Production and synthesis of a novel
Pt-labeled platinum complex and evaluation of its biodistribution in healthy mice
新規
Pt標識白金錯体の製作・合成と健康マウスにおける生体内分布の評価
面川 真里奈*; 木村 寛之*; 初川 雄一*; 河嶋 秀和*; 塚田 和明
; 屋木 祐介*; 内藤 行基*; 安井 裕之*
Omokawa, Marina*; Kimura, Hiroyuki*; Hatsukawa, Yuichi*; Kawashima, Hidekazu*; Tsukada, Kazuaki; Yagi, Yusuke*; Naito, Yuki*; Yasui, Hiroyuki*
Pt was produced via the (n,2n) reaction induced by accelerator neutrons. [
Pt]FGC-Pt was obtained through the accelerator neutron irradiation of FGC-Pt and K
PtCl
. Highly purified [
Pt]FGC-Pt was obtained using the latter method, which suggests that the synthetic method using a
Pt-labeled platinum reagent is suitable for the radioactivation of platinum complexes. We also investigated whether a significant correlation existed between the biodistribution of FGC-Pt and [
Pt]FGC-Pt in healthy mice 24 h after tail vein administration. These results suggest that
Pt-labeled compounds, synthesized using radioactive platinum reagents, can be used to confirm the biodistribution of platinum compounds. Our study on the biodistribution of [
Pt]FGC-Pt is expected to contribute to the development of novel platinum-based drugs in the future.