DK2947111T3 - Monofunktionel forgrenet polyethylenglycol og biorelateret stof modificeret af samme - Google Patents
Monofunktionel forgrenet polyethylenglycol og biorelateret stof modificeret af samme Download PDFInfo
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- DK2947111T3 DK2947111T3 DK13871951.3T DK13871951T DK2947111T3 DK 2947111 T3 DK2947111 T3 DK 2947111T3 DK 13871951 T DK13871951 T DK 13871951T DK 2947111 T3 DK2947111 T3 DK 2947111T3
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- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 description 1
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- 150000003905 phosphatidylinositols Chemical class 0.000 description 1
- SHUZOJHMOBOZST-UHFFFAOYSA-N phylloquinone Natural products CC(C)CCCCC(C)CCC(C)CCCC(=CCC1=C(C)C(=O)c2ccccc2C1=O)C SHUZOJHMOBOZST-UHFFFAOYSA-N 0.000 description 1
- 230000008560 physiological behavior Effects 0.000 description 1
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- 229920001308 poly(aminoacid) Polymers 0.000 description 1
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- TZLVRPLSVNESQC-UHFFFAOYSA-N potassium azide Chemical compound [K+].[N-]=[N+]=[N-] TZLVRPLSVNESQC-UHFFFAOYSA-N 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
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- ZNCXUFVDFVBRDO-UHFFFAOYSA-N pyridine;sulfuric acid Chemical compound [H+].[O-]S([O-])(=O)=O.C1=CC=[NH+]C=C1 ZNCXUFVDFVBRDO-UHFFFAOYSA-N 0.000 description 1
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- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- XJBLDMYABBOCCD-UHFFFAOYSA-N sulfuryl dichloride 2,2,2-trifluoroacetic acid Chemical compound S(=O)(=O)(Cl)Cl.FC(C(=O)O)(F)F XJBLDMYABBOCCD-UHFFFAOYSA-N 0.000 description 1
- FGTJJHCZWOVVNH-UHFFFAOYSA-N tert-butyl-[tert-butyl(dimethyl)silyl]oxy-dimethylsilane Chemical compound CC(C)(C)[Si](C)(C)O[Si](C)(C)C(C)(C)C FGTJJHCZWOVVNH-UHFFFAOYSA-N 0.000 description 1
- KJTULOVPMGUBJS-UHFFFAOYSA-N tert-butyl-[tert-butyl(diphenyl)silyl]oxy-diphenylsilane Chemical compound C=1C=CC=CC=1[Si](C=1C=CC=CC=1)(C(C)(C)C)O[Si](C(C)(C)C)(C=1C=CC=CC=1)C1=CC=CC=C1 KJTULOVPMGUBJS-UHFFFAOYSA-N 0.000 description 1
- QSUJAUYJBJRLKV-UHFFFAOYSA-M tetraethylazanium;fluoride Chemical compound [F-].CC[N+](CC)(CC)CC QSUJAUYJBJRLKV-UHFFFAOYSA-M 0.000 description 1
- 229940126585 therapeutic drug Drugs 0.000 description 1
- 150000007970 thio esters Chemical group 0.000 description 1
- 239000005495 thyroid hormone Substances 0.000 description 1
- 229940036555 thyroid hormone Drugs 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 239000012581 transferrin Substances 0.000 description 1
- WILBTFWIBAOWLN-UHFFFAOYSA-N triethyl(triethylsilyloxy)silane Chemical compound CC[Si](CC)(CC)O[Si](CC)(CC)CC WILBTFWIBAOWLN-UHFFFAOYSA-N 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- VBEQCZHXXJYVRD-GACYYNSASA-N uroanthelone Chemical compound C([C@@H](C(=O)N[C@H](C(=O)N[C@@H](CS)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CS)C(=O)N[C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)NCC(=O)N[C@@H](CC=1C=CC(O)=CC=1)C(=O)N[C@@H](CO)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CS)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C(C)C)[C@@H](C)O)NC(=O)[C@H](CO)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@@H](NC(=O)[C@H](CC=1NC=NC=1)NC(=O)[C@H](CCSC)NC(=O)[C@H](CS)NC(=O)[C@@H](NC(=O)CNC(=O)CNC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CS)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CS)NC(=O)CNC(=O)[C@H]1N(CCC1)C(=O)[C@H](CC=1C=CC(O)=CC=1)NC(=O)[C@H](CO)NC(=O)[C@@H](N)CC(N)=O)C(C)C)[C@@H](C)CC)C1=CC=C(O)C=C1 VBEQCZHXXJYVRD-GACYYNSASA-N 0.000 description 1
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- MYPYJXKWCTUITO-LYRMYLQWSA-N vancomycin Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C(O)=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)NC)[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-N 0.000 description 1
- 229960003165 vancomycin Drugs 0.000 description 1
- MYPYJXKWCTUITO-UHFFFAOYSA-N vancomycin Natural products O1C(C(=C2)Cl)=CC=C2C(O)C(C(NC(C2=CC(O)=CC(O)=C2C=2C(O)=CC=C3C=2)C(O)=O)=O)NC(=O)C3NC(=O)C2NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(CC(C)C)NC)C(O)C(C=C3Cl)=CC=C3OC3=CC2=CC1=C3OC1OC(CO)C(O)C(O)C1OC1CC(C)(N)C(O)C(C)O1 MYPYJXKWCTUITO-UHFFFAOYSA-N 0.000 description 1
- OGWKCGZFUXNPDA-XQKSVPLYSA-N vincristine Chemical compound C([N@]1C[C@@H](C[C@]2(C(=O)OC)C=3C(=CC4=C([C@]56[C@H]([C@@]([C@H](OC(C)=O)[C@]7(CC)C=CCN([C@H]67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)C[C@@](C1)(O)CC)CC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-XQKSVPLYSA-N 0.000 description 1
- 229960004528 vincristine Drugs 0.000 description 1
- OGWKCGZFUXNPDA-UHFFFAOYSA-N vincristine Natural products C1C(CC)(O)CC(CC2(C(=O)OC)C=3C(=CC4=C(C56C(C(C(OC(C)=O)C7(CC)C=CCN(C67)CC5)(O)C(=O)OC)N4C=O)C=3)OC)CN1CCC1=C2NC2=CC=CC=C12 OGWKCGZFUXNPDA-UHFFFAOYSA-N 0.000 description 1
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- 239000011710 vitamin D Substances 0.000 description 1
- 150000003710 vitamin D derivatives Chemical class 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 235000019168 vitamin K Nutrition 0.000 description 1
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- 229940045997 vitamin a Drugs 0.000 description 1
- 229940046008 vitamin d Drugs 0.000 description 1
- 229940046010 vitamin k Drugs 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
Classifications
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- 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
- A61K47/50—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/56—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
- A61K47/59—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes
- A61K47/60—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 the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol
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- C—CHEMISTRY; METALLURGY
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- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
- C08G65/08—Saturated oxiranes
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
- C08G65/2609—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aliphatic hydroxyl groups
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- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
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- C08G2650/28—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type
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Claims (15)
1. Monofunktionel forgrenet poly(ethylenglycol) (PEG) repræsenteret af den følgende generelle formel (1):
hvor Xi og X2 er hver uafhængigt en carbonhydridgruppe med 1 til 20 carbonatomer ved den terminale ende af de to forgrenede kæder, hvor ni og n2 er hver uafhængigt en værdi valgt fra 1 til 1000, hvor n3 er en værdi valgt fra 11 til 1000, hvor Ri er et hydrogenatom, en carbonhydridgruppe med 1 til 20 carbonatomer, eller en carbonhydridgruppe med 1 til 20 carbonatomer med en eller flere grupper valgt fra en gruppe bestående af en amidbinding, en etherbinding, en dobbeltbinding, en tripelbinding og en tertiær aminogruppe, og hvor R er en funktionel gruppe på terminalen af hovedkæden af det forgrenede poly(ethylenglycol), og R kan reagere med den reaktive gruppe af et bio relate ret stof, hvor p er 0 eller 1, hvor Li og L2 er hver uafhængigt en linker-gruppe og kombinationen af Li og L2 er valgt fra en af en gruppe bestående af: gruppe I: Li er en divalent carbonhydridgruppe med 1 til 20 carbonatomer, og Li udelukker en methylengruppe, når p er 0, gruppe II: Li er en divalent carbonhydridgruppe med 1 til 20 carbonatomer og indeholder mindst en af en gruppe bestående af en etherbinding, en thioetherbinding, en dobbeltbinding, en tripelbinding, og en aminogruppe, når p er 0, gruppe III: Li og L· er hver uafhængigt en divalent carbonhydridgruppe med 1 til 20 carbonatomer, når p er 1, gruppe IV: Li er en divalent carbonhydridgruppe med 1 til 20 carbonatomer, udelukkende en methylengruppe, og hvor Lz er en divalent carbonhydridgruppe med 1 til 20 carbonatomer indeholdende en etherbinding, når p er 1, gruppe V: Li er en divalent carbonhydridgruppe med 1 til 20 carbonatomer, og hvor Li er en divalent carbonhydridgruppe med 1 til 20 carbonatomer indeholdende en etherbinding, når p er 1, og gruppe VI: Li og L2 er hver uafhængigt en divalent carbonhydridgruppe med 1 til 20 carbonatomer og indeholder mindst en afen gruppe bestående afen etherbinding, en thioetherbinding, en dobbeltbinding, en tripelbinding, og en aminogruppe, når p er 1, hvor Li udelukker en etherbinding, når L2 indeholder en etherbinding, og hvor L2 udelukker en etherbinding, når Li indeholder en etherbinding, hvor nævnte monofunktionelle forgrenede poly(ethylenglycol) er opnåelig med en fremgangsmåde hvori
er en startinitiator for en første polymerisering, og hvor
er et intermediat for en anden polymerisering, og PG er en beskyttelsesgruppe af en hydroxylgruppe.
2. Den monofunktionelle forgrenede PEG ifølge krav 1, hvor Xi og X2 er hver uafhængigt en gruppe valgt fra gruppen bestående af en methyl, en ethyl, en propyl, en propenyl, en propinyl, en isopropyl, en butyl, en tertiær butyl, en pentyl, en heptyl, en 2-ethylhexyl, en octyl, en nonyl, en decyl, en undecyl, en dodecyl, en tridecyl, en tetradecyl, en pentadecyl, en hexadecyl, en heptadecyl, en octodecyl, en nonadecyl, en eicosyl, en benzyl og en butylphenyl, og Xi og X2 er de samme eller forskellige fra hinanden i et molekyle.
3. Den monofunktionelle forgrenede PEG ifølge krav 1, hvor R er valgt fra de følgende grupper:
hvor Z er en alkylengruppe eller en alkylengruppe indeholdende mindst en gruppe valgt fra en gruppe bestående afen amidbinding, en etherbinding, en dobbeltbinding, en tripelbinding og en sekundær aminogruppe, hvor q er 0 eller 1, hvor Y er en carbonhydridgruppe med 1 til 10 carbonatomer eller en carbonhydridgruppe med 1 til 10 carbonatomer, der indeholder et fluoratom, hvor Q er hydrogen eller en gruppe favoriserende induktiv effekt, konjugativ effekt eller begge elektroner på en umættet binding, hvor M er et carbonatom eller et nitrogenatom på ringen, og hvor W er et halogenatom.
4. Den monofunktionelle forgrenede PEG ifølge krav 3, hvor Z er valgt fra en gruppe bestående af: en methylengruppe, en 1,2-ethylengruppe, en 1,3-propylengruppe, en 1,2-propylengruppe, en isopropylengruppe, en butylengruppe, en pentylengruppe og en hexylengruppe.
5. Den monofunktionelle forgrenede PEG ifølge krav 1, hvor hver af ni og m er uafhængigt en værdi valgt fra 10 til 800, fortrinsvis fra 25 til 800, og mere fortrinsvis fra 50 til 500.
6. Den monofunktionelle forgrenede PEG ifølge krav 1, hvor n3 er en værdi valgt fra 11 til 800, fortrinsvis fra 11 til 500, og mere fortrinsvis fra 11 til 200.
7. Den monofunktionelle forgrenede PEG ifølge krav 1, hvor det biorelatererede stof er valgt fra en gruppe bestående af polypeptid, protein, enzym, small molecule lægemiddel, farvestof, liposom, nukleosid, nukleotid, oligonukleotid, polynukleotid, nukleinsyre, polysaccharid, steroid, lipid, phospholipid, glycolipid, glycoprotein, celle og virus.
8. Den monofunktionelle forgrenede PEG ifølge krav 1, hvor den reaktive gruppe af et biorelateret stof er valgt fra en af en gruppe bestående af en aminogruppe, en mercaptogruppe, en umættet binding, en carboxylgruppe og en hydroxylgruppe.
9. Fremgangsmåde til fremstilling af den monofunktionelle forgrenede PEG ifølge et hvilket som helst af kravene 1-8, der inkluderer de følgende trin: Trin (a): I et co-initiatorsystem bestående af en small molecule-initiator (4) og en base, polymeriseres ethylenoxid til de to geometrisk symmetriske hydroxylgrupper af initiator (4) for at generere to forgrenede kæder; Derefter, deprotoneres terminalenderne af de to nydannede forgrenede kæder for at opnå et intermediat (5), Trin (b): De initierende aktive terminaler af de to forgrenede kæder af intermediat (5) alkyl-etherificeres for at opnå et intermediat (6); Trin c): Den terminale hydroxylgruppe på symmetriaksen af intermediat (6) afbeskyttes for at opnå et intermediat (7); Trin (d): Ethylenoxid polymeriseres til den afbeskyttede terminale hydroxylgruppe på symmetriaksen af intermediat (7) for at generere en hovedkæde, der efterfølgende protoneres for at opnå et intermediat (3) med en terminal hydroxylgruppe; Trin (e): Terminalen af hovedkæden af intermediat (3) funktionaliseres, og derved kan den monofunktionelle forgrenede poly(ethylenglycol) af den generelle formel (1) opnås;
hvor PG repræsenterer en beskyttelsesgruppe afen hydroxylgruppe.
10. Biorelateret stof modificeret af den monofunktionelle forgrenede PEG ifølge et hvilket som helst af kravene 1 til 8, og med en kemisk struktur vist i den generelle formel (2):
hvor D er et biorelateret stof, q er 0 eller 1, og hvor Z er en linker-gruppe igennem hvilken en funktionel gruppe i stand til at reagere med det biorelatererede stof er forbundet til hovedkæden af PEG, og kan reagere med det biorelatererede stof for at danne en restgruppe l_3.
11. Det PEG-modificerede biorelaterede stof ifølge krav 10, hvor D er valgt fra en gruppe bestående af polypeptid, protein, enzym, small molecule lægemiddel, farvestof, liposom, nukleosid, nukleotid, oligonukleotid, polynukleotid, nukleinsyre, polysaccharid, steroid, lipid, phospholipid, glycolipid, glycoprotein, celle og virus.
12. Det PEG-modificerede biorelaterede stof ifølge krav 11, hvor D er valgt fra en gruppe bestående af polypeptid, protein, enzym, farvestof, liposom, nukleosid, nukleotid, oligonukleotid, polynukleotid, nukleinsyre, polysaccharid, steroid, lipid, phospholipid, glycolipid, glycoprotein, celle og virus, fortrinsvis valgt fra en gruppe bestående af polypeptid, protein, enzym, nukleosid, nukleotid, oligonukleotid, polynukleotid og nukleinsyre, og mere fortrinsvis valgt fra en gruppe bestående af interferon, lysozym og antisense-oligodeoxynukleotid.
13. Det PEG-modificerede biorelaterede stof ifølge krav 10, hvor l_3 er valgt fra en gruppe bestående afen triazolbinding, en isoxazolbinding, en etherbinding, en amidbinding, en imidbinding, en iminogruppe, en sekundær aminogruppe, en tertiær aminogruppe, en thioesterbinding, en disulfidbinding, en urethanbinding, en thiocarbonatbinding, en sulfonatbinding, en sulfamidbinding, en carbamatbinding, en tyrosingruppe, en cysteingruppe, en histidingruppe og kombinationen deraf.
14. Forbindelse af den følgende formel (3)
hvor Xi, Xi, ni, m, n3, Li, Li og Ri er de samme som de defineret i generel formel (1) ifølge krav 1.
15. Fremgangsmåde til fremstilling af intermediatforbindelsen med formlen (3) nedenfor, hvilken inkluderer de følgende trin: Trin (a): i et co-initiatorsystem bestående af en small molecule-initiator (4) og en base, polymeriseres ethylenoxid til de to geometrisk symmetriske hydroxylgrupper af initiator (4) for at generere to forgrenede kæder; derefter, deprotoneres terminalenderne af de to nydannede forgrenede kæder for at opnå et intermediat (5), Trin (b): de initierende aktive terminaler af de to forgrenede kæder af intermediat (5) alkyl-etherificeres for at opnå et intermediat (6); Trin (c): den terminale hydroxylgruppe på symmetriaksen af intermediat (6) afbeskyttes for at opnå et intermediat (7); Trin (d): ethylenoxid polymeriseres til den afbeskyttede terminale hydroxylgruppe på symmetriaksen af intermediat (7) for at generere en hovedkæde, der efterfølgende protoneres for at opnå et intermediat (3) med en terminal hydroxylgruppe;
hvor PG repræsenterer en beskyttelsesgruppe af en hydroxylgruppe.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201310017350.4A CN103044676B (zh) | 2013-01-17 | 2013-01-17 | 一种聚乙二醇修饰的生物相关物质 |
| CN201310020124.1A CN103044675B (zh) | 2013-01-17 | 2013-01-17 | 一种单一官能化的支化聚乙二醇 |
| PCT/CN2013/073463 WO2014110867A1 (zh) | 2013-01-17 | 2013-03-29 | 一种单一官能化的支化聚乙二醇及其修饰的生物相关物质 |
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| DK2947111T3 true DK2947111T3 (da) | 2018-05-07 |
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| US (2) | US20140199750A1 (da) |
| EP (1) | EP2947111B1 (da) |
| DK (1) | DK2947111T3 (da) |
| WO (1) | WO2014110867A1 (da) |
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| MX2015014438A (es) | 2013-04-18 | 2016-05-18 | Armo Biosciences Inc | Metodos de uso de interleucina-10 para tratar enfermedades y trastornos. |
| EP3010527B1 (en) | 2013-06-17 | 2018-08-08 | Armo Biosciences, Inc. | Method for assessing protein identity and stability |
| CN105658232A (zh) | 2013-08-30 | 2016-06-08 | 阿尔莫生物科技股份有限公司 | 使用白细胞介素-10治疗疾病和病症的方法 |
| CN120242030A (zh) | 2013-11-11 | 2025-07-04 | 阿尔莫生物科技股份有限公司 | 将白细胞介素-10用于治疗疾病和病症的方法 |
| US20160361415A1 (en) | 2015-05-28 | 2016-12-15 | Armo Biosciences, Inc. | Methods of Using Interleukin-10 for Treating Diseases and Disorders |
| KR20180038553A (ko) | 2015-08-25 | 2018-04-16 | 아르모 바이오사이언시스 인코포레이티드 | 질환 및 장애를 치료하기 위한 인터류킨-10을 사용하는 방법 |
| WO2017204378A1 (ko) * | 2016-05-25 | 2017-11-30 | 엔에이치케미칼 | 폴리알킬렌 글리콜의 말단 알킬화 촉매 및 이를 이용한 폴리알킬렌 글리콜의 말단 알킬화 방법 |
| WO2018066692A1 (ja) | 2016-10-07 | 2018-04-12 | 国立大学法人東京工業大学 | 分岐型ヘテロ単分散ポリエチレングリコール、その製造方法、及びその結合体 |
| CN116348150A (zh) * | 2020-09-11 | 2023-06-27 | 箭头药业股份有限公司 | 用于递送治疗剂的脂质缀合物 |
| CN114685778B (zh) * | 2020-12-30 | 2023-10-17 | 苏州艾博生物科技有限公司 | 长循环阳离子脂质体的合成方法 |
| EP4509544A4 (en) * | 2022-04-12 | 2025-07-02 | Xiamen Sinopeg Biotech Co Ltd | NONLINEAR PEGYLATED LIPID CONTAINING TERTIARY AMINE AND ITS APPLICATION |
| CN115417984B (zh) * | 2022-08-26 | 2023-07-21 | 厦门赛诺邦格生物科技股份有限公司 | 一种聚乙二醇醛衍生物的制备方法 |
| CN116178733B (zh) * | 2023-03-03 | 2023-08-01 | 浙江博美生物技术有限公司 | 一种基于三官能团氨基酸的支化单分散peg衍生物、制备方法和应用 |
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| US5919455A (en) * | 1993-10-27 | 1999-07-06 | Enzon, Inc. | Non-antigenic branched polymer conjugates |
| US5932462A (en) * | 1995-01-10 | 1999-08-03 | Shearwater Polymers, Inc. | Multiarmed, monofunctional, polymer for coupling to molecules and surfaces |
| EP1446438A2 (en) * | 2001-11-07 | 2004-08-18 | Nektar Therapeutics Al, Corporation | Branched polymers and their conjugates |
| EP2644206B1 (en) * | 2003-05-23 | 2019-04-03 | Nektar Therapeutics | PEG derivatives containing two PEG chains |
| KR20070042567A (ko) * | 2004-08-31 | 2007-04-23 | 파마시아 앤드 업존 캄파니 엘엘씨 | 글리세롤 분지쇄 폴리에틸렌 글리콜 인간 성장 호르몬공액체, 이의 제조 방법 및 이의 사용 방법 |
| WO2007132956A1 (en) * | 2006-05-12 | 2007-11-22 | Dong-A Pharm.Co., Ltd. | Polyethylene glycol-interferon alpha conjugate |
| KR101079993B1 (ko) * | 2006-11-17 | 2011-11-04 | 동아제약주식회사 | 폴리에틸렌글리콜 과립구 콜로니 자극인자 접합체 |
| CN101831065A (zh) * | 2009-03-13 | 2010-09-15 | 复旦大学 | 一种含单一活性功能基团的多臂星型聚乙二醇及其制备方法 |
| CN102367290B (zh) * | 2011-04-26 | 2013-05-08 | 厦门赛诺邦格生物科技有限公司 | 链官能化的多级支化聚乙二醇及其合成方法 |
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- 2013-03-29 WO PCT/CN2013/073463 patent/WO2014110867A1/zh not_active Ceased
- 2013-03-29 DK DK13871951.3T patent/DK2947111T3/da active
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Also Published As
| Publication number | Publication date |
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| EP2947111A1 (en) | 2015-11-25 |
| EP2947111B1 (en) | 2018-03-07 |
| US20140199750A1 (en) | 2014-07-17 |
| WO2014110867A1 (zh) | 2014-07-24 |
| EP2947111A4 (en) | 2016-01-13 |
| US20220118100A1 (en) | 2022-04-21 |
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