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作 者:楚进锋[1] 孔德靖[2] 李彬[2] 王学斌[2] 陆洁[2] 王金城[3] 米宏志[3] 赵建冬[3]
机构地区:[1]北京化工大学理学院,北京100029 [2]北京师范大学化学系,北京100875 [3]北京安贞医院核医学科,北京100029
出 处:《高等学校化学学报》2006年第6期1016-1019,共4页Chemical Journal of Chinese Universities
摘 要:通过配体交换反应制备了[99mTcN(PNP5)(DEDC)]+和[99mTcN(PNP5)(DPODC)]+两种新配合物,其放化纯度均大于90%.生物性能研究结果表明:两种配合物在小鼠心肌中的初始摄取高,肝、肺等非靶组织清除快,靶/非靶比高,有利于早期心肌显像.其中,[99mTcN(PNP5)(DEDC)]+在小鼠中的性质较优,且其在狗体内的性质接近99mTc-tetrofosm in,有望成为一种新型心肌灌注显像剂.To develop a new potential myocardial imaging agent, [^99mTcN(PNP5)(DEDC)] ^+ and [ ^99mTcN( PNP5 ) (DPODC) ] ^+ were prepared through ligand exchange reaction. Their radiochemical purities were over 90%. The results of biodistribution in mice indicate that they possessed a high myocardial uptake, rapid clearance from non-target tissues and good ratios of target to non-target. And [^99mTcN(PNP5). (DEDC) ]^+ is superior. SPECT imaging in dog shows that its properties were similar to those of ^99m Tctetrofosmin. Based on its promising characters, it may be suitable for myocardial perfusion imaging.
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