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兔巩膜不同区域葡萄糖的差异渗透速率和清除百分比。

Differential permeability rate and percent clearing of glucose in different regions in rabbit sclera.

作者信息

Ghosn Mohamad G, Carbajal Esteban F, Befrui Natasha A, Tuchin Valery V, Larin Kirill V

机构信息

University of Houston, Biomedical Engineering Program, N207 Engineering Building 1, Houston, Texas 77204, USA.

出版信息

J Biomed Opt. 2008 Mar-Apr;13(2):021110. doi: 10.1117/1.2907699.

Abstract

Imaging of biological tissues with optical coherence tomography (OCT) poses a great interest for its capability to noninvasively outline subsurface microstructures within tissues. However, a major limitation for many optical imaging techniques is inadequate depth penetration of light in turbid media, which is bounded to just a few millimeters. There have been several attempts to improve light penetration depth in biological tissues, including application of different tissue optical clearing methods. In this study, an aqueous solution of glucose (40%) is added to rabbit sclera in vitro, where depth-resolved permeability coefficients and optical clearing are calculated with OCT. The permeability rate in regions in the upper 80- to 100-microm region is found to be different from that of regions in the deeper 100-microm region: (6.01+/-0.37)x10(-6) cmsec and (2.84+/-0.68)x10(-5) cmsec, respectively. A difference in percent clearing is also noted. Optical clearing of the upper region is about 10% and increased to 17 to 22% in the one beneath. These results demonstrate the capability of OCT-based methods to not only measure the diffusion rate and optical clearing of a tissue, but also its ability of functional differentiation between layers of epithelial tissues.

摘要

利用光学相干断层扫描(OCT)对生物组织进行成像,因其能够无创地勾勒出组织内的亚表面微观结构而备受关注。然而,许多光学成像技术的一个主要限制是光在浑浊介质中的穿透深度不足,仅局限于几毫米。人们已经进行了几次尝试来提高光在生物组织中的穿透深度,包括应用不同的组织光学透明化方法。在本研究中,将40%的葡萄糖水溶液体外添加到兔巩膜中,并用OCT计算深度分辨的渗透系数和光学透明化情况。发现80至100微米上层区域的渗透率与更深的100微米区域的渗透率不同:分别为(6.01±0.37)×10(-6)厘米/秒和(2.84±0.68)×10(-5)厘米/秒。还注意到透明化百分比的差异。上层区域的光学透明化约为10%,而其下方区域则增加到17%至22%。这些结果表明,基于OCT的方法不仅能够测量组织的扩散速率和光学透明化,还能够区分上皮组织各层之间的功能差异。

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