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3669B130 |
Department of Ophthalmology and Visual Science, Nagoya City University Graduate School of Medical Science, Nagoya, Japan
Commercial Relationships: T. Ito, None; M. Yoshida, None; A. Kato, None; Y. Ogura, None.
Grant Identification: none
Abstract
Purpose: To evaluate the toxicity of trypan blue and indocyanin green (ICG) on ocular tissues.
Methods: Human retinal pigment epithelial cells (ARPE19, ATCC) were cultured in a 1:1 mixture of Dulbeccos modified medium and Hams F12 with 2.5 mM Lglutamine. The cells were incubated for 4 and 12 hours in the media containing various amounts of trypan blue (4x103
4 mg/ml) or ICG (1.5x103
2.5 mg/ml). After the incubation, survival cells were quantified by XTT assay (SigmaAldrich Fine Chemicals, USA). Trypan blue (0.6 mg/ml and 6 mg/ml) and ICG (0.1 mg/ml and 1 mg/ml) solutions were injected into the vitreous cavity of New Zealand white rabbits. Electroretinogram was studied 4 weeks after the administration. The eyes were then enucleated and processed for histological examinations.
Results: The survival rate of RPE cells was not statistically different between trypan blue treated and control groups both in 4hour and 12hour incubation. ICG, however, reduced the survival rate of RPE cells from the concentration of 0.50 mg/ml (4hour incubation). With 12hour incubation, the lower concentration (0.15 mg/ml) showed the toxic effect on the RPE cells.
Conclusions: Although trypan blue did not show any toxic effects on the cultured RPE cells, ICG significantly reduced the survival rate of RPE cells. These results may explain the mechanism of ICGrelated retinal toxicity during ICGassisted vitreous surgery.
Keywords: retinal pigment epithelium retina drug toxicity/drug effects
© 2004, The Association for Research in Vision and Ophthalmology, Inc., all rights reserved. For permission to reproduce any part of this abstract, contact the ARVO Office at arvo{at}arvo.org.
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