Digital confocal microscopy through a multimode fiber

被引:146
|
作者
Loterie, Damien [1 ]
Farahi, Salma [1 ,2 ]
Papadopoulos, Ioannis [2 ]
Goy, Alexandre [2 ,3 ]
Psaltis, Demetri [2 ]
Moser, Christophe [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Sch Engn, Lab Appl Photon Devices, CH-1015 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Sch Engn, Lab Opt, CH-1015 Lausanne, Switzerland
[3] Princeton Univ, Dept Elect Engn, Imaging Phys Grp, Princeton, NJ 08544 USA
来源
OPTICS EXPRESS | 2015年 / 23卷 / 18期
基金
瑞士国家科学基金会;
关键词
REAL-TIME; IN-VIVO; PHASE-CONJUGATION; OPTICAL-FIBER; TRANSMISSION; PROPAGATION; SCANNER; SYSTEM; BUNDLE; MATRIX;
D O I
10.1364/OE.23.023845
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Acquiring high-contrast optical images deep inside biological tissues is still a challenging problem. Confocal microscopy is an important tool for biomedical imaging since it improves image quality by rejecting background signals. However, it suffers from low sensitivity in deep tissues due to light scattering. Recently, multimode fibers have provided a new paradigm for minimally invasive endoscopic imaging by controlling light propagation through them. Here we introduce a combined imaging technique where confocal images are acquired through a multimode fiber. We achieve this by digitally engineering the excitation wavefront and then applying a virtual digital pinhole on the collected signal. In this way, we are able to acquire images through the fiber with significantly increased contrast. With a fiber of numerical aperture 0.22, we achieve a lateral resolution of 1.5 mu m, and an axial resolution of 12.7 mu m. The point-scanning rate is currently limited by our spatial light modulator (20Hz). (C)2015 Optical Society of America
引用
收藏
页码:23845 / 23858
页数:14
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