From: Corneal Cross-Linking with Riboflavin and UV-A in the Mouse Cornea in Vivo: Morphological, Biochemical, and Physiological Analysis Trans. Vis. Sci.

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From: Corneal Cross-Linking with Riboflavin and UV-A in the Mouse Cornea in Vivo: Morphological, Biochemical, and Physiological Analysis Trans. Vis. Sci. Tech.. 2017;6(1):7. doi:10.1167/tvst.6.1.7 Figure Legend: Histological analysis of the central cornea for different CXL protocols at 24 hours after treatment: 9 mW/cm2, 10 minutes, 0.5% riboflavin = 5.4 J/cm2 (A), 9 mW/cm2, 2:50 minutes, 0.27% riboflavin = 1.53 J/cm2 (B), 3 mW/cm2, 1 minute, 0.1% riboflavin = 0.18 J/cm2 (C), 3 mW/cm2, 30 seconds, 0.1% riboflavin = 0.09 J/cm2 (D). Keratocyte apoptosis in the central cornea reached a similar depth (black arrows) in all CXL protocols and was independent of irradiation time (30 seconds – 10 minutes) and UV fluence (0.09 – 5.4 J/cm2). However, keratocyte density was lower at higher UV fluences (A, B). Date of download: 12/27/2017 The Association for Research in Vision and Ophthalmology Copyright © 2017. All rights reserved.