Revealing fine microstructural morphology in the living human retina using Optical Coherence Tomography with pancorrection

C. Torti, B. Povazay, B. Hofer, A. Unterhuber, B. Hermann, W. Drexler
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Abstract

Ultra-high speed optical coherence tomography employing an ultra-broadband light source has been combined with adaptive optics utilizing a single high stroke deformable mirror and chromatic aberration compensation. The reduction of motion artefacts, geometric and chromatic aberrations (pancorrection) permits to achieve an isotropic resolution of 2-3 μm in the human eye. The performance of this non-invasive imaging modality enables to resolve cellular structures including cone photoreceptors, nerve fibre bundles and collagenous plates of the lamina cribrosa, and retinal pigment epithelial (RPE) cells in the human retina in vivo with superior detail. Alterations of cellular morphology due to cone degeneration in a colour-blind subject are investigated in ultra-high resolution with selective depth sectioning for the first time.
全校正光学相干断层扫描显示活体视网膜精细显微结构形态
采用超宽带光源的超高速光学相干层析成像与利用单高行程可变形镜和色差补偿的自适应光学相结合。减少运动伪像,几何和色差(全校正)允许在人眼中实现2-3 μm的各向同性分辨率。这种非侵入性成像方式的性能使其能够以优异的细节分辨人体视网膜中的细胞结构,包括锥状光感受器、神经纤维束和筛层的胶原板,以及视网膜色素上皮(RPE)细胞。本文首次采用选择性深度切片的超高分辨率技术研究了色盲受试者因锥体变性而引起的细胞形态学改变。
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