Pandiyan Vimal Prabhu, Jiang Xiaoyun, Maloney-Bertelli Aiden, Kuchenbecker James A, Sharma Utkarsh, Sabesan Ramkumar
Department of Ophthalmology, University of Washington School of Medicine, Seattle, WA 98109, USA.
Catapult Sky LLC, 34116 Blue Heron Dr, Solon, OH 44139, USA.
Biomed Opt Express. 2020 Aug 26;11(9):5274-5296. doi: 10.1364/BOE.399034. eCollection 2020 Sep 1.
Optoretinography-the non-invasive, optical imaging of light-induced functional activity in the retina-stands to provide a critical biomarker for testing the safety and efficacy of new therapies as well as their rapid translation to the clinic. Optical phase change in response to light, as readily accessible in phase-resolved OCT, offers a path towards all-optical imaging of retinal function. However, typical human eye motion adversely affects phase stability. In addition, recording fast light-induced retinal events necessitates high-speed acquisition. Here, we introduce a high-speed line-scan spectral domain OCT with adaptive optics (AO), aimed at volumetric imaging and phase-resolved acquisition of retinal responses to light. By virtue of parallel acquisition of an entire retinal cross-section (B-scan) in a single high-speed camera frame, depth-resolved tomograms at speeds up to 16 kHz were achieved with high sensitivity and phase stability. To optimize spectral and spatial resolution, an anamorphic detection paradigm was introduced, enabling improved light collection efficiency and signal roll-off compared to traditional methods. The benefits in speed, resolution and sensitivity were exemplified in imaging nanometer-millisecond scale light-induced optical path length changes in cone photoreceptor outer segments. With 660 nm stimuli, individual cone responses readily segregated into three clusters, corresponding to long, middle, and short-wavelength cones. Recording such optoretinograms on spatial scales ranging from individual cones, to 100 µm-wide retinal patches offers a robust and sensitive biomarker for cone function in health and disease.
视网膜光成像——对视网膜中光诱导功能活动进行的非侵入性光学成像——有望为测试新疗法的安全性和有效性以及将其快速转化至临床提供关键生物标志物。如在相分辨光学相干断层扫描(OCT)中易于获取的那样,对光响应的光学相位变化为视网膜功能的全光学成像提供了一条途径。然而,典型的人眼运动会对相位稳定性产生不利影响。此外,记录快速的光诱导视网膜事件需要高速采集。在此,我们介绍一种带有自适应光学(AO)的高速线扫描光谱域OCT,旨在对视网膜对光的反应进行体积成像和相分辨采集。借助在单个高速相机帧中并行采集整个视网膜横截面(B扫描),以高达16 kHz的速度实现了具有高灵敏度和相位稳定性的深度分辨断层扫描。为了优化光谱和空间分辨率,引入了一种变形检测模式,与传统方法相比,可提高光收集效率并减少信号滚降。在对锥体细胞光感受器外段中纳米 - 毫秒级光诱导光程长度变化进行成像时,展示了速度、分辨率和灵敏度方面的优势。使用660 nm刺激时,单个锥体细胞反应很容易分为三类,分别对应长、中、短波长的锥体细胞。在从单个锥体细胞到100 µm宽的视网膜区域等空间尺度上记录此类视网膜光成像,可为健康和疾病状态下的锥体细胞功能提供一种强大且灵敏的生物标志物。