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POLARIZED SPATIAL FREQUENCY DOMAIN IMAGING OF HEART VALVE FIBER STRUCTURE

机译:心脏瓣膜纤维结构的极化空间频率域成像

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摘要

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:我们的小组先前引入了极化空间频域成像(PSFDI),这是一种宽视野的反射成像技术,我们使用该技术以经验的方式绘制猪肺心瓣小叶(PHVL)中的纤维方向,而无需光学清除或对样品进行物理切片。本文介绍了使用偏光散射的逆Mueller矩阵模型对我们的PSFDI结果进行的扩展分析,该模型允许附加的纤维取向分布图,以及可以提高动态PHVL纤维测量成像速度的仪器。然后将这些测量结果与针对相同体模收集的SEM数据进行比较。然后将PHVL成像并与光学清除的相同小叶的结果进行比较,并用小角度光散射(SALS)进行成像。静态PHVL图像显示了纤维取向分布的明显区域差异,与我们的SALS结果相符。我们使用提高的成像速度来观察使用双轴拉伸装置动态加载的牛腱。我们的动态成像实验显示了负载下生物组织纤维微结构的可追踪变化。我们新的PSFDI分析模型和仪器可以表征心脏瓣膜组织内的纤维结构(已通过SALS测量验证),以及动态纤维重塑的成像。实验数据将被用作我们的PHVL组织本构模型的输入,以充分表征这些组织的弹性行为,并立即应用于确定用作生物假体植入物的PHVL的结构和功能衰竭的机制。

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