CN110092920A - 一种pnaga增强醛肼交联型可注射水凝胶及其制备方法 - Google Patents
一种pnaga增强醛肼交联型可注射水凝胶及其制备方法 Download PDFInfo
- Publication number
- CN110092920A CN110092920A CN201910409511.1A CN201910409511A CN110092920A CN 110092920 A CN110092920 A CN 110092920A CN 201910409511 A CN201910409511 A CN 201910409511A CN 110092920 A CN110092920 A CN 110092920A
- Authority
- CN
- China
- Prior art keywords
- pnaga
- naga
- preparation
- polymer
- hydrogel
- 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.)
- Granted
Links
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 title claims abstract description 50
- 238000002360 preparation method Methods 0.000 title claims abstract description 23
- 238000004132 cross linking Methods 0.000 title claims description 13
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 title claims description 11
- 238000002347 injection Methods 0.000 title claims description 6
- 239000007924 injection Substances 0.000 title claims description 6
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 title claims 5
- 230000002708 enhancing effect Effects 0.000 title claims 4
- 239000000017 hydrogel Substances 0.000 claims abstract description 48
- 239000007864 aqueous solution Substances 0.000 claims abstract description 30
- 229920000642 polymer Polymers 0.000 claims abstract description 24
- 229940079593 drug Drugs 0.000 claims abstract description 19
- 239000003814 drug Substances 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 11
- 239000003999 initiator Substances 0.000 claims abstract description 10
- 239000000463 material Substances 0.000 claims abstract description 6
- 229920001282 polysaccharide Polymers 0.000 claims abstract description 6
- 239000005017 polysaccharide Substances 0.000 claims abstract description 6
- 238000010526 radical polymerization reaction Methods 0.000 claims abstract description 6
- 150000004676 glycans Chemical class 0.000 claims abstract description 5
- 238000011065 in-situ storage Methods 0.000 claims abstract description 4
- WKNMKGVLOWGGOU-UHFFFAOYSA-N 2-aminoacetamide;hydron;chloride Chemical compound Cl.NCC(N)=O WKNMKGVLOWGGOU-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000012876 carrier material Substances 0.000 claims abstract description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 18
- -1 hydrazine compound Chemical class 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 238000000465 moulding Methods 0.000 claims description 6
- 239000000047 product Substances 0.000 claims description 5
- 230000035484 reaction time Effects 0.000 claims description 5
- 229920001353 Dextrin Polymers 0.000 claims description 4
- 239000004375 Dextrin Substances 0.000 claims description 4
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 4
- 235000019425 dextrin Nutrition 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 230000000977 initiatory effect Effects 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- 238000003860 storage Methods 0.000 claims description 3
- 229910001870 ammonium persulfate Inorganic materials 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 238000000746 purification Methods 0.000 claims description 2
- 238000001291 vacuum drying Methods 0.000 claims description 2
- 238000005406 washing Methods 0.000 claims description 2
- 238000007037 hydroformylation reaction Methods 0.000 claims 3
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 claims 2
- VYBHLZOLHCQLHT-UHFFFAOYSA-N 1-(2-methylpropyl)-4,5-dihydroimidazole hydrochloride Chemical compound Cl.C(C(C)C)N1C=NCC1 VYBHLZOLHCQLHT-UHFFFAOYSA-N 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- 230000007717 exclusion Effects 0.000 claims 1
- BEBCJVAWIBVWNZ-UHFFFAOYSA-N glycinamide Chemical compound NCC(N)=O BEBCJVAWIBVWNZ-UHFFFAOYSA-N 0.000 claims 1
- UWNADWZGEHDQAB-UHFFFAOYSA-N i-Pr2C2H4i-Pr2 Natural products CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 claims 1
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 239000002244 precipitate Substances 0.000 claims 1
- 239000002131 composite material Substances 0.000 abstract description 4
- GVGGWUXGMRTNIK-UHFFFAOYSA-N n-(2-amino-2-oxoethyl)prop-2-enamide Chemical compound NC(=O)CNC(=O)C=C GVGGWUXGMRTNIK-UHFFFAOYSA-N 0.000 abstract description 3
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 abstract description 2
- 229920003213 poly(N-isopropyl acrylamide) Polymers 0.000 description 13
- 239000000499 gel Substances 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 238000013268 sustained release Methods 0.000 description 6
- 239000012730 sustained-release form Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- MEAPRSDUXBHXGD-UHFFFAOYSA-N 3-chloro-n-(4-propan-2-ylphenyl)propanamide Chemical compound CC(C)C1=CC=C(NC(=O)CCCl)C=C1 MEAPRSDUXBHXGD-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- LXEKPEMOWBOYRF-UHFFFAOYSA-N [2-[(1-azaniumyl-1-imino-2-methylpropan-2-yl)diazenyl]-2-methylpropanimidoyl]azanium;dichloride Chemical compound Cl.Cl.NC(=N)C(C)(C)N=NC(C)(C)C(N)=N LXEKPEMOWBOYRF-UHFFFAOYSA-N 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000002105 nanoparticle Substances 0.000 description 2
- 229960004604 propranolol hydrochloride Drugs 0.000 description 2
- AQHHHDLHHXJYJD-UHFFFAOYSA-N propranolol hydrochloride Natural products C1=CC=C2C(OCC(O)CNC(C)C)=CC=CC2=C1 AQHHHDLHHXJYJD-UHFFFAOYSA-N 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- 239000012620 biological material Substances 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000010382 chemical cross-linking Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000012567 medical material Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 1
- 239000002114 nanocomposite Substances 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 238000004626 scanning electron microscopy Methods 0.000 description 1
- 239000002520 smart material Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/32—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers, poly(meth)acrylates, or polyvinyl pyrrolidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/36—Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/06—Ointments; Bases therefor; Other semi-solid forms, e.g. creams, sticks, gels
-
- 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
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/26—Mixtures of macromolecular compounds
-
- 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
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
-
- 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
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L27/52—Hydrogels or hydrocolloids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F122/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides or nitriles thereof
- C08F122/36—Amides or imides
- C08F122/38—Amides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/04—Azo-compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
- C08J3/075—Macromolecular gels
-
- 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
- A61L2400/00—Materials characterised by their function or physical properties
- A61L2400/06—Flowable or injectable implant compositions
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2333/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2333/24—Homopolymers or copolymers of amides or imides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2403/00—Characterised by the use of starch, amylose or amylopectin or of their derivatives or degradation products
- C08J2403/04—Starch derivatives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2435/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Derivatives of such polymers
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Dermatology (AREA)
- Pharmacology & Pharmacy (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Dispersion Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Medicinal Preparation (AREA)
- Materials For Medical Uses (AREA)
Abstract
本发明公开了一种PNAGA增强醛肼交联型可注射水凝胶及其制备方法，属于生物医用材料技术领域。该方法具体为：首先将甘氨酰胺盐酸盐与丙烯酰氯反应得到N‑丙烯酰基甘氨酰胺，记为NAGA；再通过引发剂引发自由基聚合得到聚合物PNAGA，提纯干燥；然后配制聚合物PNAGA水溶液；再将醛化多糖与肼化物分别溶解在聚合物PNAGA水溶液中，最后将两种复合水溶液通过双针筒注射器注射后原位形成水凝胶。经PNAGA补强后的水凝胶强度提升显著，该类水凝胶可作为组织工程支架材料或水溶性药物的载体材料，有望应用于生物医用领域。
Description
技术领域
本发明属于生物医用材料技术领域，特别涉及一种PNAGA增强醛肼交联型可注射水凝胶及其制备方法。
背景技术
水凝胶在外用医疗材料、组织工程支架、生物传感、药物传输与载体等领域具有广泛的应用。聚(N-异丙基丙烯酰胺)(PNIPAM)由于聚合物链上存在亲水和疏水基团，对温度有很好地敏感响应性，其临界相转变温度(LCST)在32℃左右与人体体温相近，在生物智能材料领域具有广泛的应用前景。醛肼交联注射型PNIPAM水凝胶通过醛基和肼基在室温下快速发生交联反应制得，但由于反应时间短，形成的腙键共价键网络存在缺陷，导致水凝胶的力学性能较差。在水凝胶中引入淀粉纳米粒子，制备的纳米复合PNIPAM水凝胶(石淑先,李珊珊,夏宇正,et al.一种纳米淀粉粒子补强的醛肼交联型可注射PNIPAM水凝胶的制备方法:中国,20161115097.9[P].2017-06-13.)的凝胶强度虽可提高，但淀粉纳米粒子在微生物的作用下易腐败变质，限制了其潜在应用。
氢键是一种非常重要的分子间作用力，在许多生物和化学体系中有着不可替代的作用。利用聚合物之间的协同氢键作用可获得高强度的水凝胶(Gong J P,Katsuyama Y,Kurokawa T,et al.Double ㎞ etwork Hydrogels with Extremely High MechanicalStrength[J].Advanced Materials,2003,15(14):1155-1158.Mati I K,Cockroft SL.Molecular balances for quantifying non-covalent interactions[J].ChemicalSociety Reviews,2010,39(11):4195.)，凝胶中均匀分布的柔性物理交联位点及它们之间的长聚合物链使凝胶能有效地分散施加的载荷。
氢键作用增强方式不仅简单高效，而且无需添加额外的交联剂，生物毒性低，特别适用于生物材料的制备。N-丙烯酰基甘氨酰胺(NAGA)在没有任何化学交联剂的情况下，其水溶液经光引发聚合可以形成超分子聚(N-丙烯酰基甘氨酰胺)(PNAGA)水凝胶，表现出了优异的机械性能，这是由其内部双酰胺氢键合微区域增强所致，使其水凝胶在水中具有高稳定性。但是NAGA溶液聚合制备PNAGA一般使用过硫酸盐等热引发剂引发聚合，存在反应时间长、用量大等缺点。PNAGA与醛肼交联的聚(N-异丙基丙烯酰胺)(PNIPAM)化学结构相似，而且还具有良好的生物相容性，将其引入PNIPAM水凝胶体系，通过醛肼化学交联和多重氢键交联，增加交联点的数量，从而提高凝胶强度。但是PNAGA水溶液由于氢键作用在常温下表现为凝胶状态，无法和醛肼交联型PNIPAM实现室温注射成型；只有升高温度至90℃以上，才可使PNAGA水凝胶中的氢键破坏使其形成水溶液，但是温敏型的PNIPAM分子链(LCST＝32℃)在此高温下是蜷缩状态，因此也无法和PGANA共混形成均匀的交联网络，而这也失去了醛肼交联型PNIPAM水凝胶的室温注射成型特性。本发明在AIBA引发(催化效率高，分解速率常数小，聚合恒速聚合，过程不会改变pH，不含腈基，且分解产物无毒本)下，通过NAGA在水溶液中进行自由基聚合制得PNAGA，调节PNAGA水溶液的浓度，保证其在室温下的溶解状态，并分别将其与醛化多糖和肼化的PNIPAM混合，成功通过室温共注射，原位制备了PNAGA增强的PNIPAM基温敏水凝胶，凝胶强度可提高至5.6倍。
发明内容
本发明提供了一种PNAGA增强醛肼交联型可注射水凝胶及其制备方法。经PNAGA补强后的水凝胶强度提升显著。
所述的PNAGA增强醛肼交联型可注射水凝胶的制备方法为：通过引发剂引发NAGA在水中进行自由基聚合制得聚合物PNAGA，提纯干燥；然后配制聚合物PNAGA水溶液；再将醛化多糖与肼化物分别溶解在聚合物PNAGA水溶液中，最后将两种复合水溶液通过双针筒注射器注射后原位形成水凝胶。
所述的NAGA是由甘氨酰胺盐酸盐与丙烯酰氯反应得到N-丙烯酰基甘氨酰胺，记为NAGA。
所述的NAGA在水中的质量分数为1-3％。
所述的聚合物PNAGA的制备方法的具体步骤为：配制质量浓度为1-3％的NAGA水溶液，通入氮气排除体系中的氧气，之后加入引发剂引发自由基聚合，反应时间为1-30min，随后加入无水甲醇使产物沉淀，离心过滤，甲醇洗涤提纯，真空干燥得到白色粉末即为聚合物PNAGA。
所述的引发剂选自偶氮二异丁基脒盐酸盐、偶氮二异丁咪唑啉盐酸盐、偶氮二氰基戊酸、偶氮二异丙基咪唑啉、过硫酸铵、过硫酸钾中的一种或几种，引发剂的用量为NAGA质量的0.5％-10％，引发温度为45-70℃。
所述的配制聚合物PNAGA水溶液的方法为：将聚合物PNAGA溶于水中并在90-100℃下加热溶解12-30h，聚合物PNAGA的浓度为0.001-2wt％。
所述的肼化物为P(NIPAM-co-AA)-hdz。
所述的醛化多糖为醛化糊精。
所述的PNAGA增强醛肼交联型可注射水凝胶的储存方法为：将上述制得的PNAGA增强醛肼交联型可注射水凝胶注入到模具之中，将模具置于30-40℃的烘箱之中固化成型后取出。
将上述制得的PNAGA增强醛肼交联型可注射水凝胶作为组织工程支架材料或水溶性药物的载体材料的应用。
本发明结合了PNAGA的优异的机械性能和醛肼交联反应室温快速交联成型和醛肼交联形成腙键的可注射等特点，得到一种机械强度强，温度敏感性高，具有解交联特性的可注射PNIPAM复合水凝胶，在生物医药方面具有良好的应用前景。
附图说明
图1为实施例1制备的水凝胶断面的扫描电镜图：(a)醛肼交联型水凝胶；(b)PNAGA增强醛肼交联型水凝胶；
图2为实施例1制备的醛肼交联水凝胶的动态模量；
图3为图为实施例3制备的PNAGA增强醛肼交联型水凝胶的药物缓释曲线。
具体实施方式
下面结合具体实施和附图说明进一步说明技术实现方案：
实施例1
(1)PNAGA水溶液的制备：将1.0g单体NAGA溶解于5.0g去离子水中形成质量分数为2％的NAGA溶液，通入氮气30min排除体系中的氧气，之后加入引发剂AIBA在60℃引发聚合，反应时间为30min得到聚合物浊液，随后加入无水甲醇使产物沉淀，然后5000r/min的条件下离心30min，过滤并用甲醇洗涤粗产品，放入到60℃的真空箱中干燥48h，最后收集得到白色的聚合物粉末即为PNAGA。将2.0g的PNAGA溶于水中并在90℃下加热24h以得到质量分数0-1.5％的PNAGA水溶液。
(2)1.5％PNAGA水溶液增强醛肼交联型PNIPANM水凝胶的制备：先把99.70mg肼化物P(NIPAM-co-AA)-hdz和98.95mg醛化糊精分别溶解在1g的1.5％PNAGA水溶液中，之后二者的复合水溶液在注射器中混合，挤出注入到模具之中，将模具置于37℃的烘箱之中固化成型后取出，得到1.5％PNAGA稀溶液增强醛肼交联型PNIPANM水凝胶。将水凝胶样品在液氮中快速冷冻10分钟后并立即冷冻干燥24h以除去水。通过扫描电镜可以看出，水凝胶呈现出连续的大孔结构，有利于水凝胶的药物释放。
实施例2
PNAGA增强醛肼交联型PNIPANM水凝胶的制备：把99.70mg肼化物P(NIPAM-co-AA)-hdz和98.95mg醛化糊精分别溶解在1.0g的1.5％PNAGA水溶液中，之后二者的水溶液在注射器中混合，用平行板流变仪对水凝胶的动态模量进行测定，实验中将混合后的溶液注射到板上成型，在37℃下保持40min完全固化成型。样品直径25mm，厚度1mm，实验温度37℃。设置角频率0.1到100rad·s-1，制备PNAGA增强醛肼交联型PNIPANM水凝胶的弹性性能最大为未增强水凝胶的5倍，最大储能模量达到527.0kPa，而未增强水凝胶的弹性模量为93.6kPa。、
实施例3
载药1.5％PNAGA水溶液增强醛肼交联型PNIPANM水凝胶的制备：选用水溶性药物盐酸普萘洛尔作为负载药物进行水凝胶药物缓释性能研究。将6.0mg，12.0mg，18.0mg，24.0mg盐酸普萘洛尔分别溶解在12mL质量分数为1.5％PNAGA水溶液中，从而制备药物含量分别为0.5mg/mL,1.0mg/mL,1.5mg/mL,2.0mg/mL的PNAGA溶液。分别把99.70mg肼化物P(NIPAM-co-AA)-hdz和98.95mg醛化糊精溶解在不同药物浓度的1.0g的1.5％PNAGA水溶液中，二者的水溶液在注射器中混合，之后挤出注入到模具之中，将模具置于37℃的烘箱之中固化成型后取出，得到载药浓度为0.5mg/mL,1.0mg/mL,1.5mg/mL,2.0mg/mL的1.5％PNAGA水溶液增强醛肼交联型PNIPANM水凝胶。将载药水凝胶置于离心管之中，在离心管中各加入10mLPBS缓冲液，之后置于37℃环境中，每隔24h取出3mL液体并同时补加等体积的PBS缓冲液，重复上述操作直至药物缓释测试结束。取出的液体用紫外分光光度计在291.8nm处测定药物浓度，根据数据测试结果计算出得到不同时间点的药物释放量。药物缓释实验表明该水凝胶表现出良好的药物缓释性能，缓释时间最长可达20天，释药率可达99.0％。
本发明可用其他的不违背本发明的精神或主要特征的具体形式来概述。本发明的上述实施方案都只能认为是对本发明的示例性说明描述，权利要求书指出了本发明的范围，而上述的说明并未指出本发明的范围，因此，在不脱离本发明的权利要求书相当的含义和范围内的任何简单变化、修改或者其他本领域技术人员能够不花费创造性劳动的等同替换都应认为是包括在权利要求书的保护范围内。
Claims (10)
1.一种PNAGA增强醛肼交联型可注射水凝胶的制备方法，其特征在于，该制备方法为：通过引发剂引发NAGA在水中进行自由基聚合制得聚合物PNAGA，提纯干燥；然后配制聚合物PNAGA水溶液；再将醛化多糖与肼化物分别溶解在聚合物PNAGA水溶液中，最后将两种复合水溶液通过双针筒注射器注射后原位形成水凝胶。
2.根据权利要求1所述的制备方法，其特征在于，所述的NAGA是由甘氨酰胺盐酸盐与丙烯酰氯反应得到N-丙烯酰基甘氨酰胺，记为NAGA。
3.根据权利要求1所述的制备方法，其特征在于，所述的NAGA在水中的质量分数为1-3％。
4.根据权利要求1所述的制备方法，其特征在于，所述的聚合物PNAGA的制备方法的具体步骤为：配制质量浓度为1-3％的NAGA水溶液，通入氮气排除体系中的氧气，之后加入引发剂引发自由基聚合，反应时间为1-30min，随后加入无水甲醇使产物沉淀，离心过滤，甲醇洗涤提纯，真空干燥得到白色粉末即为聚合物PNAGA。
5.根据权利要求4所述的制备方法，其特征在于，所述的引发剂选自偶氮二异丁基脒盐酸盐、偶氮二异丁咪唑啉盐酸盐、偶氮二氰基戊酸、偶氮二异丙基咪唑啉、过硫酸铵、过硫酸钾中的一种或几种，引发剂的用量为NAGA质量的0.5％-10％，引发温度为45-70℃。
6.根据权利要求1所述的制备方法，其特征在于，所述的配制聚合物PNAGA水溶液的方法为：将聚合物PNAGA溶于水中并在90-100℃下加热溶解12-30h，聚合物PNAGA的浓度为0.001-2wt％。
7.根据权利要求1所述的制备方法，其特征在于，所述的肼化物为P(NIPAM-co-AA)-hdz。
8.根据权利要求1所述的制备方法，其特征在于，所述的醛化多糖为醛化糊精。
9.根据权利要求1所述的方法制备得到的PNAGA增强醛肼交联型可注射水凝胶，其特征在于，所述水凝胶的储存方法为：将PNAGA增强醛肼交联型可注射水凝胶注入到模具之中，将模具置于30-40℃的烘箱之中固化成型后取出。
10.根据权利要求1-8任一所述的方法制备得到的PNAGA增强醛肼交联型可注射水凝胶作为组织工程支架材料或水溶性药物的载体材料的应用。
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201910409511.1A CN110092920B (zh) | 2019-05-17 | 2019-05-17 | 一种pnaga增强醛肼交联型可注射水凝胶及其制备方法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201910409511.1A CN110092920B (zh) | 2019-05-17 | 2019-05-17 | 一种pnaga增强醛肼交联型可注射水凝胶及其制备方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN110092920A true CN110092920A (zh) | 2019-08-06 |
| CN110092920B CN110092920B (zh) | 2020-07-24 |
Family
ID=67448273
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201910409511.1A Active CN110092920B (zh) | 2019-05-17 | 2019-05-17 | 一种pnaga增强醛肼交联型可注射水凝胶及其制备方法 |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN110092920B (zh) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111995769A (zh) * | 2020-07-30 | 2020-11-27 | 东南大学 | 一种可调控双温敏水凝胶及其制备方法 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH066610B2 (ja) * | 1987-05-13 | 1994-01-26 | 工業技術院長 | 親水性―疎水性熱可逆型高分子材料及びその製造方法 |
| CN106336474A (zh) * | 2015-04-21 | 2017-01-18 | 天津大学 | 基于丙烯酰基甘氨酰胺的高强度水凝胶作为热塑性聚合物的应用 |
| CN106832342A (zh) * | 2016-12-14 | 2017-06-13 | 北京化工大学 | 一种纳米淀粉粒子补强的醛肼交联型可注射pnipam水凝胶的制备方法 |
| CN106947012A (zh) * | 2017-03-17 | 2017-07-14 | 天津大学 | 基于甲基丙烯酰基甘氨酰胺的水凝胶及其作为自修复材料的应用 |
-
2019
- 2019-05-17 CN CN201910409511.1A patent/CN110092920B/zh active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH066610B2 (ja) * | 1987-05-13 | 1994-01-26 | 工業技術院長 | 親水性―疎水性熱可逆型高分子材料及びその製造方法 |
| CN106336474A (zh) * | 2015-04-21 | 2017-01-18 | 天津大学 | 基于丙烯酰基甘氨酰胺的高强度水凝胶作为热塑性聚合物的应用 |
| CN106832342A (zh) * | 2016-12-14 | 2017-06-13 | 北京化工大学 | 一种纳米淀粉粒子补强的醛肼交联型可注射pnipam水凝胶的制备方法 |
| CN106947012A (zh) * | 2017-03-17 | 2017-07-14 | 天津大学 | 基于甲基丙烯酰基甘氨酰胺的水凝胶及其作为自修复材料的应用 |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111995769A (zh) * | 2020-07-30 | 2020-11-27 | 东南大学 | 一种可调控双温敏水凝胶及其制备方法 |
| CN111995769B (zh) * | 2020-07-30 | 2022-06-10 | 东南大学 | 一种可调控双温敏水凝胶及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN110092920B (zh) | 2020-07-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Liao et al. | Preparation, properties and drug controlled release of chitin-based hydrogels: An updated review | |
| Lu et al. | The formation mechanism of hydrogels | |
| Fu et al. | The chitosan hydrogels: From structure to function | |
| CN110522948B (zh) | 可注射水凝胶及其制备方法和应用 | |
| Ebhodaghe | Hydrogel–based biopolymers for regenerative medicine applications: a critical review | |
| CN103724455A (zh) | 一种透明质酸衍生物及其水凝胶的制备方法 | |
| CN112089685B (zh) | 一种温度响应型细菌纤维素抗菌纳米凝胶的制备方法 | |
| CN113583257B (zh) | 一种电致黏附水凝胶及其制备方法 | |
| Kumar et al. | Synthetic polymer hydrogels | |
| CN107233629A (zh) | 可注射水凝胶及其制备和应用 | |
| CN103965491A (zh) | 一种丝素蛋白复合凝胶的制备方法 | |
| CN106380990B (zh) | 含有醛基的磷酰胆碱聚合物与多巴胺交联涂层的制备方法 | |
| CN103396545B (zh) | 聚合物、葡萄糖敏感纳米凝胶、葡萄糖敏感载药纳米凝胶及其制备方法 | |
| CN101024697A (zh) | 聚n－异丙基丙烯酰胺－聚氨基酸两嵌段共聚物及制备方法 | |
| Wei et al. | Injectable poly (γ-glutamic acid)-based biodegradable hydrogels with tunable gelation rate and mechanical strength | |
| CN106832342B (zh) | 一种纳米淀粉粒子补强的醛肼交联型可注射pnipam水凝胶的制备方法 | |
| CN113185725B (zh) | 一种原位快速制备银纳米粒子/明胶复合水凝胶的方法 | |
| CN108341913A (zh) | 天然高分子模板引导聚合制备自修复水凝胶的方法 | |
| CN108129687B (zh) | 一种表面为磷酰胆碱的仿细胞外层膜结构涂层的制备方法 | |
| CN110092920B (zh) | 一种pnaga增强醛肼交联型可注射水凝胶及其制备方法 | |
| CN112807439A (zh) | 一种可植入原位成型的壳聚糖水凝胶的制备方法及应用 | |
| CN114569786B (zh) | 一种用于体内创伤的化学稳定性水凝胶敷料及其制备方法 | |
| CN115536919B (zh) | 一种改性壳聚糖粘附水凝胶及其制备方法和应用 | |
| CN106750416B (zh) | 一种拥有自愈合和pH响应性能的可注射水凝胶及其制备方法和应用 | |
| CN103214625A (zh) | 一种具有抗蛋白质吸附的温敏性接枝水凝胶及其制备方法 |
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 | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant |