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Excitation and emission dual-wavelength confocal metalens designed directly in the biological tissue environment for two-photon micro-endoscopy

机译:直接在双光子微内窥镜检查的生物组织环境中设计的励磁和发射双波长共聚合金属

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摘要

With the advantages of completely controlling the phase, amplitude, and polarization in subwavelength range, metalenses have drawn intensive attentions in high resolution two-photon micro-endoscopic fluorescence imaging system. However, chromatic dispersion and severe scattering of biological tissue significantly reduce excitation-collection efficiency in the traditional two-photon imaging system based on traditional metalenses designed in the air background. Here, an excitation and emission dual-wavelength confocal and polarization-insensitive metalens designed in the biological tissue environment was proposed by adopting the composite embedding structure and spatial multiplexing approach. The metalens with numerical aperture (NA) of 0.895 can focus the excitation (915 nm) and emission (510 nm) beams to the same focal spot in the mouse cortex. According to the theoretical simulation of two-photon fluorescence imaging, the lateral resolution of the collected fluorescent spots via the proposed metalens can be up to 0.42 µm. Compared to the metalens designed in the air environment, the collection efficiency of fluorescent spot is improved from 5.92% to 14.60%. Our investigation has opened a new window of high resolution and minimally invasive imaging in deep regions of biological tissues.
机译:凭借完全控制亚波长范围内的相位,幅度和偏振的优点,金属纤维在高分辨率双光子微内窥镜荧光成像系统中绘制了密集的关注。然而,基于空气背景中设计的传统金属透析,生物组织的色散和生物组织的严重散射显着降低了传统的双光子成像系统中的激励收集效率。这里,通过采用复合嵌入结构和空间复用方法,提出了在生物组织环境中设计的激发和发射双波长共聚焦和偏振不敏感金属。具有0.895的数值孔径(NA)的金属可以将激发(915nm)和发射(510nm)光束聚焦到小鼠皮质中的相同焦点。根据双光子荧光成像的理论模拟,通过所提出的金属的收集的荧光点的横向分辨率可以高达0.42μm。与在空气环境中设计的金属相比,荧光点的收集效率从5.92%提高至14.60%。我们的调查开辟了在生物组织的深层地区的高分辨率和微创成像的新窗口。

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