Journal
CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
Volume 43, Issue 9, Pages 820-829Publisher
WILEY
DOI: 10.1111/ceo.12568
Keywords
retina; retinal light toxicity; surgery
Categories
Funding
- Discovery Eye Foundation
- Henry L. Guenther Foundation
- The Iris and B. Gerald Cantor Foundation
- The Skirball Molecular Ophthalmology Program
- Poly and Michael Smith Foundation
- Research to Prevent Blindness Foundation
- Fight for Sight [1906] Funding Source: researchfish
- Medical Research Council [MR/K008722/1] Funding Source: researchfish
- MRC [MR/K008722/1] Funding Source: UKRI
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Background: The aim of this study is to evaluate the safety profile of Brilliant Blue G (BBG) with and without exposure to light (L) on three different retinal cell lines. Method: ARPE-19, R28 and MIO-M1 cells were treated with BBG: 0.125 mg/mL (0.5x clinical concentration), 0.25 mg/mL (1x) or 0.5 mg/mL (2x) with or without surgical illumination of halogen light exposure for 10 min, 15 min or 30 min. Cells were further cultured after 24 h and then analysed for cell viability, late stages of apoptosis and mitochondrial damage associated with early apoptosis using assays that measure trypan blue dye exclusion, increases in caspase-3/7 activity or changes in mitochondrial membrane potential (Delta Psi m), respectively. Result: All three cell lines that were exposed to BBG in the presence or absence of light exposure for 30 min were found to have cell viability and caspase-3/7 activity levels similar to the untreated cultures. The mitochondrial membrane potential (Delta Psi m) was decreased significantly at the 2x + L dose and 2x dose in all three retinal cell lines compared to their respective untreated control cells. At the lower doses of BBG, with or without exposure to light, the Delta Psi m values were similar to the untreated control cultures. Conclusion: Exposure to BBG dye concentrations that are used clinically (0.125 mg/mL and 0.25 mg/mL) in the presence up to 30 min of surgically equivalent light intensity is safe for retinal cells.
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