CN110452337A - A kind of degradable medical high molecular material and preparation method thereof - Google Patents

A kind of degradable medical high molecular material and preparation method thereof Download PDF

Info

Publication number
CN110452337A
CN110452337A CN201910719078.1A CN201910719078A CN110452337A CN 110452337 A CN110452337 A CN 110452337A CN 201910719078 A CN201910719078 A CN 201910719078A CN 110452337 A CN110452337 A CN 110452337A
Authority
CN
China
Prior art keywords
parts
high molecular
molecular material
medical high
degradable medical
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
CN201910719078.1A
Other languages
Chinese (zh)
Inventor
不公告发明人
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.)
Zhou Qingying
Original Assignee
Zhou Qingying
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 Zhou Qingying filed Critical Zhou Qingying
Priority to CN201910719078.1A priority Critical patent/CN110452337A/en
Publication of CN110452337A publication Critical patent/CN110452337A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F283/00Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
    • C08F283/01Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to unsaturated polyesters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

The invention discloses a kind of degradable medical high molecular materials, it is characterized in that, it is made of each raw material of following parts by weight: 30-40 parts of vinyl modified star polylactic acid, 3-6 parts of Diacetone Acrylamide, 3-6 parts of 1- vinyl imidazole, 10-15 parts of end-vinyl ultra-branching polyester, 25-35 parts, 1-2 parts of initiator of ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer.The invention also discloses the preparation methods of the degradable medical high molecular material.Degradable medical high molecular material disclosed by the invention has good tissue sticking nature and degradable metabolic capability, and its quality is stablized, and mechanical mechanics property is excellent, can effectively kill germ, prevents the growth of germ.

Description

A kind of degradable medical high molecular material and preparation method thereof
Technical field
The present invention relates to medical material tech field more particularly to a kind of degradable medical high molecular material and its preparation sides Method.
Background technique
As economic fast development and scientific and technological are constantly progressive, the medical and health care system in China also achieves very big , powerful guarantee is provided to the raising of people's physical fitness, these achievements have driven medical macromolecular materials rapidly to develop. Urgent need with the continuous expansion of medical macromolecular materials application range and people to medical level is improved, to medical high More stringent requirements are proposed for the performance of molecular material, and degradable medical high molecular material is exactly one of demand for meeting people And the medical macromolecular materials with high added value, it is widely used in the production of the medical devices such as syringe, transfusion bottle, perfusion tube With the artificial repair materials of human tissue organ.
Medical instrument made of degradable high polymer material is voluntarily degraded after completing set treatment purpose, is not deposited for a long time It stays, can avoid biological inflammatory reaction that permanent implanted instrument causes in body long-term existence and biomethanics is not adapted to etc. asks Topic, and catabolite is metabolizable, has no toxic side effect, and is increasingly becoming current researcher and doctor defends the heat of staff's research Point.Current common degradable high polymer material mainly includes the materials such as polylactic acid, polycaprolactone, hydroxymethyl cellulose, these The generally existing matter of material is crisp uneven, and flexibility is poor, non-stretchable, intensity is too low, often occurs during clinical use Accidents, the clinical applicabilities such as fracture are extremely restricted.
108795003 A of Chinese invention patent CN discloses a kind of preparation method of Biodegradable medical material.It is described A kind of Biodegradable medical material composition are as follows: the polydactyl acid of 100-120 part of mass fraction meter, 60-80 parts Poly- carbonic acid fiber, 4-8 parts of reinforcing agent, 1-2 parts of lubricant, 2-5 parts of toughener, 2-3 parts of dispersing agent, 1-2 parts of antioxygens Agent;The medical material function admirable, intensity is high, it is corrosion-resistant, can itself is degradable, will not cause damages to environment, simultaneously Preparation method is simple, is suitable for large-scale production and application, but this material addition auxiliary agent is more, compatible between each ingredient Property and material comprehensive performance need to be further increased.
Therefore, developing one kind has good tissue sticking nature and degradable metabolic capability, and quality is stablized, mechanical mechanics The excellent degradable medical high molecular material of energy has very important significance.
Summary of the invention
In order to overcome the defects of the prior art, the present invention provides a kind of degradable medical high molecular material and its preparation side Method, the preparation method simple process is easy to operate, of less demanding to equipment and reaction condition, and raw material sources are abundant, and price is low It is honest and clean, it is nontoxic, it is suitble to large-scale production, there is biggish value for clinical application;The degradable medical macromolecule being prepared Material has good tissue sticking nature and degradable metabolic capability, and its quality is stablized, and mechanical mechanics property is excellent, Neng Gouyou Effect kills germ, prevents the growth of germ.
To achieve the above object of the invention, the technical solution adopted by the present invention is that: a kind of degradable medical high molecular material, It is characterized in that, is made of each raw material of following parts by weight: 30-40 parts of vinyl modified star polylactic acid, Diacetone Acrylamide 3-6 parts, 3-6 parts of 1- vinyl imidazole, 10-15 parts of end-vinyl ultra-branching polyester, ethenyl blocking polycaprolactone glycol 2,5- 25-35 parts of furandicarboxylic acid condensation polymer, 1-2 parts of initiator.
Further, the initiator is selected from azodiisobutyronitrile, azobisisoheptonitrile, lauroyl peroxide, peroxidating At least one of diisopropylbenzene (DIPB).
Further, the preparation method of the ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer, packet It includes as follows: polycaprolactone glycol, 2,5-furandicarboxylic acid being added in high boiling solvent and form solution, then will be dissolved in addition Into polymerization reaction kettle, in 3-4 hours progress esterifications of 220-240 DEG C of back flow reaction, catalyst is then added in sealing, is dropped Be depressed into 100-300Pa, polycondensation reaction 12-18 hours at 240-250 DEG C, after polymerization inhibitor and prenol is added thereto again, Continue insulation reaction 1-2 hours, after be cooled to room temperature, separate out polymer in water, then with mass fraction be successively 3-5%'s Sodium hydroxide solution, ether washing, finally pass through drying, obtain the contracting of ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid Polymers.
Further, the polycaprolactone glycol, 2,5-furandicarboxylic acid, high boiling solvent, catalyst, polymerization inhibitor, different The mass ratio of pentenol is 1:1:(6-10): (0.3-0.6): (0.05-0.1): 0.1.
Preferably, the high boiling solvent is selected from dimethyl sulfoxide, n,N-Dimethylformamide, N-Methyl pyrrolidone, N, At least one of N- dimethyl acetamide.
Preferably, the catalyst is selected from one or more of antimony oxide, antimony acetate, antimony glycol.
Preferably, the polymerization inhibitor is selected from tetrachloroquinone, l, one or more of 4- naphthoquinones, p-hydroxyanisole.
Further, the preparation method of the degradable medical high molecular material includes the following steps: each raw material by weight Amount part is mixed to form mixture, then adds mixture into and melts co-extrusion in double screw extruder, using cooling, is formed, Obtain degradable medical high molecular material.
Preferably, the melting extrusion technological parameter are as follows: control screw speed 55-75r/min, extrusion temperature 210-230 ℃。
The beneficial effects of adopting the technical scheme are that
(1) a kind of degradable medical high molecular material provided by the invention, preparation method simple process is easy to operate, right Equipment and reaction condition are of less demanding, and raw material sources are abundant, cheap, nontoxic, are suitble to large-scale production, have larger Value for clinical application.
(2) a kind of degradable medical high molecular material provided by the invention, overcoming conventional medical high molecular material can drop Solution performance is bad, and biocompatibility is bad, and mechanical mechanics property needs the technical issues of being further increased, and has good tissue Sticking nature and degradable metabolic capability, and its quality is stablized, mechanical mechanics property is excellent, can effectively kill germ, prevent disease The growth of bacterium.
(3) a kind of degradable medical high molecular material provided by the invention has vinyl on each bulk composition, is squeezing Out in forming process, under the action of initiator, each ingredient is copolymerized, and is formed organic whole, is constructed three-dimensional cross-linked net Lattice structure is conducive to the normal growth of new histoorgan, secondly, these nets when being applied to the reparation of human body artificial organ organ Lattice structure also provides reaction compartment for biodegrade, so that material has more excellent degradability.
(4) a kind of degradable medical high molecular material provided by the invention, bulk composition includes star polylactic acid, hyperbranched Polyester and polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer, these ingredients are linked together in the form of chemical bond, are mentioned High material property stability, so that the advantages of material has both standby these types of material, good biocompatibility is nontoxic, can give birth to Object degradation property is good, also in relation with the excellent good processing performance of mechanical property and condensation polymer of addition polymers;So that material is more It is soluble, there is lower crystallinity, molecular surface there are the performances such as higher functionality, lesser hydrodynamic volume, melting is viscous Spend it is lower, it is easy to produce and process;The addition of this biomaterial of polycaprolactone glycol 2,5- furandicarboxylic acid is so that material is comprehensive More preferably, furan structure introduces main chain to performance, so that biodegradability is stronger.
(5) a kind of degradable medical high molecular material provided by the invention introduces Diacetone Acrylamide, carbonyl structure Introducing processing can improve outside the mechanical mechanics property of material, moreover it is possible to photosensitization is played, when carbonyl content is higher, and this discarded kind Material has preferable light degradation ability, that is to say, that the material combines light degradation and biodegrade, so that material is degradable Ability enhancing;1- vinyl imidazole is introduced, the introducing of glyoxaline structure can improve material antibiotic property, make it have antibacterial sterilizing energy Power.
Specific embodiment
In order to make those skilled in the art more fully understand technical solution of the present invention, and make features described above of the invention, Purpose and advantage are more clear understandable, and the present invention will be further explained with reference to the examples below.Embodiment is only used for It is bright the present invention rather than limit the scope of the invention.
Involved vinyl modified star polylactic acid is previously prepared in the following embodiments of the present invention, preparation method ginseng It examines: the synthesis of vinyl modified star polylactic acid and performance study, Xu Qiongnan, Wuhan Engineering Univ, 2017;Other raw materials are It is commercially available.
Embodiment 1
A kind of degradable medical high molecular material, which is characterized in that be made of each raw material of following parts by weight: vinyl changes Property 30 parts of star polylactic acid, 3 parts of Diacetone Acrylamide, 3 parts of 1- vinyl imidazole, 10 parts of end-vinyl ultra-branching polyester, second 25 parts, 1 part of azodiisobutyronitrile of condensation polymer of alkenyl terminated polycaprolactone glycol 2,5- furandicarboxylic acid.
The preparation method of the ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer, include the following: by Polycaprolactone glycol, 2,5-furandicarboxylic acid, which are added in dimethyl sulfoxide, forms solution, then will be dissolved in and be added to polymerization reaction In kettle, sealing in 220 DEG C of back flow reactions, 3 hours progress esterifications, is then added antimony oxide, is depressurized to 100Pa, In Polycondensation reaction 12 hours at 240 DEG C, after tetrachloroquinone and prenol is added thereto again, continue insulation reaction 1 hour, it is rear cold But to room temperature, separate out polymer in water, then successively with mass fraction be 3% sodium hydroxide solution, ether wash, finally By drying, ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer is obtained;The polycaprolactone glycol, 2,5- Furandicarboxylic acid, dimethyl sulfoxide, antimony oxide, tetrachloroquinone, prenol mass ratio be 1:1:6:0.3:0.05:0.1.
The preparation method of the degradable medical high molecular material includes the following steps: by weight to mix each raw material Mixture is formed, then adds mixture into and melts co-extrusion in double screw extruder, using cooling, sizing, obtains to drop Solve medical macromolecular materials;The melting extrusion technological parameter are as follows: control screw speed 55r/min, 210 DEG C of extrusion temperature.
Embodiment 2
A kind of degradable medical high molecular material, which is characterized in that be made of each raw material of following parts by weight: vinyl changes Property 33 parts of star polylactic acid, 4 parts of Diacetone Acrylamide, 4 parts of 1- vinyl imidazole, 11 parts of end-vinyl ultra-branching polyester, second 27 parts, 1.2 parts of azobisisoheptonitrile of condensation polymer of alkenyl terminated polycaprolactone glycol 2,5- furandicarboxylic acid.
The preparation method of the ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer, include the following: by Polycaprolactone glycol, 2,5-furandicarboxylic acid, which are added in n,N-Dimethylformamide, forms solution, then will be dissolved in and be added to In polymerization reaction kettle, sealing in 225 DEG C of back flow reactions, 3.3 hours progress esterifications, is then added antimony acetate, is depressurized to 150Pa, polycondensation reaction 14 hours at 242 DEG C, after be added l, 4- naphthoquinones and prenol thereto again, continue insulation reaction 1.2 hours, after be cooled to room temperature, separate out polymer in water, then successively with mass fraction be 3.5% sodium hydroxide it is molten Liquid, ether washing, finally pass through drying, obtain ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer;It is described Polycaprolactone glycol, 2,5- furandicarboxylic acid, N,N-dimethylformamide, antimony acetate, l, the mass ratio of 4- naphthoquinones, prenol For 1:1:7:0.4:0.06:0.1.
The preparation method of the degradable medical high molecular material includes the following steps: by weight to mix each raw material Mixture is formed, then adds mixture into and melts co-extrusion in double screw extruder, using cooling, sizing, obtains to drop Solve medical macromolecular materials;The melting extrusion technological parameter are as follows: control screw speed 60r/min, 215 DEG C of extrusion temperature.
Embodiment 3
A kind of degradable medical high molecular material, which is characterized in that be made of each raw material of following parts by weight: vinyl changes Property 35 parts of star polylactic acid, 4.5 parts of Diacetone Acrylamide, 4.5 parts of 1- vinyl imidazole, end-vinyl ultra-branching polyester 13 Part, 30 parts, 1.5 parts of lauroyl peroxide of ethenyl blocking polycaprolactone glycol 2,5- furandicarboxylic acid condensation polymer.
The preparation method of the ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer, include the following: by Polycaprolactone glycol, 2,5-furandicarboxylic acid, which are added in N-Methyl pyrrolidone, forms solution, then will be dissolved in be added to it is poly- It closes in reaction kettle, sealing in 230 DEG C of back flow reactions, 3.5 hours progress esterifications, is then added antimony glycol, is depressurized to 200Pa, polycondensation reaction 16 hours at 245 DEG C, after p-hydroxyanisole and prenol is added thereto again, it is anti-to continue heat preservation Answer 1.5 hours, after be cooled to room temperature, separate out polymer in water, then successively with mass fraction be 4% sodium hydroxide it is molten Liquid, ether washing, finally pass through drying, obtain ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer;It is described Polycaprolactone glycol, 2,5- furandicarboxylic acid, N-Methyl pyrrolidone, antimony glycol, p-hydroxyanisole, the matter of prenol Amount is than being 1:1:8:0.5:0.07:0.1.
The preparation method of the degradable medical high molecular material includes the following steps: by weight to mix each raw material Mixture is formed, then adds mixture into and melts co-extrusion in double screw extruder, using cooling, sizing, obtains to drop Solve medical macromolecular materials;The melting extrusion technological parameter are as follows: control screw speed 65r/min, 220 DEG C of extrusion temperature.
Embodiment 4
A kind of degradable medical high molecular material, which is characterized in that be made of each raw material of following parts by weight: vinyl changes 38 parts of star polylactic acid of property, 5.5 parts of Diacetone Acrylamide, 5 parts of 1- vinyl imidazole, 14 parts of end-vinyl ultra-branching polyester, 33 parts, 1.9 parts of initiator of ethenyl blocking polycaprolactone glycol 2,5- furandicarboxylic acid condensation polymer;The initiator is azo two Isobutyronitrile, azobisisoheptonitrile, lauroyl peroxide, cumyl peroxide 1:2:3:2 in mass ratio are mixed.
The preparation method of the ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer, include the following: by Polycaprolactone glycol, 2,5-furandicarboxylic acid, which are added in n,N-dimethylacetamide, forms solution, then will be dissolved in and be added to In polymerization reaction kettle, in 235 DEG C of back flow reactions, 3.8 hours progress esterifications, antimony oxide is then added in sealing, is depressured To 250Pa, polycondensation reaction 17 hours at 248 DEG C, after tetrachloroquinone and prenol is added thereto again, continue insulation reaction 1.9 hours, after be cooled to room temperature, separate out polymer in water, then successively with mass fraction be 4.5% sodium hydroxide it is molten Liquid, ether washing, finally pass through drying, obtain ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer;It is described The matter of polycaprolactone glycol, 2,5- furandicarboxylic acid, DMAC N,N' dimethyl acetamide, antimony oxide, tetrachloroquinone, prenol Amount is than being 1:1:9:0.5:0.09:0.1.
The preparation method of the degradable medical high molecular material includes the following steps: by weight to mix each raw material Mixture is formed, then adds mixture into and melts co-extrusion in double screw extruder, using cooling, sizing, obtains to drop Solve medical macromolecular materials;The melting extrusion technological parameter are as follows: control screw speed 73r/min, 225 DEG C of extrusion temperature.
Embodiment 5
A kind of degradable medical high molecular material, which is characterized in that be made of each raw material of following parts by weight: vinyl changes Property 40 parts of star polylactic acid, 6 parts of Diacetone Acrylamide, 6 parts of 1- vinyl imidazole, 15 parts of end-vinyl ultra-branching polyester, second 35 parts, 2 parts of lauroyl peroxide of condensation polymer of alkenyl terminated polycaprolactone glycol 2,5- furandicarboxylic acid.
The preparation method of the ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer, include the following: by Polycaprolactone glycol, 2,5-furandicarboxylic acid, which are added in high boiling solvent, forms solution, then will be dissolved in and be added to polymerization instead It answers in kettle, seals, in 240 DEG C of back flow reactions, 4 hours progress esterifications, catalyst is then added, is depressurized to 300Pa, 250 Polycondensation reaction 18 hours at DEG C, after polymerization inhibitor and prenol is added thereto again, continue insulation reaction 2 hours, after be cooled to Room temperature separates out polymer in water, then successively with mass fraction be 5% sodium hydroxide solution, ether wash, finally pass through It is dry, obtain ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer;The polycaprolactone glycol, 2,5- furans Dioctyl phthalate, high boiling solvent, catalyst, polymerization inhibitor, prenol mass ratio be 1:1:10:0.6:0.1:0.1;It is described high boiling Point solvent is dimethyl sulfoxide, N,N-dimethylformamide, N-Methyl pyrrolidone, DMAC N,N' dimethyl acetamide 1:3 in mass ratio: 2:2 is mixed;The catalyst is that antimony oxide, antimony acetate, antimony glycol 1:3:5 in mass ratio are mixed;It is described Polymerization inhibitor is tetrachloroquinone, l, and 4- naphthoquinones, p-hydroxyanisole 1:2:4 in mass ratio are mixed.
The preparation method of the degradable medical high molecular material includes the following steps: by weight to mix each raw material Mixture is formed, then adds mixture into and melts co-extrusion in double screw extruder, using cooling, sizing, obtains to drop Solve medical macromolecular materials;The melting extrusion technological parameter are as follows: control screw speed 75r/min, 230 DEG C of extrusion temperature.
Comparative example 1
A kind of degradable medical high molecular material, it is essentially identical with the formula and preparation method of embodiment 1, the difference is that not having There is addition vinyl modified star polylactic acid.
Comparative example 2
A kind of degradable medical high molecular material, it is essentially identical with the formula and preparation method of embodiment 1, the difference is that not having There is addition Diacetone Acrylamide.
Comparative example 3
A kind of degradable medical high molecular material, it is essentially identical with the formula and preparation method of embodiment 1, the difference is that not having There is addition 1- vinyl imidazole.
Comparative example 4
A kind of degradable medical high molecular material, it is essentially identical with the formula and preparation method of embodiment 1, the difference is that not having There is addition ethenyl blocking polycaprolactone glycol 2,5- furandicarboxylic acid condensation polymer.
Comparative example 5
A kind of degradable medical high molecular material, it is essentially identical with the formula and preparation method of embodiment 1, the difference is that not having There is addition end-vinyl ultra-branching polyester.
Comparative example 6
A kind of commercially available degradable medical high molecular material, main component is polylactic acid.
The degradable medical high molecular material described in above-described embodiment 1-5 and comparative example 1-6 is respectively according to country or industry Standard is tested for the property, and test result is shown in Table 1, and the strain that wherein antibiotic rate test is used to test is staphylococcus aureus.
Table 1
Test item Tensile strength Cytositimulation reaction Degradation rate (soil buries method, 30 days) Antibiotic rate
Unit MPa % %
Embodiment 1 62 It is non-stimulated 91 98.6
Embodiment 2 65 It is non-stimulated 93 98.8
Embodiment 3 67 It is non-stimulated 94 99.0
Embodiment 4 68 It is non-stimulated 94 99.1
Embodiment 5 70 It is non-stimulated 95 99.3
Comparative example 1 54 It is non-stimulated 83 98.2
Comparative example 2 55 It is non-stimulated 82 98.0
Comparative example 3 52 It is non-stimulated 84 85.0
Comparative example 4 53 It is non-stimulated 83 97.5
Comparative example 5 53 It is non-stimulated 81 97.8
Comparative example 6 48 It is non-stimulated 78 79.0
As seen from Table 1, degradable medical high molecular material disclosed by the embodiments of the present invention has compared with commercial product More excellent mechanical mechanics property, biocompatibility and antibiotic property, and degradation capability is more preferable.
The basic principles, main features and advantages of the present invention have been shown and described above.The technology of the industry Personnel are it should be appreciated that the present invention is not limited to the above embodiments, and what is described in the above embodiment and the description is only the present invention Principle, various changes and improvements may be made to the invention without departing from the spirit and scope of the present invention, these variation and Improvement is both fallen in the range of claimed invention.The present invention claims protection scope by appended claims and its Equivalent defines.

Claims (9)

1. a kind of degradable medical high molecular material, which is characterized in that be made of each raw material of following parts by weight: vinyl modified 30-40 parts of star polylactic acid, 3-6 parts of Diacetone Acrylamide, 3-6 parts of 1- vinyl imidazole, end-vinyl ultra-branching polyester 10- 15 parts, 25-35 parts, 1-2 parts of initiator of ethenyl blocking polycaprolactone glycol 2,5- furandicarboxylic acid condensation polymer.
2. a kind of degradable medical high molecular material according to claim 1, which is characterized in that the initiator is selected from even At least one of nitrogen bis-isobutyronitrile, azobisisoheptonitrile, lauroyl peroxide, cumyl peroxide.
3. a kind of degradable medical high molecular material according to claim 1, which is characterized in that the ethenyl blocking is poly- The preparation method of caprolactone diol 2,5-furandicarboxylic acid condensation polymer includes the following: by polycaprolactone glycol, 2,5- furans diformazan Acid, which is added in high boiling solvent, forms solution, then will be dissolved in and be added in polymerization reaction kettle, and sealing is returned in 220-240 DEG C Stream 3-4 hours progress esterifications of reaction, are then added catalyst, are depressurized to 100-300Pa, polycondensation is anti-at 240-250 DEG C Answer 12-18 hours, after polymerization inhibitor and prenol is added thereto again, continue insulation reaction 1-2 hours, after be cooled to room temperature, Separate out polymer in water, then be successively 3-5% with mass fraction sodium hydroxide solution, ether wash, finally through overdrying It is dry, obtain ethenyl blocking polycaprolactone glycol 2,5-furandicarboxylic acid condensation polymer.
4. a kind of degradable medical high molecular material according to claim 3, which is characterized in that the polycaprolactone two Alcohol, 2,5- furandicarboxylic acid, high boiling solvent, catalyst, polymerization inhibitor, prenol mass ratio be 1:1:(6-10): (0.3- 0.6):(0.05-0.1):0.1。
5. a kind of degradable medical high molecular material according to claim 3, which is characterized in that the high boiling solvent choosing From at least one of dimethyl sulfoxide, N,N-dimethylformamide, N-Methyl pyrrolidone, DMAC N,N' dimethyl acetamide.
6. a kind of degradable medical high molecular material according to claim 3, which is characterized in that the catalyst is selected from three Aoxidize one or more of two antimony, antimony acetate, antimony glycol.
7. a kind of degradable medical high molecular material according to claim 3, which is characterized in that the polymerization inhibitor is selected from four Chloranil, l, one or more of 4- naphthoquinones, p-hydroxyanisole.
8. a kind of degradable medical high molecular material according to claim 1-7, which is characterized in that described to drop The preparation method for solving medical macromolecular materials, includes the following steps: each raw material being mixed to form mixture by weight, then will Mixture, which is added in double screw extruder, melts co-extrusion, using cooling, sizing, obtains degradable medical high molecular material.
9. a kind of degradable medical high molecular material according to claim 8, which is characterized in that the melting extrusion technique Parameter are as follows: control screw speed 55-75r/min, 210-230 DEG C of extrusion temperature.
CN201910719078.1A 2019-08-05 2019-08-05 A kind of degradable medical high molecular material and preparation method thereof Pending CN110452337A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910719078.1A CN110452337A (en) 2019-08-05 2019-08-05 A kind of degradable medical high molecular material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910719078.1A CN110452337A (en) 2019-08-05 2019-08-05 A kind of degradable medical high molecular material and preparation method thereof

Publications (1)

Publication Number Publication Date
CN110452337A true CN110452337A (en) 2019-11-15

Family

ID=68484961

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910719078.1A Pending CN110452337A (en) 2019-08-05 2019-08-05 A kind of degradable medical high molecular material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN110452337A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111840637A (en) * 2020-05-08 2020-10-30 陈艳 Material for artificial liver and preparation method thereof
CN113755021A (en) * 2021-09-11 2021-12-07 中国人民解放军总医院第三医学中心 3D printing bone material and preparation method thereof
CN114989585A (en) * 2022-05-27 2022-09-02 江苏康宝医疗器械有限公司 Degradable medical material suitable for infusion apparatus and preparation method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104004143A (en) * 2014-04-25 2014-08-27 湖北工业大学 Photoactive polylactic acid acrylate degradation material
CN107118309A (en) * 2017-06-26 2017-09-01 浙江海轩科技有限公司 A kind of biodegradable polyesters alloy and preparation method thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104004143A (en) * 2014-04-25 2014-08-27 湖北工业大学 Photoactive polylactic acid acrylate degradation material
CN107118309A (en) * 2017-06-26 2017-09-01 浙江海轩科技有限公司 A kind of biodegradable polyesters alloy and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
徐琼楠: ""乙烯基改性星形聚乳酸的合成与性能研究"", 《中国优秀硕士学位论文全文数据库(电子期刊) 工程科技I辑》 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111840637A (en) * 2020-05-08 2020-10-30 陈艳 Material for artificial liver and preparation method thereof
CN113755021A (en) * 2021-09-11 2021-12-07 中国人民解放军总医院第三医学中心 3D printing bone material and preparation method thereof
CN114989585A (en) * 2022-05-27 2022-09-02 江苏康宝医疗器械有限公司 Degradable medical material suitable for infusion apparatus and preparation method thereof

Similar Documents

Publication Publication Date Title
CN110452337A (en) A kind of degradable medical high molecular material and preparation method thereof
CN103467760B (en) A kind of method preparing high-strength chitosan/cellulose composite hydrogel film
CN101381500B (en) Chitin/polyvinyl alcohol composite foam material and preparation method thereof
EP2764146B1 (en) Polysaccharide fibres for wound dressings
CN102585037A (en) Enoxaparin sodium and production purification method thereof
CN109627498A (en) A kind of sodium alginate-cellulose derivative blended membrane/fiber and preparation method thereof
CN102040813A (en) PLA (polylactic acid) resin-ABS (acrylonitrile-butadiene-styrene) resin composite material and method for preparing same
CN106310389A (en) Bacterial cellulose patch used for gynecology and preparation method thereof
CN102935248A (en) PLA absorbable bone screw with PBC as toughening agent, and preparation method thereof
CN102373514A (en) Glucomannan fiber and preparation method thereof
CN101642584B (en) Medical cassava starch composite film and preparation method thereof
CN101559238A (en) Method for preparing biodegradable blood vessel external scaffold material used in tissue engineering
CN104387669A (en) Medical PP inorganic antibacterial composite and preparation method thereof
CN112359594A (en) Medical fiber material, preparation method and application thereof
CN107815079A (en) A kind of medical nano fiber-reinforced composites and preparation method thereof
CN103160087A (en) Completely-biodegradable plasticizing polylactic resin and method for preparing same
KR100912644B1 (en) The preparing method of chemically transformed chitosan fiber
CN113802207A (en) Nano antibacterial composite fiber for processing non-woven fabric and preparation method thereof
CN102071491B (en) Medicinal gullet scaffold fiber and preparation method thereof
CN104073904B (en) A kind of spandex waste silk that utilizes prepares the method for hygienic material with thick dawn spandex fibre
CN111298190A (en) Hemostatic material for infants and preparation method thereof
US20210061960A1 (en) Polymer gels, method of preparation and uses thereof
CN103709452A (en) Chitin/polyvinyl alcohol composite foam material and preparation method thereof
CN110423442A (en) A kind of degradable composite membrane and preparation method thereof
CN1260282C (en) Preparation process and use of blending film

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
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20191115