Grierson J R, Shields A F
Research Imaging Laboratory, University of Washington Medical Center, Seattle, Washington 98195, USA.
Nucl Med Biol. 2000 Feb;27(2):143-56. doi: 10.1016/s0969-8051(99)00104-3.
A reliable radiosynthesis of 3'-deoxy-3'-[(18)F]fluorothymidine ([(18)F]FLT) has been developed based on [(18)10 mCi (370 MBq) of radiochemically pure [(18)1 Ci/micromol (37 GBq/micromol) at EOS within 100 min and in 13% radiochemical yield (end of bombardment (EOB); 7% end of synthesis (EOS)). [(18)F]FLT has been designed as a new positron emission tomography imaging agent for visualizing cellular proliferation in vivo based on the metabolism of thymidine.
基于[(18)F]氟代胸苷([(18)F]FLT)的可靠放射性合成方法已被开发出来。在100分钟内,以1居里/微摩尔(37吉贝可/微摩尔)的比活度,在轰击结束时(EOB)获得了10毫居里(370兆贝可)的放射化学纯[(18)F]FLT,在合成结束时(EOS)产率为13%(EOB时为7%)。[(18)F]FLT被设计为一种新的正电子发射断层显像剂,用于基于胸苷代谢在体内可视化细胞增殖。