CN105078651A - Multifunctional wet medical wound dressing and preparation method thereof - Google Patents
Multifunctional wet medical wound dressing and preparation method thereof Download PDFInfo
- Publication number
- CN105078651A CN105078651A CN201510500878.6A CN201510500878A CN105078651A CN 105078651 A CN105078651 A CN 105078651A CN 201510500878 A CN201510500878 A CN 201510500878A CN 105078651 A CN105078651 A CN 105078651A
- Authority
- CN
- China
- Prior art keywords
- multifunctional
- dressing
- layer
- medical
- wound
- 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
- 238000002360 preparation method Methods 0.000 title claims abstract description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 65
- 239000004814 polyurethane Substances 0.000 claims abstract description 21
- 239000004698 Polyethylene Substances 0.000 claims abstract description 13
- 229920000573 polyethylene Polymers 0.000 claims abstract description 13
- 229920002635 polyurethane Polymers 0.000 claims abstract description 13
- -1 polyethylene Polymers 0.000 claims abstract description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 39
- 239000012153 distilled water Substances 0.000 claims description 18
- 230000002439 hemostatic effect Effects 0.000 claims description 17
- 239000012528 membrane Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 13
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 13
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 13
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 13
- 239000000022 bacteriostatic agent Substances 0.000 claims description 11
- 239000002202 Polyethylene glycol Substances 0.000 claims description 9
- 229920001223 polyethylene glycol Polymers 0.000 claims description 9
- 229920001661 Chitosan Polymers 0.000 claims description 7
- 230000001954 sterilising effect Effects 0.000 claims description 7
- 239000008367 deionised water Substances 0.000 claims description 6
- 229910021641 deionized water Inorganic materials 0.000 claims description 6
- 238000010894 electron beam technology Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 6
- 239000011265 semifinished product Substances 0.000 claims description 6
- 238000010030 laminating Methods 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 3
- 239000003292 glue Substances 0.000 claims description 3
- 239000010410 layer Substances 0.000 abstract description 57
- 239000000017 hydrogel Substances 0.000 abstract description 37
- 239000010408 film Substances 0.000 abstract description 30
- 230000000694 effects Effects 0.000 abstract description 9
- 239000004820 Pressure-sensitive adhesive Substances 0.000 abstract description 8
- 208000002193 Pain Diseases 0.000 abstract description 4
- 230000036407 pain Effects 0.000 abstract description 4
- 239000010409 thin film Substances 0.000 abstract description 3
- 206010061218 Inflammation Diseases 0.000 abstract description 2
- 230000023597 hemostasis Effects 0.000 abstract description 2
- 230000004054 inflammatory process Effects 0.000 abstract description 2
- 230000003467 diminishing effect Effects 0.000 abstract 1
- 231100000331 toxic Toxicity 0.000 abstract 1
- 230000002588 toxic effect Effects 0.000 abstract 1
- 206010052428 Wound Diseases 0.000 description 71
- 208000027418 Wounds and injury Diseases 0.000 description 71
- 239000000499 gel Substances 0.000 description 24
- 238000012360 testing method Methods 0.000 description 16
- 239000000047 product Substances 0.000 description 15
- 238000000034 method Methods 0.000 description 13
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 11
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 11
- 210000001519 tissue Anatomy 0.000 description 10
- 230000029663 wound healing Effects 0.000 description 10
- 230000033228 biological regulation Effects 0.000 description 9
- 230000005540 biological transmission Effects 0.000 description 7
- 229920003023 plastic Polymers 0.000 description 7
- 230000003385 bacteriostatic effect Effects 0.000 description 6
- 239000002131 composite material Substances 0.000 description 6
- 239000002250 absorbent Substances 0.000 description 5
- 230000003110 anti-inflammatory effect Effects 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 210000000416 exudates and transudate Anatomy 0.000 description 5
- 230000035876 healing Effects 0.000 description 5
- 208000015181 infectious disease Diseases 0.000 description 5
- 244000005700 microbiome Species 0.000 description 5
- 239000003755 preservative agent Substances 0.000 description 5
- 230000002335 preservative effect Effects 0.000 description 5
- 239000011241 protective layer Substances 0.000 description 5
- 238000010998 test method Methods 0.000 description 5
- 241000894006 Bacteria Species 0.000 description 4
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 4
- 230000000202 analgesic effect Effects 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000008014 freezing Effects 0.000 description 4
- 238000007710 freezing Methods 0.000 description 4
- 230000005251 gamma ray Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- JLFNLZLINWHATN-UHFFFAOYSA-N pentaethylene glycol Chemical compound OCCOCCOCCOCCOCCO JLFNLZLINWHATN-UHFFFAOYSA-N 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- 208000006313 Delayed Hypersensitivity Diseases 0.000 description 2
- 241000521257 Hydrops Species 0.000 description 2
- 206010030113 Oedema Diseases 0.000 description 2
- 230000001133 acceleration Effects 0.000 description 2
- 230000000172 allergic effect Effects 0.000 description 2
- 208000010668 atopic eczema Diseases 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000005213 imbibition Methods 0.000 description 2
- 230000036512 infertility Effects 0.000 description 2
- 208000014674 injury Diseases 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- 230000009545 invasion Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000008733 trauma Effects 0.000 description 2
- 230000037314 wound repair Effects 0.000 description 2
- 206010011409 Cross infection Diseases 0.000 description 1
- 102000010834 Extracellular Matrix Proteins Human genes 0.000 description 1
- 108010037362 Extracellular Matrix Proteins Proteins 0.000 description 1
- 206010017533 Fungal infection Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- 206010029803 Nosocomial infection Diseases 0.000 description 1
- 206010040943 Skin Ulcer Diseases 0.000 description 1
- 208000028990 Skin injury Diseases 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- 206010070835 Skin sensitisation Diseases 0.000 description 1
- 206010072170 Skin wound Diseases 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 206010053615 Thermal burn Diseases 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 206010048038 Wound infection Diseases 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000004964 aerogel Substances 0.000 description 1
- 210000001367 artery Anatomy 0.000 description 1
- 230000000721 bacterilogical effect Effects 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 230000004663 cell proliferation Effects 0.000 description 1
- 230000007541 cellular toxicity Effects 0.000 description 1
- 210000000589 cicatrix Anatomy 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000003013 cytotoxicity Effects 0.000 description 1
- 231100000135 cytotoxicity Toxicity 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 210000002919 epithelial cell Anatomy 0.000 description 1
- 210000002744 extracellular matrix Anatomy 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 239000003102 growth factor Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 230000000774 hypoallergenic effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000002085 irritant Substances 0.000 description 1
- 231100000021 irritant Toxicity 0.000 description 1
- 230000033001 locomotion Effects 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 239000012567 medical material Substances 0.000 description 1
- 210000004877 mucosa Anatomy 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000010603 pastilles Nutrition 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000012056 semi-solid material Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 231100000370 skin sensitisation Toxicity 0.000 description 1
- 231100000019 skin ulcer Toxicity 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000638 stimulation Effects 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 230000017423 tissue regeneration Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000820 toxicity test Toxicity 0.000 description 1
- 230000000472 traumatic effect Effects 0.000 description 1
- 201000008827 tuberculosis Diseases 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
- 210000003954 umbilical cord Anatomy 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/01—Non-adhesive bandages or dressings
- A61F13/01021—Non-adhesive bandages or dressings characterised by the structure of the dressing
- A61F13/01029—Non-adhesive bandages or dressings characterised by the structure of the dressing made of multiple layers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/00051—Accessories for dressings
- A61F13/00063—Accessories for dressings comprising medicaments or additives, e.g. odor control, PH control, debriding, antimicrobic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/01—Non-adhesive bandages or dressings
- A61F13/01034—Non-adhesive bandages or dressings characterised by a property
- A61F13/01042—Absorbency
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/01—Non-adhesive bandages or dressings
- A61F13/01034—Non-adhesive bandages or dressings characterised by a property
- A61F13/01046—Air-vapor permeability
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/02—Adhesive bandages or dressings
- A61F13/0203—Adhesive bandages or dressings with fluid retention members
- A61F13/0213—Adhesive bandages or dressings with fluid retention members the fluid retention member being a layer of hydrocolloid, gel forming material
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/02—Adhesive bandages or dressings
- A61F13/0203—Adhesive bandages or dressings with fluid retention members
- A61F13/0223—Adhesive bandages or dressings with fluid retention members characterized by parametric properties of the fluid retention layer, e.g. absorbency, wicking capacity, liquid distribution
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/02—Adhesive bandages or dressings
- A61F13/0276—Apparatus or processes for manufacturing adhesive dressings or bandages
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F13/00—Bandages or dressings; Absorbent pads
- A61F13/02—Adhesive bandages or dressings
- A61F13/0276—Apparatus or processes for manufacturing adhesive dressings or bandages
- A61F13/0283—Apparatus or processes for manufacturing adhesive dressings or bandages for making adhesive or cohesive tape or fabrics therefor, e.g. coating or mechanical treatments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
- A61L15/28—Polysaccharides or their derivatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/44—Medicaments
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
- A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
- A61L15/42—Use of materials characterised by their function or physical properties
- A61L15/46—Deodorants or malodour counteractants, e.g. to inhibit the formation of ammonia or bacteria
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/40—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
- A61L2300/418—Agents promoting blood coagulation, blood-clotting agents, embolising agents
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Materials Engineering (AREA)
- Hematology (AREA)
- Manufacturing & Machinery (AREA)
- Dispersion Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Materials For Medical Uses (AREA)
Abstract
The invention relates to a multifunctional wet medical wound dressing and a preparation method thereof. The multifunctional wet medical wound dressing comprises a polyethylene release film layer, a polyurethane thin film layer, a medical pressure-sensitive adhesive layer, a multifunctional hydrogel layer, a release paper layer and a release paper tearing opening formed in the release paper layer, wherein the polyethylene release film layer, the polyurethane thin film layer, the medical pressure-sensitive adhesive layer, the multifunctional hydrogel layer and the release paper layer are sequentially laminated. The invention further provides the preparation method of the multifunctional wet medical wound dressing. By the adoption of the multifunctional wet medical wound dressing and the preparation method thereof, the effects of being water resistible and breathable, achieving hemostasis and bacteriostasis, diminishing inflammation and stopping pains are achieved; a closed moist environment can be kept around the surface of a wound and in a wound surface area, no toxic and side effects exist, the texture is soft and elastic, the mechanical property is good, and great practical value is achieved.
Description
Technical field
The present invention relates to medical applications, particularly medical dressing, specifically refer to a kind of Multifunctional Moisture medical wound dressing and preparation method thereof.
Background technology
Wound repair is the bioprocess that body response skin injury one of showing is complicated, mainly comprises the local inflammation stage of reaction, cell proliferation stage and tissue reconstruction stage.The change of local environment, comprising wound local various cell, extracellular matrix and growth factor etc. must interact, and has great impact to wound healing.Wet wound healing is the theory of scientists through 30 or 40 years Researching and practicing formation, and namely epithelial cell could must grow fast under moistening environment, and wound healing rate when moistening is accelerated.
Moistening healing is the main trend of following trauma care and Wound care, therefore creates moistening healing environment, promotes wound healing, reduces to infect probability, the generation of minimizing cicatrix and reduce and look after the primary condition that cost etc. is an advanced dressing.And the volume production technology of the inner face material of dynamical absorbing material, high bio-compatibility, water-proof antibiotic coating surfacing and advanced person determines the successful key of advanced dressing commercialization.
The development of present dressing is very fast, but does not still have a kind of dressing can reach the requirement of desirable dressing at present.Traditional dressing is as good in cystose dressing absorbability, water vapo(u)r transmission is good, but it can bring secondary damage to wound, and leaves over detritus in wound surface; Film dressing can stop bacteriological infection, provides gas exchange, have the advantages such as good mechanical performance, but the too little and easy hydrops of its moisture-vapor transmission.All have various deficiency, various new material dressing also emerges in an endless stream, and as dressing such as glue, hydrogel, polymeric membrane and artificial skin, it all belongs to the dressing of wet wound healing type.There is the interaction of multiple pattern between dressing and wound, as absorbed sepage and noxious substance, permission gas exchange, and is the desirable environment of healing creation one; Barrier layer structure, to prevent in environment microorganism invasion, and prevention wound cross infection etc. are multi-functional, wherein has more transparent, soft, moisture absorption with aerogel dressing again, breathes freely and to prevent in environment the characteristics such as microorganism invasion.Hydrogel medical dressing is a kind of novel wound dressing that development in recent years is got up, it is the novel biomaterial that a class performance is better than traditional dressing and biological dressing, can promote that wound heals better, alleviate the pain of patient, it can improve the microenvironment of wound surface, the growth of anti-bacteria, has investigation and application widely at biomedical engineering field.
Desirable medical dressing except to protect wound by secondary damage, provide benefit wound healing moist environment, prevent excessively scattering and disappearing of moisture and body fluid, also should possess and protect from infection and the performance such as acceleration of tissue repair process.But the level of present medical dressing does not also reach above-mentioned level far away.
Summary of the invention
The object of the invention is to overcome shortcoming of the prior art, Multifunctional Moisture wound dressing that a kind of waterproof and breathable, hemostatic bacteriostatic, anti-inflammatory analgetic are provided and preparation method thereof.
To achieve these goals, first aspect present invention provides the dressing of a kind of Multifunctional Moisture medical wound, it is characterized in that, comprise the polyethylene release film layer, thin polyurethane rete, medical pressure-sensing glue-line, multifunctional water gel layer, the off-style paper layer that stack gradually, and be located at the release paper tearing notch on described off-style paper layer.Wherein polyethylene release film layer and thin polyurethane rete are combined into PU layer.
Preferably, described multifunctional water gel layer comprises the composition of following mass percent:
Glycerol 15-25%;
Polyethylene Glycol 5-15%;
Polyvinylpyrrolidone 2-8%;
Hemostatic bacteriostatic agent 5-15%;
Deionized water 40-70%.
More preferably, described hemostatic bacteriostatic agent is water-soluble chitosan.
Preferably, the thickness of described multifunctional water gel layer is between 0.2-0.4mm.
Preferably, the preparation method of described multifunctional water gel layer comprises the following steps:
Step (1): be dissolved in by glycerol in distilled water and be configured to the first solution, is dissolved in polyvinylpyrrolidone in distilled water and is configured to the second solution, hemostatic bacteriostatic agent is dissolved in distilled water and is configured to the 3rd solution;
Step (2): by the first described solution, the second described solution, the 3rd described solution mixing, add Polyethylene Glycol, be placed in autoclave sterilizer heating and obtain the 4th solution;
Step (3): medical thermoplastic polyurethane (TPU) film is laid on the irradiation plate of covering one deck preservative film, the 4th described solution is painted on after in TPU membrane, adopt electron beam irradiation, obtain the rete after irradiation;
Step (4): freezingly under described rete being placed in-5 DEG C to 5 DEG C conditions be placed on 15-35 DEG C of environment, is cycled to repeat repeatedly, obtains described multifunctional water gel layer.
Preferably, described multifunctional water gel layer comprises the composition of following mass percent:
Glycerol 18-25%, is more preferably 20-23%;
Polyethylene Glycol 8-15%, is more preferably 10-12%;
Polyvinylpyrrolidone 5-8%;
Hemostatic bacteriostatic agent 5-10%, is more preferably 6-8%;
Deionized water 40-70%, is more preferably 50-60%.
Second aspect present invention provides a kind of preparation method according to the dressing of above-mentioned Multifunctional Moisture medical wound, it is characterized in that, comprises the following steps:
Step (1): polyethylene release film layer, thin polyurethane rete, medical pressure-sensing glue-line are stacked gradually the PU film of laminating formation with medical pressure-sensing glue-line;
Step (2): fitted by the medical pressure-sensing glue layer of the upper surface of multifunctional water gel layer and described PU film, fits described multifunctional water gel layer lower surface and the off-style paper layer be provided with from paper mold tearing notch, obtains semi-finished product of fitting;
Step (3): described laminating semi-finished product are cut into sheet-like hydrous gel according to setting specification, obtains Multifunctional Moisture wound dressing semi-finished product;
Step (4): by sterilizing after described semi finished package, obtains described Multifunctional Moisture wound dressing.
Adopt Multifunctional Moisture medical wound of the present invention dressing and preparation method thereof, its waterproof and breathable, hemostatic bacteriostatic, anti-inflammatory analgetic, extremely have use value, and it can make around wound surface and wound surface district keeps closed moist environment, without any side effects; Quality softness is flexible, good mechanical property; Have very strong liquid-absorbent, 2 times of transudates of Absorbable rod own vol, namely move back sticky after imbibition, effectively prevent the wound again of wound tissue; There is splendid ductility, good with tissue attaching property, be specially adapted to the crooked position of the activities such as joint, make wound tissue produce constant moisture and happy curative effect, significantly reduce pain; Hemostatic bacteriostatic, prevents bacterial micro-organism from invading, prevention infection, for wound surface structure provides a good reparation platform, can effectively promote wound tissue quickly-healing.Its preparation method, technique is simple, is easy to industrialization, is applicable to the quick procedure for producing of continuous industryization, can effectively reduces costs, and improves yield.
Accompanying drawing explanation
Fig. 1 and Fig. 2 is the structure of the Multifunctional Moisture medical wound dressing in the embodiment of the present invention.
Detailed description of the invention
In order to more clearly understand technology contents of the present invention, below specific embodiment of the invention method is described further.
As depicted in figs. 1 and 2; Multifunctional Moisture wound dressing of the present invention; the multifunctional water gel comprised as main body applies core 4; the upper surface that described multifunctional water gel applies core 4 is pasted with the transparent plastic protecting film (i.e. polyethylene 1/ polyurethane 2 composite membrane) that one deck scribbles medical pressure-sensitive adhesive 3, and the lower surface stickup that described multifunctional water gel applies core 4 is provided with the release paper protective layer 5 facilitating tearing notch 6.
Hydrogel applies core (multifunctional water gel layer), utilize the hydrophilic group in hydrogel structure to absorb wound exudate and evacuation of pus, form the semi-solid material of similar gels, be attached to wound base portion, prevent wound dehydrates, provide and maintain the moist environment of wound healing; Utilize its viscosity to form the healing environment of wound surface enclosed, prevent bacterial micro-organism from invading, prevention infection.Hydrogel layer is water white transparency, is convenient to the recovery situation observing wound surface like this.
Glycerol has hygroscopicity, and therefore obtained multifunctional water gel has very strong liquid-absorbent.Polyethylene Glycol has antibacterial, plasticization, has excellent moisture retention, dispersibility, lubricity, bonding agent and softening agent etc., and for U.S. FDA approval medical material.By changing the material proportion of glycerol and Polyethylene Glycol, solving mechanical property and the absorbent of hydrogel, maintaining the moist environment of wound surface, effectively prevent the damage again of wound tissue, be conducive to wound surface quickly-healing.Polyvinylpyrrolidone is a kind of synthesizing water-solubility macromolecular compound, has the general aspects of water-soluble high-molecular compound, colloid protective effect, film property, caking property, hygroscopicity, solubilising or cohesion.Polyvinylpyrrolidone is both water-soluble, is dissolved in majority of organic solvent again, has excellent physiological inertia and biocompatibility, and toxicity is very low, does not produce any stimulation to skin, mucosa, eye etc.By changing its content in multifunctional water gel, the film property of controlled controlling the water circulation gel and viscosity.Deionized water, for regulating concentration during each component cross-link, also can regulate the moist of hydrogel in addition.Hemostatic bacteriostatic agent as chitosan, then makes hydrogel layer have hemostasis, antiinflammatory, sterilizing, promotion wound healing, absorb the effect such as Wound exudate, not easily syneresis, can also figuration, and hydrogel layer can be made to form moist g., jelly-like material.
Embodiment 1
Step (1): glycerol is dissolved in appropriate distilled water, is made into solution A; Polyvinylpyrrolidone is dissolved in appropriate distilled water, joins to obtain B solution; Chitosan is dissolved in appropriate distilled water, joins to obtain C solution.
Step (2): above-mentioned three kinds of solution are pressed different proportion mixing, then add a certain amount of PEG400, shake up, is then placed in the solution D that autoclave sterilizer 125 DEG C heating 2h obtains mix homogeneously.
Step (3): TPU membrane be laid on the irradiation plate of covering one deck preservative film, uses brush a certain amount of solution D to be painted in TPU membrane.
Step (4): adopt electron beam irradiation, beam energy is 10MeV, and electric current is 8.5mA, and device transmission speed is 3m/min, and irradiation dose is 42kGy.
Step (5): put into-20 DEG C of refrigerator freezings after irradiation terminates 4 hours, to be then placed at room temperature 25 DEG C 2 hours, to be cycled to repeat 2 times, to obtain the hydrogel layer of thickness 0.4mm.The multifunctional water gel prepared is placed in 4 DEG C of Refrigerator stores.Hydrogel layer specification is 5cm × 5cm, and the percentage by weight composition of each component of hydrogel layer sees the following form 1.
Step (6): the transparent plastic protecting film (i.e. polyethylene/polyurethane composite membrane) scribbling medical pressure-sensitive adhesive on hydrogel layer upper surface is pasted; the release paper protective layer facilitating tearing notch is provided with on hydrogel layer lower surface is pasted; after gamma-ray irradiation sterilizing, obtain Multifunctional Moisture wound dressing.
Embodiment 2:
Step (1): glycerol is dissolved in appropriate distilled water, is made into solution A; Polyvinylpyrrolidone is dissolved in appropriate distilled water, joins to obtain B solution; Chitosan is dissolved in appropriate distilled water, joins to obtain C solution.
Step (2): above-mentioned three kinds of solution are pressed different proportion mixing, then add a certain amount of PEG400, shake up, is then placed in the solution D that autoclave sterilizer 120 DEG C heating 3h obtains mix homogeneously.
Step (3): TPU membrane be laid on the irradiation plate of covering one deck preservative film, uses brush a certain amount of solution D to be painted in TPU membrane.
Step (4): adopt electron beam irradiation, beam energy is 10MeV, and electric current is 8.5mA, and device transmission speed is 3m/min, and irradiation dose is 38kGy.
Step (5): put into-10 DEG C of refrigerator freezings after irradiation terminates 2 hours, to be then placed at room temperature 25 DEG C 2 hours, to be cycled to repeat 2 times, to obtain the hydrogel layer of thickness 0.3mm.The multifunctional water gel prepared is placed in 4 DEG C of Refrigerator stores.Hydrogel layer specification is 5cm × 14cm, and the percentage by weight composition of each component of hydrogel layer sees the following form 1.
Step (6): the transparent plastic protecting film (i.e. polyethylene/polyurethane composite membrane) scribbling medical pressure-sensitive adhesive on hydrogel layer upper surface is pasted; the release paper protective layer facilitating tearing notch is provided with on hydrogel layer lower surface is pasted; after gamma-ray irradiation sterilizing, obtain Multifunctional Moisture wound dressing.
Embodiment 3:
Step (1): glycerol is dissolved in appropriate distilled water, is made into solution A; Polyvinylpyrrolidone is dissolved in appropriate distilled water, joins to obtain B solution; Chitosan is dissolved in appropriate distilled water, joins to obtain C solution.
Step (2): above-mentioned three kinds of solution are pressed different proportion mixing, then add a certain amount of PEG400, shake up, is then placed in the solution D that autoclave sterilizer 130 DEG C heating 1.5h obtains mix homogeneously.
Step (3): TPU membrane be laid on the irradiation plate of covering one deck preservative film, uses brush a certain amount of solution D to be painted in TPU membrane.
Step (4): adopt electron beam irradiation, beam energy is 10MeV, and electric current is 8.5mA, and device transmission speed is 3m/min, and irradiation dose is 30kGy.
Step (5): put into-15 DEG C of refrigerator freezings after irradiation terminates 3 hours, to be then placed at room temperature 25 DEG C 2 hours, to be cycled to repeat 2 times, to obtain the hydrogel layer of thickness 0.35mm.The multifunctional water gel prepared is placed in 4 DEG C of Refrigerator stores.Hydrogel layer specification is 10cm × 10cm, and the percentage by weight composition of each component of hydrogel layer sees the following form 1.
Step (6): the transparent plastic protecting film (i.e. polyethylene/polyurethane composite membrane) scribbling medical pressure-sensitive adhesive on hydrogel layer upper surface is pasted; the release paper protective layer facilitating tearing notch is provided with on hydrogel layer lower surface is pasted; after gamma-ray irradiation sterilizing, obtain Multifunctional Moisture wound dressing.
Embodiment 4:
Step (1): glycerol is dissolved in appropriate distilled water, is made into solution A; Polyvinylpyrrolidone is dissolved in appropriate distilled water, joins to obtain B solution; Chitosan is dissolved in appropriate distilled water, joins to obtain C solution.
Step (2): above-mentioned three kinds of solution are pressed different proportion mixing, then add a certain amount of PEG400, shake up, is then placed in the solution D that autoclave sterilizer 125 DEG C heating 2h obtains mix homogeneously.
Step (3): TPU membrane be laid on the irradiation plate of covering one deck preservative film, uses brush a certain amount of solution D to be painted in TPU membrane.
Step (4): adopt electron beam irradiation, beam energy is 10MeV, and electric current is 8.5mA, and device transmission speed is 3m/min, and irradiation dose is 35kGy.
Step (5): put into-20 DEG C of refrigerator freezings after irradiation terminates 4 hours, to be then placed at room temperature 25 DEG C 2 hours, to be cycled to repeat 2 times, to obtain the hydrogel layer of thickness 0.4mm.The multifunctional water gel prepared is placed in 4 DEG C of Refrigerator stores.Hydrogel layer specification is 10cm × 20cm, and the percentage by weight composition of each component of hydrogel layer sees the following form 1.
Step (6): the transparent plastic protecting film (i.e. polyethylene/polyurethane composite membrane) scribbling medical pressure-sensitive adhesive on hydrogel layer upper surface is pasted; the release paper protective layer facilitating tearing notch is provided with on hydrogel layer lower surface is pasted; after gamma-ray irradiation sterilizing, obtain Multifunctional Moisture wound dressing.
The percentage by weight composition of each component of table 1 hydrogel layer:
The present invention is disposable sterile product, will notice that product list packaging is necessary for the unabroken state of sealing, if there is breakage not use before using.The Multifunctional Moisture wound dressing of dimension is selected according to wound surface size; tear along packaging bag opening and take out this product; release paper is opened along tearing notch; hydrogel face is affixed on cleaned wound location; guarantee that dressing covers wound completely; press gently, then remove outer transparent plastic protecting film.Can combinationally use with sterile gauze or binder, also can as required fixation adhesive tape be cut into corresponding size with the use of.Use in time behind Kaifeng, do not reuse.The present invention is applicable to otch or the wound surface such as skin trauma, skin ulcer (comprising decubital ulcer, tuberculosis, mycete, fungal infection etc.), I degree or shallow II degree burn wound, scald, incised wound, various surgical operation and plastic operation; also be applicable to indwelling artery and vein conduit and stick use, and infant umbilical cord protecting wound surface etc.
The change of dressing time is how many and determine according to wound fluid, when sepage is more, according to circumstances change in time or replacing in 1 ~ 2 hour once; When sepage is less or nothing is oozed out, within 2-3 days, change once, until healing.If patient is exposed to wound surface in the environment of especially dry or high temperature, the present invention includes the depletion rate of effective ingredient can than faster under room temperature.
Points for attention:
1. normal saline or iodine tincture Sterile surgery or traumatic surface and surrounding skin should be used if desired before use, in case infect.
2. the present invention is sterile product, can only single use, packages in damaged condition or exceed useful life, prohibits the use.3. use and appropriate to the occasionly exceed wound surface edge 0.5cm, to guarantee that multifunctional water gel can flap coverage completely.Sealing is singly packed and is just lost aseptic immediately once opening, therefore needs to use as soon as possible in time.
4. sticky by automatically moving back after dressing absorbs transudate, should change in time, to maintain the environment that wound effectively heals.
5. the present invention is hypoallergenic product, generally there will not be allergic phenomena.As there is allergic phenomena or uncomfortable reaction, should doctor be submitted in time to dispose.
6. the present invention is sterile product, should aseptically use.
Product standard and the method for inspection:
This standard specifies Multifunctional Moisture wound dressing of the present invention, forms, not pastille by scribbling the polyurethane/polyethylene composite film (be called for short PU film) of medical pressure-sensitive adhesive, multifunctional water gel and release paper.
1, outward appearance
With visual observations and touch inspection.Multifunctional Moisture wound dressing and single packaging bag surface should smooth, free from smutting during, without damaged, hydrogel layer should be coated with uniform ground, without starved phenomenon.Colloid part answers water white transparency, and PU film, hydrogel layer, release paper must not have break-off.
2, size
With general gage measuring.Size conforms design code of the present invention, given size ± the 2mm margin of tolerance in.
3, viscosity is held
According in Appendix B in YY/T0148-2006 the B.2 chapter test time, duration of test in baking oven, the top being affixed on adhesive film on corrosion resistant plate glides and should be no more than 2.5mm.
4, breathability
Test according to " water vapo(u)r transmission test method " regulation in appendix C in YY/T0148-2006, the vapor permeation of every 24h is no less than 500g/ (m224h).
5, water absorption
Test according to part 1 " water absorption test method " regulation of contact Wound dressing test method in YY/T0471.1-2004, the average magnitude being affixed on the dressing absorbing fluid in 30 minutes on wound surface is not less than 11.5g/100cm2.
Note: tested sample dressing is as the criterion with effective area, and its backed film need not be peeled off, removes thicker mould release membrance and edge adjuvant.
6, content of beary metal
Content of beary metal is tested according to 5.6.1 in GB/T14233.1-2008 " heavy metal total content method one " regulation, and content of beary metal is less than 10 μ g/g.
Test liquid preparation method in content of beary metal: sample thief is 1:30 by example weight (g) and water (ml) ratio, under 37 DEG C ± 1 DEG C condition, lixiviate 24h, by sample and fluid separation applications (filtration), be chilled to room temperature, as test liquid.Get consubstantiality hydrops and be placed in glass container, with legal system for blank liquid.
7, comfortableness
When testing according to YY/T0471.4-2004, extensibility is not more than 14Ncm-1, and permanent deformation is not more than 5%.
8, heat resistant test
Get product of the present invention, removing release paper and protecting film, be placed in 60 DEG C of calorstats and heat 0.5h, and take out and put to room temperature gel-free trickling phenomenon, hydrogel layer hands touches toughness.
9, low temperature resistant test
Get product of the present invention, removing release paper and protecting film, be placed in 0 DEG C of refrigerator and place 24h, takes out and observe hydrogel layer without icing phenomenon.
10, water preventing ability
Get product of the present invention, removing release paper and protecting film, according to YY/T0471.3-2004 contact Wound dressing test method the 3rd part: the regulation of water preventing ability is tested, and its water preventing ability meets the requirement of standard YY/T0471.3-2004 defined.
11, bacterium property is hindered
Get product of the present invention, removing release paper and protecting film, according to YY/T0471.5-2004 contact Wound dressing test method the 5th part: the regulation of resistance bacterium property is tested, under semi-humid state, there is resistance bacterium property.
12, the detection of biological property
12.1 sterility tests
Carry out according to 3 " sterility test " method regulation in GB/T14233.2-2005, product is aseptic.
12.2 cell toxicity tests
Carry out according to 8.2 " lixiviating solution test " method regulation in GB/T16886.5-2003, cytotoxicity is not more than I level.
12.3 Skin Irritation Test
Carry out according to 6.3 " animal skin irritant test " method regulation in GB/T16886.10-2005, it is 0 that test specimen and solvent control are on average scored, namely without skin wound repair.
12.4 Skin sensitization
Carry out according to 7.4 " test of delayed hypersensitivity maximal dose " method regulation in GB/T16886.10-2005, level of reaction is 0, namely without delayed hypersensitivity.
The embodiment of the present invention is compared with similar products and preparation method thereof at present from the foregoing, has the following advantages:
(1) glycerol, Polyethylene Glycol, hemostatic bacteriostatic agent, deionized water and polyvinylpyrrolidone are cross-linked, independent innovational design molecular structure, develops the Multifunctional Moisture wound dressing obtained and has excellent physical and chemical performance and good biocompatibility;
(2) the PU thin film of multifunctional water gel and waterproof and breathable is arranged in pairs or groups be made into medical wound dressing, easy-to-use, the moist environment that is closed is provided simultaneously, effectively forms the environment of antibacterial resistance bacterium, avoid wound infection;
(3) by adding hemostatic bacteriostatic agent etc., comparatively like product has better hemostatic bacteriostatic, anti-inflammatory analgesic effect;
(4) the Multifunctional Moisture wound dressing obtained by the present invention has stronger liquid-absorbent, and its Liquid Absorption rate can reach the gel-like of having gone on the market and to apply ointment or plaster more than 6 times of product, makes wound healing acceleration in moist environment, shortens wound healing time;
(5) the Multifunctional Moisture wound dressing obtained by the present invention has splendid elasticity, ductility and conformable, is specially adapted to the crooked position that joint etc. is movable, does not affect body movement;
(6) be easy to industrialization production rolling, can be applicable to the quick procedure for producing of wound dressing, substantially increase prouctiveness.
Adopt Multifunctional Moisture medical wound of the present invention dressing and preparation method thereof, its waterproof and breathable, hemostatic bacteriostatic, anti-inflammatory analgetic, extremely have use value, and it can make around wound surface and wound surface district keeps closed moist environment, without any side effects; Quality softness is flexible, good mechanical property; Have very strong liquid-absorbent, 2 times of transudates of Absorbable rod own vol, namely move back sticky after imbibition, effectively prevent the wound again of wound tissue; There is splendid ductility, good with tissue attaching property, be specially adapted to the crooked position of the activities such as joint, make wound tissue produce constant moisture and happy curative effect, significantly reduce pain; Hemostatic bacteriostatic, prevents bacterial micro-organism from invading, prevention infection, for wound surface structure provides a good reparation platform, can effectively promote wound tissue quickly-healing.Its preparation method, technique is simple, is easy to industrialization, is applicable to the quick procedure for producing of continuous industryization, can effectively reduces costs, and improves yield.
In this description, the present invention is described with reference to its specific embodiment.But, still can make various amendment and conversion obviously and not deviate from the spirit and scope of the present invention.Therefore, description is regarded in an illustrative, rather than a restrictive.
Claims (7)
1. Multifunctional Moisture medical wound dressing, it is characterized in that, comprise the polyethylene release film layer, thin polyurethane rete, medical pressure-sensing glue-line, multifunctional water gel layer, the off-style paper layer that stack gradually, and be located at the release paper tearing notch on described off-style paper layer.
2. Multifunctional Moisture medical wound according to claim 1 dressing, is characterized in that, described multifunctional water gel layer comprises the composition of following mass percent:
Glycerol 15-25%;
Polyethylene Glycol 5-15%;
Polyvinylpyrrolidone 2-8%;
Hemostatic bacteriostatic agent 5-15%;
Deionized water 40-70%.
3. Multifunctional Moisture medical wound according to claim 2 dressing, is characterized in that, described hemostatic bacteriostatic agent is water-soluble chitosan.
4. Multifunctional Moisture medical wound according to claim 1 and 2 dressing, is characterized in that, the thickness of described multifunctional water gel layer is between 0.2-0.4mm.
5. Multifunctional Moisture medical wound according to claim 2 dressing, is characterized in that, the preparation method of described multifunctional water gel layer comprises the following steps:
Step (1): be dissolved in by glycerol in distilled water and be configured to the first solution, is dissolved in polyvinylpyrrolidone in distilled water and is configured to the second solution, hemostatic bacteriostatic agent is dissolved in distilled water and is configured to the 3rd solution;
Step (2): by the first described solution, the second described solution, the 3rd described solution mixing, add Polyethylene Glycol, be placed in autoclave sterilizer heating and obtain the 4th solution;
Step (3): be painted on after in TPU membrane by the 4th described solution, adopts electron beam irradiation, obtains the rete after irradiation;
Step (4): freezingly under described rete being placed in-5 DEG C to 5 DEG C conditions be placed on 15-35 DEG C of environment, is cycled to repeat repeatedly, obtains described multifunctional water gel layer.
6. Multifunctional Moisture medical wound according to claim 2 dressing, is characterized in that, described multifunctional water gel layer comprises the composition of following mass percent:
Glycerol 18-25%;
Polyethylene Glycol 8-15%;
Polyvinylpyrrolidone 5-8%;
Hemostatic bacteriostatic agent 5-10%;
Deionized water 40-70%.
7. a preparation method for Multifunctional Moisture medical wound according to claim 1 dressing, is characterized in that, comprise the following steps:
Step (1): polyethylene release film layer, thin polyurethane rete, medical pressure-sensing glue-line are stacked gradually the PU film of laminating formation with medical pressure-sensing glue-line;
Step (2): fitted by the medical pressure-sensing glue layer of the upper surface of multifunctional water gel layer and described PU film, fits described multifunctional water gel layer lower surface and the off-style paper layer be provided with from paper mold tearing notch, obtains semi-finished product of fitting;
Step (3): described laminating semi-finished product are cut into sheet-like hydrous gel according to setting specification, obtains Multifunctional Moisture wound dressing semi-finished product;
Step (4): by sterilizing after described semi finished package, obtains described Multifunctional Moisture wound dressing.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510500878.6A CN105078651A (en) | 2015-08-14 | 2015-08-14 | Multifunctional wet medical wound dressing and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201510500878.6A CN105078651A (en) | 2015-08-14 | 2015-08-14 | Multifunctional wet medical wound dressing and preparation method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN105078651A true CN105078651A (en) | 2015-11-25 |
Family
ID=54560601
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201510500878.6A Pending CN105078651A (en) | 2015-08-14 | 2015-08-14 | Multifunctional wet medical wound dressing and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN105078651A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108705838A (en) * | 2018-05-29 | 2018-10-26 | 中新科技集团股份有限公司 | A kind of preparation method of laminated film |
CN108742750A (en) * | 2018-06-21 | 2018-11-06 | 广州迈普再生医学科技股份有限公司 | It organizes plugging material and preparation method thereof and blocks product |
CN111134957A (en) * | 2020-01-07 | 2020-05-12 | 苏州汇涵医用科技发展有限公司 | Hydrogel wound dressing and preparation method thereof |
CN112206093A (en) * | 2019-07-10 | 2021-01-12 | 广西美丽肤医疗器械有限公司 | Waterproof breathable wet dressing |
CN112494211A (en) * | 2016-08-29 | 2021-03-16 | 唐山市博世德医疗器械有限公司 | Silica gel dressing, multifunctional silica gel negative pressure drainage device and preparation method thereof |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN202844321U (en) * | 2012-10-31 | 2013-04-03 | 上海华舟压敏胶制品有限公司 | Visible polyurethane retention needle stick |
CN203829153U (en) * | 2014-02-28 | 2014-09-17 | 人福医药集团医疗用品有限公司 | Self-adhesion type medical wound dressing |
CN204072475U (en) * | 2014-08-12 | 2015-01-07 | 上海典范医疗科技有限公司 | A kind of composite aquogel wound dressing |
CN204306964U (en) * | 2014-11-03 | 2015-05-06 | 黄箭林 | A kind of waterproof ventilating type cesarean waterproof is applied ointment or plaster |
CN204319351U (en) * | 2014-12-11 | 2015-05-13 | 南阳市汇博生物技术有限公司 | A kind of medical composite aquogel dressing |
-
2015
- 2015-08-14 CN CN201510500878.6A patent/CN105078651A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN202844321U (en) * | 2012-10-31 | 2013-04-03 | 上海华舟压敏胶制品有限公司 | Visible polyurethane retention needle stick |
CN203829153U (en) * | 2014-02-28 | 2014-09-17 | 人福医药集团医疗用品有限公司 | Self-adhesion type medical wound dressing |
CN204072475U (en) * | 2014-08-12 | 2015-01-07 | 上海典范医疗科技有限公司 | A kind of composite aquogel wound dressing |
CN204306964U (en) * | 2014-11-03 | 2015-05-06 | 黄箭林 | A kind of waterproof ventilating type cesarean waterproof is applied ointment or plaster |
CN204319351U (en) * | 2014-12-11 | 2015-05-13 | 南阳市汇博生物技术有限公司 | A kind of medical composite aquogel dressing |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112494211A (en) * | 2016-08-29 | 2021-03-16 | 唐山市博世德医疗器械有限公司 | Silica gel dressing, multifunctional silica gel negative pressure drainage device and preparation method thereof |
CN108705838A (en) * | 2018-05-29 | 2018-10-26 | 中新科技集团股份有限公司 | A kind of preparation method of laminated film |
CN108742750A (en) * | 2018-06-21 | 2018-11-06 | 广州迈普再生医学科技股份有限公司 | It organizes plugging material and preparation method thereof and blocks product |
CN108742750B (en) * | 2018-06-21 | 2020-09-22 | 广州迈普再生医学科技股份有限公司 | Tissue plugging material, preparation method thereof and plugging product |
CN112206093A (en) * | 2019-07-10 | 2021-01-12 | 广西美丽肤医疗器械有限公司 | Waterproof breathable wet dressing |
CN111134957A (en) * | 2020-01-07 | 2020-05-12 | 苏州汇涵医用科技发展有限公司 | Hydrogel wound dressing and preparation method thereof |
CN111134957B (en) * | 2020-01-07 | 2022-01-14 | 苏州汇涵医用科技发展有限公司 | Hydrogel wound dressing and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN105078651A (en) | Multifunctional wet medical wound dressing and preparation method thereof | |
Corkhill et al. | Synthetic hydrogels VI. Hydrogel composites as wound dressings and implant materials | |
Zhou et al. | Rational design of intelligent and multifunctional dressing to promote acute/chronic wound healing | |
CN102625677B (en) | Alleviate method and the product of tissue injury with water imbibition stress distribution material | |
CN101249274B (en) | Preparation of bletilla striata polyose water gelatin of promoting wound healing and uses thereof | |
WO2009107189A1 (en) | Wound-covering hydrogel material | |
Chopra et al. | Strategies and therapies for wound healing: a review | |
JPH10505769A (en) | Spirosorbent bandage for exudate treatment | |
CN110507845A (en) | Biological composite ventilating dressing and preparation method thereof | |
CN103394116A (en) | Hydrogel dressing capable of promoting wound healing and preparation method thereof | |
KR101763368B1 (en) | Silicon adhesvie compositoin with hyaluronic acid for moisturizing skin | |
CN208448217U (en) | A kind of anti-bacterial hydrogel dressing | |
CN105086318B (en) | A kind of antibacterial transparent dressing and its preparation method and application | |
CN106139239A (en) | Full-service fluid dressing and preparation method thereof | |
CN106963973B (en) | A kind of chitosan combine dressing and preparation method thereof | |
CN106267316B (en) | Anti- dehydration gecko hydrogel application of one kind and preparation method thereof | |
Burd | Evaluating the use of hydrogel sheet dressings in comprehensive burn wound care | |
CN111407919B (en) | Chitosan quaternary ammonium salt sterilization gauze and preparation method thereof | |
AU649475B2 (en) | Bilayer wound dressing | |
CN204971863U (en) | Moist dressing of aquogel | |
CN101147744A (en) | Chitin water soluble aerosol and wound applied block composite medicine | |
CN110916900A (en) | Hydrogel medical dressing and preparation method thereof | |
CN112957519A (en) | Composition for preparing hydrogel for promoting wound healing, hydrogel and preparation method thereof | |
RU2312658C1 (en) | Film-forming aerosol for wound protection in treatment and method for its using | |
JPH0751139B2 (en) | Wound dressing |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20151125 |
|
WD01 | Invention patent application deemed withdrawn after publication |