Adaptive optics optical coherence tomography at 120,000 depth scans/s for non-invasive cellular phenotyping of the living human retina

被引:110
作者
Torti, Cristiano [1 ]
Povazay, Boris [1 ]
Hofer, Bernd [1 ]
Unterhuber, Angelika [1 ]
Carroll, Joseph [2 ]
Ahnelt, Peter Kurt [3 ]
Drexler, Wolfgang [1 ]
机构
[1] Cardiff Univ, Sch Optometry & Vis Sci, Biomed Imaging Grp, Cardiff CF24 4LU, S Glam, Wales
[2] Med Coll Wisconsin, Dept Ophthalmol, Milwaukee, WI 53226 USA
[3] Med Univ Vienna, Dept Physiol, A-1090 Vienna, Austria
关键词
SCANNING LASER OPHTHALMOSCOPY; CHROMATIC ABERRATION CORRECTION; PIGMENT EPITHELIAL-CELLS; ULTRAHIGH-RESOLUTION; HIGH-SPEED; HUMAN EYE; LAMINA-CRIBROSA; IMAGE QUALITY; POPULATION; TOPOGRAPHY;
D O I
10.1364/OE.17.019382
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
This paper presents a successful combination of ultra-high speed (120,000 depth scans/s), ultra-high resolution optical coherence tomography with adaptive optics and an achromatizing lens for compensation of monochromatic and longitudinal chromatic ocular aberrations, respectively, allowing for non-invasive volumetric imaging in normal and pathologic human retinas at cellular resolution. The capability of this imaging system is demonstrated here through preliminary studies by probing cellular intraretinal structures that have not been accessible so far with in vivo, noninvasive, label-free imaging techniques, including pigment epithelial cells, micro-vasculature of the choriocapillaris, single nerve fibre bundles and collagenous plates of the lamina cribrosa in the optic nerve head. In addition, the volumetric extent of cone loss in two colour-blinds could be quantified for the first time. This novel technique provides opportunities to enhance the understanding of retinal pathogenesis and early diagnosis of retinal diseases. (c) 2009 Optical Society of America
引用
收藏
页码:19382 / 19400
页数:19
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