186305-06-6Relevant academic research and scientific papers
Synthesis and preliminary evaluation of a 99mTc-labeled folate-PAMAM dendrimer for FR imaging
Song, Manli,Guo, Zhide,Gao, Mengna,Shi, Changrong,Xu, Duo,You, Linyi,Wu, Xiaowei,Su, Xinhui,Zhuang, Rongqiang,Pan, Weimin,Liu, Ting,Zhang, Xianzhong
, p. 755 - 761 (2017)
Folate receptor is an ideal target for tumor-specific diagnostic and therapeutic. The aim of this study was to synthesize 99mTc-labeled folate-polyamidoamine dendrimer modified with 2-hydrazinonicotinic acid (99mTc-HP3FA)
Synthesis and evaluation of 99mTc-labeled dimeric folic acid for FR-targeting
Guo, Zhide,Gao, Mengna,Song, Manli,Shi, Changrong,Zhang, Pu,Xu, Duo,You, Linyi,Zhuang, Rongqiang,Su, Xinhui,Liu, Ting,Du, Jin,Zhang, Xianzhong
, (2016)
The folate receptor (FR) is overexpressed in a wide variety of human tumors. In our study, the multimeric concept was used to synthesize a dimeric folate derivative via a click reaction. The novel folate derivative (HYNIC-D1-FA2) was radiolabeled with 99mTc using tricine and trisodium triphenylphosphine-3,3′,3″-trisulfonate (TPPTS) as coligands (99mTc-HYNIC-D1-FA2) and its in vitro physicochemical properties, ex vivo biodistribution and in vivo micro-SPECT/CT imaging as a potential FR targeted agent were evaluated. It is a hydrophilic compound (log P = -2.52 ± 0.13) with high binding affinity (IC50 = 19.06 nM). Biodistribution in KB tumor-bearing mice showed that 99mTc-HYNIC-D1-FA2 had high uptake in FR overexpressed tumor and kidney at all time-points, and both of them could obviously be inhibited when blocking with free FA in the blocking studies. From the in vivo micro-SPECT/CT imaging results, good tumor uptake of 99mTc-HYNIC-D1-FA2 was observed in KB tumor-bearing mice and it could be blocked obviously. Based on the results, this new radiolabeled dimeric FA tracer might be a promising candidate for FR-targeting imaging with high affinity and selectivity.
