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ASSEMBLY OF TRABECULAR BONE DERIVED SCAFFOLD MICRO-ARCHITECTURES FOR PATIENT SPECIFIC APPLICATIONS   *Wettergreen, M A; *Bucklen, B S; *Liebschner, M A K  *Dept. of Bioengineering, Rice University, Houston, TX,  [email_address] INTRODUCTION Orthopedic tissue engineering incorporates the use of scaffolds which act as a temporary conduit for cell attachment and tissue growth. The clinical need arises in the areas of tissue degeneration due to osteoporosis, voids caused by tumor resection, and a variety of other genetic diseases and trauma affecting mature bone.  When autografts and allografts are non-ideal, tissue scaffolds must be designed.  Unfortunately, the interplay of factors thought to be critical in the process (such as stiffness, strength, permeability, surface-volume ratio, mechanical surface environment) is virtually unknown. At the very least, the design must incorporate the apparent mechanical properties of the trabecular bone we are trying to replace.  Here, we discuss a framework for the design of an implant from design to manufacture. FUTURE OF COMPUTER-AIDED TISSUE ENGINEERING TISSUE MODELING: SELECTION, OPTIMIZATION, AND ASSEMBLY Figure 2.  Optimization of Surface Mechanical Properties.  A heuristic voxel-based procedure was used to improve the surface stress environment of initial unit cells toward a uniform stress state. Figure 3.   Unit Cell Characterization.  Finite Element Modeling (FEM) helped characterize tissue primitives at their average native porosity. Figure 1.   Tissue Modeling (Identification of Tissue Primitives).  Repeated shapes witnessed in the trabecular portion of human T-9 vertebral bodies were documented and transferred into CAD models.  Figure 4.   Unit Scaffold Assembly.  The vertebral body is scanned, density values of subregions corresponding to the unit cell size are ranked.  Unit Cells are placed according to the density map, and interfaces from an interface library are selected to match adjacent faces of the unit cells.  The selection is determined by a system which indexes the unit-cell – interface intersection volume and interface – interface intersection surface area. Computer-Aided Tissue Engineering.  Patient-specific CT data is used to develop tissue models which replicate the apparent properties of trabecular bone (i.e. modulus, permeability, etc.). Models are manufactured, validated  ex vivo , then implanted   Figure 6.  Mechanical Usage and Implant/Tissue Degradation Profiles. The mechanical usage window  (left)  hypothesizes that metabolic changes in bone mass occur with strain at the micro-architectural level.  Large strains result in an irreversible, pathological overload and tissue necrosis. Tissue engineered implants must provide initial mechanical support. Yet, as the scaffold degrades and new tissue is formed, increased strain nearing the pathological window may be induced  (right) .  Depending on the scaffold architecture, regional differences exist.  Implant design must take this into account. MANUFACTURE / FABRICATION Figure 5.   Fabrication of CATE Library into a Global Construct.  Assembly of a partial, human vertebral body  (top, left)  is translated for 3-D printing via a fused deposition rapid prototyping system which uses a thermoplastic wax material  (top, right) .  Other methods of fabrication include selective laser sintering, which cures a powder polymer in a layer-by-layer fashion by heating the material to just above its glass transition temperature  (bottom, right). Acknowledgements: Chris Chen, Jeremy Lemoine, Stefan Lohfeld. Funding provided by NSF.

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Assembly of Trabecular Bone Derived Scaffold Micro-Architectures for Patient Specific Applications, 10/2006

  • 1. ASSEMBLY OF TRABECULAR BONE DERIVED SCAFFOLD MICRO-ARCHITECTURES FOR PATIENT SPECIFIC APPLICATIONS *Wettergreen, M A; *Bucklen, B S; *Liebschner, M A K *Dept. of Bioengineering, Rice University, Houston, TX, [email_address] INTRODUCTION Orthopedic tissue engineering incorporates the use of scaffolds which act as a temporary conduit for cell attachment and tissue growth. The clinical need arises in the areas of tissue degeneration due to osteoporosis, voids caused by tumor resection, and a variety of other genetic diseases and trauma affecting mature bone. When autografts and allografts are non-ideal, tissue scaffolds must be designed. Unfortunately, the interplay of factors thought to be critical in the process (such as stiffness, strength, permeability, surface-volume ratio, mechanical surface environment) is virtually unknown. At the very least, the design must incorporate the apparent mechanical properties of the trabecular bone we are trying to replace. Here, we discuss a framework for the design of an implant from design to manufacture. FUTURE OF COMPUTER-AIDED TISSUE ENGINEERING TISSUE MODELING: SELECTION, OPTIMIZATION, AND ASSEMBLY Figure 2. Optimization of Surface Mechanical Properties. A heuristic voxel-based procedure was used to improve the surface stress environment of initial unit cells toward a uniform stress state. Figure 3. Unit Cell Characterization. Finite Element Modeling (FEM) helped characterize tissue primitives at their average native porosity. Figure 1. Tissue Modeling (Identification of Tissue Primitives). Repeated shapes witnessed in the trabecular portion of human T-9 vertebral bodies were documented and transferred into CAD models. Figure 4. Unit Scaffold Assembly. The vertebral body is scanned, density values of subregions corresponding to the unit cell size are ranked. Unit Cells are placed according to the density map, and interfaces from an interface library are selected to match adjacent faces of the unit cells. The selection is determined by a system which indexes the unit-cell – interface intersection volume and interface – interface intersection surface area. Computer-Aided Tissue Engineering. Patient-specific CT data is used to develop tissue models which replicate the apparent properties of trabecular bone (i.e. modulus, permeability, etc.). Models are manufactured, validated ex vivo , then implanted Figure 6. Mechanical Usage and Implant/Tissue Degradation Profiles. The mechanical usage window (left) hypothesizes that metabolic changes in bone mass occur with strain at the micro-architectural level. Large strains result in an irreversible, pathological overload and tissue necrosis. Tissue engineered implants must provide initial mechanical support. Yet, as the scaffold degrades and new tissue is formed, increased strain nearing the pathological window may be induced (right) . Depending on the scaffold architecture, regional differences exist. Implant design must take this into account. MANUFACTURE / FABRICATION Figure 5. Fabrication of CATE Library into a Global Construct. Assembly of a partial, human vertebral body (top, left) is translated for 3-D printing via a fused deposition rapid prototyping system which uses a thermoplastic wax material (top, right) . Other methods of fabrication include selective laser sintering, which cures a powder polymer in a layer-by-layer fashion by heating the material to just above its glass transition temperature (bottom, right). Acknowledgements: Chris Chen, Jeremy Lemoine, Stefan Lohfeld. Funding provided by NSF.