Université Bordeaux Segalen, CNRS, UMR 5084, 146 rue Leo Saignat, 33076 Bordeaux, France.
Pharmaceutics. 2011 Mar 9;3(1):88-106. doi: 10.3390/pharmaceutics3010088.
PET (Positron Emission Tomography) allows imaging of the in vivo distribution of biochemical compounds labeled with a radioactive tracer, mainly 18F-FDG (2-deoxy-2-[18F] fluoro-D-glucose). 18F only allows a relatively poor spatial resolution (2-3 mm) which does not allow imaging of small tumors or specific small size tissues, e.g. vasculature. Unfortunately, angiogenesis is a key process in various physiologic and pathologic processes and is, for instance, involved in modern anticancer approaches. Thus ability to visualize angiogenesis could allow early diagnosis and help to monitor the response of cancer to specific chemotherapies. Therefore, indirect analytical techniques are required to assess the localization of fluorinated compounds at a micrometric scale. Multimodality imaging approaches could provide accurate information on the metabolic activity of the target tissue. In this article, PIGE method (Particle Induced Gamma-ray Emission) was used to determine fluorinated tracers by the nuclear reaction of 19F(p,p'γ)19F in tissues. The feasibility of this approach was assessed on polyfluorinated model glucose compounds and novel peptide-based tracer designed for angiogenesis imaging. Our results describe the first mapping of the biodistribution of fluorinated compounds in both vascularized normal tissue and tumor tissue.
正电子发射断层扫描(PET)允许使用放射性示踪剂标记的生化化合物的体内分布成像,主要是 18F-FDG(2-脱氧-2-[18F]氟代-D-葡萄糖)。18F 仅允许相对较差的空间分辨率(2-3 毫米),无法对小肿瘤或特定小尺寸组织(例如血管)进行成像。不幸的是,血管生成是各种生理和病理过程中的关键过程,例如,涉及现代抗癌方法。因此,能够可视化血管生成可以允许早期诊断并有助于监测癌症对特定化疗的反应。因此,需要间接分析技术来评估氟化物化合物在微米级别的定位。多模态成像方法可以提供有关目标组织代谢活性的准确信息。在本文中,使用粒子感生伽马射线发射(PIGE)方法通过组织中的 19F(p,p'γ)19F 核反应来确定氟化示踪剂。在多氟化模型葡萄糖化合物和用于血管生成成像的新型基于肽的示踪剂上评估了这种方法的可行性。我们的结果描述了氟代化合物在血管化正常组织和肿瘤组织中的生物分布的首次映射。