Division of Imaging Sciences & Biomedical Engineering, King's College London, Thomas' Hospital, London, UK.
Bioconjug Chem. 2011 Mar 16;22(3):455-65. doi: 10.1021/bc100483k. Epub 2011 Feb 21.
The combination of radionuclide-based imaging modalities such as single photon emission computed tomography (SPECT) and positron emission tomography (PET) with magnetic resonance imaging (MRI) is likely to become the next generation of clinical scanners. Hence, there is a growing interest in the development of SPECT- and PET-MRI agents. To this end, we report a new class of dual-modality imaging agents based on the conjugation of radiolabeled bisphosphonates (BP) directly to the surface of superparamagnetic iron oxide (SPIO) nanoparticles. We demonstrate the high potential of BP-iron oxide conjugation using (⁹⁹m)Tc-dipicolylamine(DPA)-alendronate, a BP-SPECT agent, and Endorem/Feridex, a liver MRI contrast agent based on SPIO. The labeling of SPIOs with (⁹⁹m)Tc-DPA-alendronate can be performed in one step at room temperature if the SPIO is not coated with an organic polymer. Heating is needed if the nanoparticles are coated, as long as the coating is weakly bound as in the case of dextran in Endorem. The size of the radiolabeled Endorem (⁹⁹m)Tc-DPA-ale-Endorem) was characterized by TEM (5 nm, Fe₃O₄ core) and DLS (106 ± 60 nm, Fe₃O₄ core + dextran). EDX, Dittmer-Lester, and radiolabeling studies demonstrate that the BP is bound to the nanoparticles and that it binds to the Fe₃O₄ cores of Endorem, and not its dextran coating. The bimodal imaging capabilities and excellent stability of these nanoparticles were confirmed using MRI and nanoSPECT-CT imaging, showing that (⁹⁹m)Tc and Endorem co-localize in the liver and spleen In Vivo, as expected for particles of the composition and size of (⁹⁹m)Tc-DPA-ale-Endorem. To the best of our knowledge, this is the first example of radiolabeling SPIOs with BP conjugates and the first example of radiolabeling SPIO nanoparticles directly onto the surface of the iron oxide core, and not its coating. This work lays down the basis for a new generation of SPECT/PET-MR imaging agents in which the BP group could be used to attach functionality to provide targeting, stealth/stability, and radionuclides to Fe₃O₄ nanoparticles using very simple methodology readily amenable to GMP.
基于放射性核素的成像方式(如单光子发射计算机断层扫描[SPECT]和正电子发射断层扫描[PET])与磁共振成像[MRI]的结合,可能成为下一代临床扫描仪。因此,人们对开发 SPECT 和 PET-MRI 造影剂越来越感兴趣。为此,我们报告了一类基于放射性标记双膦酸盐(BP)直接偶联到超顺磁氧化铁(SPIO)纳米粒子表面的新型双模成像剂。我们使用(99m)Tc-二吡啶甲酰胺(DPA)-阿仑膦酸盐(一种 BP-SPECT 试剂)和 Endorem/Feridex(一种基于 SPIO 的肝 MRI 造影剂)证明了 BP-氧化铁偶联的高潜力。如果 SPIO 没有用有机聚合物包裹,则可以在室温下一步完成 SPIO 与(99m)Tc-DPA-阿仑膦酸盐的标记。如果纳米粒子被包裹,则需要加热,只要涂层像 Endorem 中的葡聚糖一样弱结合即可。放射性标记的 Endorem(99m)Tc-DPA-ale-Endorem)的大小通过 TEM(5nm,Fe3O4核心)和 DLS(106±60nm,Fe3O4核心+葡聚糖)进行表征。EDX、Dittmer-Lester 和放射性标记研究表明,BP 与纳米粒子结合,并与 Endorem 的 Fe3O4 核心结合,而不是其葡聚糖涂层。通过 MRI 和纳米 SPECT-CT 成像证实了这些纳米粒子的双模态成像能力和优异的稳定性,表明(99m)Tc 和 Endorem 在体内肝和脾中共同定位,正如预期的那样,对于(99m)Tc-DPA-ale-Endorem 的组成和大小的颗粒。据我们所知,这是首例用 BP 缀合物标记 SPIO 的实例,也是首例直接在氧化铁核表面而不是其涂层上标记 SPIO 纳米粒子的实例。这项工作为新一代 SPECT/PET-MRI 造影剂奠定了基础,其中 BP 基团可用于通过非常简单的方法将功能附着到 Fe3O4 纳米粒子上,提供靶向性、隐身/稳定性和放射性核素,这些方法很容易适用于 GMP。