Construction method of functional imitation cell outer layer membrane three-dimensional structure coating

A technology imitating the outer membrane of cells and a three-dimensional structure, applied in coatings and other directions, can solve problems such as unsatisfactory biocompatibility, and achieve the effects of convenient and flexible functionalization, wide application range, and simple use process

Active Publication Date: 2019-01-25
NORTHWEST UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0002] In the clinical application of existing biomedical materials and devices, there are still problems such as infection, blood coagulation, and postoperative tissue hyperplasia to varying degrees. key factor

Method used

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  • Construction method of functional imitation cell outer layer membrane three-dimensional structure coating
  • Construction method of functional imitation cell outer layer membrane three-dimensional structure coating

Examples

Experimental program
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Effect test

preparation example Construction

[0016] 1. Preparation of polydopamine-mediated coating: prepare a 0.1-2 mg / mL dopamine aqueous solution (pH 7.5-8.6), and dip-coat it on the surface of the material to be modified at room temperature to form a stable polydopamine coating.

[0017] 2. On the surface of the polydopamine layer, construct a functional coating imitating the three-dimensional structure of the outer layer of the cell membrane:

[0018] 1) Immerse the polydopamine-coated material in an activated carboxypolyethylene glycol aqueous solution, and bond a designed amount of polyethylene glycol on the surface of polydopamine through amidation reaction to extend outward as a three-dimensional structure imitating the outer layer of the cell membrane flexible long chain;

[0019] 2) Then dip-coat in the aqueous solution of the imitation cell outer membrane structure copolymer (PMEN) containing the active ester group and the side chain of the phosphorylcholine group, and continue to coat the surface of the mate...

Embodiment 1

[0028]Example 1: Preparation of binary polymer PMEN containing active lipid groups and phosphorylcholine groups. Take a three-necked flask, add a dropping funnel, a reflux tube with a drying tube, and a device for venting nitrogen to the three ports respectively, add 20 ml of absolute ethanol to a 100 mL dry and clean three-necked flask, keep the temperature at 70°C, and keep the temperature for 30 min, weighed and added 0.05 g AIBN dissolved in 6 ml THF solution. 40 ml of anhydrous ethanol solution containing 1.05 g of active ester monomer MEONP and 2.98 g of phosphorylcholine group-containing monomer MPC were added dropwise, and the addition was completed within 4 h, and the reaction was carried out for 20 h. The resulting PMEN binary random copolymer solution was concentrated and put into a dialysis bag with a molecular weight cut-off of 7000, and dialyzed against pH 3.93 phosphoric acid aqueous solution for 48 h. PMEN flocculent solid was obtained after freeze-drying. 1 ...

Embodiment 2

[0029] Embodiment 2: the preparation that contains active ester functional polymer PMENP. Add 10 mL of absolute ethanol into a 100 mL three-necked flask, pass through nitrogen, stir with a magnetic force and gradually raise the temperature to 70 °C. Weigh 0.140 g of active ester monomer NPCEMA, 2.726 g of carboxyl chain monomer PEGA and 0.805 g of MPC in sequence, and add 34 mL of absolute ethanol to dissolve them. Weigh 0.037 gAIBN and add it to the monomer mixture. Use the dropping funnel to drop the mixed solution of the monomers, and the dropwise addition is completed in about 2 h. Change to a closed system and allow it to continue to react for 24 h. After the reaction was stopped, part of the reaction solution was taken out and put into a dialysis bag with a molecular weight cut off of 7000, and dialyzed in an acidic aqueous solution with a pH of 3~4. Freeze dried. D. 2 O solvent 1 H-NMR characterizes its structure, and its composition is polymer PMENP containing ac...

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Abstract

The invention discloses a method for constructing a three-dimensional coating imitating the outer membrane of cells on the surface of almost any material. First, the material is immersed in an aqueous solution of dopamine to coat polydopamine, and then dicarboxypolyethylene glycol HOOC‑PEG‑ COOH or carboxy-polyethylene glycol PEG-COOH, the imitation cell outer membrane structure copolymer PMEN containing active ester groups and phosphorylcholine group side chains reacts with the amino groups on the surface of polydopamine coating in aqueous solution and fixes them on On the surface of the material, an anti-bio-fouling coating imitating the three-dimensional structure of the outer membrane of cells is formed, and finally a targeting molecule containing amino groups is covalently bonded to the carboxyl group at the end of polyethylene glycol on the coating surface to obtain a coating with a three-dimensional structure imitating the outer membrane of cells. The invention improves the biocompatibility of materials and endows them with designed functions. The coating is constructed on the surface of nano drug-loaded particles, which can greatly improve the "invisible" effect of nano drugs in vivo and the circulation time in blood, and significantly enhance the Enriched release at the lesion site.

Description

technical field [0001] The invention relates to the construction and performance optimization of a three-dimensional structure coating imitating the outer membrane of cells, and belongs to the technical field of surface modification. technical background [0002] In the clinical application of existing biomedical materials and devices, there are still problems such as infection, blood coagulation, and postoperative tissue hyperplasia to varying degrees. key factor. Currently, surface modification of materials is a very effective way to improve their biocompatibility. However, how to improve the stability and biocompatibility of modified substances on the surface of materials simply and efficiently is the key to current research and application. [0003] Generally speaking, improving the biocompatibility of materials can improve the biocompatibility of materials in vivo by increasing the hydrophilicity of the material surface, forming a hydration layer, and utilizing the re...

Claims

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Application Information

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Patent Type & AuthorityPatents(China)
IPC IPC(8): C08J7/06C08J3/12C03C17/28C08L23/12C08L67/04
CPCC03C17/002C03C17/28C08J3/126C08J7/065C08J2323/12C08J2367/04C08J2479/00
Inventor宫永宽邢成美鲍丽丽姜海涛
OwnerNORTHWEST UNIV