Massachusetts Institute of Technology, Department of Mechanical Engineering, Cambridge, Massachusetts 02139, USA.
J Biomed Opt. 2010 Jul-Aug;15(4):046022. doi: 10.1117/1.3475954.
The imaging depth of two-photon excitation fluorescence microscopy is partly limited by the inhomogeneity of the refractive index in biological specimens. This inhomogeneity results in a distortion of the wavefront of the excitation light. This wavefront distortion results in image resolution degradation and lower signal level. Using an adaptive optics system consisting of a Shack-Hartmann wavefront sensor and a deformable mirror, wavefront distortion can be measured and corrected. With adaptive optics compensation, we demonstrate that the resolution and signal level can be better preserved at greater imaging depth in a variety of ex-vivo tissue specimens including mouse tongue muscle, heart muscle, and brain. However, for these highly scattering tissues, we find signal degradation due to scattering to be a more dominant factor than aberration.
双光子激发荧光显微镜的成像深度部分受到生物样本中折射率不均匀性的限制。这种不均匀性导致激发光的波前失真。这种波前失真导致图像分辨率下降和信号水平降低。使用由 Shack-Hartmann 波前传感器和变形镜组成的自适应光学系统,可以测量和校正波前失真。通过自适应光学补偿,我们证明在包括小鼠舌肌、心肌和脑在内的各种离体组织标本中,可以在更大的成像深度更好地保持分辨率和信号水平。然而,对于这些高度散射的组织,我们发现由于散射导致的信号降级比像差更为重要。