CN107875433A - A kind of preparation method of quick-acting haemostatic powder type looped fabric - Google Patents

A kind of preparation method of quick-acting haemostatic powder type looped fabric Download PDF

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Publication number
CN107875433A
CN107875433A CN201711241962.6A CN201711241962A CN107875433A CN 107875433 A CN107875433 A CN 107875433A CN 201711241962 A CN201711241962 A CN 201711241962A CN 107875433 A CN107875433 A CN 107875433A
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China
Prior art keywords
mass parts
looped fabric
preparation
quick
stirring
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CN201711241962.6A
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Chinese (zh)
Inventor
郭新华
张会良
叶萍
韩建钢
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Thai Fashion Apparel (suzhou) Co Ltd
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Thai Fashion Apparel (suzhou) Co Ltd
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Priority to CN201711241962.6A priority Critical patent/CN107875433A/en
Publication of CN107875433A publication Critical patent/CN107875433A/en
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/28Polysaccharides or their derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/18Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing inorganic materials
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/20Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing organic materials
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42Use of materials characterised by their function or physical properties
    • A61L15/62Compostable, hydrosoluble or hydrodegradable materials
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F11/00Chemical after-treatment of artificial filaments or the like during manufacture
    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F9/00Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04BKNITTING
    • D04B1/00Weft knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes
    • D04B1/14Other fabrics or articles characterised primarily by the use of particular thread materials
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04BKNITTING
    • D04B21/00Warp knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2400/00Materials characterised by their function or physical properties
    • A61L2400/04Materials for stopping bleeding
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2201/00Cellulose-based fibres, e.g. vegetable fibres
    • D10B2201/20Cellulose-derived artificial fibres
    • D10B2201/22Cellulose-derived artificial fibres made from cellulose solutions
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2509/00Medical; Hygiene
    • D10B2509/02Bandages, dressings or absorbent pads
    • D10B2509/022Wound dressings

Abstract

A kind of preparation method of quick-acting haemostatic powder type looped fabric, belongs to looped fabric technical field.Dissolve the chitosan in dilute acetic acid solutions, then add urea and zinc acetate is prepared into chitosan spinning solution;Structure directing agent is added in deionized water, sodium hydroxide is added after stirring, absolute ethyl alcohol is added after stirring and dissolving, tetraethoxysilance is then added dropwise heats and continues stirring and obtain colloidal sol;Colloidal sol to be prepared is filtered after being cooled to room temperature, washs, dried, and then obtains mesoporous silicon oxide in roasting;Take mesoporous silicon oxide to add in NaOH solution to stir;Make its solidification in the mixed liquor that chitosan spinning solution is sprayed into after stirring through spinning head, dry after stretching, washing, then spinned in a tensioned state, spin the yarn come and be made into looped fabric by knitting machine.The product clotting time prepared by the present invention is short, and anthemorrhagic speed is fast, and preparation method is easy and effective, is dipped in water in colourless or slightly yellow translucent thick gel, no insoluble fibre.

Description

A kind of preparation method of quick-acting haemostatic powder type looped fabric
Technical field
The invention belongs to looped fabric technical field, and in particular to a kind of preparation method of quick-acting haemostatic powder type looped fabric.
Background technology
Place's horse back of bleeding allows blood stopping flowing being called hemostasis.Four kinds of conventional Hemostasis:1. pressure, is used when wounds streamed blood Hand pins bleeding area.2. bag, it is that gauze, bandage, elastoplast or clean cotton or use cotton goods is done to wrap up material used Into pad.3. plug.It is to use cotton goods for the hemostasis with packs method at armpit, shoulder, mouth and nose or other blindgut wounds and tissue defect To tightly it be clogged at the cavity or tissue defect of bleeding, until arresting hemorrhage really.4. bundle, hemostasis with tourniquet, is generally used for It is effective to control extremity hemorrhage during operation, but the damage of N&M may be caused, can also causes because of limb ischemia Systemic complications, not in the case of last resort, this method is not used.
Emergency haemostatic is developed mainly for the emergency that The blood streamed down in wound.In a short period of time (3 min) just can control the emergency as bleeding sustainer, for further medical treatment win preciousness when Between.The 80's of 20th century Francis X.Hursey be not intended to be found that zeolite molecular sieve have excellent anastalsis and in Patent is applied within 1989.At the beginning of 2002, Z-Medica companies set up the new of special Development and Production trade name Quikclot Type hemostatic material, the material are to be made with 75% synthetic zeolite (A type zeolites, LTA structures) for substrate and 25% clay The composite type zeolite hemostatic material mixed for adhesive, at present using the new hemostatic material that zeolite molecular sieve material is main body Material Quikclot has obtained U.S. FDA approval listing, no matter in laboratory or in practice (especially in field operation battlefield ), its haemostatic effect and the aspect of raising survival rate two are better than traditional hemostatic material.Put because Quikclot hemostatic materials have The characteristics of heat is high, wound tissue can be burnt.
China Patent No. CN100345597C has been disclosed mesopore molecular sieve hemostatic material and preparation method thereof, still They simply emphasize simple mesoporous material (main component is silica and other oxides), but due to not passing through Others processing, haemostatic effect are relatively poor.Thus exploitation has the excellent haemostatic effect low hemostatic material of side effect simultaneously, is The consistent target of researcher.
The content of the invention
The technical problem of solution:For above-mentioned technical problem, the present invention provides a kind of preparation of quick-acting haemostatic powder type looped fabric Method, possess anthemorrhagic speed it is fast, without insoluble fibre, preparation process is simple the advantages that.
Technical scheme:A kind of preparation method of quick-acting haemostatic powder type looped fabric, the preparation method comprise the following steps:
5 ~ 10 mass parts chitosans are dissolved in 75 ~ 86 mass parts 2 ~ 5wt.% dilute acetic acid solutions by step 1, then add 2 ~ 5 Mass parts urea and 1 ~ 3 mass parts zinc acetate are prepared into chitosan spinning solution;
Step 2 adds 0.5 ~ 1 mass parts structure directing agent in 100 ~ 130 mass parts deionized waters, after stirring 10 ~ 15min 1 ~ 2 mass parts sodium hydroxide is added, 4 ~ 6 mass parts absolute ethyl alcohols is added after stirring and dissolving, 1 ~ 2 mass parts is then added dropwise Tetraethoxysilance is heated to 80 ~ 90 DEG C and continues the h of stirring 15 ~ 18 to obtain colloidal sol;
Step 3 is filtered after colloidal sol prepared by step 2 is cooled to room temperature, washed, drying, then at a temperature of 300 ~ 420 DEG C 4 ~ 5.5 h of roasting obtain mesoporous silicon oxide;
It is molten that the mesoporous silicon oxide that step 4 takes 2 ~ 4 mass parts step 3 to prepare adds the wt.% NaOH of 60 ~ 75 mass parts 2 ~ 4 Stirred in liquid;
Chitosan spinning solution prepared by step 1 is sprayed into step 4 through a diameter of 0.1mm ~ 1mm spinning heads and prepared by step 5 Stir after mixed liquor in make its solidification, dry at a temperature of 75 ~ 78 DEG C 30 after stretching, washing in a tensioned state ~ 60min, then spinned, spin the yarn come and be made into looped fabric by knitting machine.
Preferably, 6 mass parts chitosans are dissolved in the wt.% dilute acetic acid solutions of 80 mass parts 4 in the step 1, Then 3 mass parts urea are added and 2 mass parts zinc acetates are prepared into chitosan spinning solution.
Preferably, structure directing agent is TPAOH in the step 2.
Preferably, 1 mass parts structure directing agent is added in 120 mass parts deionized waters in the step 2, stirring 1.5 mass parts sodium hydroxides are added after 14 min, 5 mass parts absolute ethyl alcohols are added after stirring and dissolving, are then added dropwise 1.5 Mass parts tetraethoxysilance be heated to 85 DEG C and continue stir 16 h obtain colloidal sol.
Preferably, obtain mesoporous silicon oxide in 350 DEG C of h of roasting temperature 5 in the step 3.
Preferably, the mesoporous silicon oxide for taking 3 mass parts step 3 to prepare in the step 4 adds 66 mass parts 3 Stirred in wt.% NaOH solutions.
Preferably, 45 min are dried in the step 5 at a temperature of 77 DEG C.
Beneficial effect:1. quick-acting haemostatic powder type of the present invention knitting is arranged in warm water, solution is in colourless or slightly yellow half Transparent thick gel, no insoluble fibre;
2. preparation process of the present invention strictly observes sterile working standard, Sterility testing is qualified;
3. quick-acting haemostatic powder type looped fabric of the present invention is short by adding the material clotting time such as chitosan, tetraethoxysilance, only Blood speed is fast, and preparation method is easy and effective.
Embodiment
Embodiment 1
A kind of preparation method of quick-acting haemostatic powder type looped fabric, the preparation method comprise the following steps:
5 mass parts chitosans are dissolved in 75 mass parts 2wt.% dilute acetic acid solutions by step 1, then add 2 mass parts urea Chitosan spinning solution is prepared into 1 mass parts zinc acetate;
Step 2 adds 0.5 mass parts structure directing agent in 100 mass parts deionized waters, and 1 matter is added after stirring 10min Part sodium hydroxide is measured, 4 mass parts absolute ethyl alcohols are added after stirring and dissolving, the heating of 1 mass parts tetraethoxysilance is then added dropwise To 80 DEG C and continue stir 15 h obtain colloidal sol;
Step 3 is filtered after colloidal sol prepared by step 2 is cooled to room temperature, washed, drying, then in 300 DEG C of roasting temperatures 4 h obtain mesoporous silicon oxide;
The mesoporous silicon oxide that step 4 takes 2 mass parts step 3 to prepare, which is added in the wt.% NaOH solutions of 60 mass parts 2, to be stirred Uniformly;
Chitosan spinning solution prepared by step 1 is sprayed into step 4 through a diameter of 0.1mm ~ 1mm spinning heads and prepared by step 5 Stir after mixed liquor in make its solidification, 30min is dried at a temperature of 75 DEG C in a tensioned state after stretching, washing, Then spinned, spin the yarn come and be made into looped fabric by knitting machine.
Detection experiment is carried out to quick-acting haemostatic powder type looped fabric made from the present embodiment, the looped fabric of preparation is folded, cut, By average piece weight 0.8g, area needed for hemostatic gauze is cut into, it is long:A width of 10:7 ratio, claims during cutting every 20min Weight successively, it is found that deviation adjusts in time, specific test result is as follows:
1st, dissolubility detects:The quick-acting haemostatic powder type looped fabric 0.5g of the present invention, warm water 100mL is taken to be dissolved, solution is in nothing Color or slightly yellow translucent sticky colloid, micro-strip opalescence, no insoluble fibre.
2nd, acid-base value detects:The quick-acting haemostatic powder type looped fabric 0.5g of the present invention is taken, after adding water 100mL to dissolve, pH is measured and exists In the range of 6.0-8.0.
3rd, Sterility testing:Preparation process of the present invention strictly observes sterile working standard, up to specification after testing.
4th, anthemorrhagic performance is tested:Take 4 mL pigs whole bloods in advance in 25 DEG C of constant temperature water bath half an hour, first determination nature blood coagulation Between, take 2 mL 0.2M CaCl2 Solution, the whole blood of 2 mL constant temperature is then added, it is 10 min to measure the nature clotting time.Then Take the g of quick-acting haemostatic powder type looped fabric 0.5 of the present invention to add in 10 mL centrifuge tube, add 2 mL 0.2M CaCl2, finally add Enter the pig whole blood after 2 mL constant temperature, start simultaneously at timing, the time of whole blood coagulation is 3min.
Embodiment 2
A kind of preparation method of quick-acting haemostatic powder type looped fabric, the preparation method comprise the following steps:
10 mass parts chitosans are dissolved in 86 mass parts 5wt.% dilute acetic acid solutions by step 1, then add 5 mass parts urine Element and 3 mass parts zinc acetates are prepared into chitosan spinning solution;
Step 2 adds 1 mass parts structure directing agent in 130 mass parts deionized waters, and 2 mass are added after stirring 15min Part sodium hydroxide, 6 mass parts absolute ethyl alcohols are added after stirring and dissolving, 2 mass parts tetraethoxysilances are then added dropwise and are heated to 90 DEG C and continue stir 18 h obtain colloidal sol;
Step 3 is filtered after colloidal sol prepared by step 2 is cooled to room temperature, washed, drying, then in 420 DEG C of roasting temperatures 5.5 h obtain mesoporous silicon oxide;
The mesoporous silicon oxide that step 4 takes 4 mass parts step 3 to prepare, which is added in the wt.% NaOH solutions of 75 mass parts 4, to be stirred Uniformly;
Chitosan spinning solution prepared by step 1 is sprayed into step 4 through a diameter of 0.1mm ~ 1mm spinning heads and prepared by step 5 Stir after mixed liquor in make its solidification, 60min is dried at a temperature of 78 DEG C in a tensioned state after stretching, washing, Then spinned, spin the yarn come and be made into looped fabric by knitting machine.
Detection experiment is carried out to quick-acting haemostatic powder type looped fabric made from the present embodiment, the looped fabric of preparation is folded, cut, By average piece weight 0.8g, area needed for hemostatic gauze is cut into, it is long:A width of 10:7 ratio, claims during cutting every 20min Weight successively, it is found that deviation adjusts in time, specific test result is as follows:
1st, dissolubility detects:The quick-acting haemostatic powder type looped fabric 0.5g of the present invention, warm water 100mL is taken to be dissolved, solution is in nothing Color or slightly yellow translucent sticky colloid, micro-strip opalescence, no insoluble fibre.
2nd, acid-base value detects:The quick-acting haemostatic powder type looped fabric 0.5g of the present invention is taken, after adding water 100mL to dissolve, pH is measured and exists In the range of 6.0-8.0.
3rd, Sterility testing:Preparation process of the present invention strictly observes sterile working standard, up to specification after testing.
4th, anthemorrhagic performance is tested:Take 4 mL pigs whole bloods in advance in 25 DEG C of constant temperature water bath half an hour, first determination nature blood coagulation Between, take 2 mL 0.2M CaCl2 Solution, the whole blood of 2 mL constant temperature is then added, it is 10 min to measure the nature clotting time.Then Take the g of quick-acting haemostatic powder type looped fabric 0.5 of the present invention to add in 10 mL centrifuge tube, add 2 mL 0.2M CaCl2, finally add Enter the pig whole blood after 2 mL constant temperature, start simultaneously at timing, the time of whole blood coagulation is 2.5 min.
Embodiment 3
A kind of preparation method of quick-acting haemostatic powder type looped fabric, the preparation method comprise the following steps:
6 mass parts chitosans are dissolved in 80 mass parts 4wt.% dilute acetic acid solutions by step 1, then add 3 mass parts urea Chitosan spinning solution is prepared into 2 mass parts zinc acetates;
Step 2 adds 1 mass parts structure directing agent in 120 mass parts deionized waters, and 1.5 matter are added after stirring 14min Part sodium hydroxide is measured, 5 mass parts absolute ethyl alcohols is added after stirring and dissolving, 1.5 mass parts tetraethoxysilances is then added dropwise and add Heat to 85 DEG C and continue stir 16 h obtain colloidal sol;
Step 3 is filtered after colloidal sol prepared by step 2 is cooled to room temperature, washed, drying, then in 350 DEG C of roasting temperatures 5 h obtain mesoporous silicon oxide;
The mesoporous silicon oxide that step 4 takes 2 ~ 4 mass parts step 3 to prepare, which is added in the wt.% NaOH solutions of 66 mass parts 3, to be stirred Mix uniformly;
Chitosan spinning solution prepared by step 1 is sprayed into step 4 through a diameter of 0.1mm ~ 1mm spinning heads and prepared by step 5 Stir after mixed liquor in make its solidification, 45 min are dried at a temperature of 77 DEG C in a tensioned state after stretching, washing, Then spinned, spin the yarn come and be made into looped fabric by knitting machine.
Detection experiment is carried out to quick-acting haemostatic powder type looped fabric made from the present embodiment, the looped fabric of preparation is folded, cut, By average piece weight 0.8g, area needed for hemostatic gauze is cut into, it is long:A width of 10:7 ratio, claims during cutting every 20min Weight successively, it is found that deviation adjusts in time, specific test result is as follows:
1st, dissolubility detects:The quick-acting haemostatic powder type looped fabric 0.5g of the present invention, warm water 100mL is taken to be dissolved, solution is in nothing Color or slightly yellow translucent sticky colloid, micro-strip opalescence, no insoluble fibre.
2nd, acid-base value detects:The quick-acting haemostatic powder type looped fabric 0.5g of the present invention is taken, after adding water 100mL to dissolve, pH is measured and exists In the range of 6.0-8.0.
3rd, Sterility testing:Preparation process of the present invention strictly observes sterile working standard, up to specification after testing.
4th, anthemorrhagic performance is tested:Take 4 mL pigs whole bloods in advance in 25 DEG C of constant temperature water bath half an hour, first determination nature blood coagulation Between, take 2 mL 0.2M CaCl2 Solution, the whole blood of 2 mL constant temperature is then added, it is 10 min to measure the nature clotting time.Then Take the g of quick-acting haemostatic powder type looped fabric 0.5 of the present invention to add in 10 mL centrifuge tube, add 2 mL 0.2M CaCl2, finally add Enter the pig whole blood after 2 mL constant temperature, start simultaneously at timing, the time of whole blood coagulation is 1.5 min.
Comparative example 1
With embodiment 3, difference is not add zinc acetate, and specific preparation process is as follows:
6 mass parts chitosans are dissolved in 80 mass parts 4wt.% dilute acetic acid solutions by step 1, then add 3 mass parts urea It is prepared into chitosan spinning solution;
Step 2 adds 1 mass parts structure directing agent in 120 mass parts deionized waters, and 1.5 matter are added after stirring 14min Part sodium hydroxide is measured, 5 mass parts absolute ethyl alcohols is added after stirring and dissolving, 1.5 mass parts tetraethoxysilances is then added dropwise and add Heat to 85 DEG C and continue stir 16 h obtain colloidal sol;
Step 3 is filtered after colloidal sol prepared by step 2 is cooled to room temperature, washed, drying, then in 350 DEG C of roasting temperatures 5 h obtain mesoporous silicon oxide;
The mesoporous silicon oxide that step 4 takes 2 ~ 4 mass parts step 3 to prepare, which is added in the wt.% NaOH solutions of 66 mass parts 3, to be stirred Mix uniformly;
Chitosan spinning solution prepared by step 1 is sprayed into step 4 through a diameter of 0.1mm ~ 1mm spinning heads and prepared by step 5 Stir after mixed liquor in make its solidification, 45 min are dried at a temperature of 77 DEG C in a tensioned state after stretching, washing, Then spinned, spin the yarn come and be made into looped fabric by knitting machine.
Detection experiment is carried out to quick-acting haemostatic powder type looped fabric made from the present embodiment, the looped fabric of preparation is folded, cut, By average piece weight 0.8g, area needed for hemostatic gauze is cut into, it is long:A width of 10:7 ratio, claims during cutting every 20min Weight successively, it is found that deviation adjusts in time, specific test result is as follows:
1st, dissolubility detects:The quick-acting haemostatic powder type looped fabric 0.5g of the present invention, warm water 100mL is taken to be dissolved, solution is in nothing Color or slightly yellow translucent sticky colloid, micro-strip opalescence, no insoluble fibre.
2nd, acid-base value detects:The quick-acting haemostatic powder type looped fabric 0.5g of the present invention is taken, after adding water 100mL to dissolve, pH is measured and exists In the range of 6.0-8.0.
3rd, Sterility testing:Preparation process of the present invention strictly observes sterile working standard, up to specification after testing.
4th, anthemorrhagic performance is tested:Take 4 mL pigs whole bloods in advance in 25 DEG C of constant temperature water bath half an hour, first determination nature blood coagulation Between, take 2 mL 0.2M CaCl2 Solution, the whole blood of 2 mL constant temperature is then added, it is 10 min to measure the nature clotting time.Then Take the g of quick-acting haemostatic powder type looped fabric 0.5 of the present invention to add in 10 mL centrifuge tube, add 2 mL 0.2M CaCl2, finally add Enter the pig whole blood after 2 mL constant temperature, start simultaneously at timing, the time of whole blood coagulation is 5.5 min.
Comparative example 2
With embodiment 3, difference is not add tetraethoxysilance, and specific preparation process is as follows:
6 mass parts chitosans are dissolved in 80 mass parts 4wt.% dilute acetic acid solutions by step 1, then add 3 mass parts urea Chitosan spinning solution is prepared into 2 mass parts zinc acetates;
Step 2 adds 1 mass parts structure directing agent in 120 mass parts deionized waters, and 1.5 matter are added after stirring 14min Measure part sodium hydroxide, add 5 mass parts absolute ethyl alcohols after stirring and dissolving, be then heated to 85 DEG C and continue to stir 16 h obtain it is molten Glue;
Chitosan spinning solution prepared by step 1 is sprayed into step 2 through a diameter of 0.1mm ~ 1mm spinning heads and prepared by step 3 Stir after mixed liquor in make its solidification, 45 min are dried at a temperature of 77 DEG C in a tensioned state after stretching, washing, Then spinned, spin the yarn come and be made into looped fabric by knitting machine.
Detection experiment is carried out to quick-acting haemostatic powder type looped fabric made from the present embodiment, the looped fabric of preparation is folded, cut, By average piece weight 0.8g, area needed for hemostatic gauze is cut into, it is long:A width of 10:7 ratio, claims during cutting every 20min Weight successively, it is found that deviation adjusts in time, specific test result is as follows:
1st, dissolubility detects:The quick-acting haemostatic powder type looped fabric 0.5g of the present invention, warm water 100mL is taken to be dissolved, solution is in nothing Color or slightly yellow translucent sticky colloid, micro-strip opalescence, no insoluble fibre.
2nd, acid-base value detects:The quick-acting haemostatic powder type looped fabric 0.5g of the present invention is taken, after adding water 100mL to dissolve, pH is measured and exists In the range of 6.0-8.0.
3rd, Sterility testing:Preparation process of the present invention strictly observes sterile working standard, up to specification after testing.
4th, anthemorrhagic performance is tested:Take 4 mL pigs whole bloods in advance in 25 DEG C of constant temperature water bath half an hour, first determination nature blood coagulation Between, take 2 mL 0.2M CaCl2 Solution, the whole blood of 2 mL constant temperature is then added, it is 10 min to measure the nature clotting time.Then Take the g of quick-acting haemostatic powder type looped fabric 0.5 of the present invention to add in 10 mL centrifuge tube, add 2 mL 0.2M CaCl2, finally add Enter the pig whole blood after 2 mL constant temperature, start simultaneously at timing, the time of whole blood coagulation is 8 min.

Claims (7)

1. a kind of preparation method of quick-acting haemostatic powder type looped fabric, it is characterised in that the preparation method comprises the following steps:
5 ~ 10 mass parts chitosans are dissolved in 75 ~ 86 mass parts 2 ~ 5wt.% dilute acetic acid solutions by step 1, then add 2 ~ 5 Mass parts urea and 1 ~ 3 mass parts zinc acetate are prepared into chitosan spinning solution;
Step 2 adds 0.5 ~ 1 mass parts structure directing agent in 100 ~ 130 mass parts deionized waters, after stirring 10 ~ 15min 1 ~ 2 mass parts sodium hydroxide is added, 4 ~ 6 mass parts absolute ethyl alcohols is added after stirring and dissolving, 1 ~ 2 mass parts is then added dropwise Tetraethoxysilance is heated to 80 ~ 90 DEG C and continues the h of stirring 15 ~ 18 to obtain colloidal sol;
Step 3 is filtered after colloidal sol prepared by step 2 is cooled to room temperature, washed, drying, then at a temperature of 300 ~ 420 DEG C 4 ~ 5.5 h of roasting obtain mesoporous silicon oxide;
It is molten that the mesoporous silicon oxide that step 4 takes 2 ~ 4 mass parts step 3 to prepare adds the wt.% NaOH of 60 ~ 75 mass parts 2 ~ 4 Stirred in liquid;
Chitosan spinning solution prepared by step 1 is sprayed into step 4 through a diameter of 0.1mm ~ 1mm spinning heads and prepared by step 5 Stir after mixed liquor in make its solidification, dry at a temperature of 75 ~ 78 DEG C 30 after stretching, washing in a tensioned state ~ 60min, then spinned, spin the yarn come and be made into looped fabric by knitting machine.
A kind of 2. preparation method of quick-acting haemostatic powder type looped fabric according to claim 1, it is characterised in that the step 1 It is middle that 6 mass parts chitosans are dissolved in the wt.% dilute acetic acid solutions of 80 mass parts 4, then add 3 mass parts urea and 2 mass Part zinc acetate is prepared into chitosan spinning solution.
A kind of 3. preparation method of quick-acting haemostatic powder type looped fabric according to claim 1, it is characterised in that the step 2 Middle structure directing agent is TPAOH.
A kind of 4. preparation method of quick-acting haemostatic powder type looped fabric according to claim 1, it is characterised in that the step 2 It is middle to add 1 mass parts structure directing agent in 120 mass parts deionized waters, add 1.5 mass parts hydrogen-oxygens after stirring 14 min Change sodium, add 5 mass parts absolute ethyl alcohols after stirring and dissolving, 1.5 mass parts tetraethoxysilances are then added dropwise and are heated to 85 DEG C And continue 16 h of stirring and obtain colloidal sol.
A kind of 5. preparation method of quick-acting haemostatic powder type looped fabric according to claim 1, it is characterised in that the step 3 In in 350 DEG C of h of roasting temperature 5 obtain mesoporous silicon oxide.
A kind of 6. preparation method of quick-acting haemostatic powder type looped fabric according to claim 1, it is characterised in that the step 4 In take 3 mass parts step 3 prepare mesoporous silicon oxide add the wt.% NaOH solutions of 66 mass parts 3 in stir.
A kind of 7. preparation method of quick-acting haemostatic powder type looped fabric according to claim 1, it is characterised in that the step 5 In at a temperature of 77 DEG C dry 45 min.
CN201711241962.6A 2017-11-30 2017-11-30 A kind of preparation method of quick-acting haemostatic powder type looped fabric Pending CN107875433A (en)

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Application publication date: 20180406