Viscoelasticity and wearability of hyaluronate solutions

Abstract This work systematically studied the viscoelastic properties of hyaluronic acid (HA) solution, a major component of synovial fluid, under various testing conditions. The optimum relaxation time of HA solution is around 4.5 s at pH 6.8, in the absence of salt at room temperature, indicating that synovial fluid is viscous when the shear rate is less than 1/4.5 s−1 but elastic when the shear rate exceeds this critical value. HA viscosity declines markedly as the following factors are increased in their order, salt concentration > pH level > temperature, demonstrating that these factors weaken the intermolecular attraction among HA molecules. The non-thixotropic behavior of the HA solution suggests that the breakdown and recovery of the HA structure proceed through the same intermediate states, reconfirming the strong performance of HA as a main component of synovial fluid. The wear results reveal that when the shear rate exceeds a critical value of around 20 s−1, the drop in viscosity leveled out independent of any further increase in shear rate. However, in a broad range of wear rates (20–300 s−1), the HA viscosity sustains for wearing time less than 20 min but declines without leveling off as the wear duration increases thereafter. Finally, experimental results verify that bovine albumin (BA), in HA solution, acts as both hydrodynamic and boundary lubricant, substantially improving the wearability of HA.

[1]  Warren P. Mason,et al.  Introduction to polymer viscoelasticity , 1972 .

[2]  K. Nishinari,et al.  Rheology of hyaluronan solutions under extensional flow. , 2001, Biorheology.

[3]  A. Ogston,et al.  The composition and physicochemical properties of hyaluronic acids prepared from ox synovial fluid and from a case of mesothelioma. , 1965, The Biochemical journal.

[4]  S. Rwei,et al.  Cascade analysis of mixed gels of xanthan and locust bean gum , 2006 .

[5]  R. Gilli,et al.  FTIR studies of sodium hyaluronate and its oligomers in the amorphous solid phase and in aqueous solution. , 1994, Carbohydrate research.

[6]  F. Devínsky,et al.  Aggregates of sodium hyaluronate with cationic and aminoxide surfactants in aqueous solution — light scattering study , 2001 .

[7]  Toshijiro Yamaguchi,et al.  Temporary network formation of hyaluronate under a physiological condition. 1. Molecular‐weight dependence , 1990, Biopolymers.

[8]  S. Arnott,et al.  Hyaluronic acid: molecular conformations and interactions in two sodium salts. , 1980, Journal of molecular biology.

[9]  Stefaan De Smedt,et al.  HYALURONAN : PREPARATION, STRUCTURE, PROPERTIES, AND APPLICATIONS , 1998 .

[10]  E. Morris,et al.  Conformation and dynamic interactions in hyaluronate solutions. , 1980, Journal of molecular biology.

[11]  Yan Sun,et al.  Dependence of pore diffusivity of protein on adsorption density in anion-exchange adsorbent , 2003 .

[12]  E. Balazs,et al.  Rheology of hyaluronic acid , 1968, Biopolymers.

[13]  L. Archer,et al.  Principles of Polymer Systems , 1982 .

[14]  R. Larson The Structure and Rheology of Complex Fluids , 1998 .

[15]  G. Phillips,et al.  The application of shear and extensional viscosity measurements to assess the potential of hylan in viscosupplementation. , 1996, Biorheology.

[16]  S. Rwei,et al.  Sol/gel transition of chitosan solutions , 2005, Journal of biomaterials science. Polymer edition.

[17]  B. Love,et al.  Fabrication and characterization of dipalmitoylphosphatidylcholine-attracting elastomeric material for joint replacements. , 1995, Biomaterials.

[18]  K. Nishinari,et al.  Effect of alkali metal ions on the viscoelasticity of concentrated kappa-carrageenan and agarose gels , 1982 .

[19]  V. Mow,et al.  Constituents and pH changes in protein rich hyaluronan solution affect the biotribological properties of artificial articular joints. , 2001, Journal of biomechanics.

[20]  A. Teŕamoto,et al.  Chain-stiffness and excluded-volume effects in solutions of sodium hyaluronate at high ionic strength , 1995 .

[21]  Hayek,et al.  Adsorption and desorption kinetics of bovine serum albumin in ion exchange and hydrophobic interaction chromatography on silica matrices. , 2000, Biochemical engineering journal.

[22]  F. Devínsky,et al.  Viscometric study of the sodium hyaluronate-sodium chloride-alkyl-(n)-ammonium surfactant system , 1999 .

[23]  J. Demeester,et al.  Viscoelastic and transient network properties of hyaluronic acid as a function of the concentration. , 1993, Biorheology.

[24]  J. Scott,et al.  A water molecule participates in the secondary structure of hyaluronan. , 1988, The Biochemical journal.

[25]  Christopher W. Macosko,et al.  Rheology: Principles, Measurements, and Applications , 1994 .

[26]  Wei-Chih Huang,et al.  The role of dissolved oxygen and function of agitation in hyaluronic acid fermentation , 2006 .