He Jiang, Feng Jinjin, Su Yang, Seo Youngho, Liu Bin
Department of Radiology and Medical Imaging, University of Virginia, Charlottesville, Virginia 22908, United States.
Department of Radiology and Biomedical Imaging, University of California, San Francisco, California 94143, United States.
Bioconjug Chem. 2020 Jul 15;31(7):1750-1755. doi: 10.1021/acs.bioconjchem.0c00319. Epub 2020 Jul 6.
Single chain antibody fragment (scFv) is a promising agent for imaging and targeted therapy. The objective of the study is to evaluate a kit formulation for Tc labeling of scFv for tumor imaging. The scFv was engineered to contain a cysteine tag to accommodate the specific conjugation of HYNIC and subsequent Tc labeling. The labeling conditions were formulated to allow instantaneous one-pot quantitative labeling. The reproducibility of labeling was evaluated at various time points during kit storage at -20 °C. In vitro cell binding experiments and HPLC analysis were performed to assess binding affinity and radiolabel stability, respectively. In vivo tumor targeting study was performed in xenograft models with biodistribution studied at 1, 3, and 24 h post-injection. The optimized kit with 5 μg SnF, pH 5.5, and 50 μg GH along with as low as 15 μg of HYNIC-cys-scFv provided high labeling yield (>95%), high specific activity (1.8 × 10 Ci/Mol), and robust reproducibility with shelf life up to 90 days when stored at -20 °C. The in vitro cell binding study showed the labeled scFv maintained the binding capability with an apparent of ∼27 nM. The animal study using tumor-bearing mice showed high tumor uptake at 16.9%ID/g 24 h post-injection along with rapid blood clearance (0.18%ID/g) and kidney excretion (44%ID/g), resulting in very high contrast (tumor/muscle >200:1). A kit formulation for Tc labeling of scFvs targeting mesothelioma was developed based on specific HYNIC conjugation and GH (Glucoheptonate) as a coligand, producing not only high specific activity, but also improved tumor uptake. This convenient one-pot labeling method has the potential for translation into clinical use and is applicable to other scFvs as well.
单链抗体片段(scFv)是一种用于成像和靶向治疗的有前景的药物。本研究的目的是评估一种用于肿瘤成像的scFv的锝标记试剂盒配方。对scFv进行工程改造,使其包含一个半胱氨酸标签,以适应HYNIC的特异性偶联及随后的锝标记。制定标记条件以实现即时一锅法定量标记。在试剂盒于-20°C储存的不同时间点评估标记的重现性。分别进行体外细胞结合实验和高效液相色谱分析,以评估结合亲和力和放射性标记稳定性。在异种移植模型中进行体内肿瘤靶向研究,并在注射后1、3和24小时研究生物分布。优化后的试剂盒含有5μg SnF、pH 5.5、50μg葡庚糖酸盐(GH)以及低至15μg的HYNIC-半胱氨酸-scFv,提供了高标记产率(>95%)、高比活度(1.8×10 Ci/mol),并且在-20°C储存时具有高达90天的保质期,重现性良好。体外细胞结合研究表明,标记后的scFv保持了结合能力,表观解离常数约为27 nM。使用荷瘤小鼠的动物研究表明,注射后24小时肿瘤摄取率高,为16.9%ID/g,同时血液清除迅速(0.18%ID/g),肾脏排泄率为(44%ID/g),从而产生非常高的对比度(肿瘤/肌肉>200:1)。基于特定的HYNIC偶联和作为共配体的葡庚糖酸盐(GH),开发了一种用于靶向间皮瘤的scFv的锝标记试剂盒配方,不仅产生了高比活度,还提高了肿瘤摄取。这种便捷的一锅法标记方法有转化为临床应用的潜力,并且也适用于其他scFv。