Single-exposure optical focusing inside scattering media using binarized time-reversed adapted perturbation

被引:42
作者
Ma, Cheng [1 ]
Zhou, Fengbo [1 ]
Liu, Yan [1 ]
Wang, Lihong V. [1 ]
机构
[1] Washington Univ, Dept Biomed Engn, Opt Imaging Lab, St Louis, MO 63130 USA
基金
美国国家卫生研究院;
关键词
DIGITAL PHASE-CONJUGATION; IN-VIVO; TURBIDITY SUPPRESSION; LIGHT; MICROSCOPY; SAMPLES; TISSUE; FIBER; DEEP;
D O I
10.1364/OPTICA.2.000869
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Light scattering inhibits high-resolution optical imaging, manipulation, and therapy deep inside biological tissue by preventing focusing. To form deep foci, wavefront-shaping techniques that break the optical diffusion limit have been developed. For in vivo applications, such focusing must provide a high gain, high speed, and a high focal peak-tobackground ratio. However, none of the previous techniques meet these requirements simultaneously. Here, we overcome this challenge by rapidly measuring the perturbed optical field within a single camera exposure followed by adaptively time-reversing the phase-binarized perturbation. Consequently, a phase-conjugated wavefront is synthesized within a millisecond, two orders of magnitude shorter than the digitally achieved record. We demonstrate real-time focusing in dynamic scattering media and extend laser speckle contrast imaging to new depths. The unprecedented combination of a fast response, high gain, and high focusing contrast makes this work a major stride toward in vivo deep-tissue optical imaging, manipulation, and therapy. (C) 2015 Optical Society of America
引用
收藏
页码:869 / 876
页数:8
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