Poroelastic response of articular cartilage by nanoindentation creep tests at different characteristic lengths

M. Taffetani, R. Gottardi, D. Gastaldi, R. Raiteri, P. Vena

Research output: Contribution to journalArticle


Nanoindentation is an experimental technique which is attracting increasing interests for the mechanical characterization of articular cartilage. In particular, time dependent mechanical responses due to fluid flow through the porous matrix can be quantitatively investigated by nanoindentation experiments at different penetration depths and/or by using different probe sizes. The aim of this paper is to provide a framework for the quantitative interpretation of the poroelastic response of articular cartilage subjected to creep nanoindentation tests. To this purpose, multiload creep tests using spherical indenters have been carried out on saturated samples of mature bovine articular cartilage achieving two main quantitative results. First, the dependence of indentation modulus in the drained state (at equilibrium) on the tip radius: a value of 500kPa has been found using the large tip (400μm radius) and of 1.7MPa using the smaller one (25μm). Secon, the permeability at microscopic scale was estimated at values ranging from 4.5×10-16m4/Ns to 0.1×10-16m4/Ns, from low to high equivalent deformation. Consistently with a poroelastic behavior, the size-dependent response of the indenter displacement disappears when characteristic size and permeability are accounted for. For comparison purposes, the same protocol was applied to intrinsically viscoelastic homogeneous samples of polydimethylsiloxane (PDMS): both indentation modulus and time response have been found size-independent.

Original languageEnglish
Pages (from-to)850-858
Number of pages9
JournalMedical Engineering and Physics
Issue number7
Publication statusPublished - 2014



  • Articular cartilage
  • Nanoindentation
  • Poroelasticity size effect
  • Time-dependence

ASJC Scopus subject areas

  • Biomedical Engineering
  • Biophysics
  • Medicine(all)

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