Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
ACS Nano. 2012 Jun 26;6(6):5209-19. doi: 10.1021/nn300974s. Epub 2012 May 8.
A novel strategy based on metal-free "click" chemistry was developed for the copper-64 radiolabeling of the core in shell-cross-linked nanoparticles (SCK-NPs). Compared with Cu(I)-catalyzed click chemistry, this metal-free strategy provides the following advantages for Cu-64 labeling of the core of SCK-NPs: (1) elimination of copper exchange between nonradioactive Cu in the catalyst and DOTA-chelated Cu-64; (2) elimination of the internal click reactions between the azide and acetylene groups in the same NPs; and (3) increased efficiency of the click reaction because water-soluble Cu(I) does not need to reach the hydrophobic core of the NPs. When 50 mCi Cu-64 was used for the radiolabeling, the specific activity of the radiolabeled product was 975 Ci/μmol at the end of synthesis, which represents the attachment of ca. 500 Cu-64 atoms per SCK-NP, giving in essence a 500-fold amplification of specific activity of the NP over that of the Cu-64 chelate. To the best of our knowledge, this is the highest specific activity obtained for Cu-64-labeled nanoparticles.
一种基于无金属“点击”化学的新策略被开发用于壳交联纳米颗粒(SCK-NPs)内核的铜-64 放射性标记。与 Cu(I)-催化的点击化学相比,这种无金属策略为 SCK-NPs 内核的 Cu-64 标记提供了以下优势:(1)消除了催化剂中非放射性 Cu 与 DOTA 螯合的 Cu-64 之间的铜交换;(2)消除了同一 NPs 中叠氮化物和乙炔基之间的内部点击反应;(3)由于不需要水相溶性的 Cu(I) 到达 NPs 的疏水核心,因此点击反应的效率提高。当使用 50 mCi 的 Cu-64 进行放射性标记时,放射性标记产物的比活度在合成结束时达到 975 Ci/μmol,这代表每个 SCK-NP 上约附着 500 个 Cu-64 原子,实质上使 NP 的比活度相对于 Cu-64 螯合物提高了 500 倍。据我们所知,这是获得的铜-64 标记纳米颗粒的最高比活度。