首页> 外文会议>Conference on Optical Elastography and Tissue Biomechanics III >POLARIZED SPATIAL FREQUENCY DOMAIN IMAGING OF HEART VALVE FIBER STRUCTURE
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POLARIZED SPATIAL FREQUENCY DOMAIN IMAGING OF HEART VALVE FIBER STRUCTURE

机译:心阀纤维结构的偏振空间频域成像

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Our group previously introduced Polarized Spatial Frequency Domain Imaging (PSFDI), a wide-field, reflectance imaging technique which we used to empirically map fiber direction in porcine pulmonary heart valve leaflets (PHVL) without optical clearing or physical sectioning of the sample. Presented is an extended analysis of our PSFDI results using an inverse Mueller matrix model of polarized light scattering that allows additional maps of fiber orientation distribution, along with instrumentation permitting increased imaging speed for dynamic PHVL fiber measurements. We imaged electrospun fiber phantoms with PSFDI, and then compared these measurements to SEM data collected for the same phantoms. PHVL was then imaged and compared to results of the same leaflets optically cleared and imaged with small angle light scattering (SALS). The static PHVL images showed distinct regional variance of fiber orientation distribution, matching our SALS results. We used our improved imaging speed to observe bovine tendon subjected to dynamic loading using a biaxial stretching device. Our dynamic imaging experiment showed trackable changes in the fiber microstructure of biological tissue under loading. Our new PSFDI analysis model and instrumentation allows characterization of fiber structure within heart valve tissues (as validated with SALS measurements), along with imaging of dynamic fiber remodeling. The experimental data will be used as inputs to our constitutive models of PHVL tissue to fully characterize these tissues' elastic behavior, and has immediate application in determining the mechanisms of structural and functional failure in PHVLs used as bio-prosthetic implants.
机译:我们组先前引入的极化空间频域成像(PSFDI),我们使用以经验映射猪肺心脏瓣膜小叶(PHVL)而没有光透明或样品的物理切片纤维方向上的宽视场,反射成像技术。呈现是使用偏振光散射的逆穆勒矩阵模型以使纤维取向分布的更多的地图,与仪表允许增加用于动态PHVL纤维测量成像速度沿我们PSFDI结果的扩展分析。我们进行成像的电纺丝纤维幻影与PSFDI,然后比较这些测量所收集的针对相同幻影SEM数据。然后PHVL进行成像和相比,在相同的小叶的结果光学清除并被小角光散射(SALS)成像。静态PHVL图像显示纤维取向分布的不同区域方差,匹配我们SALS结果。我们使用我们的改进的成像速度,观察进行使用双轴拉伸装置动态加载牛腱。我们的动态成像实验表明在生物组织中的在负载下的纤维的微结构可跟踪的变化。我们的新PSFDI分析模型和仪表允许纤维结构的表征心脏瓣膜组织内(如用SALS测量验证)中,用动态纤维重塑的成像沿。实验数据将被用作输入,以我们的PHVL组织的构模型完全表征这些组织弹性行为,并且在确定在用作生物假体植入物PHVLs结构和功能故障的机制直接应用。

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