The ocular toxicity and pharmacokinetics of simvastatin following intravitreal injection in mice
Author(s) -
Dennis Y. Tse,
Seong Jae Kim,
In Young Chung,
Feng He,
Theodore G. Wensel,
Samuel M. Wu
Publication year - 2017
Publication title -
international journal of ophthalmology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.634
H-Index - 29
eISSN - 2227-4898
pISSN - 2222-3959
DOI - 10.18240/ijo.2017.09.05
Subject(s) - simvastatin , medicine , retina , pharmacokinetics , electroretinography , retinal , ophthalmology , toxicity , histology , erg , pharmacology , pathology , biology , neuroscience
To investigate the retinal toxicity and pharmacokinetics of simvastatin intravitreally injected into mice.Forty-eight 6-8-week-old C57BL/6J mice were used in this study. Simvastatin was intravitreally injected into the right eye of each mouse; the left eye was injected with vehicle and was used as a control. Bilateral dark-adapted electroretinography (ERG) was performed 1 and 7d following injection. Histology was examined using a combination of light, fluorescence and electron microscopy. High-performance liquid chromatography (HPLC) was used to determine the decay in the retinal simvastatin concentration.ERG revealed no significant changes in the simvastatin-injected eyes compared to control. Histologic studies showed normal retinal morphology in eyes injected with simvastatin up to a final vitreal concentration of 200 µmol/L. No significant changes in the number of photoreceptors, bipolar cells or ganglion cells were found. The retinal simvastatin concentration decayed exponentially, with a half-life of 1.92-2.41h.Intravitreal injection of up to 200 µmol/L simvastatin produced no signs of adverse effects in the mouse retina. Simvastatin reaches the retina shortly after intravitreal injectionand has a short half-life.
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