Biphasic Poroviscoelastic Characteristics of Proteoglycan-Depleted Articular Cartilage: Simulation of Degeneration

AbstractThis study investigated the biphasic poroviscoelastic properties of normal and proteoglycan-depleted articular cartilage to validate this model for use in the diagnosis of degenerated cartilage. A normal control group, a buffer-treated control group, and a trypsin-treated proteoglycan-depleted experimental group were investigated. Water content and glycosaminoglycan concentration were measured for each group in order to assess the affects of buffer treatment and trypsin treatment on normal articular cartilage. Histological staining with toluidine blue confirmed the depletion of proteoglycan molecules by trypsin treatment. Specimens from each group were tested in unconfined compression, and the biphasic poroviscoelastic model was fit to the data obtained. No significant difference in water content was found between any of the three groups. Glycosaminoglycan concentration was found to be significantly lower in the trypsin-treated group when compared to both the normal and buffer-treated groups, while no difference between normal and buffer-treated specimens was found. Specimens from the normal and buffer-treated groups behaved the same mechanically. Model parameters from these two groups were not statistically different. However, model parameters for the trypsin-treated group were statistically different from those from the other two groups, suggesting that the biphasic poroviscoelastic model may be a powerful diagnostic tool for degenerative articular cartilage. © 2002 Biomedical Engineering Society. PAC2002: 8780Rb, 8719Rr, 8715Rn

[1]  J. Suh,et al.  A cross-validation of the biphasic poroviscoelastic model of articular cartilage in unconfined compression, indentation, and confined compression. , 2001, Journal of biomechanics.

[2]  J. Suh,et al.  Biphasic Poroviscoelastic Behavior of Hydrated Biological Soft Tissue , 1999 .

[3]  V C Mow,et al.  Variations in the intrinsic mechanical properties of human articular cartilage with age, degeneration, and water content. , 1982, The Journal of bone and joint surgery. American volume.

[4]  J. Suh,et al.  Biphasic poroviscoelastic simulation of the unconfined compression of articular cartilage: II--Effect of variable strain rates. , 2001, Journal of biomechanical engineering.

[5]  A F Mak,et al.  Viscoelastic properties of proteoglycan subunits and aggregates in varying solution concentrations. , 1984, Journal of biomechanics.

[6]  J. Peyron,et al.  Articular Cartilage and Osteoarthritis, Workshop Conference Hoechst Werk Kalle-Albert , 1993 .

[7]  Rainer Storn,et al.  Differential Evolution – A Simple and Efficient Heuristic for global Optimization over Continuous Spaces , 1997, J. Glob. Optim..

[8]  J. Suh,et al.  Finite element formulation of biphasic poroviscoelastic model for articular cartilage. , 1998, Journal of biomechanical engineering.

[9]  A Ratcliffe,et al.  Mechanical and biochemical changes in the superficial zone of articular cartilage in canine experimental osteoarthritis , 1994, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[10]  J S Jurvelin,et al.  Biphasic poroviscoelastic simulation of the unconfined compression of articular cartilage: I--Simultaneous prediction of reaction force and lateral displacement. , 2001, Journal of biomechanical engineering.

[11]  H. Muir,et al.  Demonstration of increased proteoglycan turnover in cartilage explants from dogs with experimental osteoarthritis , 1984, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[12]  A F Mak,et al.  The apparent viscoelastic behavior of articular cartilage--the contributions from the intrinsic matrix viscoelasticity and interstitial fluid flows. , 1986, Journal of biomechanical engineering.

[13]  G E Kempson,et al.  The effects of proteolytic enzymes on the mechanical properties of adult human articular cartilage. , 1976, Biochimica et biophysica acta.

[14]  D. Buttle,et al.  Improved quantitation and discrimination of sulphated glycosaminoglycans by use of dimethylmethylene blue. , 1986, Biochimica et biophysica acta.