Universidad de Murcia, Instituto Universitario de Investigación en Óptica y Nanofísica, Laboratorio de Óptica, Campus de Espianrdo, Murcia, Spain.
J Biomed Opt. 2014 Jan;19(1):011007. doi: 10.1117/1.JBO.19.1.011007.
Despite the inherent confocality and optical sectioning capabilities of multiphoton microscopy, three-dimensional (3-D) imaging of thick samples is limited by the specimen-induced aberrations. The combination of immersion objectives and sensorless adaptive optics (AO) techniques has been suggested to overcome this difficulty. However, a complex plane-by-plane correction of aberrations is required, and its performance depends on a set of image-based merit functions. We propose here an alternative approach to increase penetration depth in 3-D multiphoton microscopy imaging. It is based on the manipulation of the spherical aberration (SA) of the incident beam with an AO device while performing fast tomographic multiphoton imaging. When inducing SA, the image quality at best focus is reduced; however, better quality images are obtained from deeper planes within the sample. This is a compromise that enables registration of improved 3-D multiphoton images using nonimmersion objectives. Examples on ocular tissues and nonbiological samples providing different types of nonlinear signal are presented. The implementation of this technique in a future clinical instrument might provide a better visualization of corneal structures in living eyes.
尽管多光子显微镜具有固有共聚焦和光学切片能力,但厚样品的三维(3-D)成像受到样品诱导像差的限制。已经提出了将浸液物镜和无传感器自适应光学(AO)技术相结合的方法来克服这一困难。然而,需要对像差进行复杂的逐平面校正,并且其性能取决于一组基于图像的优点函数。我们在这里提出了一种替代方法来增加 3-D 多光子显微镜成像的穿透深度。它基于在使用 AO 设备进行快速断层多光子成像时对入射光束的球面像差(SA)进行操纵。当诱导 SA 时,最佳焦点处的图像质量会降低;然而,从样品内部更深的平面获得了质量更好的图像。这是一种折衷方案,允许使用非浸液物镜对改进的 3-D 多光子图像进行配准。提供不同类型非线性信号的眼部组织和非生物样本的示例。在未来的临床仪器中实施这项技术可能会提供对活体眼睛中角膜结构的更好可视化。