Lin Weifeng, Klein Jacob
Department of Molecular Chemistry and Materials Science, Weizmann Institute of Science, Rehovot 76100, Israel.
Acc Mater Res. 2022 Feb 25;3(2):213-223. doi: 10.1021/accountsmr.1c00219. Epub 2022 Feb 9.
In the course of evolution, nature has achieved remarkably lubricated surfaces, with healthy articular cartilage in the major (synovial) joints being the prime example, that can last a lifetime as they slide past each other with ultralow friction (friction coefficient μ = the force to slide surfaces past each other/load compressing the surfaces < 0.01) under physiological pressures (up to 10 MPa or more)). Such properties are unmatched by any man-made materials. The precise mechanism of low friction between such sliding cartilage tissues, which is closely related to osteoarthritis (OA), the most widespread joint disease, affecting hundreds of millions worldwide, has been studied for nearly a century, but is still not fully understood. Traditionally, the roles of load bearing by interstitial fluid within the cartilage bulk and that of thin exuded fluid films at the interface between the sliding cartilage surfaces have been proposed as the main lubrication mechanism. More recent work, however, suggests that molecular boundary layers at the surfaces of articular cartilage and other tissues play a major role in their lubrication. In particular, in recent years hydration lubrication has emerged as a new paradigm for boundary lubrication in aqueous media based on subnanometer hydration shells which massively reduce frictional dissipation. The vectors of hydration lubrication include trapped hydrated ions, hydrated surfactants, biological macromolecules, biomimetic polymers, polyelectrolytes and polyzwitterionic brushes, and close-packed layers of phosphatidylcholine (PC) vesicles, all having in common the exposure of highly hydrated groups at the slip plane. Among them, vesicles (or bilayers) of PC lipids, which are the most widespread lipid class in mammals, are exceptionally efficient lubricating elements as a result of the high hydration of the phosphocholine headgroups they expose. Such lipids are ubiquitous in joints, leading to the proposal that macromolecular surface complexes exposing PC bilayers are responsible for the remarkable lubrication of cartilage. Cartilage, comprising ∼70% water, may be considered to be a complex biological hydrogel, and studying the frictional properties of hydrogels may thus provide new insights into its lubrication mechanisms, leading in turn to novel, highly lubricious hydrogels that may be used in a variety of biomedical and other applications. A better understanding of cartilage lubrication could moreover lead to better treatments for OA, for example, through intra-articular injections of appropriate lubricants or through the creation of low-friction hydrogels that may be used as tissue engineering scaffolds for diseased cartilage. In this Account, we begin by introducing the concept and origin of hydration lubrication, extending from the seminal study of lubrication by hydrated simple ions to more complex systems. We then briefly review different modes of lubrication in synovial joints, focusing primarily on boundary lubrication. We consider modes of hydrogel lubrication and different kinds of such low-friction synthetic gels and then focus on cartilage-inspired, boundary-lubricated hydrogels. We conclude by discussing challenges and opportunities.
在进化过程中,自然界创造出了表面润滑效果极佳的结构,主要(滑膜)关节中的健康关节软骨就是典型例子。在生理压力(高达10兆帕或更高)下,这些关节软骨能以超低摩擦(摩擦系数μ = 使表面相互滑动的力/压缩表面的载荷 < 0.01)相互滑动,从而终身使用。这种特性是任何人造材料都无法比拟的。这种滑动软骨组织间低摩擦的确切机制与骨关节炎(OA)密切相关,骨关节炎是最常见的关节疾病,全球数亿人受其影响。近一个世纪以来,人们一直在研究这一机制,但仍未完全理解。传统观点认为,软骨主体内间质液的承载作用以及滑动软骨表面间薄的渗出液膜的作用是主要润滑机制。然而,最近的研究表明,关节软骨和其他组织表面的分子边界层在其润滑过程中起主要作用。特别是近年来,水合润滑已成为水介质中边界润滑的一种新范式,它基于亚纳米水合壳层,能大幅降低摩擦耗散。水合润滑的载体包括捕获的水合离子、水合表面活性剂、生物大分子、仿生聚合物、聚电解质和聚两性离子刷,以及紧密堆积的磷脂酰胆碱(PC)囊泡层,它们的共同特点是在滑移面暴露高度水合的基团。其中,PC脂质的囊泡(或双层膜)是哺乳动物中分布最广的脂质类别,由于其暴露的磷酸胆碱头部基团具有高水合性,是特别有效的润滑元件。这种脂质在关节中普遍存在,这使得人们提出,暴露PC双层膜的大分子表面复合物是软骨卓越润滑性能的原因。软骨约含70%的水,可以被认为是一种复杂的生物水凝胶,因此研究水凝胶的摩擦特性可能会为其润滑机制提供新的见解,进而开发出可用于各种生物医学和其他应用的新型高润滑水凝胶。此外,更好地理解软骨润滑可能会带来更好的骨关节炎治疗方法,例如,通过关节内注射合适的润滑剂或通过制造可作为患病软骨组织工程支架使用的低摩擦水凝胶。在本综述中,我们首先介绍水合润滑的概念和起源,从关于水合简单离子润滑的开创性研究扩展到更复杂的系统。然后我们简要回顾滑膜关节中的不同润滑模式,主要关注边界润滑。我们考虑水凝胶润滑的模式以及不同类型的低摩擦合成凝胶,然后重点讨论受软骨启发的边界润滑水凝胶。最后我们讨论挑战和机遇。