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Two-Photon Autofluorescence Lifetime and SHG Imaging of Healthy and Diseased Human Corneas

机译:健康和患病人体角膜的双光子自发荧光寿命和SHG成像

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Corneal function can be drastically affected by several degenerations and dystrophies, leading to blindness. Early diagnosis of corneal disease is of major importance and it may be accomplished by monitoring changes of the metabolic state and structural organization, the first detectable pathological signs, by two-photon excitation autofluorescence lifetime and second-harmonic generation imaging. In this study, we propose to use these imaging techniques to differentiate between healthy and pathological corneas. Images were acquired using a laser-scanning microscope with a broadband sub-15 femtosecond near-infrared pulsed laser and a 16-channel photomultiplier tube detector for signal collection. This setup allows the simultaneous excitation of metabolic co-factors and to identify them based on their fluorescence spectra. We were able to discriminate between healthy and pathological corneas using two-photon excitation autofluorescence lifetime and second-harmonic generation imaging from corneal epithelium and stroma. Furthermore, differences between different pathologies were observed. Alterations in the metabolic state of corneal epithelial cells were observed using the autofluorescence lifetime of the metabolic co-factors. In the corneal stroma, we observed not only alterations in the collagen fibril structural organization but also alterations in the autofluorescence lifetime. Further tests are required as the number of pathological samples must be increased. In the future, we intend to establish a correlation between the metabolic and structural changes and the disease stage. This can be a step forward in achieving early diagnosis.
机译:几种变性和营养不良会严重影响角膜功能,导致失明。角膜疾病的早期诊断非常重要,可以通过监测代谢状态和结构组织的变化,通过两个光子激发自发荧光寿命和第二谐波产生的成像来监测第一个可检测到的病理体征。在这项研究中,我们建议使用这些成像技术来区分健康角膜层和病理性角膜。使用具有宽带亚15飞秒近红外脉冲激光和16通道光电倍增管检测器的激光扫描显微镜采集图像,以采集信号。此设置允许同时激发代谢辅因子,并根据其荧光光谱识别它们。我们能够使用双光子激发自发荧光寿命和来自角膜上皮和间质的二次谐波成像来区分健康和病理性角膜。此外,观察到不同病理之间的差异。使用代谢辅因子的自发荧光寿命观察到角膜上皮细胞代谢状态的改变。在角膜基质中,我们不仅观察到了胶原纤维结构的改变,而且还观察到了自体荧光寿命的改变。由于必须增加病理样本的数量,因此需要进一步测试。将来,我们打算在代谢和结构变化与疾病阶段之间建立关联。这可以是实现早期诊断的一步。

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