NUS Graduate School for Integrative Science and Engineering, National University of Singapore , Kent Ridge, Singapore 117576.
Institute of Materials Research and Engineering, A*STAR (Agency for Science, Technology and Research , 2 Fusionopolis Way, Singapore 138634.
ACS Appl Mater Interfaces. 2016 Nov 9;8(44):30552-30563. doi: 10.1021/acsami.6b09481. Epub 2016 Oct 31.
Surface charge and wettability, the two prominent physical factors governing protein adsorption and cell adhesion, have been extensively investigated in the literature. However, a comparison between these driving forces in terms of their independent and cooperative effects in affecting adhesion is rarely explored on a systematic and quantitative level. Herein, we formulate a protocol that features two-dimensional control over both surface charge and wettability with limited cross-parameter influence. This strategy is implemented by controlling both the polyion charge density in the layer-by-layer (LbL) assembly process and the polyion side-chain chemical structures. The 2D property matrix spans surface isoelectric points ranging from 5 to 9 and water contact angles from 35 to 70°, with other interferential factors (e.g., roughness) eliminated. The interplay between these two surface variables influences protein (bovine serum albumin, lysozyme) adsorption and 3T3 fibroblast cell adhesion. For proteins, we observe the presence of thresholds for surface wettability and electrostatic driving forces necessary to affect adhesion. Beyond these thresholds, the individual effects of electrostatic forces and wettability are observed. For fibroblast, both surface charge and wettability have an effect on its adhesion. The combined effects of positive charge and hydrophilicity lead to the highest cell adhesion, whereas negative charge and hydrophobicity lead to the lowest cell adhesion. Our design strategy can potentially form the basis for studying the distinct behaviors of electrostatic force or wettability driven interfacial phenomena and serve as a reference in future studies assessing protein adsorption and cell adhesion to surfaces with known charge and wettability within the property range studied here.
表面电荷和润湿性是控制蛋白质吸附和细胞黏附的两个重要物理因素,这两个因素已在文献中得到了广泛研究。然而,很少有研究从系统和定量的角度比较这两个驱动力在独立和协同作用下对黏附的影响。在此,我们提出了一种方案,通过控制层层组装过程中的聚离子电荷密度和聚离子侧链化学结构,实现了对表面电荷和润湿性的二维控制,且两种参数的影响较小。这种策略可以将二维特性矩阵的表面等电点范围控制在 5 到 9 之间,水接触角范围控制在 35 到 70°之间,同时消除了其他干扰因素(例如粗糙度)。这两个表面变量的相互作用影响了蛋白质(牛血清白蛋白、溶菌酶)的吸附和 3T3 成纤维细胞的黏附。对于蛋白质,我们观察到表面润湿性和静电力这两个黏附驱动力存在阈值。超过这些阈值后,静电力和润湿性的单独作用就会显现出来。对于成纤维细胞,表面电荷和润湿性都会影响其黏附。正电荷和亲水性的联合作用会导致细胞黏附性最高,而负电荷和疏水性则会导致细胞黏附性最低。我们的设计策略可能为研究静电力或润湿性驱动的界面现象的独特行为提供基础,并为未来在已知电荷和润湿性范围内研究蛋白质吸附和细胞黏附到表面的研究提供参考。