Chau Allison L, Rosas Jonah, Degen George D, Månsson Lisa K, Chen Jonathan, Valois Eric, Pitenis Angela A
Materials Department University of California, Santa Barbara, CA 93106, USA.
Biomolecular Science and Engineering Department University of California, Santa Barbara, CA 93106, USA.
J Mater Chem B. 2020 Aug 21;8(31):6782-6791. doi: 10.1039/d0tb00582g. Epub 2020 May 4.
Aqueous surface gels are fragile yet resilient biopolymer-based networks capable of sustaining extremely low friction coefficients despite tribologically-challenging environments. These superficial networks are ubiquitous in natural sliding interfaces and protect mechanosensitive cells from excessive contact pressures and frictional shear stresses from cell-fluid, cell-cell, or cell-solid interactions. Understanding these complex lubrication mechanisms may aid in the development of materials-based strategies for increasing biocompatibility in medical devices and implants. Equally as important is characterizing the interplay between soft and passive yet mobile implant materials and cellular reactions in response to direct contact and frictional shear stresses. Physically interrogating living biological systems without rupturing them in the process is nontrivial. To this end, custom biotribometers have been designed to precisely modulate contact pressures against living human telomerase-immortalized corneal epithelial (hTCEpi) cell layers using soft polyacrylamide membrane probes. Reverse-transcription quantitative polymerase chain-reaction (RT-qPCR) indicated that increased duration and, to a much greater extent, the magnitude of frictional shear stress lead to increased production of pro-inflammatory (IL-1β, IL-6, MMP9) and pro-apoptotic (DDIT3, FAS) genes, which in clinical studies are linked to pathological pain. The hierarchical structure often found in biological systems has also been investigated through the fabrication of high-water content (polyacrylamide) hydrogels through free-radical polymerization inhibition. Nanoindentation experiments and friction coefficient measurements indicate that these "gradient surface gels" reduce contact pressures and frictional shear stresses at the surface of the material while still maintaining stiffness within the bulk. Reducing frictional shear stresses through informed materials and surface design may concomitantly increase lubricity and quiet the immune response, and thus provide bio-inspired routes to improve patient outcomes and quality of life.
水表面凝胶是脆弱但具有弹性的基于生物聚合物的网络,尽管处于摩擦学挑战性环境中,仍能维持极低的摩擦系数。这些表面网络在天然滑动界面中无处不在,并保护机械敏感细胞免受来自细胞-流体、细胞-细胞或细胞-固体相互作用的过度接触压力和摩擦剪切应力。了解这些复杂的润滑机制可能有助于开发基于材料的策略,以提高医疗设备和植入物的生物相容性。同样重要的是表征柔软、被动但可移动的植入材料与细胞对直接接触和摩擦剪切应力的反应之间的相互作用。在不破坏活体生物系统的情况下对其进行物理探究并非易事。为此,已设计出定制的生物摩擦计,使用柔软的聚丙烯酰胺膜探针精确调节对永生人端粒酶角膜上皮(hTCEpi)细胞层的接触压力。逆转录定量聚合酶链反应(RT-qPCR)表明,摩擦剪切应力的持续时间增加,以及在更大程度上其大小增加,会导致促炎(IL-1β、IL-6、MMP9)和促凋亡(DDIT3、FAS)基因的产生增加,在临床研究中这些基因与病理性疼痛有关。还通过自由基聚合抑制制备高含水量(聚丙烯酰胺)水凝胶,对生物系统中常见的层次结构进行了研究。纳米压痕实验和摩擦系数测量表明,这些“梯度表面凝胶”降低了材料表面的接触压力和摩擦剪切应力,同时仍保持整体的刚度。通过明智的材料和表面设计降低摩擦剪切应力可能会相应地增加润滑性并平息免疫反应,从而提供受生物启发的途径来改善患者的治疗效果和生活质量。