体内分布
化学
亲脂性
Pet成像
神经降压素
体内
放射合成
体外
分子成像
正电子发射断层摄影术
限制
临床前影像学
示踪剂
显像剂
癌症研究
核医学
放射化学
核成像
代谢稳定性
部分
药代动力学
Spect成像
放射性示踪剂
比活度
药理学
神经降压素受体
受体
作者
Jiamin Zhu,Hui Yuan,Boyu Tan,Xiufeng Liu,Kun Qian,Yuanpeng Jiang,Renda Li,Wenqing Zhang,Chunrong Qu,Zhen Cheng,Lei Jiang,Jiamin Zhu,Hui Yuan,Boyu Tan,Xiufeng Liu,Kun Qian,Yuanpeng Jiang,Renda Li,Wenqing Zhang,Chunrong Qu
标识
DOI:10.1021/acs.jmedchem.5c02195
摘要
Neurotensin receptor 1 (NTSR1) is overexpressed in various cancers, making it an attractive target for tumor imaging and therapy. However, current NTSR1-targeting peptides derived from neurotensin (NT) analogs face challenges including rapid metabolic clearance and insufficient tumor uptake, limiting their clinical translation. To address this, we developed a novel probe, [68Ga]Ga-DOTA-NT-20.3-IPBA, by conjugating the DOTA-NT-20.3 probe with an albumin-binding moiety (4-(p-iodophenyl)butyric acid [IPBA]). The resulting tracer exhibited enhanced lipophilicity and albumin-binding capacity, while maintaining reasonable in vitro stability, radiochemical yield, and purity (all >95%). In vitro and in vivo evaluations confirmed its high affinity and specificity for NTSR1. Clinical PET/CT imaging demonstrated significant tracer accumulation in lung adenocarcinoma, with a tumor-to-lung ratio of 7.89 ± 0.76 at 60 min postinjection and a favorable biodistribution profile. Collectively, [68Ga]Ga-DOTA-NT-20.3-IPBA shows high potential as a PET tracer for NTSR1-expressing tumors and DOTA-NT-20.3-IPBA may be a promising candidate for future theranostic development.
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