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中红外光热显微镜高灵敏度心脏组织高光谱振动成像。

High-sensitivity hyperspectral vibrational imaging of heart tissues by mid-infrared photothermal microscopy.

机构信息

Institute of Post-LED Photonics, Tokushima University, 2-1 Minamijosanjima-cho, Tokushima, Tokushima, 770-8506, Japan.

Innovative Photon Manipulation Research Team, RIKEN Center for Advanced Photonics, Wako, Saitama, 351-0198, Japan.

出版信息

Anal Sci. 2022 Dec;38(12):1497-1503. doi: 10.1007/s44211-022-00182-8. Epub 2022 Sep 7.

DOI:10.1007/s44211-022-00182-8
PMID:36070070
Abstract

Visualizing the spatial distribution of chemical compositions in biological tissues is of great importance to study fundamental biological processes and origin of diseases. Raman microscopy, one of the label-free vibrational imaging techniques, has been employed for chemical characterization of tissues. However, the low sensitivity of Raman spectroscopy often requires a long acquisition time of Raman measurement or a high laser power, or both, which prevents one from investigating large-area tissues in a nondestructive manner. In this work, we demonstrated chemical imaging of heart tissues using mid-infrared photothermal (MIP) microscopy that simultaneously achieves the high sensitivity benefited from IR absorption of molecules and the high spatial resolution down to a few micrometers. We successfully visualized the distributions of different biomolecules, including proteins, phosphate-including proteins, and lipids/carbohydrates/amino acids. Further, we experimentally compared MIP microscopy with Raman microscopy to evaluate the sensitivity and photodamage to tissues. We proved that MIP microscopy is a highly sensitive technique for obtaining vibrational information of molecules in a broad fingerprint region, thereby it could be employed for biological and diagnostic applications, such as live-tissue imaging.

摘要

可视化生物组织中化学成分的空间分布对于研究基本生物过程和疾病的起源非常重要。拉曼显微镜是一种无标记的振动成像技术,已被用于组织的化学特征分析。然而,拉曼光谱的低灵敏度通常需要较长的拉曼测量采集时间或较高的激光功率,或者两者兼而有之,这使得人们无法以非破坏性的方式研究大面积的组织。在这项工作中,我们使用中红外光热(MIP)显微镜演示了心脏组织的化学成像,该显微镜同时实现了得益于分子红外吸收的高灵敏度和高达几微米的高空间分辨率。我们成功地可视化了不同生物分子的分布,包括蛋白质、含磷蛋白和脂质/碳水化合物/氨基酸。此外,我们通过实验将 MIP 显微镜与拉曼显微镜进行了比较,以评估对组织的灵敏度和光损伤。我们证明 MIP 显微镜是一种非常灵敏的技术,可用于获取分子在广泛指纹区域内的振动信息,因此可用于生物和诊断应用,如活体组织成像。

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