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扫描声学显微镜用于绘制人眼角膜组织的微观弹性特性图。

Scanning acoustic microscopy for mapping the microelastic properties of human corneal tissue.

机构信息

Carys Bannister Building, Faculty of Life Sciences, The University of Manchester, Manchester, UK.

出版信息

Curr Eye Res. 2013 Apr;38(4):437-44. doi: 10.3109/02713683.2012.753094. Epub 2013 Feb 12.

Abstract

PURPOSE

To assess the feasibility of applying scanning acoustic microscopy (SAM) on UV cross-linked corneal tissue for mapping and analyzing its biomechanical properties.

MATERIALS AND METHODS

Five corneal pairs (10 corneas) were used. In each pair, one cornea was cross-linked (epithelium removed, riboflavin application for 45 min and UVA irradiation for 30 min) and the contralateral control cornea was epithelial debrided and treated only with riboflavin for 45 min. Histological sections were prepared and their mechanical properties were examined using SAM. A line profile technique and 2D analysis was used to analyze the mechanical properties of the corneas. Then the corneal paraformaldehyde and unfixed sections were examined histologically using hematoxylin and eosin (H&E) staining.

RESULTS

In the frozen fresh corneal tissue, the speed of sound of the treated corneas was 1672.5 ± 36.9 ms(-1), while it was 1584.2 ± 25.9 ms(-1) in the untreated corneas. In the paraformaldehyde fixed corneal tissue, the speed of sound of the treated corneas was 1863.0 ± 12.7 ms(-1), while it was 1739.5 ± 30.4 ms(-1) in the untreated corneas. The images obtained from the SAM technique corresponded well with the histological images obtained with H&E staining.

CONCLUSION

SAM is a novel tool for examining corneal tissue with a high spatial resolution, providing both histological and mechanical data.

摘要

目的

评估扫描声学显微镜(SAM)在交联角膜组织上进行绘图和分析其生物力学特性的可行性。

材料与方法

使用 5 对(10 只)角膜。每对中一只角膜交联(去除上皮,应用核黄素 45 分钟,UVA 照射 30 分钟),对侧对照角膜仅去除上皮并应用核黄素 45 分钟。制备组织学切片并用 SAM 检查其力学性能。采用线轮廓技术和 2D 分析来分析角膜的力学性能。然后用苏木精和伊红(H&E)染色对角膜多聚甲醛和未固定切片进行组织学检查。

结果

在冷冻新鲜角膜组织中,处理过的角膜的声速为 1672.5±36.9ms(-1),而未处理的角膜的声速为 1584.2±25.9ms(-1)。在多聚甲醛固定的角膜组织中,处理过的角膜的声速为 1863.0±12.7ms(-1),而未处理的角膜的声速为 1739.5±30.4ms(-1)。SAM 技术获得的图像与 H&E 染色获得的组织学图像非常吻合。

结论

SAM 是一种用于检查具有高空间分辨率的角膜组织的新工具,可提供组织学和力学数据。

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