Plössl Karl, Chandra Rajesh, Qu Wenchao, Lieberman Brian P, Kung Mei-Ping, Zhou Rong, Huang Bin, Kung Hank F
Department of Radiology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Nucl Med Biol. 2008 Jan;35(1):83-90. doi: 10.1016/j.nucmedbio.2007.08.002. Epub 2007 Nov 19.
The development of new myocardial perfusion imaging agents for positron emission tomography (PET) may improve the resolution and quantitation of changes in regional myocardial perfusion measurement. It is known that a (68)Ge/(68)Ga generator can provide a convenient source of PET tracers because of the long physical half-life of (68)Ge (271 days). A new ligand, 7,8-dithia-16,24-diaza-trispiro[5.2.5.2.5.3]pentacosa-15,24-diene, which consists of a N(2)S(2)-chelating core incorporated into three cyclohexyl rings, was prepared. To test feasibility and potential utility, the N(2)S(2) ligand was successfully labeled and tested with (67)Ga (half-life=3.26 day; gamma=93.3, 184.6 and 300.2 keV), which showed >92% radiochemical purity. The corresponding "cold" Ga complex was synthesized, and its structure containing a pyramidal N(2)S(2) chloride core was elucidated with X-ray crystallography. In vivo biodistribution of this novel (67)Ga complex, evaluated in normal rats, exhibited excellent heart uptake and retention, with 2.1% and 0.9% initial dose/organ at 2 and 60 min, respectively, after an intravenous injection. Autoradiography was performed in normal rats and in rats that had the left anterior descending coronary artery permanently ligated surgically. Autoradiography showed an even uptake of activity in the normal heart, and there was a distinctively lower uptake in the damaged side of the surgically modified heart. In conclusion, the new N(2)S(2) ligand was readily prepared and labeled with radioactive (67)Ga. Biodistribution in rats revealed high initial heart uptake and relatively high retention reflecting regional myocardial perfusion.
用于正电子发射断层扫描(PET)的新型心肌灌注显像剂的研发,可能会提高局部心肌灌注测量变化的分辨率和定量分析能力。众所周知,由于(68)Ge的物理半衰期较长(271天),(68)Ge/(68)Ga发生器可为PET示踪剂提供便利的来源。制备了一种新的配体,即7,8-二硫杂-16,24-二氮杂-三螺[5.2.5.2.5.3]二十五碳-15,24-二烯,它由一个并入三个环己基环的N(2)S(2)螯合核心组成。为测试其可行性和潜在用途,该N(2)S(2)配体成功地用(67)Ga进行了标记和测试(半衰期=3.26天;γ射线能量=93.3、184.6和300.2 keV),其放射化学纯度>92%。合成了相应的“冷”Ga配合物,并用X射线晶体学阐明了其含有一个金字塔形N(2)S(2)氯核心的结构。在正常大鼠中评估的这种新型(67)Ga配合物的体内生物分布显示,静脉注射后2分钟和60分钟时,心脏摄取和保留情况良好,分别为初始剂量的2.1%和0.9%/器官。在正常大鼠和通过手术永久结扎左前降支冠状动脉的大鼠中进行了放射自显影。放射自显影显示正常心脏中放射性摄取均匀,而在手术改造心脏的受损侧摄取明显较低。总之,新的N(2)S(2)配体易于制备并用放射性(67)Ga进行标记。大鼠体内生物分布显示心脏初始摄取高且保留相对较高,反映了局部心肌灌注情况。