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arXiv 2003.09500physics.opticsphysics.app-ph

使用双光梳拍频的二维光谱映射和频率复用实现无扫描全场荧光寿命双梳显微成像

Scan-less full-field fluorescence-lifetime dual-comb microscopy using two-dimensional spectral mapping and frequency multiplexing of dual-optical-comb beats

Takahiko Mizuno, Eiji Hase, Takeo Minamikawa, Yu Tokizane, Ryo Oe, Hidenori Koresawa, Hirotsugu Yamamoto, Takeshi Yasui

AI总结:

本文提出一种基于双光梳拍频二维光谱映射和频率复用的无扫描全场荧光寿命显微成像方法,无需机械扫描即可实现高定量性的荧光幅度与寿命双模态成像。

摘要:

荧光寿命成像显微术(FLIM)是定量荧光成像的强大工具,因为荧光寿命独立于荧光分子浓度和激发/探测效率,且对光漂白具有鲁棒性。然而,由于FLIM基于逐点测量,需要通过机械扫描焦点来形成图像,这阻碍了快速成像。本文演示了基于二维图像像素与频率复用射频信号之间逐点对应关系的无扫描全场FLIM。大量双光梳拍频(dual-optical-comb beats)有效地用于射频区域高密度频率复用的二维光谱映射。通过荧光射频梳模式的幅度和相位光谱,无需机械扫描即可获得荧光幅度和寿命的双模态图像,且具有高定量性。所提出的方法将有助于生命科学中的快速定量荧光成像。

英文摘要:

Fluorescence lifetime imaging microscopy (FLIM) is a powerful tool for quantitative fluorescence imaging because fluorescence lifetime is independent of concentration of fluorescent molecules or excitation/detection efficiency and is robust to photobleaching. However, since FLIM is based on point-to-point measurements, mechanical scanning of a focal spot is needed for forming an image, which hampers rapid imaging. In this article, we demonstrate scan-less full-field FLIM based on a one-to-one correspondence between two-dimensional (2D) image pixels and frequency-multiplexed RF signals. A vast number of dual-optical-comb beats between dual optical frequency combs is effectively adopted for 2D spectral mapping and high-density frequency multiplexing in radio-frequency region. Bimodal images of fluorescence amplitude and lifetime are obtained with high quantitativeness from amplitude and phase spectra of fluorescence RF comb modes without the need for mechanical scanning. The proposed method will be useful for rapid quantitative fluorescence imaging in life science.

机构、总结、中文摘要均由AI分析而来,可能存在错误,请以论文正文为准。

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