Mechanics: – Applied (or Engineering) Mechanics: – the science of applying the principles of mechanics Rigid Body Mech. Applied Mechanics a branch of physics that is concerned with the motion and deformation of bodies in response to forces Statics Dynamics Deformable Body Mech Elasticity Plasticity Viscoelasticity Fluid Mechanics Kinematics and Kinetics Gases and Liquids Poroelasticity Physical Properties of Spinal Elements Spinal Elements: – Bone • Vertebral body: Cortical bone, cancellous bone, and bony endplate • Posterior bony elements – Soft Tissues • Ligaments and intervertebral disc Physical Properties: – Mass: • Bone density • Mass moment of inertia for dynamic analysis – Morphology: • Structure, shape, size, location, area and polar moment of inertia – Mechanical (Elastic, elastic, and poroelastic) Properties: • Stiffness: compression, tension, share, bending, torsion • Moduli and Poisson’s ratio • Permeability Measurement of Physical Properties Mass Measurement: – – – Morphology Measurement: – – – – Direct measurement Dual X-ray Absorption metry for BMD measurement QCT Direct measurement from cadaveric specimens Video system Plain X-rays CT and MRI Mechanical Properties – Elastic Property Measurement: • – Viscoelastic Property measurement: • – Static mechanical tests in compression, tension, shear, bending and torsion tests Creep, relaxation, cyclic loading tests Poroelastic Property Measurement: • Elastic property measurement techniques combined with diffusion tests Measurement of Mechanical Properties Mechanical Tests: – Based on Loading Direction • • • – Based on Loading Speed • Static or dynamic Tests Input and Output: – Input • – loading by Displacement control vs. Load Control Output • • Compression/Tension Test Bending/Torsion Tests Creep and Relaxation Tests measuring resultant force or displacement stress-strain curve Factors for Consideration: – – – – Boundary condition Loading direction and loading speed Parameter measurement: Prevention of dehydration of specimens Spinal Ligaments Ligaments: – – – Uniaxial structures Effective in carrying tensile loads along the direction in which the fiber runs Spinal ligaments provide tensile resistance to external loads by developing tension when the spinal segment is subjected to complex loads Functions – – – – of Ligaments: Allow adequate physiologic motion and fixed postural attitudes between vertebrae with a minimum expenditure of muscle energy Protect the spinal cord by restricting the motions within well-defined limits Share with the muscles the role of providing stability to the spine within its physiologic ranges of motion Protect the spinal cord in traumatic situations (energy absorption) Quantitative Anatomy Quantities for describing the functional role of ligaments: – – Length, X-sectional Area, 3-D coordinates of the attachment position Precise data are not available Region Cervical Lumbar Level C1-C2 Ligament Transverse Alar X-area (mm2) 18 22 Length(mm) 20 11 ALL PLL LF CL ISL SSL 53 16 67 26 23 13 11 19 11 Tensile Tests Loading Methods – – F-d and Stress-Strain Curves – Stiffness and/or elastic modulus Displacement or Force Measurements – – – Load Control Displacement Control LVDT installed in MTS machine Extensometer Image Analysis of markers on the tissue Important Factors of Consideration – – – Loading speed or loading rate Cross-sectional area measurement for stress calculation Prevention of dehydration Typical Load-displacement Curve of Ligaments Load or Stress Failure Physiologic Range NZ EZ PZ Traumatic Range NZ = Neutral Zone EX = Elastic Zone PZ = Plastic Zone Deformation of Strain Physical Properties of Ligaments Ligament Ant. Atlantooccip. Memb. Post. Atlantooccip. Memb. C1-C2 ALL LF CL Transverse Lig. C2-C7 ALL PLL LF CL ISL SSL Failure Load (N) Deformation (mm) 233 83 18.9 18.1 281 113 157 354 (170-700) 12.3 8.7 11.4 111.5 (47-176) 74.5 (47-102) 138.5 (56-221) 204 (144-264) 35.5 (26-45) 8.95 (4.2-13.7) 6.4 (3.4-9.4) 8.3 (3.7-12.9) 8.4 (6.8-10) 7.4 (5.5-9.2) *Range of values are listed in parentheses. Stress (MPa) Strain (%) Elastic Properties of Ligaments Ligament Modulus (MPa) Thoracic ALL PLL LF CL ISL SSL Lumbar ALL PLL LF CL ISL SSL TL 7.8 (<12%) 20 (>12%) 10 (<11%) 20 (>11%) 15 (<6.2%) 19.5 (>6.2%) 7.5 (<25%) 32.9 (>25%) 10 (<14%) 11.6 (>14%) 8.0 (<20%) 15 (>20%) 10 (<18%) 58.7 (>18%) Failure Load (N) Deformation (mm) 296 (123-468) 106 (74-138) 200 (135-265) 168 (63-273) 75.5 (31-120) 320 (101-538) 10.3 (6.3-14.2) 5.25 (3.2-7.3) 8.65 (6.3-11) 6.75 (3.9-9.6) 5.25 (3.8-6.7) 14.1 (7.2-21) 450 (390-510) 324 (264-384) 285 (230-340) 222 (160-284) 125 (120-130) 150 (100-200) 15.2 (7-20) 5.1 (4.2-7) 12.7 (12-14.5) 11.3 (9.8-12.8) 13.0 (7.4-17.8) 25.9 (22.1-28.1) *Range of values are listed in parentheses. Stress (MPa) Strain (%) 11.6 (2.4-21) 11.5 (2.9-20) 8.7 (2.4-15) 7.6 (7.6) 3.4 (1.8-4.6) 5.4 (2.0-8.7) 36.5 (16-57) 26.0 (8-44) 26.0 (10-46) 12.0 (12.0) 13.0 (13.0) 32.5 (26-39) Functional Biomechanics Functional properties of a ligament are described as a combination of physical properties and orientation and location with respect to the moving vertebra Physiological Strain in Ligaments Future Studies Physical Properties of Spinal Ligaments: – Tkaczauk et al. (Acta Scand Orthop, 115, 1968) • Decreases in maximum deformation, the residual (or permanent) deformation, and the energy loss of hysteresis of anterior and posterior longitudinal ligaments with age • Decrease in maximum deformation and residual deformation with the disc degeneration – Property changes with age and disc degeneration may be related with segmental instability and low back pain. Further studies on the changes in the physical properties of spinal ligament with respect to the pathology THE VERTEBRA Vertebra: – – Vertebral body Posterior bony ring (neural arch) • two pedicles and laminae from which arise seven processes of articular, transverse, and spinous processes – Basic design of the vertebrae from C3-L5 is almost same, but the size and mass increase from the first cervical to the last lumbar vertebra (Mechanical adaptation to the progressively increasing loads). Functions – – – of the Vertebra: Protect the spinal cord Maintain the posture Provide major load bearing Pedicles – – Pedicle Height and Pedicle Width (PDH and PDW) Inclination angles to the sagittal and transverse planes (PDIs and PDIt) Region C3 C5 C7 T1 T5 T9 T12 L1 L2 L3 L4 L5 PDW (mm) 6 (4 - 8) 6 (4 - 8) 7 (5 - 9) 8 (5 -10) 5 (3 - 7) 6 (4 - 9) 7 (3 - 11) 9 (5 - 13) 9 (4 -13) 10 (5 - 16) 13 (9 - 17) 18 (9 - 29) PDH (mm) 8 (6 -10) 7 (5 - 9) 8 (6 -10) 10 (7 - 15) 12 (7 - 14) 14 (11 - 16) 16 (12 - 20) 15 (11 - 21) 15 (10 - 18) 15 (8 - 18) 15 (9 - 19) 14 (10 -19) PDIs (deg) 41 (20 - 55) 39 (24 - 54) 30 (15 - 45) 27 (16 - 34) 9 (2 - 19) 8 (0 - 11) -4 (-17 - 15) 11 (7 - 15) 12 (5 - 18) 14 (8 - 24) 18 (6 - 28) 30 (19 -44) PDIt (deg) -6 (-16 - 4) 0 (-10 - 10) 6 (4 -16) 13 (4 - 25) 15 (7 - 20) 16 (9 -14) 12 (7 - 16) 2 (-13 - 15) 2 (-10 - 13) 0 (-10 - 12) 0 (-6 - 7) -2 (-8 - 6) Neural Arch - Most failures occurred through the pedicles. - In Lamy et al.’s study, 1/3 of the failures were through the pars interarticularis (Spondylolysis). This number increased when the tests were conducted at higher rates of loading. - No strength difference between males and females as well as between normal and degenerated discs Facet Joints - Shape and position of the articulating processes are the important factors for determining the pattern of spinal motion. - Cervical spine - Thoracic spine - Lumbar spine: - Curved mating surfaces not plane - Facet orientations in the figure are only approximate Facet Joints Physical Properties of the Vertebral Body - The variation in the vertebral strength with the spinal level is most probably due to the size of the vertebrae alone. - Strength decreases with age. A rapid rate of decrease was observed from age 20 - 40 years, while the strength remained more or less constant after age 40. Physical Properties of the Vertebral Body - Strength decrease with relative ash content or osseous tissue of the vertebrae. - 25% osseous tissue loss results in a more than 50% strength decrease. - Bone mineral content (BMC) decrease with age. - Mechanical Strength BMC Cortical Shell and Cancellous Core F Cancellous Bone Endplate Fcan The vertebral body carries most of the compressive loads that are transmitted from the superior to the inferior endplate. Mechanical properties of the vertebral cortical shell has not been clearly investigated yet. Rockoff et al. (Calcif. Tissue Res 3:163, 1969) – Fcor Fcor – McBroom et al, (JBJS 67A:1206, 1985) – Cortical Bone Endplate F Trabecular bone contributes 25 - 55% of the strength depending upon the ash content of the bone. 55% vs 35% carried under and after 40 yrs of age. The cortical shell provides only 10% (in average) of the total compressive load even in specimens came from an old population (63 - 99 yrs) Cancellous Bone - Failure Type I: decreasing strength after the maximum load reached (13% of the specimens) - Failure Type II: maintaining strength (about 50% of the specimens) - Failure Type III: increasing strength (38% of the specimens) - Type III failure was found most frequently in males under 40 yrs of age and least frequently in women over 40. Compressive Properties of Vertebral Cancellous Bone - Despite of much variation after the maximum strength in the loaddisplacement curve, the mechanical properties represented in the early part of the curve were quite consistent. Compressive properties of cancellous bone of vertebrae Physical Property Proportional-limit stress Compression at proportional limit Modulus of elasticity Failure stress Compression at failure Magnitude 1.37 - 4.0 MPa 6.0 - 6.7 % 22.8 - 55.6 MPa 1.55 - 4.6 MPa 7.4 - 9.5% Functional Biomechanics of Vertebral Trabecular Bone Presence of Bone marrow in Cancellous Core: – – Effect of aging on the vertebral trabecular bone structure: – – – significantly increase the compressive strength as well as the energy capacity. This suggests that the function of cancellous core is not only to share the load with the cortical shell but also to act as the main resistor of the dynamic peak loads. Loss of the horizontal trabeculae with simultaneous thickening of the vertebral trabeculae Loss of the horizontal trabeculae occurs in the central region of the vertebral body while those in the peripheral regions remained unaltered. In another study, however, it was found that both trabeculae get thinner and decrease at the same rate, but the horizontal trabeculae are lesser in number than the vertical trabeculae at all density levels. Thus, the spacing between horizontal trabeculae increases more rapidly than the spacing between vertical trabeculae. Biomechanical adaptation: – – – Changes in the trabecular bone was found with the disc degeneration. With less disc degeneration, the trabecular bone is stronger in the center. In case of degenerated discs, the trabecular bone strength has uniform distribution. Biomechanical Factors for Bone Tests Experimental Artifacts: – – – – Boundary and Loading Conditions: – – Specimen preparation methods: Damages on the specimen surface Orientation and anatomical site of the specimen Specimen condition: wet or dry; repeated use of specimens Specimen shape and size: A cylindrical specimen with at least 1:2 aspect ratio End-artifact: Friction between the specimen and the platen and also the deformation measurement points Loading rates Effect of bone marrow on the mechanical properties of the trabecular bone (poroelastic effect) BIOMECHANICAL ANALYSIS OF TRABECULAR BONE AS A POROELASTIC MATERIAL STUDIES OF TRABECULAR BONE MECHANICS Bone behavior in vivo Effects of aging, disease, and instrumentation, etc. STUDIES OF TRABECULAR BONE MECHANICS Age-related bone fracture Total joint loosening Bone remodeling, etc. TRABECULAR BONE (ELASTIC MATERIAL) Elastic – Properties Young’s Modulus (E), Shear Modulus (G), and Poisson’s ratio () Stiffness – and Strength Relationship with Bone Density Anisotropy – Transversely isotropic or orthotropic Effect of the Architectural Features of Trabecular Bone TRABECULAR BONE (ELASTIC MATERIAL) Micromechanics – – Mathematical models Material properties of individual trabecular tissue Experimental – friction artifacts at specimen-platen interface, damage artifact during specimen preparation, and specimen geometry, etc. Limitations – – Errors in using the Theory of Elasticity Considering trabecular bone as a single-phase solid material; unable to describe the time-dependent behaviors. TIME-DEPENDENT BEHAVIORS OF TRABECULAR BONE Creep – and Stress Relaxation Zilich et al., 1980; Schoerfeld et al., 1974; Deligianni et al., 1994; Bowman et al., 1994 Influence Stiffness – of Loading Rate on Strength and Carter and Hayes, 1977; Ducheyne, et al., 1977; Galante et al.; Linde et al., 1991 TIME-DEPENDENT BEHAVIORS OF TRABECULAR BONE Trabecular – – Kafka et al. Deligianni et al. Limitations – – Bone as a Viscoelastic Material of a Viscoelastic Theory Unable to experimentally determine the time-dependent viscoelastic properties of trabecular bone; Difficult to describe the mechanical role of fluid-phase. BONE STRUCTURE Solid – mineralized bone tissue with pores Fluid – Phase Phase blood vessels, blood, red and yellow marrow, nerve tissue, miscellaneous cells, and interstitial ROLE OF FLUID PHASE Physiological – Transporting nutrients and waste products Mechanical – – Role: Role: Postulated to cause time-dependent behaviors of trabecular bone; Not fully understood yet. HYPOTHESES Fluid phase may change the mechanical behaviors of trabecular bone . Two Coupled Interaction Mechanisms between the Interstitial Fluid and the Porous Trabecular Tissue – Compression of trabecular bone causes a rise of pore pressure; – An increase in pore pressure induces dilation of trabecular bone. HYPOTHESES The apparent elastic and time-dependent behaviors of trabecular bone can be well described by using the theory of poroelasticity. Trabecular bone can be characterized using poroelastic properties. THREE STUDIES Poroelastic Model of Trabecular Bone; Effect of the Fluid Flow in Trabecular Bone on the Relaxation Behavior; Measurement of Poroelastic Properties of Trabecular Bone. PURPOSE To investigate: if the apparent mechanical behavior of trabecular bone can be well described with poroelasticity theory. what affects the poroelastic behavior. HISTORY OF POROELASTICITY THEORY Consolidation – – Terzaghi: 1-D model Rendulic: 3-D model Theory – – of Poroelasticity: Biot; Verrjuit Rice and Cleary Mixture – Model: Theories: Atkin; Bowen; Morland COMPARISON OF POROELASTIC THEORIES Biot’s – – Use of model parameters that are not identifiable and difficult measure. For simplification, Incompressibility of both the solid and fluid phases was assumed. Rice – – – Formulation: and Cleary’s Formulation: Use of model parameters that are elastically identifiable and measurable. Full incorporation of the compressibility. Simplified the interpretation of asymptotic poroelastic phenomena Poroelastic Equations (Rice and Cleary, 1976) Constitutive Equation: 3(u - ) 2G p = 2Gij + ij + kk ij (1 - 2 ) B(1 - 2 )(1 + u) ij = Total Stress Tensor (MPa) ij = Strain Tensor p = Pore Pressure (MPa) Poroelastic Equations (Rice and Cleary, 1976) Diffusion Equation: p t - 2GB 2(1 - 2)(1 + u)2 9(u - )(1 - 2 u) 2GB (1 + u) kk p=3 (1 - 2 u) t 2 - Governing pore pressure generation with volumetric deformation of the control element - Rate of flow through the pores is proportional to the gradient of pore pressure (p): Darcy’s Law Asymptotic Poroelastic Phenomena Drained Deformation: – – Quasi-static deformation in a drained condition in which free-fluid flow is allowed; No pore pressure generation and thus elastic behavior only Undrained Deformation: – Deformation in an undrained condition in which the fluid is prevented from flowing out across the boundary; 3 = 2G(1 - u) 1 - 2 u 3 POROELASTIC PROPERTIES G: drained shear modulus (MPa) : drained Poisson’s ratio u: undrained Poisson’s ratio – – Poisson’s ratio for an undrained deformation; Theoretical range 0.5 < u < B: – : Skempton’s coefficient describes the undrained pore pressure change with a change in mean stress (0.0 < B < 1.0). permeability (m2/MPa/sec) UNIAXIAL STRAIN CONDITION Strain Input Rigid Porous Loading Platen •Loading Condition d3/dt = Constant 2 •Boundary Conditions: p(0,t) = 0 p(l,t)/ x3 = 0 Bone Specimen Impermeable 3 Rigid Boundary Carters and Hayes, 1977 •Initial Condition: p(x3,0) = 0 Constitutive Euqations in Uniaxial Strain Condition: 3 = 2G(1 - ) (1 - 2) 1 = 2 = (1 ) 3p(u - ) d3 t dt B(1 - 2)(1 + u) 3 - 3p(u - ) B(1 - 2)(1 + u) p p Diffusion Equation: p t 2GB(1 - 2)(1 + u)2 2p 9(u - )(1 - 2 u) x32 = - 2GB (1 + u) d3 3 (1 - 2 u) dt 1-D Poroelastic Model in Uniaxial Strain Condition Pore Pressure: p(x3, t) = 6(u - )(d3/dt) - n = 1 BL n ,where eignevalues 3(1 - 2)(1 + u) [1 - exp(-n2t)]sin(n x3) n = (2n - 1)p/2L, and = 2GB2 (1 - 2u)(1 + u)2 9(u - ) (1 - 2) Total Stress: 3 (x3 , t) = 2G(1 - ) (1 - 2) 3(u - ) d3 t dt B(1 - 2)(1 + u) p(x3, t) Assumptions for Poroelastic Modeling of Trabecular Bone Interconnective Pores (Proven) Rate of flow through the pores proportional to the gradient of pore pressure (Proven) Solid trabecular tissue is assumed to be isotropic and elastic. Pores are assumed to be uniformly distributed. Compression Tests of Trabecular Bone in Uniaxial Strain Condition (Carter and Hayes, 1977) Carter – – Specimens with and without marrow in situ; Loading with different strain rates (0.001, 0.01, 0.1, 1, 10 /second). Luo – and Hayes, 1977: et al., 1993: Effect of specimen size on hydraulic stiffening of cancellous bone. ESTIMATION OF MODEL PARAMETERS = 0.3 – G = 16.17 (MPa) – assumed based on literature comp modulus of 56.6 of the specimen with marrow responding to the slowest strain rate, 0.001/sec (Carter and Hayes, 1977) u = 0.459 – comp modulus of 211.1 of the specimen with marrow responding to the fastest strain rate, 10.0/sec (Carter and Hayes, 1977) B = 0.91 (0.82 ~ 1.0) = 3.54 x 10-5 (m2/MPa/sec) – Permeability of bovine proximal tibia measured by Ochoa and Hilbery, 1992. Compressive Modulus (MPa) Compressive Modulus vs. Strain Rate 250 Carter and Hayes’ Experimental Results 200 150 100 50 0 0.001 Model prediction (= 3.4 x 10-5 m2 / MPa-sec) 0.01 0.1 1.0 10.0 Strain Rate (/sec) Predicted Compressive Moduli of Trabecular Bones of Different Lengths (B = 0.91 and = 3.4 x 10-5) Strain Rate (/sec) 0.001 0.01 0.1 1.0 10.0 Compressive Moduli (MPa) 5 mm 10 mm 25 mm 54.03 54.27 54.76 54.30 56.74 61.61 57.04 81.38 123.98 84.40 188.69 209.40 192.32 212.33 214.48 Effect of Trabecular Bone Length At a strain of 0.001/sec, near zero change in the compressive modulus was predicted for the longer trabecular bones. Greater strain rate effect on the compressive modulus was in the longer specimens. Similar effects were observed in the study of bovine tibial cancellous bone (Luo et al., 1993) Total Stress vs. and B (Strain Rate = 0.001/s) Total Stress (MPa) B K (m2 / MPa/sec) , B (No unit) Total Stress vs. and B (Strain Rate = 0.1/s) Total Stress (MPa) K (m2 / MPa/sec) , B (No unit) B Total Stress vs. and B (Strain Rate = 10/s) Total Stress (MPa) B K (m2 / MPa/sec) , B (No unit) Poroelastic Equations (Rice and Cleary, 1976) Constitutive Equation: 3(u - ) 2G p = 2Gij + ij + (1 - 2 B(1 - 2 )(1 + u) ) ij = Total Stress Tensor (MPa) ij = Strain Tensor p = Pore Pressure (MPa) kk ij Poroelastic Equations (Rice and Cleary, 1976) Diffusion Equation: p t - 2GB 2(1 - 2)(1 + u)2 9(u - )(1 - 2 u) 2GB (1 + u) kk p=3 (1 - 2 u) t 2 - Governing pore pressure generation with volumetric deformation of the control element - Rate of flow through the pores is proportional to the gradient of pore pressure (p): Darcy’s Law Permeability Measurement A total of 40 bovine and 22 human lumbar vertebrae were used. Cylindrical Trabecular Specimens (9.8 mm in diameter and 15 mm in length) were obtained using a diamond coring tool and a low-speed bone saw. Bone marrow was removed by a water jet. Diffusion Apparatus for Permeability Measurement Constant Force for producing a hydraulic pressure of 7 kPa LVDT to measure the piston displacement h (m) O-Ring Trabecular Specimen Piston Spacer Reservoir filled with saline solution Since the rate of flow (Q/t; m3/sec) is proportional to the pressure difference (p; Pa) according to Darcy’s law; = L Asp p Q t ,where t = time (sec); Asp = specimen X-area (301.7 x 10-6 m2); p = pressure diff. (7.0 kPa); and L = specimen length (0.015 m). Flow Volume (Q; m3) = h x piston X-area Typical Relationship of Flow Volume vs. Time Flow Volume (m3) 2.0 E-5 1.5 E-5 1.0 E-5 r2 > 0.99 5.0 E-6 0.0 0.0 0.5 1.0 1.5 Time (sec) 2.0 Uniaxial Strain Tests Loading Piston MTS Load Cell Rigid Stainless Steel Annulus * u - u and u - p curves were obtained. O-Ring Marrow In Situ Trabecular Specimen * The specimen was subjected to a 0.7% strain using a displacement control (0.002 mm/sec). Ram Pressure Transducer Uniaxial Stress Tests MTS Load Cell LVDTs * The specimen was subjected to a 1.0% strain using a displacement control (0.002 mm/sec). * - and L - curves were obtained. MTS Ram Data Analyses (Uniaxial Stress Tests) From the Elasticity Theory: Young’s Modulus: Drained Poisson’s ratio: Shear Modulus: E= L = - E G = 2(1 + ) * 5th order polynomial curves were used to determine the - and L - relationships. (Slope at = 0.0065) Lateral Strain vs. Axial Strain 1. 0 0. 8 0. 6 0.4 0.18 Lateral Strain L (%) Stress (MPa) Stress vs. Strain 0.2 0.0 0.3 0.6 0.9 Axial Strain (%) 0.15 0.12 0.09 0.06 0.03 0.0 0.3 0.6 0.9 Axial Strain (%) Data Analyses (Uniaxial Strain Tests) From the stress-strain relationship in an undrained uniaxial condition and the definition B: u 2G(1 - u) Undrained Poisson’s ratio: = u (1 - 2u) Skempton’s Coefficient: 3(1 - u) u B= (1 + u) u * 5th order polynomial curves were used to determine the u - u and p - u relationships. (Slope at u = 0.0065) Stress (or Pore Pressure) vs. Strain Pore Pressure) vs. Stress 4.0 4.0 Undrained Condition 3.0 2.0 Pore Pressure 1.0 0.0 Pore Pressure (MPa) u or Pressure (MPa) 5.0 3.0 2.0 1.0 0.0 0.1 0.2 0.3 0.4 0.5 u (%) 0.6 1.0 2.0 3.0 4.0 u (MPa) 5.0 Permeability of Human Vertebral Trabecular Bone Level Mean Permeability (SD) L1 L2 L3 L4 L5 Total (x10-8 m2/Pa/sec) 61.3 (10.4) 53.6 (7.30) 50.4 (6.30) 38.6 (10.7) 45.7 (8.30) 52.2 (10.8) Permeability of Bovine Vertebral Trabecular Bone Level L1 L2 L3 L4 L5 Total Mean Permeability (SD) (x10-8 m2/Pa/sec) 14.91 (9.83) 12.39 (7.85) 19.03 (8.55) 18.50 (6.74) 16.85 (6.23) 16.31 (8.02) RESULTS All curves were well represented by a 5th order polynomial curve (r2 0.97). Mean (SD) values of the poroelastic parameters G u B (x10-8 m2 /Pa/sec) (MPa) 90.85 (59.59) 0.242 (0.099) 0.399 (0.083) 0.851 (0.144) 16.31 (8.02) DISCUSSION First measurement of the poroelastic properties of trabecular bone. Feasibility for measuring the poroelastic properties of human trabecular bone. Similar methods can be used for the measurement of cortical bone properties. Knowledge of these parameters may improve our understanding of the mechanical behavior of trabecular bone in vivo. DISCUSSION Linear relationship between the fluid flow (Q) and time (t) – The fluid flow in trabecular bone follows Darcy’s law as observed in another study (Simkin, 1985). First measurement of permeability for human trabecular bone Significantly larger permeability in human trabecular bone than in bovine trabecular bone In vivo, permeability would be smaller because of 67 times higher viscosity of bone marrow than that of water Measurement of G, , u, and B Uniaxial Strain Tests in an Undrained Condition: – Uniaxial Stress Tests in a Drained Condition: – B and u measurements E, , and G measurements Each bovine vertebral trabecular specimen (9.8 mm in diameter and 20 mm in length) was used for both tests. – Uniaxial strain tests were always performed first to minimize the loss of bone marrow.