Purpose: To evaluate the retinal toxicity of intravitreal minocycline in rabbit eyes. Methods: Intravitreal injection of minocycline with concentrations of 1000, 500, 250, 125 and 62.5 μg in 0.1 ml was performed in 10 New Zealand albino rabbits. Each concentration was injected into two rabbit eyes. For each dose, normal saline was injected in one contralateral eye and the other fellow eye remained non-injected. Electrophysiologic testing was performed before and 4 weeks after injections. The eyes were enucleated 4 weeks after injections and examined using light microscopy. Results: The clinical examination was unremarkable after injections. Electroretinography recordings were significantly affected at all doses in at least one of the a- or...
Purpose: To compare the intravitreal pharmacokinetic profile of a triamcinolone acetonide formulatio...
Purpose: To determine the maximum non-toxic dose of recombinant human erythropoietin (EPO) in rabbit...
Purpose: To evaluate the safety and tolerability of a single intracameral administration of a combin...
Purpose To determine the possible adverse effects and safe dose range of intravitreal colistin, an a...
Purpose: To evaluate the ocular toxicity of escalating doses of intravitreous adalimumab (Humira (R)...
Purpose: To evaluate the toxic effects of two triamcinolone acetonide (TA) vehicles on rabbit retina...
Purpose: The aim of this study was to evaluate whether intravitreal triamcinolone hexace-tonide (TH)...
Purpose: To report the clinical, electrophysiologic, and histologic findings of different concentrat...
Purpose. To assess the safety of biosimilar intravitreal aflibercept (CinnaGen Co., Iran) compared t...
Background: To investigate the highest nontoxic intravitreal dose of piperacillin/tazobactam in rabb...
Purpose: To evaluate the safety of intravitreal injection of Stivant, a biosimilar to bevacizumab, i...
Purpose: The purpose of this prospective experimental study was to evaluate the safety/toxicity of α...
Objective: This study was designed to determine the effects of trauma and infection on vitreous cipr...
Purpose To evaluate the ocular toxicity of escalating doses of intravitreous adalimumab (Humira) in ...
PubMed ID: 25285465Purpose: The purpose of this experiment was to investigate the possible toxic eff...
Purpose: To compare the intravitreal pharmacokinetic profile of a triamcinolone acetonide formulatio...
Purpose: To determine the maximum non-toxic dose of recombinant human erythropoietin (EPO) in rabbit...
Purpose: To evaluate the safety and tolerability of a single intracameral administration of a combin...
Purpose To determine the possible adverse effects and safe dose range of intravitreal colistin, an a...
Purpose: To evaluate the ocular toxicity of escalating doses of intravitreous adalimumab (Humira (R)...
Purpose: To evaluate the toxic effects of two triamcinolone acetonide (TA) vehicles on rabbit retina...
Purpose: The aim of this study was to evaluate whether intravitreal triamcinolone hexace-tonide (TH)...
Purpose: To report the clinical, electrophysiologic, and histologic findings of different concentrat...
Purpose. To assess the safety of biosimilar intravitreal aflibercept (CinnaGen Co., Iran) compared t...
Background: To investigate the highest nontoxic intravitreal dose of piperacillin/tazobactam in rabb...
Purpose: To evaluate the safety of intravitreal injection of Stivant, a biosimilar to bevacizumab, i...
Purpose: The purpose of this prospective experimental study was to evaluate the safety/toxicity of α...
Objective: This study was designed to determine the effects of trauma and infection on vitreous cipr...
Purpose To evaluate the ocular toxicity of escalating doses of intravitreous adalimumab (Humira) in ...
PubMed ID: 25285465Purpose: The purpose of this experiment was to investigate the possible toxic eff...
Purpose: To compare the intravitreal pharmacokinetic profile of a triamcinolone acetonide formulatio...
Purpose: To determine the maximum non-toxic dose of recombinant human erythropoietin (EPO) in rabbit...
Purpose: To evaluate the safety and tolerability of a single intracameral administration of a combin...