自愈水凝胶
蛋白质吸附
聚合
乙二醇
PEG比率
肿胀 的
磷酰胆碱
化学工程
聚合物
化学
材料科学
吸附
高分子化学
有机化学
生物化学
复合材料
财务
工程类
经济
作者
Kristopher W. Kolewe,Kerianne M. Dobosz,Todd Emrick,Stephen S. Nonnenmann,Jessica D. Schiffman
出处
期刊:ACS applied bio materials
[American Chemical Society]
日期:2018-06-08
卷期号:1 (1): 33-41
被引量:17
标识
DOI:10.1021/acsabm.8b00001
摘要
Biofilm-associated infections stemming from medical devices are increasingly challenging to treat due to the spread of antibiotic resistance. In this study, we present a simple strategy that significantly enhances the antifouling performance of covalently cross-linked poly(ethylene glycol) (PEG) and physically cross-linked agar hydrogels by incorporation of the fouling-resistant polymer zwitterion, poly(2-methacryloyloxyethyl phosphorylcholine) (pMPC). Dopamine polymerization was initiated during swelling of the hydrogels, which provided dopamine and pMPC, an osmotic driving force into the hydrogel interior. Both PEG and agar hydrogels were synthesized over a broad range of storage moduli (1.7–1300 kPa), which remained statistically equivalent after being functionalized with pMPC and polydopamine (PDA). When challenged with fibrinogen, a model blood-clotting protein, the pMPC/PDA-functionalized PEG and agar hydrogels displayed a >90% reduction in protein adsorption compared to hydrogel controls. Further, greater than an order-of-magnitude reduction in Escherichia coli and Staphylococcus aureus adherence was observed. This study demonstrates a versatile material platform to enhance the fouling resistance of hydrogels through a pMPC/PDA incorporation strategy that is independent of the chemical composition and network structure of the original hydrogel.
科研通智能强力驱动
Strongly Powered by AbleSci AI