Journal of Clinical Medicine Research, ISSN 1918-3003 print, 1918-3011 online, Open Access
Article copyright, the authors; Journal compilation copyright, J Clin Med Res and Elmer Press Inc
Journal website http://www.jocmr.org

Original Article

Volume 7, Number 7, July 2015, pages 517-524


Effect of Distance and Duration of Illumination on Retinal Ganglion Cells Exposed to Varying Concentrations of Brilliant Blue Green

Figures

Figure 1.
Figure 1. Schematic representation explaining the exposure of RGCs to BBG during intraocular surgery as well as cell culture setup. (a) Diffuse light illumination. (b) Focal illumination. LS: light source; LP: light pipe; D: distance; RGC: retinal ganglion cell; BBG: brilliant blue green.
Figure 2.
Figure 2. Experimental illustration. (a) Measurement of metal halide light illumination using a light meter at a certain distance from the light source. (b) Measurement of metal halide light illumination using a light meter directly from the light source. (c) Exposure of cultured RGCs to metal halide illumination. LS: light source; LP: light pipe; LM: light meter; dist: distance; RGC: retinal ganglion cell; BBG: brilliant blue green.
Figure 3.
Figure 3. Evaluating the cytotoxic effect of brilliant blue green at 1 cm metal halide distance illumination on retinal ganglion cells using WST-1 assay at high (a) and medium illumination (b). X-axis represents the time dependent exposure in minutes; Y-axis represents number of viable cells expressed as percent of control (N = 4); (c) represents the trend line.
Figure 4.
Figure 4. Evaluating the cytotoxic effect of brilliant blue green at 2.5 cm metal halide distance illumination on retinal ganglion cells using WST-1 assay at high (a) and medium illumination (b). X-axis represents the time dependent exposure in minutes; Y-axis represents number of viable cells expressed as percent of control (N = 4); (c) represents the trend line.
Figure 5.
Figure 5. Evaluating the cytotoxic effect of brilliant blue green at 1 cm metal halide distance illumination on retinal ganglion cells using CellTiter 96® AQueous One proliferation assay at high (a) and medium illumination (b). X-axis represents the time dependent exposure in minutes; Y-axis represents number of viable cells expressed as percent of control (N = 4); (c) represents the trend line.
Figure 6.
Figure 6. Evaluating the cytotoxic effect of brilliant blue green at 2.5 cm metal halide distance illumination on retinal ganglion cells using CellTiter 96® AQueous One proliferation assay at high (a) and medium illumination (b). X-axis represents the time dependent exposure in minutes; Y-axis represents number of viable cells expressed as percent of control (N = 4); (c) represents the trend line.

Tables

Table 1. Viability of RGCs After Illumination at 1 cm and 2.5 cm Distance With Higher and Medium Illumination of Metal Halide Light Source Using the WST-1 Assay
 
Distance of illumination (cm)Concentration of dye (mg/mL)Higher illumination cell viability ± SD (%)Medium illumination cell viability ± SD (%)
1 min5 min15 min1 min5 min15 min
10.2589.8 ± 7.479.6 ± 4.956.7 ± 4.099.1 ± 14.594.4 ± 18.873.7 ± 16.0
0.579 ± 13.166.7 ± 13.653.1 ± 11.396.5 ± 8.584.5 ± 11.072.3 ± 12.8
2.50.2597.5 ± 16.496.7 ± 15.292.4 ± 15.295.1 ± 7.293.8 ± 7.293.0 ± 1.8
0.598.9 ± 12.694.8 ± 12.482.7 ± 15.794.5 ± 3.994.0 ± 2.987.0 ± 7.0

 

Table 2. Viability of RGCs After Illumination at 1 cm and 2.5 cm Distance With Higher and Medium Illumination of Metal Halide Light Source Using the CellTiter 96® AQueous One Assay
 
Distance of illumination (cm)Concentration of dye (mg/mL)Higher illumination cell viability ± SD (%)Medium illumination cell viability ± SD (%)
1 min5 min15 min1 min5 min15 min
10.2593.5 ± 5.390.4 ± 3.188.2 ± 6.798.9 ± 6.597.8 ± 7.994.2 ± 4.8
0.588.2 ± 5.585.3 ± 7.983.6 ± 4.196.2 ± 8.196.4 ± 5.988.9 ± 7.1
2.50.2595.6 ± 1.891.2 ± 3.284 ± 2.397.2 ± 7.693.7 ± 8.691.4 ± 7.9
0.593.3 ± 1.383.2 ± 2.083.1 ± 2.896.3 ± 8.591.6 ± 6.988.2 ± 7.8