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偏振解析二次谐波显微镜。

Polarization resolved second harmonic microscopy.

机构信息

Department of Biophysics, School of Life Sciences, Manipal University, Manipal 576104, India.

Department of Physics, National Taiwan University, No. 1, Sec. 4, Roosevelt Road, Taipei 10617, Taiwan.

出版信息

Methods. 2017 Sep 1;128:105-118. doi: 10.1016/j.ymeth.2017.06.012. Epub 2017 Jun 15.

DOI:10.1016/j.ymeth.2017.06.012
PMID:28624539
Abstract

Second harmonic (SH) microscopy has proven to be a powerful imaging modality over the past years due to its intrinsic advantages as a multiphoton process with endogenous contrast specificity, which allows pinhole-less optical sectioning, non-invasive observation, deep tissue penetration, and the possibility of easier signal detection at visible wavelengths. Depending on the relative orientation between the polarization of the incoming light and the second-order susceptibility of non-centrosymmetric structures, SH microscopy provides the unique capacity to probe the absolute molecular structure of a broad variety of biological tissues without the necessity for additional labeling. In addition, SH microscopy, when working with polarimetry, provides clear and in-depth insights on the details of molecular orientation and structural symmetry. In this review, the working principles of the polarization resolving techniques and the corresponding implements of SH microscopy are elucidated, with focus on Stokes vector based polarimetry. An overview of the advancements on SH anisotropy measurements are also presented. Specifically, the recent progresses on the following three topics in polarization resolved SH microscopy will be elucidated, which include Stokes vector resolving for imaging molecular structure and orientation, 3-D structural chirality by SH circular dichroism, and correlation with fluorescence lifetime imaging (FLIM) for in vivo wound healing diagnosis. The potentials and challenges for future researches in exploring complex biological tissues are also discussed.

摘要

二次谐波 (SH) 显微镜在过去几年中已被证明是一种强大的成像方式,因为它作为一种具有内源性对比特异性的多光子过程具有固有优势,允许无针孔光学切片、非侵入性观察、深层组织穿透以及在可见波长处更容易检测信号。根据入射光的偏振和非中心对称结构的二阶极化率之间的相对取向,SH 显微镜提供了独特的能力,可以在不进行额外标记的情况下探测广泛的生物组织的绝对分子结构。此外,当与偏振测量结合使用时,SH 显微镜可以提供关于分子取向和结构对称性细节的清晰和深入的见解。在这篇综述中,阐述了偏振解析技术的工作原理及其在 SH 显微镜中的相应实现,重点是基于 Stokes 矢量的偏振测量。还介绍了 SH 各向异性测量的进展。具体来说,将阐明偏振分辨 SH 显微镜中的以下三个主题的最新进展,包括用于成像分子结构和取向的 Stokes 矢量解析、SH 圆二色性的 3D 结构手性以及与荧光寿命成像 (FLIM) 的相关性,用于体内伤口愈合诊断。还讨论了探索复杂生物组织的未来研究的潜力和挑战。

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