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The ocular toxicity and pharmacokinetics of simvastatin following intravitreal injection in mice

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dc.contributor.authorTse, Dennis Y.-
dc.contributor.authorKim, Seong Jae-
dc.contributor.authorChung, Inyoung-
dc.contributor.authorHe, Feng-
dc.contributor.authorWensel, Theodore G.-
dc.contributor.authorWu, Samuel M.-
dc.date.accessioned2022-12-26T18:32:59Z-
dc.date.available2022-12-26T18:32:59Z-
dc.date.issued2017-09-18-
dc.identifier.issn2222-3959-
dc.identifier.issn2227-4898-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/13476-
dc.description.abstractAIM: To investigate the retinal toxicity and pharmacokinetics of simvastatin intravitreally injected into mice. METHODS: 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. RESULTS: 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 mu mol/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 1.92-2.41 h. CONCLUSION: Intravitreal injection of up to 200 mu mol/L simvastatin produced no signs of adverse effects in the mouse retina. Simvastatin reaches the retina shortly after intravitreal injection and has a short half-life.-
dc.format.extent9-
dc.language영어-
dc.language.isoENG-
dc.publisherIJO PRESS-
dc.titleThe ocular toxicity and pharmacokinetics of simvastatin following intravitreal injection in mice-
dc.typeArticle-
dc.publisher.location중국-
dc.identifier.doi10.18240/ijo.2017.09.05-
dc.identifier.scopusid2-s2.0-85029156540-
dc.identifier.wosid000409558000005-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF OPHTHALMOLOGY, v.10, no.9, pp 1361 - 1369-
dc.citation.titleINTERNATIONAL JOURNAL OF OPHTHALMOLOGY-
dc.citation.volume10-
dc.citation.number9-
dc.citation.startPage1361-
dc.citation.endPage1369-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOphthalmology-
dc.relation.journalWebOfScienceCategoryOphthalmology-
dc.subject.keywordPlusRETINAL GANGLION-CELLS-
dc.subject.keywordPlusDIABETIC-RETINOPATHY-
dc.subject.keywordPlusMOUSE MODEL-
dc.subject.keywordPlusVASCULAR-PERMEABILITY-
dc.subject.keywordPlusMACULAR DEGENERATION-
dc.subject.keywordPlusRAT RETINA-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusSTATINS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusGLAUCOMA-
dc.subject.keywordAuthorsimvastatin-
dc.subject.keywordAuthorretina-
dc.subject.keywordAuthorelectroretinography-
dc.subject.keywordAuthorhigh-performance liquid chromatography-
dc.subject.keywordAuthorelectron microscopy-
dc.subject.keywordAuthorintravitreal injection-
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