Compressive cyclic ratcheting and fatigue of synthetic, soft biomedical polymers in solution.

Published

Journal Article

The use of soft, synthetic materials for the replacement of soft, load-bearing tissues has been largely unsuccessful due to a lack of materials with sufficient fatigue and wear properties, as well as a lack of fundamental understanding on the relationship between material structure and behavior under cyclic loads. In this study, we investigated the response of several soft, biomedical polymers to cyclic compressive stresses under aqueous conditions and utilized dynamic mechanical analysis and differential scanning calorimetry to evaluate the role of thermo-mechanical transitions on such behavior. Studied materials include: polycarbonate urethane, polydimethylsiloxane, four acrylate copolymers with systematically varied thermo-mechanical transitions, as well as bovine meniscal tissue for comparison. Materials showed compressive moduli between 2.3 and 1900MPa, with polycarbonate urethane (27.3MPa) matching closest to meniscal tissue (37.0MPa), and also demonstrated a variety of thermo-mechanical transition behaviors. Cyclic testing resulted in distinct fatigue-life curves, with failure defined as either classic fatigue fracture or a defined increased in maximum strain due to ratcheting. Our study found that polymers with sufficient dissipation mechanisms at the testing temperature, as evidenced by tan delta values, were generally tougher than those with less dissipation and exhibited ratcheting rather than fatigue fracture much like meniscal tissue. Strain recovery tests indicated that, for some toughened polymers, the residual strain following our cyclic loading protocol could be fully recovered. The similarity in ratcheting behavior, and lack of fatigue fracture, between the meniscal tissue and toughened polymers indicates that such polymers may have potential as artificial soft tissue.

Full Text

Duke Authors

Cited Authors

  • Miller, AT; Safranski, DL; Smith, KE; Guldberg, RE; Gall, K

Published Date

  • February 2016

Published In

Volume / Issue

  • 54 /

Start / End Page

  • 268 - 282

PubMed ID

  • 26479427

Pubmed Central ID

  • 26479427

Electronic International Standard Serial Number (EISSN)

  • 1878-0180

International Standard Serial Number (ISSN)

  • 1751-6161

Digital Object Identifier (DOI)

  • 10.1016/j.jmbbm.2015.09.034

Language

  • eng