Centre for Advanced Biomedical Imaging (CABI), University College of London, Paul O'Gorman Building, 72 Huntley Street, London, UK
Centre for Tissue and Cell Research, University College of London, Royal National Orthopeadic Hospital, London, UK.
J R Soc Interface. 2017 Dec;14(137). doi: 10.1098/rsif.2017.0653.
The growth of bubbles within the body is widely believed to be the cause of decompression sickness (DCS). Dive computer algorithms that aim to prevent DCS by mathematically modelling bubble dynamics and tissue gas kinetics are challenging to validate. This is due to lack of understanding regarding the mechanism(s) leading from bubble formation to DCS. In this work, a biomimetic tissue phantom and a three-dimensional computational model, comprising a hyperelastic strain-energy density function to model tissue elasticity, were combined to investigate key areas of bubble dynamics. A sensitivity analysis indicated that the diffusion coefficient was the most influential material parameter. Comparison of computational and experimental data revealed the bubble surface's diffusion coefficient to be 30 times smaller than that in the bulk tissue and dependent on the bubble's surface area. The initial size, size distribution and proximity of bubbles within the tissue phantom were also shown to influence their subsequent dynamics highlighting the importance of modelling bubble nucleation and bubble-bubble interactions in order to develop more accurate dive algorithms.
人们普遍认为,体内气泡的生长是减压病 (DCS) 的原因。旨在通过数学模拟气泡动力学和组织气体动力学来预防减压病的潜水计算机算法很难得到验证。这是因为缺乏对导致气泡形成到减压病的机制的理解。在这项工作中,结合了仿生组织模型和一个三维计算模型,其中包括一个超弹性应变能密度函数来模拟组织弹性,以研究气泡动力学的关键领域。敏感性分析表明,扩散系数是最具影响力的材料参数。计算数据与实验数据的比较表明,气泡表面的扩散系数比组织中体相的扩散系数小 30 倍,并且取决于气泡的表面积。组织模型中气泡的初始大小、大小分布和接近程度也会影响它们随后的动力学,这突出了在开发更准确的潜水算法时对气泡成核和气泡-气泡相互作用进行建模的重要性。