Aerospace Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Orthopaedic Surgery, Washington University, St. Louis, MO 60613, USA.
Acta Biomater. 2018 Oct 15;80:217-227. doi: 10.1016/j.actbio.2018.09.027. Epub 2018 Sep 19.
As the fundamental structural protein in mammals, collagen transmits cyclic forces that are necessary for the mechanical function of tissues, such as bone and tendon. Although the tissue-level mechanical behavior of collagenous tissues is well understood, the response of collagen at the nanometer length scales to cyclical loading remains elusive. To address this major gap, we cyclically stretched individual reconstituted collagen fibrils, with average diameter of 145 ± 42 nm, to small and large strains in the partially hydrated conditions of 60% relative humidity. It is shown that cyclical loading results in large steady-state hysteresis that is reached immediately after the first loading cycle, followed thereafter by limited accumulation of inelastic strain and constant initial elastic modulus. Cyclic loading above 20% strain resulted in 70% increase in tensile strength, from 638 ± 98 MPa to 1091 ± 110 MPa, and 70% increase in toughness, while maintaining the ultimate tensile strain of collagen fibrils not subjected to cyclic loading. Throughout cyclic stretching, the fibrils maintained a steady-state hysteresis, yielding loss coefficients that are 5-10 times larger than those of known homogeneous materials in their modulus range, thus establishing damping of nanoscale collagen fibrils as a major component of damping in tissues. STATEMENT OF SIGNIFICANCE: It is shown that steady-state energy dissipation occurs in individual collagen fibrils that are the building blocks of hard and soft tissues. To date, it has been assumed that energy dissipation in tissues takes place mainly at the higher length scales of the tissue hierarchy due to interactions between collagen fibrils and fibers, and in limited extent inside collagen fibrils. It is shown that individual collagen fibrils need only a single loading cycle to assume a highly dissipative, steady-state, cyclic mechanical response. Mechanical cycling at large strains leads to 70% increase in mechanical strength and values exceeding those of engineering steels. The same cyclic loading conditions also lead to 70% increase in toughness and loss properties that are 5-10 times higher than those of engineering materials with comparable stiffness.
作为哺乳动物的基本结构蛋白,胶原蛋白传递着组织(如骨骼和肌腱)机械功能所必需的循环力。尽管胶原蛋白组织的组织水平力学行为已得到很好的理解,但胶原蛋白在纳米长度尺度上对循环加载的反应仍然难以捉摸。为了解决这一主要差距,我们在相对湿度为 60%的部分水合条件下,对平均直径为 145±42nm 的单个重建胶原蛋白原纤维进行了小到大的应变循环拉伸。结果表明,循环加载会导致大的稳态滞后,在第一个加载循环后立即达到稳态滞后,随后弹性应变的积累有限,初始弹性模量保持不变。在 20%以上的应变循环加载下,拉伸强度增加了 70%,从 638±98MPa 增加到 1091±110MPa,韧性增加了 70%,同时保持了未经历循环加载的胶原蛋白原纤维的极限拉伸应变。在整个循环拉伸过程中,原纤维保持稳态滞后,其损耗系数比其模量范围内已知均匀材料的损耗系数大 5-10 倍,从而确定纳米级胶原蛋白原纤维的阻尼是组织阻尼的主要组成部分。
结果表明,在构建硬组织和软组织的单个胶原蛋白原纤维中会发生稳态能量耗散。迄今为止,人们一直认为,由于胶原蛋白原纤维和纤维之间的相互作用,以及胶原蛋白原纤维内部的相互作用,能量耗散主要发生在组织层次结构的较高长度尺度上,而且在胶原蛋白原纤维内部的能量耗散也很有限。结果表明,单个胶原蛋白原纤维只需一个加载循环即可呈现高度耗散的、稳态的循环力学响应。在大应变下的机械循环会导致机械强度增加 70%,并且超过工程钢的强度值。相同的循环加载条件还会导致韧性增加 70%,损耗特性比具有可比刚度的工程材料高 5-10 倍。