乙二醇
高分子化学
化学
甲基丙烯酸酯
束缚水
分子
差示扫描量热法
吸附
PEG比率
吸热过程
蛋白质吸附
化学工程
聚合物
单体
有机化学
物理
财务
工程类
经济
热力学
作者
Jiang Wu,Weifeng Lin,Zhen Wang,Shengfu Chen,Yung Chang
出处
期刊:Langmuir
[American Chemical Society]
日期:2012-04-18
卷期号:28 (19): 7436-7441
被引量:361
摘要
The strong surface hydration layer of nonfouling materials plays a key role in their resistance to nonspecific protein adsorption. Poly(sulfobetaine methacrylate) (polySBMA) is an effective material that can resist nonspecific protein adsorption and cell adhesion. About eight water molecules are tightly bound with one sulfobetaine (SB) unit, and additional water molecules over 8:1 ratio mainly swell the polySBMA matrix, which is obtained through the measurement of T(2) relaxation time by low-field nuclear magnetic resonance (LF-NMR). This result was also supported by the endothermic behavior of water/polySBMA mixtures measured by differential scanning calorimetry (DSC). Furthermore, by comparing both results of polySBMA and poly(ethylene glycol) (PEG), it is found that (1) the hydrated water molecules on the SB unit are more tightly bound than on the ethylene glycol (EG) unit before saturation, and (2) the additional water molecules after forming the hydration layer in polySBMA solutions show higher freedom than those in PEG. These results might illustrate the reason for higher resistance of zwitterionic materials to nonspecific protein adsorptions compared to that of PEGs.
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