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Article
November 1986

Ocular Penetration, Toxicity, and Radiosensitization Effects of Two Hypoxic Cell Radiosensitizers on Retinoblastoma

Author Affiliations

From the Department of Ophthalmology and Pathology, Faculty of Medicine, University of British Columbia, Vancouver (Drs Rootman, Kumi, and Bussanich), The Ontario Cancer Institute and the Department of Ophthalmology, University of Toronto (Dr Gallie and Ms Rogers), and the Medical Biophysics Unit, British Columbia Cancer Research Center, Vancouver (Dr Palcic).

Arch Ophthalmol. 1986;104(11):1693-1697. doi:10.1001/archopht.1986.01050230131048
Abstract

• Two new radiosensitizing drugs, SR-2508 and SR-2555, were studied for their in vivo toxicity and absorption properties. For both drugs, 100 mg dissolved in 0.5 mL of normal saline resulted in the maximum acceptable level of toxicity when injected subconjunctivally in rabbit eyes as determined by ocular and histopathologic changes. SR-2508 showed higher ocular and systemic absorption than SR-2555. The radiosensitizing ability of these drugs was studied using Chinese hamster ovary cells and the retinoblastoma cell line, V79c6. Results of the in vitro radiation experiments indicate that both drugs are comparable with misonidazole in their radiosensitizing ability, with SR-2508 being slightly more effective than SR-2555. Because of their relative high ocular absorption and low toxicity in comparison with misonidazole, these two drugs, particularly SR-2508, may be of clinical value and could be considered for adjunctive use as radiosensitizers of hypoxic tumors such as retinoblastoma.

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