红外光谱法分析核黄素和紫外线对角膜胶原的影响

Vikas Sharma, V. Kansal, Jayd Lukenchuk, M. Dodd, M. Hackett
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摘要

目的:角膜胶原交联(CCL)是一种将角膜暴露在紫外线和/或核黄素下以阻止角膜扩张性疾病进展的方法。目前,使用傅里叶变换红外光谱(FTIR)对CCL后角膜变化的研究大多集中在角膜超微结构上,而不是在分子水平上的变化。本研究的目的是研究角膜胶原连接的时间和空间分离,这是CCL成功的基础。材料与方法:对照实验。5例患者(n = 10)对供体球体分为介入组和对照组。介入组(n = 5)角膜按照改良的Dresden方案暴露于0.1%核黄素和UVA光下,收获,冷冻切片,置于玻片上。对照组角膜(n = 5)行无CCL的冷冻显微切片。在加拿大光源下使用同步加速器中红外光束线对分子变化进行成像。结果:总蛋白的傅里叶变换红外光谱成像,酰胺I波段下的集成面积为1,700至1,600 cm−1,胶原三螺旋结构的FTIR成像,二阶导数强度为1,666 cm−1,聚集蛋白的FTIR成像,二阶导数强度为1,625 cm−1,在介入和对照角膜之间的分子内交联没有差异。胶原蛋白的二级结构既没有明显改变,也没有在角膜内聚集或变性的证据。结论:我们的数据表明,分子内交联在CCL中并不起主要作用,更有可能是分子间连接的增加导致了角膜强度的增加。临床意义:分子间键的增加可能是CCL后角膜强度增加的原因。我们希望这些结果将指导未来优化CCL技术的工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Analysis of the Change Induced by Riboflavin and Ultraviolet Light on Corneal Collagen by Infrared Spectrometry
Ab s t r Ac t Aim: Corneal collagen cross-linking (CCL) is a procedure that exposes the cornea to ultraviolet light and/or riboflavin to halt the progression of corneal ectatic disease. Currently, most investigations using Fourier-transform infrared spectroscopy (FTIR) of corneal changes following CCL focus on corneal ultrastructure, and not on changes at the molecular level. The aim of this study was to investigate the temporal and spatial separation of corneal collagen linkages that underlie the success of CCL. Materials and methods: Controlled experimental trial. Pairs of donor globes from five patients (n = 10) were divided into interventional and control groups. Interventional group corneas (n = 5) were exposed to riboflavin 0.1% and ultraviolet-A (UVA) light according to the modified Dresden protocol, harvested, cryo-microtomed, and placed on glass slides. Control group corneas (n = 5) underwent cryo-microtoming without CCL. Molecular changes were imaged using the synchrotron mid-infrared beamline at the Canadian Light Source. Results: Fourier-transform infrared spectroscopy imaging of total protein, integrated area under the amide I band from 1,700 to 1,600 cm− 1, FTIR imaging of collagen triple helix structures, second-derivative intensity as 1,666 cm− 1, and FTIR imaging of aggregated proteins, secondderivative intensity as 1,625 cm− 1 detected no difference in intramolecular cross-links between the interventional and control corneas. The secondary structure of collagen was neither significantly altered nor was their evidence of aggregation or denaturation within the cornea. Conclusion: Our data suggest that intramolecular cross-linking does not play a major role in CCL and that it is more likely an increase in intermolecular linkages that accounts for increased corneal strength. Clinical significance: An increase in intermolecular linkages likely accounts for the increased corneal strength observed following CCL. We hope that these results will guide future work to optimize techniques for CCL.
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