Biomedical subjects

John C Gardiner

Publications and source records attributed to John C Gardiner.

4 recordsLinked to original sources

PubMed2005

Three-dimensional finite element modeling of ligaments: technical aspects.

The objective of this paper is to describe strategies for addressing technical aspects of the computational modeling of ligaments with the finite element (FE) method. Strategies for FE modeling of ligament mechanics are described, differentiating between whole-joint models and models of individual ligaments. Common approaches to obtain three-dimensional ligament geometry are reviewed, with an emphasis on techniques that rely on volumetric medical image data. Considerations for the three-dimensional constitutive modeling of ligaments are reviewed in the context of ligament composition and structure. A novel approach to apply in situ strain to FE models of ligaments is described, and test problems are presented that demonstrate the efficacy of the approach. Approaches for the verification and validation of ligament FE models are outlined. The paper concludes with a discussion of future research directions.

Algorithms↗

PubMed2003

Subject-specific finite element analysis of the human medial collateral ligament during valgus knee loading.

The objectives of this study were (1) to develop subject-specific experimental and finite element (FE) techniques to study the three-dimensional stress-strain behavior of ligaments, with application to the human medial collateral ligament (MCL), and (2) to determine the importance of subject-specific material properties and initial (in situ) strain distribution for prediction of the strain distribution in the MCL under valgus loading. Eight male knees were subjected to varus-valgus loading at flexion angles of 0 degrees, 30 degrees, and 60 degrees. Three-dimensional joint kinematics and MCL strains were recorded during kinematic testing. Following testing, the MCL of each knee was removed to allow measurement of the in situ strain distribution and to perform material testing. A FE model of the femur-MCL-tibia complex was constructed for each knee to simulate valgus loading at each flexion angle, using subject-specific bone and ligament geometry, material properties, and joint kinematics. A transversely isotropic hyperelastic material model was used to represent the MCL. The MCL in situ strain distribution at full extension was used to apply in situ strain to each MCL FE model. FE predicted MCL strains during valgus loading were compared to experimental measurements using regression analysis. The subject-specific FE predictions of strain correlated reasonably well with experimentally measured MCL strains (R(2)=0.83, 0.72, and 0.66 at 0 degrees, 30 degrees, and 60 degrees, respectively). Despite large inter-subject variation in MCL material properties, MCL strain distributions predicted by individual FE models that used average MCL material properties were strongly correlated with subject-specific FE strain predictions (R(2)=0.99 at all flexion angles). However, predictions by FE models that used average in situ strain distributions yielded relatively poor correlations with subject-specific FE predictions (R(2)=0.44, 0.35, and 0.33 at flexion angles of 0 degrees, 30 degrees, and 60 degrees, respectively). The strain distribution within the MCL was nonuniform and changed with flexion angle. The highest MCL strains occurred at full extension in the posterior region of the MCL proximal to the joint line during valgus loading, suggesting this region may be most vulnerable to injury under these loading conditions. This work demonstrates that subject-specific FE models can predict the complex, nonuniform strain fields that occur in ligaments due to external loading of the joint.

Adult↗

PubMed2003

Control of cellulose synthase complex localization in developing xylem.

Cellulose synthesis in the developing xylem vessels of Arabidopsis requires three members of the cellulose synthase (CesA) gene family. In young vessels, these three proteins localize within the cell, whereas in older vessels, all three CesA proteins colocalize with bands of cortical microtubules that mark the sites of secondary cell wall deposition. In the absence of one subunit, however, the remaining two subunits are retained in the cell, demonstrating that all three CesA proteins are required to assemble a functional complex. CesA proteins with altered catalytic activity localize normally, suggesting that cellulose synthase activity is not required for this localization. Cortical microtubule arrays are required continually to maintain normal CesA protein localization. By contrast, actin microfilaments do not colocalize with the CesA proteins and are unlikely to play a direct role in their localization. Green fluorescent protein-tagged CesA reveals a novel process in which the structure and/or local environment of the cellulose synthase complex is altered rapidly.

Arabidopsis↗

PubMed2002

Ligament material behavior is nonlinear, viscoelastic and rate-independent under shear loading.

The material behavior of ligament is determined by its constituents, their organization and their interaction with each other. To elucidate the origins of the multiaxial material behavior of ligaments, we investigated ligament response to shear loading under both quasi-static and rate-dependent loading conditions. Stress relaxation tests demonstrated that the tissue was highly viscoelastic in shear, with peak loads dropping over 40% during 30 min of stress relaxation. The stress relaxation response was unaffected by three decades of change in shear strain rate (1.3, 13 and 130%/s). A novel parameter estimation technique was developed to determine material coefficients that best described the experimental response of each test specimen to shear. The experimentally measured clamp displacements and reaction forces from the simple shear tests were used with a nonlinear optimization strategy based around function evaluations from a finite element program. A transversely isotropic material with an exponential matrix strain energy provided an excellent fit to experimental load-displacement curves. The shear modulus of human MCL showed a significant increase with increasing shear strain (p<0.001), reaching a maximum of 1.72+/-0.4871 MPa. The results obtained from this study suggest that viscoelasticity in shear does not likely result from fluid flow. Gradual loading of transversely oriented microstructural features such as intermolecular collagen crosslinks or collagen-proteoglycan crosslinking may be responsible for the stiffening response under shear loading.

Adult↗