TESTING INTRAVITREAL TOXICITY OF BEVACIZUMAB (AVASTIN)MANZANO, ROBERTA P. A. MD; PEYMAN, GHOLAM A. MD; KHAN, PALWASHA MD; KIVILCIM, MUHAMET MDRetina: March 2006 - Volume 26 - Issue 3 - pp 257-261 Original Articles Abstract In Brief Author Information Abstract Purpose: To evaluate the retinal toxicity of varying doses of bevacizumab when injected intravitreally in rabbits. Bevacizumab has been approved by the US Food and Drug Administration for the treatment of metastatic colorectal cancer. Materials and Methods: Twelve New Zealand albino rabbits were used for this study and divided into four groups. Four concentrations of bevacizumab were prepared: 500 μg/0.1 mL, 1.0 mg/0.1 mL, 2.5 mg/0.1 mL, and 5.0 mg/0.2 mL. Each concentration was injected intravitreally in one eye of each of three rabbits; 0.1 mL volume of sterile balanced saline solution was injected into the contralateral eyes. Slit-lamp and funduscopic examinations were performed and the animals were observed for 2 weeks for signs of infection, inflammation, or toxicity. A baseline electroretinogram (ERG) was performed before the drug treatment and at day 14 before the animals were killed. The enucleated eyes were prepared for histologic evaluation of retinal toxicity. Results: Histologic and ERG results in all groups showed no retinal toxicity. However, some inflammatory cells were found in the vitreous at the 5–mg dose. Conclusions: Intravitreal bevacizumab did not appear toxic to the retina in albino rabbits at a concentration of 2.5 mg. Intravitreally injected bevacizumab should be evaluated for efficacy in choroidal neovascularization and macular edema. In Brief Bevacizumab, a monoclonal antibody against vascular endothelial growth factor, was evaluated for retinal toxicity in the albino rabbit eye. At a concentration of 5 mg/0.2 mL, there was no evidence of toxicity upon clinical, electroretinographic, or histologic examinations. Author Information From the Department of Ophthalmology, Tulane University Health Sciences Center, New Orleans, Louisiana. None of the authors has any proprietary interest in any technique or product described herein. Reprint requests: Gholam A. Peyman, MD, Tulane University Health Science Center, 1430 Tulane Avenue SL-69, New Orleans, LA 70112-2699; e-mail: firstname.lastname@example.org © The Ophthalmic Communications Society, Inc.