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Investigation of Neovascularization in Three-Dimensional Porous Scaffolds In Vivo by a Combination of Multiscale Photoacoustic Microscopy and Optical Coherence Tomography

机译:多尺度光声显微镜和光学相干断层扫描相结合的三维三维多孔支架体内新生血管的研究。

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摘要

It is a grand challenge to visualize and assess in vivo neovascularization in a three-dimensional (3D) scaffold noninvasively, together with high spatial resolution and deep penetration depth. Here we used multiscale photoacoustic microscopy (PAM), including acoustic-resolution PAM (AR-PAM) and optical-resolution PAM (OR-PAM), to chronically monitor neovascularization in an inverse opal scaffold implanted in a mouse model up to 6 weeks by taking advantage of the optical absorption contrast intrinsic to hemoglobin molecules in red blood cells. By combining with optical coherence tomography (OCT) based on optical scattering contrast, we also demonstrated the capability to simultaneously image and analyze the vasculature and the scaffold in the same mouse. The hybrid system containing OR-PAM and OCT offered a fine lateral resolution of ∼5 μm and a penetration depth of ∼1 mm into the scaffold/tissue construct. AR-PAM further extended the penetration depth up to ∼3 mm at a lateral resolution of ∼45 μm. By quantifying the 3D PAM data, we further examined the effect of pore size (200 vs. 80 μm) of a scaffold on neovascularization. The data collected from PAM were consistent with those obtained from traditional invasive, labor-intensive histologic analyses.
机译:无损地可视化和评估三维(3D)支架中的体内新血管形成以及高空间分辨率和深穿透深度是一项巨大的挑战。在这里,我们使用多尺度光声显微镜(PAM),包括声学分辨率PAM(AR-PAM)和光学分辨率PAM(OR-PAM),来长期监测植入小鼠模型的反蛋白石支架中的新血管形成情况,该过程长达6周,利用红细胞中血红蛋白分子固有的光学吸收对比。通过结合基于光学散射对比的光学相干断层扫描(OCT),我们还展示了在同一只小鼠中同时成像和分析脉管系统和支架的能力。包含OR-PAM和OCT的混合系统可提供约5μm的精细横向分辨率,并能进入支架/组织构建体的约1μmm的穿透深度。 AR-PAM以约45μm的横向分辨率将穿透深度进一步扩展至约3μmm。通过量化3D PAM数据,我们进一步检查了支架的孔径(200 vs.80μm)对新生血管形成的影响。从PAM收集的数据与从传统的侵入性劳动密集型组织学分析获得的数据一致。

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