Lanzini Manuela, Curcio Claudia, Spoerl Eberhard, Calienno Roberta, Mastropasqua Alessandra, Colasante Martina, Mastropasqua Rodolfo, Nubile Mario, Mastropasqua Leonardo
Department of Medicine and Ageing Sciences, Ophthalmology Clinic, University "G. d' Annunzio" of Chieti-Pescara, 66100, Chieti-Pescara, Italy.
Department of Medicine and Ageing Sciences, Visual Science Laboratory, CeSI, University "G. d' Annunzio" of Chieti-Pescara, Chieti-Pescara, Italy.
Int Ophthalmol. 2017 Feb;37(1):235-243. doi: 10.1007/s10792-016-0266-8. Epub 2016 May 24.
The aim of this study is to determine modifications in stromal fluorescence intensity after different corneal cross-linking (CXL) procedures and to correlate stromal fluorescence to corneal biomechanical resistance. For confocal microscopy study, 15 human cadaver corneas were examined. Three served as control (group 1), three were just soaked with iontophoresis procedure (group 2), three were treated with standard epi-off technique (group 3), and six underwent iontophoresis imbibition. Three of later six were irradiated for 30 min with 3 mW/cm UVA (group 4) and three for 9 min at 10 mW/cm UVA (group 5). Confocal microscopy was performed to quantify the fluorescence intensity in the cornea at different stromal depths. For biomechanical study, 30 human cadaver corneas were randomly divided into five groups and treated as previously described. Static stress-strain measurements of the corneas were performed. Iontophoresis imbibition followed by 10mW/cm irradiation proved to increase stromal fluorescence into the corneal stroma and significant differences were revealed between group 3 and 5 both at 100 (p = 0.0171) and 250 µm (p = 0.0024), respectively. Biomechanical analysis showed an improvement of corneal resistance in group 5. Iontophoresis imbibition followed by accelerated irradiation increased the stromal fluorescence and is related to an improvement of biomechanical resistance. This approach may represent a new strategy to achieve greater concentrations of riboflavin without removing corneal epithelium and improve clinical results while reducing the side effects of CXL.
本研究的目的是确定不同角膜交联(CXL)程序后基质荧光强度的变化,并将基质荧光与角膜生物力学阻力相关联。对于共聚焦显微镜研究,检查了15个人类尸体角膜。3个作为对照(第1组),3个仅用离子导入程序浸泡(第2组),3个用标准上皮剥离技术治疗(第3组),6个进行离子导入吸收。后6个中的3个用3 mW/cm的紫外线A照射30分钟(第4组),3个用10 mW/cm的紫外线A照射9分钟(第5组)。进行共聚焦显微镜检查以量化角膜不同基质深度处的荧光强度。对于生物力学研究,将30个人类尸体角膜随机分为五组,并按先前描述进行处理。对角膜进行静态应力-应变测量。离子导入吸收后用10mW/cm照射可增加角膜基质中的基质荧光,并且在第3组和第5组之间分别在100(p = 0.0171)和250 µm(p = 0.0024)处显示出显著差异。生物力学分析显示第5组角膜阻力有所改善。离子导入吸收后加速照射可增加基质荧光,并与生物力学阻力的改善有关。这种方法可能代表了一种新策略,即在不去除角膜上皮的情况下实现更高浓度的核黄素,并改善临床结果,同时减少CXL的副作用。