Biomechanics of Bone / Bone Biomechanics
Ahmad Raeisi Najafi; Ahmad Reza Arshi; Mohammad Reza Eslami; Shahriar Fariborz; Mansour Moeinzadeh
Volume 1, Issue 3 , June 2007, , Pages 177-188
Abstract
A two dimensional finite element model for the human Haversian cortical bone is represented. The interstitial bone tissue, the osteons and the cement line were modeled as the matrix, the fibers and the interface, respectively. This was due to similarities between fiber-ceramic composite materials and ...
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A two dimensional finite element model for the human Haversian cortical bone is represented. The interstitial bone tissue, the osteons and the cement line were modeled as the matrix, the fibers and the interface, respectively. This was due to similarities between fiber-ceramic composite materials and the human Haversian cortical bone. The stress intensity factor in the microcrack tips vicinity was computed using the linear elastic fracture mechanics theory and assuming a plane strain condition. It was therefore possible to study the effect of microstructure and mechanical properties of Haversian cortical bone on microcrack propagation trajectory. The results indicated that this effect was limited to the vicinity of the osteon. If both osteon and cement line were assumed to be softer than the interstitial tissue, the stress intensity factor was increased when the crack distance to the osteon reduced. The stress intensity factor decreased if both osteon and cement line were assumed to be stiffer than the interstitial tissue. The resulting simulation indicated that the effect of existence of osteon on the stress intensity factor was no significance, if both the interstitial tissue and cement line were assumed either stiffer or softer than the osteon. Microcrack trajectory was observed to deviate from the osteon under tensile loading; indicating an independence from the mechanical properties of various tissues. In fact, the microcrack adopts a trajectory between the osteons, thereby increasing the necessary absorbed energy for fracture. This results in an increase in the human Haversian cortical bone toughness. The result of this finite element modeling has been confirmed by through evaluation and comparison made with experimental results.
Cell Biomechanics / Cell Mechanics / Mechanobiology
Farhad Tabatabaei Ghomshe; Ahmad Reza Arshi; Masoud Mahmoudian; Mahyar Janahmadi
Volume -1, Issue 1 , June 2004, , Pages 77-92
Abstract
Effective pharmacological analysis encompassing both the pharmacodynamics and the pharmacokinetics of the heart, dictates the necessity for responses made by the main channel receptors, to be appropriately modelled. This approach is of critical value when the pharmacological responses of the organ during ...
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Effective pharmacological analysis encompassing both the pharmacodynamics and the pharmacokinetics of the heart, dictates the necessity for responses made by the main channel receptors, to be appropriately modelled. This approach is of critical value when the pharmacological responses of the organ during pathological states are under investigation. To this effect, the electrochemical phenomenon in the heart was simulated using a specifically simplified three dimensional model based on the cellular physiological concepts. Various advanced models for different types of heart cells were combined to produce a three dimensional model capable of describing the electrophysiological, electrochemical and geometric characteristics of a heart in a non-pathological state. Various cell type models such as central and peripheral SA node, AV node, atrial myocyte, ventricular myocyte, and specialized cells for rapid conductance like purkinje fibres were included in the 3D model. The cellular architecture in the model follows the non-heterogeneity of the heart structure accompanied by gap junctions representing cellular interconnections. Here the transport of Na+, Ca++, K+ and CL- was primarily governed by such factors as electrical and chemical potential gradients along with other energetic mechanisms. The simplified heart geometry is introduced through 18 layers with 25 cells in each layer. Model equations were solved to simulate a one second using a 2.6 GHz Pentium IV PC. The simulation was performed utilizing MA TLAB programming language which provides effective visualization capabilities. The CEP model could be adopted as a preliminary basis towards individualizations in pharmacology and electrophysiology.
