Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/75880
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dc.contributorSchool of Optometryen_US
dc.creatorTse, DYen_US
dc.creatorKim, SJen_US
dc.creatorChung, Ien_US
dc.creatorHe, Fen_US
dc.creatorWensel, TGen_US
dc.creatorWu, SMen_US
dc.date.accessioned2018-05-10T02:54:50Z-
dc.date.available2018-05-10T02:54:50Z-
dc.identifier.issn2222-3959en_US
dc.identifier.urihttp://hdl.handle.net/10397/75880-
dc.language.isoenen_US
dc.publisherInternational Council of Ophthalmologyen_US
dc.rightsAll content of the IJO is published with open access under the Creative Commons Attribution-NonCommercial-NoDerivs License (CC BY-NC-ND 4.0) (https://creativecommons.org/licenses/by-nc-nd/4.0/). All articles published with open access will be immediately and permanently free for everyone to read, download, copy, and distribute as defined by the applied license.en_US
dc.rightsThe following publication :Y D. Tse,Seong Jae Kim,Inyoung Chung,Feng He,Theodore G. Wensel,Samuel M. Wu.The ocular toxicity and pharmacokinetics of simvastatin following intravitreal injection in mice.Int J Ophthalmol 2017;10(9):1361-1369 is available at 10.18240/ijo.2017.09.05.en_US
dc.subjectSimvastatinen_US
dc.subjectRetinaen_US
dc.subjectElectroretinographyen_US
dc.subjectHigh-performance liquid chromatographyen_US
dc.subjectElectron microscopyen_US
dc.subjectIntravitreal injectionen_US
dc.titleThe ocular toxicity and pharmacokinetics of simvastatin following intravitreal injection in miceen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1361en_US
dc.identifier.epage1369en_US
dc.identifier.volume10en_US
dc.identifier.issue9en_US
dc.identifier.doi10.18240/ijo.2017.09.05en_US
dcterms.abstractAIM: To investigate the retinal toxicity and pharmacokinetics of simvastatin intravitreally injected into mice.en_US
dcterms.abstractMETHODS: 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.en_US
dcterms.abstractRESULTS: 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.en_US
dcterms.abstractCONCLUSION: 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.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationInternational journal of ophthalmology, 2017, v. 10, no. 9, p. 1361-1369en_US
dcterms.isPartOfInternational journal of ophthalmologyen_US
dcterms.issued2017-
dc.identifier.isiWOS:000409558000005-
dc.identifier.pmid28944193-
dc.identifier.eissn2227-4898en_US
dc.identifier.rosgroupid2017005530-
dc.description.ros2017-2018 > Academic research: refereed > Publication in refereed journalen_US
dc.description.validate201805 bcrcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberSO-0075-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Institute of Health; Retina Research Foundation(Houston); Research to Prevent Blindness Inc. ; Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6780528-
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