Use of adaptive optics to increase nonlinear imaging signal in mouse bone morrow

SPIE MOEMS-MEMS Pub Date : 2008-02-07 DOI:10.1117/12.769506
Yaopeng Zhou, T. Bifano, Charles P. Lin
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Abstract

In a recent effort, researchers from Wellman Center of Photomedicine use fluorescence signal provided by single- or two-photon excitation, second harmonic generation and coherent anti-Stokes Raman spectroscopy (CARS) to illustrate the cell level detail of mouse bone marrow [1]. However, the several non-linear imaging techniques suffered on a common base: signal degradation with deeper light penetration. The fluorescence signal weakening from the mouse skull is caused by the decreased excitation light intensity. With deeper imaging depth, the excitation light suffers tissue scattering, absorption and optical aberration. The last one of the causes spreads the light intensity away from its diffraction limited focal spot. In consequence, less fluorescence light is produced in the enlarged focal volume. In this paper, I will introduce Adaptive Optics (AO), a system for real time optical aberration compensation, to improve the non-linear fluorescence signal in the mouse bone marrow imaging. A parallel stochastic gradient decent algorithm based on Zernike polynomial is employed to control the deformable mirror in real time aberration compensation.
利用自适应光学增强小鼠骨神经非线性成像信号
最近,Wellman Center of Photomedicine的研究人员利用单光子或双光子激发、二次谐波产生和相干反斯托克斯拉曼光谱(CARS)提供的荧光信号来说明小鼠骨髓的细胞水平细节[1]。然而,几种非线性成像技术在一个共同的基础上遭受:随着更深的光穿透信号退化。小鼠颅骨的荧光信号减弱是由激发光强度降低引起的。随着成像深度的加深,激发光受到组织散射、吸收和光学像差的影响。最后一种原因使光强远离其衍射极限焦斑。因此,在放大的焦体积中产生较少的荧光。本文将介绍一种实时光学像差补偿系统——自适应光学(AO),以改善小鼠骨髓成像中的非线性荧光信号。在实时像差补偿中,采用基于Zernike多项式的并行随机梯度校正算法控制变形镜。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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