CN108721679B - Anti-inflammatory and antibacterial medical dressing - Google Patents
Anti-inflammatory and antibacterial medical dressing Download PDFInfo
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- CN108721679B CN108721679B CN201810741349.9A CN201810741349A CN108721679B CN 108721679 B CN108721679 B CN 108721679B CN 201810741349 A CN201810741349 A CN 201810741349A CN 108721679 B CN108721679 B CN 108721679B
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- 230000003110 anti-inflammatory effect Effects 0.000 title claims abstract description 25
- 230000000844 anti-bacterial effect Effects 0.000 title abstract description 23
- 239000000835 fiber Substances 0.000 claims abstract description 123
- 229940111630 tea tree oil Drugs 0.000 claims abstract description 42
- 239000010677 tea tree oil Substances 0.000 claims abstract description 42
- 239000002502 liposome Substances 0.000 claims abstract description 32
- 244000025254 Cannabis sativa Species 0.000 claims abstract description 21
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 claims abstract description 21
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 claims abstract description 21
- 229920001661 Chitosan Polymers 0.000 claims abstract description 21
- 229920000297 Rayon Polymers 0.000 claims abstract description 21
- 235000009120 camo Nutrition 0.000 claims abstract description 21
- 235000005607 chanvre indien Nutrition 0.000 claims abstract description 21
- 239000011487 hemp Substances 0.000 claims abstract description 21
- 238000005470 impregnation Methods 0.000 claims abstract description 19
- 239000002131 composite material Substances 0.000 claims abstract description 14
- 238000013329 compounding Methods 0.000 claims abstract description 13
- 239000007788 liquid Substances 0.000 claims abstract description 10
- 238000002360 preparation method Methods 0.000 claims abstract description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 33
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 20
- 239000000243 solution Substances 0.000 claims description 18
- 238000005303 weighing Methods 0.000 claims description 18
- 239000012528 membrane Substances 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- 238000005520 cutting process Methods 0.000 claims description 12
- 150000002632 lipids Chemical class 0.000 claims description 12
- 238000005507 spraying Methods 0.000 claims description 12
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 claims description 10
- 235000012000 cholesterol Nutrition 0.000 claims description 10
- NRHMKIHPTBHXPF-TUJRSCDTSA-M sodium cholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 NRHMKIHPTBHXPF-TUJRSCDTSA-M 0.000 claims description 10
- 229940083466 soybean lecithin Drugs 0.000 claims description 10
- 229920000742 Cotton Polymers 0.000 claims description 9
- 238000009960 carding Methods 0.000 claims description 9
- 239000005662 Paraffin oil Substances 0.000 claims description 6
- 230000003385 bacteriostatic effect Effects 0.000 claims description 6
- 210000000795 conjunctiva Anatomy 0.000 claims description 6
- 238000010828 elution Methods 0.000 claims description 6
- 238000001914 filtration Methods 0.000 claims description 6
- 238000006703 hydration reaction Methods 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 239000011259 mixed solution Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 6
- 238000004806 packaging method and process Methods 0.000 claims description 6
- 238000003825 pressing Methods 0.000 claims description 6
- 238000002390 rotary evaporation Methods 0.000 claims description 6
- 238000003892 spreading Methods 0.000 claims description 6
- 230000007480 spreading Effects 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- 239000008363 phosphate buffer Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 10
- 238000010521 absorption reaction Methods 0.000 abstract description 7
- 230000035699 permeability Effects 0.000 abstract description 7
- 230000000694 effects Effects 0.000 abstract description 5
- 239000002994 raw material Substances 0.000 abstract description 4
- 206010020112 Hirsutism Diseases 0.000 abstract description 3
- 229940127554 medical product Drugs 0.000 abstract description 3
- 230000003115 biocidal effect Effects 0.000 abstract description 2
- 238000007731 hot pressing Methods 0.000 abstract description 2
- 230000002787 reinforcement Effects 0.000 abstract description 2
- 206010052428 Wound Diseases 0.000 description 31
- 208000027418 Wounds and injury Diseases 0.000 description 31
- 210000000416 exudates and transudate Anatomy 0.000 description 13
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 10
- 239000003242 anti bacterial agent Substances 0.000 description 8
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 5
- 239000007853 buffer solution Substances 0.000 description 5
- 230000029663 wound healing Effects 0.000 description 5
- 230000009286 beneficial effect Effects 0.000 description 4
- 230000002980 postoperative effect Effects 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 230000007794 irritation Effects 0.000 description 3
- 238000002791 soaking Methods 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 206010048038 Wound infection Diseases 0.000 description 2
- 229940088710 antibiotic agent Drugs 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000000857 drug effect Effects 0.000 description 2
- 230000002439 hemostatic effect Effects 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 230000037314 wound repair Effects 0.000 description 2
- 208000035143 Bacterial infection Diseases 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 208000022362 bacterial infectious disease Diseases 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 230000009545 invasion Effects 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 210000004877 mucosa Anatomy 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
-
- 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
- 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
- A61F13/02—Adhesive bandages or dressings
- A61F13/0276—Apparatus or processes for manufacturing adhesive dressings or bandages
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- 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
- A61L15/20—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing organic materials
-
- 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
- A61L15/40—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing ingredients of undetermined constitution or reaction products thereof, e.g. plant or animal extracts
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- A—HUMAN NECESSITIES
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- 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
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- 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
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- 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
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- 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
- A61L2300/20—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing organic materials
- A61L2300/30—Compounds of undetermined constitution extracted from natural sources, e.g. Aloe Vera
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- 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
- A61L2300/404—Biocides, antimicrobial agents, antiseptic agents
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- A—HUMAN NECESSITIES
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- 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
- A61L2300/41—Anti-inflammatory agents, e.g. NSAIDs
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- 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
- A61L2300/60—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a special physical form
- A61L2300/602—Type of release, e.g. controlled, sustained, slow
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
- A61L2300/60—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a special physical form
- A61L2300/62—Encapsulated active agents, e.g. emulsified droplets
- A61L2300/626—Liposomes, micelles, vesicles
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- Health & Medical Sciences (AREA)
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- Heart & Thoracic Surgery (AREA)
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Abstract
The invention relates to an anti-inflammatory and antibacterial medical dressing, and belongs to the field of dressing preparation. The method comprises the steps of preparing tea tree oil liposome and chitosan solution to obtain impregnation liquid, carrying out spunlace reinforcement on hemp and viscose composite fibers, immersing the hemp and viscose composite fibers into the impregnation liquid for ultrasonic loading, and carrying out hot pressing to obtain the anti-inflammatory and antibacterial medical dressing, wherein the problems of strong volatility and poor stability of the tea tree oil liposome are solved, the liposome has a slow release effect and can prolong the effective duration of antibiosis and antiphlogosis, the chitosan has better biocompatibility due to compounding, the fiber dressing prepared by the spunlace method has the advantages of softness, sanitation, air permeability, moisture absorption and no hairiness, and the medical dressing prepared by compounding integrates the advantages of various raw materials, so that the dressing is a comfortable and effective medical product.
Description
Technical Field
The invention relates to an anti-inflammatory and bacteriostatic medical dressing, and belongs to the field of dressing preparation.
Background
The skin is the largest organ of the human body, has the important functions of resisting external microorganism invasion, excreting, preventing water evaporation, adjusting body temperature, maintaining the stability of the internal environment of the body and the like, and various scholars are trying to actively promote wound repair and healing through various methods. The medical dressing is used as a covering of a wound, can replace damaged skin to play a role of temporary barrier in the process of wound healing, avoids or controls wound infection, and provides an environment beneficial to wound healing.
The dressing which is most clinically used at present is mainly made of gauze, cotton pads and the like, and is mostly made of cotton, linen and linen, belongs to an inert dressing, and has no obvious promotion effect on the healing of wound surfaces. The dressing has the advantages of low price, wide raw material sources, simple preparation, certain absorbability to wound exudate, wound protection and reusability. However, with the continuous and deep research on wound repair, the dressing has limitations due to the defects of being not beneficial to wound healing, easily causing wound infection, poor hemostatic effect and the like.
The addition of the functional antibacterial agent is an important way for improving the antibacterial performance of the novel dressing. Commonly used antibacterial agents include silver-based, iodine-based, organic small molecule antibacterial agents, antibiotics, and the like. However, silver is expensive and easily causes heavy metal residue; the stability of iodine is poor, and the irritation to skin and mucosa is strong; the organic micromolecule antibacterial agent has poor antibacterial broad spectrum and antibacterial effect; antibiotics have been increasingly limited in use in recent years.
The natural tea tree oil has wide antibacterial, anti-inflammatory and bacteriostatic effects, and as the most effective natural antibacterial agent so far, the tea tree oil has excellent effect when being applied to medical dressings, but the tea tree oil has volatility and larger irritation, is difficult to store and poor in stability, influences the exertion of the drug effect and brings inconvenience to the clinical application, so that the development of a high-efficiency and stable tea tree oil product has important significance.
Disclosure of Invention
The invention mainly solves the technical problems that: aiming at the defects that the dressing which is most clinically used at present mainly comprises gauze, a cotton pad and the like, belongs to an inert dressing, is not beneficial to wound healing, is easy to cause wound bacterial infection and has poor hemostatic effect, and as a natural antibacterial agent, tea tree oil has volatility and larger irritation, is not easy to store, has poor stability, influences the exertion of drug effect and brings inconvenience to clinical application, the preparation method of the tea tree oil liposome anti-inflammatory and antibacterial medical dressing is provided, the preparation method comprises the steps of preparing impregnation liquid by compounding the tea tree oil liposome and chitosan solution, then carrying out spunlace reinforcement on the hemp and viscose composite fibers, immersing the impregnation liquid in ultrasonic load, and carrying out hot pressing to obtain the anti-inflammatory and antibacterial medical dressing, wherein the problem of strong volatility and poor stability of the tea tree oil liposome is solved by preparing the tea tree oil liposome, the liposome has a slow release effect, and can prolong the effective duration of anti-inflammatory and antibacterial effects, the compounding of chitosan makes it have better biocompatibility, the fiber dressing made by the spunlace method has the advantages of softness, sanitation, air permeability, moisture absorption and no hairiness, and the medical dressing made by compounding integrates the advantages of various raw materials, and is a comfortable and effective medical product.
In order to solve the technical problems, the technical scheme adopted by the invention is as follows:
(1) weighing 150-250 g of soybean lecithin, 20-30 g of cholesterol and 2-4 g of sodium cholate, dissolving the soybean lecithin, the 20-30 g of cholesterol and the 2-4 g of sodium cholate together in 500-600 mL of absolute ethyl alcohol, placing the mixture on a shaking table, oscillating and dissolving the mixture for 1-2 h, pouring the mixture into a 1L flask, placing the flask on a rotary evaporator, and performing rotary evaporation at a rotating speed of 50-60 r/min to remove the absolute ethyl alcohol, so that a layer of uniform lipid membrane is formed on the inner wall of the flask;
(2) weighing 50-100 mL of tea tree oil and 100-200 mL of phosphate buffer with pH of 6.5, pouring into a flask with a conjunctiva, putting into a vortex oscillator, oscillating and eluting a lipid membrane on the wall of the flask with power of 30-40W, transferring the flask into a microwave reactor after elution is finished, carrying out hydration reaction for 40-50 min at 45-55 ℃, and filtering through a microporous filter membrane to obtain tea tree oil liposome for later use;
(3) weighing 300-400 g of China hemp fiber and 200-300 g of viscose fiber, uniformly spreading the China hemp fiber and the viscose fiber on a screen mesh, uniformly spraying 30-40 mL of paraffin oil on the fiber in a fog point shape, standing the fiber after spraying is finished, moistening the fiber for 20-30 h, and then putting the fiber into a cotton mixing box for opening treatment;
(4) putting the opened fibers into a fixed cover plate type carding machine to be carded into 3-4 fiber bundles, cutting the fiber bundles into short fibers of 35-40 mm, and lapping the short fibers into short fibers with the gram weight of 40-60 g/m by using a cross lapping machine2The web of (a);
(5) placing the laid fiber web into a spunlace machine, and carrying out spunlace compounding on the front surface and the back surface of the composite fiber web for 2-3 times respectively at a spunlace pressure of 2-3 MPa and a spunlace production speed of 5-7 m/min, so that the hemp and viscose mixed fiber web is tightly entangled together under the spunlace pressure to prepare a dressing base layer fiber web;
(6) putting 200-300 mL of chitosan acetic acid solution into a beaker, adding 20-30 g of standby tea tree oil liposome when the mass concentration of chitosan in the chitosan acetic acid solution is 30%, magnetically stirring for 10-20 min, putting the mixed solution into a concentration tank, and reducing the pressure to 900-1000 Pa to obtain a concentrated impregnation solution;
(7) and (3) immersing the dressing base layer fiber net into the prepared concentrated impregnation liquid, performing ultrasonic impregnation treatment for 2-3 h at the power of 100-200W, taking out, putting into a hot press, performing pressure maintaining pressing at the normal temperature under the pressure of 5-7 MPa for 20-30 min, cutting into 5 x 5cm square blocks, and packaging to obtain the anti-inflammatory and bacteriostatic medical dressing for the tea tree oil liposome.
The application method of the invention comprises the following steps: the anti-inflammatory and antibacterial medical tea tree oil liposome dressing prepared by the invention can be used for postoperative incisions or wound surfaces of various surgical operations and plastic operations, before use, the skin around the wound surface is wiped dry by using sterile gauze, then the wound is covered by selecting a composite medical dressing which is 4-6 cm longer than the wound, and then the composite medical dressing is bound by using the sterile gauze, so that the dressing is tightly attached to the wound, the replacement time is determined according to the exudate of the wound surface, the exudate is more, the dressing is timely replaced after being saturated in absorption, the exudate is less, the dressing can be replaced at intervals of 2-3 days, the air permeability of the dressing is excellent, and the effective time of anti-inflammatory and antibacterial is 2-3 times that of the.
The invention has the beneficial effects that: the anti-inflammatory and bacteriostatic medical dressing prepared by the invention solves the problems of strong volatility and poor stability by preparing the tea tree oil into the liposome, the liposome has a slow release effect, the effective duration of antibiosis and antiphlogosis can be prolonged, the chitosan has better biocompatibility by compounding, the fiber dressing prepared by the spunlace method has the advantages of softness, sanitation, air permeability, moisture absorption and no hairiness, and the medical dressing prepared by compounding integrates the advantages of various raw materials, thereby being a comfortable and effective medical product.
Detailed Description
Weighing 150-250 g of soybean lecithin and 20-30 g of soybean lecithinDissolving cholesterol and sodium cholate 2-4 g together in 500-600 mL of absolute ethyl alcohol, placing the mixture on a shaking table to oscillate and dissolve for 1-2 h, pouring the mixture into a 1L flask, placing the flask on a rotary evaporator to remove the absolute ethyl alcohol by rotary evaporation at a rotating speed of 50-60 r/min, and forming a layer of uniform lipid membrane on the inner wall of the flask; weighing 50-100 mL of tea tree oil and 100-200 mL of phosphoric acid buffer solution with the pH value of 6.5, pouring the tea tree oil and the phosphoric acid buffer solution into a flask with a conjunctiva, putting the flask into a vortex oscillator, oscillating and eluting a lipid membrane on the wall of the flask with the power of 30-40W, transferring the flask into a microwave reactor after the elution is finished, carrying out hydration reaction at the temperature of 45-55 ℃ for 40-50 min, and filtering the mixture by using a microporous filter membrane to obtain tea tree oil liposome for later use; weighing 300-400 g of China hemp fiber and 200-300 g of viscose fiber, uniformly spreading the China hemp fiber and the viscose fiber on a screen mesh, uniformly spraying 30-40 mL of paraffin oil on the fiber in a fog point shape, standing the fiber after spraying is finished, moistening the fiber for 20-30 h, and then putting the fiber into a cotton mixing box for opening treatment; putting the opened fibers into a fixed cover plate type carding machine to be carded into 3-4 fiber bundles, cutting the fiber bundles into short fibers with the length of 35-40 mm, and lapping the short fibers into short fibers with the weight of 40-60 g/m by using a cross lapping machine2The web of (a); placing the laid fiber web into a spunlace machine, and carrying out spunlace compounding on the front surface and the back surface of the composite fiber web for 2-3 times respectively at the spunlace pressure of 2-3 MPa and the spunlace production speed of 5-7 m/min, so that the hemp and viscose mixed fiber web is tightly entangled together under the spunlace pressure to prepare a dressing base layer fiber web; putting 200-300 mL of chitosan acetic acid solution into a beaker, adding 20-30 g of standby tea tree oil liposome when the mass concentration of chitosan in the chitosan acetic acid solution is 30%, magnetically stirring for 10-20 min, putting the mixed solution into a concentration tank, and reducing the pressure to 900-1000 Pa to obtain a concentrated impregnation solution; and (3) immersing the dressing base layer fiber net into the prepared concentrated impregnation liquid, performing ultrasonic impregnation treatment for 2-3 h at the power of 100-200W, taking out, putting into a hot press, pressing at the normal temperature under the pressure of 5-7 MPa for 20-30 min under the pressure maintaining condition, cutting into 5 x 5cm square blocks, and packaging to obtain the anti-inflammatory and antibacterial medical dressing for the tea tree oil liposome.
Example 1
Weighing 150g of soybean lecithin, 20g of cholesterol and 2g of sodium cholate, dissolving in 500mL of absolute ethanol, placing on a shaking table, and shaking to dissolveAfter the solution is decomposed for 1 hour, pouring the solution into a 1L flask, placing the flask on a rotary evaporator, and performing rotary evaporation at a rotating speed of 50r/min to remove the absolute ethyl alcohol, so as to form a layer of uniform lipid film on the inner wall of the flask; weighing 50mL of tea tree oil and 100mL of phosphoric acid buffer solution with the pH value of 6.5, pouring into a flask with a conjunctiva, putting into a vortex oscillator, oscillating and eluting a lipid membrane on the wall of the flask with the power of 30W, transferring the flask into a microwave reactor after the elution is finished, carrying out hydration reaction for 40min at the temperature of 45 ℃, and filtering by using a microporous filter membrane to obtain tea tree oil liposome for later use; weighing 300g of China hemp fiber and 200g of viscose fiber, uniformly spreading the China hemp fiber and the viscose fiber on a screen mesh, uniformly spraying 30mL of paraffin oil on the fiber in a fog point shape, standing the fiber after spraying, moistening the fiber for 20 hours, and then putting the fiber into a cotton mixing box for opening treatment; carding the opened fibers in a fixed cover plate type carding machine into 3 fiber bundles, cutting the fiber bundles into short fibers with the diameter of 35mm, and lapping the short fibers into short fibers with the gram weight of 40g/m by a cross lapping machine2A fiber web; placing the laid fiber web into a spunlace machine, carrying out spunlace compounding on the front surface and the back surface of the composite fiber web for 2 times respectively at the spunlace pressure of 2MPa and the spunlace production speed of 5m/min, and tightly twisting the hemp and viscose mixed fiber web together under the spunlace pressure to obtain a dressing base layer fiber web; putting 200mL of chitosan acetic acid solution into a beaker, adding 20g of standby tea tree oil liposome when the mass concentration of chitosan in the chitosan acetic acid solution is 30%, magnetically stirring for 10min, putting the mixed solution into a concentration tank, and reducing the pressure to 900Pa to prepare a concentrated steeping solution; soaking the dressing base layer fiber net in the prepared concentrated impregnation liquid, performing ultrasonic impregnation treatment for 2h at the power of 100W, taking out, putting into a hot press, pressing at the normal temperature under the pressure of 5MPa for 20min under the pressure maintaining condition, cutting into 5 x 5cm squares, and packaging to obtain the anti-inflammatory and antibacterial medical dressing containing tea tree oil liposome.
The application method of the invention comprises the following steps: the tea tree oil liposome anti-inflammatory and antibacterial medical dressing prepared by the invention can be used for postoperative incisions or wound surfaces of various surgical operations and plastic operations, before use, the skin around the wound surface is wiped dry by using sterile gauze, then the wound is covered by selecting a composite medical dressing which is 4cm longer than the wound, and then the dressing is bound by using the sterile gauze, so that the dressing is tightly attached to the wound, the replacement time is determined according to wound exudate, the exudate is more, the dressing is timely replaced after being saturated in absorption, the exudate is less, the dressing can be replaced at intervals of 2 days, the air permeability of the dressing is excellent, and the effective time of anti-inflammatory and antibacterial is 2 times that of the common dressing.
Example 2
Weighing 200g of soybean lecithin, 25g of cholesterol and 3g of sodium cholate, dissolving the soybean lecithin, the 25g of cholesterol and the 3g of sodium cholate together in 550mL of absolute ethyl alcohol, placing the mixture on a shaking table, oscillating and dissolving the mixture for 1.5h, pouring the mixture into a 1L flask, placing the flask on a rotary evaporator, and performing rotary evaporation at a rotating speed of 55r/min to remove the absolute ethyl alcohol, so that a layer of uniform lipid membrane is formed on the inner wall of the flask; weighing 80mL of tea tree oil and 150mL of phosphoric acid buffer solution with the pH value of 6.5, pouring into a flask with a conjunctiva, putting into a vortex oscillator, oscillating and eluting a lipid membrane on the wall of the flask at the power of 35W, transferring the flask into a microwave reactor after the elution is finished, carrying out hydration reaction for 45min at the temperature of 50 ℃, and filtering by using a microporous filter membrane to obtain tea tree oil liposome for later use; weighing 350g of China hemp fiber and 250g of viscose fiber, uniformly spreading the China hemp fiber and the viscose fiber on a screen mesh, uniformly spraying 35mL of paraffin oil on the fiber in a foggy point shape, standing the fiber after spraying, moistening the fiber for 25 hours, and then putting the fiber into a cotton mixing box for opening treatment; carding the opened fibers in a fixed cover plate type carding machine into 3 fiber bundles, cutting the fiber bundles into 38mm short fibers, and lapping the short fibers into short fibers with the gram weight of 50g/m by using a cross lapping machine2A fiber web; placing the laid fiber web into a spunlace machine, carrying out spunlace compounding on the front surface and the back surface of the composite fiber web for 2 times respectively at the spunlace pressure of 3MPa and the spunlace production speed of 6m/min, and tightly twisting the hemp and viscose mixed fiber web together under the spunlace pressure to obtain a dressing base layer fiber web; putting 250mL of chitosan acetic acid solution into a beaker, adding 25g of standby tea tree oil liposome when the mass concentration of chitosan in the chitosan acetic acid solution is 30%, magnetically stirring for 15min, putting the mixed solution into a concentration tank, and reducing the pressure to 950Pa to prepare a concentrated impregnation solution; soaking the dressing base layer fiber net in the prepared concentrated impregnation liquid, performing ultrasonic impregnation treatment for 2h at the power of 150W, taking out, putting into a hot press, pressing at the normal temperature under the pressure of 6MPa for 25min under the pressure maintaining condition, cutting into 5 x 5cm squares, and packaging to obtain the anti-inflammatory and antibacterial medical dressing containing tea tree oil liposome.
The application method of the invention comprises the following steps: the tea tree oil liposome anti-inflammatory and antibacterial medical dressing prepared by the invention can be used for postoperative incisions or wound surfaces of various surgical operations and plastic operations, before use, the skin around the wound surface is wiped dry by using sterile gauze, then the composite medical dressing which is 5cm longer than the wound is selected to cover the wound, and then the wound is wrapped by using the sterile gauze, so that the dressing is tightly attached to the wound, the replacement time is determined according to wound exudate, the exudate is more, the dressing is timely replaced after being saturated in absorption, the exudate is less, the dressing can be replaced at intervals of 2 days, the air permeability of the dressing is excellent, and the effective time of anti-inflammatory and antibacterial is 2 times that of the common dressing.
Example 3
Weighing 250g of soybean lecithin, 30g of cholesterol and 4g of sodium cholate, dissolving the soybean lecithin, the cholesterol and the sodium cholate together in 600mL of absolute ethyl alcohol, placing the mixture on a shaking table, oscillating the mixture for dissolving for 2 hours, pouring the mixture into a 1L flask, placing the flask on a rotary evaporator, and performing rotary evaporation at a rotating speed of 60r/min to remove the absolute ethyl alcohol, so that a layer of uniform lipid membrane is formed on the inner wall of the flask; weighing 100mL of tea tree oil and 200mL of phosphoric acid buffer solution with pH of 6.5, pouring into a flask with a conjunctiva, putting into a vortex oscillator, oscillating and eluting a lipid membrane on the wall of the flask with 40W power, transferring the flask into a microwave reactor after elution is finished, carrying out hydration reaction for 50min at 55 ℃, and filtering with a microporous filter membrane to obtain tea tree oil liposome for later use; weighing 400g of hemp fiber and 300g of viscose fiber, uniformly spreading the hemp fiber and the viscose fiber on a screen mesh, uniformly spraying 40mL of paraffin oil on the fiber in a fog point shape, standing the fiber after spraying, moistening the fiber for 30 hours, and then putting the fiber into a cotton mixing box for opening treatment; carding the opened fibers into 4 fiber bundles in a fixed cover plate type carding machine, cutting the fiber bundles into short fibers with the diameter of 40mm, and lapping the short fibers into short fibers with the gram weight of 60g/m by a cross lapping machine2A fiber web; putting the laid fiber web into a spunlace machine, and carrying out spunlace compounding on the front surface and the back surface of the composite fiber web for 3 times respectively at the spunlace pressure of 3MPa and the spunlace production speed of 7m/min, so that the hemp and viscose mixed fiber web is tightly entangled together under the spunlace pressure to prepare a dressing base layer fiber web; adding 300mL of chitosan acetic acid solution into a beaker, adding 30g of standby tea tree oil liposome, magnetically stirring for 20min, adding the mixed solution into a concentration tank, and reducing pressure to 1000Pa to obtain the final productObtaining concentrated steeping liquor; soaking the dressing base layer fiber net in the prepared concentrated impregnation liquid, performing ultrasonic impregnation treatment for 3h at 200W power, taking out, putting into a hot press, pressing at the normal temperature under the pressure of 7MPa for 30min, cutting into 5 x 5cm squares, and packaging to obtain the anti-inflammatory and antibacterial medical dressing of tea tree oil liposome.
The application method of the invention comprises the following steps: the tea tree oil liposome anti-inflammatory and antibacterial medical dressing prepared by the invention can be used for postoperative incisions or wound surfaces of various surgical operations and plastic operations, before use, the skin around the wound surface is wiped dry by using sterile gauze, then the composite medical dressing which is 6cm longer than the wound is selected to cover the wound, and then the wound is wrapped by using the sterile gauze, so that the dressing is tightly attached to the wound, the replacement time is determined according to wound exudate, the exudate is more, the dressing is timely replaced after being saturated in absorption, the exudate is less, the dressing can be replaced at intervals of 3 days, the air permeability of the dressing is excellent, and the effective time of anti-inflammatory and antibacterial is 3 times that of the common dressing.
Claims (1)
1. The anti-inflammatory and bacteriostatic medical dressing containing tea tree oil lipidosome is characterized by being prepared by the following preparation method, and the preparation method comprises the following specific steps:
(1) weighing 150-250 g of soybean lecithin, 20-30 g of cholesterol and 2-4 g of sodium cholate, dissolving the soybean lecithin, the 20-30 g of cholesterol and the 2-4 g of sodium cholate together in 500-600 mL of absolute ethyl alcohol, placing the mixture on a shaking table, oscillating and dissolving the mixture for 1-2 h, pouring the mixture into a 1L flask, placing the flask on a rotary evaporator, and performing rotary evaporation at a rotating speed of 50-60 r/min to remove the absolute ethyl alcohol, so that a layer of uniform lipid membrane is formed on the inner wall of the flask;
(2) weighing 50-100 mL of tea tree oil and 100-200 mL of phosphate buffer with pH of 6.5, pouring into a flask with a conjunctiva, putting into a vortex oscillator, oscillating and eluting a lipid membrane on the wall of the flask with power of 30-40W, transferring the flask into a microwave reactor after elution is finished, carrying out hydration reaction for 40-50 min at 45-55 ℃, and filtering through a microporous filter membrane to obtain tea tree oil liposome for later use;
(3) weighing 300-400 g of China hemp fiber and 200-300 g of viscose fiber, uniformly spreading the China hemp fiber and the viscose fiber on a screen mesh, uniformly spraying 30-40 mL of paraffin oil on the fiber in a fog point shape, standing the fiber after spraying is finished, moistening the fiber for 20-30 h, and then putting the fiber into a cotton mixing box for opening treatment;
(4) putting the opened fibers into a fixed cover plate type carding machine to be carded into 3-4 fiber bundles, cutting the fiber bundles into short fibers of 35-40 mm, and lapping the short fibers into short fibers with the gram weight of 40-60 g/m by using a cross lapping machine2The web of (a);
(5) placing the laid fiber web into a spunlace machine, and carrying out spunlace compounding on the front surface and the back surface of the composite fiber web for 2-3 times respectively at a spunlace pressure of 2-3 MPa and a spunlace production speed of 5-7 m/min, so that the hemp and viscose mixed fiber web is tightly entangled together under the spunlace pressure to prepare a dressing base layer fiber web;
(6) putting 250mL of chitosan acetic acid solution into a beaker, adding 20-30 g of standby tea tree oil liposome when the mass concentration of chitosan in the chitosan acetic acid solution is 30%, magnetically stirring for 10-20 min, putting the mixed solution into a concentration tank, and reducing the pressure to 900-1000 Pa to obtain a concentrated steeping liquor;
(7) and (3) immersing the dressing base layer fiber net into the prepared concentrated impregnation liquid, performing ultrasonic impregnation treatment for 2-3 h at the power of 100-200W, taking out, putting into a hot press, performing pressure maintaining pressing at the normal temperature under the pressure of 5-7 MPa for 20-30 min, cutting into 5 x 5cm square blocks, and packaging to obtain the anti-inflammatory and bacteriostatic medical dressing for the tea tree oil liposome.
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CN107823695B (en) * | 2017-09-19 | 2022-03-15 | 华东理工大学 | Intelligent antibacterial dressing and preparation method thereof |
CN109364290A (en) * | 2018-11-12 | 2019-02-22 | 新疆维吾尔自治区分析测试研究院 | A kind of Lavender liposome liquid adhesive bandage and preparation method thereof |
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CN108721679A (en) | 2018-11-02 |
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Effective date of registration: 20201105 Address after: No.39 middle street, Xiaocheng Town, LUANNAN COUNTY, Tangshan City, Hebei Province Applicant after: TANGSHAN BOSHIDE MEDICAL DEVICES Co.,Ltd. Address before: 213000 Liaohe Road, Xinbei District, Changzhou, Jiangsu Province, No. 29 Applicant before: Ding Yongxin |
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