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Zwitter-ion hydrogel coating for anticoagulation and preparation method of zwitter-ion hydrogel coating

A zwitterion and hydrogel technology, which is applied in anticoagulation treatment, coating, packaging food, etc., can solve the problems of cumbersome coating curing process, low interface bonding strength, and insufficient long-term stability, and achieve long-lasting anticoagulation Blood effect, enhanced mechanical properties, excellent superhydrophilic effect

Active Publication Date: 2022-06-24
TIANJIN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0004] In view of this, the purpose of the present invention is to overcome the shortcomings of the existing zwitterionic hydrogel coatings such as cumbersome curing process, weak mechanical properties, low interfacial bonding strength and insufficient long-term stability, and provide a simple preparation process with good mechanical properties. Zwitterionic hydrogel coating with strong adhesion and long-term durability for anticoagulation and preparation method thereof

Method used

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  • Zwitter-ion hydrogel coating for anticoagulation and preparation method of zwitter-ion hydrogel coating
  • Zwitter-ion hydrogel coating for anticoagulation and preparation method of zwitter-ion hydrogel coating
  • Zwitter-ion hydrogel coating for anticoagulation and preparation method of zwitter-ion hydrogel coating

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Experimental program
Comparison scheme
Effect test

Embodiment 1

[0054] (1) 1.5g of 3-[3-(acrylamidopropyl)dimethylamino]-propionate (CBAA), 75mg of N,N-methylenebisacrylamide and 10.5mg of ammonium persulfate were weighed and dissolved in 10 mL of deionized water to prepare the aqueous phase. Then, 0.87 g of Tween-80 and 5.28 g of Span-80 were dissolved in 615 mL of n-hexane to prepare an oil phase. The aqueous phase was slowly added to the oil phase and treated by ultrasonic cell disintegrator in an ice bath to give a pale blue emulsion. The resulting emulsion was transferred to a three-necked flask, followed by heating to 80° C. and carrying out a polymerization reaction in a nitrogen atmosphere. After 2 hours of reaction, the reaction solution was cooled to room temperature, the microgel suspension was centrifuged at high speed to obtain the lower layer precipitate, and finally, the purified polycarboxybetaine microgel was obtained by dialysis and freeze-drying. like figure 1 As shown, the particle size and morphology of the prepared...

Embodiment 2

[0060] (1) Weigh any mass of SBMA monomer, 2-hydroxy-2-methyl-1-phenyl-1-propanone and N,N-methylenebisacrylamide into 20 mL of aqueous solution. It was then dissolved by magnetic stirring in the dark to prepare a hydrogel pre-solution.

[0061] (2) Using polyvinyl chloride as the modified substrate, the polyvinyl chloride plate was treated by oxygen plasma for 3 minutes, and then immersed in 100 mL of acetone solution containing 10 wt % benzophenone for 10 minutes. The treated polyvinyl chloride plates were washed sequentially with ethanol and water and dried under vacuum. The pre-gel solution prepared in step (1) was transferred to a polyvinyl chloride plate, then exposed to UV light for 12 hours under nitrogen atmosphere, and then rinsed with deionized water to remove unreacted reagents to obtain no microagglomeration. A traditional zwitterionic hydrogel coating for glue.

[0062] Figure 4The results of the anti-fibrinogen, L929 cell and platelet adhesion tests of the m...

Embodiment 3

[0066] (1) 1.5g of 3-[3-(acrylamidopropyl)dimethylamino]-propionate (CBAA), 75mg of N,N-methylenebisacrylamide and 10.5mg of ammonium persulfate were weighed and dissolved in 10 mL of deionized water to prepare the aqueous phase. Then, 0.87 g of Tween-80 and 5.28 g of Span-80 were dissolved in 615 mL of n-hexane to prepare an oil phase. The aqueous phase was slowly added to the oil phase and treated by ultrasonic cell disintegrator in an ice bath to give a pale blue emulsion. The resulting emulsion was transferred to a three-necked flask, followed by heating to 80° C. and carrying out a polymerization reaction in a nitrogen atmosphere. After 2 hours of reaction, the reaction solution was cooled to room temperature, the microgel suspension was centrifuged at high speed to obtain the lower layer precipitate, and finally, the purified polycarboxybetaine microgel was obtained by dialysis and freeze-drying.

[0067] (2) 0.5 g of polycarboxybetaine microgel prepared in step (1), 1...

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Abstract

The invention relates to a zwitter-ion hydrogel coating for anticoagulation and a preparation method of the zwitter-ion hydrogel coating. The coating comprises the following components in percentage by weight: 0.1 to 5 percent of polycarboxylic acid betaine microgel, 10 to 60 percent of sulfobetaine polymer, 0.001 to 0.06 percent of 2-hydroxy-2-methyl-1-phenyl-1-acetone, 0.01 to 0.3 percent of N, N '-methylene bisacrylamide and the balance of water. Dispersing the polycarboxylic acid betaine microgel in the sulfobetaine monomer pre-solution; transferring the solution to the surface of a base material pretreated by an initiator, and initiating polymerization by ultraviolet light to obtain a microgel reinforced zwitter-ion hydrogel coating; the mechanical property and the interface bonding force of the prepared coating are improved, and the problems that a traditional zwitter-ion hydrogel coating is prone to falling off and the like are solved. The zwitterionic hydrogel coating has excellent anticoagulation performance and can be widely applied to blood contact medical equipment.

Description

technical field [0001] The invention relates to a zwitterionic hydrogel coating for anticoagulation and a preparation method thereof, and belongs to the field of medical polymer materials. Background technique [0002] Blood-contacting biomedical devices, such as interventional catheters, vascular stents, and mechanical heart valves, have been widely used in clinical therapy. However, thrombus formation remains a major challenge in its clinical application. Studies have shown that the adhesion of proteins to biomedical devices is the main cause of thrombosis. Zwitterionic polymers are polymers with equal amounts of positive and negative charges in the molecule, which form a tight hydration layer through electrostatic interactions, and are currently ideal candidates for preventing non-specific adhesion of proteins. In recent years, patent documents CN109563199A, CN108822326A, CN110204650A, etc. have prepared zwitterionic polymer coatings on the surface of substrates by graf...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61L33/00A61L33/06A61L31/10A61L27/34
CPCA61L33/0082A61L33/0064A61L31/10A61L27/34Y02A50/30
Inventor 李俊杰姚蒙蒙姚芳莲张宏
Owner TIANJIN UNIV