首页> 外文会议>ASME Bioengineering Conference >ARTICULAR CARTILAGE BIOMECHANICS MODELED VIA AN INTRINSICALLY COMPRESSIBLE BIPHASIC MODEL: IMPLICATIONS AND DEVIATIONS FROM AN INCOMPRESSIBLE BIPHASIC APPROACH
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ARTICULAR CARTILAGE BIOMECHANICS MODELED VIA AN INTRINSICALLY COMPRESSIBLE BIPHASIC MODEL: IMPLICATIONS AND DEVIATIONS FROM AN INCOMPRESSIBLE BIPHASIC APPROACH

机译:通过本质可压缩的双相模型建模的关节软骨生物力学:含义和不可压缩的双相方法的含义和偏差

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Biphasic continuum models have been extensively deployed for modeling macroscopic articular cartilage biomechanics [1,2]. This consolidated theoretical approach schematizes tissue as a mixture of an elastic solid matrix embedded in a fluid phase. In physiological conditions, intrinsic compressibility of each phase is very limited when compared to the whole tissue macroscopic counterpart. Based on such experimental evidence, intrinsic phase compressibility is generally reasonably neglected [3]. Hence, traditionally, cartilage biomechanics models have been developed on the basis of incompressible biphasic formulations [3-5], often referred to as Incompressible Theories of Mixtures (ITM). Alternatively, a more general biphasic model for cartilage biomechanics, accounting for full intrinsic compressibility of phases, may be considered. A consistent theoretical formulation of this type has been recently made available [6,7], hereby referred to as Theory of Microscopically Compressible Porous Media (TMCPM). In the present contribution, a new model for articular cartilage biomechanics, based on TMCPM, was developed. Predictions of this new model, and its deviations from a traditional ITM approach were studied. In particular, deviations between compressible and incompressible theoretical frameworks were investigated with a specific focus on the repercussions on models' capability of characterizing fundamental tissue properties, such as hydraulic permeability, via established experimental testing procedures.
机译:Biphasic Continuum模型已被广泛地部署用于建模宏观关节软骨生物力学[1,2]。该综合理论方法将组织与嵌入流体相中嵌入的弹性固体基质的混合物示意。在生理条件下,与整个组织宏观对应物相比,每相的固有压缩性非常有限。基于这种实验证据,内在相位可压缩性通常是合理忽略的[3]。因此,传统上,软骨生物力学模型已经基于不可压缩的双相制剂[3-5],通常被称为混合物(ITM)的不可压缩理论。或者,可以考虑更普遍的软骨生物力学的双相模型,占相间阶段的全部压缩性。最近已经提供了这种类型的一致理论制剂[6,7],特此称为显微可压缩多孔介质(TMCPM)的理论。在本贡献中,开发了一种基于TMCPM的关节软骨生物力学模型。研究了这种新模型的预测,以及其与传统ITM方法的偏差。特别地,通过建立的实验测试程序,研究了对模型的特异性关注模型表征基本组织特性的影响的特定重点突出的偏差。

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