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一种用于眼部组织宏观和微观评估的万向节安装式加压室。

A gimbal-mounted pressurization chamber for macroscopic and microscopic assessment of ocular tissues.

作者信息

Keyes Joseph T, Yan Dongmei, Rader Jacob H, Utzinger Urs, Vande Geest Jonathan P

机构信息

Graduate Interdisciplinary Program in Biomedical Engineering, The University of Arizona, Tucson, AZ 85721, USA.

出版信息

J Biomech Eng. 2011 Sep;133(9):095001. doi: 10.1115/1.4004921.

Abstract

The biomechanical model of glaucoma considers intraocular pressure-related stress and resultant strain on load bearing connective tissues of the optic nerve and surrounding peripapillary sclera as one major causative influence that effects cellular, vascular, and axonal components of the optic nerve. By this reasoning, the quantification of variations in the microstructural architecture and macromechanical response of scleral shells in glaucomatous compared to healthy populations provides an insight into any variations that exist between patient populations. While scleral shells have been tested mechanically in planar and pressure-inflation scenarios the link between the macroscopic biomechanical response and the underlying microstructure has not been determined to date. A potential roadblock to determining how the microstructure changes based on pressure is the ability to mount the spherical scleral shells in a method that does not induce unwanted stresses to the samples (for instance, in the flattening of the spherical specimens), and then capturing macroscopic and microscopic changes under pressure. Often what is done is a macroscopic test followed by sample fixation and then imaging to determine microstructural organization. We introduce a novel device and method, which allows spherical samples to be pressurized and macroscopic and microstructural behavior quantified on fully hydrated ocular specimens. The samples are pressurized and a series of markers on the surface of the sclera imaged from several different perspectives and reconstructed between pressure points to allow for mapping of nonhomogenous strain. Pictures are taken from different perspectives through the use of mounting the pressurization scheme in a gimbal that allows for positioning the sample in several different spherical coordinate system configurations. This ability to move the sclera in space about the center of the globe, coupled with an upright multiphoton microscope, allows for collecting collagen, and elastin signal in a rapid automated fashion so the entire globe can be imaged.

摘要

青光眼的生物力学模型认为,与眼压相关的应力以及对视神经和周围视乳头周围巩膜的承重结缔组织产生的应变是影响视神经细胞、血管和轴突成分的一个主要致病因素。据此推断,与健康人群相比,对青光眼患者巩膜壳的微观结构和宏观力学反应变化进行量化,有助于深入了解不同患者群体之间存在的差异。虽然已经在平面和压力充气场景下对巩膜壳进行了力学测试,但迄今为止,宏观生物力学反应与潜在微观结构之间的联系尚未确定。确定微观结构如何随压力变化的一个潜在障碍是,能否以一种不会对样本产生不必要应力的方式(例如,在球形样本扁平化过程中)安装球形巩膜壳,然后在压力下捕捉宏观和微观变化。通常的做法是先进行宏观测试,然后固定样本,再进行成像以确定微观结构组织。我们介绍了一种新颖的设备和方法,它能够对球形样本进行加压,并对完全水合的眼部标本的宏观和微观结构行为进行量化。对样本进行加压,并从几个不同角度对巩膜表面的一系列标记进行成像,并在压力点之间进行重建,以实现非均匀应变的映射。通过将加压方案安装在万向架中,允许在几个不同的球坐标系配置中定位样本,从而从不同角度拍摄照片。这种使巩膜围绕眼球中心在空间中移动的能力,再加上一台直立式多光子显微镜,能够以快速自动化的方式收集胶原蛋白和弹性蛋白信号,从而可以对整个眼球进行成像。

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