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首页> 外文期刊>Nuclear Medicine and Biology >Kit-like 18F-labeling of RGD-19F-Arytrifluroborate in high yield and at extraordinarily high specific activity with preliminary in vivo tumor imaging
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Kit-like 18F-labeling of RGD-19F-Arytrifluroborate in high yield and at extraordinarily high specific activity with preliminary in vivo tumor imaging

机译:初步体内肿瘤显像的试剂盒样18F-标记的RGD-19F-三氟硼酸高产率,高比活

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摘要

Introduction: Positron Emission Tomography (PET) is a rapidly expanding, cutting edge technology for preclinical evaluation, cancer diagnosis and staging, and patient management. A one-step aqueous 18F-labeling method, which can be applied to peptides to provide functional in vivo images, has been a long-standing challenge in PET imaging. Over the past few years, we have sought a rapid and mild radiolabeling method based on the aqueous radiosynthesis of in vivo stable aryltrifluoroborate (ArBF3 -) conjugates. Recent access to production levels of 18F-Fluoride led to a fluorescent-18F-ArBF3 - at unprecedentedly high specific activities of 15Ci/μmol. However, extending this method to labeling peptides as imaging agents has not been explored. Methods: In order to extend these results to a peptide of clinical interest in the context of production-level radiosynthesis, we applied this new technology for labeling RGD, measured its specific activity by standard curve analysis, and carried out a preliminary evaluation of its imaging properties. Results: RGD was labeled in excellent radiochemical yields at exceptionally high specific activity (~. 14. Ci/μmol) (n = 3). Preliminary tumor-specific images corroborated by ex vivo biodistribution data with blocking controls show statistically significant albeit relatively low tumor uptake along with reasonably high tumor:blood ratios (n = 3). Conclusions: Isotope exchange on a clinically useful 18F-ArBF3 - radiotracer leads to excellent radiochemical yields and exceptionally high specific activities while the anionic nature of the aryltrifluoroborate prosthetic results in very rapid clearance. Since rapid clearance of the radioactive tracer is generally desirable for tracer development, these results suggest new directions for varying linker arm composition to slightly retard clearance rather than enhancing it. Advances in Knowledge and Implications for patient Care: This work is the first to use production levels of 18F-activity to directly label RGD at specific activities that are an order of magnitude higher than most reports and thereby increases the distribution window for radiotracer production and delivery.
机译:简介:正电子发射断层扫描(PET)是一种快速扩展的尖端技术,用于临床前评估,癌症诊断和分期以及患者管理。一步法18F水性标记方法可应用于肽以提供功能性体内图像,这一直是PET成像领域的长期挑战。在过去的几年中,我们已经基于体内稳定的三氟硼酸芳基酯(ArBF3-)缀合物的水性放射性合成,寻求了一种快速且温和的放射性标记方法。最近获得的18F-氟化物生产水平导致了荧光18F-ArBF3-前所未有的高比活度15Ci /μmol。然而,尚未探索将该方法扩展至将肽标记为显像剂。方法:为了将这些结果扩展到在生产水平放射合成的背景下具有临床意义的肽,我们应用了这项新技术来标记RGD,通过标准曲线分析测量其比活,并对其成像进行了初步评估属性。结果:RGD以极高的比活(〜。14. Ci /μmol)(n = 3)以出色的放射化学产率标记。尽管有相对较低的肿瘤摄取率和相当高的肿瘤:血液比例(n = 3),但由离体生物分布数据和阻断剂对照证实的初步肿瘤特异性图像显示出统计学意义。结论:在临床上有用的18F-ArBF3-放射性示踪剂上进行同位素交换可导致出色的放射化学收率和异常高的比活,而芳基三氟硼酸酯假体的阴离子性质可实现非常快速的清除。由于放射性示踪剂的快速清除通常是示踪剂开发所希望的,因此这些结果提出了改变连接臂组成以稍微延迟清除而不是增加清除的新方向。知识进步和对患者护理的意义:这项工作是第一个使用18F活性生产水平直接在比大多数报告高一个数量级的特定活动上标记RGD的方法,从而增加了放射性示踪剂生产和交付的分布范围。

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