Inhibition of experimental corneal neovascularisation by bevacizumab (Avastin)
- Roberta P A Manzano1,2,
- Gholam A Peyman1,
- Palwasha Khan1,
- Petros E Carvounis1,
- Muhamet Kivilcim3,
- Min Ren1,
- Jonathan C Lake2,
- Patricia Chévez-Barrios1
- 1Department of Ophthalmology, Tulane University Health Sciences Center, New Orleans, Louisiana, USA
- 2Department of Ophthalmology, Santa Casa de Misericórdia de São Paulo, São Paulo, Brazil
- 3Department of Ophthalmology, University of Arizona, Arizona Health Sciences Center, Tucson, Arizona, USA
- Correspondence to: Dr G A Peyman Department of Ophthalmology, University of Arizona, 655 N Alvernon Way, Ste 108, Tucson, AZ 85711, USA; ccole{at}eyes.arizona.edu
- Accepted 9 December 2006
- Published Online First 19 December 2006
Abstract
Aim: To evaluate the effect of topically administered bevacizumab (Avastin) on experimental corneal neovascularisation in rats.
Methods: Silver nitrate sticks (75% silver nitrate, 25% potassium nitrate) were used to perform chemical cauterisation on the corneas of 16 eyes from 16 male Long Evans rats. For the following 7 days, the 10 eyes in the treatment group were instilled with bevacizumab 4 mg/ml drops twice daily, whereas the 6 eyes in the control group received placebo (normal saline drops twice daily). Digital photographs of the cornea were analysed to determine the area of cornea covered by neovascularisation as a percentage of the total corneal area.
Results: In the bevacizumab-treated eyes, neovascularisation covered, on average, 38.2% (15.5%) (mean (SD)) of the corneal surface compared with 63.5% (5.0%) in the control group (p<0.02, Mann–Whitney U test).
Conclusion: Topically administered bevacizumab (Avastin) at a concentration of 4 mg/ml limits corneal neovascularisation following chemical injury in the male Long Evans rat model.
Footnotes
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Published Online First 19 December 2006
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Competing interests: None.







