CN113402661A - Zwitterionic polymer-based nitric oxide-driven nano motor and preparation method and application thereof - Google Patents
Zwitterionic polymer-based nitric oxide-driven nano motor and preparation method and application thereof Download PDFInfo
- Publication number
- CN113402661A CN113402661A CN202110503975.6A CN202110503975A CN113402661A CN 113402661 A CN113402661 A CN 113402661A CN 202110503975 A CN202110503975 A CN 202110503975A CN 113402661 A CN113402661 A CN 113402661A
- Authority
- CN
- China
- Prior art keywords
- nanomotor
- arginine
- reaction
- zwitterionic polymer
- driven
- 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
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 title claims abstract description 187
- 229920000642 polymer Polymers 0.000 title claims abstract description 32
- 238000002360 preparation method Methods 0.000 title claims abstract description 17
- 239000003642 reactive oxygen metabolite Substances 0.000 claims description 44
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 39
- -1 diselenide compound Chemical class 0.000 claims description 34
- 238000006243 chemical reaction Methods 0.000 claims description 28
- 206010028980 Neoplasm Diseases 0.000 claims description 24
- ODKSFYDXXFIFQN-BYPYZUCNSA-N L-arginine Chemical compound OC(=O)[C@@H](N)CCCN=C(N)N ODKSFYDXXFIFQN-BYPYZUCNSA-N 0.000 claims description 23
- 229930064664 L-arginine Natural products 0.000 claims description 23
- 235000014852 L-arginine Nutrition 0.000 claims description 23
- 125000002059 L-arginyl group Chemical class O=C([*])[C@](N([H])[H])([H])C([H])([H])C([H])([H])C([H])([H])N([H])C(=N[H])N([H])[H] 0.000 claims description 22
- 239000003431 cross linking reagent Substances 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 20
- 238000003756 stirring Methods 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 16
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 15
- 239000008367 deionised water Substances 0.000 claims description 15
- 229910021641 deionized water Inorganic materials 0.000 claims description 15
- 230000035484 reaction time Effects 0.000 claims description 15
- 239000003999 initiator Substances 0.000 claims description 14
- 230000004044 response Effects 0.000 claims description 14
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 13
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 12
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 10
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims description 9
- DCUFMVPCXCSVNP-UHFFFAOYSA-N methacrylic anhydride Chemical compound CC(=C)C(=O)OC(=O)C(C)=C DCUFMVPCXCSVNP-UHFFFAOYSA-N 0.000 claims description 8
- VHRYZQNGTZXDNX-UHFFFAOYSA-N methacryloyl chloride Chemical compound CC(=C)C(Cl)=O VHRYZQNGTZXDNX-UHFFFAOYSA-N 0.000 claims description 8
- 238000005119 centrifugation Methods 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 7
- 238000005199 ultracentrifugation Methods 0.000 claims description 7
- MBMJDELICBDLEE-UHFFFAOYSA-N ethanamine;dihydrochloride Chemical compound Cl.Cl.CCN MBMJDELICBDLEE-UHFFFAOYSA-N 0.000 claims description 6
- 239000012074 organic phase Substances 0.000 claims description 6
- 230000002829 reductive effect Effects 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 5
- 208000024172 Cardiovascular disease Diseases 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 239000003208 petroleum Substances 0.000 claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 4
- 239000002994 raw material Substances 0.000 claims description 4
- 230000008685 targeting Effects 0.000 claims description 4
- 239000007810 chemical reaction solvent Substances 0.000 claims description 3
- 238000001704 evaporation Methods 0.000 claims description 3
- 230000008020 evaporation Effects 0.000 claims description 3
- 238000004108 freeze drying Methods 0.000 claims description 3
- 239000012535 impurity Substances 0.000 claims description 3
- ZQMHJBXHRFJKOT-UHFFFAOYSA-N methyl 2-[(1-methoxy-2-methyl-1-oxopropan-2-yl)diazenyl]-2-methylpropanoate Chemical compound COC(=O)C(C)(C)N=NC(C)(C)C(=O)OC ZQMHJBXHRFJKOT-UHFFFAOYSA-N 0.000 claims description 3
- 239000012046 mixed solvent Substances 0.000 claims description 3
- 239000007832 Na2SO4 Substances 0.000 claims description 2
- 239000011203 carbon fibre reinforced carbon Chemical group 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 238000001816 cooling Methods 0.000 claims description 2
- 230000000977 initiatory effect Effects 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 238000010898 silica gel chromatography Methods 0.000 claims description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 2
- 230000003902 lesion Effects 0.000 claims 2
- 125000000524 functional group Chemical group 0.000 claims 1
- 230000033001 locomotion Effects 0.000 abstract description 21
- 230000003399 chemotactic effect Effects 0.000 abstract description 6
- 210000004881 tumor cell Anatomy 0.000 abstract description 3
- 210000004027 cell Anatomy 0.000 description 47
- 239000000243 solution Substances 0.000 description 20
- 201000011510 cancer Diseases 0.000 description 17
- 230000000694 effects Effects 0.000 description 11
- 238000011534 incubation Methods 0.000 description 10
- 239000000463 material Substances 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 230000035605 chemotaxis Effects 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000015556 catabolic process Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000006731 degradation reaction Methods 0.000 description 5
- 239000002105 nanoparticle Substances 0.000 description 5
- 238000005303 weighing Methods 0.000 description 5
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 238000003917 TEM image Methods 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 239000005457 ice water Substances 0.000 description 4
- 239000012299 nitrogen atmosphere Substances 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- 239000004971 Cross linker Substances 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- XIMIGUBYDJDCKI-UHFFFAOYSA-N diselenium Chemical compound [Se]=[Se] XIMIGUBYDJDCKI-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000006073 displacement reaction Methods 0.000 description 3
- 230000002526 effect on cardiovascular system Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 description 3
- 230000002147 killing effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 230000001376 precipitating effect Effects 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 206010006187 Breast cancer Diseases 0.000 description 2
- 208000026310 Breast neoplasm Diseases 0.000 description 2
- 206010061218 Inflammation Diseases 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
- 238000004113 cell culture Methods 0.000 description 2
- 230000001413 cellular effect Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 2
- 210000002889 endothelial cell Anatomy 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000001963 growth medium Substances 0.000 description 2
- 230000004054 inflammatory process Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002840 nitric oxide donor Substances 0.000 description 2
- 210000000056 organ Anatomy 0.000 description 2
- 230000001766 physiological effect Effects 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000010526 radical polymerization reaction Methods 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 230000002459 sustained effect Effects 0.000 description 2
- 229940124597 therapeutic agent Drugs 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- OZAIFHULBGXAKX-VAWYXSNFSA-N AIBN Substances N#CC(C)(C)\N=N\C(C)(C)C#N OZAIFHULBGXAKX-VAWYXSNFSA-N 0.000 description 1
- 230000005653 Brownian motion process Effects 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 231100000570 acute poisoning Toxicity 0.000 description 1
- 238000004115 adherent culture Methods 0.000 description 1
- 230000033115 angiogenesis Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000001093 anti-cancer Effects 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000005537 brownian motion Methods 0.000 description 1
- 201000011529 cardiovascular cancer Diseases 0.000 description 1
- 208000013527 cardiovascular neoplasm Diseases 0.000 description 1
- 210000000748 cardiovascular system Anatomy 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 208000026106 cerebrovascular disease Diseases 0.000 description 1
- 230000003034 chemosensitisation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001962 electrophoresis Methods 0.000 description 1
- 230000012202 endocytosis Effects 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 230000028993 immune response Effects 0.000 description 1
- 210000000987 immune system Anatomy 0.000 description 1
- 230000005847 immunogenicity Effects 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000002086 nanomaterial Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 238000011275 oncology therapy Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000001991 pathophysiological effect Effects 0.000 description 1
- 210000001539 phagocyte Anatomy 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000007065 protein hydrolysis Effects 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 230000009182 swimming Effects 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 238000009210 therapy by ultrasound Methods 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
- 230000005909 tumor killing Effects 0.000 description 1
- 238000001132 ultrasonic dispersion Methods 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 230000024883 vasodilation Effects 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
Images
Classifications
-
- 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
- C08F220/00—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 a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/52—Amides or imides
- C08F220/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
- C08F220/60—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing nitrogen in addition to the carbonamido nitrogen
- C08F220/603—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide containing nitrogen in addition to the carbonamido nitrogen and containing oxygen in addition to the carbonamido oxygen and nitrogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/74—Synthetic polymeric materials
- A61K31/785—Polymers containing nitrogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y40/00—Manufacture or treatment of nanostructures
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
- B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
Abstract
The invention discloses a preparation method and application of a zwitterionic polymer-based Nitric Oxide (NO) driven nano motor. The nanomotor disclosed by the invention can respond to the ROS concentration gradient to generate chemotactic behavior, and reacts with ROS in the nanomotor under the environment of tumor cells to generate NO to drive the NO to move and gradually degrade. The preparation method of the zwitterionic polymer-based NO driving nano motor is simple and efficient, has excellent biocompatibility, has active movement capability in a ROS microenvironment, and has a wide application prospect in the field of biomedicine.
Description
Technical Field
The invention belongs to a novel biomedical nano material, and particularly relates to a zwitterionic polymer based Nitric Oxide (NO) driven nano motor and a preparation method and application thereof.
Background
NO is a key signaling molecule in the cardiovascular, immune and central nervous systems and shows versatility in biomedical applications, such as playing a prominent role in regulating vasodilation, angiogenesis, chemosensitization, bactericidal and cancer-related physiological/pathophysiological activities. However, NO delivery techniques are still severely limited due to the physiological properties of NO, such as short half-life (<5s), short diffusion distance (20-160 μm), high reactivity with oxygen species, and concentration-dependent therapeutic outcome. To address these problems, a variety of NO-donor-based delivery systems have been developed for various NO-delivery platforms for cancer therapy, antimicrobial and cardiovascular therapy. Currently small molecule NO donors do not address the problem of sustained NO release. In the prior art, a post-load type NO driving nano motor with autonomous movement capability is constructed by utilizing a polymer and L-arginine electrostatic combination mode, and the problem of continuous NO release is solved, but the method of combining the polymer and the L-arginine by weak electrostatic action may face the problems of low load efficiency of L-arginine (fuel) and unstable load and possible shedding in the nano motor driving process, so that the release period and the release amount are not satisfactory. There is therefore a need to develop new types of NO-driven nanomotors with higher, high sustained NO release capabilities.
Disclosure of Invention
The purpose of the invention is as follows: aiming at the problems in the prior art, the invention provides a zwitterionic polymer based Nitric Oxide (NO) driven nano motor, which mainly solves the problems that the existing NO driven nano motor is low in fuel load efficiency and the load is unstable and can fall off in the nano motor driving process, so that the release period and the release amount of NO are improved.
The invention also provides a preparation method and application of the zwitterionic polymer-based Nitric Oxide (NO) driven nanomotor.
The technical scheme is as follows: in order to achieve the purpose, the invention provides a zwitterionic polymer-based Nitric Oxide (NO) driven nano motor which is formed by initiating a free radical polymerization reaction through an initiator by using an L-arginine derivative as a monomer and a diselenide compound as a cross-linking agent; the L-arginine derivative is a compound with a high-density active guanidyl crown energy group and a carbon-carbon double bond at the chain end; the diselenide compound is a Reactive Oxygen Species (ROS) -responsive diselenide compound; the nanomotors can produce chemotactic behavior in response to ROS concentration gradients.
Wherein the structural formulas of the L-arginine derivative and the diselenide compound are respectively shown as follows:
preferably, the initiator is one of azobisisobutyronitrile, azobisisoheptonitrile or dimethyl azobisisobutyrate.
The preparation method of the zwitterionic polymer based Nitric Oxide (NO) driven nanomotor comprises the following steps:
(1) dissolving L-arginine in a mixed solvent of deionized water and 1, 4-dioxane, adding triethylamine, cooling the solution by using an ice-water bath, dropwise adding methacrylic anhydride while stirring, removing the ice-water bath, stirring for reaction, and precipitating a product in acetone to obtain an L-arginine derivative;
(2) adding 2,2' -diselenide diethyl bis (1-ethylamine) dihydrochloride and triethylamine into an anhydrous dichloromethane solution, and slowly adding methacryloyl chloride; then stirring the reaction mixture to react under the nitrogen atmosphere; extracting and drying the reaction system, and removing an organic phase; purifying to obtain a diselenide compound cross-linking agent with ROS response type;
(3) dissolving the L-arginine derivative obtained in the step (1) and the diselenide compound cross-linking agent with ROS response type obtained in the step (2) in a solvent, adding an initiator to carry out polymerization reaction, and carrying out centrifugal washing to obtain the zwitterionic polymer-based NO driving nanomotor.
Wherein the molar ratio of the L-arginine to the methacrylic anhydride in the step (1) is 0.5-1, the volume ratio of the deionized water to the 1, 4-dioxane is 1-5, the volume ratio of the 1, 4-dioxane to the triethylamine is 1-5, the stirring reaction temperature is 20-30 ℃, and the reaction time is 10-48 h.
Preferably, the molar ratio of L-arginine to methacrylic anhydride is 0.6; the volume ratio of the deionized water to the 1, 4-dioxane is 2.4; the volume ratio of the 1, 4-dioxane to the triethylamine is 1.9; the reaction temperature is 25 ℃, and the reaction time is 12 h.
Wherein the molar ratio of the 2,2' -diselenodiethylbis (1-ethylamine) dihydrochloride to the methacryloyl chloride in the step (2) is 0.1-0.5, the stirring reaction temperature is 0-30 ℃, and the reaction time is 10-48 h;
wherein the volume of the anhydrous dichloromethane is 30-100mL, and the dosage of the triethylamine is 1-5 mL.
Preferably, the molar ratio of 2, 2-diselenodiethylbis (1-ethylamine) dihydrochloride to methacryloyl chloride is 0.25; the volume of the anhydrous dichloromethane is 60 mL; the dosage of triethylamine is 3.6 mL; the reaction temperature is 25 ℃, and the reaction time is 24 h.
Further, the reaction system in the step (2) is extracted by deionized water to remove impurities, namely anhydrous Na2SO4Drying overnight, removing an organic phase by reduced pressure evaporation, and purifying by silica gel column chromatography with ethyl acetate/petroleum ether as a raw material to obtain the ROS-responsive diselenide compound cross-linking agent.
Preferably, the ratio of the purified separation solvent is ethyl acetate/petroleum ether volume ratio of 1:2, 1:1, 2: 1.
Wherein, in the step (3), the molar ratio of the L-arginine zwitterionic derivative to the diselenide compound cross-linking agent is 5-20, the molar ratio of the L-arginine zwitterionic derivative to the initiator is 1-20, the reaction solvent is one of acetonitrile or dimethyl sulfoxide, the dosage of the solvent is generally 10-50mL, the reaction temperature is 80-100 ℃, and the reaction time is 1-5 h.
Preferably, the molar ratio of the L-arginine zwitterion derivative to the diselenide compound cross-linking agent is 10; the molar ratio of the L-arginine zwitterionic derivative to the initiator is 16.7; the solvent of the reaction is dimethyl sulfoxide; the dosage of the solvent is 20 mL; the initiator is azobisisobutyronitrile; the reaction temperature is 90 ℃ and the reaction time is 4 h.
And (3) performing centrifugal washing on the collected nanogel by ultracentrifugation, washing, freezing and drying to obtain the zwitterionic polymer-based NO driving nano motor, wherein the ultracentrifugation rotation speed is 10000-12000rpm, and the centrifugation time is 10-30 min.
Preferably, the speed of the ultracentrifugation is 12000rpm, and the centrifugation time is 10 min.
The zwitterionic polymer-based Nitric Oxide (NO) driven nano motor disclosed by the invention is applied to the biomedical field of treatment of cardiovascular and cerebrovascular diseases, cancer and the like.
The invention relates to application of a zwitterionic polymer-based Nitric Oxide (NO) driven nano motor in preparation of a medicine for targeting cardiovascular diseases and tumor focuses. The nano motor can respond to ROS concentration gradient in a microenvironment and embody chemotactic behavior, and is expected to achieve the aim of targeting diseases including cardiovascular diseases and tumors through microenvironment targeting.
The zwitterionic polymer-based Nitric Oxide (NO) driving nano motor prepared by the invention has high-density active guanidino sites by using a polymer polymerized by taking an L-arginine derivative as a monomer, and can efficiently react with ROS in a tumor microenvironment to generate NO which is used as a fuel for driving the motor to move and a therapeutic agent for playing a therapeutic role; and can respond to the ROS concentration gradient to generate chemotactic behavior, namely the nanomotor can perform self-diffusion electrophoresis movement towards a tumor site or an inflammation site with higher ROS concentration. The nano motor can be broken and degraded in the presence of ROS due to the diselenide ether bond in the structure, and the nano motor can be broken into low molecular segments and can be eliminated by a human body through the metabolism of each organ.
In the invention, the nano motor is added into the culture environment of cancer cells, and the motion condition of the nano motor is tracked by using a laser confocal microscope and a fluorescence microscope; the effective demonstration is that: the nano motor can respond to the concentration gradient of ROS to generate chemotactic behavior, reacts with ROS in the tumor cell environment to generate NO to drive the tumor cell to move and gradually degrade, has excellent biocompatibility, has active movement capability in the ROS microenvironment, and has wide application prospect in the field of biomedicine.
The invention synthesizes a novel NO driving nano motor with high-density guanidyl active sites by a method of free radical polymerization and covalent grafting. Wherein, the monomer is the L-arginine derivative of the zwitterionic polymer group, so the monomer has good biocompatibility; the cross-linking agent is a diselenide compound with Reactive Oxygen Species (ROS) response type, so the cross-linking agent has response degradation performance, and the invention synthesizes a brand new NO driving nano motor by using the L-arginine derivative and the diselenide compound for the first time. Compared with electrostatic combination, the nano motor prepared by adopting the covalent combination mode has richer active guanidine-based sites capable of releasing NO, so that the nano motor has longer-lasting and larger-amount NO releasing performance. Eventually providing faster motion speed to the nanomotor.
The invention adopts a covalent grafting method to prepare a nano particle with rich active guanidyl sites on the surface, but not a micromolecular NO donor, so the nano particle has longer NO release capacity than the donor. In addition, the monomers used for synthesizing the nano motor are L-arginine derivatives based on zwitterionic polymers, so that the nano motor has unique good biocompatibility of zwitterions, and the risk of rapid clearance, degradation and even acute poisoning in vivo can be avoided. The synthesized nano motor is prepared by combining free polymerization and covalent bonds, and has high-density guanidine active sites (sites for generating NO), so that the performance of generating NO is more stable and durable, a theoretical basis is provided for the nano motor to react with ROS in a tumor microenvironment to continuously release NO, and the problems of short half-life period and short release time of NO are solved.
Has the advantages that: compared with the prior art, the invention has the following advantages:
1. the NO driving nano motor based on the zwitterionic polymer base has the advantages that the material main body of the nano motor is an L-arginine derivative, so that the nano motor has good biocompatibility and dense guanidyl active sites; the diselenide compound with Reactive Oxygen Species (ROS) response type is a cross-linking agent, so that the diselenide compound has response degradation performance. Due to the fact that high-density guanidino active sites provide theoretical basis for the guanidino active sites to react with ROS in a tumor microenvironment to continuously release NO, the problems of short half-life period and short release time of NO are solved. In addition, NO can be used as a driving force for driving the nano motor to move, and can also be used as a therapeutic agent for treating tumors.
2. The preparation method is simple and efficient, the synthesis conditions are mild, the material dispersion performance is good, and the synthesized nano motor has the following characteristics: (1) excellent biocompatibility, the zwitterionic polymer matrix material has low immunogenicity, which is beneficial to maintaining the bioavailability and the treatment effect of the material in the long-term administration process, and inhibits the activation of phagocytes by reducing protein endocytosis, interfering protein hydrolysis, physically blocking MHCII-epitope combination and the like, thereby weakening the immune response; (2) degrading the performance of the nanomotor as required, the Se-Se bond has low energy, reacts even under mild stimuli, is particularly sensitive to reductive or oxidative stimuli, can be cleaved in the presence of active oxygen, and triggers the disintegration of the nanogel. The small molecular fragment can be metabolized by human organs and discharged out of the body, and has good biological safety.
3. The zwitterionic polymer-based Nitric Oxide (NO) driven nano motor prepared by the invention has the advantages of long NO release time, large release amount and the like, has spontaneous chemotactic performance, and can generate self-diffusion swimming movement and tumor killing performance towards a tumor part or an inflammation part with higher ROS concentration.
Drawings
FIG. 1 is a nuclear magnetic spectrum of a derivative of L-arginine of example 1;
FIG. 2 is a nuclear magnetic spectrum of the diselenide ether crosslinker of example 2;
FIG. 3 is a transmission electron micrograph (scale: 500nm) of the zwitterion-based NO-driven nanomotor obtained in example 3;
FIG. 4 is a transmission electron micrograph of PAMSe in example 4 after incubation at 37 ℃ for 12h,24h and 48h in 0.002% hydrogen peroxide solution;
FIG. 5 is the NO release of the nanomotor in the cancer cell environment of example 5;
FIG. 6 is the movement trace of the nanomotor in the cancer cell environment in example 6;
FIG. 7 is a Mean Square Displacement (MSD) quadratic fit curve of the nanomotor motion trajectory in the cancer cell environment of example 6;
FIG. 8 is a linear fit curve of Mean Square Displacement (MSD) of the nanomotor motion trajectory in the cancer cell environment of example 6;
FIG. 9 is a model of the chemotaxis assay of the concentration of nanomotor ROS in example 7;
FIG. 10 is the fluorescence intensity of nanomotors in example 7 at b-terminus in chemotaxis model with/without ROS gradient
FIG. 11 is a graph showing the cell activity of the nanomotors incubated with endothelial cells at different concentrations for different periods of time in example 8 to evaluate the biocompatibility of the nanomotors;
FIG. 12 is the cell activity of the degraded nanomotor of example 8 after incubation with cancer cells for various times to evaluate the biocompatibility of the nanomotor;
FIG. 13 is an evaluation of the killing performance of the nanomotor on cancer cells in example 9;
FIG. 14 is a transmission electron micrograph (lower right angle scale: 500nm) of the nanomotor prepared in comparative example 1;
FIG. 15 shows NO release of the supported PMSE/A nanomotor of comparative example 1 under a cellular environment;
FIG. 16 is a graph of the movement of the supported PMSE/A nanomotor of comparative example 1 in a cellular environment;
fig. 17 is a MSD quadratic fit curve of the moving trajectory of the supported PMSe/a nanomotor of comparative example 1 in a cancer cell environment.
Detailed Description
The experimental methods described in the examples are all conventional methods unless otherwise specified; the reagents and materials are commercially available, unless otherwise specified.
Example 1
Preparation of L-arginine derivative:
(1) weighing 11.5mmol L-arginine, dissolving in a mixed solvent of deionized water (20mL) and 1, 4-dioxane (8.5mL), ultrasonically dispersing, and magnetically stirring at room temperature;
(2) 4.5mL of triethylamine is added into the reaction system in the step (1), and the solution is cooled to 0 ℃ by using an ice water bath;
(3) adding 18.9mmol of methacrylic anhydride dropwise under stirring, removing the ice-water bath, and reacting under stirring at 25 ℃ for 12 hours.
(4) And (3) dropwise adding the solution obtained in the step (3) into 400mL of acetone for precipitation, then re-dissolving the precipitate in water, and precipitating in acetone again, wherein the precipitation step is repeated twice to dissolve in water.
(5) Centrifuging the solution of (4) at 8000rpm for 15min, discarding the upper liquid, precipitating the lower layer, and vacuum drying at 60 deg.C to obtain L-arginine derivative: n- (2-methyl-1-OXO-2-propen-1-yl) -L-arginine.
FIG. 1 is a nuclear magnetic spectrum of N- (2-methyl-1-OXO-2-propen-1-yl) -L-arginine,1H NMR(400MHz,D2o) δ 5.61(s,1H),5.35(s,1H),4.13(dd, J ═ 8.0,5.1Hz,1H),3.09(t, J ═ 6.8Hz,2H),1.83(s,3H), 1.81-1.59 (m,2H), 1.56-1.46 (m, 2H). As a result, it was confirmed that the L-arginine derivative was successfully produced.
Example 2
Synthesis of diselenide compound cross-linker with Reactive Oxygen Species (ROS):
(1) 1.0g of 2,2' -diselenediylbis (1-ethylamine) dihydrochloride (CAS number: 3542-13-0) and 3.6mL of triethylamine were weighed into 60mL of dichloromethane, and the mixture was cooled to 0 ℃.
(2) To the solution obtained in step (1), 1.3g of methacryloyl chloride was slowly added, followed by a reaction at 25 ℃ for 24 hours in a nitrogen atmosphere.
(3) And (3) extracting the solution reacted in the step (2) by using a large amount of deionized water to remove impurities, and collecting an organic solvent phase.
(4) The organic phase collected in step (3) was dried over anhydrous sodium sulfate overnight to give a crude product, and the organic phase was removed by evaporation under reduced pressure.
(5) And (3) respectively taking ethyl acetate/petroleum ether (volume ratio is 1:2, 1:1 and 2:1) with different proportions as raw materials for the crude product obtained in the step (4), and separating and purifying the raw materials through a silica gel column to obtain a product, namely light yellow solid powder and a diselenide compound with Reactive Oxygen Species (ROS) response type.
FIG. 2 is a nuclear magnetic spectrum of a synthesized diselenide compound having a Reactive Oxygen Species (ROS) response pattern.1HNMR(400MHz,CDCl3) δ 6.54(s,2H),5.77(s,2H),5.43-5.34(m,2H),3.70(q, J ═ 6.5Hz,4H),3.16-3.04(m,4H),2.03-1.94(m,6H),1.68(s, 4H). The successful synthesis of a diselenide compound having a Reactive Oxygen Species (ROS) response can be seen in fig. 2.
Example 3
Preparation of the NO-driven nanomotor based on the zwitterionic polymer group:
(1) weighing 0.5mmol of L-arginine derivative and 0.05mmol of diselenide ether cross-linking agent with active oxygen response type in a three-neck flask;
(2) removing air in the flask in the step (1) by using a vacuum pump, and continuously introducing nitrogen;
(3) adding 20mL of dry dimethyl sulfoxide solution into the step (2), and performing ultrasonic dispersion and dissolution;
(4) weighing 0.03mmol of azobisisobutyronitrile, adding 500 mu L of dry dimethyl sulfoxide solution, ultrasonically dispersing and dissolving, and injecting into the reaction system in the step (3) by using an injector;
(5) transferring the three-necked flask into an oil bath kettle, magnetically stirring at 300rpm, and polymerizing at the reaction temperature of 90 ℃ for 4 hours in a nitrogen atmosphere to obtain a milky uniformly dispersed zwitter-ion nitric oxide nanomotor solution;
(6) the obtained zwitterion-based NO-driven nano motor solution is placed in a high-speed centrifuge to be centrifuged at 12000rpm for 10min, the upper layer liquid is discarded, and the precipitate is repeatedly washed with deionized water for 3 times. And (3) freeze-drying the finally obtained precipitate in a freeze-drying machine to obtain the final zwitter ion-based nitric oxide nanomotor (PAMSe). As shown in fig. 3, the synthesized nanomotor has a particle size of about 230nm and appears as uniformly dispersed and irregular quasi-spherical nanoparticles.
Example 4
Degradation of zwitterionic NO-driven nanomotors:
(1) the PAMSe nanomotor prepared in example 3 was weighed out and dispersed in 1mL of 0.002% hydrogen oxide solution to a final concentration of 200. mu.g mL-1And reacting in a 37 ℃ water bath environment, and observing the morphology change of the nano motor by using a transmission electron microscope at 12h,24h and 48h respectively. As shown in FIG. 4, it can be seen that the PAMSe nanomotor is associated with H2O2(0.002%) incubation time was prolonged, the size of the nanoparticles gradually increased until finally the spheroidal particle structure completely collapsed and degraded, indicating that the PAMSe nanomotor of the present invention can be degraded in response in the ROS environment.
Example 5
Zwitterionic NO-driven nanomotor release of NO:
(1) 3mg of the zwitterionic-based NO nanomotor prepared in example 3 was added to MCF-7 cells seeded in 24-well plates, respectively. Cell seeding density of 5 x 106cell/well, complete medium volume of 1mL, cell 37 degrees C after 24h incubation and adding the nanometer motor.
(2) The cells were incubated with zwitterionic nitric oxide nanomotors (0, 1h, 3h, 6h, 9h, 12h,24h, 36h, 72h, 96h and 108h), respectively. After the reaction, the mixture was centrifuged at 12000rpm for 10min, and the supernatant was collected for further use.
(3) The obtained supernatants were each assayed for the amount of NO produced using a nitric oxide kit (bi yun day). As shown in fig. 5, the nano-motor NO release amount is continuously increased with the time extension in the time range set by the experiment, i.e. the nano-motor can continuously release NO 96h, and the release amount is 4.7 μ M. The nano motor NO of the invention is proved to have long release time and high release amount.
Example 6
The movement performance of the zwitterion-based NO-driven nanomotor in a cancer cell environment is researched:
(1) weighing 1mg of the nano motor prepared in the embodiment 3, adding 5mL of deionized water, and performing ultrasonic treatment for 20min to fully disperse the solution to obtain a uniformly dispersed nano motor solution of 200 mug/mL;
(2) breast cancer cells MCF-7 with 5 x 105Inoculating the cell/mL into a 14mm cell culture dish, wherein the volume of a complete culture medium is 1mL, and placing the cell culture dish in a constant-temperature incubator at 37 ℃ to allow the cells to adhere to the wall overnight;
(3) and taking 10 mu L of the uniformly dispersed nano motor solution of 200 mu g/mL, directly adding the solution into the adherent cell culture dish, and immediately observing and recording the motion state of the nano motor by using a fluorescence microscope.
(4) Fig. 6 is a motion trace of the nanomotor, which proves that the nanomotor can move in the cell environment. And the motion speed is calculated to be about 3.48 mu m/s according to the motion track, parabolic fitting and linear fitting are respectively carried out on the mean square displacement (fig. 7 and 8), as shown in fig. 7 and 8, the result shows high correlation with the parabola, and the motion mode of the nanomotor in the cell environment is proved to be self-driven rather than Brownian motion.
Example 7
Zwitterionic NO-driven nanomotor chemotaxis study:
(1) weighing 1mg of the nanomotor prepared in example 3, adding 1mL of deionized water, and performing ultrasonic full dispersion to obtain 1mg mL-1A uniformly dispersed nanomotor solution. Breast cancer cells MCF-7 with 5 x 105cell/mL was inoculated into the right chamber of the chemotaxis model apparatus shown in fig. 9, placed in a 37 ℃ incubator at a constant temperature to allow cells to adhere overnight, and a ROS concentration gradient was constructed in the apparatus from right to left with the ROS concentration varying from high to low. As a control not inThe right chamber was seeded with cells to provide an environment free of ROS concentration gradients.
(2) To the left chamber of both devices with and without ROS concentration gradient was added 250. mu.L of 1mg mL-1The zwitterion-based NO of (a) drives the nanomotor solution. After 20min, the solution in the right chamber of the model was pipetted 100. mu.L to measure its fluorescence intensity. As shown in fig. 10, the fluorescence intensity of the nanomotors detected in the model right chamber with ROS concentration gradient was about 8 times higher than that of the control group (without ROS concentration gradient), demonstrating that the zwitterionic NO-driven nanomotor chemotaxis has high ROS concentration chemotaxis.
Example 8
Evaluation of biocompatibility of the NO-driven nanomotors of zwitterionic derivatives;
(1) endothelial Cells (HUVECs) were treated with 5X 104cells/mL are inoculated in a 96-well plate, after the cells are attached to the wall, the nano motor prepared in example 3 is dispersed in a culture medium, and nano motors (20,50, 100,150,200 mu g mL) with different concentrations are prepared-1) After incubation with HUVECs for different times (12h,24h,48h), cell activity was detected using MTT reagent;
(2) from fig. 11, it can be seen that the cell activities of HUVECs do not change significantly after incubation with HUVECs for different time periods (12h,24h and 48h) at the above concentration of nanomotors, which preliminarily proves the biocompatibility of nanomotors;
(3) then, 5mg nanomotor was added to 5mL of hydrogen oxide solution (0.002%) and reacted in a water bath environment at 37 ℃ for 48 hours sufficiently, and the degraded product in the lower layer was centrifuged to take out, at which time it was considered that NO was continuously generated in the cancer cell environment. Mixing MCF-7 with 5 x 105cells/mL were seeded in 96-well plates and after cells were attached, the degraded material was treated with different concentrations of product (20,50, 100,150, 200. mu.g mL)-1) Incubating the cells and the cancer cells in an incubator at 37 ℃ for different time (12h,24h and 48h) to check the activity of the cells;
(4) from fig. 12, it can be seen that the cancer cell activity was hardly affected by the increase of the material concentration (after degradation) and the extension of the incubation time, thus demonstrating that the zwitterionic substrate has good biocompatibility.
Example 9
Evaluation of anticancer Properties of NO-driven nanomotors of zwitterionic derivatives
(1) Mixing MCF-7 with 5 x 105cell/mL was seeded in 96-well plates, and after cells were attached to the wall, the nanomotors prepared in example 3 were formulated into dispersions using complete medium at different final concentrations (20,50, 100,150, 200. mu.g mL)-1) Detecting the cell activity of the cells after incubation with cancer cells for different time periods (12h,24h and 48 h);
(2) it can be seen from fig. 13 that the killing performance of nanomotors against cancer cells is concentration and time dependent. Specifically, the cell activity of the cancer cells gradually decreased with the increase in the concentration of the material incubated with the cells at the same time, and the concentration of the material was adjusted from 20. mu.g mL at a time point of 48 hours-1Increase to 200. mu.g mL-1When the cell activity is reduced to 49.7% from 87.4%; and when the concentration of the nano motor is constant, the cell activity is gradually reduced along with the prolonging of the incubation time of the nano motor and the cells. The reason for the above results may be that the NO produced by the nanomotor in the cell environment has concentration and time dependency, and the killing ability to the cell is gradually enhanced as the concentration of the nanomotor is increased and the NO production amount is gradually increased with the prolongation of the cell incubation time.
Comparative example 1
The nano-particle PMSE is prepared by using methacrylic acid with double bonds at end groups as a monomer and a diselenide compound as a cross-linking agent, and then is subjected to electrostatic combination with L-arginine in a weak electrostatic combination mode to prepare the rear-loading nano-motor PMSE/A nano-motor.
The specific experimental steps are as follows: methacrylic acid (500mg, 5.81mmol), AIBN (11.10mg, 0.07mmol) and diselenide crosslinker (55.60mg, 0.15mmol, prepared in inventive example 2) were dissolved in 40mL acetonitrile in a three-neck flask and kept under nitrogen atmosphere at reflux for 1 h. The resulting nanogels were collected by centrifugation (5000rpm, 10min), washed at least three times with deionized water and freeze-dried. Next, 50mg of the prepared product is weighed and dispersed in 5mL of aqueous solution, 5mg of L-arginine is added and stirred at room temperature for 24 hours, then the mixture is washed with distilled water for 3 times, and the product is obtained by centrifugation and dried, so that the supported NO-driven nanomotor is obtained, wherein a TEM image of the supported NO-driven nanomotor is shown in fig. 14, and the particle size of the supported NO-driven nanomotor is close to that of the nanomotor prepared in example 3.
The NO release amount and the moving speed were measured by the method of example 5, respectively, as shown in FIGS. 15 to 17, and as a result, it was found that the NO release amount of the supported PMSE/A nanomotor was 1.57. mu.M as compared with PAMSe (4.71. mu.M). The movement speed obtained by the movement track of the load type PMSE/A nano motor in the cell environment and MSD quadratic term fitting curve is about 1.8 +/-0.4 mu m/s, which is far less than the movement speed (3.48 +/-0.9 mu m/s) of the covalent grafting nano motor provided by the invention. Therefore, the PAMSe nano motor provided by the invention has higher fuel load efficiency, so that the release period and the release amount of NO are improved, and the movement speed of the nano motor is also improved.
Example 10
Example 10 preparation of zwitterionic polymer based Nitric Oxide (NO) driven nanomotors. Wherein an L-arginine derivative was prepared by the method of example 1, except that: the mol ratio of L-arginine to methacrylic anhydride is 0.5, the volume ratio of deionized water to 1, 4-dioxane is 1, the volume ratio of 1, 1, 4-dioxane to triethylamine is 1, the stirring reaction temperature is 20 ℃, and the reaction time is 48 hours;
wherein the diselenide compound cross-linking agent is prepared by the method of example 2, except that: the molar ratio of 2, 2-diselenodiethylbis (1-ethylamine) dihydrochloride to methacryloyl chloride is 0.1, the reaction temperature is 0 ℃ under stirring, and the reaction time is 48 hours.
The method of example 3 was used to prepare a nanomotor, except that: the molar ratio of the L-arginine zwitterionic derivative to the diselenide compound cross-linking agent is 5, the molar ratio of the L-arginine zwitterionic derivative to the initiator is 1, the initiator is azodiisoheptanonitrile, the reaction solvent is acetonitrile, the reaction temperature is 80 ℃, the reaction time is 5h, the rotation speed of ultracentrifugation is 10000rpm, and the centrifugation time is 30 min.
Example 11
Example 11 preparation of zwitterionic Nitric Oxide (NO) -driven nanomotors. Wherein an L-arginine derivative was prepared by the method of example 1, except that: the mol ratio of L-arginine to methacrylic anhydride is 1, the volume ratio of deionized water to 1, 4-dioxane is 5, the volume ratio of 1, 4-dioxane to triethylamine is 5, the stirring reaction temperature is 30 ℃, and the reaction time is 10 hours;
wherein the diselenide compound cross-linking agent is prepared by the method of example 2, except that: the molar ratio of 2, 2-diselenodiethylbis (1-ethylamine) dihydrochloride to methacryloyl chloride is 0.5, the reaction temperature is 30 ℃ under stirring, and the reaction time is 10 hours.
The method of example 3 was used to prepare a nanomotor, except that: the molar ratio of the L-arginine zwitterionic derivative to the diselenide compound cross-linking agent is 20, the molar ratio of the L-arginine zwitterionic derivative to the initiator is 20, the initiator is one of dimethyl azodiisobutyrate, the reaction temperature is 100 ℃, the reaction time is 1h, the ultracentrifugation rotating speed is 12000rpm, and the centrifugation time is 10 min.
Claims (10)
1. A zwitterionic polymer-based NO-driven nano motor is characterized in that the zwitterionic polymer-based NO-driven nano motor is formed by initiating polymerization reaction through an initiator by taking an L-arginine derivative as a monomer and a diselenide compound as a cross-linking agent; the L-arginine derivative is a compound with a high-density active guanidyl functional group and a carbon-carbon double bond at the chain end; the diselenide compound is a Reactive Oxygen Species (ROS) responsive diselenide compound.
3. the zwitterionic polymer-based nitric oxide-driven nanomotor of claim 1, wherein the initiator is preferably one of azobisisobutyronitrile, azobisisoheptonitrile, or dimethyl azobisisobutyrate.
4. A method for preparing the zwitterionic polymer-based nitric oxide-driven nanomotor of claim 1, comprising the steps of:
(1) dissolving L-arginine in a mixed solvent of deionized water and 1, 4-dioxane, adding triethylamine, cooling the solution, dropwise adding methacrylic anhydride while stirring, and stirring for reaction to obtain an L-arginine derivative;
(2) adding 2,2' -diselenide diethyl bis (1-ethylamine) dihydrochloride and triethylamine into an anhydrous dichloromethane solution, slowly adding methacryloyl chloride, and stirring for reaction; extracting and drying the reaction system, and removing an organic phase; purifying to obtain a diselenide compound cross-linking agent with ROS response type;
(3) dissolving the L-arginine derivative obtained in the step (1) and the diselenide compound cross-linking agent with ROS response type obtained in the step (2) in a solvent, adding an initiator to carry out polymerization reaction, and carrying out centrifugal washing to obtain the zwitterionic polymer-based NO driving nanomotor.
5. The preparation method according to claim 4, wherein the molar ratio of L-arginine to methacrylic anhydride in step (1) is 0.5-1, the volume ratio of deionized water to 1, 4-dioxane is 1-5, the volume ratio of 1, 4-dioxane to triethylamine is 1-5, the stirring reaction temperature is 20-30 ℃, and the reaction time is 10-48 h.
6. The preparation method according to claim 4, wherein the molar ratio of the 2,2' -diselenediylbis (1-ethylamine) dihydrochloride to the methacryloyl chloride in the step (2) is 0.1 to 0.5, the reaction temperature is 0 to 30 ℃ and the reaction time is 10 to 48 hours.
7. The method according to claim 4, wherein the reaction system of step (2) is extracted with deionized water to remove impurities, anhydrous Na2SO4Drying overnight, removing an organic phase by reduced pressure evaporation, and purifying by silica gel column chromatography with ethyl acetate/petroleum ether as a raw material to obtain the ROS-responsive diselenide compound cross-linking agent.
8. The preparation method according to claim 4, wherein the molar ratio of the L-arginine zwitterionic derivative to the diselenide compound cross-linking agent in the step (3) is 5-20, the molar ratio of the L-arginine zwitterionic derivative to the initiator is 1-20, the reaction solvent is one of acetonitrile or dimethyl sulfoxide, the reaction temperature is 80-100 ℃, and the reaction time is 1-5 h.
9. The preparation method according to claim 4, wherein the centrifugal washing in step (3) is collecting the obtained nanogel by ultracentrifugation, and washing and freeze-drying to obtain the zwitterionic polymer-based NO-driven nanomotor, wherein the rotation speed of the ultracentrifugation is 10000-12000rpm, and the centrifugation time is 10-30 min.
10. Use of the zwitterionic polymer-based nitric oxide-driven nanomotor of claim 1 in the manufacture of a medicament for targeting a cardiovascular disease lesion or a tumor lesion.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110503975.6A CN113402661B (en) | 2021-05-08 | 2021-05-08 | Zwitterionic polymer-based nitric oxide-driven nano motor and preparation method and application thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202110503975.6A CN113402661B (en) | 2021-05-08 | 2021-05-08 | Zwitterionic polymer-based nitric oxide-driven nano motor and preparation method and application thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN113402661A true CN113402661A (en) | 2021-09-17 |
CN113402661B CN113402661B (en) | 2022-07-26 |
Family
ID=77678399
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202110503975.6A Active CN113402661B (en) | 2021-05-08 | 2021-05-08 | Zwitterionic polymer-based nitric oxide-driven nano motor and preparation method and application thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN113402661B (en) |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004050795A2 (en) * | 2002-11-27 | 2004-06-17 | Tufts University | Antioxidant-functionalized polymers |
CN101115514A (en) * | 2005-02-11 | 2008-01-30 | 诺拉布斯有限公司 | Device method, and use for treatment of neuropathy involving nitric oxide |
US20100081159A1 (en) * | 2008-09-26 | 2010-04-01 | Lebedeva Irina V | Profiling reactive oxygen, nitrogen and halogen species |
US20120003155A1 (en) * | 2009-06-15 | 2012-01-05 | National Institutes Of Health | Dendrimer based nanodevices for therapeutic and imaging purposes |
CN108379219A (en) * | 2018-02-08 | 2018-08-10 | 复旦大学 | Amphoteric ion polymer nanogel and its preparation method and application |
CN108773831A (en) * | 2018-06-11 | 2018-11-09 | 南京师范大学 | L-arginine nano-particle and the degradable nano-motor and preparation method thereof that nitric oxide is power source |
-
2021
- 2021-05-08 CN CN202110503975.6A patent/CN113402661B/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004050795A2 (en) * | 2002-11-27 | 2004-06-17 | Tufts University | Antioxidant-functionalized polymers |
CN101115514A (en) * | 2005-02-11 | 2008-01-30 | 诺拉布斯有限公司 | Device method, and use for treatment of neuropathy involving nitric oxide |
US20100081159A1 (en) * | 2008-09-26 | 2010-04-01 | Lebedeva Irina V | Profiling reactive oxygen, nitrogen and halogen species |
US20120003155A1 (en) * | 2009-06-15 | 2012-01-05 | National Institutes Of Health | Dendrimer based nanodevices for therapeutic and imaging purposes |
CN108379219A (en) * | 2018-02-08 | 2018-08-10 | 复旦大学 | Amphoteric ion polymer nanogel and its preparation method and application |
CN108773831A (en) * | 2018-06-11 | 2018-11-09 | 南京师范大学 | L-arginine nano-particle and the degradable nano-motor and preparation method thereof that nitric oxide is power source |
Non-Patent Citations (4)
Title |
---|
WAN M M, ET AL.: "Nitric oxide‐driven nanomotor for deep tissue penetration and multidrug resistance reversal in cancer therapy", 《ADVANCED SCIENCE》 * |
WAN M, CHEN H, ET AL.: "Bio-inspired nitric-oxide-driven nanomotor", 《NATURE COMMUNICATIONS》 * |
YANG Y,ET AL.: "Advanced nitric oxide donors: Chemical structure of NO drugs, NO nanomedicines and biomedical applications", 《NANOSCALE》 * |
YUAN Z, ET AL.: "Near-infrared light-triggered nitric-oxide-enhanced photodynamic therapy and low-temperature photothermal therapy for biofilm elimination", 《ACS NANO》 * |
Also Published As
Publication number | Publication date |
---|---|
CN113402661B (en) | 2022-07-26 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN107550921B (en) | Nanoparticle-polymer injectable composite hydrogel double-drug-loading system and preparation method thereof | |
Li et al. | Glucose and H 2 O 2 dual-sensitive nanogels for enhanced glucose-responsive insulin delivery | |
Wang et al. | Heparin− paclitaxel conjugates as drug delivery system: synthesis, self-assembly property, drug release, and antitumor activity | |
KR102144749B1 (en) | Biodegradable amphiphilic polymer, polymer vesicle produced therefrom, and use in the manufacture of therapeutic agents for lung cancer | |
CN108752541B (en) | Amphiphilic block polymer with hypoxia and temperature dual responsiveness and taking azo bond as connecting bond and preparation method thereof | |
CN101474411B (en) | Anti-tumor prodrug using novel amphipathic hyperbranched polyesters as carrier and preparation method | |
JP2017517622A (en) | Carbonate polymer having dithio 5-membered ring functional group in side chain and its application | |
US20220257589A1 (en) | Drug carrier and preparation method thereof | |
WO2021179843A1 (en) | Anti-tumor nano adjuvant based on vesicle formed by cross-linked biodegradable polymer, preparation method therefor and use thereof | |
CN101045033A (en) | Ply-glycosyl modified acid-sensitive nanometer gel | |
Wu et al. | Novel hydroxyl-containing reduction-responsive pseudo-poly (aminoacid) via click polymerization as an efficient drug carrier | |
CN107266384B (en) | N- carboxyl inner-acid anhydride monomer and polyaminoacid based on 2- aminohexadecanoic acid and preparation method thereof | |
Chen et al. | Real-time monitoring of a controlled drug delivery system in vivo: construction of a near infrared fluorescence monomer conjugated with pH-responsive polymeric micelles | |
JP6296381B2 (en) | Disulfur 5-membered ring functional group-containing cyclic carbonate monomer and method for preparing the same | |
CN113402661B (en) | Zwitterionic polymer-based nitric oxide-driven nano motor and preparation method and application thereof | |
CN109821025B (en) | Light and redox dual-stimulus response type amphiphilic polymer drug carrier and preparation method and application thereof | |
WO2023237060A1 (en) | Amphiphilic block polymer, chemoradiotherapy nano sensitizer, and method for preparing same | |
CN1869099A (en) | Method of preparing nanometer and micron self assembling body from poly peptide-b-polytetrahydrofuran-b-polypeptide triblock copolymer | |
CN114668745B (en) | Glucose and H 2 O 2 Double-response double-layer crosslinked polymer nano drug delivery system and preparation method and application thereof | |
CN105879048A (en) | Preparation method of functional biodegradable nano particle based on polyamino acid | |
CN113995850B (en) | Cascade amplification nano-drug with tyrosinase response and preparation and application thereof | |
CN110642968B (en) | Double-enzyme responsive dumbbell-shaped super-amphiphilic molecule and preparation method and application thereof | |
CN112625252B (en) | PH response permeability-enhanced modified dendritic PAMAM polymer and preparation and application thereof | |
CN111423571B (en) | Biodegradable zwitterionic polycarbonate and application thereof | |
CN111777711B (en) | Polymer for photo-thermal controlled release of hydrogen sulfide and preparation method and application thereof |
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 |