Severin Gregory W, Jørgensen Jesper T, Wiehr Stefan, Rolle Anna-Maria, Hansen Anders E, Maurer Andreas, Hasenberg Mike, Pichler Bernd, Kjær Andreas, Jensen Andreas I
The Hevesy Laboratory, DTU Nutech, Technical University of Denmark; Center for Nanomedicine and Theranostics, Technical University of Denmark.
Dept. of Clinical Physiology, Nuclear Medicine & PET, Rigshospitalet and Cluster for Molecular Imaging, Faculty of Health Science, University of Copenhagen, Denmark.
Nucl Med Biol. 2015 Apr;42(4):360-8. doi: 10.1016/j.nucmedbio.2014.11.005. Epub 2014 Nov 22.
Preclinical studies involving (89)Zr often report significant bone accumulation, which is associated with dissociation of the radiometal from the tracer. However, experiments determining the uptake of unbound (89)Zr in disease models are not performed as routine controls. The purpose of the present study was to investigate the impact of free or weakly bound (89)Zr on PET quantifications in disease models, in order to determine if such control experiments are warranted.
Chemical studies were carried out to find a (89)Zr compound that would solubilize the (89)Zr as a weak chelate, thus mimicking free or weakly bound (89)Zr released in circulation. (89)Zr oxalate had the desired characteristics, and was injected into mice bearing FaDu and HT29 solid tumor xenografts, and mice infected in the lungs with the mold Aspergillus fumigatus, as well as in healthy controls (naïve). PET/CT or PET/MR imaging followed to quantify the distribution of the radionuclide in the disease models.
(89)Zr oxalate was found to have a plasma half-life of 5.1 ± 2.3 h, accumulating mainly in the bones of all animals. Both tumor types accumulated (89)Zr on the order of 2-4 %ID/cm(3), which is comparable to EPR-mediated accumulation of certain species. In the aspergillosis model, the concentration of (89)Zr in lung tissue of the naïve animals was 6.0 ± 1.1 %ID/g. This was significantly different from that of the animals with advanced disease, showing 11.6 ± 1.8 %ID/g.
Given the high levels of (89)Zr accumulation in the disease sites in the present study, we recommend control experiments mapping the biodistribution of free (89)Zr in any preclinical study employing (89)Zr where bone uptake is observed. Aqueous (89)Zr oxalate appears to be a suitable compound for such studies. This is especially relevant in studies where the tracer accumulation is based upon passive targeting, such as EPR.
涉及(89)Zr的临床前研究经常报告有显著的骨聚集,这与放射性金属从示踪剂中的解离有关。然而,在疾病模型中确定未结合的(89)Zr摄取的实验并未作为常规对照进行。本研究的目的是调查游离或弱结合的(89)Zr对疾病模型中PET定量的影响,以确定是否需要进行此类对照实验。
进行化学研究以找到一种能将(89)Zr作为弱螯合物溶解的(89)Zr化合物,从而模拟循环中释放的游离或弱结合的(89)Zr。草酸(89)Zr具有所需特性,并被注射到携带FaDu和HT29实体瘤异种移植的小鼠、肺部感染烟曲霉的小鼠以及健康对照(未处理)中。随后进行PET/CT或PET/MR成像以量化疾病模型中放射性核素的分布。
发现草酸(89)Zr的血浆半衰期为5.1±2.3小时,主要积聚在所有动物的骨骼中。两种肿瘤类型摄取(89)Zr的量约为2-4%ID/cm³,这与某些物质通过增强渗透滞留(EPR)介导的摄取相当。在曲霉病模型中,未处理动物肺组织中(89)Zr的浓度为6.0±1.1%ID/g。这与晚期疾病动物的浓度有显著差异,晚期疾病动物的浓度为11.6±1.8%ID/g。
鉴于本研究中疾病部位(89)Zr的高积聚水平,我们建议在任何观察到骨摄取的使用(89)Zr的临床前研究中进行对照实验,以绘制游离(89)Zr的生物分布。草酸(89)Zr水溶液似乎是进行此类研究的合适化合物。这在示踪剂积聚基于被动靶向(如EPR)的研究中尤为重要。