首页> 外文OA文献 >Pre-concentration of positron-emitting 18Ffluoride and radiosynthesis of fluoride-based prosthetic compounds for PET imaging using magnetic droplet microfluidics (MDM)
【2h】

Pre-concentration of positron-emitting 18Ffluoride and radiosynthesis of fluoride-based prosthetic compounds for PET imaging using magnetic droplet microfluidics (MDM)

机译:使用磁滴微流控技术(MDM)进行正电子发射18F氟化物的预浓缩和放射性合成的基于氟的辅料,用于PET成像

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The radioisotope 18F is often considered the best choice for PET imaging, owing to its desirable chemical and radiochemical properties. However, nucleophilic 18F fluorination of large, water soluble biomolecules, based on C-F bond formation, has been difficult. Thus, several aqueous fluorination approach have been developed which offers significant development in radiopharmaceutical synthesis. Furthermore, since 18F decays rapidly, production of these 18F-labelled compounds requires an automated process to reduce production time, reduce radiation exposure and also minimize transfer of reagents during tracer synthesis to reduce sample transfer loss. Herein, a method called magnetic droplet microfluidics (MDM) has been developed which aims to conduct [18F]fluoride pre-concentration and synthesis of 18F-labeled compound on a microfluidic platform. Using this method, we have demonstrated 18F pre-concentration in a small-volume droplet through the use of anion exchanging magnetic particles. By using MDM, the pre-concentration step took approximately 5 min. and the [18F]fluoride solution was pre-concentrated by 15-fold from a volume of 1 mL to 0.05 mL. After the pre-concentration step, an 18F-labelling reaction was performed on the MDM platform using the S-F bond formation in aqueous conditions to produce an arylsulfonyl [18F]fluoride which can be used as a prosthetic group to label PET targeting ligands. The high radiochemical purity of 95 ± 1% was comparable with 96% which was previously reported using conventional method. In addition, when using MDM, the total synthesis time was improved to 15 min. with lower reagent volumes (50-60 µL) used. The MDM method was also used to produce an 18F-labelled aryltrifluoroborate through B-F bond formation. The synthesis of aryltrifluoroborate compound at low activities (~5 mCi), gave radiochemical purities which were low for both MDM (5.8%) and conventional method (6.0%).
机译:放射性同位素18F由于其理想的化学和放射化学特性,通常被认为是PET成像的最佳选择。然而,基于C-F键形成的大型水溶性生物分子的亲核18F氟化很难。因此,已经开发了几种水性氟化方法,这些方法在放射性药物合成中提供了重要的发展。此外,由于18F迅速衰减,因此这些18F标记的化合物的生产需要自动化的过程以减少生产时间,减少辐射暴露并在示踪剂合成过程中使试剂的转移最小化以减少样品转移损失。在本文中,已经开发了一种称为磁滴微流体(MDM)的方法,该方法旨在在微流体平台上进行[18F]氟化物的预浓缩和18F标记化合物的合成。使用这种方法,我们已通过使用阴离子交换磁性颗粒证明了小体积液滴中18 F的预浓缩。通过使用MDM,预浓缩步骤大约需要5分钟。将[18F]氟化物溶液从1 mL的体积预浓缩15倍至0.05 mL。在预浓缩步骤之后,在水性条件下使用S-F键形成在MDM平台上进行18F标记反应,生成芳基磺酰基[18F]氟化物,该基团可以用作辅基来标记PET靶向配体。 95±1%的高放射化学纯度与以前使用常规方法报道的96%相当。此外,使用MDM时,总合成时间缩短到15分钟。使用较低的试剂量(50-60 µL)。 MDM方法还用于通过B-F键形成来生产18F标记的芳基三氟硼酸酯。低活性(〜5 mCi)的芳基三氟硼酸酯化合物的合成产生的放射化学纯度对于MDM(5.8%)和常规方法均较低(6.0%)。

著录项

  • 作者

    Fiel Somewhere Albacite;

  • 作者单位
  • 年度 2014
  • 总页数
  • 原文格式 PDF
  • 正文语种
  • 中图分类

相似文献

  • 外文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号