Suzuki Yoshimasa, Fujii Shintaro, Watanabe Satoshi, Hayashi Shinichi
Advanced Optics R&D Department, Evident Corporation, Hachioji, Tokyo 192-0033, Japan.
Biomed Opt Express. 2025 Jul 29;16(8):3437-3453. doi: 10.1364/BOE.569674. eCollection 2025 Aug 1.
Confocal laser scanning microscopy (CLSM) is widely used in biological research, but imaging the deep regions of three-dimensional samples like spheroids is challenging due to scattering. We propose a computational method that estimates the refractive index distribution from CLSM images, calculates position-dependent point-spread functions (PSFs) using a multi-diffraction propagation model for both excitation and emission light, and applies shift-variant deconvolution. This approach enables the resolution of deep spheroid structures that could not be resolved in conventional CLSM images. It requires no hardware modifications to conventional CLSM systems, enabling high-quality three-dimensional imaging of scattering samples using conventional equipment.
共聚焦激光扫描显微镜(CLSM)在生物学研究中被广泛应用,但由于散射,对诸如球体等三维样本的深部区域进行成像具有挑战性。我们提出了一种计算方法,该方法从CLSM图像估计折射率分布,使用激发光和发射光的多衍射传播模型计算位置相关的点扩散函数(PSF),并应用平移可变去卷积。这种方法能够解析传统CLSM图像中无法分辨的深部球体结构。它不需要对传统CLSM系统进行硬件修改,从而能够使用传统设备对散射样本进行高质量的三维成像。