CN106474537A - A kind of method preparing the liquid bandage for War injury - Google Patents

A kind of method preparing the liquid bandage for War injury Download PDF

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Publication number
CN106474537A
CN106474537A CN201610906715.2A CN201610906715A CN106474537A CN 106474537 A CN106474537 A CN 106474537A CN 201610906715 A CN201610906715 A CN 201610906715A CN 106474537 A CN106474537 A CN 106474537A
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CN
China
Prior art keywords
liquid bandage
war injury
method preparing
war
gross weight
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
CN201610906715.2A
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Chinese (zh)
Inventor
谢和辉
邱彦
仲伯蒙
王亚威
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Nanjing Sheng Chun Medical Technology Co Ltd
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Nanjing Sheng Chun Medical Technology Co Ltd
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Priority to CN201610906715.2A priority Critical patent/CN106474537A/en
Publication of CN106474537A publication Critical patent/CN106474537A/en
Pending legal-status Critical Current

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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
    • A61L26/00Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0061Use of materials characterised by their function or physical properties
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L26/00Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0009Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form containing macromolecular materials
    • A61L26/0023Polysaccharides
    • 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
    • A61L26/00Chemical aspects of, or use of materials for, wound dressings or bandages in liquid, gel or powder form
    • A61L26/0061Use of materials characterised by their function or physical properties
    • A61L26/008Hydrogels or hydrocolloids

Abstract

The invention discloses a kind of method preparing the liquid bandage for War injury is it is characterised in that comprise the following steps:Step one:Sulfydryl matter acid derivative, viscosifier, wetting agent, preservative are dissolved in deionized water, form component A;Step 2:Acrylate derivative, preservative are dissolved in deionized water, add borate buffer solution, form component B;Step 3:Component A is ejected into wound surface, then again component B is ejected into wound surface, quickly crosslinked within 10 second time, form the liquid bandage for War injury.The liquid bandage for War injury of present invention preparation has excellent biocompatibility, no skin irritation and cytotoxicity it is adaptable to the War injury such as the less gunshot wound of wound, burn and incised wound.The present invention is easy to make simple, quick, has high practical value.

Description

A kind of method preparing the liquid bandage for War injury
Technical field
The present invention relates to prepared by a kind of method preparing the liquid bandage for War injury, especially one kind be applied to wound The method of the liquid bandage of the War injury such as less gunshot wound, burn and incised wound.
Background technology
Interim in modern war, various types of burns increase, and how to be occurred in the form of combined injury, all have more wound Face.For scars of war, widely used conventional bandages (gauze) are mainly using cotton yarn as base material, and its major function is wrapping Wound or hemostasis.This conventional bandages is bound up a wound loaded down with trivial details, and will consume about up to ten thousand tons of cotton yarns every year.As conventional bandages Deformation-common adhesive bandage is by gauze, rubber adhesive and to be attached to the active drug composition two on rubber adhesive Part forms.Gauze plays support in effect, and has the function of absorbing wound transudate;Rubber adhesive adheres to skin table Fixation is played in face;Active drug composition plays antibacterial, antiinflammatory, the function of hemostasis.But limited in one's ability due to absorbing sepage, and should Class tourniquet bandage (gauze) is also subject to certain impact and restriction due to its mechanical performance that limits of its material, also can shadow during use Sound is attractive in appearance.The greatest problem that the use of conventional bandages is restricted is in wound healing process, and binder is easy to regenerating tissues and occurs Adhesion, when recovering from injury removing it is easy to cause secondary damage.
It is desirable to hydrogel is liquid when using in a lot of biological medicine applications, but fast after reaching appointed part Speed forms gel, loses flowability." liquid bandage " overcomes many drawbacks of traditional wound surface protective material, imparts wound shield Manage new function:As binder, adhesive bandage etc. to irregular wound face or some human body protective capacities of being inconvenient to use poor, Water-proof breathable properties are bad, helpless to the bacterium infection of wound, use inaesthetic shortcoming.However, " liquid bandage " For wound care, there is obviously advantage:Ratio, if the shape fully according to wound forms one layer of hydrogel, sticks Hydrogel thin film can stop blooding, using being easily removed after terminating etc..Up to the present, research worker has investigated various ways in fact The quick-gelatinizing of existing hydrogel.For example, the unsaturated derivant of water-soluble polyethylene glycol and derivant pass through photo-initiated crosslinking Prepare gel;The solution of the triblock copolymer of the Polyethylene Glycol of specific composition and polypropylene glycol has the solidifying of temperature change initiation Gel behavior;Cyanoacrylate polymerizable is cross-linked to form gel, gluing for organizing;Glutaraldehyde cross-linking material of gelatin etc.. In general, there are various defects in these above-mentioned hydrogels, such as poor biocompatibility, poor biodegradation Performance etc..Quick-gelatinizing typically requires the cross-linking agent of high activity, and these compounds generally have larger toxic and side effects.
Sulfydryl is the naturally occurring functional group with good biocompatibility in vivo.It has good reaction Activity, at identical conditions its reactivity generally than amino high several orders of magnitude.The crosslinking of sulfydryl may be selected activity relatively Low bio-compatible cross-linking agent, prepared hydrogel has more preferable biocompatibility.Wallace etc. multi-arm (four arms or 12 arms) Polyethylene Glycol mercapto derivatives are dissolved in the sodium phosphate/sodium carbonate buffer (pH=9.6) of 0.3mol/L, multi-arm (four Arm or 12 arms) Polyethylene Glycol butanediol succimide activated derivatives are dissolved in the sodium phosphate buffer of 0.0005mol/L (pH=6.0), it is prepared for hydrogel by mixing above two solution, in wound care art, there is obvious advantage (Wallace etc., US6,624,245).
From the point of view of the research, patent or the product that have just disclosed at present, will have antibacterial bacteriostatic, promote the functions such as wound healing Macromole combined by various modes and make the research of hydrogel moist dressing and compare and receive publicity, and before market Scape is huge.But although this hydrogel functionally meets, on wound surface formed gel have on earth how soon how good, still not The requirement of emergency care of trauma can be reached.
Content of the invention
The technical problem to be solved is to overcome prior art defect, provides that a kind of prepare can Quick cross-linking Method for the liquid bandage of War injury.
In order to solve above-mentioned technical problem, the method that the preparation that the present invention provides is used for the liquid bandage of War injury, including Following steps:
Step one:Sulfydryl matter acid derivative, viscosifier, wetting agent, preservative are dissolved in deionized water, form component A;
Step 2:Acrylate derivative, preservative are dissolved in deionized water, add borate buffer solution, formation group Divide B;
Step 3:Component A is ejected into wound surface, then again component B is ejected into wound surface, formed for War injury Liquid bandage.
As improvement, in the liquid bandage of described War injury, described sulfydryl matter acid derivative accounts for gross weight ratio and is:0.5- 5%, described acrylate derivative accounts for gross weight than for 0.5-5%, and described viscosifier account for gross weight than for 3-20%, described guarantor Humectant accounts for gross weight than for 5-35%, and described preservative accounts for gross weight than for 0.05-1%, and described deionized water accounts for gross weight ratio For 20-60%.
As improvement, described sulfydryl matter acid derivative is one kind of H-1, H-2 or two kinds.
As improvement, described sulfydryl matter acid derivative at least contains three sulfydryls.
As improvement, described acrylate derivative is tetramethyl acrylate derivative.
As improvement, described acrylate derivative be one kind of PEG-2, PEG-4, H-3 or two kinds and more than.
As improvement, described viscosifier are water soluble starch, Polyvinylpyrrolidone, polyvinyl alcohol, gelatin, carboxymethyl are fine One or more of dimension element, polyvidone, collagen protein, vegetable polysaccharidess.
As improvement, described wetting agent is one of glycerol, propylene glycol, Polyethylene Glycol, glycerol, Sorbitol or many Kind.
As improvement, described preservative is parabenses, benzoic acid and its salt, sorbic acid and its salt, Ben Zha Bromo-amine, one or more of chlorhexidine acetate.
As improvement, the pH value of described borate buffer solution is 9.5-11.0.
The beneficial effects of the present invention is:The biocompatibility of primary raw material matter containing sulfydryl acid derivative used by the present invention By-product that is good, not producing side reaction and do not produce toxic side effect, each component stability being used is good, consumption is few, one-tenth This is cheap, easy to use be easily achieved quick-gelatinizing, be easily achieved quick-gelatinizing spray preparation, be suitable for multiple not The advantages of with medical usage;Blending ingredients A and bis- kinds of solution of component B, can occur gelation within 20 seconds.The present invention is especially suitable Field emergency field with War injury.
Brief description
Fig. 1 is sulfydryl matter acid derivative of the present invention and hyaluronic acid1H NMR spectra.
Specific embodiment
Below in conjunction with accompanying drawing, the present invention is elaborated.
Embodiment 1
The preparation of the acid derivative H-1 of matter containing sulfydryl:
10 grams of hyaluronic acids are dissolved in 1L distilled water.It is subsequently added 12 grams of dithio dipropyl two hydrazides, be sufficiently stirred for dissolving. With 0.1mol/L dilute hydrochloric acid, above solution ph is adjusted to 4.75, add 19.2 grams of 1- ethyl -3- (3- dimethylamine propyl) Carbodiimide hydrochloride, continuing stirring makes it fully dissolve.Reaction 12 hours, and keep reacting solution pH value 4.75.
With the sodium hydroxide solution of 1.0mol/L, the pH value of solution in 1 is adjusted to 7.0, is subsequently adding 50 grams of dithiothreitol, DTTs, And adjust pH value of solution for 8.5.After normal-temperature reaction 24 hours, the hydrochloric acid conditioning solution pH using 1mol/L is 3.5.Then by sample Load in bag filter and dialyse (molecular cut off 3500), dialysed 4-5 days using pure water, change a dialysis solution for every eight hours.Finally Collect the solution in Dialysis tubing, lyophilization obtains white fluffy solid.
Embodiment 2
The preparation of the PEG-2 of polyethyleneglycol derivative containing dimethacrylate:
4g Polyethylene Glycol is added in the dichloromethane of 50mL, adds 1g triethylamine, mixed liquor is cooled to 0 DEG C.Then The dichloromethane solution of 1g methacrylic chloride is added dropwise in reaction system, reacts continuously stirred 12 hours.By three times two Chloromethanes dissolving and ether deposition and purification finally give end-product.
Embodiment 3
The preparation of the derivant PEG-4 of polyalkylene glycol acrylate containing tetramethyl:
4g Polyethylene Glycol is added in the dichloromethane of 50mL, adds 1g triethylamine, mixed liquor is cooled to 0 DEG C.Then The dichloromethane solution of 1g methacrylic chloride is added dropwise in reaction system, reacts continuously stirred 12 hours.Then by sample Load in bag filter and dialyse (molecular cut off 3500), dialysed 4 days using pure water, change a dialysis solution for every eight hours.Finally receive Solution in collection Dialysis tubing, lyophilization obtains white fluffy solid.
Embodiment 4
The preparation of acrylate derivative H-3:
The 1,4- dioxane of 50mL water for injection and 75mL is added in the hyaluronic acid aqueous solution of the 1wt% of 100mL;Thereto plus Enter 3mL glycidyl thiophene acrylate, then stir 24 hours in 50 DEG C of thermostatic container;Add sodium chloride to gained To solution in, be followed by stirring for, and pour the mixture into and in 800mL ethanol, obtain continuous shape precipitation.Fully rinse institute with ethanol The H-3 precipitating and obtaining after being dried 1.1g obtaining.
Hyaluronic acid preferred molecular weight 20000 to 3000000, more preferably molecular weight 100000 to 2000000, and more preferably Molecular weight 200000 to 1200000.
Embodiment 5
Configuration component solution A:By 0.5mL2% (mass ratio) sulfydryl matter acid derivative, 0.5mL15% (mass ratio) water solublity forms sediment Powder solution, 1mL20 polyvinyl alcohol, 0.5mL propylene glycol is added to standby in 20mL syringe;
Configuration component B solution:Borate buffer solution configuration 2% (mass ratio) acrylate derivative being 9.5 with pH, standby; Component solution A is sprayed on glass plate, then component B is sprayed on component solution A, it is possible to find after 10s, form one layer of tool There are certain viscosity and the hydrogel layer of elasticity.
Embodiment 6
The impact to crosslinking time for the pH:
Embodiment 7
The impact to crosslinking time for the concentration (mass ratio) of component A and component B:
1With distilling water dissolution, concentration is 2% (mass ratio)
2With boric acid-sodium hydrate buffer solution (pH=11.0) dissolving.Concentration is A+B after 2% (mass ratio) mixing, and concentration is respectively 1% (mass ratio).
Embodiment 8
The present invention is used for the test of the liquid bandage water retention property of War injury.Test shows, sample 4, No. 5 and No. 9 performances Go out excellent water retention property.Preferably propylene glycol is as water-retaining agent.
Embodiment 9
The present invention is used for the optimization Test of each component of the liquid bandage of War injury.The experimental condition of preferred sample 8.
The above is only the preferred embodiment of the present invention it is noted that ordinary skill people for the art For member, some improvement can also be made under the premise without departing from the principles of the invention, these improvement also should be regarded as the present invention's Protection domain.

Claims (10)

1. a kind of method preparing the liquid bandage for War injury is it is characterised in that comprise the following steps:
Step one:Sulfydryl matter acid derivative, viscosifier, wetting agent, preservative are dissolved in deionized water, form component A;
Step 2:Acrylate derivative, preservative are dissolved in deionized water, add borate buffer solution, formation group Divide B;
Step 3:Component A is ejected into wound surface, then again component B is ejected into wound surface, formed for War injury Liquid bandage.
2. the preparation according to claim 1 be used for War injury liquid bandage method it is characterised in that:Described for In the liquid bandage of War injury, sulfydryl matter acid derivative accounts for gross weight ratio and is:0.5-5%, described acrylate derivative accounts for gross weight Than being 0.5-5%, described viscosifier account for gross weight ratio for 3-20% to amount, and described wetting agent accounts for gross weight ratio for 5-35%, described anti-corrosion Agent accounts for gross weight than for 0.5-1%, and described deionized water accounts for gross weight than for 20-60%.
3. the method preparing the liquid bandage for War injury according to claim 1 and 2 it is characterised in that:Described mercapto Substrate acid derivative is one kind of H-1, H-2 or two kinds.
4. the method preparing the liquid bandage for War injury according to claim 1 and 2 it is characterised in that:Described mercapto Substrate acid derivative at least contains three sulfydryls.
5. the method preparing the liquid bandage for War injury according to claim 1 and 2 it is characterised in that:Described third Olefin(e) acid ester derivant is tetramethyl acrylate derivative.
6. the method preparing the liquid bandage for War injury according to claim 1 and 2 it is characterised in that:Described third Olefin(e) acid ester derivant be one kind of PEG-2, PEG-4, H-3 or two kinds and more than.
7. the method preparing the liquid bandage for War injury according to claim 1 and 2 it is characterised in that:Described increasing Stick is water soluble starch, Polyvinylpyrrolidone, polyvinyl alcohol, gelatin, carboxymethyl cellulose, polyvidone, collagen protein, plant One or more of thing polysaccharide.
8. the method preparing the liquid bandage for War injury according to claim 1 and 2 it is characterised in that:Described guarantor Humectant is one or more of glycerol, propylene glycol, Polyethylene Glycol, glycerol, Sorbitol.
9. the method preparing the liquid bandage for War injury according to claim 1 and 2 it is characterised in that:Described anti- Rotten agent be parabenses, benzoic acid and its salt, sorbic acid and its salt, this bundle bromo-amine, one kind of chlorhexidine acetate or Multiple.
10. the preparation according to claim 1 be used for War injury liquid bandage method it is characterised in that:Borate buffer The pH value of solution is 9.5-11.0.
CN201610906715.2A 2016-10-18 2016-10-18 A kind of method preparing the liquid bandage for War injury Pending CN106474537A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110755676A (en) * 2019-10-21 2020-02-07 浙江大学 Composite dressing for promoting wound healing and regeneration and loading traditional Chinese medicine exosomes and preparation method thereof
US11446256B1 (en) 2021-08-20 2022-09-20 Advantice Health, Llc Aqueous wound healing formulation

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103613686A (en) * 2013-11-12 2014-03-05 广州市一杰医药科技有限公司 Preparation method and application of sulfhydryl hyaluronic acid
CN103665397A (en) * 2013-11-12 2014-03-26 广州市一杰医药科技有限公司 Preparation method and application of hydrogel
CN103732264A (en) * 2011-04-20 2014-04-16 卡比兰生物外科公司 In-situ gel forming compositions
US20150266986A1 (en) * 2014-03-20 2015-09-24 National University Of Ireland, Galway Multifunctional Hyperbranched Polymers

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103732264A (en) * 2011-04-20 2014-04-16 卡比兰生物外科公司 In-situ gel forming compositions
CN103613686A (en) * 2013-11-12 2014-03-05 广州市一杰医药科技有限公司 Preparation method and application of sulfhydryl hyaluronic acid
CN103665397A (en) * 2013-11-12 2014-03-26 广州市一杰医药科技有限公司 Preparation method and application of hydrogel
US20150266986A1 (en) * 2014-03-20 2015-09-24 National University Of Ireland, Galway Multifunctional Hyperbranched Polymers

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
HASSAN 等: "Encapsulation and 3D culture of human adipose-derived stem cells in an in-situ crosslinked hybrid hydrogel composed of PEG-based hyperbranched copolymer and hyaluronic acid", 《STEM CELL RESEARCH & THERAPY》 *
XIAO ZHENG SHU 等: "In situ crosslinkable hyaluronan hydrogels for tissue engineering", 《BIOMATERIALS》 *
梁嘉碧 等: "原位交联透明质酸水凝胶的制备及体外生物相容性研究", 《中国修复重建外科杂志》 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110755676A (en) * 2019-10-21 2020-02-07 浙江大学 Composite dressing for promoting wound healing and regeneration and loading traditional Chinese medicine exosomes and preparation method thereof
CN110755676B (en) * 2019-10-21 2021-06-15 浙江大学 Composite dressing for promoting wound healing and regeneration and loading traditional Chinese medicine exosomes and preparation method thereof
US11446256B1 (en) 2021-08-20 2022-09-20 Advantice Health, Llc Aqueous wound healing formulation
US11844869B2 (en) 2021-08-20 2023-12-19 Advantice Health, Llc Aqueous wound healing formulation

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