May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Fullerol Cytotoxicity And Phototoxicity In Human Retinal Pigment Epithelial Cells
Author Affiliations & Notes
  • J.E. Roberts
    Natural Sciences, Fordham University, New York, NY
  • D. Hu
    Tissue Culture Center, New York Eye and Ear Infirmary, New York, NY
  • C.F. Chignell
    Laboratory of Pharmacology and Chemistry, NIEHS, Research Triangle Park, NC
  • D.S. Miller
    Laboratory of Pharmacology and Chemistry, NIEHS, Research Triangle Park, NC
  • P.P. Bilski
    Laboratory of Pharmacology and Chemistry, NIEHS, Research Triangle Park, NC
  • A.R. Wielgus
    Laboratory of Pharmacology and Chemistry, NIEHS, Research Triangle Park, NC
  • Footnotes
    Commercial Relationships  J.E. Roberts, None; D. Hu, None; C.F. Chignell, None; D.S. Miller, None; P.P. Bilski, None; A.R. Wielgus, None.
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 2078. doi:
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      J.E. Roberts, D. Hu, C.F. Chignell, D.S. Miller, P.P. Bilski, A.R. Wielgus; Fullerol Cytotoxicity And Phototoxicity In Human Retinal Pigment Epithelial Cells . Invest. Ophthalmol. Vis. Sci. 2006;47(13):2078.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : Water–soluble fullerenes [nano–C60 ,fullerol] have recently been shown to exhibit antibacterial and antiviral activity including inhibition of HIV protease. In addition to their potential to be used as drugs, they are also being tested as carriers to deliver drugs to the brain. To assess ocular toxicity of these nanoparticles which might limit their use, we determined the cytotoxicity and visible light induced phototoxicity of fullerol in vitro with human retinal pigment epithelial (hRPE) cells.

Methods: : Human RPE cells from donor eyes were incubated in the dark for 22 hours with 1–50 µM fullerol in F–12 medium supplemented with 10% FBS. Cells were washed and placed in Hanks Balanced Salt Solution. Then they were exposed to visible light emitted by 2 Philips, F40 AX50, 5000 K Advantage lamps equipped with a filter which transmitted only wavelengths above 400 nm. The visible light exposures used in our experiments (60 – 12000 mJ/cm2) are lower than the daily dose that reaches the human retina. Cell viability and cytotoxicity were estimated using MTS and LDH assays, respectively. Dose and light dependent changes of TBARS concentration were monitored. Protein content was determined by the BCA method. The potential of fullerol to photoproduce 1O2 was measured by direct detection of its steady state phosphorescence at 1270 nm, achieved by using an Oriel 500 W Hg lamp that was equipped with an interference filter with maximal transmittance at 366nm.

Results: : MTS and LDH assays have shown that fullerol is toxic toward RPE cells in the dark at concentrations of 20–50 µM. When cells preincubated with fullerol are exposed to light (> 400nm) cytotoxicity is increased. Increased TBARS production induced by light correlates to fullerol concentration in hRPE cells. We have also determined that fullerol produces singlet oxygen (Φ = 0.07).

Conclusions: : Fullerol is both cytotoxic in the dark and phototoxic to hRPE cells at low concentrations and weak visible light. The mechanism of this damage is, at least in part, through singlet oxygen production resulting in lipid peroxidation. Lipid peroxidation is an important risk factor in the induction of retinal and choroidal neovascularization and diabetic retinopathy.

Keywords: oxidation/oxidative or free radical damage • radiation damage: light/UV • retinal pigment epithelium 
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