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RIBOFLAVIN FOR CORNEAL CROSS-LINKING

机译:用于角膜交联的核黄素

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Corneal collagen cross-linking (CXL) with riboflavin and ultraviolet A (UVA) radiation is the first therapeutic modality that appears to arrest the progression of keratoconus and other corneal ectasias. Riboflavin is central to the process, acting as a photosensitizer for the production of oxygen singlets and riboflavin triplets. These free radicals drive the CXL process within the proteins of the corneal stroma, altering its biomechanical properties. Riboflavin also absorbs the majority of the UVA radiation, which is potentially cytotoxic and mutagenic, within the anterior stroma, preventing damage to internal ocular structures, such as the corneal endothelium, lens and retina. Clinical studies report cessation of ectatic progression in over 90% of cases and the majority document significant improvements in visual, keratometric and topographic parameters. Clinical follow-up is limited to 5-10 years, but suggests sustained stability and enhancement in corneal shape. Sight-threatening complications are rare. The optimal stromal riboflavin dosage for CXL is as yet undetermined.
机译:角膜胶原蛋白与核黄素和紫外线A(UVA)辐射的交联(CXL)是刺激角蛋白酶和其他角膜异构酶的进展的第一种治疗模态。核黄素是该方法的核心,作为用于生产氧单曲和核黄素三胞胎的光敏剂。这些自由基在角膜基质的蛋白质内驱动CXL过程,改变其生物力学性质。核黄素还吸收大部分UVA辐射,这是潜在的细胞毒性和致突变性,在前基质内,防止对内部眼部结构的损伤,例如角膜内皮,透镜和视网膜。临床研究报告在90%的案例中停止孤立的进展,并且大多数文件在视觉,腔简体和地形参数中的显着改善。临床随访限于5 - 10年,但表明角膜形状的持续稳定性和增强。威胁威胁性并发症很少见。 CXL的最佳基质核糖蛋白剂量尚未确定。

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