Synthesis and biodistribution of 1-[2(-cyclopentadienyltricarbonyltechnetium-99m)-2-oxo-ethoxyphenyl]-1,2-di- (p-hydroxyphenyl)but-1-ene for tumor imaging

被引:5
|
作者
Dallagi, Tesnim [1 ]
Saidi, Mouldi [1 ]
Jaouen, Gerard [2 ,3 ]
Top, Siden [3 ]
机构
[1] Ctr Natl Sci & Technol Nucl, Lab Biotechnol & Technol Nucl, Technopole Sidi Thabet, Sidi Thabet 2020, Tunisia
[2] Chim ParisTech, PSL, 11 Rue Pierre & Marie Curie, F-75005 Paris, France
[3] UPMC Univ Paris 6, Sorbonne Univ, CNRS, IPCM,UMR 8232, Pl Jussieu, F-75005 Paris, France
关键词
Estrogen receptor; Tc-99m radiolabelling; SPECT; Tumor imaging; Biodistribution; Tumor; BREAST-CANCER; BIOLOGICAL EVALUATION; AROMATASE INHIBITORS; TC-99M; DERIVATIVES; FERROCENYL; COMPLEXES; PROBE;
D O I
10.1016/j.jorganchem.2019.04.006
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The high incidence and mortality of breast cancer and other estrogen receptor related tumors motivates efforts to develop innovative imaging probes to effectively diagnose, evaluate the extent of the tumor, and predict the efficacy of treatments while concurrently and selectively delivering anticancer agents to the cancer tissues. In the present study, 1-[2-(cyclopentadienyltricarbonyltechnetium-99m)-2-oxoethoxy-phenyl]-1,2-di-(p-hydroxyphenyl) but-1-ene was prepared and investigated as a potential agent for imaging estrogen receptors (ERs) in associated tumors. The compound was obtained in high radiochemical purity and radiochemical yields. The biodistribution of the radioactive compound in mature female rats showed an ER-mediation in the ovarian target tissues as the uptake was reduced by a blocking dose of estradiol. The nonspecific uptake in muscle was relatively low. (C) 2019 Published by Elsevier B.V.
引用
收藏
页码:1 / 6
页数:6
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