Anssari-Benam Afshin, Barber Asa H, Bucchi Andrea
School of Engineering, University of Portsmouth, Anglesea Road, Portsmouth, PO1 3DJ, UK.
J Mater Sci Mater Med. 2016 Feb;27(2):42. doi: 10.1007/s10856-015-5657-2. Epub 2015 Dec 29.
A matrix-fibril shear stress transfer approach is devised and developed in this paper to analyse the primary biomechanical factors which initiate the structural degeneration of the bioprosthetic heart valves (BHVs). Using this approach, the critical length of the collagen fibrils l c and the interface shear acting on the fibrils in both BHV and natural aortic valve (AV) tissues under physiological loading conditions are calculated and presented. It is shown that the required critical fibril length to provide effective reinforcement to the natural AV and the BHV tissue is l c = 25.36 µm and l c = 66.81 µm, respectively. Furthermore, the magnitude of the required shear force acting on fibril interface to break a cross-linked fibril in the BHV tissue is shown to be 38 µN, while the required interfacial force to break the bonds between the fibril and the surrounding extracellular matrix is 31 µN. Direct correlations are underpinned between these values and the ultimate failure strength and the failure mode of the BHV tissue compared with the natural AV, and are verified against the existing experimental data. The analyses presented in this paper explain the role of fibril interface shear and critical length in regulating the biomechanics of the structural failure of the BHVs, for the first time. This insight facilitates further understanding into the underlying causes of the structural degeneration of the BHVs in vivo.
本文设计并开发了一种基质-纤维剪切应力传递方法,以分析引发生物人工心脏瓣膜(BHV)结构退变的主要生物力学因素。利用该方法,计算并给出了生理负荷条件下BHV和天然主动脉瓣(AV)组织中胶原纤维的临界长度lc以及作用在纤维上的界面剪切力。结果表明,为天然AV和BHV组织提供有效增强所需的临界纤维长度分别为lc = 25.36 µm和lc = 66.81 µm。此外,在BHV组织中,使交联纤维断裂所需作用在纤维界面上的剪切力大小为38 µN,而使纤维与周围细胞外基质之间的键断裂所需的界面力为31 µN。这些值与BHV组织相对于天然AV的极限破坏强度和破坏模式之间存在直接关联,并通过现有实验数据进行了验证。本文的分析首次解释了纤维界面剪切和临界长度在调节BHV结构破坏生物力学中的作用。这一见解有助于进一步理解体内BHV结构退变的潜在原因。