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基于(64)铜和(68)镓的叶酸受体阳性肿瘤的正电子发射断层显像:白蛋白结合型NODAGA-叶酸的研发与评估

(64)Cu- and (68)Ga-Based PET Imaging of Folate Receptor-Positive Tumors: Development and Evaluation of an Albumin-Binding NODAGA-Folate.

作者信息

Farkas Renáta, Siwowska Klaudia, Ametamey Simon M, Schibli Roger, van der Meulen Nicholas P, Müller Cristina

机构信息

Center for Radiopharmaceutical Sciences ETH-PSI-USZ, Paul Scherrer Institut , Villigen-PSI, Switzerland.

Department of Chemistry and Applied Biosciences, ETH Zurich , Zurich, Switzerland.

出版信息

Mol Pharm. 2016 Jun 6;13(6):1979-87. doi: 10.1021/acs.molpharmaceut.6b00143. Epub 2016 May 4.

Abstract

A number of folate-based radioconjugates have been synthesized and evaluated for nuclear imaging purposes of folate receptor (FR)-positive tumors and potential therapeutic application. A common shortcoming of radiofolates is, however, a significant accumulation of radioactivity in the kidneys. This situation has been faced by modifying the folate conjugate with an albumin-binding entity to increase the circulation time of the radiofolate, which led to significantly improved tumor-to-kidney ratios. The aim of this study was to develop an albumin-binding folate conjugate with a NODAGA-chelator (rf42) for labeling with (64)Cu and (68)Ga, allowing application for PET imaging. The folate conjugate rf42 was synthesized in 8 steps, with an overall yield of 5%. Radiolabeling with (64)Cu and (68)Ga was carried out at room temperature within 10 min resulting in (64)Cu-rf42 and (68)Ga-rf42 with >95% radiochemical purity. (64)Cu-rf42 and (68)Ga-rf42 were stable (>95% intact) in phosphate-buffered saline over more than 4 half-lives of the corresponding radionuclide. In vitro, the plasma protein-bound fraction of (64)Cu-rf42 and (68)Ga-rf42 was determined to be >96%. Cell experiments proved FR-specific uptake of both radiofolates, as it was reduced to <1% when KB tumor cells were coincubated with excess folic acid. In vivo, high accumulation of (64)Cu-rf42 and (68)Ga-rf42 was found in KB tumors of mice (14.52 ± 0.99% IA/g and 11.92 ± 1.68% IA/g, respectively) at 4 h after injection. The tumor-to-kidney ratios were in the range of 0.43-0.55 over the first 4 h of investigation. At later time points (up to 72 h p.i. of (64)Cu-rf42) the tumor-to-kidney ratio increased to 0.73. High-quality PET/CT images were obtained 2 h after injection of (64)Cu-rf42 and (68)Ga-rf42, respectively, allowing distinct visualization of tumors and kidneys. Comparison of PET/CT images obtained with (64)Cu-rf42 and a (64)Cu-labeled DOTA-folate conjugate (cm10) clearly proved the superiority of NODAGA for stable coordination of (64)Cu. (64)Cu-cm10 showed high liver uptake, most probably as a consequence of released (64)Cu(2+). The data reported in this study clearly proved the promising features of (64)Cu-rf42, particularly in terms of favorable tumor-to-kidney ratios. The relatively long half-life of (64)Cu (T1/2 = 12.7 h) matches well with the enhanced circulation time of the albumin-binding NODAGA-folate, allowing PET imaging at longer time points after injection than is possible when using (68)Ga (T1/2 = 68 min).

摘要

已经合成了多种基于叶酸的放射性缀合物,并对其进行评估,用于叶酸受体(FR)阳性肿瘤的核成像以及潜在的治疗应用。然而,放射性叶酸的一个常见缺点是肾脏中放射性的大量蓄积。通过用白蛋白结合实体修饰叶酸缀合物以延长放射性叶酸的循环时间,解决了这一问题,这使得肿瘤与肾脏的比值得到显著改善。本研究的目的是开发一种与NODAGA螯合剂结合的白蛋白结合叶酸缀合物(rf42),用于用(64)Cu和(68)Ga进行标记,以便应用于PET成像。叶酸缀合物rf42通过8步合成,总产率为5%。在室温下10分钟内用(64)Cu和(68)Ga进行放射性标记,得到放射化学纯度>95%的(64)Cu-rf42和(68)Ga-rf42。(64)Cu-rf42和(68)Ga-rf42在磷酸盐缓冲盐水中超过相应放射性核素的4个半衰期保持稳定(>95%完整)。在体外,(64)Cu-rf42和(68)Ga-rf42与血浆蛋白结合的部分测定为>96%。细胞实验证明两种放射性叶酸均有FR特异性摄取,当KB肿瘤细胞与过量叶酸共同孵育时,摄取率降至<1%。在体内,注射后4小时,在小鼠的KB肿瘤中发现(64)Cu-rf42和(68)Ga-rf42有高蓄积(分别为14.52±0.99%IA/g和11.92±1.68%IA/g)。在研究的前4小时内,肿瘤与肾脏的比值在0.43 - 0.55范围内。在稍后的时间点(注射(64)Cu-rf42后长达72小时),肿瘤与肾脏的比值增加到0.73。分别在注射(64)Cu-rf42和(68)Ga-rf42后2小时获得高质量的PET/CT图像,能够清晰地显示肿瘤和肾脏。用(64)Cu-rf42和(64)Cu标记的DOTA-叶酸缀合物(cm10)获得的PET/CT图像比较清楚地证明了NODAGA对(64)Cu稳定配位的优越性。(64)Cu-cm10显示出高肝脏摄取,很可能是释放的(64)Cu(2+)导致的。本研究报告的数据清楚地证明了(64)Cu-rf42的良好特性,特别是在有利的肿瘤与肾脏比值方面。(64)Cu相对较长的半衰期(T1/2 = 12.7小时)与白蛋白结合的NODAGA-叶酸延长的循环时间非常匹配,使得在注射后比使用(68)Ga(T1/2 = 68分钟)更长的时间点进行PET成像成为可能。

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