Cao Jing, Yang Qiang, Miao Yusi, Li Yan, Qiu Saijun, Zhu Zhikai, Wang Pinghe, Chen Zhongping
Beckman Laser Institute, University of California, Irvine, Irvine, CA, 92612, USA.
Key Laboratory of Biomedical Engineering of Hainan Province, School of Biomedical Engineering, Hainan University, 570228, Hainan, China.
Light Sci Appl. 2022 Apr 24;11(1):108. doi: 10.1038/s41377-022-00795-8.
Multiple light scattering is considered as the major limitation for deep imaging and focusing in turbid media. In this paper, we present an innovative method to overcome this limitation and enhance the delivery of light energy ultra-deep into turbid media with significant improvement in focusing. Our method is based on a wide-field reflection matrix optical coherence tomography (RM-OCT). The time-reversal decomposition of the RM is calibrated with the Tikhonov regularization parameter in order to get more accurate reversal results deep inside the scattering sample. We propose a concept named model energy matrix, which provides a direct mapping of light energy distribution inside the scattering sample. To the best of our knowledge, it is the first time that a method to measure and quantify the distribution of beam intensity inside a scattering sample is demonstrated. By employing the inversion of RM to find the matched wavefront and shaping with a phase-only spatial light modulator, we succeeded in both focusing a beam deep (9.6 times of scattering mean free path, SMFP) inside the sample and increasing the delivery of light energy by an order of magnitude at an ultra-deep (14.4 SMFP) position. This technique provides a powerful tool to understand the propagation of photon in a scattering medium and opens a new way to focus light inside biological tissues.
多重光散射被认为是浑浊介质中深度成像和聚焦的主要限制因素。在本文中,我们提出了一种创新方法来克服这一限制,并将光能超深度地传输到浑浊介质中,同时显著提高聚焦效果。我们的方法基于宽场反射矩阵光学相干断层扫描(RM-OCT)。通过用蒂霍诺夫正则化参数校准RM的时间反转分解,以便在散射样品内部获得更准确的反转结果。我们提出了一个名为模型能量矩阵的概念,它提供了散射样品内部光能分布的直接映射。据我们所知,这是首次展示一种测量和量化散射样品内部光束强度分布的方法。通过利用RM的反演来找到匹配的波前,并使用仅相位空间光调制器进行整形,我们成功地在样品内部深处(约为散射平均自由程,SMFP的9.6倍)聚焦了一束光,并在超深(约14.4 SMFP)位置将光能传输提高了一个数量级。这项技术为理解光子在散射介质中的传播提供了一个强大的工具,并为在生物组织内部聚焦光开辟了一条新途径。