CN110527075A - A kind of preparation method for remembering biological support for the biodegradable body temperature inductive material of 4D printing and the induction of degradable body temperature - Google Patents
A kind of preparation method for remembering biological support for the biodegradable body temperature inductive material of 4D printing and the induction of degradable body temperature Download PDFInfo
- Publication number
- CN110527075A CN110527075A CN201910860265.1A CN201910860265A CN110527075A CN 110527075 A CN110527075 A CN 110527075A CN 201910860265 A CN201910860265 A CN 201910860265A CN 110527075 A CN110527075 A CN 110527075A
- Authority
- CN
- China
- Prior art keywords
- body temperature
- preparation
- biodegradable
- norbornene
- inductive material
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims abstract description 83
- 230000036760 body temperature Effects 0.000 title claims abstract description 82
- 238000007639 printing Methods 0.000 title claims abstract description 62
- 238000002360 preparation method Methods 0.000 title claims abstract description 56
- 230000001939 inductive effect Effects 0.000 title claims abstract description 52
- 230000006698 induction Effects 0.000 title claims abstract description 18
- -1 norbornene small molecule Chemical class 0.000 claims abstract description 56
- 238000006243 chemical reaction Methods 0.000 claims abstract description 48
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 claims abstract description 35
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 21
- 230000009477 glass transition Effects 0.000 claims abstract description 20
- 229920002521 macromolecule Polymers 0.000 claims abstract description 18
- 150000003384 small molecules Chemical class 0.000 claims abstract description 17
- 238000002844 melting Methods 0.000 claims abstract description 11
- 230000008018 melting Effects 0.000 claims abstract description 11
- 239000000178 monomer Substances 0.000 claims description 41
- 238000000034 method Methods 0.000 claims description 32
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical group ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 28
- 238000007789 sealing Methods 0.000 claims description 28
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 27
- 239000003999 initiator Substances 0.000 claims description 27
- 239000002904 solvent Substances 0.000 claims description 27
- 229920001577 copolymer Polymers 0.000 claims description 22
- 229920005862 polyol Polymers 0.000 claims description 17
- 150000003077 polyols Chemical class 0.000 claims description 17
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical group ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 15
- 239000003054 catalyst Substances 0.000 claims description 14
- 238000012545 processing Methods 0.000 claims description 14
- BIMKUWCEBYOHHG-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol;3-sulfanylpropanoic acid Chemical class OC(=O)CCS.OCC(CO)(CO)CO BIMKUWCEBYOHHG-UHFFFAOYSA-N 0.000 claims description 12
- 239000002202 Polyethylene glycol Substances 0.000 claims description 12
- 229920001223 polyethylene glycol Polymers 0.000 claims description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 11
- 229920001610 polycaprolactone Polymers 0.000 claims description 11
- 239000004632 polycaprolactone Substances 0.000 claims description 11
- 230000008569 process Effects 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims description 11
- 229920000570 polyether Polymers 0.000 claims description 10
- RKDVKSZUMVYZHH-UHFFFAOYSA-N 1,4-dioxane-2,5-dione Chemical compound O=C1COC(=O)CO1 RKDVKSZUMVYZHH-UHFFFAOYSA-N 0.000 claims description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 9
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 9
- 125000004122 cyclic group Chemical group 0.000 claims description 9
- 229910052698 phosphorus Inorganic materials 0.000 claims description 9
- 239000011574 phosphorus Substances 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 8
- 238000007334 copolymerization reaction Methods 0.000 claims description 7
- KOUKXHPPRFNWPP-UHFFFAOYSA-N pyrazine-2,5-dicarboxylic acid;hydrate Chemical compound O.OC(=O)C1=CN=C(C(O)=O)C=N1 KOUKXHPPRFNWPP-UHFFFAOYSA-N 0.000 claims description 7
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 7
- SORGMJIXNUWMMR-UHFFFAOYSA-N lanthanum(3+);propan-2-olate Chemical compound [La+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SORGMJIXNUWMMR-UHFFFAOYSA-N 0.000 claims description 6
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 6
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical group [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- 229920000858 Cyclodextrin Polymers 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 4
- 230000035484 reaction time Effects 0.000 claims description 4
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 150000005846 sugar alcohols Chemical class 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 239000012299 nitrogen atmosphere Substances 0.000 claims description 2
- OTEKOJQFKOIXMU-UHFFFAOYSA-N 1,4-bis(trichloromethyl)benzene Chemical compound ClC(Cl)(Cl)C1=CC=C(C(Cl)(Cl)Cl)C=C1 OTEKOJQFKOIXMU-UHFFFAOYSA-N 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims 1
- 238000010792 warming Methods 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 7
- 230000008901 benefit Effects 0.000 abstract description 7
- 230000005764 inhibitory process Effects 0.000 abstract description 7
- 239000001301 oxygen Substances 0.000 abstract description 7
- 229910052760 oxygen Inorganic materials 0.000 abstract description 7
- 238000011084 recovery Methods 0.000 abstract description 6
- 230000015556 catabolic process Effects 0.000 abstract description 5
- 230000006835 compression Effects 0.000 abstract description 5
- 238000007906 compression Methods 0.000 abstract description 5
- 238000006731 degradation reaction Methods 0.000 abstract description 5
- 230000009467 reduction Effects 0.000 abstract description 3
- 239000011800 void material Substances 0.000 abstract 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 42
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 229920000642 polymer Polymers 0.000 description 11
- 238000010146 3D printing Methods 0.000 description 10
- 239000000376 reactant Substances 0.000 description 10
- YFHICDDUDORKJB-UHFFFAOYSA-N trimethylene carbonate Chemical compound O=C1OCCCO1 YFHICDDUDORKJB-UHFFFAOYSA-N 0.000 description 10
- 239000002244 precipitate Substances 0.000 description 9
- 210000004204 blood vessel Anatomy 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 6
- MZRQZJOUYWKDNH-UHFFFAOYSA-N diphenylphosphoryl-(2,3,4-trimethylphenyl)methanone Chemical class CC1=C(C)C(C)=CC=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MZRQZJOUYWKDNH-UHFFFAOYSA-N 0.000 description 6
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 238000000016 photochemical curing Methods 0.000 description 6
- 238000004132 cross linking Methods 0.000 description 5
- 238000013461 design Methods 0.000 description 5
- 238000005516 engineering process Methods 0.000 description 5
- 238000001125 extrusion Methods 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000006166 lysate Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000007246 mechanism Effects 0.000 description 4
- 238000007146 photocatalysis Methods 0.000 description 4
- 230000001699 photocatalysis Effects 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 229920000431 shape-memory polymer Polymers 0.000 description 4
- 238000007493 shaping process Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 230000002792 vascular Effects 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229920006237 degradable polymer Polymers 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 230000005284 excitation Effects 0.000 description 3
- ZQTYQMYDIHMKQB-UHFFFAOYSA-N exo-norborneol Chemical group C1CC2C(O)CC1C2 ZQTYQMYDIHMKQB-UHFFFAOYSA-N 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 239000012467 final product Substances 0.000 description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- ZKJNETINGMOHJG-GGWOSOGESA-N (e)-1-[(e)-prop-1-enoxy]prop-1-ene Chemical compound C\C=C\O\C=C\C ZKJNETINGMOHJG-GGWOSOGESA-N 0.000 description 2
- 208000024172 Cardiovascular disease Diseases 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- WRLRISOTNFYPMU-UHFFFAOYSA-N [S].CC1=CC=CC=C1 Chemical compound [S].CC1=CC=CC=C1 WRLRISOTNFYPMU-UHFFFAOYSA-N 0.000 description 2
- FYGUSUBEMUKACF-UHFFFAOYSA-N bicyclo[2.2.1]hept-2-ene-5-carboxylic acid Chemical compound C1C2C(C(=O)O)CC1C=C2 FYGUSUBEMUKACF-UHFFFAOYSA-N 0.000 description 2
- 229920002988 biodegradable polymer Polymers 0.000 description 2
- 239000004621 biodegradable polymer Substances 0.000 description 2
- 239000008280 blood Substances 0.000 description 2
- 210000004369 blood Anatomy 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 239000004567 concrete Substances 0.000 description 2
- 210000004351 coronary vessel Anatomy 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- JBFHTYHTHYHCDJ-UHFFFAOYSA-N gamma-caprolactone Chemical compound CCC1CCC(=O)O1 JBFHTYHTHYHCDJ-UHFFFAOYSA-N 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000002513 implantation Methods 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- 230000006386 memory function Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 2
- 238000006552 photochemical reaction Methods 0.000 description 2
- 229920000747 poly(lactic acid) Polymers 0.000 description 2
- 239000004626 polylactic acid Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000010526 radical polymerization reaction Methods 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- KKJUPNGICOCCDW-UHFFFAOYSA-N 7-N,N-Dimethylamino-1,2,3,4,5-pentathiocyclooctane Chemical compound CN(C)C1CSSSSSC1 KKJUPNGICOCCDW-UHFFFAOYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- 102400001284 Vessel dilator Human genes 0.000 description 1
- 239000003377 acid catalyst Substances 0.000 description 1
- 150000001263 acyl chlorides Chemical class 0.000 description 1
- 238000002399 angioplasty Methods 0.000 description 1
- 239000002473 artificial blood Substances 0.000 description 1
- 108010090012 atrial natriuretic factor prohormone (31-67) Proteins 0.000 description 1
- 230000006399 behavior Effects 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000003519 biomedical and dental material Substances 0.000 description 1
- 238000009954 braiding Methods 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical class ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 1
- 238000012650 click reaction Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000005138 cryopreservation Methods 0.000 description 1
- 238000001723 curing Methods 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- KZNICNPSHKQLFF-UHFFFAOYSA-N dihydromaleimide Natural products O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 238000010109 expendable mold casting Methods 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000001976 improved effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 1
- 230000003902 lesion Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000012567 medical material Substances 0.000 description 1
- CXHHBNMLPJOKQD-UHFFFAOYSA-N methyl hydrogen carbonate Chemical compound COC(O)=O CXHHBNMLPJOKQD-UHFFFAOYSA-N 0.000 description 1
- 230000002073 mitogenetic effect Effects 0.000 description 1
- 239000002114 nanocomposite Substances 0.000 description 1
- 125000003518 norbornenyl group Chemical group C12(C=CC(CC1)C2)* 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 239000012781 shape memory material Substances 0.000 description 1
- 230000000192 social effect Effects 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 230000008093 supporting effect Effects 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- QVTVDJWJGGEOGX-UHFFFAOYSA-N urea;cyanide Chemical compound N#[C-].NC(N)=O QVTVDJWJGGEOGX-UHFFFAOYSA-N 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
- A61L31/04—Macromolecular materials
- A61L31/06—Macromolecular materials obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
- A61L31/14—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L31/145—Hydrogels or hydrocolloids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS 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
- A61L31/00—Materials for other surgical articles, e.g. stents, stent-grafts, shunts, surgical drapes, guide wires, materials for adhesion prevention, occluding devices, surgical gloves, tissue fixation devices
- A61L31/14—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L31/148—Materials at least partially resorbable by the body
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B33—ADDITIVE MANUFACTURING TECHNOLOGY
- B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
- B33Y10/00—Processes of additive manufacturing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B33—ADDITIVE MANUFACTURING TECHNOLOGY
- B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
- B33Y70/00—Materials specially adapted for additive manufacturing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B33—ADDITIVE MANUFACTURING TECHNOLOGY
- B33Y—ADDITIVE MANUFACTURING, i.e. MANUFACTURING OF THREE-DIMENSIONAL [3-D] OBJECTS BY ADDITIVE DEPOSITION, ADDITIVE AGGLOMERATION OR ADDITIVE LAYERING, e.g. BY 3-D PRINTING, STEREOLITHOGRAPHY OR SELECTIVE LASER SINTERING
- B33Y80/00—Products made by additive manufacturing
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/06—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
- C08G63/08—Lactones or lactides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/91—Polymers modified by chemical after-treatment
- C08G63/912—Polymers modified by chemical after-treatment derived from hydroxycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/18—Block or graft polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/20—General preparatory processes
- C08G64/30—General preparatory processes using carbonates
- C08G64/305—General preparatory processes using carbonates and alcohols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/42—Chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2230/00—Compositions for preparing biodegradable polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Surgery (AREA)
- Vascular Medicine (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Manufacturing & Machinery (AREA)
- General Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Materials For Medical Uses (AREA)
Abstract
The invention discloses the preparation methods of a kind of biodegradable body temperature inductive material for 4D printing and degradable body temperature induction memory biological support, material preparation method is comprising steps of using end as based on the Biodegradable high-molecular of hydroxyl, preparation end is the multicomponent biodegradable macromolecule of sulfydryl or norbornene;The preparation method of biological support is comprising steps of polyfunctional group sulfydryl small molecule or norbornene small molecule and biodegradable body temperature inductive material print generation norbornene-sulfydryl photopolymerization reaction by 4D and obtain biological support;Biological support is heated to melting temperature or glass transition temperature or more and diametrically compression reduction size, then incudes memory biological support in the fixed temporary shapes of near zero to get degradable body temperature.The present invention have print speed it is fast, without oxygen inhibition and the characteristics of shrinkage-void, have that heat deflection peak width is narrow, it is fast to reply speed, recovery temperature is accurate, takes into account the advantages such as controllable degradation rate.
Description
Technical field
The invention belongs to 4D printed material technical fields, and in particular to a kind of biodegradable body temperature sense for 4D printing
Material and degradable body temperature is answered to incude the preparation method of memory biological support.
Background technique
Cardiovascular disease has become No.1 Health Killer in world wide.Treatment maximally efficient for this disease at present
Means are the intracavitary Balloon Angioplasties of coronary artery (PTCA), i.e., provide radial support to blood vessel using timbering material, prevent again narrow
It is narrow, to achieve the purpose that treatment.The implantation of presently the most common balloon-expandable bracket is that bracket pressure is held on end band
Have on the seal wire of sacculus, sent bracket to Coronary Artery Lesions by foley's tube, then utilizes the pressure expanded release branch of sacculus
Frame.It shows according to statistics, in the annual cardiovascular interventional operation about 2,400,000 in the whole world in 2006, and every year with 40% speed
Degree increases.Therefore, there is very high scientific value and social effect for the exploration of new timbering material and technology.
Intravascular stent experienced revolutionary development three times at present, be first generation bare metal stent, second generation drug respectively
FirebirdTM and third generation biodegradable polymer stent.Discovered in recent years, current most reliable method are using completely may be used
Degradation bracket, after playing a supporting role in a short time, does not leave any metal or polymer, while drug release in human body
It finishes.Thus the concept for proposing Wholly-degradable bracket, is considered as third time revolution in cardiovascular disease interventional therapy.
The implantation of current biodegradable stent can only can be just implanted under the conditions of assisting operation using adminiclies such as sacculus
Human body, operation is highly inconvenient, and surgical procedure is cumbersome, and needs the circumscribed wound of mask placement device larger when treatment.It can drop
Bracket manufacture view is solved, intravascular stent generallys use the modes such as traditional injection molding, braiding, laser processing, and equipment is complicated, technique is multiple
It needs to reject burr after miscellaneous, waste material, molding and forms the problems such as capilary bracket is difficult, personalized customization difficult to realize is set
Meter.3D printing forming technique is the novel digital forming technique for quickly manufacturing arbitrarily complicated 3 dimensional coil geometry object, is had
Precision is high, speed is fast and can flexible design the features such as.Currently, the degradable thermoplastics bio-medical material such as polylactic acid, polycaprolactone
Material has used fused glass pellet method 3D printing to prepare various bio-medical materials.
It 2013, holds in TED (Technology, Entertainment, Design) conference, comes from California, USA
The Skylar Tibbits of the Massachusetts Institute of Technology is first public to demonstrate 4D printing technique.The cardinal principle of 4D printing technique be
On the basis of 3D printing technique, using intelligent alterable shape material (shape-memory material is most widely used) as driving execution unit,
Using the deformability characteristics of material, the design parameter of shaped component, moulding process, deformational behavior and final structure target etc. are believed
Breath is designed into initial configuration.It is stimulated after molding using outfield excitable media, by bending, distortion, expansion etc., self deformation is obtained
Three-dimensional space configuration must be preset, is the innovative technology that a kind of design of integrated products, manufacture, assembly are integrated, i.e. 4D Method of printing.
For degradable polymer bracket presently, there are technical bottleneck problem, newest 4D printing technique can prepare
The intelligentized complete absorbable polymer intravascular stent with shape memory function.Using the blood of 4D printing technique machine-shaping
Pipe holder self deformation such as can expand under the excitation of body temp, be finally reached preset three-dimensional space configuration, make
It can be deformed by self without balloon expandable when being implanted into human body and realize that bracket is bonded with the close stabilization of blood vessel, this
Kind adaptivity can reduce intense impact, reduction vascular wall tearing risk of the balloon expandable process to vascular wall, greatly reduce
The size of circumscribed wound mitigates sufferer pain.Meanwhile forming process is not limited by structural complexity, with classical production process
It compares, it is easier to meet mechanical property and the requirement with medical performance.
There are pertinent literature report and patented technology using 4D printing technique printing shape memory vascular stent material.Specially
Sharp a kind of 201410344228.2 (methods of 4D printing shaping artificial blood vessel bracket) are prepared for shape memory using 3D printing and gather
Object intravascular stent is closed, using fusion sediment 3D printing, intravascular stent does not have degradability.Patent 201410832997.7
(a kind of to can absorb macromolecule intravascular stent and preparation method thereof completely) is prepared for degradable shape memory using melting extrusion 3D
Bracket, the timbering material do not have body temperature induction shape memory function.(one kind is based on 3D printing skill to patent 201610232704.0
The method that art prepares biodegradable polymer self-expanding type blood vessel dilator) it is prepared for gathering cream using melting extrusion formula 3D printing
Acid/ferric oxide nano composite material, shape memory respond temperature close to human body temperature.Patent 201710064389.X (is based on shape
Degradable self expandable 4D intravascular stent of shape memory polyurethane and preparation method thereof) it is prepared for incuding temperature using melting extrusion 3D printing
Spend the Biodegradable Shape-Memory Polyurethane close to human body temperature.(a kind of visualization shape memory is high by patent 201710215735.X
The preparation method of molecule intravascular stent) using six terminal-modified arm degradable macromolecules of photocuring 3D printing double bond it is prepared for blood
Pipe holder, since macromolecular end is the photocatalysis self-polymeric reaction of acrylic double bond, photopolymerization rate is slow, has oxygen inhibition and receipts
The shortcomings that contracting.Document (ACS Appl.Mater.Interfaces, 2017,9,876-883) reports a kind of extrusion posterior photocuring
Mode be prepared for polylactic acid/iron oxide intravascular stent, since preparation process is first to squeeze out to be crosslinked in illumination, preparation process is slow
Slowly, processing step is complicated, and shape memory response temperature is much higher than human body temperature.
The degradable shape memory intravascular stent of achievable 4D printing is largely by melting extrusion 3D printing skill at present
Art preparation, bracket is to be printed by piling up layer by layer, and be not crosslinked mutually, and mechanical property is relatively weak.For current
The intravascular stent of direct photocuring 4D printing is to be prepared by the macromolecular of acrylate end functionalization by photo-crosslinking, due to
The photopolymerization of acrylic acid ester bond, there are chance oxygen inhibitions, and photocuring is incomplete, and extend curing time.In addition, acrylate
Key is an auto polymerization system, is easy to happen gel and occurs to early, and generates stress and concentrates, and can cause sample corrugation and warpage.Step
Increasing sulfydryl-alkene light reaction not only has collaboration photopolymerization reaction and walks the advantage of Propagating Radical polymerization reaction, is also equipped with nothing
Oxygen inhibition, unstressed concentration, the feature that initiator amount is few and polymerization rate is fast.
Light-initiated sulfydryl and can be in the photochemical reaction system of homopolymerization type double bond monomer a chain growth mechanism and by
The photopolymerization reaction that step Growth Mechanism is vied each other, and be simple in sulfydryl and non-homopolymerizing type double bond monomer photochemical reaction system
Gradually mechanism of polymerization.According to the double bond monomer reactivity of click-reaction sequence (J.Am.Chem.Soc.2012,134,
13804-13817), as shown in figure 11, at present only norbornene (Norbornene), vinyl ethers (Vinyl ether) and
The monomer of the minority such as propenyl ether (Propenyl ether) takes simple gradually mechanism of polymerization, and norbornene group
Sulfydryl alkene photopolymer reaction speed is most fast.
In consideration of it, also lacking at present, a kind of shaping speed is fast, prints degradable body temperature sense without oxygen inhibition and shrinkage-free 4D
Answer material and using shape memory intravascular stent made of the material.
Summary of the invention
In order to solve the above problems existing in the present technology, it is an object of that present invention to provide a kind of biologies for 4D printing
The preparation method of degradable body temperature inductive material and degradable body temperature induction memory biological support.
The technical scheme adopted by the invention is as follows:
A kind of preparation method of the biodegradable body temperature inductive material for 4D printing, comprising steps of in physiology temperature
It spends based on the Biodegradable high-molecular that lower end is hydroxyl, by being prepared in life to the processing of body ends sealing endization
Degradable at a temperature of reason, end is the multicomponent biodegradable macromolecule of sulfydryl or norbornene, is printed as 4D
Biodegradable body temperature inductive material use.
Further, the glass transition temperature of the main body or melting temperature are 20 DEG C -40 DEG C.
Further, the preparation method of the main body includes: with D, and L- lactide or caprolactone are main monomer;L- third is handed over
One of ester, caprolactone, glycolide, cyclic acid anhydride, cyclic carbonate ester, cyclic phosphorus or Lanthanum Isopropoxide are a variety of single as copolymerization
Body;Copolymerization obtains multicomponent copolymer after catalyst, initiator effect.
Further, the initiator is dihydroxylic compound, multi-hydroxy compound or oligomer.
Further, the initiator be ethylene glycol, pentaerythrite, small molecule polyhydroxy-alcohol, oligomeric two arms polyethylene glycol,
Multi-arm polyethylene glycol, oligomeric two arms polycaprolactone polyol, multi-arm polycaprolactone polyol, oligomeric two arms polyether polyol, three
Arm polyether polyol, cyclodextrin or sugar alcohol.
Further, the catalyst is stannous octoate.
Further, when the main body that preparation glass transition temperature is 20 DEG C -40 DEG C, the main monomer of use and the matter of comonomer
Score is measured to determine according to formula (1):
TgBased on glass transition temperature;Tg1、Tg2…TgnThe segment vitrifying temperature of respectively each monomer for participating in reaction
Degree;N is the positive integer more than or equal to 2;W1、W2…WnRespectively each monomer for participating in reaction accounts for the quality point of all monomers
Number.
Further, when the main body that preparation glass transition temperature is 20 DEG C -40 DEG C, it is total that the mole of initiator accounts for all monomers
The 0.02mol% of mole.
Further, the molecular weight for the main body that the glass transition temperature is 20 DEG C -40 DEG C is 400-2000.
Further, when preparing the main body that fusing point is 20 DEG C -40 DEG C, the molar ratio of initiator and each monomer is according to
The molecular weight for the main body that fusing point is 20 DEG C -40 DEG C determines.
Further, when preparing the main body that fusing point is 30 DEG C -40 DEG C, initiator amount is the gross weight of all monomers
0.1wt%;The molecular weight of main body is 1000-4000.
Further, the body ends sealing endization processing is norbornene termination process, the norbornene envelope
End processing is comprising steps of it is norborneol that main body, norbornene acyl chlorides and triethylamine solvent, which are mixed reaction end is prepared,
The multicomponent biodegradable macromolecule of alkenyl.
Further, the solvent is methylene chloride;The molar ratio of the norbornene acyl chlorides, triethylamine and main body hydroxyl
For 1.2:1.2:1;Reaction time is 48h;Reaction temperature is room temperature.
Further, the body ends sealing endization processing is sulfydryl termination process, and the sulfydryl termination process includes step
It is rapid: can by main body, thioacetic acid, the catalysts and solvents multicomponent biological that back flow reaction obtains that end is sulfydryl under nitrogen atmosphere
Degraded macromolecular.
Further, in the body ends sealing endization processing, the hydroxyl of the main body and the molar ratio of thioacetic acid are
1:10。
Further, catalyst is a water p-methyl benzenesulfonic acid in the body ends sealing endization processing;One water is to toluene sulphur
The mass fraction that acid accounts for monomer mass is 1wt%;The temperature of the reaction is 120 DEG C -126 DEG C, and the reaction time is for 24 hours.
A kind of biodegradable body temperature inductive material 4D prints the preparation method of degradable body temperature induction memory biological support,
Comprising steps of by the biodegradable body temperature inductive material, solvent, photoinitiator and polyfunctional group sulfydryl small molecule or drop ice
The mixing of piece alkene small molecule is adjusted to be suitble to printing viscosity after, the polyfunctional group sulfydryl small molecule or norbornene small molecule and life
Biodegradable body temperature inductive material obtains biological support after printing generation norbornene-sulfydryl photopolymerization reaction by 4D;It will give birth to
Object bracket is heated to melting temperature or glass transition temperature or more and diametrically compression reduction size, then near zero
Fixed temporary shapes remember biological support to get to the induction of degradable body temperature.
Further, the biological support is intravascular stent, and the print conditions of the 4D printing are ultraviolet ray intensity 30mW/
cm-2;Print speed: 50mm/h, print carriage size: length 40mm, outer diameter 4mm, internal diameter 2mm.
Further, the biodegradable body temperature inductive material is that the multicomponent biological that end is norbornene can drop
Solve macromolecule;The preparation of the biological support includes the following steps: the biodegradable body temperature inductive material, solvent, light
After initiator and the mixing of polyfunctional group sulfydryl small molecule are adjusted to suitable printing viscosity, print to obtain biological support by 4D;Institute
Stating polyfunctional group sulfydryl small molecule is four (3- mercaptopropionic acid) pentaerythritol esters.
Further, the biodegradable body temperature inductive material is the multicomponent biodegradable high score that end is sulfydryl
Son;The preparation of the biological support includes the following steps: the biodegradable body temperature inductive material, solvent, photoinitiator
It is adjusted to the mixing of norbornene small molecule after being suitble to printing viscosity, prints to obtain biological support by 4D;The norbornene
Small molecule is 5- norbornene -2- carboxylic acid trimethylolpropane triester.
Further, the photoinitiator is 2,4,6 (trimethylbenzoyl) diphenyl phosphine oxides;The solvent is three
Chloromethanes;The mass fraction that photoinitiator accounts for each substance gross weight is 0.5wt%.
The invention has the benefit that a kind of biodegradable body temperature inductive material for 4D printing of the invention and can
Degrade body temperature induction memory biological support preparation method, by end be hydroxyl Biodegradable high-molecular based on, lead to
Cross the multicomponent biodegradable macromolecule for the processing of body ends sealing endization being prepared end is sulfydryl or norbornene
The shortcomings that being printed for 4D, contraction can be generated when overcoming traditional 4D printing using acrylate monomer photopolymerization;The present invention
Biological support is small for the multicomponent biodegradable macromolecule and sulfydryl or norbornene of sulfydryl or norbornene by end
Molecule prepares the memory biological support of degradable body temperature induction by norbornene-sulfydryl photocuring printing;This norbornene-
The printing of sulfydryl photocuring have the advantages that shaping speed fastly, without oxygen inhibition and shrinkage-free.Meanwhile with acrylate-based radical polymerization
Conjunction is compared, and the polymer network that norbornene-sulfydryl step increases polymerization formation has regularity, and heat deflection peak width is narrow, shape
It replys faster, the more accurate advantage of recovery temperature, in addition, it can also take into account controllable degradation rate;Biology branch of the invention
Frame such as can expand at self deformation under the excitation of body temp, be finally reached preset three-dimensional space configuration, make its
It can be deformed by self when being implanted into human body without balloon expandable and realize that bracket is bonded with the close stabilization of blood vessel.Due to life
Object bracket has biodegradability, takes out without second operation, can mitigate sufferer pain significantly.
Detailed description of the invention
Fig. 1 is based on norbornene-sulfydryl photopolymerization 4D printing technique printing schematic diagram.
Fig. 2 norbornene blocks the poly- D of four arms, the nucleus magnetic hydrogen spectrum figure of L- lactide.
Fig. 3 sulfydryl blocks the poly- D of four arms, the nucleus magnetic hydrogen spectrum of L- lactide.
Fig. 4 norbornene blocks the poly- D of four arms, and L- lactide and four (3- mercaptopropionic acid) pentaerythritol esters are 10mW/m2's
1~2s forms the schematic diagram of gel under ultraviolet light.
Fig. 5 norbornene blocks the poly- D of four arms, and L- lactide and four (3- mercaptopropionic acid) pentaerythritol esters are crosslinked shape memory
Polymer glass transition area figure (narrow half-peak breadth).
Fig. 6 norbornene blocks the poly- D of four arms, and L- lactide and four (3- mercaptopropionic acid) pentaerythritol esters are crosslinked shape memory
Shape-memory properties figure of the polymer under differently strained.
Fig. 7 norbornene blocks the poly- D of four arms, and L- lactide and four (3- mercaptopropionic acid) pentaerythritol esters are crosslinked shape memory
The memory cycle performance map of polymer.
Fig. 8 norbornene blocks the poly- D of four arms, and L- lactide and four (3- mercaptopropionic acid) pentaerythritol esters are crosslinked shape memory
The shape memory of polymer replys display diagram (1s can be replied in the hot water of glass transition temperature).
Tan δ-temperature curve of Fig. 9 hydroxy-end capped four arms poly- D, L- lactide-co- trimethylene carbonate copolymer.
Figure 10 hydroxy-end capped poly- (caprolactone-co- trimethylene carbonate) melting point curve.
Figure 11 is double bond monomer reactivity precedence diagram in sulfydryl alkene reaction.
Specific embodiment
With reference to the accompanying drawing and specific embodiment does further explaination to the present invention.
A kind of biodegradable body temperature inductive material and the induction memory life of degradable body temperature for 4D printing of the invention
The preparation method of object bracket, preparation method and degradable body temperature induction memory biology including biodegradable body temperature inductive material
Two big technical solutions of preparation method of bracket.It is described as follows respectively:
The preparation method of biodegradable body temperature inductive material is the Biodegradable high-molecular of hydroxyl by using end
(i.e. hydroxy-end capped Biodegradable high-molecular) is basic body material, that preparation can degrade under physiological temp, last
End is the multicomponent biodegradable macromolecule of sulfydryl or norbornene, i.e. the multiple groups of sulfydryl or norbornene sealing end are mitogenetic
Biodegradable macromolecule.The material application prints field to 4D, is the multicomponent biological blocked by sulfydryl or norbornene
The degradable macromolecular that degradable macromolecule is blocked with corresponding two arm or multi-arm norbornene or sulfydryl, in photocatalysis
Under, photocatalysis norbornene-sulfydryl click chemistry reaction occurs and realizes.The biological support as made from the reaction, such as blood vessel
Bracket has shape design and replys the advantage that speed is fast, recovery temperature is more accurate and degradation rate is controllable.
In order to enable biodegradable body temperature inductive material of the invention (the i.e. biological intracorporal maintenance life under physiological temp
Manage movable temperature) it degrades, the present invention is the Biodegradable high-molecular of hydroxyl to the end as material of main part first
Degradable improvement is carried out.
Guarantee especially by the following two kinds mode.First is that by the glass transition temperature of control material of main part at 20 DEG C -40
℃;Second is that being realized by the fusing point for controlling material of main part at 20 DEG C -40 DEG C.
Glass transition temperature of the invention is with D in 20 DEG C -40 DEG C of main body, and L- lactide or caprolactone are main monomer;L-
One of lactide, caprolactone, glycolide, cyclic acid anhydride, cyclic carbonate ester, cyclic phosphorus or Lanthanum Isopropoxide are a variety of as altogether
Polycondensation monomer;Copolymerization obtains multicomponent copolymer after catalyst, initiator effect, and the composition of product is controlled by formula (1)
And molecular weight obtains.Specifically, it is exemplified below:
Using stannous octoate as catalyst, binary or multi-hydroxy compound or oligomer are initiator, with D, L- lactide
For main monomer, in L- lactide, caprolactone, glycolide, cyclic acid anhydride, cyclic carbonate ester, cyclic phosphorus, Lanthanum Isopropoxide etc. one
Kind, two or three the above are comonomers.Anhydrous and oxygen-free reaction is added in reactant needed for will be above-mentioned, initiator and catalyst
Bottle, vacuumizes, and leads to nitrogen, repeatedly for three times.It is reacted for 24 hours under 130 DEG C of oil bath after reaction system sealing.After completion of the reaction, instead
It answers system to be down to room temperature, suitable chloroform lysate is added.Reaction mixture is slowly dropped in cold methanol and is precipitated,
Wherein the volume of methanol is the chloroform soln volume of 5-10 times of reactant, dissolves and precipitates again after filtering, continuous precipitation
Three times, the final product obtained.Wherein, the mole dosage of initiator accounts for the mole percent of all monomer integral molar quantities and is
0.02mol%;The molar ratio of initiator and monomer is calculated according to required molecular weight, and the macromolecular molecular weight finally synthesized is 400
~2000 or so;The proportion of main monomer and comonomer makes its glass transition temperature on 20~40 DEG C of left sides according to FOX equation calculation
The right side, for example, the calculating of three kinds of monomers copolymerization is as follows:
In formula: Tg=34~37 DEG C, shape memory transition temperature is made to be close to human body temperature;Tg1、Tg2And Tg3It is D,
The vitrifying of L- lactide (55-60 DEG C), L- lactide (60-65 DEG C) and Trimethylene Carbonate (- 15 DEG C) three kinds of segments
Temperature;W1、W2And W3It is D, the mass fraction of three kinds of L- lactide, L- lactide and Trimethylene Carbonate segments.
Fusing point of the invention is with D in 20 DEG C -40 DEG C of main body, and L- lactide or caprolactone are main monomer;L- lactide,
One of caprolactone, glycolide, cyclic acid anhydride, cyclic carbonate ester, cyclic phosphorus or Lanthanum Isopropoxide are a variety of as comonomer;
Copolymerization obtains multicomponent copolymer after catalyst, initiator effect, and the molecular weight of the main body finally synthesized by constraint is
1000-4000 or so, and the 0.1wt% for the gross weight that initiator amount is all monomers is controlled to realize.Concrete example is as follows:
Using stannous octoate as catalyst, binary or multi-hydroxy compound or oligomer are initiator, based on caprolactone
Monomer, D, L- lactide, L- lactide, caprolactone, glycolide, cyclic acid anhydride, cyclic carbonate ester, cyclic phosphorus, Lanthanum Isopropoxide etc.
One of, two or three the above are comonomers.Anhydrous and oxygen-free is added in reactant needed for will be above-mentioned, initiator and catalyst
Reaction flask vacuumizes, and leads to nitrogen, repeatedly for three times.It is reacted for 24 hours under 130 DEG C of oil bath after reaction system sealing.End of reaction
Afterwards, reaction system is down to room temperature, and suitable chloroform lysate is added.Reaction mixture is slowly dropped in cold methanol
Precipitating, wherein the volume of methanol is the chloroform soln volume of 5-10 times of reactant, dissolves and precipitates again after filtering, continuously
It precipitates three times, obtained final product.Wherein, initiator amount is the 0.1wt% of (all) monomers;Initiator and monomer
Molar ratio is calculated according to required molecular weight, and the macromolecular molecular weight finally synthesized is 1000~4000 or so, and fusing point is 30~40
℃。
The present invention end be hydroxyl Biodegradable high-molecular carried out degradable improved on the basis of, further into
Row norbornene termination process and sulfydryl termination process, to obtain degradable 4D printed material.Concrete example is as follows:
The synthesis of norbornene sealing end Biodegradable high-molecular is added hydroxy-end capped degradable big in reaction flask
Molecule, norbornene acyl chlorides and triethylamine.Wherein, the molar ratio of norbornene acyl chlorides, triethylamine and hydroxyl is 1.2:1.2:1,
Solvent is dry methylene chloride, reacts at room temperature 48h, filters after the reaction was completed, filtrate is precipitated three times in cold methanol, room temperature
Cryo-conservation is spare after vacuum drying.
The synthesis of sulfydryl sealing end Biodegradable high-molecular takes hydroxy-end capped degradable macromolecular to be placed in connection water segregator
Two mouth flask in, be added 10 times of hydroxyl mole thioacetic acid and monomer mass 1wt% a water Catalyzed by p-Toluenesulfonic Acid
Then solvent is added in agent, lead to nitrogen.Back flow reaction is for 24 hours under the conditions of 120~126 DEG C for reactant.After reaction, cooling, it is molten
Liquid precipitates three times in methyl alcohol, stored refrigerated after room temperature in vacuo is dry.
After the completion of degradable 4D printed material, biological support is prepared by 4D printing.The basic skills of the printing be by
The biodegradable body temperature inductive material, solvent, photoinitiator and polyfunctional group sulfydryl small molecule or norbornene small molecule
Mixing is adjusted to be suitble to printing viscosity after, the polyfunctional group sulfydryl small molecule or norbornene small molecule and biodegradable body
Warm inductive material is printed by 4D, and norbornene-sulfydryl photopolymerization reaction occurs under the catalysis of ultraviolet light;By biological support plus
More than heat to melting temperature or glass transition temperature and diametrically compressing reduces size, then fixed interim near zero
Shape remembers biological support to get to the induction of degradable body temperature.
After the biological support is implanted to human body, it self deformation such as can expand under the excitation of body temp, finally
Reach preset three-dimensional space configuration, make its when being implanted into human body without balloon expandable can by self deform realize bracket with
The close of blood vessel stablizes fitting.
The polymer network of the biological support is the three-dimensional network of crosslinking, has excellent shape memory fixed rate, replys
Rate, memory cycle performance, height can recovery strain and degradabilities.
The printing principle that 4D of the invention prints degradable body temperature induction shape memory intravascular stent is dropped based on photocatalysis
The reaction of bornylene-sulfydryl click chemistry, have the advantages that print speed fastly, without oxygen inhibition and shrinkage-free.It is prepared based on the method
Shape memory vascular stent material have recovery of shape speed it is fast, the more accurate and controllable degradation rate of recovery temperature.
Print conditions after optimization are as follows: the print conditions of the 4D printing are ultraviolet ray intensity 30mW/cm-2;Printing speed
Degree: 50mm/h, print carriage size: length 40mm, outer diameter 4mm, internal diameter 2mm.
The different biodegradable body temperature inductive materials of above-mentioned synthesis can be respectively adopted such as under type, progress 4D
Printing and making biological support.
When biodegradable body temperature inductive material is the multicomponent biodegradable macromolecule that end is norbornene, institute
The preparation for stating biological support includes the following steps: the biodegradable body temperature inductive material, solvent, photoinitiator and more officials
Sulfydryl small molecule can be rolled into a ball and mix to be adjusted to and be suitble to printing viscosity (such as the solid content of solution when printing is made to be maintained at 40% or so)
Afterwards, it prints to obtain biological support by 4D;The polyfunctional group sulfydryl small molecule is four (3- mercaptopropionic acid) pentaerythritol esters.It is excellent
Selection of land, photoinitiator 2,4,6 (trimethylbenzoyl) diphenyl phosphine oxide;Solvent is chloroform;Photoinitiator accounts for respectively
The mass fraction of substance gross weight is 0.5wt%.
When biodegradable body temperature inductive material is the multicomponent biodegradable macromolecule that end is sulfydryl, biological support
Preparation include the following steps: the biodegradable body temperature inductive material, solvent, photoinitiator and norbornene small molecule
After mixing is adjusted to suitable printing viscosity, print to obtain biological support by 4D;The norbornene small molecule is 5- norborneol
Alkene -2- carboxylic acid trimethylolpropane triester.Preferably, photoinitiator 2,4,6 (trimethylbenzoyl) diphenyl phosphine oxides;
Solvent is chloroform;The mass fraction that photoinitiator accounts for each substance gross weight is 0.5wt%.
Embodiment 1
By 0.076mmol stannous octoate, 69.6mmol trimethylene carbonate, 309.6mmol D, L- lactide and
Anhydrous and oxygen-free reaction flask is added in 50mmol pentaerythrite, vacuumizes, and leads to nitrogen, repeatedly for three times.At 130 DEG C after reaction system sealing
Oil bath under react for 24 hours.After completion of the reaction, reaction system is down to room temperature, and suitable chloroform lysate is added.It will reaction
Mixture is slowly dropped in cold methanol and precipitates, and wherein the volume of methanol is the chloroform soln volume of 5-10 times of reactant,
It dissolves and precipitates again after filtering, obtain four hydroxy-end capped arm Poly D,L-lactide-co- trimethylene carbonate copolymers
(Mn=1568;Mw=1770;Tg=34~36 DEG C), the four hydroxy-end capped Sanyas arm Poly D,L-lactide-co- as shown in Figure 9
Tan δ-temperature curve of methyl carbonic acid ester copolymer.
By hydroxy-end capped four arms poly- D, L- lactide-co- trimethylene carbonate copolymer, norbornene acyl chlorides and three
Ethamine is put into there-necked flask.Wherein, the molar ratio of norbornene acyl chlorides, triethylamine and hydroxyl is 1.2:1.2:1, and solvent is dry
Methylene chloride reacts at room temperature 48h, filters after the reaction was completed, and filtrate is precipitated three times in cold methanol, after room temperature in vacuo is dry
Four arms poly- D, the L- lactide-co- trimethylene carbonate copolymer blocked to norbornene.
Using chloroform as solvent, the four arm Poly D,L-lactide-co- trimethylene carbonates copolymerization of norbornene sealing end
Object, four (3- mercaptopropionic acid) pentaerythritol esters, 2,4,6 (trimethylbenzoyl) diphenyl phosphine oxides are uniformly mixed, norborneol
Alkenyl and sulfydryl molar ratio 1:1, photoinitiator mass fraction 0.5wt%.The solid content for adjusting solution is 40%, passes through norborneol
Alkene-sulfydryl Stereolithography printing technique print carriage material, ultraviolet ray intensity 20mW/cm-2;Print carriage size: length
40mm, outer diameter 4mm, internal diameter 2mm;Print speed: 80mm/h.Material glass temperature has 3 DEG C of increase after photo-crosslinking.It will
Printed bracket is heated to 40 DEG C, and diametrical direction compression reduces size, then in the fixed temporary shapes of near zero, can obtain
Shape-memory polymer intravascular stent is incuded to degradable body temperature.
Embodiment 2
Compared with Example 1, in addition to having following difference, remaining is identical for the present embodiment.Different is simply that four
(3- mercaptopropionic acid) pentaerythritol ester replaces with trimethylolpropane tris (3-thiopropionate).
Embodiment 3
Compared with Example 1, in addition to having following difference, remaining is identical for the present embodiment.Different is simply that four
(3- mercaptopropionic acid) pentaerythritol ester replaces with isocyanuric acid three [2- (3- mercaptopropionyl oxygroup) ethyl ester].
Embodiment 4
Compared with Example 1, in addition to having following difference, remaining is identical for the present embodiment.It is not both: by Ji Wusi
Alcohol replaces with 1,4-butanediol, obtains line style Poly D,L-lactide-co- trimethylene carbonate copolymer.In addition, selected
The sulfydryl quantity of polyfunctional group sulfhydryl compound is at least three.
Ethylene glycol, pentaerythrite, small molecule polyhydroxy-alcohol, oligomeric two arms polyethylene glycol, multi-arm polyethylene glycol, oligomeric two arm
Polycaprolactone polyol, multi-arm polycaprolactone polyol, oligomeric two arms polyether polyol, three arm polyether polyol, cyclodextrin or
Sugar alcohol
Embodiment 5
Compared with Example 1, in addition to having following difference, remaining is identical for the present embodiment.It is not both: will
The replacement of 69.6mmol trimethylene carbonate are as follows: the L- lactide or glycolide of 90mmol trimethylene carbonate and 10mmol or
One of cyclic acid anhydride or cyclic phosphorus are a variety of.
Embodiment 6
Compared with Example 1, in addition to having following difference, remaining is identical for the present embodiment.It is not both: by Ji Wusi
Alcohol replaces with oligomeric two arms polyethylene glycol, oligomeric two arms polycaprolactone polyol or oligomeric two arms polyether polyol, obtains line style
Poly- D, L- lactide-co- trimethylene carbonate copolymer.In addition, the sulfydryl number of selected polyfunctional group sulfhydryl compound
Amount is at least three.
Embodiment 7
Compared with Example 1, in addition to having following difference, remaining is identical for the present embodiment.It is not both: by Ji Wusi
Alcohol replaces with multi-arm polyethylene glycol, multi-arm polycaprolactone polyol or three arm polyether polyol oligomer, obtains the poly- D of line style, L-
Lactide-co- trimethylene carbonate copolymer.In addition, the sulfydryl quantity of selected polyfunctional group sulfhydryl compound is at least
It is two.
Embodiment 8
Compared with Example 1, in addition to having following difference, remaining is identical for the present embodiment.It is not both: by Ji Wusi
Alcohol replaces with dipentaerythritol, obtains six arm Poly D,L-lactide-co- trimethylene carbonate copolymers.Polyfunctional group sulfydryl
Small molecule may is that dithioglycol, 1,4- succinimide mercaptans, 1,6- ethanthiol, four (3- mercaptopropionic acid) pentaerythritol esters, isocyanide
Urea acid three [2- (3- mercaptopropionyl oxygroup) ethyl ester], trimethylolpropane tris (3-thiopropionate) etc..
Embodiment 9
In the present embodiment the synthesis of hydroxy-end capped four arms poly- D, L- lactide-co- trimethylene carbonate copolymer with
Embodiment 1 is identical.
Hydroxy-end capped four arms poly- D, L- lactide-co- trimethylene carbonate copolymer is placed in connection water segregator
In two mouth flask, 10 times of hydroxyl mole of thioacetic acid and a water Catalyzed by p-Toluenesulfonic Acid agent of monomer mass 1wt% is added,
Then solvent is added, leads to nitrogen.Back flow reaction is for 24 hours under the conditions of 120~126 DEG C for reactant.After reaction, cooling, solution
It precipitates in methyl alcohol three times, it is stored refrigerated after room temperature in vacuo is dry.
Using chloroform as solvent, four arm Poly D,L-lactide-co- trimethylene carbonate copolymers of sulfydryl sealing end,
5- norbornene -2- carboxylic acid trimethylolpropane triester, 2,4,6 (trimethylbenzoyl) diphenyl phosphine oxides) it is uniformly mixed,
Norbornene and sulfydryl molar ratio 1:1, photoinitiator mass fraction 0.5wt%.The solid content for adjusting solution is 40%, is passed through
Norbornene-sulfydryl Stereolithography printing technique print carriage material, ultraviolet ray intensity 30mW/cm-2;Print carriage ruler
It is very little: length 40mm, outer diameter 4mm, internal diameter 2mm;Print speed: 50mm/h.Material glass temperature has 3 DEG C after photo-crosslinking
Increase.Printed bracket is heated to 40 DEG C, diametrical direction compression reduces size, then in the fixed interim shape of near zero
Degradable body temperature induction shape-memory polymer intravascular stent can be obtained in shape.
Embodiment 10
Compared with Example 9, in addition to having following difference, remaining is identical for the present embodiment.Different is simply that 5-
Norbornene -2- carboxylic acid trimethylolpropane triester replaces with four ester of 5- norbornene -2- carboxylic acid tetra methylol propane.
Embodiment 11
Compared with Example 9, in addition to having following difference, remaining is identical for the present embodiment.Different is simply that 5-
Norbornene -2- carboxylic acid trimethylolpropane triester replaces with 1,6-HD 5- norbornene-2-carboxylic ether.
Embodiment 12
6-caprolactone, trimethylene carbonate, 1,6- butanediol and stannous octoate are added in anhydrous and oxygen-free reaction flask is
Catalyst, decompression vacuum pumping three times, react for 24 hours under 130 DEG C of oil bath after reaction system sealing.After completion of the reaction, reactant
System is down to room temperature, and suitable chloroform lysate is added.Reaction mixture is slowly dropped in cold methanol and is precipitated, wherein
The volume of methanol is the chloroform soln volume of 5-10 times of reactant, dissolves and precipitates again after filtering, continuous precipitation three times,
Poly- (caprolactone-co- trimethylene carbonate) of obtained final product linear hydroxy sealing end.Wherein, initiator amount is single
The 0.1wt% of body;The molar ratio of 6-caprolactone and trimethylene carbonate is 80:20;The molar ratio 1:25 of initiator and monomer,
Hydroxy-end capped poly- (caprolactone-co- trimethylene carbonate) fusing point finally synthesized is at 34~38 DEG C, attached drawing 10.
Poly- (caprolactone-co- trimethylene carbonate) copolymer that hydroxy-end capped linear hydroxy blocks is placed in connection
In the two mouth flask of water segregator, the thioacetic acid of 10 times of hydroxyl mole of addition and a water of monomer mass 1wt% are to toluene sulphur
Then solvent is added in acid catalyst, lead to nitrogen.Back flow reaction is for 24 hours under the conditions of 120~126 DEG C for reactant.After reaction,
Cooling, solution precipitates three times in methyl alcohol, stored refrigerated after room temperature in vacuo is dry.
Using chloroform as solvent, poly- (caprolactone-co- trimethylene carbonate), the 5- norborneol of line style sulfydryl sealing end
Alkene -2- carboxylic acid trimethylolpropane triester, 2,4,6 (trimethylbenzoyl) diphenyl phosphine oxides are uniformly mixed, norbornene
Base and sulfydryl molar ratio 1:1, photoinitiator mass fraction 0.5wt%.The solid content for adjusting solution is 40%, passes through norborneol
Alkene-sulfydryl Stereolithography printing technique print carriage material, ultraviolet ray intensity 30mW/cm-2;Print carriage size: length
40mm, outer diameter 4mm, internal diameter 2mm;Print speed: 50mm/h.Material glass temperature has 3 DEG C of increase after photo-crosslinking.It will
Printed bracket is heated to 40 DEG C, and diametrical direction compression reduces size, then in the fixed temporary shapes of near zero, can obtain
Shape-memory polymer intravascular stent is incuded to degradable body temperature.
Embodiment 13
The present embodiment is compared with embodiment 12, and in addition to having following difference, remaining is identical.Different is simply that
5- norbornene -2- carboxylic acid trimethylolpropane triester replaces with four ester of 5- norbornene -2- carboxylic acid tetra methylol propane.
Embodiment 14
The present embodiment is compared with embodiment 12, and in addition to having following difference, remaining is identical.Different is simply that
5- norbornene -2- carboxylic acid trimethylolpropane triester replaces with the dissaving polymer of norbornene sealing end.
Embodiment 15
The present embodiment is compared with embodiment 12, and in addition to having following difference, remaining is identical.Different is simply that
5- norbornene -2- carboxylic acid trimethylolpropane triester replaces with 1,6-HD 5- norbornene-2-carboxylic ether.
Embodiment 16
The present embodiment is compared with embodiment 12, and in addition to having following difference, remaining is identical.Unlike: 1,6-
Hexylene glycol replaces with polyethylene glycol, and molecular weight is 500~1000;Trimethylene carbonate monomer removes;Polyethylene glycol is prepared to draw
The linear polycaprolactone for sending out polymerization, is similarly obtained degradable polymer of the fusing point at 38~40 DEG C.
Embodiment 17
The present embodiment is compared with embodiment 12, and in addition to having following difference, remaining is identical.Unlike: 1,6-
Hexylene glycol replaces with pentaerythrite or cyclodextrin or sugar alcohol.
Embodiment 18
The present embodiment is compared with embodiment 12, and in addition to having following difference, remaining is identical.Unlike: 1,6-
Hexylene glycol replaces with hydroxy-end capped dissaving polymer.
Embodiment 19
The present embodiment is compared with embodiment 12, and in addition to having following difference, remaining is identical.It is not both: by Sanya
Methyl carbonic replacement are as follows: one kind or more of trimethylene carbonate and L- lactide or glycolide or cyclic acid anhydride or cyclic phosphorus
Kind.
Embodiment 20
The present embodiment is compared with embodiment 12, and in addition to having following difference, remaining is identical.It is not both: by Sanya
Methyl carbonic replacement are as follows: D, L- lactide and L- lactide or glycolide or cyclic acid anhydride or cyclic phosphorus it is one or more.
Embodiment 21
The synthesis of poly- (caprolactone-co- trimethylene carbonate) copolymer of linear hydroxy sealing end is same as Example 9.
Poly- (caprolactone-co- trimethylene carbonate) copolymer, norbornene that hydroxy-end capped linear hydroxy is blocked
Acyl chlorides and triethylamine are put into there-necked flask.Wherein, the molar ratio of norbornene acyl chlorides, triethylamine and hydroxyl is 1.2:1.2:1, solvent
For dry methylene chloride, 48h is reacted at room temperature, is filtered after the reaction was completed, filtrate is precipitated three times in cold methanol, room temperature in vacuo
Poly- (caprolactone-co- trimethylene carbonate) copolymer of line style of norbornene sealing end is obtained after drying.
The print procedure of copolymer is substantially the same manner as Example 12.The difference is that poly- (the caprolactone-of line style sulfydryl sealing end
Co- trimethylene carbonate) and 5- norbornene -2- carboxylic acid trimethylolpropane triester replace with respectively norbornene sealing end
Poly- (caprolactone-co- trimethylene carbonate) copolymer of line style and four (3- mercaptopropionic acid) pentaerythritol esters.
Embodiment 22
The present embodiment is compared with embodiment 21, and in addition to having following difference, remaining is identical.Different is simply that
Four (3- mercaptopropionic acid) pentaerythritol esters replace with the dissaving polymer of sulfydryl sealing end.
Embodiment 23
The present embodiment is compared with embodiment 21, and in addition to having following difference, remaining is identical.Unlike: 1,6-
Hexylene glycol replaces with oligomeric two arms polyethylene glycol, multi-arm polyethylene glycol, oligomeric two arms polyether polyol or three arm polyether polyol
One of or it is a variety of, molecular weight be 500~1000;Trimethylene carbonate monomer removes;It prepares polyethylene glycol and causes polymerization
Linear polycaprolactone, be similarly obtained degradable polymer of the fusing point at 38~40 DEG C.
Embodiment 24
The present embodiment is compared with embodiment 21, and in addition to having following difference, remaining is identical.Unlike: 1,6-
Hexylene glycol replaces with pentaerythrite.
Embodiment 25
The present embodiment is compared with embodiment 21, and in addition to having following difference, remaining is identical.Unlike: 1,6-
Hexylene glycol replaces with hydroxy-end capped dissaving polymer.
The present invention is not limited to above-mentioned optional embodiment, anyone can show that other are each under the inspiration of the present invention
The product of kind form.Above-mentioned specific embodiment should not be understood the limitation of pairs of protection scope of the present invention, the foregoing is merely
Preferred embodiment of the invention, is not intended to restrict the invention.In the case of without prejudice to the principle of the invention, the present invention can be carried out
Various modifications and variations, all any modifications made for the present invention, equivalent replacement is modified etc., should be included in guarantor of the invention
It protects in range.
Claims (21)
1. a kind of preparation method of the biodegradable body temperature inductive material for 4D printing, it is characterised in that: comprising steps of with
Based on the Biodegradable high-molecular that physiological temp lower end is hydroxyl, by the processing of body ends sealing endization, preparation
The multicomponent biodegradable macromolecule that the degradable, end under physiological temp is sulfydryl or norbornene is obtained, is made
Biodegradable body temperature inductive material for 4D printing uses.
2. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 1,
Be characterized in that: the glass transition temperature or melting temperature of the main body are 20 DEG C -40 DEG C.
3. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 2,
Be characterized in that: the preparation method of the main body includes: with D, and L- lactide or caprolactone are main monomer;L- lactide, caprolactone,
One of glycolide, cyclic acid anhydride, cyclic carbonate ester, cyclic phosphorus or Lanthanum Isopropoxide are a variety of as comonomer;Through being catalyzed
Copolymerization obtains multicomponent copolymer after agent, initiator effect.
4. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 3,
Be characterized in that: the initiator is dihydroxylic compound, multi-hydroxy compound or oligomer.
5. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 3,
Be characterized in that: the initiator is ethylene glycol, pentaerythrite, small molecule polyhydroxy-alcohol, oligomeric two arms polyethylene glycol, the poly- second of multi-arm
Glycol, oligomeric two arms polycaprolactone polyol, multi-arm polycaprolactone polyol, oligomeric two arms polyether polyol, three arm polyethers are more
First alcohol, cyclodextrin or sugar alcohol.
6. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 3,
Be characterized in that: the catalyst is stannous octoate.
7. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 6,
Be characterized in that: when the main body that preparation glass transition temperature is 20 DEG C -40 DEG C, the main monomer of use and the mass fraction of comonomer are pressed
It is determined according to formula (1):
TgBased on glass transition temperature;Tg1、Tg2…TgnThe segment glass transition temperature of respectively each monomer for participating in reaction;n
For the positive integer more than or equal to 2;W1、W2…WnRespectively each monomer for participating in reaction accounts for the mass fraction of all monomers.
8. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 7,
Be characterized in that: when the main body that preparation glass transition temperature is 20 DEG C -40 DEG C, the mole of initiator accounts for all monomer integral molar quantities
0.02mol%.
9. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 8,
Be characterized in that: the molecular weight for the main body that the glass transition temperature is 20 DEG C -40 DEG C is 400-2000.
10. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 6,
Be characterized in that: when preparing the main body that fusing point is 20 DEG C -40 DEG C, the molar ratio of initiator and each monomer is 20 according to the fusing point
The molecular weight of DEG C -40 DEG C of main body determines.
11. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 10,
It is characterized by: initiator amount is the 0.1wt% of the gross weight of all monomers when preparing the main body that fusing point is 30 DEG C -40 DEG C;It is main
The molecular weight of body is 1000-4000.
12. a kind of biodegradable body temperature inductive material for 4D printing described in -11 any one according to claim 1
Preparation method, which is characterized in that the body ends sealing endization processing is norbornene termination process, the norbornene
Termination process is comprising steps of it is drop ice that main body, norbornene acyl chlorides and triethylamine solvent, which are mixed reaction end is prepared,
The multicomponent biodegradable macromolecule of piece alkenyl.
13. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 12,
It is characterized in that, the solvent is methylene chloride;The molar ratio of the norbornene acyl chlorides, triethylamine and main body hydroxyl is 1.2:
1.2:1;Reaction time is 48h;Reaction temperature is room temperature.
14. a kind of biodegradable body temperature inductive material for 4D printing described in -11 any one according to claim 1
Preparation method, which is characterized in that the body ends sealing endization processing is sulfydryl termination process, and the sulfydryl termination process includes
Step: by main body, thioacetic acid, catalysts and solvents, back flow reaction obtains the multicomponent biological that end is sulfydryl under nitrogen atmosphere
Degradable macromolecule.
15. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 14,
It is characterized in that, the hydroxyl of the main body and the molar ratio of thioacetic acid are 1:10 in the body ends sealing endization processing.
16. a kind of preparation method of biodegradable body temperature inductive material for 4D printing according to claim 15,
It is characterized in that, catalyst is a water p-methyl benzenesulfonic acid in the body ends sealing endization processing;One water p-methyl benzenesulfonic acid accounts for list
The mass fraction of weight is 1wt%;The temperature of the reaction is 120 DEG C -126 DEG C, and the reaction time is for 24 hours.
17. a kind of print degradable body using biodegradable body temperature inductive material 4D described in claim 1-16 any one
Warming should remember the preparation method of biological support, which is characterized in that comprising steps of the biodegradable body temperature is incuded material
After material, solvent, photoinitiator and polyfunctional group sulfydryl small molecule or the mixing of norbornene small molecule are adjusted to suitable printing viscosity,
The polyfunctional group sulfydryl small molecule or norbornene small molecule and biodegradable body temperature inductive material are printed by 4D to be occurred
Biological support is obtained after norbornene-sulfydryl photopolymerization reaction;By biological support be heated to melting temperature or glass transition temperature with
Compressing above and diametrically reduces size, then fixes temporary shapes near zero to get the induction of degradable body temperature is arrived
Remember biological support.
18. biodegradable body temperature inductive material 4D according to claim 17 prints degradable body temperature induction memory biology
The preparation method of bracket, which is characterized in that the biological support is intravascular stent, and the print conditions of the 4D printing are ultraviolet light
Intensity 30mW/cm-2;Print speed: 50mm/h, print carriage size: length 40mm, outer diameter 4mm, internal diameter 2mm.
19. biodegradable body temperature inductive material 4D according to claim 17 prints degradable body temperature induction memory biology
The preparation method of bracket, which is characterized in that the biodegradable body temperature inductive material is the multiple groups that end is norbornene
Decomposing biological degradable macromolecule;The preparation of the biological support includes the following steps: the biodegradable body temperature incuding material
After material, solvent, photoinitiator and the mixing of polyfunctional group sulfydryl small molecule are adjusted to suitable printing viscosity, are printed and given birth to by 4D
Object bracket;The polyfunctional group sulfydryl small molecule is four (3- mercaptopropionic acid) pentaerythritol esters.
20. biodegradable body temperature inductive material 4D according to claim 17 prints degradable body temperature induction memory biology
The preparation method of bracket, which is characterized in that the biodegradable body temperature inductive material is the multicomponent biological that end is sulfydryl
Degradable macromolecule;The preparation of the biological support includes the following steps: the biodegradable body temperature inductive material, molten
After agent, photoinitiator and the mixing of norbornene small molecule are adjusted to suitable printing viscosity, print to obtain biological support by 4D;Institute
Stating norbornene small molecule is 5- norbornene -2- carboxylic acid trimethylolpropane triester.
21. biodegradable body temperature inductive material 4D described in 7-20 any one prints degradable body temperature according to claim 1
The preparation method of induction memory biological support, which is characterized in that the photoinitiator is 2,4,6 (trimethylbenzoyl) hexichol
Base phosphine oxide;The solvent is chloroform;The mass fraction that photoinitiator accounts for each substance gross weight is 0.5wt%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910860265.1A CN110527075A (en) | 2019-09-11 | 2019-09-11 | A kind of preparation method for remembering biological support for the biodegradable body temperature inductive material of 4D printing and the induction of degradable body temperature |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201910860265.1A CN110527075A (en) | 2019-09-11 | 2019-09-11 | A kind of preparation method for remembering biological support for the biodegradable body temperature inductive material of 4D printing and the induction of degradable body temperature |
Publications (1)
Publication Number | Publication Date |
---|---|
CN110527075A true CN110527075A (en) | 2019-12-03 |
Family
ID=68668433
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201910860265.1A Pending CN110527075A (en) | 2019-09-11 | 2019-09-11 | A kind of preparation method for remembering biological support for the biodegradable body temperature inductive material of 4D printing and the induction of degradable body temperature |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN110527075A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111497220A (en) * | 2020-03-24 | 2020-08-07 | 深圳大学 | Shape memory sensor and method for manufacturing the same |
CN112126075A (en) * | 2020-09-23 | 2020-12-25 | 兰州大学第二医院 | Degradable shape memory polymer and preparation method thereof, and 4D printing degradable lower limb vascular stent and preparation method thereof |
-
2019
- 2019-09-11 CN CN201910860265.1A patent/CN110527075A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111497220A (en) * | 2020-03-24 | 2020-08-07 | 深圳大学 | Shape memory sensor and method for manufacturing the same |
CN112126075A (en) * | 2020-09-23 | 2020-12-25 | 兰州大学第二医院 | Degradable shape memory polymer and preparation method thereof, and 4D printing degradable lower limb vascular stent and preparation method thereof |
CN112126075B (en) * | 2020-09-23 | 2022-06-07 | 兰州大学第二医院 | Degradable shape memory polymer and preparation method thereof, and 4D printing degradable lower limb vascular stent and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6730772B2 (en) | Degradable polymers from derivatized ring-opened epoxides | |
CN101443055B (en) | Removal of tubular tissue supports | |
JPH06122Y2 (en) | Synthetic copolymer surgical suture | |
US20040077797A1 (en) | Crosslinked hydrogel copolymers | |
US20140357806A1 (en) | Thermal-responsive polymer networks, compositions, and methods and applications related thereto | |
AU2005304567B2 (en) | Photocrosslinkable poly(caprolactone fumarate) | |
CN101370447A (en) | Compressible tubular tissue supports | |
US8912247B2 (en) | Hydrophilic/hydrophobic polymer networks based on poly(caprolactone fumarate), poly(ethylene glycol fumarate), and copolymers thereof | |
EP1498147B1 (en) | Absorbable biocompatible block copolymer | |
CN110527075A (en) | A kind of preparation method for remembering biological support for the biodegradable body temperature inductive material of 4D printing and the induction of degradable body temperature | |
Bizzarri et al. | Synthesis and characterization of new malolactonate polymers and copolymers for biomedical applications | |
CN100372578C (en) | Composite support material, composite support, and its production process | |
KR102208921B1 (en) | Shape memory polymer, preparation method thereof, and the use of the same | |
CN110366434A (en) | Functionalized poly (fumaric acid acrylic ester) polymer prepared using Mg catalyst by ring-opening polymerisation | |
CN103374208A (en) | Gradient degradable polymeric material and preparation method thereof | |
Chen et al. | Biodegradable poly (trimethylene carbonate‐b‐(L‐lactide‐ran‐glycolide)) terpolymers with tailored molecular structure and advanced performance | |
CN100400115C (en) | Composite stent material, composite stent and production method thereof | |
Uto et al. | Design of super-elastic biodegradable scaffolds with longitudinally oriented microchannels and optimization of the channel size for Schwann cell migration | |
CN111053951A (en) | Elastic degradable 3D printing porous scaffold and preparation method thereof | |
KR102521685B1 (en) | Substrate for inseting a nasolacrimal duct including shape memory polymers | |
US20080267901A1 (en) | Biocompatible Polymer Networks | |
Lei et al. | Synthesis, characterization and cytocompatibility of a degradable polymer using ferric catalyst for esophageal tissue engineering | |
Zhao et al. | Review of crosslinked and non‐crosslinked copolyesters for tissue engineering and drug delivery | |
US20230148372A1 (en) | Degradable, Printable Poly(Propylene Fumarate)-Based ABA Triblock Elastomers | |
KR20220118848A (en) | Shape memory polymer and manufacturing method thereof, and the use of the same |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20191203 |
|
WD01 | Invention patent application deemed withdrawn after publication |