Graves Stephen A, Hernandez Reinier, Fonslet Jesper, England Christopher G, Valdovinos Hector F, Ellison Paul A, Barnhart Todd E, Elema Dennis R, Theuer Charles P, Cai Weibo, Nickles Robert J, Severin Gregory W
Technical University of Denmark , Center for Nuclear Technologies, 4000 Roskilde, Denmark.
TRACON Pharmaceuticals , San Diego, California 92122, United States.
Bioconjug Chem. 2015 Oct 21;26(10):2118-24. doi: 10.1021/acs.bioconjchem.5b00414. Epub 2015 Sep 10.
(52)Mn (t1/2 = 5.59 d, β(+) = 29.6%, Eβave = 0.24 MeV) shows promise in positron emission tomography (PET) and in dual-modality manganese-enhanced magnetic resonance imaging (MEMRI) applications including neural tractography, stem cell tracking, and biological toxicity studies. The extension to bioconjugate application requires high-specific-activity (52)Mn in a state suitable for macromolecule labeling. To that end a (52)Mn production, purification, and labeling system is presented, and its applicability in preclinical, macromolecule PET is shown using the conjugate (52)Mn-DOTA-TRC105. (52)Mn is produced by 60 μA, 16 MeV proton irradiation of natural chromium metal pressed into a silver disc support. Radiochemical separation proceeds by strong anion exchange chromatography of the dissolved Cr target, employing a semiorganic mobile phase, 97:3 (v:v) ethanol:HCl (11 M, aqueous). The method is 62 ± 14% efficient (n = 7) in (52)Mn recovery, leading to a separation factor from Cr of (1.6 ± 1.0) × 10(6) (n = 4), and an average effective specific activity of 0.8 GBq/μmol (n = 4) in titration against DOTA. (52)Mn-DOTA-TRC105 conjugation and labeling demonstrate the potential for chelation applications. In vivo images acquired using PET/CT in mice bearing 4T1 xenograft tumors are presented. Peak tumor uptake is 18.7 ± 2.7%ID/g at 24 h post injection and ex vivo (52)Mn biodistribution validates the in vivo PET data. Free (52)Mn(2+) (as chloride or acetate) is used as a control in additional mice to evaluate the nontargeted biodistribution in the tumor model.
(半衰期 t1/2 = 5.59 天,β(+) = 29.6%,平均β能量 Eβave = 0.24 兆电子伏特)在正电子发射断层扫描(PET)以及双模态锰增强磁共振成像(MEMRI)应用中显示出前景,这些应用包括神经纤维束成像、干细胞追踪和生物毒性研究。将其扩展到生物共轭应用需要处于适合大分子标记状态的高比活度(52)Mn。为此,本文介绍了一种(52)Mn 的生产、纯化和标记系统,并使用共轭物(52)Mn-DOTA-TRC105 展示了其在临床前大分子 PET 中的适用性。(52)Mn 通过以 60 微安、16 兆电子伏特的质子辐照压制在银盘载体中的天然铬金属来生产。通过对溶解的铬靶进行强阴离子交换色谱法进行放射化学分离,采用半有机流动相,97:3(体积比)乙醇:盐酸(11 摩尔/升,水溶液)。该方法在(52)Mn 回收方面的效率为 62 ± 14%(n = 7),与铬的分离因子为(1.6 ± 1.0)× 10(6)(n = 4),在与 DOTA 滴定中平均有效比活度为 0.8 吉贝可/微摩尔(n = 4)。(52)Mn-DOTA-TRC105 的共轭和标记证明了螯合应用的潜力。展示了在携带 4T1 异种移植肿瘤的小鼠中使用 PET/CT 获取的体内图像。注射后 24 小时肿瘤摄取峰值为 18.7 ± 2.7%注射剂量/克,离体(52)Mn 生物分布验证了体内 PET 数据。游离的(52)Mn(2+)(以氯化物或乙酸盐形式)在另外的小鼠中用作对照,以评估肿瘤模型中的非靶向生物分布。