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Superpenetration optical microscopy by iterative multiphoton adaptive compensation technique

机译:迭代多光子自适应补偿技术的超穿透光学显微镜

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摘要

Biological tissues are rarely transparent, presenting major challenges for deep tissue optical microscopy. The achievable imaging depth is fundamentally limited by wavefront distortions caused by aberration and random scattering. Here, we report an iterative wavefront compensation technique that takes advantage of the nonlinearity of multiphoton signals to determine and compensate for these distortions and to focus light inside deep tissues. Different from conventional adaptive optics methods, this technique can rapidly measure highly complicated wavefront distortions encountered in deep tissue imaging and provide compensations for not only aberration but random scattering. The technique is tested with a variety of highly heterogeneous biological samples including mouse brain tissue, skull, and lymph nodes. We show that high quality three-dimensional imaging can be realized at depths beyond the reach of conventional multiphoton microscopy and adaptive optics methods, albeit over restricted distances for a given correction. Moreover, the required laser excitation power can be greatly reduced in deep tissues, deviating from the power requirement of ballistic light excitation and thus significantly reducing photo damage to the biological tissue.
机译:生物组织很少透明,这对深层组织光学显微镜提出了重大挑战。可达到的成像深度从根本上受到像差和随机散射引起的波阵面畸变的限制。在这里,我们报告了一种迭代波前补偿技术,该技术利用了多光子信号的非线性来确定和补偿这些畸变,并将光聚焦在深层组织内部。与传统的自适应光学方法不同,该技术可以快速测量在深部组织成像中遇到的高度复杂的波阵面畸变,不仅可以补偿像差,还可以补偿随机散射。该技术已通过多种高度异质的生物样品进行了测试,包括小鼠脑组织,颅骨和淋巴结。我们表明,即使对于给定的校正,在有限的距离内,也可以在传统的多光子显微镜和自适应光学方法无法达到的深度实现高质量的三维成像。此外,可以在深部组织中大大降低所需的激光激发功率,这与弹道光激发的功率要求不同,从而显着减少了对生物组织的光损伤。

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