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使用超导纳米线单光子探测器阵列的深度小鼠脑双光子近红外荧光成像

Deep Mouse Brain Two-Photon Near-Infrared Fluorescence Imaging Using a Superconducting Nanowire Single-Photon Detector Array.

作者信息

Tamimi Amr, Caldarola Martin, Hambura Sebastian, Boffi Juan C, Noordzij Niels, Los Johannes W N, Guardiani Antonio, Kooiman Hugo, Wang Ling, Kieser Christian, Braun Florian, Castaneda Mario A Usuga, Fognini Andreas, Prevedel Robert

机构信息

Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, Heidelberg 69117, Germany.

Single Quantum B.V, Delft, HH 2629, The Netherlands.

出版信息

ACS Photonics. 2024 Sep 11;11(10):3960-3971. doi: 10.1021/acsphotonics.4c00111. eCollection 2024 Oct 16.

Abstract

Two-photon microscopy (2PM) has become an important tool in biology to study the structure and function of intact tissues . However, adult mammalian tissues such as the mouse brain are highly scattering, thereby putting fundamental limits on the achievable imaging depth, which typically reside at around 600-800 μm. In principle, shifting both the excitation as well as (fluorescence) emission light to the shortwave near-infrared (SWIR, 1000-1700 nm) region promises substantially deeper imaging in 2PM, yet this shift has proven challenging in the past due to the limited availability of detectors and probes in this wavelength region. To overcome these limitations and fully capitalize on the SWIR region, in this work, we introduce a novel array of superconducting nanowire single-photon detectors (SNSPDs) and associated custom detection electronics for use in near-infrared 2PM. The SNSPD array exhibits high efficiency and dynamic range as well as low dark-count rates over a wide wavelength range. Additionally, the electronics and software permit a seamless integration into typical 2PM systems. Together with an organic fluorescent dye emitting at 1105 nm, we report imaging depth of >1.1 mm in the in vivo mouse brain, limited mostly by available labeling density and laser properties. Our work establishes a promising, and ultimately scalable, new detector technology for SWIR 2PM that facilitates deep tissue biological imaging.

摘要

双光子显微镜(2PM)已成为生物学中研究完整组织的结构和功能的重要工具。然而,成年哺乳动物组织,如小鼠大脑,具有高度散射性,从而对可实现的成像深度构成了基本限制,其成像深度通常在600 - 800微米左右。原则上,将激发光以及(荧光)发射光都转移到短波近红外(SWIR,1000 - 1700纳米)区域有望在双光子显微镜中实现更深的成像,但由于该波长区域探测器和探针的可用性有限,过去这种转移已被证明具有挑战性。为了克服这些限制并充分利用SWIR区域,在这项工作中,我们引入了一种新型的超导纳米线单光子探测器(SNSPD)阵列以及相关的定制检测电子设备,用于近红外双光子显微镜。该SNSPD阵列在很宽的波长范围内表现出高效率、高动态范围以及低暗计数率。此外,这些电子设备和软件允许无缝集成到典型的双光子显微镜系统中。结合一种在1105纳米处发射的有机荧光染料,我们报告了在活体小鼠大脑中成像深度大于1.1毫米,其主要受限于可用的标记密度和激光特性。我们的工作为SWIR双光子显微镜建立了一种有前景且最终可扩展的新探测器技术,有助于深部组织生物学成像。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/572b/11487655/0975e30e2971/ph4c00111_0001.jpg

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