Institute for Medicine and Engineering, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6202, USA.
Langmuir. 2010 Sep 7;26(17):14126-34. doi: 10.1021/la102315j.
In this work, we report the preparation of photoactive dextran and demonstrate its utility by photochemically attaching it onto various polymeric substrates. The attachment of homogeneous and patterned dextran films was performed on polyurethane and polystyrene, with detailed analysis of surface morphology, swelling behavior, and the protein resistance of these substrates. The described photoactive dextran and attachment procedure is applicable to a wide variety of substrates while accommodating surfaces with complex surface geometries. Dextran with azide content between 22 and 0.3 wt % was produced by esterification with p-azidobenzoic acid. Dextran (1.2 wt % azide) was photografted onto plasma oxidized polyurethane and polystyrene and displayed thicknesses of 5 +/- 3 and 7 +/- 3 nm, respectively. The patterned dextran on oxidized polyurethane was patchy with a nominal height difference between dextranized and nondextranized regions. The azidated dextran on oxidized polystyrene exhibited a distinct step in height. In the presence of phosphate buffered saline (PBS), the dextranized regions became smoother and more uniform without affecting the height difference at the oxidized polyurethane boundary. However, the dextranized regions on oxidized polyurethane were observed to swell by a factor of 3 relative to the dried thickness. These dissimilarities were attributed to hydrogen bonding between the dextran and oxidized polyurethane and were confirmed by the photoimmobiliization in the presence of LiCl. The resulting surface was the smoothest of all the azidated dextran samples (R(rms) = 1 +/- 0.3 nm) and swelled up to 2 times its dried thickness in PBS. The antifouling properties of dextran functionalized surfaces were verified by the selective adsorption of FITC-labeled human albumin only on the nondextranized regions of the patterned polyurethane and polystyrene substrates.
在这项工作中,我们报告了光活性葡聚糖的制备,并通过将其光化学附着在各种聚合物基底上来展示其用途。在聚氨酯和聚苯乙烯上进行了均匀和图案化的葡聚糖薄膜的附着,对这些基底的表面形态、溶胀行为和蛋白质抗性进行了详细分析。所描述的光活性葡聚糖和附着程序适用于各种基底,同时适应具有复杂表面几何形状的表面。通过与对氨基苯甲酸酯化,制备了含叠氮基的葡聚糖(22wt%和 0.3wt%)。将 1.2wt%叠氮基的葡聚糖光接枝到等离子体氧化的聚氨酯和聚苯乙烯上,分别显示出 5±3nm 和 7±3nm 的厚度。在氧化的聚氨酯上,图案化的葡聚糖是斑驳的,在葡聚糖化和非葡聚糖化区域之间存在名义上的高度差。在氧化的聚苯乙烯上的叠氮基葡聚糖表现出明显的高度台阶。在磷酸盐缓冲盐水(PBS)存在下,葡聚糖化区域变得更加平滑和均匀,而不会影响氧化的聚氨酯边界处的高度差。然而,在氧化的聚氨酯上的葡聚糖化区域观察到相对于干燥厚度膨胀了 3 倍。这些差异归因于葡聚糖与氧化的聚氨酯之间的氢键,并通过在 LiCl 存在下的光固定化得到证实。所得表面是所有叠氮基葡聚糖样品中最光滑的(R(rms)=1±0.3nm),在 PBS 中膨胀至其干燥厚度的 2 倍。葡聚糖功能化表面的抗污染性能通过仅在图案化的聚氨酯和聚苯乙烯基底的非葡聚糖化区域选择性吸附 FITC 标记的人白蛋白得到了验证。