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dc.contributor.author김선일-
dc.date.accessioned2018-03-15T05:19:50Z-
dc.date.available2018-03-15T05:19:50Z-
dc.date.issued2012-11-
dc.identifier.citationInvestigative Ophthalmology and Visual Science, November 2012, 53(12), P.7693-7700en_US
dc.identifier.issn0146-0404-
dc.identifier.issn1552-5783-
dc.identifier.urihttp://iovs.arvojournals.org/article.aspx?articleid=2127410-
dc.identifier.urihttp://hdl.handle.net/20.500.11754/47117-
dc.description.abstractPURPOSE. We evaluated the potential of dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) as a noninvasive biomarker of choroidal neovascularization (CNV) and its utility as a tool for monitoring therapeutic response in laser-induced rat CNV models.METHODS. CNV was induced in the right eyes of 14 rats using a laser. Rats (n = 7) were treated daily for 14 days with a candidate drug (KR-31831, 50 mg/kg of body weight) having antiangiogenic effects, whereas control rats (n - 7) were treated with the vehicle alone (10% cremophor, 10% absolute ethyl alcohol, and 80% saline). DCE-MRI examinations were performed on the day before surgery (D - 1), and 3, 7, and 14 days after surgery (D + 3, D + 7, and D + 14), from which pharmacokinetic parameters (K-trans, v(e), v(p)) were calculated. Angiography was performed to visualize CNV using FITC-labeled high molecular weight dextran after MRI on D + 14. The paired Wilcoxon test and Mann-Whitney U test were performed for statistical analysis.RESULTS. The K-trans and v(e) values of the CNV-induced right eyes were significantly higher than those of the intact eyes in control rats at D+14 (P < 0.05). In the CNV-induced eyes, the relative K-trans and v(e) values of the KR-31831-treated group were significantly lower than those of the nontreated group at D + 14 (P < 0.05). The angiography showed that decreased CNV was observed in rats treated with KR-31831.CONCLUSIONS. Quantitative DCE-MRI produces noninvasive biomarker of CNV, thus allowing monitoring of therapeutic response of antiangiogenic drugs in neovascular age-related macular degeneration (AMD). (Invest Ophthalmol Vis Sci. 2012;53:7693-7700) DOI:10.1167/iovs.12-9805en_US
dc.description.sponsorshipSupported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science, and Technology (2011-0031520 and 2010-0023606).en_US
dc.language.isoenen_US
dc.publisherASSOC RESEARCH VISION OPHTHALMOLOGY INCen_US
dc.subjectBLOOD-RETINAL BARRIERen_US
dc.subjectANTIANGIOGENIC AGENT KR-31831en_US
dc.subjectMACULAR DEGENERATIONen_US
dc.subjectPARAMETERSen_US
dc.subjectANGIOGENESISen_US
dc.subjectPERMEABILITYen_US
dc.subjectBEVACIZUMABen_US
dc.subjectMACULOPATHYen_US
dc.subjectTUMORSen_US
dc.subjectDTPAen_US
dc.titleDynamic Contrast-Enhanced MRI for Assessing Therapeutic Response of Choroidal Neovascularization in a Rat Modelen_US
dc.typeArticleen_US
dc.relation.no12-
dc.relation.volume53-
dc.identifier.doi10.1167/iovs.12-9805-
dc.relation.page7693-7700-
dc.relation.journalINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE-
dc.contributor.googleauthorKim, Jae-Hun-
dc.contributor.googleauthorIm, Geun Ho-
dc.contributor.googleauthorYoon, Jaemoon-
dc.contributor.googleauthorYang, Jehoon-
dc.contributor.googleauthorChung, Julius Juhyun-
dc.contributor.googleauthorCha, Ji Hoon-
dc.contributor.googleauthorHam, Don-il-
dc.contributor.googleauthorLee, Jung Hee-
dc.contributor.googleauthorKim, Sun I-
dc.relation.code2012204427-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDIVISION OF ELECTRICAL AND BIOMEDICAL ENGINEERING-
dc.identifier.pidsunkim-
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COLLEGE OF ENGINEERING[S](공과대학) > ELECTRICAL AND BIOMEDICAL ENGINEERING(전기·생체공학부) > Articles
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