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Springer Science and Business Media LLC PhotoniX 6(1)
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    초록·키워드

    Abstract Miniaturized two-photon microscopes (m2PMs) enable high-resolution, deep-brain imaging in freely behaving animals. However, the trade-offs among weight, form factor, and optical performance in conventional refractive objectives present major obstacles to achieving large field-of-view (FOV), high-resolution imaging in weight-sensitive or multiregion applications. Metalenses offer ultralight, high-NA, aberration-corrected alternatives, but face persistent challenges, including restricted FOV, off-axis aberrations, and dual-band optimization for two-photon imaging. Here, we present Meta-m2PM 2.0, a 1.06 g headpiece featuring a compound metalens architecture with a two-stage imaging design that decouples scanning and focusing. We designed and fabricated a large-angle (± 12°) metalens-based scan lens and a high-NA (0.48) dual-layer metalens-based objective, both derived from our established polarization-insensitive Si₃N₄ meta-atom library co-optimized for focusing and transmission at 920 nm excitation and 500–560 nm fluorescence collection. Meta-m2PM 2.0 achieves a 350 × 330 µm 2 FOV (> 50 × that of Meta-m2PM 1.0), with 1.17 µm lateral and 19.85 µm axial resolution at the center, while maintaining > 80% lateral resolution uniformity across the FOV, and extending imaging depth to 210 µm (~ 3 × deeper). We demonstrate dendritic imaging in head-fixed awake mice and, to our knowledge, the first metalens-based two-photon calcium imaging in freely behaving mice with a high signal-to-noise ratio, paving the way for ultralight multiregion neuroimaging and compact nonlinear microendoscopy.

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