CN110496242A - A kind of rapid hemostatic material based on nucleopore membranes - Google Patents

A kind of rapid hemostatic material based on nucleopore membranes Download PDF

Info

Publication number
CN110496242A
CN110496242A CN201910895909.0A CN201910895909A CN110496242A CN 110496242 A CN110496242 A CN 110496242A CN 201910895909 A CN201910895909 A CN 201910895909A CN 110496242 A CN110496242 A CN 110496242A
Authority
CN
China
Prior art keywords
hemostatic
nucleopore membranes
layer
material based
hemostatic material
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201910895909.0A
Other languages
Chinese (zh)
Inventor
阎尔坤
白红升
闫小强
崔贝
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tianjin Co Ltd Of Saden Medicine Research Academy
Original Assignee
Tianjin Co Ltd Of Saden Medicine Research Academy
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Tianjin Co Ltd Of Saden Medicine Research Academy filed Critical Tianjin Co Ltd Of Saden Medicine Research Academy
Priority to CN201910895909.0A priority Critical patent/CN110496242A/en
Publication of CN110496242A publication Critical patent/CN110496242A/en
Pending legal-status Critical Current

Links

Classifications

    • 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
    • A61L15/44Medicaments
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/12Layered products comprising a layer of synthetic resin next to a fibrous or filamentary layer
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/36Layered products comprising a layer of synthetic resin comprising polyesters
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B5/00Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
    • B32B5/02Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by structural features of a fibrous or filamentary layer
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B7/00Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
    • B32B7/04Interconnection of layers
    • B32B7/12Interconnection of layers using interposed adhesives or interposed materials with bonding properties
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/20Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing organic materials
    • A61L2300/23Carbohydrates
    • A61L2300/232Monosaccharides, disaccharides, polysaccharides, lipopolysaccharides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/20Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices containing or releasing organic materials
    • A61L2300/30Compounds of undetermined constitution extracted from natural sources, e.g. Aloe Vera
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2300/00Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
    • A61L2300/40Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices characterised by a specific therapeutic activity or mode of action
    • A61L2300/45Mixtures of two or more drugs, e.g. synergistic mixtures
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Hematology (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Materials For Medical Uses (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Abstract

The invention discloses a kind of rapid hemostatic materials based on nucleopore membranes, including hemostatic layer, are disposed with nucleopore membranes and water absorption layer in the lower surface of hemostatic layer.The present invention uses filter layer of the nucleopore membranes as blood, the effectively hemostatic composition such as blood platelet in blood and red blood cell can be trapped in hemostatic layer side, and the small molecule of water etc is only allowed to pass through, increase effective hemostatic compositions concentration, plays the effect of concentrate blood quick-acting haemostatic powder.Meanwhile the hemostatic material also possess prepare simple, cheap, safe and non-toxic, scar is small, use when without the advantages that feeling of burning.

Description

A kind of rapid hemostatic material based on nucleopore membranes
Technical field
The present invention relates to medical material fields, and in particular to a kind of rapid hemostatic material based on nucleopore membranes.
Background technique
Traumatic hemorrhage is always the main reason for leading to death in field battlefield and all kinds of major traffic accidents.Especially It is in severe war environment and burst incident complicated and changeable, even if if thering is medical staff to be on the scene the bleeding feelings of patient Condition does not obtain good inhibition, still suffers from the very high death rate and late complication.Therefore in no good medical item When part first aid, realize that quickly and effectively hemostasis is of great significance.A kind of ideal rapid hemostatic material should have following several A feature: being 1. used directly for wound face, and main artery and phleborrhagia are controlled in 2-3min;2. using material safety, Bacterium or cell superinfection will not be generated;3. not needing the follow-up works such as to be prepared and mixed before use;4. using being not required to Training, easily operated, Non-medical-staff can also be used skillfully in complex environment;5. convenient for carrying;It is cheap.
Main hemostatic material can be divided into three classes by hemostatic mechanism currently on the market: the first kind is the blood coagulation of fibrin class Material, fibrinogen of the material containing high concentration itself, fibrin ferment, can accelerate in human body final step Coagulation test to Realize hemostatic function, but its disadvantage is that environmental suitability is poor, expensive, storage time is short;Second class is alpha-cyanoacrylate Esters, material main function mechanism is sealing bleeding wound site to reach anastalsis, but it is very high to operation requirement; These two types of materials use obvious deficiency for fine when hospital uses in complicated outdoor environment.Third class is more micropores Class inorganic material and high molecular polysaccharide achieve the purpose that quick-acting haemostatic powder by promoting wound site itself blood coagulation.Wherein, more Micropore class inorganic material hemostatic mechanism is the moisture absorbed in blood to improve red blood cell in blood, blood platelet and coagulation factor Concentration wound site can be generated and be burnt but the disadvantage is that a large amount of thermal energy can be released after absorbing moisture.Macromolecule polysaccharide Most popular class hemostatic material is chitosan, and hemostatic mechanism does not depend on coagulation factor, but with the red blood cell in blood To form sludged blood blocking wound Deng acting on by physical crosslinking and stop blooding, but also have lighter weight be difficult to blutpunkte it is fixed and Later period wound face is difficult to the deficiencies of handling.
United States Patent (USP) US2009/018685 1A1 describes a kind of graininess chitosan hemostatic material (formation product Celox styptic powder), there is significant effect compared with gash bleeding to larger, U.S. army's first-aid dressing is included in by the U.S. in 2010 Standard content object.But Celox hemostasis granules shape lighter weight, saves oneself in severe complex environment calumniator and is difficult to be fixed in Blutpunkte, haemostatic effect are difficult to play, and its particulate matter can be attached to wound surface, increase later period treatment of wounds difficulty.
107412843 A of Chinese patent CN (publication date: on December 1st, 2017) discloses a kind of with anti-microbial property Starch base micropore hemostatic material.The material first prepares micropore starch, then loads amino ion, and prepared poromerics stops Quickly absorb water concentrate blood when blood, has antibacterial functions again while hemostasis, can be with accelerating wound healing.But it is being absorbed A large amount of thermal energy can be discharged when moisture in blood, and then will lead to the burn of tissue, influence therapeutic effect.
102648985 B of Chinese patent CN (publication date: on March 26th, 2014), which discloses a kind of Chitosan first aid, to be stopped Blood material, using chitosan as hemostatic layer, Sodium Polyacrylate grafted chitosan laying and water absorption layer, but Sodium Polyacrylate is grafted Chitosan is only a component of material, and only limited come concentrate blood effect by its water absorbing capacity, quick-acting haemostatic powder is ineffective.
Summary of the invention
The purpose of the present invention is overcome the deficiencies of the prior art and provide a kind of rapid hemostatic material based on nucleopore membranes.
Technical solution of the present invention is summarized as follows:
A kind of rapid hemostatic material based on nucleopore membranes, including hemostatic layer 1 are disposed with core in the lower surface of hemostatic layer Pore membrane 2 and water absorption layer 3.
Nucleopore membranes top surface edge is connect by adhesive with hemostatic layer, and nucleopore membranes lower surface edge is by adhesive and inhales Water layer connection.
Adhesive preferred starch, polyester, acrylic acid or latex.
Preferably, hemostatic layer is made of following methods: hemostasis component is added in deionized water, mixed liquor is made in stirring, Supporting layer is immersed in mixed liquor, 10-30min is impregnated, is taken out, freeze-drying.
Hemostasis group is divided into Yunnan Baiyao powder, chitosan shield creates powder, pseudo-ginseng hemostatic dissipates and one kind or several of Colox styptic powder Kind.
Supporting layer is hospital gauze or degreasing cotton yarn.
For nucleopore membranes with a thickness of 10~30 μm, aperture is 1~5 μm, and hole density is 4 × 102/cm2~8.0 × 1010/cm2
Water absorption layer is hospital gauze or degreasing cotton yarn.
The beneficial effects of the present invention are:
1. the present invention, can be according to nucleopore membranes using nucleopore membranes on the basis of using hemostasis component is stopped blooding in hemostatic layer Aperture carry out selectivity filtering, make effective hemostatic compositions such as blood platelet and the red blood cell in blood, stay in hemostatic layer side, Make the moisture in blood through nucleopore membranes, achievees the purpose that the concentrate blood in hemostatic layer, to accelerate to stop blooding.
2. water absorption layer of the invention can rapidly water absorbing capacity, increase nucleopore membranes two sides permeable pressure head improve blood using it Moisture in liquid penetrates the rate of nucleopore membranes, accelerates the dense of concentration hemostatic layer side blood platelet and red blood cell etc. effectively hemostatic compositions Degree makes it easier to assemble in blutpunkte, quick-acting haemostatic powder.
3. haemostatic effect of the present invention is significant, have it is easy to operate, cheap, safe and non-toxic, use when without sense of burning, scar The advantages that trace is small, without particle attachment.
Detailed description of the invention
Fig. 1 is a kind of structural schematic diagram of the rapid hemostatic material based on nucleopore membranes of the present invention.
Specific embodiment
Nucleopore membranes are purchased from Tianjin Li Yuan Science and Technology Ltd., and material is polyester material.
Yunnan Baiyao powder is purchased from Yunnan Paiyao Group Corp., Ltd.
Chitosan shield wound powder, is purchased from Dezhou Haili'an Biotechnology Co., Ltd..
Pseudo-ginseng hemostatic dissipates, and is purchased from the prosperous Lu Da medical supplies in Anhui Co., Ltd.
Colox styptic powder is purchased from Medtrade Products Limited.
The production firm of above-mentioned material of the present invention and material are to enable those skilled in the art to more fully understand The present invention, but the present invention is not limited in any way, substance similar with above-mentioned material property can be used for the present invention, and be Protection scope of the present invention.
Hemostatic layer is made of following methods: hemostasis component being added in deionized water, stirring, it is 100mg/ that concentration, which is made, Supporting layer is immersed in the mixed liquor by the mixed liquor of mL-300mg/mL, and supporting layer and hemostasis constituent mass ratio are 100:5- 20,10-30min is impregnated, is taken out, freeze-drying.
The present invention is further illustrated with reference to the accompanying drawings and examples.
Embodiment 1
A kind of rapid hemostatic material based on nucleopore membranes, including hemostatic layer 1 are disposed with core in the lower surface of hemostatic layer Pore membrane 2 and water absorption layer 3 (see Fig. 1).
Nucleopore membranes top surface edge is connect by binder starch with hemostatic layer, and nucleopore membranes lower surface edge passes through adhesive Starch is connect with water absorption layer.
Hemostatic layer is made of following methods:
Hemostasis component Colox styptic powder is added in deionized water, the mixed liquor of concentration 200mg/mL is made in stirring, will Supporting layer hospital gauze is immersed in mixed liquor, and the mass ratio of hospital gauze and Colox styptic powder is 100:10, impregnates 20min, It takes out, freeze-drying.
For nucleopore membranes with a thickness of 20 μm, aperture is 3 μm, and hole density is 3.0 × 1010/cm2
Water absorption layer is hospital gauze.
Embodiment 2
A kind of rapid hemostatic material based on nucleopore membranes, including hemostatic layer 1 are disposed with core in the lower surface of hemostatic layer Pore membrane 2 and water absorption layer 3.
Nucleopore membranes top surface edge is connect by bonding agent emulsion with hemostatic layer, and nucleopore membranes lower surface edge passes through adhesive Latex is connect with water absorption layer.
Hemostatic layer is made of following methods:
Hemostasis component Yunnan Baiyao powder is added in deionized water, stirring is made the mixed liquor of concentration 100mg/mL, will prop up Support layer degreasing cotton yarn is immersed in mixed liquor, and the mass ratio of degreasing cotton yarn and Yunnan Baiyao powder is 100:5, is impregnated 10min, is taken Out, it is freeze-dried.
For nucleopore membranes with a thickness of 30 μm, aperture is 5 μm, and hole density is 4.0 × 102/cm2
Water absorption layer is degreasing cotton yarn.
Embodiment 3
A kind of rapid hemostatic material based on nucleopore membranes, including hemostatic layer 1 are disposed with core in the lower surface of hemostatic layer Pore membrane 2 and water absorption layer 3.
Nucleopore membranes top surface edge is connect by adhesive acrylic acid with hemostatic layer, and nucleopore membranes lower surface edge passes through bonding Agent acrylic acid is connect with water absorption layer.
Hemostatic layer is made of following methods:
Hemostasis component pseudo-ginseng hemostatic is dissipated and is added in deionized water, stirring is made the mixed liquor of concentration 300mg/mL, will prop up Support layer hospital gauze is immersed in mixed liquor, and hospital gauze is 100:20 with the mass ratio that pseudo-ginseng hemostatic dissipates, and is impregnated 30min, is taken Out, it is freeze-dried.
For nucleopore membranes with a thickness of 10 μm, aperture is 1 μm, and hole density is 8.0 × 1010/cm2
Water absorption layer is hospital gauze.
The acrylic acid for looking for the present embodiment, the chitosan for mass ratio being 1:1 shield wound powder and pseudo-ginseng hemostatic is replaced to dissipate with polyester The pseudo-ginseng hemostatic that composition substitutes the present embodiment dissipates, and other same the present embodiment can be prepared a kind of based on the quick of nucleopore membranes Hemostatic material.
Haemostatic effect evaluation:
1, rabbit ear edge arteriovenous wound hemorrhage model
Taking the new zealand white rabbit (coagulation function is normal) of 20 health, adult, average weight is in 2-3kg, half male and half female, It is randomly divided into 5 groups, i.e. blank group, embodiment 1, embodiment 2, embodiment 3, Colox styptic powder.
The Nembutal sodium solution of anesthetic selection 3% after rabbit weighing, calculates anesthetic in the ratio of 1ml/kg and uses Amount, is anaesthetized using auricular vein injection method.After rabbit anesthesia, with 75% ethanol disinfection, use scalpel in ear afterwards 1cm × 1cm size surface of a wound is done in outside center, is stopped blooding immediately by grouping after blood is filled with the entire surface of a wound, record hemostasis Time simultaneously calculates hemostasis amount.
Bleeding stopping period recording method: in bleeding surface of a wound apply pressure and fixed hemostatic material, one layer of medical yarn is covered again in periphery Cloth, and certain pressure compression is given, until no longer bleeding, records bleeding stopping period.
Amount of bleeding calculation method: the matter of hemostasis front and back hemostatic material and covering hospital gauze is weighed respectively with assay balance Amount, the calculation formula of amount of bleeding are as follows: cover hospital gauze quality after amount of bleeding (g)=hemostasis after hemostatic material quality (g)+hemostasis (g) hospital gauze quality (g) is covered before-preceding hemostatic material quality (g)-hemostasis of stopping blooding.
Table 1: hemostatic material of the present invention and other hemostatic materials are to new zealand rabbit ear edge arteriovenous wound hemostasis time and mistake Blood volume compares
Group Bleeding stopping period (s) Blood loss (g)
Blank control group 810±30 7.9568±0.003
Celox group 40±2 0.0186±0.002
Embodiment 1 27±1 0.0085±0.002
Embodiment 2 25±1 0.0062±0.002
Embodiment 3 29±1 0.0093±0.002
As shown in table 1, compared with blank control group, Celox group, embodiment have significant difference, the embodiment of the present invention Hemostatic material group and Celox styptic powder group ratio have significant difference, and bleeding stopping period and blood loss are better than Celox styptic powder Group.2, rabbit femoral artery bleeding animal model
Taking the new zealand white rabbit (coagulation function is normal) of 20 health, adult, average weight is in 2-3kg, half male and half female, It is randomly divided into 5 groups, i.e. blank group, embodiment 1, embodiment 2, embodiment 3, Colox styptic powder.
The Nembutal sodium solution of anesthetic selection 3% after rabbit weighing, calculates anesthetic in the ratio of 1ml/kg and uses Amount, is anaesthetized using auricular vein injection method.Rabbit is fixed on operating table after anesthesia, remove leg hours is carried out, is used in combination 75% ethanol disinfection.Leg skin is cut off, femoral artery is carried out using scalpel laterally to cut 3/4, blood is made to gush And go out, stopped blooding immediately using hemostatic material after bleeding 3 seconds, and record bleeding stopping period and hemostasis amount.
Table 2: novel hemostatic material and other hemostatic materials are to new zealand rabbit femoral artery wound hemostasis time and blood loss ratio Compared with
Group Bleeding stopping period (s) Blood loss (g)
Blank control group Without hemostasis Without hemostasis
Celox group 53±4 30.716±0.376
Embodiment 1 33±3 20.269±0.257
Embodiment 2 31±3 18.495±0.314
Embodiment 3 37±3 23.326±0.365
As shown in table 2, compared with blank control group, Celox group, embodiment have significant difference;The embodiment of the present invention Hemostatic material group and Celox styptic powder group ratio have significant difference, and bleeding stopping period and blood loss are better than Celox styptic powder Group.
To sum up the hemostasis of above-mentioned new zealand rabbit the experimental results showed that, it is of the present invention to be stopped blooding based on nucleopore membranes hemostatic material Time and control amount of bleeding in terms of effect be superior to Celox powder, and it is easy to operate be easily fastened at blutpunkte, more be applicable in In field emergency hemostasis operation.

Claims (8)

1. a kind of rapid hemostatic material based on nucleopore membranes, including hemostatic layer (1), it is characterized in that the lower surface of hemostatic layer successively It is provided with nucleopore membranes (2) and water absorption layer (3).
2. a kind of rapid hemostatic material based on nucleopore membranes according to claim 1, it is characterized in that table in the nucleopore membranes Face edge is connect by adhesive with hemostatic layer, and nucleopore membranes lower surface edge is connect by adhesive with water absorption layer.
3. a kind of rapid hemostatic material based on nucleopore membranes according to claim 2, it is characterized in that described adhesive is to form sediment Powder, polyester, acrylic acid or latex.
4. a kind of rapid hemostatic material based on nucleopore membranes according to claim 1 or 2, it is characterized in that the hemostatic layer It is made of following methods: hemostasis component is added in deionized water, mixed liquor is made in stirring, supporting layer is immersed in described mixed It closes in liquid, impregnates 10-30min, take out, freeze-drying.
5. a kind of rapid hemostatic material based on nucleopore membranes according to claim 4, it is characterized in that the hemostasis component For Yunnan Baiyao powder, chitosan shield wound powder, pseudo-ginseng hemostatic dissipates and the one or more of Colox styptic powder.
6. a kind of rapid hemostatic material based on nucleopore membranes according to claim 4, it is characterized in that the supporting layer is doctor With gauze or degreasing cotton yarn.
7. a kind of rapid hemostatic material based on nucleopore membranes according to claim 1, it is characterized in that the nucleopore film thickness It is 10~30 μm, aperture is 1~5 μm, and hole density is 4 × 102/cm2~8.0 × 1010/cm2
8. a kind of rapid hemostatic material based on nucleopore membranes according to claim 1, it is characterized in that the water absorption layer is Hospital gauze or degreasing cotton yarn.
CN201910895909.0A 2019-09-21 2019-09-21 A kind of rapid hemostatic material based on nucleopore membranes Pending CN110496242A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910895909.0A CN110496242A (en) 2019-09-21 2019-09-21 A kind of rapid hemostatic material based on nucleopore membranes

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910895909.0A CN110496242A (en) 2019-09-21 2019-09-21 A kind of rapid hemostatic material based on nucleopore membranes

Publications (1)

Publication Number Publication Date
CN110496242A true CN110496242A (en) 2019-11-26

Family

ID=68592358

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910895909.0A Pending CN110496242A (en) 2019-09-21 2019-09-21 A kind of rapid hemostatic material based on nucleopore membranes

Country Status (1)

Country Link
CN (1) CN110496242A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114699926A (en) * 2022-03-31 2022-07-05 邻得膜(厦门)医疗科技有限公司 PRF preparation device and preparation method

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030125654A1 (en) * 2001-12-19 2003-07-03 Kimberly-Clark Worldwide, Inc. Bandage, methods of producing and using same
CN1775301A (en) * 2005-12-08 2006-05-24 长春吉原生物科技有限公司 Nuclear pore membrane composite medical dressing
US20070003529A1 (en) * 2003-02-21 2007-01-04 King's College London Generating teeth from bone marrow cells
CN103611184A (en) * 2013-11-27 2014-03-05 长春吉原生物科技有限公司 Hydrogel of composite semipermeable membrane and preparation method thereof
CN208551919U (en) * 2018-03-06 2019-03-01 秦先明 A kind of Paediatric special-purpose tourniquet

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030125654A1 (en) * 2001-12-19 2003-07-03 Kimberly-Clark Worldwide, Inc. Bandage, methods of producing and using same
US20070003529A1 (en) * 2003-02-21 2007-01-04 King's College London Generating teeth from bone marrow cells
CN1775301A (en) * 2005-12-08 2006-05-24 长春吉原生物科技有限公司 Nuclear pore membrane composite medical dressing
CN103611184A (en) * 2013-11-27 2014-03-05 长春吉原生物科技有限公司 Hydrogel of composite semipermeable membrane and preparation method thereof
CN208551919U (en) * 2018-03-06 2019-03-01 秦先明 A kind of Paediatric special-purpose tourniquet

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
上海市医师协会组等: "《医师考核培训规范教程 烧伤外科分册》", 31 July 2018, 上海科学技术出版社 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114699926A (en) * 2022-03-31 2022-07-05 邻得膜(厦门)医疗科技有限公司 PRF preparation device and preparation method
CN114699926B (en) * 2022-03-31 2023-12-08 邻得膜(厦门)医疗科技有限公司 PRF preparation device and preparation method

Similar Documents

Publication Publication Date Title
Chan et al. PolySTAT-modified chitosan gauzes for improved hemostasis in external hemorrhage
CN101991875B (en) Mesoporous bioactive glass and chitosan composite porous hemostatic material and preparation method thereof
US10159762B2 (en) Hemostatic compositions and dressings for bleeding
CN102139123B (en) Method for preparing intra-operative hemostatic material by cross emulsification of plant starch
CN103800940B (en) A kind of bleeding-stopping dressing and preparation method
CN101596207A (en) Be used for rapid hemostatic Pharmaceutical composition and preparation method
CN102908652A (en) Composite hemostatic material mainly used for emergency aid
CN110496242A (en) A kind of rapid hemostatic material based on nucleopore membranes
CN108310450A (en) A kind of the medical haemostatic material and application process of quick injection film forming
CN107496973B (en) Chitosan sponge pad band-aid capable of rapidly stopping bleeding and preparation method thereof
CN108686103B (en) Hemostatic traditional Chinese medicine composition and multifunctional emergency hemostatic composite material
CN105561370A (en) Novel hemostatic material and preparation method thereof
CN105251036A (en) Medical hemostatic material and preparation method thereof
CN113975452A (en) Kaolin hemostatic composition, hemostatic dressing containing kaolin hemostatic composition and preparation method of kaolin hemostatic dressing
CN106902383A (en) A kind of nanogel hemostatic material of modified glucan modification and its preparation and application
CN208287272U (en) A kind of skin face restoration care dressing inhibiting scar
CN106039383A (en) Compound pseudo-ginseng, kaolin and bamboo fiber hemostatic gauze and preparation method thereof
CN105688266A (en) Composite medical biofiber bleeding-arresting powder material and preparation method thereof
CN105233326A (en) Preparation method and preparation of absorbable micropore vacuum polysaccharide particles
CN114748670A (en) Non-woven hemostatic gauze and preparation method and application thereof
CN105770970A (en) Compound polysaccharide anti-hemorrhagic thin film and preparation method thereof
CN108619556B (en) Preparation method of porous fiber composite hemostatic material
CN102988407A (en) Starch-hyaluronic acid hemostatic agent and preparation method thereof
CN106075563A (en) A kind of preparation method of medical bio base compound hemostatic dressing
CN111001034A (en) Degradable polyvinyl alcohol-based composite hemostatic material

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20191126