Department of Agricultural, Food and Nutritional Science, University of Alberta, Edmonton T6G 2P5, Canada.
Department of Chemical and Materials Engineering, University of Alberta, Edmonton T6G 1H9, Canada.
ACS Appl Mater Interfaces. 2024 Sep 4;16(35):46909-46922. doi: 10.1021/acsami.4c09771. Epub 2024 Aug 22.
Developing efficient aqueous biolubricants has become a significant focus of research due to their prevalence in biotribological contacts and enormous potential in soft matter applications. In this study, size-controllable, pH-sensitive whey protein microgels were prepared using a water-in-water emulsion template method from protein-polysaccharide phase separation. The granular hydrogel from the protein microgels exhibited superior lubricity, obtaining 2.7-fold and 1.7-fold reductions in coefficient of friction (μ) compared to native protein and human saliva (μ = 0.30 compared to 0.81 and 0.52, respectively). The microgels also exhibited outstanding load-bearing capabilities, sustaining lubrication under normal forces up to 5 N. Microgels with a smaller size (1 μm) demonstrated better lubricating performance than 6 and 20 μm microgels. The exceptional lubricity was from a synergistic effect of the ball-bearing mechanism and the hydration state of the microgels. Particularly at pH 7.4, the hydration layer surrounding highly negative charges contributed to the electrostatic repulsion among the swollen microgels, leading to an improved buffer ability to separate contact surfaces and effective rolling behavior. Such pH-dependent repulsion was evidenced using a surface forces apparatus that the adhesion between the whey protein-coated surfaces and protein-mica surfaces decreased from 4.49 to 0.97 mN/m and from 7.89 to 0.36 mN/m, respectively, with pH increasing from the isoelectronic point to 7.4. Our findings fundamentally elucidated the tribo-rheological properties and lubrication mechanisms of the whey protein microgels with excellent biocompatibility and environmental responsiveness, offering novel insights for their food and biomedical applications requiring aqueous biolubrication.
制备高效的水基生物润滑剂已成为研究的重点,因为它们在生物摩擦学接触中普遍存在,并且在软物质应用中具有巨大的潜力。在这项研究中,使用水包水乳液模板法从蛋白质-多糖相分离制备了尺寸可控、pH 敏感的乳清蛋白微凝胶。蛋白质微凝胶的颗粒水凝胶表现出优异的润滑性,与天然蛋白质和人唾液相比,摩擦系数(μ)降低了 2.7 倍和 1.7 倍(μ分别为 0.30 比 0.81 和 0.52)。微凝胶还表现出出色的承载能力,在高达 5 N 的法向力下仍能维持润滑。尺寸较小(1 μm)的微凝胶比 6 μm 和 20 μm 的微凝胶具有更好的润滑性能。优异的润滑性来自于球轴承机制和微凝胶水合状态的协同效应。特别是在 pH 7.4 时,围绕带负电荷的微凝胶的水合层有助于膨胀的微凝胶之间的静电排斥,从而提高了分离接触表面的缓冲能力和有效的滚动行为。使用表面力仪证明了这种 pH 依赖性排斥,乳清蛋白涂层表面之间以及蛋白-云母表面之间的粘附力分别从 4.49 降低到 0.97 mN/m 和从 7.89 降低到 0.36 mN/m,随着 pH 值从等电点增加到 7.4。我们的发现从根本上阐明了具有良好生物相容性和环境响应性的乳清蛋白微凝胶的摩擦学性质和润滑机制,为需要水基生物润滑的食品和生物医学应用提供了新的见解。