PEG-Based Hydrogel Coatings: Design Tools for Biomedical Applications

被引:9
|
作者
Wancura, Megan [1 ]
Nkansah, Abbey [2 ]
Robinson, Andrew [2 ]
Toubbeh, Shireen [2 ]
Talanker, Michael [2 ]
Jones, Sarah [2 ]
Cosgriff-Hernandez, Elizabeth [2 ,3 ]
机构
[1] Univ Texas Austin, Dept Chem, Austin, TX 78712 USA
[2] Univ Texas Austin, Dept Biomed Engn, Austin, TX 78712 USA
[3] Univ Texas Austin, Dept Biomed Engn, 107 W Dean Keeton,BME Bldg,Room 3 503D, Austin, TX 78712 USA
基金
美国国家卫生研究院;
关键词
Hydrogel coatings; Redox initiation; Photoinitiation; Poly(ethylene glycol) hydrogels; CROSS-LINKING; BIOACTIVE HYDROGELS; RADICAL INITIATORS; VOLUME RELAXATION; POLYMERIZATION; SCAFFOLDS; KINETICS; ACRYLONITRILE; MECHANISM;
D O I
10.1007/s10439-023-03154-9
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Device failure due to undesired biological responses remains a substantial roadblock in the development and translation of new devices into clinical care. Polyethylene glycol (PEG)-based hydrogel coatings can be used to confer antifouling properties to medical devices-enabling minimization of biological responses such as bacterial infection, thrombosis, and foreign body reactions. Application of hydrogel coatings to diverse substrates requires careful consideration of multiple material factors. Herein, we report a systematic investigation of two coating methods: (1) traditional photoinitiated hydrogel coatings; (2) diffusion-mediated, redox-initiated hydrogel coatings. The effects of method, substrate, and compositional variables on the resulting hydrogel coating thickness are presented. To expand the redox-based method to include high molecular weight macromers, a mechanistic investigation of the role of cure rate and macromer viscosity was necessary to balance solution infiltration and gelation. Overall, these structure-property relationships provide users with a toolbox for hydrogel coating design for a broad range of medical devices.
引用
收藏
页码:1804 / 1815
页数:12
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