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A kind of polyethylene glycol chemical hydrogel based on enzyme cross-linking and preparation method thereof

A polyethylene glycol and enzyme cross-linking technology, applied in the field of biomedical materials, can solve problems such as complex reaction processes, achieve the effects of improving modification rate, good biocompatibility, and broadening application prospects

Active Publication Date: 2020-09-22
FUDAN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the synthesis of polyethylene glycol involves anionic polymerization and post-treatment reactions. The entire reaction process is complex, requiring strict control of anhydrous and oxygen-free conditions, and there are many influencing factors. The route of ethylene glycol is particularly important

Method used

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  • A kind of polyethylene glycol chemical hydrogel based on enzyme cross-linking and preparation method thereof
  • A kind of polyethylene glycol chemical hydrogel based on enzyme cross-linking and preparation method thereof
  • A kind of polyethylene glycol chemical hydrogel based on enzyme cross-linking and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] In a 1L three-necked flask, first add polyethylene glycol diacrylate (PEG400DA) and 1,4-dimercapto-2-butanol with a molar ratio of 1:1, then add 400mL dimethylsulfoxide, and stir until the magnet Dissolve completely; then measure 0.2 mL of triethylamine and dissolve it in 10 mL of dimethyl sulfoxide, and slowly inject it into the above reaction system through a micro syringe pump, and catalyze the Michael addition reaction at room temperature. After the system was reacted at room temperature for 24 hours, 0.40 g of N-isopropylacrylamide was added to end capping and the reaction was continued for 4 hours. After the reaction was completed, most of the dimethyl sulfoxide was removed by distillation under reduced pressure, and the crude product was settled in a large amount of toluene; after settled at -20°C for 24 hours, the upper toluene solution was carefully poured and vacuum dried for 24 hours to obtain linear polymer 1a. Using polystyrene as a standard sample, the numb...

Embodiment 2

[0040] In a 1L three-necked flask, first add polyethylene glycol diacrylate (PEG700DA) and dithiothreitol (DTT) with a molar ratio of 1:1, and then add 400 mL of dimethyl sulfoxide, and stir until the magnet is completely dissolved; Subsequently, 0.2 mL of triethylamine was measured and dissolved in 10 mL of dimethyl sulfoxide, and slowly injected into the above reaction system through a micro syringe pump, and the Michael addition reaction was catalyzed at room temperature. After the system was reacted at room temperature for 24 hours, 0.40 g of acrylamide was added for capping and the reaction was continued for 4 hours. After the reaction was completed, most of the dimethyl sulfoxide was removed by distillation under reduced pressure, and the crude product was settled in a large amount of toluene; after settled at -20°C for 24 hours, the upper toluene solution was carefully poured and dried under vacuum for 24 hours to obtain linear polymer 1bPEG700DA- DTT. Using polystyrene...

Embodiment 3

[0042] In a 1L three-necked flask, first add polyethylene glycol diacrylate (PEG1500DA) and 3,4-dimercapto-1-butanol with a molar ratio of 1:1, then add 400mL dimethylsulfoxide, and stir until the magnet Dissolve completely; then measure 0.2 g of sodium ethoxide and dissolve it in 10 mL of dimethyl sulfoxide, slowly inject it into the above reaction system through a micro syringe pump, and catalyze the Michael addition reaction at room temperature. After the system was reacted at room temperature for 48 hours, 0.40 g of N-isopropylacrylamide was added to cap the reaction and the reaction was continued for 8 hours. After the reaction was completed, most of the dimethyl sulfoxide was removed by distillation under reduced pressure, and the crude product was settled in a large amount of toluene; after 24 hours of settling at -20°C, the upper toluene solution was carefully poured and vacuum dried for 24 hours to obtain linear polymer 1c. Using polystyrene as a standard sample, the n...

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Abstract

The invention discloses polyethylene glycol chemical crosslinking hydrogel based on enzyme cross linkage. A preparation method comprises the steps of modifying phenolic hydroxy modified on a side chain of a polyethylene glycol linear polymer macromonomer solution, taking a horse radish peroxidase solution as a catalyst, and giving an in-situ enzyme cross-linking reaction in the presence of an enzyme catalysis reaction substrate, namely a hydrogen peroxide solution, to form a three-dimensional net structure. The prepared polyethylene glycol chemical crosslinking hydrogel has good biocompatibility, degradability and gel flexibility; physical and chemical properties such as gelation time and mechanical strength of the hydrogel can be regulated conveniently; and the hydrogel has wide application prospects in the fields of tissue engineering, drug controlled release, regenerative medicine and the like.

Description

Technical field [0001] The invention belongs to the field of biomedical materials, and specifically relates to a polyethylene glycol chemical hydrogel based on enzyme crosslinking and a preparation method thereof. Background technique [0002] Hydrogels have become an important class of biomedical materials due to their high water content and good biocompatibility, and they have great application prospects in many fields. At present, injectable chemically cross-linked hydrogels have received extensive attention due to their ease of operation, minimal invasiveness, good matching of the lesion space and the controllability of gel performance. The injectable chemically cross-linked hydrogel can be prepared by mixing two-component or multi-component precursor solutions. The precursor solution can be loaded with growth factors, cells and drugs due to its good fluidity before mixing. Once the component precursor solution is mixed and injected into the body, it will form a chemically c...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08J3/075A61K47/10A61L27/52A61L27/18A61L27/38C08L71/02
CPCA61K47/34A61L27/18A61L27/38A61L27/52C08J3/075C08J2371/02C08L71/02
Inventor 俞麟王丹妮丁建东
Owner FUDAN UNIV