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Evaluation of Corneal Cross-Linking for Treatment of Fungal Keratitis: Using Confocal Laser Scanning Microscopy on an Ex Vivo Human Corneal Model

机译:角膜交联治疗真菌性角膜炎的评价:在共聚焦的人角膜模型上使用共聚焦激光扫描显微镜。

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Purpose: Some previous reports have established the use of photoactivated chromophore-induced corneal cross-linking (PACK-CXL) in treating fungal keratitis. The results of these case reports have often been conflicting. To systematically study the effect of PACK-CXL in the management of Fusarium keratitis, we have developed an ex vivo model of human corneal infection using eye-banked human corneas. Methods: Sixteen healthy ex vivo human corneas were divided into four study groups: (1) untreated control, (2) cross-linked, (3) infected with fungal spores, and (4) infected with fungal spores and then cross-linked. All infected corneas were inoculated with Fusarium oxysporum spores. The PACK-CXL procedure was performed 24 hours post inoculation for group 4. For PACK-CXL treatment, the corneas were debrided of epithelium; then 1% (wt/vol) isotonic riboflavin was applied dropwise at 5-minute intervals for 30 minutes and during the course of UV-A cross-linking for another 30 minutes. The corneas were imaged using a confocal microscope at 48 hours post inoculation, and the Fusarium hyphal volume and spore concentration were calculated. Results: The infected and then cross-linked group had a significantly lower volume of Fusarium hyphae, compared to the infected (P = 0.001) group. In the infected and then cross-linked group there was significant inhibition of Fusarium sporulation compared with the infected (P = 0.007) group. Conclusions: A model of human corneal infection was successfully developed for investigation of the effects of PACK-CXL on fungal keratitis. A treatment regimen of combined UV-A/riboflavina??induced corneal cross-linking appears to be a valuable approach to inhibit the growth and sporulation of Fusarium and suppress the progression of fungal keratitis.
机译:目的:以前的一些报道已经建立了光活化生色团诱导的角膜交联(PACK-CXL)在治疗真菌性角膜炎中的用途。这些案例报告的结果常常是矛盾的。为了系统地研究PACK-CXL在镰刀菌性角膜炎治疗中的作用,我们已经开发了使用眼库人角膜的人角膜感染的离体模型。方法:将十六个健康的离体健康人角膜分为四个研究组:(1)未经处理的对照;(2)交联;(3)感染真菌孢子;(4)感染真菌孢子然后交联。所有感染的角膜均接种尖孢镰刀菌孢子。对于第4组,在接种后24小时进行PACK-CXL程序。对于PACK-CXL治疗,将角膜上皮清除。然后以5分钟的间隔滴加1%(wt / vol)的等渗核黄素30分钟,并在UV-A交联过程中再滴加30分钟。接种后48小时,使用共聚焦显微镜对角膜成像,并计算镰刀菌菌丝的菌丝量和孢子浓度。结果:与感染(P = 0.001)组相比,感染后再交联的组镰刀菌菌丝的体积明显减少。与感染组(P = 0.007)相比,感染后交联的组对镰刀菌孢子形成有明显的抑制作用。结论:成功开发了人类角膜感染模型,以研究PACK-CXL对真菌性角膜炎的影响。联合UV-A /核黄素诱导的角膜交联的治疗方案似乎是抑制镰刀菌的生长和孢子形成并抑制真菌性角膜炎进展的有价值的方法。

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