Hemphill Ashton S, Tay Jian Wei, Wang Lihong V
Washington University in St. Louis, Optical Imaging Laboratory, Department of Biomedical Engineering, One Brookings Drive, Saint Louis, Missouri 63130, United States.
J Biomed Opt. 2016 Dec 1;21(12):121502. doi: 10.1117/1.JBO.21.12.121502.
One of the prime limiting factors of optical imaging in biological applications is the diffusion of light by tissue, which prevents focusing at depths greater than the optical diffusion limit (typically ?1??mm). To overcome this challenge, wavefront shaping techniques that use a spatial light modulator (SLM) to correct the phase of the incident wavefront have recently been developed. These techniques are able to focus light through scattering media beyond the optical diffusion limit. However, the low speeds of typically used liquid crystal SLMs limit the focusing speed. Here, we present a method using a digital micromirror device (DMD) and an electro-optic modulator (EOM) to measure the scattering-induced aberrations, and using a liquid crystal SLM to apply the correction to the illuminating wavefront. By combining phase modulation from an EOM with the DMD’s ability to provide selective illumination, we exploit the DMD’s higher refresh rate for phase measurement. We achieved focusing through scattering media in less than 8 ms, which is sufficiently short for certain in vivo applications, as it is comparable to the speckle correlation time of living tissue.
光学成像在生物应用中的主要限制因素之一是组织对光的散射,这使得无法在大于光学扩散极限(通常为1毫米左右)的深度进行聚焦。为了克服这一挑战,最近开发了一些波前整形技术,这些技术使用空间光调制器(SLM)来校正入射波前的相位。这些技术能够使光透过散射介质聚焦到超过光学扩散极限的深度。然而,通常使用的液晶空间光调制器速度较慢,限制了聚焦速度。在此,我们提出一种方法,使用数字微镜器件(DMD)和电光调制器(EOM)来测量散射引起的像差,并使用液晶空间光调制器对照明波前进行校正。通过将电光调制器的相位调制与数字微镜器件提供选择性照明的能力相结合,我们利用数字微镜器件较高的刷新率进行相位测量。我们在不到8毫秒的时间内实现了透过散射介质的聚焦,对于某些体内应用来说这个时间足够短,因为它与活体组织的散斑相关时间相当。