2013
DOI: 10.1002/jbm.a.34914
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Strain rate viscoelastic analysis of soft and highly hydrated biomaterials

Abstract: Measuring the viscoelastic behavior of highly hydrated biological materials is challenging because of their intrinsic softness and labile nature. In these materials, it is difficult to avoid prestress and therefore to establish precise initial stress and strain conditions for lumped parameter estimation using creep or stress-relaxation (SR) tests. We describe a method ( or epsilon dot method) for deriving the viscoelastic parameters of soft hydrated biomaterials which avoids prestress and can be used to rapidl… Show more

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Cited by 75 publications
(80 citation statements)
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“…However, the impact of these effects should be minimal as compression and relaxation are performed on timescales faster than tissue viscoelastic relaxation rates, typically several seconds. [28][29][30] Future work should investigate the impact of tissue viscoelastic properties on perfusion-rate estimation and account for heterogeneity in tissue mechanical properties. …”
Section: Discussionmentioning
confidence: 99%
“…However, the impact of these effects should be minimal as compression and relaxation are performed on timescales faster than tissue viscoelastic relaxation rates, typically several seconds. [28][29][30] Future work should investigate the impact of tissue viscoelastic properties on perfusion-rate estimation and account for heterogeneity in tissue mechanical properties. …”
Section: Discussionmentioning
confidence: 99%
“…Moreover, they often require a long testing phase which may result in significant sample deterioration in case of highly hydrated and labile specimens [23]. To address these issues we proposed the epsilon dot method ( _ eM) to derive material viscoelastic constants through measurements performed rapidly at different strain rates within the linear viscoelastic region [10]. As it avoids sample pre-stress and/or degradation during measurements, the _ eM is particularly suited for hepatic and other soft tissues.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, we suggest that tissue and soft material characterisation for in-vitro applications be performed on equilibrium swollen samples at physiological temperature (or at least at the same temperature at which the biomimetic material is tested) using methods which are non force-or strain-triggered and rapid measurements (e.g. _ eM [10], nano-_ eM [90]). Equilibrium swelling ensures that the samples are in a physiologically relevant, stable and reproducible state before the experiment, while quick, non-triggered testing avoids sample pre-stress and minimises status alterations during testing [23].…”
Section: Ex-vivo Mechanical Testing Guidelines For In-vitro Applicationsmentioning
confidence: 99%
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“…Kinetics modeling, including loss factor and nature frequency, is a key issue [3]. In recent years, many researchers have investigated the kinetics parameters of damping structures [4][5][6][7][8]. However, viscoelastic dynamic performance is difficult to precisely predict owing to the complex stiffness matrix of viscoelastic structures.…”
Section: Introductionmentioning
confidence: 99%