CN100558781C - A kind of Polyurethane Thermoplastic Elastomer and synthetic method that contains the poly-polypeptide block of polyethers - Google Patents
A kind of Polyurethane Thermoplastic Elastomer and synthetic method that contains the poly-polypeptide block of polyethers Download PDFInfo
- Publication number
- CN100558781C CN100558781C CNB2006100986707A CN200610098670A CN100558781C CN 100558781 C CN100558781 C CN 100558781C CN B2006100986707 A CNB2006100986707 A CN B2006100986707A CN 200610098670 A CN200610098670 A CN 200610098670A CN 100558781 C CN100558781 C CN 100558781C
- Authority
- CN
- China
- Prior art keywords
- poly
- amino
- polytetrahydrofuran
- peptide
- reaction
- 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.)
- Expired - Fee Related
Links
Images
Landscapes
- Polyurethanes Or Polyureas (AREA)
- Polyamides (AREA)
Abstract
The present invention is a kind of Polyurethane Thermoplastic Elastomer and synthetic method that contains the poly-polypeptide block of polyethers.Synthetic method of the present invention was divided into for three steps: 1) amino acid and derivative thereof and two (trichloromethyl) carbonic ether generates a-amino acid-N-carboxyl inner-acid anhydride (NCA); 2) be that initiator causes NCA ring-opening polymerization generation polyamino acid-polytetrahydrofuran-amino prepolymer of polyamino acid three block ends to hold amino polytetrahydrofuran; 3) (MDI, TDI HDI) wait and chainextender 1,4-butyleneglycol (BDO) or polytetrahydrofuran-1000 (PTHF-1000) reaction in synthetic thermoplastic polyurethane elastomer with vulcabond without separating again.The performance of the poly-peptide polyurethane elastomer of polyethers of the present invention is by the molar feed ratio of NCA and initiator, initiator molecule amount, mol ratio ([NCO]/[NH of isocyanate groups and initiator middle-end amino
2]) regulated.This polyurethane elastomer has good biocompatibility and degradability, and the mechanical property excellence is easy to process, can be widely used in biomedical materials field.
Description
Technical field
The present invention relates generally to a kind of Polyurethane Thermoplastic Elastomer and synthetic method that contains the poly-polypeptide block of polyethers, belongs to the bioabsorbable polymer material field.
Background technology
Polyurethane elastomer is normally by soft section and the hard section segmented copolymer of alternately forming, the carbamate groups that is contained in the molecular chain (NHCOO-) can make intramolecularly and intermolecular generation intensive interaction of hydrogen bond, by selecting suitable soft, hard segment structure and ratio thereof, can obtain the good macromolecular material of physical and mechanical properties, as good toughness and elasticity, but the thermoplastic processed-type, good wear resistance, soft sense of touch, moisture-proof gas, the medicine of anti-number of chemical performance etc.Meanwhile, polyurethane elastomer also has good anticoagulation function and biocompatibility, and does not have performance such as anaphylaxis, thereby is widely used at biomedical sector, is the preferred material of making artificial heart, artificial blood vessel, artificial conduit etc.
Along with polyurethane elastomer constantly the widening of Application Areas in biomedical sector, the non-biodegradable shortcoming of conventional polyurethanes material causes people's attention day by day.Therefore, develop an important symbol [the J Biomed Master Res 2001 that biodegradable polyurethane material has become this field development; 55 (2): 141].At present, in the biodegradable polyurethane material that people have developed, there is a class to utilize natural polyhydroxy compound or polymkeric substance and isocyanic ester direct reaction to obtain, as utilizes xylogen [Idustrial Crops and Products2004,20,231; Polymer Int 1996,41:13], starch [Cell Polym 1999,18 (1): 21] and Mierocrystalline cellulose [Euro Polym J 2004,40:2803] wait and prepare polyurethane elastomer.This class polyurethane elastomer is good mechanical performance not only, also all has favorable biological degradability and biocompatibility simultaneously.Present this method has become one of the main path of preparation Biodegradable polyurethane material [J M S-Pure Appl Chem1995,32 (4): 743].
Another kind of biodegradable polyurethane material mainly is biodegradable polyester dibasic alcohol [J ApplPolym Sci 2000,76 (7): 1074], as poly(lactic acid), poly-epsilon-caprolactone [Biomaterials2005,26 (20): 4219] and poly-beta-hydroxy-butanoic acid ester [Polymer, 1999,40 (11): 3153] etc. and di-isocyanate reaction, utilize 1,4-butyleneglycol etc. carries out chain extension and comes the synthesized degradable polyurethane elastomer.Soft by regulating, hard section molecular weight and ratio can reach main character and purposes such as its degradation rate of control elastomerics, Young's modulus, degree of crystallinity, tensile strength, Young's modulus.With biodegradable natural macromolecular material (as Mierocrystalline cellulose, chitin, starch, collagen etc.) and the chemosynthesis macromolecular material (as poly(lactic acid), poly-epsilon-caprolactone) and the poly-beta-hydroxy-butanoic acid ester that obtains of fermentation using bacteria compare, the biodegradation type polyurethane material because of have excellent biological compatibility, the physical and mechanical properties variable range is big, machine-shaping is easy, of many uses, price is lower etc., and advantage has become bio-medical material hot of research and development in recent years.[J Biomed Master Res1991 such as Alok; 25 (10): 1249] prepare a kind of the have high again biological degradation type polyurethane of excellent machinability, physical strength, especially its excellent toughness and elasticity, make it be particularly suitable as medical operation suture thread and use.Bruin etc. [J Biomed Mat] develop a kind of polyurethane skin surrogate; its top layer is the fungi-proofing polyether-polyurethane elastomerics of micro-porous permeable; and isolate bottom is biodegradable polyester type polyurethane elastomerics reticulated structure; by clinical and histological observation, confirm that this material has the advantages of good skin defencive function.[Biomaterials 1998 for Borkenhagen etc.; 19 (23): 2155] synthetic biodegradable polyurethane elastomerics has utmost point low thermal expansion, good elasticity and biocompatibility, the process of growth of its degradation time and newborn nervous tissue is more identical, and the degraded product reaction that can not cause inflammation is the desirable selection of guiding property twice-laid stufves such as nerve.
Chemosynthesis polyamino acid or poly-peptide have the structure and properties similar to natural protein or polypeptide, demonstrate and cell and highly organized biocompatibility; Owing to have a large amount of peptide bonds on the poly-peptide main chain, in body, very easily be subjected to the effect of enzyme simultaneously, generate little peptide or the amino acid product of not having, participate in the absorption and the metabolism of body, thereby have excellent biodegradability and security thereby can degrade.Hayashi etc. [Polym J 1993,25:481] confirm that the poly-peptide of artificial synthetic has with the similar multi-polar structure of protein and cell and tissue and other biotic component and demonstrate good consistency; Owing to have a large amount of peptide bonds on the poly-peptide main chain, very easily be subjected to the effect of enzyme in human body simultaneously, degraded generates nontoxic polypeptide or amino acid, thereby has excellent biodegradability again.[Biomed Mater Symp 1970 such as Anderson, 5:197] preparation γ-benzyl-L-glutamate and leucic multipolymer have very good tissue affinity, after 200 days, observing has fairly obvious growth of new tissue around implant in implanting the experiment mice body.This multipolymer also has the favorable biological degradability energy simultaneously, and degradation speed changes with the change of copolymer component.
The synthesize polypeptide distinctive molecular structure makes it be different from traditional synthetic macromolecule, and has a not available performance of a lot of traditional polymers, except excellent biological compatibility, degradability, self-assembly behavior, liquid crystal phenomenon and mechanical property etc., they also have good mechanical performance, film-forming properties and spinning property.No matter be to obtain after the ring-opening polymerization; or the synthesize polypeptide that after the deprotection base is handled, forms; the timbering material of all can be directly cultivating as cell and organizational project; formed support not only has controlled biodegradability and suitable mechanical property, also has the avtive spot that can supply the cell adhesion growth to discern in a large number simultaneously.In addition, the self-assembly behavior of poly-peptide has been created condition for the new controlled release drug novel form of exploitation, but makes medicine have plurality of advantages such as controlled release, targeted, the insoluble drug absorption rate of raising and degradable.Therefore synthesize polypeptide can be widely used in the support that cell and organizational project are cultivated in the regenerative medicine, medicine controlled release carrier, biomaterial surface modification, the medical aspect such as operating sutures that absorbs.
Although the present degradable polyurethane elastomerics that synthesizes generally all has good physical and mechanical properties, degradability, process easy to usely, they all lack the avtive spot that can discern for cell adhesion growth in molecular structure.Because polyamino acid or poly-peptide have excellent biological compatibility and biodegradable, urethane has the good mechanical performance again, and therefore many researchists attempt both are combined the Novel Polyurethane Elastomer that preparation contains poly-polypeptide block.As Zhang Jianying[Biomaterials 2000,21:1247] at first prepare prepolymer with nontoxic lysinediisocyanate (LDI) and glycerol reaction, and then preparation urethane.And Guan Jianjun etc. [Biomacromolecules 2005,6:2833] use the segmented copolymer of polyoxyethylene glycol and polycaprolactone as soft section and isocyanate reaction,, prepared and contained the poly-of Aly-Aly-Lys tripeptides as chainextender with the Ala-Ala-Lys tripeptides by ester.McClung etc. [Biomaterials 2001,22:1919] have prepared the polyurethane elastomer by the Methionin modification.[J Poly Sci A:Polym Chem1999 such as Uchida; 37:383; Polymer 2000,41:473; U S Pat 3594351,1971] then at first synthetic γ-methyl-L-L-glutamic acid-N-carboxyl inner-acid anhydride (NCA), use polytetrahydrofuran and phenylbenzene methylene radical isocyanic ester (MDI) reaction prepolymer then, both as the initiator of NCA ring-opening polymerization, prepared the poly-peptide polyurethane elastomer of cross-linking type as chainextender with anhydrous hydrazine again.This elastomerics can be used as ePTFE artificial blood vessel coating on inner surface and uses, and can obviously improve the degree of blood vessel endotheliumization, can suppress thrombosis.[Biomaterials 2000 for Jian etc.; 21 (12): 1247] recent development goes out a kind of timbering material that contains the foam type polyurea polyurethanes of poly-polypeptide block as organizational project.This foam type polyurea polyurethanes has excellent biological compatibility and mechanical property, and that can well promote the cell growth, as tissue engineering bracket material good prospects for application is arranged.
Summary of the invention
The present invention seeks to the poly-polypeptide block of chemosynthesis is incorporated into the poly-polypeptide block prepolymer of formation polyethers on the polyethers section, and then with different hydrogen acid ether and/or chainextender prepared in reaction Polyurethane Thermoplastic Elastomer, the performance of this polyurethane elastomer can be by changing the molecular weight and the composition thereof of polyethers and poly-peptide, and the kind of different hydrogen acid ether and chainextender and content are regulated, support for cell in the regenerative medicine and organizational project cultivation, the carrier of medicine controlled releasing, the surface modification of inertia biomaterial, and the medical operating sutures etc. of absorbing provides a kind of degradable biomedical material, promptly the invention provides a kind of novel thermoplastic polyurethane elastomer and synthetic method of containing the poly-polypeptide block of polyethers with good biodegradability properties and biocompatibility.
Its preparation process totally three the step as follows:
1) preparation of amino acid-N-carboxyl inner-acid anhydride (NCA)
Amino acid and derivative and two (trichloromethyl) carbonic ether thereof and solvent anhydrous tetrahydro furan added be equipped with in the there-necked flask of reflux condensing tube, thermometer, alkali absorption unit, stirring reaction, 25 ℃～65 ℃ reactions of temperature, the time is 0.5～6 hour.After the question response suspension liquid becomes clarification, inflated with nitrogen 1-2 hour, to remove hydrogenchloride and the remaining phosgene that generates in the reaction process.Cooling and concentration of reaction solution, the dry oil ether of pouring 1: 10～1: 15 excessive volume ratio into precipitates, and places 12h down, filters to such an extent that white, needle-shaped crystals is crude product for-10 ℃～20 ℃.Crude product is amino acid-N-carboxyl inner-acid anhydride (NCA) with the needle crystal that ethyl acetate/petroleum ether (1: 10～1: 15 volume ratio) recrystallization obtains.Productive rate 92%.
Among the above-mentioned preparation method, each seed amino acid and derivative thereof comprise: as γ-benzyl-L-glutamate, and γ-methyl-L-glutamate, γ-ethyl-L-glutamate etc.; Methionin (Lys) and derivative thereof, as ε-carbobenzoxy-(Cbz)-Methionin, ε-tertbutyloxycarbonyl-Methionin, ε-trifluoroacetyl group-Methionin etc.;
Among the above-mentioned preparation method, the preparation of different aminoacids NCA, temperature generally can be controlled in 25 ℃～65 ℃ reactions, and the time is 0.5～6 hour.Inflated with nitrogen 1～2 hour, to remove hydrogenchloride and the remaining phosgene that generates in the reaction process, different aminoacids NCA uses anhydrous ethyl acetate/dry oil ether (1: 10～1: 15 volume ratio) respectively, and recrystallization repeatedly, fusing point conforms to literature value, and ultimate analysis measured value and theoretical value differ less than 3 ‰.
2) the amino poly-peptide of prepolymer end-poly-peptide three block prepolymers preparation of b-polytetrahydrofuran-b-
To hold amino polytetrahydrofuran macromole evocating agent to add in the flask, vacuum-drying is 2～12 hours under 40 ℃～140 ℃ following vacuum-dryings, is cooled to 20～25 ℃ then.Under anhydrous and protection of inert gas; with anhydrous N; dinethylformamide is a solvent; under vacuum condition, be that macromole evocating agent causes corresponding amino acid whose NCA ring-opening polymerization with the amino polytetrahydrofuran of different molecular weight end; reaction times is 3～12 hours, forms the poly-peptide of the amino ABA type of end-poly-peptide three block prepolymers of b-polytetrahydrofuran-b-.Molecular weight by the amino polytetrahydrofuran macromole evocating agent in adjustable side and with the molar feed ratio of different aminoacids NCA, can obtain the amino ABA type of the end block prepolymer of different molecular weight and composition thereof.
Among the above-mentioned preparation method, the molecular weight ranges of holding amino polytetrahydrofuran macromole evocating agent is from 800-10000.The amino polytetrahydrofuran polyethers of wherein said end initiator also can be other macromole such as Amino Terminated polyether(ATPE), polyester, polysiloxane, and their molecular weight is identical with the molecular weight ranges of holding amino polytetrahydrofuran macromole evocating agent.
Among the above-mentioned preparation method, the molar feed ratio example of holding amino polytetrahydrofuran and NCA is 1: 5 to 1: 200, and polyreaction is controlled in this scope, and the molecular weight of multipolymer can be regulated and control by changing feed ratio.
Among the above-mentioned preparation method, hold amino prepolymer to gather the poly-peptide triblock copolymer of peptide-b-polytetrahydrofuran-b-, wherein the molecular weight ranges of this multipolymer is from 1,800-50,000.
Among the above-mentioned preparation method, hold amino polytetrahydrofuran macromole evocating agent, be cooled to 20～25 ℃ then 40 ℃～140 ℃ following vacuum-dryings 2～12 hours.Holding amino polytetrahydrofuran to cause the NCA ring-opening polymerization time is 3～12 hours, 20 ℃～60 ℃ of range of reaction temperature.
Among the above-mentioned preparation method, hold amino prepolymer to gather in the synthetic method of the poly-peptide triblock copolymer of peptide-b-polytetrahydrofuran-b-two kinds of feeding modes are arranged, promptly in proper order reinforced method and one pot of feeding method, thus, formed the poly-peptide of the amino prepolymer of the end-poly-peptide triblock copolymer of b-polytetrahydrofuran-b-of different structure form.If by the order charging process, the poly-peptide of the amino prepolymer of institute's synthetic end in the step 2-poly-peptide triblock copolymer of b-polytetrahydrofuran-b-, wherein poly-polypeptide block can cause one or both and two or more amino acid-N-carboxyl inner-acid anhydride monomer ring-opening polymerization prepares homopolymerization or the poly-peptide multipolymer of block by the amino polytetrahydrofuran of end.If by one pot of feeding method, the poly-peptide of the amino prepolymer of institute's synthetic end-poly-peptide triblock copolymer of b-polytetrahydrofuran-b-in the step 2, wherein poly-polypeptide block is caused two or more the poly-peptide random copolymers that amino acid-ring-opening polymerization of N-carboxyl inner-acid anhydride monomer prepares by the amino polytetrahydrofuran of end.But these two kinds of methods do not influence the novel thermoplastic polyurethane elastomer agent structure formula that contains the poly-polypeptide block of polyethers.
3) Polyurethane Thermoplastic Elastomer must prepare
2) described in same reactor in, the poly-peptide three block prepolymers of the amino poly-peptide of end-b-polytetrahydrofuran-b-are without separation, according to [NCO]/[NH
2]) mol ratio is 0.5～2.5, and a certain amount of vulcabond was dropwise added in 3～6 hours, continues reaction 6～72 hours again.After reaction finishes, with precipitating in reactant pour volume ratio into 1: 8～1: 15 the ether, filter, vacuum-drying obtains Polyurethane Thermoplastic Elastomer of the present invention.
Among the above-mentioned preparation method, wherein said vulcabond is MDI (MDI), 2, and 4-or 2,6-tolylene diisocyanate (TDI) or its mixture, hexamethylene diisocyanate (HDI) also can be other vulcabond.
Among the above-mentioned preparation method, the mol ratio of isocyanate groups and prepolymer middle-end amino is 0.5～2.5 in the wherein said vulcabond.
Among the above-mentioned preparation method, after prepolymer generates, directly add di-isocyanate reaction.This Polyurethane Thermoplastic Elastomer is at 20 ℃～60 ℃, and is reinforced by order, and employing is held amino poly-peptide-poly-peptide three block prepolymers not separated " one kettle way " of b-polytetrahydrofuran-b-to synthesize and obtained.
4) Polyurethane Thermoplastic Elastomer must prepare
The 3rd step also can be replaced with by the 4th step, according to [NCO]/[NH
2]) mol ratio is 2, a certain amount of vulcabond dropwise added vulcabond carry out end-blocking in 3～6 hours, reacts after 3～12 hours, adds chainextender BDO or PTHF-1000 again, continues reaction 6～72 hours.Pour reactant into volume ratio and precipitated in the ether in 1: 8～1: 15, filter, vacuum-drying obtains Polyurethane Thermoplastic Elastomer of the present invention.
Among the above-mentioned preparation method, wherein said vulcabond is MDI (MDI), 2, and 4-or 2,6-tolylene diisocyanate (TDI) or its mixture, hexamethylene diisocyanate (HDI) also can be other vulcabond.
Among the above-mentioned preparation method, the mol ratio of isocyanate groups and prepolymer middle-end amino is 2 in the wherein said vulcabond.Mol ratio is 0.5～2.5 in wherein said vulcabond and the chainextender.
Among the above-mentioned preparation method, after prepolymer generates, directly add di-isocyanate reaction.This Polyurethane Thermoplastic Elastomer is at 20 ℃～60 ℃, and is reinforced by order, and employing is held amino poly-peptide-poly-peptide three block prepolymers not separated " one kettle way " of b-polytetrahydrofuran-b-to synthesize and obtained.
The key distinction of the 3rd step with the 4th step is: whether use chainextender.The 3rd step was not used chainextender, [NCO]/[NH
2]) mol ratio is 0.5～2.5; And the 4th step used BDO or PTHF-1000 as chainextender, [NCO]/[NH
2]) mol ratio is 2, but can't change a kind of body portion minor that contains the thermoplastic elastomer of the poly-polypeptide block of polyethers like this.
With poly-(γ-phenmethyl-L-glutamate) the three block prepolymers of amino poly-(γ-phenmethyl-L-the glutamate)-b-polytetrahydrofuran-b-of following end is that example is narrated concrete implementation step:
Hold amino prepolymer:
In the formula: B=OCH
2CH
2CH
2CH
2R=CH
2CH
2COOCH
2C
6H
5
M is 10-200; N is 10-400
Below for containing the body portion minor that polyethers gathers the thermoplastic elastomer of polypeptide block:
R=CH
2CH
2COOCH
2C
6H
5M is 10-200; N is 10-400; Y is 5-100
This molecular formula is the body portion minor of this invention; different according to macromole evocating agent, amino acid N CA, different hydrogen acid ether and chainextender wherein; molecular formula has partial adjustment, but can not influence the molecule agent structure, all will be considered as within protection scope of the present invention.
Mainly can develop molecular formula and be (1)
R=CH
2CH
2COOCH
2C
6H
5M is 10-200; N is 10-400; X is 5-100
Mainly can develop molecular formula and be (2)
R=CH
2CH
2COOCH
2C6H5 m is 10-200; N is 10-400; Z is 5-100
Mainly can develop molecular formula and be (3)
R=CH
2CH
2COOCH
2C
6H
5M is 10-200; N is 10-400; Y ' is 5-100
In the formula: m; N; X; Y; Z; Y ' is a polymerization degree index
Figure of description
Fig. 1 preparation process 1
Fig. 2 preparation process 2
Fig. 3 preparation process 3
Fig. 4 preparation process 4 replacement step 3
A kind of Polyurethane Thermoplastic Elastomer body portion minor that contains the poly-polypeptide block of polyethers of Fig. 5
A kind of Polyurethane Thermoplastic Elastomer body portion minor evolution molecular formula 1 that contains the poly-polypeptide block of polyethers of Fig. 6
A kind of Polyurethane Thermoplastic Elastomer body portion minor evolution molecular formula 2 that contains the poly-polypeptide block of polyethers of Fig. 7
A kind of Polyurethane Thermoplastic Elastomer body portion minor evolution molecular formula 3 that contains the poly-polypeptide block of polyethers of Fig. 8
Embodiment
Embodiment one
The preparation of 1L-glutamic acid gamma-benzyl ester-N-carboxyl inner-acid anhydride (BLG-NCA)
With 8gL-glutamic acid gamma-benzyl ester, 4.0g three surpalites and the adding of 100mL anhydrous tetrahydro furan are equipped with in the 250mL there-necked flask of reflux condensing tube, thermometer, alkali absorption unit, are warming up to 60 ℃ under stirring.After the question response suspension liquid became clarification, inflated with nitrogen 120min was to remove hydrogenchloride and the remaining phosgene that generates in the reaction process.Cooling and concentration of reaction solution are poured in the excessive sherwood oil, place 12h down, filter to such an extent that white, needle-shaped crystals is crude product for-20 ℃.The needle crystal that crude product is obtained with recrystallization from ethyl acetate/petroleum ether is L-glutamic acid gamma-benzyl ester-N-carboxyl inner-acid anhydride (BLG-NCA).
The amino poly-γ-benzyl of the 2 prepolymer ends-poly-γ-benzyl of L-glutamate-b-polytetrahydrofuran-b--L-glutamate preparation
Hold amino polytetrahydrofuran to add in the flask 1.253g,, be cooled to room temperature then 60 ℃ of following vacuum-dryings 6 hours.Under anhydrous and protection of inert gas, will contain the N of 3g γ-benzyl-L-L-glutamic acid-N-carboxyl inner-acid anhydride (BLG-NCA), dinethylformamide (DMF) solution joins in the flask.Continuously stirring reaction at room temperature 3 hours.
3 Polyurethane Thermoplastic Elastomer must prepare
Slowly drip the DMF solution that contains 0.259g MDI in above-mentioned reaction flask, the continuously stirring reaction is 24 hours under the room temperature, then reactant is poured in the ether, obtains Polyurethane Thermoplastic Elastomer.
Embodiment two
The preparation of 1L-glutamic acid gamma-methyl esters-N-carboxyl inner-acid anhydride (MLG-NCA)
With 8gL-glutamic acid gamma-methyl esters, 4.0g three surpalites and the adding of 100mL anhydrous tetrahydro furan are equipped with in the 250mL there-necked flask of reflux condensing tube, thermometer, alkali absorption unit, are warming up to 60 ℃ under stirring.After the question response suspension liquid became clarification, inflated with nitrogen 120min was to remove hydrogenchloride and the remaining phosgene that generates in the reaction process.Cooling and concentration of reaction solution are poured in the excessive sherwood oil, place 12h down, filter to such an extent that white, needle-shaped crystals is crude product for-20 ℃.The needle-like crystal that crude product is obtained with recrystallization from ethyl acetate/petroleum ether is reaction product L-glutamic acid gamma-methyl esters-N-carboxyl inner-acid anhydride (MLG-NCA).
The amino poly-γ-methyl of the 2 prepolymer ends-poly-γ-methyl of L-glutamate-b-polytetrahydrofuran-b--L-glutamate preparation
Hold amino polytetrahydrofuran to be added in the flask 1.175g,, be cooled to room temperature then 60 ℃ of vacuum-dryings 6 hours.Under anhydrous and protection of inert gas, the DMF solution that will contain 2.0g γ-methyl-L-L-glutamic acid-N-carboxyl inner-acid anhydride (MLG-NCA) adds in the flask.Continuously stirring reaction at room temperature 3 hours.
The preparation of 3 Polyurethane Thermoplastic Elastomer
Slowly drip the DMF solution that contains 0.267g MDI in above-mentioned reaction flask, the continuously stirring reaction is 24 hours under the room temperature, then reactant is poured in the ether, obtains Polyurethane Thermoplastic Elastomer.
Embodiment three
The amino poly-γ-benzyl of the 1 prepolymer end-poly-γ-benzyl of L-glutamate-b-polytetrahydrofuran-b--L-glutamate preparation
Hold amino polytetrahydrofuran to join in the flask 1.253g,, naturally cool to room temperature then 60 ℃ of vacuum-dryings 6 hours.Under anhydrous and protection of inert gas, the DMF solution that will contain 3.0g γ-benzyl-L-L-glutamic acid-N-carboxyl inner-acid anhydride (BLG-NCA) joins in the flask.Continuously stirring reaction at room temperature 3 hours.
The preparation of 2 Polyurethane Thermoplastic Elastomer
Slowly drip the DMF solution that contains 0.191g HDI in above-mentioned reaction flask, the continuously stirring reaction is 24 hours under the room temperature, then reactant is poured in the ether, obtains Polyurethane Thermoplastic Elastomer.
Embodiment four
The amino poly-γ-methyl of the 1 prepolymer end-poly-γ-methyl of L-glutamate-b-polytetrahydrofuran-b--L-glutamate preparation
Hold amino polytetrahydrofuran to be added in the flask 1.176g,, naturally cool to room temperature 60 ℃ of vacuum-dryings 6 hours.Under anhydrous and protection of inert gas, will contain the N of 2.0g γ-methyl-L-L-glutamic acid-N-carboxyl inner-acid anhydride (MLG-NCA), dinethylformamide solution adds in the flask.Under room temperature, stirring, successive reaction 3 hours.
The preparation of 2 Polyurethane Thermoplastic Elastomer
Slowly drip the DMF solution that contains 0.179g HDI in above-mentioned reaction flask, the continuously stirring reaction is 24 hours under the room temperature, then reactant is poured in the ether, obtains Polyurethane Thermoplastic Elastomer.
Embodiment five
The amino poly-γ-benzyl of the 1 prepolymer end-poly-γ-benzyl of L-glutamate-b-polytetrahydrofuran-b--L-glutamate preparation
Hold amino polytetrahydrofuran to join in the flask 1.256g,, naturally cool to room temperature then 60 ℃ of vacuum-dryings 6 hours.Under anhydrous and protection of inert gas, the DMF solution that will contain 3.0g γ-benzyl-L-L-glutamic acid-N-carboxyl inner-acid anhydride (BLG-NCA) adds in the flask.Under room temperature, stirring, successive reaction 3 hours.
The preparation of 2 Polyurethane Thermoplastic Elastomer
Slowly drip the DMF solution that contains 0.571g MDI in the bottle slightly in above-mentioned reaction, under room temperature, stirring, reacted 3 hours.Dropwise add then and contain 0.103g chainextender 1, the DMF solution of 4-butyleneglycol (BDO), stirring reaction is 24 hours under the room temperature, at last reactant is poured in the ether, obtains Polyurethane Thermoplastic Elastomer.
Embodiment six
The amino poly-γ-methyl of the 1 prepolymer end-poly-γ-methyl of L-glutamate-b-polytetrahydrofuran-b--L-glutamate preparation
Hold amino polytetrahydrofuran to join in the flask 0.735g, naturally cool to room temperature after 6 hours 60 ℃ of vacuum-dryings.Under anhydrous and protection of inert gas, the DMF solution that will contain 2.5g γ-methyl-L-L-glutamic acid-N-carboxyl inner-acid anhydride (MLG-NCA) adds in the flask.Under room temperature, stirring, successive reaction 3 hours.
The preparation of 2 Polyurethane Thermoplastic Elastomer
In above-mentioned reaction flask, slowly drip the DMF solution that contains 0.335g MDI, reaction is 3 hours under the stirring at room, dropwise add then and contain 0.061g chainextender 1, the DMF solution of 4-butyleneglycol (BDO), stirring at room reaction 24 hours, at last reactant is poured in the ether, obtained Polyurethane Thermoplastic Elastomer.
Embodiment seven
The amino poly-γ-benzyl of the 1 prepolymer end-poly-γ-benzyl of L-glutamate-b-polytetrahydrofuran-b--L-glutamate preparation
Hold amino polytetrahydrofuran to be added in the flask 1.254g, naturally cool to room temperature after 6 hours 60 ℃ of vacuum-dryings.Under anhydrous and protection of inert gas, the DMF solution that will contain 3.0g γ-benzyl-L-L-glutamic acid-N-carboxyl inner-acid anhydride (BLG-NCA) adds in the dk flask.Under room temperature, stirring, successive reaction 3 hours.
The preparation of 2 Polyurethane Thermoplastic Elastomer
Slowly drip the DMF solution that contains 0.570g MDI in above-mentioned reaction flask, reaction is 3 hours under the stirring at room.Dropwise add the DMF solution that contains 1.140g chainextender polytetrahydrofuran-1000 (PTHF-1000) then, stirring at room reaction 24 hours is poured reactant in the ether at last, obtains Polyurethane Thermoplastic Elastomer.
Embodiment eight
The amino poly-γ-methyl of the 1 prepolymer end-poly-γ-methyl of L-glutamate-b-polytetrahydrofuran-b--L-glutamate preparation
Hold amino polytetrahydrofuran to join in the flask 1.469g, naturally cool to room temperature after 6 hours 60 ℃ of vacuum-dryings.Under anhydrous and protection of inert gas, the solution of weighing in the hand that will contain 2.5g γ-methyl-L-L-glutamic acid-N-carboxyl inner-acid anhydride (MLG-NCA) joins in the flask.Under room temperature, stirring, successive reaction 3 hours.
The preparation of 2 Polyurethane Thermoplastic Elastomer
In above-mentioned reaction flask, slowly drip the DMF solution that contains 0.334g MDI, reaction is 3 hours under the stirring at room, dropwise add the DMF solution that contains 1.335g chainextender polytetrahydrofuran 1000 (PTHF-1000) then, stirring at room reaction 24 hours, at last reactant is poured in the ether, obtained Polyurethane Thermoplastic Elastomer.
Claims (1)
1. one kind contains the synthetic method that polyethers gathers the Polyurethane Thermoplastic Elastomer of polypeptide block, it is characterized in that its building-up process comprises:
1) with the anhydrous tetrahydro furan is solvent, amino acid and derivative and two (trichloromethyl) carbonate reaction thereof are generated amino acid-N-carboxyl inner-acid anhydride, product precipitates with the dry oil ether of 1: 10～1: 15 volume ratio then, use the ethyl acetate and the sherwood oil recrystallization of 1: 10～1: 15 volume ratio again, filter, 20～25 ℃ of vacuum-dryings, get product, productive rate 92%, wherein, described amino acid and derivative thereof are γ-benzyl-L-glutamate, γ-methyl-L-glutamate, γ-ethyl-L-glutamate, ε-carbobenzoxy-(Cbz)-Methionin, ε-tertbutyloxycarbonyl-Methionin or ε-trifluoroacetyl group-Methionin;
2) utilize the amino polytetrahydrofuran macromole evocating agent of end to cause described amino acid-N-carboxyl inner-acid anhydride ring-opening polymerization, reaction times is 3～12 hours, form the poly-peptide of the amino ABA type of end-poly-peptide three block prepolymers of b-polytetrahydrofuran-b-, wherein, the molecular weight ranges of the amino polytetrahydrofuran macromole evocating agent of described end is 800～10,000, holding the molar feed ratio example of amino polytetrahydrofuran macromole evocating agent and amino acid-N-carboxyl inner-acid anhydride is 1: 5 to 1: 200;
3) 2) described in the poly-peptide of the amino ABA type of end-poly-peptide three block prepolymers of b-polytetrahydrofuran-b-without separation, according to [NCO]/[NH
2] mol ratio is 0.5～2.5, and a certain amount of vulcabond was dropwise added in 3～6 hours, continues reaction 6～72 hours again, after reaction finishes,, filter precipitating in reactant pour volume ratio into 1: 8～1: 15 the ether, vacuum-drying obtains Polyurethane Thermoplastic Elastomer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100986707A CN100558781C (en) | 2006-07-12 | 2006-07-12 | A kind of Polyurethane Thermoplastic Elastomer and synthetic method that contains the poly-polypeptide block of polyethers |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100986707A CN100558781C (en) | 2006-07-12 | 2006-07-12 | A kind of Polyurethane Thermoplastic Elastomer and synthetic method that contains the poly-polypeptide block of polyethers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1900134A CN1900134A (en) | 2007-01-24 |
| CN100558781C true CN100558781C (en) | 2009-11-11 |
Family
ID=37656139
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2006100986707A Expired - Fee Related CN100558781C (en) | 2006-07-12 | 2006-07-12 | A kind of Polyurethane Thermoplastic Elastomer and synthetic method that contains the poly-polypeptide block of polyethers |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100558781C (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101792528B (en) * | 2010-01-20 | 2011-10-19 | 章云祥 | Polyurethane with corrodible surface, preparation method and application thereof |
| CN102181061B (en) * | 2011-03-20 | 2012-09-12 | 山东理工大学 | Polyurethane-polypeptide graft copolymer and preparation method thereof |
| CN102181060B (en) * | 2011-03-20 | 2012-09-12 | 山东理工大学 | Polyvinyl alcohol-polypeptide-polyethylene glycol graft copolymer and preparation method thereof |
| CN109206620B (en) * | 2017-07-06 | 2021-08-20 | 香港理工大学深圳研究院 | Bionic water response shape memory polyamino acid material and preparation method thereof |
| CN109206612B (en) * | 2017-07-06 | 2021-06-04 | 香港理工大学深圳研究院 | Bionic spider silk polyamino acid biological elastomer material and preparation method thereof |
| CN109594324A (en) * | 2018-10-29 | 2019-04-09 | 赵建平 | A kind of crease proofing agent |
| CN111040422A (en) * | 2019-12-03 | 2020-04-21 | 东莞市雄林新材料科技股份有限公司 | Skin-feel TPU film and preparation method thereof |
| CN115612049A (en) * | 2021-07-16 | 2023-01-17 | 上海凯赛生物技术股份有限公司 | Spider silk structure-imitating compound and preparation method and application thereof |
-
2006
- 2006-07-12 CN CNB2006100986707A patent/CN100558781C/en not_active Expired - Fee Related
Non-Patent Citations (4)
| Title |
|---|
| Arg-Gly-Asp Peptides in Polyurethane: Design,Synthesis,and Characterization. Siew Peng Ho, Dustin H. O. Britton.Advanced Materials,Vol.6 No.2. 1994 |
| Arg-Gly-Asp Peptides in Polyurethane: Design,Synthesis,and Characterization. Siew Peng Ho, Dustin H. O. Britton.Advanced Materials,Vol.6 No.2. 1994 * |
| Synthesis of copolymers of poly(aminoacid)-urethane inN,N-dimethylformamide. S. Uchida, T. Oohori, T. Tanaka, M. Suzuki, H.Shirai.Polymer,Vol.41 . 2000 |
| Synthesis of copolymers of poly(aminoacid)-urethane inN,N-dimethylformamide. S. Uchida, T. Oohori, T. Tanaka, M. Suzuki, H.Shirai.Polymer,Vol.41. 2000 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1900134A (en) | 2007-01-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100558781C (en) | A kind of Polyurethane Thermoplastic Elastomer and synthetic method that contains the poly-polypeptide block of polyethers | |
| Winnacker et al. | Poly (ester amide) s: recent insights into synthesis, stability and biomedical applications | |
| Katsarava et al. | Amino acid‐based bioanalogous polymers. Synthesis, and study of regular poly (ester amide) s based on bis (α‐amino acid) α, ω‐alkylene diesters, and aliphatic dicarboxylic acids | |
| US8551519B2 (en) | Bioabsorbable surgical articales or components thereof | |
| CN101654508A (en) | Degradable and nontoxic medical polyurethane material and preparation method thereof | |
| US8911720B2 (en) | Poly(diol citrate) elastomers | |
| US5665831A (en) | Biocompatible block copolymer | |
| US20080140185A1 (en) | Biodegradable and Biocompatible Peg-Based Poly(Ester-Urethanes) | |
| EP0768329B1 (en) | High strength, melt processable, lactide-rich, poly(lactide-co-p-dioxanone) copolymers | |
| US9364442B2 (en) | Biodegradable phase separated segmented multi block co-polymers and release of biologically active polypeptides | |
| US5696178A (en) | Absorbable polyalkylene diglycolates | |
| US5321113A (en) | Copolymers of an aromatic anhydride and aliphatic ester | |
| CN102181061B (en) | Polyurethane-polypeptide graft copolymer and preparation method thereof | |
| JP2005533148A (en) | Biodegradable phase-separated segmented multiblock copolymer | |
| MXPA97001690A (en) | Mixtures containing polyoxamides absorbib | |
| JPH1053642A (en) | Absorbable polyoxaester | |
| CN101215377A (en) | Aliphatic polyester-polyamino acid Y-type three-arm block copolymers and synthetic method thereof | |
| CN100365043C (en) | Synthesis of ABA polypeptide -b- polytetrahydrofuran-b-polypeptide triblock copolymer | |
| US20050106120A1 (en) | Polyester containing active drugs and having amino acids in the main chain & comma; and its preparation method | |
| Liu | New biodegradable Polymers from renewable resources | |
| CN114685753B (en) | Tissue regeneration promoting type bi-component medical adhesive as well as preparation method and application thereof | |
| CN107033337A (en) | A kind of functional poly ester polyurethane alternate copolymer and its preparation and application | |
| CN101099867A (en) | Novel material compound for polyurethane macromolecular prodrug and preparation method | |
| Gigli | Novel etheroatom containing aliphatic polyesters for biomedical and environmental applications | |
| Lips et al. | Degradable aliphatic poly (ester amide) s |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| C17 | Cessation of patent right | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20091111 Termination date: 20100712 |