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用于同时进行简并和非简并双光子显微镜的同步泵浦拉曼激光器。

Synchronously pumped Raman laser for simultaneous degenerate and nondegenerate two-photon microscopy.

作者信息

Buttolph Michael L, Mejooli Menansili A, Sidorenko Pavel, Eom Chi-Yong, Schaffer Chris B, Wise Frank W

机构信息

School of Applied and Engineering Physics, Cornell University, Ithaca, NY 14853, USA.

Meinig School of Biomedical Engineering, Cornell University, Ithaca, NY 14853, USA.

出版信息

Biomed Opt Express. 2021 Mar 30;12(4):2496-2507. doi: 10.1364/BOE.421647. eCollection 2021 Apr 1.

Abstract

Two-photon fluorescence microscopy is a nonlinear imaging modality frequently used in deep-tissue imaging applications. A tunable-wavelength multicolor short-pulse source is usually required to excite fluorophores with a wide range of excitation wavelengths. This need is most typically met by solid-state lasers, which are bulky, expensive, and complicated systems. Here, we demonstrate a compact, robust fiber system that generates naturally synchronized femtosecond pulses at 1050 nm and 1200 nm by using a combination of gain-managed and Raman amplification. We image the brain of a mouse and view the blood vessels, neurons, and other cell-like structures using simultaneous degenerate and nondegenerate excitation.

摘要

双光子荧光显微镜是一种常用于深层组织成像应用的非线性成像方式。通常需要一个可调谐波长的多色短脉冲源来激发具有广泛激发波长范围的荧光团。这种需求最典型地由固态激光器来满足,而固态激光器是体积庞大、价格昂贵且复杂的系统。在此,我们展示了一种紧凑、坚固的光纤系统,该系统通过增益管理和拉曼放大相结合的方式,在1050纳米和1200纳米处产生自然同步的飞秒脉冲。我们对小鼠大脑进行成像,并使用同时简并和非简并激发来观察血管、神经元和其他类似细胞的结构。

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