在双光子显微镜 (2P-FOCUS) 中通过富里埃域强度合进行散射校正
Daniel Zepeda1, Yucheng Li1, Yi Xue1
1Department of Biomedical Engineering, University of California, Davis, 451 Health Sciences Dr., Davis, California 95616, USA.
概括
我们开发了一种新的两光子显微镜系统 (2P-FOCUS),可以纠正生物组织中的光散射. 该系统通过调节里埃域中的光强度来增强深层组织成像,从而提高了数十倍的信号.
科学领域:
- 生物医学光学 生物医学光学
- 显微镜的使用方法
- 光子学 是一个光子学.
背景情况:
- 生物组织中的光散射限制了成像深度.
- 当前的散射校正方法需要传输访问或代优化.
- 有限的光子可用性加剧了散射挑战.
研究的目的:
- 引入一种新的两光子显微镜系统用于散射校正.
- 克服现有的散射校正技术的局限性.
- 在具有挑战性的条件下启用深层组织成像.
主要方法:
- 开发了一种具有福里埃域强度合的双光子显微镜系统,用于分散校正 (2P-FOCUS).
- 在里埃域中利用强度调制,利用非线性干扰和两光子激发.
- 采用随机模式进行散射探测和一次性算法用于快速校正面罩生成.
- 启用了分区域特定的面具定制,以克服内存效果的限制.
主要成果:
- 通过骨和ex vivo小鼠大脑样本展示了聚焦和成像.
- 与未经纠正的成像相比,显著增强了两光子光信号 (几十个折叠).
- 在230 μm × 230 μm × 510 μm的体积中实现了分散校正,超过了内存效应范围.
- 在几秒钟内完成散射测量,计算和校正.
结论:
- 2P-FOCUS有效地纠正生物组织中的光散射.
- 该系统能够快速,经济高效地进行深层组织成像.
- 2P-FOCUS为先进的生物医学成像应用提供了广泛的采用潜力.
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