Department of Radiology, School of Medicine, Emory University, Atlanta, GA 30322, USA.
Bioorg Med Chem Lett. 2010 Apr 1;20(7):2140-3. doi: 10.1016/j.bmcl.2010.02.048. Epub 2010 Feb 14.
A new [(18)F] labeled amino acid anti-1-amino-2-[(18)F]fluoro-cyclobutyl-1-carboxylic acid 9 (anti-2-[(18)F]FACBC) was synthesized in 30% decay-corrected yield with high radiochemical purity over 99%. The cyclic sulfamidate precursor was very stable and highly reactive towards nucleophilic radiofluorination. Cell uptake assays with rat 9L gliosarcoma cells showed that [(18)F]9 was transported into tumor cells via multiple amino acid transport systems, including L and A systems. Biodistribution study in rats with intracranial 9L gliosarcoma tumors demonstrated that [(18)F]9 had a rapid and prolonged accumulation in tumors with 26:1 tumor to brain ratio at 120 min post-injection. In this model, [(18)F]9 is a potential PET tracer for brain tumor imaging.
一种新型的 [(18)F] 标记氨基酸抗 1-氨基-2-[(18)F] 氟环丁基-1-羧酸 9(抗 2-[(18)F]FACBC)以 30%的衰减校正产率合成,放射性化学纯度超过 99%。环状磺酰胺酯前体非常稳定,对亲核放射性氟化反应具有很高的反应性。用大鼠 9L 神经胶质瘤细胞进行的细胞摄取实验表明,[(18)F]9 通过包括 L 和 A 系统在内的多种氨基酸转运系统被转运到肿瘤细胞中。颅内 9L 神经胶质瘤肿瘤大鼠的生物分布研究表明,[(18)F]9 在注射后 120 分钟时在肿瘤中具有快速和持久的积累,肿瘤与脑的比值为 26:1。在该模型中,[(18)F]9 是一种潜在的用于脑肿瘤成像的 PET 示踪剂。