Liu Yan, Lai Puxiang, Ma Cheng, Xu Xiao, Grabar Alexander A, Wang Lihong V
1] Department of Biomedical Engineering, Optical Imaging Laboratory, Washington University in St. Louis, St. Louis, Missouri 63130, USA [2].
Department of Biomedical Engineering, Optical Imaging Laboratory, Washington University in St. Louis, St. Louis, Missouri 63130, USA.
Nat Commun. 2015 Jan 5;6:5904. doi: 10.1038/ncomms6904.
Focusing light deep inside living tissue has not been achieved despite its promise to play a central role in biomedical imaging, optical manipulation and therapy. To address this challenge, internal-guide-star-based wavefront engineering techniques--for example, time-reversed ultrasonically encoded (TRUE) optical focusing--were developed. The speeds of these techniques, however, were limited to no greater than 1 Hz, preventing them from in vivo applications. Here we improve the speed of optical focusing deep inside scattering media by two orders of magnitude, and focus diffuse light inside a dynamic scattering medium having a speckle correlation time as short as 5.6 ms, typical of living tissue. By imaging a target, we demonstrate the first focusing of diffuse light inside a dynamic scattering medium containing living tissue. Since the achieved focusing speed approaches the tissue decorrelation rate, this work is an important step towards in vivo deep tissue noninvasive optical imaging, optogenetics and photodynamic therapy.
尽管聚焦光深入活体组织有望在生物医学成像、光学操控和治疗中发挥核心作用,但目前尚未实现。为应对这一挑战,人们开发了基于内部导星的波前工程技术,例如时间反转超声编码(TRUE)光学聚焦。然而,这些技术的速度限制在不超过1赫兹,这阻碍了它们在体内的应用。在此,我们将深入散射介质内部的光学聚焦速度提高了两个数量级,并在具有短至5.6毫秒散斑相关时间(这是活体组织的典型特征)的动态散射介质中聚焦漫射光。通过对目标进行成像,我们展示了在包含活体组织的动态散射介质中首次实现漫射光聚焦。由于所实现的聚焦速度接近组织去相关速率,这项工作是朝着体内深部组织无创光学成像、光遗传学和光动力疗法迈出的重要一步。