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首页> 外文期刊>Iranian Journal of Radiology >Ocular Biodistribution of 89Zr-Bevacizumab in New Zealand Rabbits Determined Using PET/MRI: A Feasibility Study (NUCLEAR MEDICINE)
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Ocular Biodistribution of 89Zr-Bevacizumab in New Zealand Rabbits Determined Using PET/MRI: A Feasibility Study (NUCLEAR MEDICINE)

机译:PET / MRI测定89Zr-贝伐单抗在新西兰兔眼中的生物分布:一项可行性研究(核医学)

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Background: Despite studies on positron emission tomography/magnetic resonance imaging (PET/MRI) in oncological imaging with high soft-tissue contrast resolution, PET/MRI has not been studied in ophthalmology. 89Zr-bevacizumab, designed as a probe for PET, targets vascular endothelial growth factor, which is highly expressed in ocular angiogenesis. Intravitreal injections of bevacizumab agents have curative effects on ocular disease. Objectives: To study the ocular biodistribution of 89Zr-bevacizumab in New Zealand rabbits using PET/MRI. Materials and Methods: 89Zr-bevacizumab, synthesized from conjugated bevacizumab and 89Zr-oxalate, and the purity of radiolabeled antibodies were determined using radio high-performance liquid chromatography (radio-HPLC). Instant thin-layer chromatography (ITLC) was utilized to differentiate the labeled product from aggregates and unlabeled 89Zr. 89Zr-bevacizumab was injected 2 mm from the left limbus into the vitreous humor of six normal New Zealand white rabbits. Micro-PET was utilized for dynamic imaging from 5 minutes to 60 minutes postinjection and for static imaging at 4 hours, 24 hours, 48 hours, 120 hours, and 144 hours (10-minutes scans) postinjection. PET/MRI scans were fused using PMOD software. Results: 89Zr-bevacizumab with a radiochemical purity of 93. 21% was monitored via PET imaging. Radioactivity levels in the eyes plateaued approximately 5 minutes after administration of 89Zr-bevacizumab, and the measured vitreous values decreased from 340. 52 41. 6% injected dose (ID)/g to 21. 53 3. 39%ID/g by 144 hours. The half-life of the drug in the eye was calculated for 84. 25 hours. Conclusion: 89Zr-bevacizumab could be monitored in animals by PET imaging, and the radiolabel exhibited high sensitivity in the vitreous body. Radioactivity levels in the eyes plateaued approximately 5 minutes after administration. This study clearly demonstrates the biodistribution of 89Zr-bevacizumab.
机译:背景:尽管在具有高软组织对比度分辨率的肿瘤成像中对正电子发射断层扫描/磁共振成像(PET / MRI)进行了研究,但尚未在眼科领域研究PET / MRI。设计为PET探针的89Zr-贝伐单抗靶向血管内皮生长因子,该因子在眼血管生成中高度表达。玻璃体内注射贝伐单抗药物可治疗眼部疾病。目的:利用PET / MRI技术研究89Zr-贝伐单抗在新西兰兔眼中的生物分布。材料与方法:由缀合的贝伐单抗和89Zr-草酸酯合成的89Zr-贝伐单抗,使用放射高效液相色谱法(radio-HPLC)测定放射性标记抗体的纯度。利用即时薄层色谱(ITLC)将标记的产物与聚集体和未标记的89Zr进行区分。将89Zr-贝伐单抗从左边缘起2 mm处注射入六只正常新西兰白兔的玻璃体液中。 Micro-PET用于注射后5分钟到60分钟的动态成像,以及注射后4小时,24小时,48小时,120小时和144小时(10分钟扫描)的静态成像。使用PMOD软件融合PET / MRI扫描。结果:通过PET成像监测了89Zr-贝伐单抗的放射化学纯度为93. 21%。服用89Zr-贝伐单抗后约5分钟,眼睛的放射性水平趋于稳定,玻璃体测量值从340. 52 41. 6%注射剂量(ID)/ g降低至21. 53 3. 39%ID / g 144小时。计算出该药物在眼睛中的半衰期为84. 25小时。结论:PET显像可监测动物体内的89Zr-贝伐单抗,放射性标记对玻璃体具有较高的敏感性。给药后约5分钟,眼睛的放射性水平趋于稳定。这项研究清楚地证明了89Zr-贝伐单抗的生物分布。

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