Hu Zhaokang, Chen Liang, Betts Douglas E, Pandya Ashish, Hillmyer Marc A, DeSimone Joseph M
Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.
J Am Chem Soc. 2008 Oct 29;130(43):14244-52. doi: 10.1021/ja803991n. Epub 2008 Oct 4.
Amphiphilic networks of perfluoropolyethers (PFPE) and poly(ethylene glycol) (PEG) have been achieved to yield optically transparent, mechanically robust films over a wide range of compositions. Telechelic diols of these oligomers were transformed to a photocurable dimethacryloxy form (DMA) and free radically cured at various composition weight ratios to yield free-standing films. Clear and colorless amphiphilic networks could be achieved when low molar mass versions of both the PFPE-DMA (1 kg/mol) and the PEG-DMA (550 g/mol) were used. The bulk morphologies of the samples were extensively characterized by a variety of techniques including ultraviolet-visible spectroscopy, differential scanning calorimetry, dynamic mechanic thermal analysis, small-angle X-ray scattering, atomic force microscopy, X-ray photoelectron spectroscopy, and optical microscopy, which strongly suggest that nanoscopic to macroscopic phase-separated materials could be achieved. By incorporating a threshold amount of PFPEs into PEG-based hydrogel networks, water swelling could be significantly reduced, which may offer a new strategy for a number of medical device applications. Along these lines, strong inhibition of nonspecific protein adsorption could be achieved with these amphiphilic network materials compared with an oligo(ethylene glycol)-based self-assembled monolayer coated surface.
全氟聚醚(PFPE)和聚乙二醇(PEG)的两亲性网络已成功制备出在广泛组成范围内具有光学透明性和机械强度的薄膜。这些低聚物的遥爪二醇被转化为光固化的二甲基丙烯酰氧基形式(DMA),并在不同的组成重量比下进行自由基固化,从而得到自支撑薄膜。当使用低摩尔质量的PFPE-DMA(1 kg/mol)和PEG-DMA(550 g/mol)时,可以得到透明无色的两亲性网络。通过多种技术对样品的本体形态进行了广泛表征,包括紫外可见光谱、差示扫描量热法、动态热机械分析、小角X射线散射、原子力显微镜、X射线光电子能谱和光学显微镜,这些结果强烈表明可以实现从纳米级到宏观级的相分离材料。通过在基于PEG的水凝胶网络中加入阈值量的PFPE,可以显著降低水溶胀,这可能为许多医疗器械应用提供一种新策略。沿着这些思路,与基于低聚乙二醇的自组装单分子层涂层表面相比,这些两亲性网络材料可以实现对非特异性蛋白质吸附的强烈抑制。