, in order to meet the needs of the development of wound dressing technology, along with the need for terminal wound recovery, and to strive for the trust and potential market of the medical end, it is necessary to develop technologies for manufacturing wound dressings, which can achieve environmental protection purposes and save manufacturing costs. And can effectively form a protective wound antibacterial dressing.

根據前述傷口敷料的缺點,目前有必要提供一種新的傷口敷料及其製備方法以解決上述問題。因此,本發明主要的目的在於,利用生物可相容性聚合物為基質,輔以特定界面活性劑、塑化劑以及具抗菌功效的奈米銀製成具抗菌的膠體傷口敷料薄膜,且該薄膜具有高度拉張力與吸水能力之特性,可以取代目前醫療紗布的使用。 In accordance with the shortcomings of the aforementioned wound dressings, it is currently necessary to provide a new wound dressing and a method of preparing the same to solve the above problems. Therefore, the main object of the present invention is to use a biocompatible polymer as a matrix, supplemented with a specific surfactant, a plasticizer, and an antibacterial nano silver to form an antibacterial colloidal wound dressing film, and the film It has the characteristics of high tensile tension and water absorption capacity, which can replace the current use of medical gauze.

本發明的另一目的在於,含抗菌奈米銀膠體傷口敷料為薄膜,容易貼附於患者傷口處,且具有高度的吸水能力,可以減少對患者傷口敷料更換的頻率,而避免在更換敷料時,拉扯撕去患者新生的皮膚組織細胞,避免對傷患造成不適與降低疼痛。 Another object of the present invention is to provide an antibacterial nano silver colloid wound dressing as a film which is easy to adhere to a wound of a patient and has a high water absorption capacity, which can reduce the frequency of replacement of the patient's wound dressing, and avoids when changing the dressing. Pull and tear off the patient's newborn skin tissue cells to avoid discomfort and reduce pain.

本發明的再一目的在於,利用生物可相容性兩性聚合物與特殊配方比例製成薄膜,做為抗菌劑奈米銀緩慢釋放的載體。而含抗菌奈米銀膠體傷口敷料取代了抗菌劑與無菌紗布使用,加速傷口癒合,高度的吸水能力減少換藥頻率,高度的拉張延展性使其強固而不會緊緊黏牢於患者的傷口。 A further object of the present invention is to form a film using a ratio of a biocompatible amphoteric polymer to a specific formulation as a carrier for the slow release of the antibacterial agent nano silver. The antibacterial nano silver colloid wound dressing replaces the antibacterial agent and the sterile gauze to accelerate the wound healing, the high water absorption capacity reduces the dressing frequency, and the high tensile elongation makes it strong without sticking to the patient. wound.

根據上述目的,本發明揭露一種含抗菌奈米銀膠體傷口敷料 薄膜,由生物可相容性聚合物、界面活性劑、塑化劑、複數個奈米銀粒子及水溶液組成,其特徵在於:生物可相容性聚合物、界面活性劑、塑化劑、奈米銀粒子及水溶液的組成比例為30-50(W/V%):3-6(W/V%):0.3-1.6(W/V%):0.1-2(W/V%):30-60(V/V%)。藉由此比例所組成的含抗菌奈米銀膠體傷口敷料薄膜,具有高度的拉張力以及吸水能力,並且利用抗菌的奈米銀由此薄膜中緩慢釋放而對患者的傷口產生抗菌的效果。 According to the above object, the present invention discloses an antibacterial nano silver colloid wound dressing The film is composed of a biocompatible polymer, a surfactant, a plasticizer, a plurality of nano silver particles and an aqueous solution, and is characterized by: a biocompatible polymer, a surfactant, a plasticizer, and a naphthalene. The composition ratio of the rice silver particles and the aqueous solution is 30-50 (W/V%): 3-6 (W/V%): 0.3-1.6 (W/V%): 0.1-2 (W/V%): 30 -60 (V/V%). The antibacterial nano silver colloid wound dressing film composed of the ratio has a high tensile tension and water absorption capacity, and an antibacterial effect is exerted on the wound of the patient by using the antibacterial nano silver to be slowly released from the film.

根據前述含抗菌奈米銀膠體傷口敷料薄膜,本發明還揭露一種含抗菌奈米銀膠體傷口敷料薄膜的製備方法,其步驟包含:提供乙醇溶液、將聚甲基丙烯酸2-羥基乙基酯溶解於乙醇溶液中以得到聚甲基丙烯酸2-羥基乙基酯乙醇溶液、添加塑化劑、界面活性劑、含有複數個奈米銀粒子的水溶液與聚甲基丙烯酸2-羥基乙基酯乙醇溶液均勻混合以得到混合黏稠液體、將混合黏稠液體進行拉伸步驟以得到濕膜以及移除在濕膜中所殘留的乙醇溶液以得到薄膜,其中薄膜的厚度為0.05-0.06毫米,可貼附於患者的傷口,以取代現有所使用的醫療敷料。 According to the foregoing antibacterial nano silver colloid wound dressing film, the present invention also discloses a preparation method of the antibacterial nano silver colloid wound dressing film, which comprises the steps of: providing an ethanol solution and dissolving poly(2-hydroxyethyl methacrylate) In an ethanol solution to obtain a poly(2-hydroxyethyl methacrylate) ethanol solution, a plasticizer, a surfactant, an aqueous solution containing a plurality of nano silver particles, and a poly(2-hydroxyethyl methacrylate) ethanol solution. Mixing uniformly to obtain a mixed viscous liquid, subjecting the mixed viscous liquid to a stretching step to obtain a wet film, and removing the ethanol solution remaining in the wet film to obtain a film, wherein the film has a thickness of 0.05-0.06 mm and can be attached thereto. The patient's wound replaces the existing medical dressing used.

10‧‧‧提供乙醇溶液 10‧‧‧ Providing ethanol solution

12‧‧‧將聚甲基丙烯酸2-羥基乙基酯(pHEMA)溶解於乙醇溶液中以得到聚甲基丙烯酸2-羥基乙基酯乙醇溶液(pHEMA乙醇溶液) 12‧‧‧ Dissolve poly(2-hydroxyethyl methacrylate) (pHEMA) in ethanol solution to obtain poly(2-hydroxyethyl methacrylate) ethanol solution (pHEMA ethanol solution)

14‧‧‧將塑化劑、界面活性劑、含有複數個奈米銀粒子及水溶液與聚甲基丙烯酸2-羥基乙基酯乙醇溶液均勻混合以得到混合黏稠液體 14‧‧‧Where a plasticizer, a surfactant, a plurality of nano silver particles and an aqueous solution and a poly(2-hydroxyethyl methacrylate) solution are uniformly mixed to obtain a mixed viscous liquid.

16‧‧‧將混合黏稠液體進行拉伸步驟以得到濕膜 16‧‧‧Draw a mixed viscous liquid for the stretching step to obtain a wet film

18‧‧‧移除在濕膜中所殘留的乙醇溶液以固定成形而得到薄膜 18‧‧‧Removing the ethanol solution remaining in the wet film to form a film by fixed molding

第1圖是根據本發明所揭露的技術,表示含抗菌奈米銀膠體傷口敷料薄膜的製作步驟流程圖。 BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 is a flow chart showing the steps of making an antibacterial nano silver colloidal wound dressing film in accordance with the teachings of the present invention.

第2圖是根據本發明所揭露的技術,表示對含抗菌奈米銀膠體傷口敷料薄膜進行拉張力試驗的拉張長度的試驗示意圖。 Fig. 2 is a schematic view showing the test of the tensile length of the tensile strength test of the antibacterial nano silver colloid wound dressing film according to the technique disclosed in the present invention.

第3圖是根據本發明所揭露的技術,表示含抗菌奈米銀膠體傷口敷料薄膜中奈米銀離子經時釋放的試驗示意圖。 Figure 3 is a graphical representation of the test for the release of nano silver ions in an antibacterial nanosilver colloidal wound dressing film in accordance with the teachings of the present invention.

本發明揭露一種含抗菌奈米銀膠體傷口敷料薄膜,由生物可相容性聚合物、界面活性劑、塑化劑、複數個奈米銀粒子及水溶液組成,其中生物可相容性聚合物、界面活性劑、塑化劑、複數奈米銀粒子及水溶液的組成比例為30-50(W/V%):3-6(W/V%):0.3-1.6(W/V%):0.1-2(W/V%):30-60(V/V%)。 The invention discloses an antibacterial nano silver colloid wound dressing film, which is composed of a biocompatible polymer, a surfactant, a plasticizer, a plurality of nano silver particles and an aqueous solution, wherein the biocompatible polymer, The composition ratio of the surfactant, the plasticizer, the plurality of nano silver particles and the aqueous solution is 30-50 (W/V%): 3-6 (W/V%): 0.3-1.6 (W/V%): 0.1 -2 (W/V%): 30-60 (V/V%).

在本發明中,所使用的生物可相容性聚合物可以是一種水凝膠,其具有高度含水能力的聚合物質,質地軟如橡膠,低的界面張力使其具有高黏接性,容易黏附於其他物質表面。在本發明中,生物可相容性聚合物主要的成份為聚甲基丙烯酸2-羥基乙基酯(pHEMA,Poly(2-hydroxyethyl methacrylate)),意指包括甲基丙烯酸2-羥基乙基酯重覆單元之聚合物,化學式為(C6H10O3)n,具有分子量25000-100000Da以及分散性範圍為2-3.8。通常在水相中,其利用其中心的不對稱碳為支點旋轉,極性的羥乙基團轉向外側,因此變得柔韌;而在空氣中,非極性的甲基則轉向外側,因此變的易脆裂。聚甲基丙烯酸2-羥基乙基酯可含水而形成水性凝膠,但不溶解於水,因此是製作人工水晶體的材料。利用交聯預聚物,用以製造許多物件,包括親水性塗覆物、軟性隱形眼鏡與高精密度模製物件。另可做為藥物分子之載體裝置,如避孕環(NuvaRingTM),放置於子宮頸之環狀裝置,持續釋放依托孕烯與乙炔基雌二醇干擾受孕,也是實用的醫用高分子材料。 In the present invention, the biocompatible polymer used may be a hydrogel having a highly water-containing polymer substance, soft in texture such as rubber, low interfacial tension to make it highly adhesive, and easy to adhere. On the surface of other substances. In the present invention, the main component of the biocompatible polymer is poly(2-hydroxyethyl methacrylate), which means 2-hydroxyethyl methacrylate. The polymer of the repeating unit has a chemical formula of (C 6 H 10 O 3 ) n , a molecular weight of 25,000 to 100,000 Da, and a dispersibility ranging from 2 to 3.8. Usually in the aqueous phase, which uses its asymmetric carbon at the center as a fulcrum, the polar hydroxyethyl group turns to the outside and thus becomes flexible; in the air, the non-polar methyl group turns to the outside, thus making it easier Brittle. Poly(2-hydroxyethyl methacrylate) can form an aqueous gel by containing water, but does not dissolve in water, and is therefore a material for making artificial crystals. Crosslinked prepolymers are utilized to make a wide variety of articles, including hydrophilic coatings, soft contact lenses, and high precision molded articles. Another device can be used as a drug carrier molecule, such as IUD (NuvaRing TM), the ring means disposed in the cervix, sustained release of etonogestrel and ethinyl estradiol interference pregnancy, medical polymer materials are also useful.

此外,界面活性劑(Surfactant),或稱表面活性劑,是一種能 使目標溶液表面張力顯著下降的物質,可降低兩種液體或液體與固體間的表面張力,防止分散相的物質小液滴聚集凝結。界面活性劑一般為具有親水與疏水性基團的有機兩性分子,可溶於水或有機溶劑。其通常分為四類:陰離子型、陽離子型、非離子型與兩性離子型,可用作為清潔劑、潤濕劑、乳化劑、發泡劑和分散劑,應用範圍極為廣泛,包含化妝品、生活用品、食品工業、製藥醫療業等等。Span和Tween皆係山梨醇酯化衍生物的非離子型界面活性劑,在藥品與食品工業中作為乳化劑、共同乳化劑、增溶劑、分散劑,並且在大範圍的酸鹼值下穩定性佳。 In addition, a surfactant (Surfactant), or surfactant, is a kind of energy The substance which causes the surface tension of the target solution to be significantly lowered can reduce the surface tension between the two liquids or the liquid and the solid, and prevent the small droplets of the dispersed phase from agglomerating and coagulating. The surfactant is generally an organic amphiphilic molecule having hydrophilic and hydrophobic groups, and is soluble in water or an organic solvent. It is generally divided into four categories: anionic, cationic, nonionic and zwitterionic, which can be used as detergents, wetting agents, emulsifiers, foaming agents and dispersing agents, and has a wide range of applications, including cosmetics and household products. , food industry, pharmaceutical and medical industry, etc. Both Span and Tween are nonionic surfactants of sorbitan esterified derivatives, used as emulsifiers, co-emulsifiers, solubilizers, dispersants in the pharmaceutical and food industries, and are stable over a wide range of pH values. good.

在本發明中所使用的界面活性劑可以是Span或是Tween,其中,Span為脫水山梨醇酯化的脂肪酸衍生物(Sorbitan esters)系列,此分類常見有:Span 20(Sorbitanmonolaurate)、Span 40(Sorbitanmonopalmitate)、Span 60(Sorbitanmonostearate)、Span 80(Sorbitanmonooleate)、Span 83(Sorbitansesquioleate)、Span 85(Sorbitantrioleate)、Span 120(Sorbitanisostearate),其中,Span旁數字則代表不同的脂肪酸,如單月桂酸酯是由20表示,單棕櫚酸酯是由40表示,單硬脂酸酯是由60表示,單油酸酯則是由80表示,倍半油酸酯則是由83表示,三油酸酯則是由85表示,異硬脂酸酯則是由120表示。此Span系列的親水親油平衡值(HLB Value)範圍為1.8-8.6,適用於油包水(W/O)界面,疏水性值較高。 The surfactant used in the present invention may be Span or Tween, wherein Span is a series of sorbitan esterified fatty acid derivatives (Sorbitan esters), which are commonly classified as: Span 20 (Sorbitan monolaurate), Span 40 ( Sorbitanmonopalmitate), Span 60 (Sorbitanmonostearate), Span 80 (Sorbitanmonooleate), Span 83 (Sorbitansesoleoleate), Span 85 (Sorbitantrioleate), Span 120 (Sorbitanisostearate), wherein the number next to Span represents different fatty acids, such as monolaurate It is represented by 20 that monopalmitate is represented by 40, monostearate is represented by 60, monooleate is represented by 80, sesquioleate is represented by 83, and trioleate is represented by It is represented by 85, and isostearate is represented by 120. The Span series has a hydrophilic-lipophilic balance (HLB Value) ranging from 1.8 to 8.6 and is suitable for water-in-oil (W/O) interfaces with high hydrophobicity values.

而本發明所使用之Tween,則為聚乙氧基化的脫水山梨醇酯化的脂肪酸衍生物(Polyethoxylatedsorbitan esters)系列,此分類常見有:Tween 20(Polyoxyethylene-20 sorbitanmonolaurate)、Tween 21(Polyoxyethylene-4 sorbitanmonolaurate)、Tween 40(Polyoxyethylene-20 sorbitanmonopalmitate)、 Tween 60(Polyoxyethylene-20 sorbitanmonostearate)、Tween 61(Polyoxyethylene-4 sorbitanmonostearate)、Tween 65(Polyoxyethylene-20 sorbitantristearate)、Tween 80(Polyoxyethylene-20 sorbitanmonooleate),4或20指的是氧化乙烯(oxyethylene,-(CH2CH2O)-)單體的總數,其中,Tween旁數字則代表不同的脂肪酸,如單月桂酸酯是由20或21表示,單棕櫚酸酯是由40表示,單硬脂酸酯是由60或61表示,三硬脂酸酯是由65表示,單油酸酯則是由80表示。此Tween系列的親水親油平衡值(HLB Value)範圍為9.6-16.7,適用於水包油(O/W)界面,相較於Span系列親水性值較高。 The Tween used in the present invention is a series of polyethoxylated sorbitan esterified fatty acid derivatives (Polyoxylatedsorbentan esters), which are commonly classified as: Tween 20 (Polyoxyethylene-20 sorbitan monolaurate), Tween 21 (Polyoxyethylene- 4 sorbitanmonolaurate), Tween 40 (Polyoxyethylene-20 sorbitan monopalmitate), Tween 60 (Polyoxyethylene-20 sorbitan monostearate), Tween 61 (Polyoxyethylene-4 sorbitan monostearate), Tween 65 (Polyoxyethylene-20 sorbitantristearate), Tween 80 (Polyoxyethylene-20 sorbitan monooleate), 4 Or 20 refers to the total number of oxyethylene (-(CH 2 CH 2 O)-) monomers, wherein the Tween side number represents a different fatty acid, such as monolaurate is represented by 20 or 21, single palm The acid ester is represented by 40, the monostearate is represented by 60 or 61, the tristearate is represented by 65, and the monooleate is represented by 80. The Tween series has a hydrophilic-lipophilic balance (HLB Value) ranging from 9.6-16.7, which is suitable for the oil-in-water (O/W) interface and is higher in hydrophilicity than the Span series.

本發明所使用之塑化劑(Plasticizer),或稱增塑劑、可塑劑,是一種用以增加材料的柔軟性或使材料液化的添加劑。其添加的對象領域廣泛包含了塑膠材料、建築材料、食品工業、製藥業等等。同一種塑化劑使用在不同的對象上,常常有不相同的效果。塑化劑種料多達百餘種,在本發明中,由於含抗菌奈米銀膠體傷口敷料薄膜是要貼附在人體的傷口,會接觸人體的皮膚,因此使用對人體具有安全性的塑化劑種類,例如乙醯單酸甘油乙酯(Acetylated monoglyceride)、環己烷-1,2-二羧酸二異壬酯(1,2-Cyclohexane dicarboxylic acid diisononyl ester)(BASF的註冊商標為DINCH)或是檸檬酸酯類(Alkyl citrates),其中,乙醯單酸甘油乙酯(Acetylated monoglyceride)具有生物可降解性(Biodegradability),也不容易造成生物的化學反應,可用作食品添加劑。另外,環己烷-1,2-二羧酸二異壬酯(1,2-Cyclohexane dicarboxylic acid diisononyl ester),可用作食品包裝、醫療器材及兒童玩具,此塑化劑和包括PVC在內的大部份聚合物相容。檸檬酸酯類(Alkyl citrates)可以用作食品包裝、醫療器材、藥物控釋、化妝品及玩具, 檸檬酸酯類(Alkyl citrates)如:檸檬酸三乙酯(Triethyl citrate,TEC)、檸檬酸乙醯基三乙酯(Acetyl triethyl citrate,ATEC)、檸檬酸三丁酯(Tributyl citrate,TBC)、檸檬酸乙醯基三丁酯(Acetyl tributyl citrate,ATBC)、檸檬酸三辛酯(Trioctyl citrate,TOC)、檸檬酸乙醯基三辛酯(Acetyl trioctyl citrate,ATOC)、檸檬酸三己酯(Trihexyl citrate,THC)、檸檬酸乙醯基三己酯(Acetyl trihexyl citrate,ATHC)、丁醯檸檬酸三正己酯(Trihexylo-butyryl citrate,BTHC)、檸檬酸三甲酯(Trimethyl citrate,TMC)。 The plasticizer used in the present invention, or plasticizer or plasticizer, is an additive for increasing the softness of a material or liquefying a material. The added object areas include plastic materials, building materials, the food industry, the pharmaceutical industry, and so on. The same plasticizer is used on different objects and often has different effects. There are more than one hundred kinds of plasticizer seed materials. In the present invention, since the antibacterial nano silver colloid wound dressing film is attached to the wound of the human body and will contact the skin of the human body, the plastic which is safe for the human body is used. Types of agents, such as Acetylated monoglyceride, 1,2-Cyclohexane dicarboxylic acid diisononyl ester (BASF is a registered trademark of DINCH). Or Alkyl citrates, in which Acetylated monoglyceride has biodegradability and is not easily caused by biological reactions, and can be used as a food additive. In addition, 1,2-cyclohexane dicarboxylic acid diisononyl ester can be used as food packaging, medical equipment and children's toys, including plasticizers and PVC. Most of the polymers are compatible. Alkyl citrates can be used as food packaging, medical equipment, drug controlled release, cosmetics and toys, Alkyl citrates such as Triethyl citrate (TEC), citrate B Acetyl triethyl citrate (ATEC), Tributyl citrate (TBC), Acetyl tributyl citrate (ATBC), Trioctyl citrate (Trioctyl citrate, TOC), Acetyl trioctyl citrate (ATOC), Trihexyl citrate (THC), Acetyl trihexyl citrate (ATHC), Dingzhi lemon Trihexyl o- butyryl citrate (BTHC), Trimethyl citrate (TMC).

更甚者,在本發明中,為了使敷料具有抗菌的功能,因此使用具有抗菌能力的奈米銀,眾所皆知奈米銀具有殺菌效果,由於奈米化的活性銀能穿透細胞膜與細菌酶蛋白之硫醇基結合,阻斷細菌蛋白質之生化活性而達到殺菌效果,銀離子亦能阻斷去氧核醣核酸(DNA)轉譯蛋白質的能力而具有毒性。在此,奈米係指十億分之一米,即10-9nm(nanometer),相當於核苷酸對分子的大小,當物質粒徑不斷的微小化,總表面積大幅增加,界面能量大不穩定,因此微粒容易凝聚又形成大的粒子。現行的科技進步,利用保護劑吸附微粒表面可抑止銀微粒變大,只要粒徑小於100奈米即可稱奈米化銀。 Furthermore, in the present invention, in order to impart an antibacterial function to the dressing, nano silver having an antibacterial ability is used, and it is known that nano silver has a bactericidal effect, since the activated silver of nanocrystallization can penetrate the cell membrane and The thiol group of the bacterial enzyme protein binds to block the biochemical activity of the bacterial protein to achieve a bactericidal effect, and the silver ion can also block the ability of the DNA to translate the protein and is toxic. Here, the nanometer refers to a billionth of a meter, that is, 10 -9 nm (nanometer), which is equivalent to the size of the nucleotide to the molecule. When the particle size of the material is continuously miniaturized, the total surface area is greatly increased, and the interface energy is large. It is unstable, so the particles tend to aggregate and form large particles. The current scientific and technological progress, the use of a protective agent to adsorb the surface of the particles can inhibit the silver particles from becoming large, as long as the particle size is less than 100 nm, it can be called silver.

根據本發明所揭露的含抗菌奈米銀傷口敷料薄膜,本發明還揭露了一種含抗菌奈米銀膠體傷口敷料薄膜的製備方法,其步驟10-18為含抗菌奈米銀傷口敷料薄膜的製備方法的步驟流程,如第1圖所示。 According to the antibacterial nano silver wound dressing film disclosed by the present invention, the invention also discloses a preparation method of the antibacterial nano silver colloid wound dressing film, wherein the steps 10-18 are preparation of the antibacterial nano silver wound dressing film. The step flow of the method is shown in Figure 1.

於本發明實施例的第1圖所示,首先於步驟10中,提供乙醇溶液。 In the first diagram of the embodiment of the present invention, first in step 10, an ethanol solution is provided.

又於本發明實施例的第1圖之步驟12中,將聚甲基丙烯酸 2-羥基乙基酯(pHEMA)溶解於乙醇溶液中,以得到聚甲基丙烯酸2-羥基乙基酯乙醇溶液(pHEMA乙醇溶液)。 Further, in step 12 of the first embodiment of the embodiment of the present invention, polymethacrylic acid is used. 2-Hydroxyethyl ester (pHEMA) was dissolved in an ethanol solution to obtain a poly(2-hydroxyethyl methacrylate) ethanol solution (pHEMA ethanol solution).

再於本發明實施例的第1圖之步驟14中,將塑化劑、界面活性劑、含有複數個奈米銀粒子及水溶液與聚甲基丙烯酸2-羥基乙基酯乙醇溶液均勻混合,以得到混合黏稠液體。 Further, in step 14 of the first embodiment of the present invention, the plasticizer, the surfactant, the plurality of nano silver particles and the aqueous solution are uniformly mixed with the poly(2-hydroxyethyl methacrylate) ethanol solution, A mixed viscous liquid is obtained.

而於本發明實施例第1圖之步驟16中,將混合黏稠液體進行拉伸步驟以得到濕膜。 In the step 16 of the first embodiment of the present invention, the mixed viscous liquid is subjected to a stretching step to obtain a wet film.

最後,於本發明實施例第1圖之步驟18中,移除在濕膜中所殘留的乙醇溶液,藉以固定成形而得到薄膜。 Finally, in step 18 of the first embodiment of the present invention, the ethanol solution remaining in the wet film is removed, whereby the film is fixedly formed.

根據上述的步驟流程,詳細的含抗菌奈米銀傷口敷料薄膜的製備方法綜合如下所述: 首先於第1圖所示之步驟10中,將16公克的聚甲基丙烯酸2-羥基乙基酯溶於體積為100ml的乙醇溶液中。接著於第1圖之步驟12中,再分別加入適量比例的塑化劑、界面活性劑、複數個奈米銀粒子以及水溶液與聚甲基丙烯酸2-羥基乙基酯的乙醇溶液充分混合均勻。再接著於第1圖之步驟14中,將體積為100ml且濃度為2000ppm的含有複數個奈米銀粒子的水溶液加入上述的混合溶液中,充分混合均勻,形成混合黏稠液體。要說明的是,在本發明中,是利用含有複數個奈米銀粒子的水溶液進行混合,但是為了說明含抗菌奈米銀膠體傷口敷料薄膜的比例,在此將複數個奈米銀粒子和水溶液視為兩個組份來說明,但並不影響最後所形成的含抗菌奈米銀膠體傷口敷料薄膜的材料特性以及其功效。 According to the above procedure, the detailed preparation method of the antibacterial nano silver wound dressing film is as follows: First, in the step 10 shown in Fig. 1, 16 g of polyhydroxyethyl methacrylate was dissolved in a 100 ml ethanol solution. Then, in step 12 of FIG. 1, an appropriate amount of a plasticizer, a surfactant, a plurality of nano silver particles, and an aqueous solution of an aqueous solution of 2-hydroxyethyl methacrylate are uniformly mixed and uniformly mixed. Next, in step 14 of Fig. 1, an aqueous solution containing a plurality of nano silver particles having a volume of 100 ml and a concentration of 2000 ppm is added to the above mixed solution, and thoroughly mixed to form a mixed viscous liquid. It is to be noted that, in the present invention, mixing is carried out using an aqueous solution containing a plurality of nano silver particles, but in order to explain the ratio of the antibacterial nano silver colloid wound dressing film, a plurality of nano silver particles and an aqueous solution are herein. It is considered as two components, but does not affect the material properties of the resulting antibacterial nano silver colloidal wound dressing film and its efficacy.

續如第1圖之步驟16中,利用可調式濕膜塗佈器(未在圖 中表示)將混合濃稠液體於透明膠片(未在圖中表示)上拉製成薄膜,於可調式濕膜塗佈器上設定欲拉伸的薄膜厚度為0.25-0.35毫米(mm),較佳的厚度為0.3毫米(mm)。此時完成拉伸的薄膜還是濕膜,即薄膜中含有乙醇溶液,因此依第1圖之步驟18,將完成拉伸步驟的薄膜置於層流罩(未在圖中表示)中進行揮發乾燥,以移除薄膜中的乙醇溶液並且使薄膜固定成形,在此,揮發乾燥的時間約12小時。而完全移除乙醇溶液之後的薄膜即為含抗菌奈米銀膠體傷口敷料薄膜,其厚度為0.05-0.06毫米(mm),較佳的厚度為0.06毫米。在此,薄膜中各成份的比分別為:聚甲基丙烯酸2-羥基乙基酯:塑化劑:界面活性劑:複數個奈米銀粒子:水溶液的比例為30-50(W/V%):3-6(W/V%):0.3-1.6(W/V%):0.1-2(W/V%):30-60(V/V%)。 Continued as in step 16 of Figure 1, using an adjustable wet film applicator (not shown) In the middle of the film, the mixed thick liquid is drawn into a transparent film (not shown) to form a film, and the thickness of the film to be stretched is set to 0.25-0.35 mm (mm) on the adjustable wet film coater. The preferred thickness is 0.3 mm (mm). The film which is stretched at this time is also a wet film, that is, the film contains an ethanol solution. Therefore, according to the step 18 of FIG. 1, the film which has completed the stretching step is placed in a laminar flow hood (not shown) for evaporation and drying. To remove the ethanol solution in the film and to fix the film, where the evaporation is dried for about 12 hours. The film after completely removing the ethanol solution is an antibacterial nano silver colloid wound dressing film having a thickness of 0.05-0.06 mm (mm), preferably 0.06 mm. Here, the ratio of each component in the film is: polyhydroxyethyl methacrylate: plasticizer: surfactant: a plurality of nano silver particles: the ratio of the aqueous solution is 30-50 (W/V%) ): 3-6 (W/V%): 0.3-1.6 (W/V%): 0.1-2 (W/V%): 30-60 (V/V%).

最後,依所需要的形狀或尺寸,將含抗菌奈米銀膠體傷口敷料薄膜裁切成特定形狀或大小,並以密閉封套將此含抗菌奈米銀膠體傷口敷料薄膜以無菌的方式保存。 Finally, the antibacterial nano silver colloidal wound dressing film is cut to a specific shape or size according to the desired shape or size, and the antibacterial nano silver colloid wound dressing film is stored in a sterile manner in a sealed envelope.

在本發明中,可針對含抗菌奈米銀膠體傷口敷料薄膜進行物化特性評估,根據上述的製備方法以及特定比例,將所製得的含抗菌奈米銀傷口敷料薄膜進行吸水含量及吸水厚度的測試。首先,吸水含量的測試是將含抗菌奈米銀膠體傷口敷料薄膜稱重,並記錄。然後再將含抗菌奈米銀膠體傷口敷料薄膜置於盛裝有水的器皿中,讓水溶液完全覆蓋過整個含抗菌奈米銀膠體傷口敷料薄膜,經過24小時之後,再將浸過水的含抗菌奈米銀膠體傷口敷料薄膜取出去除表面水滴並進行稱重,並記錄下來。吸水厚度的測試是使用厚度計,來量測含抗菌奈米銀膠體傷口敷料薄膜不同位置的厚度,並記錄之。接著,再將含抗菌奈米銀膠體傷口敷料薄膜放置 在盛裝有水的器皿中,讓水溶液完全覆蓋過整個含抗菌奈米銀膠體傷口敷料薄膜,經過24小時之後,再將浸過水的含抗菌奈米銀膠體傷口敷料薄膜取出,並利用厚度計量測再將浸過水的含抗菌奈米銀膠體傷口敷料薄膜取出至少三點不同位置的厚度,並記錄顯示。 In the present invention, the physicochemical properties of the antibacterial nano silver colloid wound dressing film can be evaluated, and the prepared antibacterial nano silver wound dressing film can be subjected to water absorption content and water absorption thickness according to the above preparation method and specific ratio. test. First, the water content test was performed by weighing and recording the antibacterial nano silver colloid wound dressing film. Then, the antibacterial nano silver colloid wound dressing film is placed in a vessel filled with water, and the aqueous solution completely covers the entire antibacterial nano silver colloid wound dressing film. After 24 hours, the water-impregnated antibacterial film is further impregnated. The nano silver colloidal wound dressing film was removed to remove surface water droplets and weighed and recorded. The test for water absorption thickness is to measure the thickness of the antibacterial nano silver colloidal wound dressing film at different positions using a thickness gauge and record it. Next, the antibacterial nano silver colloid wound dressing film is placed In a vessel containing water, the aqueous solution is completely covered with the entire antibacterial nano silver colloid wound dressing film, and after 24 hours, the water-impregnated antibacterial nano silver colloid wound dressing film is taken out, and the thickness meter is used. The water-impregnated antibacterial nano silver colloid wound dressing film was then taken out to a thickness of at least three different positions and recorded.

由表1可以得到含抗菌奈米銀膠體傷口敷料薄膜於吸水前以及吸水後的重量以及吸水率: 表2是表示含抗菌奈米銀膠體傷口敷料薄膜在吸水前後,量測至少三點不同位置的厚度 The weight and water absorption of the antibacterial nano silver colloidal wound dressing film before and after water absorption can be obtained from Table 1: Table 2 shows the thickness of the antibacterial nano silver colloid wound dressing film measured at least three different positions before and after water absorption.

由表1及表2可以得到,本發明所揭露的含抗菌奈米銀膠體傷口敷料薄膜有良好的吸水率以及吸水膨脹率,也就表示在貼附於患者 的傷口時,對於傷口上的液體(血液或是膿)有良好的吸水性。 It can be obtained from Table 1 and Table 2 that the antibacterial nano silver colloid wound dressing film disclosed in the present invention has good water absorption rate and water swelling rate, and is also attached to the patient. The wound has good water absorption for the liquid (blood or pus) on the wound.

接著,因為含抗菌奈米銀膠體傷口敷料薄膜要貼附於人體的皮膚上,然而患者受傷的部位有可能在關節處,需要拉張力良好的薄膜才能貼附於人體皮膚上,因此本發明針對含抗菌奈米銀膠體傷口敷料薄膜進行了拉張力試驗,其中拉張力的條件為含抗菌奈米銀膠體傷口敷料薄膜長度為1公分,由第2圖可以得知,經破裂拉張之後的長度為1.87公分,因此可拉張長度比率為(1+1.87)/1=2.87倍。 Then, since the antibacterial nano silver colloid wound dressing film is attached to the skin of the human body, the injured part of the patient may be at the joint, and a film having a good tension may be attached to the human skin, so the present invention is directed to The tensile strength test was carried out on the antibacterial nano silver colloid wound dressing film, wherein the tension tension condition was that the film containing the antibacterial nano silver colloid wound dressing was 1 cm in length, and the length after the rupture was stretched from Fig. 2 It is 1.87 cm, so the stretchable length ratio is (1 + 1.87) / 1 = 2.87 times.

此外,對於本發明所揭露的含抗菌奈米銀膠體傷口敷料薄膜還進行銀離子釋放的試驗,猶如第3圖所示。由第3圖可以得知,在含抗菌奈米銀膠體傷口敷料薄膜中的奈米銀離子會隨著使用時間的增加而緩慢的釋放出來,以達到抗菌的功效。 In addition, the antibacterial nano silver colloid wound dressing film disclosed in the present invention is also subjected to silver ion release test as shown in FIG. It can be seen from Fig. 3 that the nano silver ions in the antibacterial nano silver colloid wound dressing film are slowly released as the use time is increased to achieve the antibacterial effect.

以上所述僅為本發明之較佳實施例而已,並非用以限定本發明之申請專利範圍;凡其它未脫離本發明所揭示之精神下所完成之等效改變或修飾,均應包含在下述之申請專利範圍內。 The above is only the preferred embodiment of the present invention, and is not intended to limit the scope of the present invention; all other equivalent changes or modifications which are not departing from the spirit of the present invention should be included in the following. Within the scope of the patent application.

10‧‧‧提供乙醇溶液 10‧‧‧ Providing ethanol solution

12‧‧‧將聚甲基丙烯酸2-羥基乙基酯(pHEMA,Poly(2-hydroxyethyl methacrylate))溶解於乙醇溶液中,以得到聚甲基丙烯酸2-羥基乙基酯乙醇溶液(pHEMA乙醇溶液) 12‧‧‧ Dissolve 2-hydroxyethyl methacrylate (pHEMA, Poly(2-hydroxyethyl methacrylate)) in ethanol solution to obtain poly(2-hydroxyethyl methacrylate) ethanol solution (pHEMA ethanol solution) )

14‧‧‧將塑化劑、界面活性劑、含有複數個奈米銀粒子及水溶液與聚甲基丙烯酸2-羥基乙基酯乙醇溶液均勻混合,以得到混合黏稠液體 14‧‧‧Where a plasticizer, a surfactant, a plurality of nano-silver particles and an aqueous solution and a poly(2-hydroxyethyl methacrylate) solution are uniformly mixed to obtain a mixed viscous liquid.

16‧‧‧將混合黏稠液體進行拉伸步驟以得到濕膜 16‧‧‧Draw a mixed viscous liquid for the stretching step to obtain a wet film

18‧‧‧移除在濕膜中所殘留的乙醇溶液以固定成形而得到薄膜 18‧‧‧Removing the ethanol solution remaining in the wet film to form a film by fixed molding

Claims (5)

一種含抗菌奈米銀膠體傷口敷料薄膜,係由一生物可相容性聚合物、一界面活性劑、一塑化劑、複數個奈米銀粒子及一水溶液組成,包含:一生物可相容性聚合物,其中該生物可相容性聚合物包含聚甲基丙烯酸2-羥基乙基酯(pHEMA,Poly(2-hydroxyethyl methacrylate));一界面活性劑,其中該界面活性劑係由陰離子型界面活性劑,陽離子型界面活性劑,非離子型界面活性劑,以及兩性離子型界面活性劑群組中所選出;一塑化劑,其中該塑化劑係由乙醯單酸甘油乙酯(Acetylated monoglyceride)、環己烷-1,2-二羧酸二異壬酯(1,2-Cyclohexane dicarboxylic acid diisononyl ester)以及檸檬酸酯類(Alkyl citrates)群組中所選出;複數個奈米銀粒子;以及一水溶液,其中該生物可相容性聚合物,該界面活性劑,該塑化劑,該複數個奈米銀粒子,以及該水溶液的組成比例為30-50(W/V%):3-6(W/V%):0.3-1.6(W/V%):0.1-2(W/V%):30-60(V/V%)。 An antibacterial nano silver colloid wound dressing film comprising a biocompatible polymer, a surfactant, a plasticizer, a plurality of nano silver particles and an aqueous solution, comprising: a biocompatible a polymer, wherein the biocompatible polymer comprises poly(2-hydroxyethyl methacrylate), a surfactant, wherein the surfactant is anionic. a surfactant, a cationic surfactant, a nonionic surfactant, and a zwitterionic surfactant group selected; a plasticizer, wherein the plasticizer is ethyl acetoacetate ( Selected from the group of Acetylated monoglyceride, 1,2-Cyclohexane dicarboxylic acid diisononyl ester and Alkyl citrates; a plurality of nano silver And an aqueous solution, wherein the biocompatible polymer, the surfactant, the plasticizer, the plurality of nano silver particles, and the composition ratio of the aqueous solution are 30-50 (W/V%) :3-6 (W/V%): 0.3-1.6 (W/V%) : 0.1-2 (W/V%): 30-60 (V/V%). 一種含抗菌奈米銀膠體傷口敷料薄膜的製備方法,步驟包含:提供一乙醇溶液;將一聚甲基丙烯酸2-羥基乙基酯溶解於該乙醇溶液中以得到一聚甲基丙烯酸2-羥基乙基酯乙醇溶液;添加一塑化劑、一界面活性劑、含有複數個奈米銀粒子的一水溶液與該聚甲基丙烯酸2-羥基乙基酯乙醇溶液均勻混合以得到一混合黏稠液 體;將該混合黏稠液體進行一拉伸步驟以得到一濕膜;以及移除在該濕膜中所殘留的該乙醇溶液以固定成形而得到一薄膜。 A method for preparing an antibacterial nano silver colloid wound dressing film, comprising the steps of: providing an ethanol solution; dissolving a poly(2-hydroxyethyl methacrylate) in the ethanol solution to obtain a poly(methacrylic acid) 2-hydroxyl group Ethyl ester ethanol solution; adding a plasticizer, a surfactant, an aqueous solution containing a plurality of nano silver particles and the poly(2-hydroxyethyl methacrylate) ethanol solution are uniformly mixed to obtain a mixed viscous liquid The mixed viscous liquid is subjected to a stretching step to obtain a wet film; and the ethanol solution remaining in the wet film is removed to be fixedly formed to obtain a film. 如申請專利範圍第2項所述的製備方法,其中該拉伸步驟更包括:提供一透明膠片;將該混合黏稠液體放置於該透明膠片上;以及利用一可調式濕膜塗佈器拉伸在該透明膠片上的該混合黏稠液體以形成厚度為0.25-0.35毫米(mm)的該濕膜。 The preparation method of claim 2, wherein the stretching step further comprises: providing a transparent film; placing the mixed viscous liquid on the transparent film; and stretching by using an adjustable wet film coater The mixed viscous liquid on the transparency film is formed to form the wet film having a thickness of 0.25 to 0.35 millimeters (mm). 如申請專利範圍第2項所述的製備方法,其中該移除該乙醇的方法包含:將該濕膜置於一層流罩中;以及於該層流罩中對該濕膜進行一揮發乾燥步驟,以移除在該濕膜中的該乙醇溶液。 The method of claim 2, wherein the removing the ethanol comprises: placing the wet film in a flow mask; and performing a volatile drying step on the wet film in the laminar flow hood To remove the ethanol solution in the wet film. 如申請專利範圍第2項所述的製備方法,其中該薄膜厚度為0.05-0.06毫米(mm)。 The preparation method according to claim 2, wherein the film has a thickness of 0.05 to 0.06 mm (mm).
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