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全层关节软骨深度依赖性力学性能的直接可视化

Direct Visualisation of the Depth-Dependent Mechanical Properties of Full-Thickness Articular Cartilage.

作者信息

Szarko Matthew, Xia Yang

机构信息

Division of Biomedical Sciences, St. George's, University of London, Cranmer Terrace, London, SW17 0RE, Telephone: +44 (0)20 8725 2831, ,

Department of Physics, Oakland University, Rochester MI, USA 48309, Tel: 001-248-370-3420, ,

出版信息

Open J Orthop. 2012 Jun;2. doi: 10.4236/ojo.2012.22007.

Abstract

OBJECTIVE

The structural anisotropy of articular cartilage controls its deformation response. As proteoglycans and collagen vary with depth, simple uniaxial compression results in inhomogeneous deformation with distinct depth-dependent mechanical properties. Investigations into depth-dependent mechanical properties of articular cartilage have previously required tissue modification after specimen isolation. Such modifications include histological processes, freezing, subchondral bone removal, and fluorescent staining that may alter the tissue, limiting applicability.

DESIGN

Using a custom tissue-sectioning device, 0.1 mm thick unfixed, unstained, osetochondral samples were obtained. A customized apparatus loaded samples to 12.5, 24, and 29% compression in under a microscope with 10× magnification. Equilibrium load was measured after stress relaxation. Intra-tissue displacement was measured by tracing groups of cells between the different compression levels using a digital imaging program. Cell distance from the subchondral bone was measured to identify intra-tissue displacement and calculate strain.

RESULTS

The results reveal that stress levels and intra-tissue displacement increased with greater tissue compression (p <0.05). Intra-tissue displacement decreased as depth from the articular surface increased (p<0.01). This occurred for each level of tissue compression. Overall compressive resistance is seen to increase with depth from the articular surface.

CONCLUSIONS

The current study identifies a method directly visualising and assessing the depth-dependent structural response to compression. The ability to avoid tissue modification after specimen isolation, allows this procedure to more closely approximate conditions and may provide an important method for analyzing the coordinated changes in cartilage composition and function due to ageing and disease.

摘要

目的

关节软骨的结构各向异性控制其变形反应。由于蛋白聚糖和胶原蛋白随深度变化,简单的单轴压缩会导致不均匀变形,并具有明显的深度依赖性力学性能。此前,对关节软骨深度依赖性力学性能的研究需要在标本分离后对组织进行处理。这些处理包括组织学处理、冷冻、去除软骨下骨以及荧光染色,这些可能会改变组织,限制了其适用性。

设计

使用定制的组织切片装置,获取厚度为0.1毫米的未固定、未染色的骨软骨样本。在10倍放大倍数的显微镜下,使用定制装置将样本压缩至12.5%、24%和29%。在应力松弛后测量平衡载荷。使用数字成像程序通过追踪不同压缩水平之间的细胞群来测量组织内位移。测量细胞与软骨下骨的距离以识别组织内位移并计算应变。

结果

结果显示,随着组织压缩程度的增加,应力水平和组织内位移增加(p<0.05)。随着距关节表面深度的增加,组织内位移减小(p<0.01)。在每个组织压缩水平下均出现这种情况。总体抗压强度随距关节表面深度的增加而增加。

结论

本研究确定了一种直接可视化和评估压缩深度依赖性结构反应的方法。避免标本分离后进行组织处理的能力,使该程序更接近实际情况,并可能为分析由于衰老和疾病导致的软骨成分和功能的协调变化提供一种重要方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb10/3886840/8c9567e47c9e/nihms473607f1.jpg

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