Visible-light optical coherence microscopy

D. Huang, Shanjida Khan, K. Neuhaus, Omkar Thaware, Alireza Karimi, Mary Kelley, Travis Redd, T. Acott, Y. Jian
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Abstract

Corneal diseases are the fifth leading cause of visual loss globally. Current clinical imaging instruments such as In Vivo Confocal Microscopy (IVCM) offer high lateral resolution to observe cellular structures but lack large field of view and volumetric imaging capability and require high operator skill to focus and align. To overcome these limitations, we have developed blue (450 nm) and green (510 nm) light Optical Coherence Microscopy (OCM) to image cellular structures. Imaging was demonstrated in ex vivo samples including human donor eyes. The OCM systems were based on a spectral-domain optical coherence tomography engine and achieved 750 μm × 750 µm field of view, 1.2 mm imaging depth, and 1.6 μm lateral resolution. Epithelial cells, endothelial cells, and keratocytes of ex vivo rabbit cornea were visualized. Additionally, collagen fibers were observed in stromal lamellae with striated patterns. En face and cross-sectional images of trabecular meshwork and Schlemm’s canal in a donor human eye wedge were observed at various trans-meshwork pressures controlled by cannulation of the canal. Microbes such as filamentous fungi and bacteria were observed.
可见光光学相干显微镜
角膜疾病是全球视力丧失的第五大原因。目前的临床成像仪器,如体内共聚焦显微镜(IVCM)提供高水平分辨率来观察细胞结构,但缺乏大视野和体积成像能力,并且需要很高的操作员技能来聚焦和对齐。为了克服这些限制,我们开发了蓝色(450 nm)和绿色(510 nm)光光学相干显微镜(OCM)来成像细胞结构。在包括人类供体眼睛在内的离体样品中证实了成像。OCM系统基于光谱域光学相干层析成像引擎,实现了750 μm × 750 μm视场,1.2 mm成像深度和1.6 μm横向分辨率。观察兔离体角膜上皮细胞、内皮细胞和角膜形成细胞。基质层中胶原纤维呈条纹状。在不同的跨网压力下,观察了供体人眼楔块的小梁网和施勒姆管的面部和横切面图像。观察了丝状真菌和细菌等微生物。
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