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1.
Journal of Medical Biomechanics ; (6): E126-E130, 2014.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-804392

RESUMO

Objective To establish the monosegmental transpedicular fixation model and short segmental fixation model by three-dimensional finite element technique, and evaluate the biomechanical properties of monosegmental transpedicular fixation for thoracolumbar fractures and verify its feasibility for application. Methods T10-L2 motion segment of a young healthy subject was used to establish the normal finite element model. The superior 1/2 cortical bone of the T12 segment was removed and superior 1/2 cancellous bone of the same vertebrae was assigned material property of the injured bone to simulate the thoracolumbar fracture. Transpedicular screw fixation of the T11 and T12 segment was performed in monosegmental fixation model. T11 and L1 segment were instrumented in the short segmental fixation model. All the four finite element models were applied with loading of axial compression, anteflexion, extension, lateroflexion and axial rotation, respectively. Motion difference of each functional unit and the stress of implants were measured to evaluate biomechanical behaviors of monosegmental fixation. Results The motion difference of all the functional units (T10-11, T11-12, T12-L1) in the fractured model was obviously increased under all loading conditions as compared to the normal model, but the motion difference in the fractured models was decreased after monosegmental fixation and short segmental fixation, and no significant differences were found between monosegmental fixation and short segmental fixation. The stress on screws in monosegmental fixation model was significantly lower than that in short segmental fixation under axial compression and anteflexion, but the stress on screws of two fixation models had no significant difference under extension, lateroflexion and axial rotation. The stress on the rods of monosegmental fixation model was apparently higher than that of short segmental fixation under extension and lateroflexion, and lower under axial rotation, but no significant difference was found for two fixation models under axial compression and anteflexion. Conclusions Monosegmental transpedicular screw fixation would give the similar stabilization as short segmental fixtion and could be an effective alternative to treat incomplete fractures in thoracolumbar spine.

2.
Journal of Medical Biomechanics ; (6): E454-E459, 2013.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-804286

RESUMO

Objective To study the morphology and biomechanical properties of the improved acellularized nerve scaffold using the technique of hypotonic buffer combined with freeze-drying. Methods The traditional acellularized nerve scaffold (traditional group) was made to be improved with the technique of hypotonic buffer combined with freeze-drying (improved group). After the acellularization process was completed, the histological structure of nerves in each group was observed by HE staining and scanning electron microscope. The interval porosity and void diameter in each group were measured by Mimics software. The biomechanical properties of nerves in each group were tested by mechanical apparatus (Endura TEC ELF3200). Results The acellularization effect of the improved chemical method with the technique of hypotonic buffer combined with freeze-drying was similar to that of the traditional Hudson method, but the histological structure was more porous in improved group than that in traditional group. The interval porosity of traditional group and improved group were 34.5% and 49.3%, respectively; the void diameter of traditional group and improved group were 11.96 and 17.61 μm, respectively. Biomechanical testing results showed that there was no statistical difference in ultimate load, ultimate stress, ultimate strain and mechanical work to fracture in each group (P>0.05). Conclusions The acellularized nerve prepared by hypotonic buffer combined with freeze-drying can be used as a new kind of nerve scaffold material to make better contribution to cell combination.

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