Confocal Raman Microscopy with Adaptive Optics

J. D. Munoz-Bolanos, P. Rajaeipour, K. Kummer, M. Kress, C. Ataman, M. Ritsch-Marte, A. Jesacher
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Abstract

Confocal Raman microscopy, a highly specific and label-free technique for the microscale study of thick samples, often presents difficulties due to weak Raman signals. Inhomogeneous samples introduce wavefront aberrations that further reduce these signals, requiring even longer acquisition times. In this study, we introduce adaptive optics to confocal Raman microscopy for the first time to counteract such aberrations, significantly increasing the Raman signal and image quality. The method is designed to integrate seamlessly with existing commercial microscopes without hardware modifications. It uses a wavefront sensorless approach to derive aberrations using an optofluidic, transmissive spatial light modulator that can be attached to the microscope nosepiece. Our experimental results demonstrate the compensation of aberrations caused by artificial scatterers and mouse brain tissue, improving spatial resolution and achieving up to 3.5-fold signal enhancements. Our results provide a basis for the molecular label-free study of biological systems at greater imaging depths.
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自适应光学共焦拉曼显微镜
共焦拉曼显微镜是一种高度特异性的无标记技术,可用于厚样品的微尺度研究,但由于拉曼信号较弱,常常会遇到困难。不均匀样品带来的波前像差会进一步降低这些信号,从而需要更长的采集时间。在这项研究中,我们首次在共焦拉曼显微镜中引入了自适应光学技术来抵消这种畸变,从而显著提高了拉曼信号和图像质量。该方法无需修改硬件即可与现有的商用显微镜无缝集成。它采用无波面传感器方法,利用可连接到显微镜鼻梁上的光流体、透射径向光调制器来推导像差。我们的实验结果表明,该方法可以补偿人工散射体和小鼠脑组织造成的像差,提高空间分辨率,并实现高达 3.5 倍的信号增强。我们的研究结果为在更大成像深度下对生物系统进行无分子标记研究奠定了基础。
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