201 Dynamic Compression Characteristics of GELs for Artificial Articular Cartilage

2007 ◽  
Vol 2007.46 (0) ◽  
pp. 35-36
Author(s):  
Atsushi ITOU ◽  
Hiroyuki FUJIKI ◽  
Masashi DAIMARUYA ◽  
Osamu SHIOZAKI
2008 ◽  
Vol 16 (02) ◽  
pp. 175-195 ◽  
Author(s):  
LIHAI ZHANG ◽  
BRUCE S. GARDINER ◽  
DAVID W. SMITH ◽  
PETER PIVONKA ◽  
ALAN J. GRODZINSKY

Experiments on the transport of radiolabeled Insulin-like Growth Factors (IGF-I and -II) into bovine articular cartilage show differential uptake depending on the relative proportion of IGF-I and -II. In this study, we present a mathematical model describing both the transport and competition of IGF-I and -II for binding sites represented by two functional groupings of IGF binding proteins (IGFBPs). The first grouping has approximately similar binding affinity to both IGF-I and -II (i.e. IGFBPs 1–5), whereas the second group has significantly higher binding preference for IGF-II compared to IGF-I (i.e. IGFBP-6). Using nonlinear least squares, it is shown that the experimental equilibrium competitive binding results can be described using a reversible Langmuir sorption isotherm involving two dominant IGFBP functional groups.After coupling the sorption model with a poromechanical continuum model, parametric studies are carried out to investigate the effect of model changes including IGF boundary conditions and the ratios of the two IGFBP functional groups. The results show that ignoring competitive binding leads to a significant overestimation of total IGF-I uptake, but an underestimation the rate of "free" (physiologically active) IGF-I within the cartilage. An increase of first group of IGFBPs (i.e. IGFBPs 1–5) as has been reported for osteoarthritis, is observed to hinder the bioavailability of free IGF-I in cartilage, even though the total IGF-I uptake is enhanced. Furthermore, the combination of dynamic compression and competitive binding is seen to enhance the IGF-I uptake within cartilage, but this enhancement is overestimated if competitive binding is neglected.


Author(s):  
Kevin A. Yamauchi ◽  
Christopher B. Raub ◽  
Albert C. Chen ◽  
Robert L. Sah ◽  
Scott J. Hazelwood ◽  
...  

The biomechanical properties of articular cartilage (AC) can be altered by chemical and mechanical stimuli. Dynamic unconfined compression (UCC) has been shown to increase biosynthesis at moderate strain amplitudes (1–4%) and frequencies from 0.01Hz. to 0.1Hz [1]. Furthermore, interstitial fluid velocity and maximum principle strain have been proposed as candidates for controlling glycosaminoglycan (GAG) and collagen (COL) remodeling, respectively [2,3]. The goal of this study was to integrate in vitro growth data, including biochemical and microstructural properties, into a computational continuum mixture model to elucidate potential mechanical triggers for AC tissue remodeling.


2003 ◽  
Vol 125 (1) ◽  
pp. 84-93 ◽  
Author(s):  
Chun-Yuh Huang ◽  
Michael A. Soltz ◽  
Monika Kopacz ◽  
Van C. Mow ◽  
Gerard A. Ateshian

A biphasic-CLE-QLV model proposed in our recent study [2001, J. Biomech. Eng., 123, pp. 410–417] extended the biphasic theory of Mow et al. [1980, J. Biomech. Eng., 102, pp. 73–84] to include both tension-compression nonlinearity and intrinsic viscoelasticity of the cartilage solid matrix by incorporating it with the conewise linear elasticity (CLE) model [1995, J. Elasticity, 37, pp. 1–38] and the quasi-linear viscoelasticity (QLV) model [Biomechanics: Its foundations and objectives, Prentice Hall, Englewood Cliffs, 1972]. This model demonstrates that a simultaneous prediction of compression and tension experiments of articular cartilage, under stress-relaxation and dynamic loading, can be achieved when properly taking into account both flow-dependent and flow-independent viscoelastic effects, as well as tension-compression nonlinearity. The objective of this study is to directly test this biphasic-CLE-QLV model against experimental data from unconfined compression stress-relaxation tests at slow and fast strain rates as well as dynamic loading. Twelve full-thickness cartilage cylindrical plugs were harvested from six bovine glenohumeral joints and multiple confined and unconfined compression stress-relaxation tests were performed on each specimen. The material properties of specimens were determined by curve-fitting the experimental results from the confined and unconfined compression stress relaxation tests. The findings of this study demonstrate that the biphasic-CLE-QLV model is able to describe the strain-rate-dependent mechanical behaviors of articular cartilage in unconfined compression as attested by good agreements between experimental and theoretical curvefits (r2=0.966±0.032 for testing at slow strain rate; r2=0.998±0.002 for testing at fast strain rate) and predictions of the dynamic response r2=0.91±0.06. This experimental study also provides supporting evidence for the hypothesis that both tension-compression nonlinearity and intrinsic viscoelasticity of the solid matrix of cartilage are necessary for modeling the transient and equilibrium responses of this tissue in tension and compression. Furthermore, the biphasic-CLE-QLV model can produce better predictions of the dynamic modulus of cartilage in unconfined dynamic compression than the biphasic-CLE and biphasic poroviscoelastic models, indicating that intrinsic viscoelasticity and tension-compression nonlinearity of articular cartilage may play important roles in the load-support mechanism of cartilage under physiologic loading.


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